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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.

rs10875238

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:99594044 (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
T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.497197 (131603/264690, TOPMED)
T=0.433134 (67309/155400, ALFA)
T=0.481588 (67353/139856, GnomAD) (+ 18 more)
C=0.31342 (5253/16760, 8.3KJPN)
C=0.4123 (2065/5008, 1000G)
T=0.3859 (1729/4480, Estonian)
T=0.3949 (1522/3854, ALSPAC)
T=0.3897 (1445/3708, TWINSUK)
C=0.2867 (840/2930, KOREAN)
C=0.4115 (856/2080, HGDP_Stanford)
C=0.3809 (713/1872, HapMap)
C=0.2953 (541/1832, Korea1K)
C=0.4390 (497/1132, Daghestan)
T=0.405 (404/998, GoNL)
T=0.393 (236/600, NorthernSweden)
T=0.340 (113/332, SGDP_PRJ)
C=0.431 (93/216, Qatari)
C=0.255 (55/216, Vietnamese)
T=0.36 (26/72, Ancient Sardinia)
T=0.38 (16/42, Siberian)
T=0.40 (16/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
Publications
0 citations
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 1 NC_000001.11:g.99594044T>C
GRCh37.p13 chr 1 NC_000001.10:g.100059600T>C
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 155400 T=0.433134 C=0.566866
European Sub 131878 T=0.408620 C=0.591380
African Sub 8332 T=0.6488 C=0.3512
African Others Sub 290 T=0.710 C=0.290
African American Sub 8042 T=0.6466 C=0.3534
Asian Sub 410 T=0.663 C=0.337
East Asian Sub 272 T=0.691 C=0.309
Other Asian Sub 138 T=0.609 C=0.391
Latin American 1 Sub 538 T=0.454 C=0.546
Latin American 2 Sub 4646 T=0.4718 C=0.5282
South Asian Sub 4992 T=0.6186 C=0.3814
Other Sub 4604 T=0.4820 C=0.5180


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 T=0.497197 C=0.502803
Allele Frequency Aggregator Total Global 155400 T=0.433134 C=0.566866
Allele Frequency Aggregator European Sub 131878 T=0.408620 C=0.591380
Allele Frequency Aggregator African Sub 8332 T=0.6488 C=0.3512
Allele Frequency Aggregator South Asian Sub 4992 T=0.6186 C=0.3814
Allele Frequency Aggregator Latin American 2 Sub 4646 T=0.4718 C=0.5282
Allele Frequency Aggregator Other Sub 4604 T=0.4820 C=0.5180
Allele Frequency Aggregator Latin American 1 Sub 538 T=0.454 C=0.546
Allele Frequency Aggregator Asian Sub 410 T=0.663 C=0.337
gnomAD - Genomes Global Study-wide 139856 T=0.481588 C=0.518412
gnomAD - Genomes European Sub 75788 T=0.38234 C=0.61766
gnomAD - Genomes African Sub 41862 T=0.64791 C=0.35209
gnomAD - Genomes American Sub 13616 T=0.47922 C=0.52078
gnomAD - Genomes Ashkenazi Jewish Sub 3322 T=0.4561 C=0.5439
gnomAD - Genomes East Asian Sub 3120 T=0.7115 C=0.2885
gnomAD - Genomes Other Sub 2148 T=0.4623 C=0.5377
8.3KJPN JAPANESE Study-wide 16760 T=0.68658 C=0.31342
1000Genomes Global Study-wide 5008 T=0.5877 C=0.4123
1000Genomes African Sub 1322 T=0.6717 C=0.3283
1000Genomes East Asian Sub 1008 T=0.6905 C=0.3095
1000Genomes Europe Sub 1006 T=0.4085 C=0.5915
1000Genomes South Asian Sub 978 T=0.641 C=0.359
1000Genomes American Sub 694 T=0.463 C=0.537
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.3859 C=0.6141
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.3949 C=0.6051
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.3897 C=0.6103
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.7133 C=0.2867
HGDP-CEPH-db Supplement 1 Global Study-wide 2080 T=0.5885 C=0.4115
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.713 C=0.287
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.601 C=0.399
HGDP-CEPH-db Supplement 1 Middle_Est Sub 348 T=0.506 C=0.494
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.434 C=0.566
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.740 C=0.260
HGDP-CEPH-db Supplement 1 America Sub 214 T=0.477 C=0.523
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.61 C=0.39
HapMap Global Study-wide 1872 T=0.6191 C=0.3809
HapMap American Sub 760 T=0.558 C=0.442
HapMap African Sub 686 T=0.697 C=0.303
HapMap Asian Sub 254 T=0.689 C=0.311
HapMap Europe Sub 172 T=0.477 C=0.523
Korean Genome Project KOREAN Study-wide 1832 T=0.7047 C=0.2953
Genome-wide autozygosity in Daghestan Global Study-wide 1132 T=0.5610 C=0.4390
Genome-wide autozygosity in Daghestan Daghestan Sub 626 T=0.593 C=0.407
Genome-wide autozygosity in Daghestan Near_East Sub 144 T=0.514 C=0.486
Genome-wide autozygosity in Daghestan Central Asia Sub 122 T=0.516 C=0.484
Genome-wide autozygosity in Daghestan Europe Sub 106 T=0.396 C=0.604
Genome-wide autozygosity in Daghestan South Asian Sub 98 T=0.66 C=0.34
Genome-wide autozygosity in Daghestan Caucasus Sub 36 T=0.56 C=0.44
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.405 C=0.595
Northern Sweden ACPOP Study-wide 600 T=0.393 C=0.607
SGDP_PRJ Global Study-wide 332 T=0.340 C=0.660
Qatari Global Study-wide 216 T=0.569 C=0.431
A Vietnamese Genetic Variation Database Global Study-wide 216 T=0.745 C=0.255
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 72 T=0.36 C=0.64
Siberian Global Study-wide 42 T=0.38 C=0.62
The Danish reference pan genome Danish Study-wide 40 T=0.40 C=0.60
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 T= C
GRCh38.p13 chr 1 NC_000001.11:g.99594044= NC_000001.11:g.99594044T>C
GRCh37.p13 chr 1 NC_000001.10:g.100059600= NC_000001.10:g.100059600T>C
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#.

117 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss16462177 Feb 27, 2004 (120)
2 SC_SNP ss18123335 Feb 27, 2004 (120)
3 SC_SNP ss18298289 Feb 27, 2004 (120)
4 SSAHASNP ss20609559 Apr 05, 2004 (121)
5 PERLEGEN ss24244094 Sep 20, 2004 (123)
6 ABI ss41073276 Mar 14, 2006 (126)
7 AFFY ss66277954 Nov 29, 2006 (127)
8 ILLUMINA ss66794543 Nov 29, 2006 (127)
9 ILLUMINA ss66906891 Nov 29, 2006 (127)
10 ILLUMINA ss67033293 Nov 29, 2006 (127)
11 ILLUMINA ss70383116 May 16, 2007 (127)
12 ILLUMINA ss70504412 May 26, 2008 (130)
13 ILLUMINA ss71030794 May 16, 2007 (127)
14 ILLUMINA ss75832136 Dec 07, 2007 (129)
15 AFFY ss75931822 Dec 07, 2007 (129)
16 HGSV ss78659228 Dec 07, 2007 (129)
17 HGSV ss80518577 Dec 15, 2007 (130)
18 KRIBB_YJKIM ss85021004 Dec 15, 2007 (130)
19 BCMHGSC_JDW ss87656532 Mar 23, 2008 (129)
20 HUMANGENOME_JCVI ss97961341 Feb 06, 2009 (130)
21 BGI ss102767823 Dec 01, 2009 (131)
22 1000GENOMES ss108453701 Jan 23, 2009 (130)
23 1000GENOMES ss110891062 Jan 25, 2009 (130)
24 ILLUMINA-UK ss118919217 Feb 15, 2009 (130)
25 ILLUMINA ss121408131 Dec 01, 2009 (131)
26 ENSEMBL ss138045101 Dec 01, 2009 (131)
27 ENSEMBL ss138842479 Dec 01, 2009 (131)
28 ILLUMINA ss152857799 Dec 01, 2009 (131)
29 GMI ss155415585 Dec 01, 2009 (131)
30 ILLUMINA ss159149516 Dec 01, 2009 (131)
31 COMPLETE_GENOMICS ss163739167 Jul 04, 2010 (132)
32 COMPLETE_GENOMICS ss164869148 Jul 04, 2010 (132)
33 COMPLETE_GENOMICS ss166904742 Jul 04, 2010 (132)
34 AFFY ss169297664 Jul 04, 2010 (132)
35 ILLUMINA ss169687452 Jul 04, 2010 (132)
36 ILLUMINA ss170685011 Jul 04, 2010 (132)
37 BUSHMAN ss198832780 Jul 04, 2010 (132)
38 BCM-HGSC-SUB ss205125695 Jul 04, 2010 (132)
39 1000GENOMES ss218548669 Jul 14, 2010 (132)
40 1000GENOMES ss230656753 Jul 14, 2010 (132)
41 1000GENOMES ss238323718 Jul 15, 2010 (132)
42 BL ss253315978 May 09, 2011 (134)
43 GMI ss275945329 May 04, 2012 (137)
44 PJP ss290580503 May 09, 2011 (134)
45 ILLUMINA ss479385930 May 04, 2012 (137)
46 ILLUMINA ss479389137 May 04, 2012 (137)
47 ILLUMINA ss484493114 May 04, 2012 (137)
48 ILLUMINA ss536647016 Sep 08, 2015 (146)
49 TISHKOFF ss554480702 Apr 25, 2013 (138)
50 SSMP ss648253975 Apr 25, 2013 (138)
51 ILLUMINA ss778368698 Sep 08, 2015 (146)
52 ILLUMINA ss782693061 Sep 08, 2015 (146)
53 ILLUMINA ss783661281 Sep 08, 2015 (146)
54 ILLUMINA ss825352606 Apr 01, 2015 (144)
55 ILLUMINA ss831944056 Sep 08, 2015 (146)
56 ILLUMINA ss832662136 Jul 12, 2019 (153)
57 ILLUMINA ss833823548 Sep 08, 2015 (146)
58 EVA-GONL ss975483069 Aug 21, 2014 (142)
59 JMKIDD_LAB ss1068127741 Aug 21, 2014 (142)
60 1000GENOMES ss1292107987 Aug 21, 2014 (142)
61 HAMMER_LAB ss1397255152 Sep 08, 2015 (146)
62 DDI ss1425911003 Apr 01, 2015 (144)
63 EVA_GENOME_DK ss1574271615 Apr 01, 2015 (144)
64 EVA_DECODE ss1584861374 Apr 01, 2015 (144)
65 EVA_UK10K_ALSPAC ss1600817121 Apr 01, 2015 (144)
66 EVA_UK10K_TWINSUK ss1643811154 Apr 01, 2015 (144)
67 EVA_SVP ss1712357152 Apr 01, 2015 (144)
68 ILLUMINA ss1751859117 Sep 08, 2015 (146)
69 HAMMER_LAB ss1794807725 Sep 08, 2015 (146)
70 WEILL_CORNELL_DGM ss1918682657 Feb 12, 2016 (147)
71 GENOMED ss1966820791 Jul 19, 2016 (147)
72 JJLAB ss2019862829 Sep 14, 2016 (149)
73 USC_VALOUEV ss2147881531 Dec 20, 2016 (150)
74 HUMAN_LONGEVITY ss2165031770 Dec 20, 2016 (150)
75 TOPMED ss2327382592 Dec 20, 2016 (150)
76 ILLUMINA ss2632553628 Nov 08, 2017 (151)
77 ILLUMINA ss2635001583 Nov 08, 2017 (151)
78 GRF ss2697808862 Nov 08, 2017 (151)
79 GNOMAD ss2758638626 Nov 08, 2017 (151)
80 SWEGEN ss2987305778 Nov 08, 2017 (151)
81 BIOINF_KMB_FNS_UNIBA ss3023695002 Nov 08, 2017 (151)
82 TOPMED ss3084652010 Nov 08, 2017 (151)
83 CSHL ss3343595955 Nov 08, 2017 (151)
84 ILLUMINA ss3626165296 Oct 11, 2018 (152)
85 ILLUMINA ss3630587802 Oct 11, 2018 (152)
86 ILLUMINA ss3632903286 Oct 11, 2018 (152)
87 ILLUMINA ss3633598284 Oct 11, 2018 (152)
88 ILLUMINA ss3634339259 Oct 11, 2018 (152)
89 ILLUMINA ss3635291895 Oct 11, 2018 (152)
90 ILLUMINA ss3637042351 Oct 11, 2018 (152)
91 ILLUMINA ss3637775457 Oct 11, 2018 (152)
92 ILLUMINA ss3638905836 Oct 11, 2018 (152)
93 ILLUMINA ss3639450877 Oct 11, 2018 (152)
94 ILLUMINA ss3640046619 Oct 11, 2018 (152)
95 ILLUMINA ss3642785642 Oct 11, 2018 (152)
96 URBANLAB ss3646731454 Oct 11, 2018 (152)
97 EGCUT_WGS ss3655390886 Jul 12, 2019 (153)
98 EVA_DECODE ss3687367277 Jul 12, 2019 (153)
99 ACPOP ss3727314132 Jul 12, 2019 (153)
100 ILLUMINA ss3744640228 Jul 12, 2019 (153)
101 EVA ss3746574209 Jul 12, 2019 (153)
102 ILLUMINA ss3772141465 Jul 12, 2019 (153)
103 PACBIO ss3783495906 Jul 12, 2019 (153)
104 PACBIO ss3789140940 Jul 12, 2019 (153)
105 PACBIO ss3794013784 Jul 12, 2019 (153)
106 KHV_HUMAN_GENOMES ss3799574981 Jul 12, 2019 (153)
107 EVA ss3826326608 Apr 25, 2020 (154)
108 EVA ss3836553577 Apr 25, 2020 (154)
109 EVA ss3841961574 Apr 25, 2020 (154)
110 HGDP ss3847343745 Apr 25, 2020 (154)
111 SGDP_PRJ ss3849477725 Apr 25, 2020 (154)
112 KRGDB ss3894555772 Apr 25, 2020 (154)
113 KOGIC ss3945091474 Apr 25, 2020 (154)
114 EVA ss3984814976 Apr 25, 2021 (155)
115 EVA ss4016927696 Apr 25, 2021 (155)
116 TOPMED ss4460700698 Apr 25, 2021 (155)
117 TOMMO_GENOMICS ss5145313562 Apr 25, 2021 (155)
118 1000Genomes NC_000001.10 - 100059600 Oct 11, 2018 (152)
119 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 100059600 Oct 11, 2018 (152)
120 Genome-wide autozygosity in Daghestan NC_000001.9 - 99832188 Apr 25, 2020 (154)
121 Genetic variation in the Estonian population NC_000001.10 - 100059600 Oct 11, 2018 (152)
122 The Danish reference pan genome NC_000001.10 - 100059600 Apr 25, 2020 (154)
123 gnomAD - Genomes NC_000001.11 - 99594044 Apr 25, 2021 (155)
124 Genome of the Netherlands Release 5 NC_000001.10 - 100059600 Apr 25, 2020 (154)
125 HGDP-CEPH-db Supplement 1 NC_000001.9 - 99832188 Apr 25, 2020 (154)
126 HapMap NC_000001.11 - 99594044 Apr 25, 2020 (154)
127 KOREAN population from KRGDB NC_000001.10 - 100059600 Apr 25, 2020 (154)
128 Korean Genome Project NC_000001.11 - 99594044 Apr 25, 2020 (154)
129 Northern Sweden NC_000001.10 - 100059600 Jul 12, 2019 (153)
130 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 100059600 Apr 25, 2021 (155)
131 Qatari NC_000001.10 - 100059600 Apr 25, 2020 (154)
132 SGDP_PRJ NC_000001.10 - 100059600 Apr 25, 2020 (154)
133 Siberian NC_000001.10 - 100059600 Apr 25, 2020 (154)
134 8.3KJPN NC_000001.10 - 100059600 Apr 25, 2021 (155)
135 TopMed NC_000001.11 - 99594044 Apr 25, 2021 (155)
136 UK 10K study - Twins NC_000001.10 - 100059600 Oct 11, 2018 (152)
137 A Vietnamese Genetic Variation Database NC_000001.10 - 100059600 Jul 12, 2019 (153)
138 ALFA NC_000001.11 - 99594044 Apr 25, 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)
rs17405084 Oct 07, 2004 (123)
rs60503647 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78659228, ss80518577, ss3638905836, ss3639450877 NC_000001.8:99771620:T:C NC_000001.11:99594043:T:C (self)
16454, 21637, ss66277954, ss75931822, ss87656532, ss108453701, ss110891062, ss118919217, ss163739167, ss164869148, ss166904742, ss169297664, ss198832780, ss205125695, ss253315978, ss275945329, ss290580503, ss479385930, ss825352606, ss1397255152, ss1584861374, ss1712357152, ss2635001583, ss3642785642, ss3847343745 NC_000001.9:99832187:T:C NC_000001.11:99594043:T:C (self)
2871560, 1584063, 1129134, 1628973, 687166, 1733166, 598997, 40903, 724587, 1494705, 397885, 3282869, 1584063, 341224, ss218548669, ss230656753, ss238323718, ss479389137, ss484493114, ss536647016, ss554480702, ss648253975, ss778368698, ss782693061, ss783661281, ss831944056, ss832662136, ss833823548, ss975483069, ss1068127741, ss1292107987, ss1425911003, ss1574271615, ss1600817121, ss1643811154, ss1751859117, ss1794807725, ss1918682657, ss1966820791, ss2019862829, ss2147881531, ss2327382592, ss2632553628, ss2697808862, ss2758638626, ss2987305778, ss3343595955, ss3626165296, ss3630587802, ss3632903286, ss3633598284, ss3634339259, ss3635291895, ss3637042351, ss3637775457, ss3640046619, ss3655390886, ss3727314132, ss3744640228, ss3746574209, ss3772141465, ss3783495906, ss3789140940, ss3794013784, ss3826326608, ss3836553577, ss3849477725, ss3894555772, ss3984814976, ss4016927696, ss5145313562 NC_000001.10:100059599:T:C NC_000001.11:99594043:T:C (self)
20299157, 136577, 1469475, 15309221, 24307033, 604981178, ss2165031770, ss3023695002, ss3084652010, ss3646731454, ss3687367277, ss3799574981, ss3841961574, ss3945091474, ss4460700698 NC_000001.11:99594043:T:C NC_000001.11:99594043:T:C (self)
ss16462177, ss18123335, ss18298289, ss20609559 NT_028050.13:8248543:T:C NC_000001.11:99594043:T:C (self)
ss24244094, ss41073276, ss66794543, ss66906891, ss67033293, ss70383116, ss70504412, ss71030794, ss75832136, ss85021004, ss97961341, ss102767823, ss121408131, ss138045101, ss138842479, ss152857799, ss155415585, ss159149516, ss169687452, ss170685011 NT_032977.9:70031517:T:C NC_000001.11:99594043:T:C (self)
Help

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

No publications for rs10875238

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