Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs13428

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr13:24435303 (GRCh38.p13) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
C>A / C>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.391273 (103566/264690, TOPMED)
G=0.33608 (14348/42692, ALFA)
G=0.29385 (4925/16760, 8.3KJPN) (+ 15 more)
G=0.40597 (5280/13006, GO-ESP)
G=0.3852 (1929/5008, 1000G)
G=0.3578 (1379/3854, ALSPAC)
G=0.3719 (1379/3708, TWINSUK)
G=0.2935 (860/2930, KOREAN)
G=0.2915 (534/1832, Korea1K)
G=0.380 (379/998, GoNL)
C=0.493 (301/610, Vietnamese)
G=0.390 (234/600, NorthernSweden)
G=0.345 (184/534, MGP)
C=0.355 (118/332, SGDP_PRJ)
G=0.445 (145/326, HapMap)
G=0.401 (122/304, FINRISK)
G=0.356 (77/216, Qatari)
C=0.32 (7/22, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
PARP4 : Missense Variant
Publications
1 citation
Genomic View
See rs on genome
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p13 chr 13 NC_000013.11:g.24435303C>A
GRCh38.p13 chr 13 NC_000013.11:g.24435303C>G
GRCh37.p13 chr 13 NC_000013.10:g.25009441C>A
GRCh37.p13 chr 13 NC_000013.10:g.25009441C>G
Gene: PARP4, poly(ADP-ribose) polymerase family member 4 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
PARP4 transcript NM_006437.4:c.3838G>T G [GGT] > C [TGT] Coding Sequence Variant
protein mono-ADP-ribosyltransferase PARP4 NP_006428.2:p.Gly1280Cys G (Gly) > C (Cys) Missense Variant
PARP4 transcript NM_006437.4:c.3838G>C G [GGT] > R [CGT] Coding Sequence Variant
protein mono-ADP-ribosyltransferase PARP4 NP_006428.2:p.Gly1280Arg G (Gly) > R (Arg) Missense Variant
PARP4 transcript variant X1 XM_011534931.1:c.3979G>T G [GGT] > C [TGT] Coding Sequence Variant
protein mono-ADP-ribosyltransferase PARP4 isoform X1 XP_011533233.1:p.Gly1327C…

XP_011533233.1:p.Gly1327Cys

G (Gly) > C (Cys) Missense Variant
PARP4 transcript variant X1 XM_011534931.1:c.3979G>C G [GGT] > R [CGT] Coding Sequence Variant
protein mono-ADP-ribosyltransferase PARP4 isoform X1 XP_011533233.1:p.Gly1327A…

XP_011533233.1:p.Gly1327Arg

G (Gly) > R (Arg) Missense Variant
PARP4 transcript variant X2 XM_011534932.2:c.3838G>T G [GGT] > C [TGT] Coding Sequence Variant
protein mono-ADP-ribosyltransferase PARP4 isoform X2 XP_011533234.1:p.Gly1280C…

XP_011533234.1:p.Gly1280Cys

G (Gly) > C (Cys) Missense Variant
PARP4 transcript variant X2 XM_011534932.2:c.3838G>C G [GGT] > R [CGT] Coding Sequence Variant
protein mono-ADP-ribosyltransferase PARP4 isoform X2 XP_011533234.1:p.Gly1280A…

XP_011533234.1:p.Gly1280Arg

G (Gly) > R (Arg) Missense Variant
PARP4 transcript variant X3 XR_941496.1:n.3994G>T N/A Non Coding Transcript Variant
PARP4 transcript variant X3 XR_941496.1:n.3994G>C N/A Non Coding Transcript Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 42692 C=0.66392 A=0.00000, G=0.33608
European Sub 33146 C=0.66062 A=0.00000, G=0.33938
African Sub 1890 C=0.7090 A=0.0000, G=0.2910
African Others Sub 60 C=0.63 A=0.00, G=0.37
African American Sub 1830 C=0.7115 A=0.0000, G=0.2885
Asian Sub 96 C=0.80 A=0.00, G=0.20
East Asian Sub 54 C=0.81 A=0.00, G=0.19
Other Asian Sub 42 C=0.79 A=0.00, G=0.21
Latin American 1 Sub 414 C=0.671 A=0.000, G=0.329
Latin American 2 Sub 306 C=0.990 A=0.000, G=0.010
South Asian Sub 52 C=0.96 A=0.00, G=0.04
Other Sub 6788 C=0.6481 A=0.0000, G=0.3519


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 C=0.608727 G=0.391273
8.3KJPN JAPANESE Study-wide 16760 C=0.70615 G=0.29385
GO Exome Sequencing Project Global Study-wide 13006 C=0.59403 G=0.40597
GO Exome Sequencing Project European American Sub 8600 C=0.6274 G=0.3726
GO Exome Sequencing Project African American Sub 4406 C=0.5288 G=0.4712
1000Genomes Global Study-wide 5008 C=0.6148 G=0.3852
1000Genomes African Sub 1322 C=0.5151 G=0.4849
1000Genomes East Asian Sub 1008 C=0.6399 G=0.3601
1000Genomes Europe Sub 1006 C=0.5875 G=0.4125
1000Genomes South Asian Sub 978 C=0.725 G=0.275
1000Genomes American Sub 694 C=0.653 G=0.347
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.6422 G=0.3578
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.6281 G=0.3719
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.7065 G=0.2935
Korean Genome Project KOREAN Study-wide 1832 C=0.7085 G=0.2915
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.620 G=0.380
A Vietnamese Genetic Variation Database Global Study-wide 610 C=0.493 G=0.507
Northern Sweden ACPOP Study-wide 600 C=0.610 G=0.390
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 C=0.655 G=0.345
SGDP_PRJ Global Study-wide 332 C=0.355 G=0.645
HapMap Global Study-wide 326 C=0.555 G=0.445
HapMap American Sub 120 C=0.542 G=0.458
HapMap African Sub 118 C=0.483 G=0.517
HapMap Asian Sub 88 C=0.67 G=0.33
FINRISK Finnish from FINRISK project Study-wide 304 C=0.599 G=0.401
Qatari Global Study-wide 216 C=0.644 G=0.356
Siberian Global Study-wide 22 C=0.32 G=0.68
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement C= A G
GRCh38.p13 chr 13 NC_000013.11:g.24435303= NC_000013.11:g.24435303C>A NC_000013.11:g.24435303C>G
GRCh37.p13 chr 13 NC_000013.10:g.25009441= NC_000013.10:g.25009441C>A NC_000013.10:g.25009441C>G
PARP4 transcript NM_006437.4:c.3838= NM_006437.4:c.3838G>T NM_006437.4:c.3838G>C
PARP4 transcript NM_006437.3:c.3838= NM_006437.3:c.3838G>T NM_006437.3:c.3838G>C
PARP4 transcript variant X2 XM_011534932.2:c.3838= XM_011534932.2:c.3838G>T XM_011534932.2:c.3838G>C
PARP4 transcript variant X3 XR_941496.1:n.3994= XR_941496.1:n.3994G>T XR_941496.1:n.3994G>C
PARP4 transcript variant X1 XM_011534931.1:c.3979= XM_011534931.1:c.3979G>T XM_011534931.1:c.3979G>C
protein mono-ADP-ribosyltransferase PARP4 NP_006428.2:p.Gly1280= NP_006428.2:p.Gly1280Cys NP_006428.2:p.Gly1280Arg
protein mono-ADP-ribosyltransferase PARP4 isoform X2 XP_011533234.1:p.Gly1280= XP_011533234.1:p.Gly1280Cys XP_011533234.1:p.Gly1280Arg
protein mono-ADP-ribosyltransferase PARP4 isoform X1 XP_011533233.1:p.Gly1327= XP_011533233.1:p.Gly1327Cys XP_011533233.1:p.Gly1327Arg
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

90 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 CGAP-GAI ss15756 Sep 19, 2000 (52)
2 LEE ss1524438 Oct 04, 2000 (86)
3 LEE ss4415329 May 29, 2002 (106)
4 YUSUKE ss4928180 Aug 28, 2002 (111)
5 SNP500CANCER ss5586208 Mar 31, 2003 (113)
6 WI_SSAHASNP ss12262357 Jul 11, 2003 (116)
7 CGAP-GAI ss16262968 Feb 28, 2004 (123)
8 CSHL-HAPMAP ss17484433 Feb 27, 2004 (120)
9 ABI ss40317290 Mar 15, 2006 (126)
10 AFFY ss74810630 Aug 16, 2007 (128)
11 ILLUMINA ss74909590 Dec 07, 2007 (129)
12 SI_EXO ss76889983 Dec 07, 2007 (129)
13 CORNELL ss86272100 Mar 23, 2008 (129)
14 BCMHGSC_JDW ss89535417 Mar 24, 2008 (129)
15 1000GENOMES ss114417933 Jan 25, 2009 (130)
16 ILLUMINA-UK ss118388958 Feb 14, 2009 (130)
17 KRIBB_YJKIM ss119339310 Dec 01, 2009 (131)
18 ENSEMBL ss133485243 Dec 01, 2009 (131)
19 GMI ss154535303 Dec 01, 2009 (131)
20 SEATTLESEQ ss159727866 Dec 01, 2009 (131)
21 ILLUMINA ss160337914 Dec 01, 2009 (131)
22 ENSEMBL ss161582246 Dec 01, 2009 (131)
23 COMPLETE_GENOMICS ss167713950 Jul 04, 2010 (132)
24 COMPLETE_GENOMICS ss168970408 Jul 04, 2010 (132)
25 COMPLETE_GENOMICS ss170881933 Jul 04, 2010 (132)
26 BUSHMAN ss198972773 Jul 04, 2010 (132)
27 1000GENOMES ss226080191 Jul 14, 2010 (132)
28 1000GENOMES ss236176502 Jul 15, 2010 (132)
29 1000GENOMES ss242687259 Jul 15, 2010 (132)
30 GMI ss281639165 May 04, 2012 (137)
31 GMI ss286668263 Apr 25, 2013 (138)
32 PJP ss291557327 May 09, 2011 (134)
33 NHLBI-ESP ss342373174 May 09, 2011 (134)
34 ILLUMINA ss480570034 Sep 08, 2015 (146)
35 1000GENOMES ss491056902 May 04, 2012 (137)
36 EXOME_CHIP ss491477103 May 04, 2012 (137)
37 CLINSEQ_SNP ss491677204 May 04, 2012 (137)
38 TISHKOFF ss563550111 Apr 25, 2013 (138)
39 SSMP ss659144060 Apr 25, 2013 (138)
40 JMKIDD_LAB ss974486219 Aug 21, 2014 (142)
41 EVA-GONL ss990192725 Aug 21, 2014 (142)
42 JMKIDD_LAB ss1067540182 Aug 21, 2014 (142)
43 JMKIDD_LAB ss1078937672 Aug 21, 2014 (142)
44 1000GENOMES ss1347494795 Aug 21, 2014 (142)
45 DDI ss1427128213 Apr 01, 2015 (144)
46 EVA_FINRISK ss1584086112 Apr 01, 2015 (144)
47 EVA_UK10K_ALSPAC ss1629889896 Apr 01, 2015 (144)
48 EVA_DECODE ss1642298209 Apr 01, 2015 (144)
49 EVA_UK10K_TWINSUK ss1672883929 Apr 01, 2015 (144)
50 EVA_EXAC ss1691227164 Apr 01, 2015 (144)
51 EVA_EXAC ss1691227165 Apr 01, 2015 (144)
52 EVA_MGP ss1711352322 Apr 01, 2015 (144)
53 HAMMER_LAB ss1807525806 Sep 08, 2015 (146)
54 WEILL_CORNELL_DGM ss1933561057 Feb 12, 2016 (147)
55 GENOMED ss1967734435 Jul 19, 2016 (147)
56 JJLAB ss2027534941 Sep 14, 2016 (149)
57 USC_VALOUEV ss2155898750 Dec 20, 2016 (150)
58 TOPMED ss2358949557 Dec 20, 2016 (150)
59 ILLUMINA ss2635043315 Nov 08, 2017 (151)
60 GRF ss2700270213 Nov 08, 2017 (151)
61 GNOMAD ss2740317045 Nov 08, 2017 (151)
62 GNOMAD ss2749018534 Nov 08, 2017 (151)
63 GNOMAD ss2917598473 Nov 08, 2017 (151)
64 AFFY ss2984998911 Nov 08, 2017 (151)
65 SWEGEN ss3010720973 Nov 08, 2017 (151)
66 EVA_SAMSUNG_MC ss3023068182 Nov 08, 2017 (151)
67 BIOINF_KMB_FNS_UNIBA ss3027582198 Nov 08, 2017 (151)
68 TOPMED ss3187995624 Nov 08, 2017 (151)
69 CSHL ss3350364906 Nov 08, 2017 (151)
70 ILLUMINA ss3636222148 Oct 12, 2018 (152)
71 ILLUMINA ss3642990944 Oct 12, 2018 (152)
72 OMUKHERJEE_ADBS ss3646451543 Oct 12, 2018 (152)
73 ILLUMINA ss3653769263 Oct 12, 2018 (152)
74 EVA_DECODE ss3694925556 Jul 13, 2019 (153)
75 ACPOP ss3739582243 Jul 13, 2019 (153)
76 EVA ss3751235735 Jul 13, 2019 (153)
77 KHV_HUMAN_GENOMES ss3816566690 Jul 13, 2019 (153)
78 EVA ss3824796543 Apr 27, 2020 (154)
79 EVA ss3825529011 Apr 27, 2020 (154)
80 EVA ss3825544167 Apr 27, 2020 (154)
81 EVA ss3833448121 Apr 27, 2020 (154)
82 SGDP_PRJ ss3879593052 Apr 27, 2020 (154)
83 KRGDB ss3928409970 Apr 27, 2020 (154)
84 KOGIC ss3973207237 Apr 27, 2020 (154)
85 FSA-LAB ss3984043665 Apr 26, 2021 (155)
86 EVA ss3986062088 Apr 26, 2021 (155)
87 EVA ss3986596586 Apr 26, 2021 (155)
88 TOPMED ss4939948406 Apr 26, 2021 (155)
89 TOMMO_GENOMICS ss5209177018 Apr 26, 2021 (155)
90 EVA ss5236911761 Apr 26, 2021 (155)
91 1000Genomes NC_000013.10 - 25009441 Oct 12, 2018 (152)
92 The Avon Longitudinal Study of Parents and Children NC_000013.10 - 25009441 Oct 12, 2018 (152)
93 ExAC

Submission ignored due to conflicting rows:
Row 1550752 (NC_000013.10:25009440:C:C 76640/121380, NC_000013.10:25009440:C:G 44740/121380)
Row 1550753 (NC_000013.10:25009440:C:C 121378/121380, NC_000013.10:25009440:C:A 2/121380)

- Oct 12, 2018 (152)
94 ExAC

Submission ignored due to conflicting rows:
Row 1550752 (NC_000013.10:25009440:C:C 76640/121380, NC_000013.10:25009440:C:G 44740/121380)
Row 1550753 (NC_000013.10:25009440:C:C 121378/121380, NC_000013.10:25009440:C:A 2/121380)

- Oct 12, 2018 (152)
95 FINRISK NC_000013.10 - 25009441 Apr 27, 2020 (154)
96 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 425509932 (NC_000013.11:24435302:C:A 2/140080)
Row 425509933 (NC_000013.11:24435302:C:G 56213/140030)

- Apr 26, 2021 (155)
97 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 425509932 (NC_000013.11:24435302:C:A 2/140080)
Row 425509933 (NC_000013.11:24435302:C:G 56213/140030)

- Apr 26, 2021 (155)
98 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 9558485 (NC_000013.10:25009440:C:C 251184/251192, NC_000013.10:25009440:C:A 8/251192)
Row 9558486 (NC_000013.10:25009440:C:C 159166/251192, NC_000013.10:25009440:C:G 92026/251192)

- Jul 13, 2019 (153)
99 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 9558485 (NC_000013.10:25009440:C:C 251184/251192, NC_000013.10:25009440:C:A 8/251192)
Row 9558486 (NC_000013.10:25009440:C:C 159166/251192, NC_000013.10:25009440:C:G 92026/251192)

- Jul 13, 2019 (153)
100 GO Exome Sequencing Project NC_000013.10 - 25009441 Oct 12, 2018 (152)
101 Genome of the Netherlands Release 5 NC_000013.10 - 25009441 Apr 27, 2020 (154)
102 HapMap NC_000013.11 - 24435303 Apr 27, 2020 (154)
103 KOREAN population from KRGDB NC_000013.10 - 25009441 Apr 27, 2020 (154)
104 Korean Genome Project NC_000013.11 - 24435303 Apr 27, 2020 (154)
105 Medical Genome Project healthy controls from Spanish population NC_000013.10 - 25009441 Apr 27, 2020 (154)
106 Northern Sweden NC_000013.10 - 25009441 Jul 13, 2019 (153)
107 Qatari NC_000013.10 - 25009441 Apr 27, 2020 (154)
108 SGDP_PRJ NC_000013.10 - 25009441 Apr 27, 2020 (154)
109 Siberian NC_000013.10 - 25009441 Apr 27, 2020 (154)
110 8.3KJPN NC_000013.10 - 25009441 Apr 26, 2021 (155)
111 TopMed NC_000013.11 - 24435303 Apr 26, 2021 (155)
112 UK 10K study - Twins NC_000013.10 - 25009441 Oct 12, 2018 (152)
113 A Vietnamese Genetic Variation Database NC_000013.10 - 25009441 Jul 13, 2019 (153)
114 ALFA NC_000013.11 - 24435303 Apr 26, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs3190395 Jul 03, 2002 (106)
rs3742174 Feb 20, 2003 (111)
rs11557034 Oct 08, 2004 (123)
rs52831662 Sep 21, 2007 (128)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss491677204 NC_000013.9:23907440:C:A NC_000013.11:24435302:C:A (self)
ss1691227165, ss2740317045 NC_000013.10:25009440:C:A NC_000013.11:24435302:C:A (self)
3107386213 NC_000013.11:24435302:C:A NC_000013.11:24435302:C:A
ss89535417, ss114417933, ss118388958, ss160337914, ss167713950, ss168970408, ss170881933, ss198972773, ss281639165, ss286668263, ss291557327, ss1642298209, ss2635043315, ss3642990944 NC_000013.9:23907440:C:G NC_000013.11:24435302:C:G (self)
60338183, 33509278, 82573, 1253936, 14950279, 35587364, 468082, 12867108, 15602987, 31610032, 8415104, 67146325, 33509278, 7433048, ss226080191, ss236176502, ss242687259, ss342373174, ss480570034, ss491056902, ss491477103, ss563550111, ss659144060, ss974486219, ss990192725, ss1067540182, ss1078937672, ss1347494795, ss1427128213, ss1584086112, ss1629889896, ss1672883929, ss1691227164, ss1711352322, ss1807525806, ss1933561057, ss1967734435, ss2027534941, ss2155898750, ss2358949557, ss2700270213, ss2740317045, ss2749018534, ss2917598473, ss2984998911, ss3010720973, ss3023068182, ss3350364906, ss3636222148, ss3646451543, ss3653769263, ss3739582243, ss3751235735, ss3824796543, ss3825529011, ss3825544167, ss3833448121, ss3879593052, ss3928409970, ss3984043665, ss3986062088, ss3986596586, ss5209177018 NC_000013.10:25009440:C:G NC_000013.11:24435302:C:G (self)
948093, 29585238, 97231694, 155494064, 3107386213, ss3027582198, ss3187995624, ss3694925556, ss3816566690, ss3973207237, ss4939948406, ss5236911761 NC_000013.11:24435302:C:G NC_000013.11:24435302:C:G (self)
ss12262357 NT_009799.12:5989440:C:G NC_000013.11:24435302:C:G (self)
ss17484433, ss76889983 NT_024524.13:5989440:C:G NC_000013.11:24435302:C:G (self)
ss15756, ss1524438, ss4415329, ss4928180, ss5586208, ss16262968, ss40317290, ss74810630, ss74909590, ss86272100, ss119339310, ss133485243, ss154535303, ss159727866, ss161582246 NT_024524.14:5989440:C:G NC_000013.11:24435302:C:G (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs13428
PMID Title Author Year Journal
26263974 Molecular Classification and Pharmacogenetics of Primary Plasma Cell Leukemia: An Initial Approach toward Precision Medicine. Simeon V et al. 2015 International journal of molecular sciences
Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post596+ae089ad