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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.

rs17599091

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr4:99591762 (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>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.038173 (10104/264690, TOPMED)
G=0.030973 (7749/250182, GnomAD_exome)
G=0.039582 (5548/140164, GnomAD) (+ 20 more)
G=0.033262 (3799/114216, ExAC)
G=0.03276 (2578/78700, PAGE_STUDY)
G=0.03994 (2113/52910, ALFA)
G=0.04067 (529/13006, GO-ESP)
G=0.0206 (103/5008, 1000G)
G=0.0533 (239/4480, Estonian)
G=0.0397 (153/3854, ALSPAC)
G=0.0369 (137/3708, TWINSUK)
G=0.0003 (1/2922, KOREAN)
G=0.0005 (1/1832, Korea1K)
G=0.035 (35/998, GoNL)
G=0.038 (23/600, NorthernSweden)
G=0.032 (17/534, MGP)
G=0.033 (10/304, FINRISK)
G=0.065 (14/216, Qatari)
G=0.07 (3/40, GENOME_DK)
C=0.50 (18/36, SGDP_PRJ)
G=0.50 (18/36, SGDP_PRJ)
C=0.5 (1/2, Siberian)
G=0.5 (1/2, Siberian)
Clinical Significance
Reported in ClinVar
Gene : Consequence
MTTP : Missense Variant
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 4 NC_000004.12:g.99591762C>G
GRCh37.p13 chr 4 NC_000004.11:g.100512919C>G
MTTP RefSeqGene NG_011469.1:g.32680C>G
Gene: MTTP, microsomal triglyceride transfer protein (plus strand)
Molecule type Change Amino acid[Codon] SO Term
MTTP transcript variant 1 NM_000253.4:c.730C>G Q [CAA] > E [GAA] Coding Sequence Variant
microsomal triglyceride transfer protein large subunit isoform 1 precursor NP_000244.2:p.Gln244Glu Q (Gln) > E (Glu) Missense Variant
MTTP transcript variant 3 NM_001386140.1:c.730C>G Q [CAA] > E [GAA] Coding Sequence Variant
microsomal triglyceride transfer protein large subunit isoform 1 precursor NP_001373069.1:p.Gln244Glu Q (Gln) > E (Glu) Missense Variant
MTTP transcript variant 2 NM_001300785.2:c.481C>G Q [CAA] > E [GAA] Coding Sequence Variant
microsomal triglyceride transfer protein large subunit isoform 2 NP_001287714.2:p.Gln161Glu Q (Gln) > E (Glu) Missense 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.

Allele: G (allele ID: 135073 )
ClinVar Accession Disease Names Clinical Significance
RCV000117639.2 not specified Likely-Benign
RCV000625114.3 Abetalipoproteinaemia Benign

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 52910 C=0.96006 G=0.03994
European Sub 40738 C=0.95935 G=0.04065
African Sub 3604 C=0.9498 G=0.0502
African Others Sub 122 C=0.959 G=0.041
African American Sub 3482 C=0.9495 G=0.0505
Asian Sub 170 C=1.000 G=0.000
East Asian Sub 114 C=1.000 G=0.000
Other Asian Sub 56 C=1.00 G=0.00
Latin American 1 Sub 504 C=0.956 G=0.044
Latin American 2 Sub 644 C=0.981 G=0.019
South Asian Sub 98 C=0.99 G=0.01
Other Sub 7152 C=0.9663 G=0.0337


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=0.961827 G=0.038173
gnomAD - Exomes Global Study-wide 250182 C=0.969027 G=0.030973
gnomAD - Exomes European Sub 134510 C=0.965371 G=0.034629
gnomAD - Exomes Asian Sub 48896 C=0.97914 G=0.02086
gnomAD - Exomes American Sub 34456 C=0.98822 G=0.01178
gnomAD - Exomes African Sub 16172 C=0.94719 G=0.05281
gnomAD - Exomes Ashkenazi Jewish Sub 10052 C=0.93772 G=0.06228
gnomAD - Exomes Other Sub 6096 C=0.9697 G=0.0303
gnomAD - Genomes Global Study-wide 140164 C=0.960418 G=0.039582
gnomAD - Genomes European Sub 75922 C=0.96270 G=0.03730
gnomAD - Genomes African Sub 42006 C=0.94829 G=0.05171
gnomAD - Genomes American Sub 13640 C=0.97940 G=0.02060
gnomAD - Genomes Ashkenazi Jewish Sub 3322 C=0.9449 G=0.0551
gnomAD - Genomes East Asian Sub 3130 C=1.0000 G=0.0000
gnomAD - Genomes Other Sub 2144 C=0.9627 G=0.0373
ExAC Global Study-wide 114216 C=0.966738 G=0.033262
ExAC Europe Sub 68502 C=0.96215 G=0.03785
ExAC Asian Sub 23970 C=0.97760 G=0.02240
ExAC American Sub 10958 C=0.98987 G=0.01013
ExAC African Sub 9910 C=0.9458 G=0.0542
ExAC Other Sub 876 C=0.976 G=0.024
The PAGE Study Global Study-wide 78700 C=0.96724 G=0.03276
The PAGE Study AfricanAmerican Sub 32514 C=0.94833 G=0.05167
The PAGE Study Mexican Sub 10810 C=0.98622 G=0.01378
The PAGE Study Asian Sub 8318 C=0.9995 G=0.0005
The PAGE Study PuertoRican Sub 7918 C=0.9656 G=0.0344
The PAGE Study NativeHawaiian Sub 4534 C=0.9885 G=0.0115
The PAGE Study Cuban Sub 4230 C=0.9704 G=0.0296
The PAGE Study Dominican Sub 3828 C=0.9647 G=0.0353
The PAGE Study CentralAmerican Sub 2450 C=0.9792 G=0.0208
The PAGE Study SouthAmerican Sub 1982 C=0.9808 G=0.0192
The PAGE Study NativeAmerican Sub 1260 C=0.9659 G=0.0341
The PAGE Study SouthAsian Sub 856 C=0.966 G=0.034
GO Exome Sequencing Project Global Study-wide 13006 C=0.95933 G=0.04067
GO Exome Sequencing Project European American Sub 8600 C=0.9664 G=0.0336
GO Exome Sequencing Project African American Sub 4406 C=0.9455 G=0.0545
1000Genomes Global Study-wide 5008 C=0.9794 G=0.0206
1000Genomes African Sub 1322 C=0.9523 G=0.0477
1000Genomes East Asian Sub 1008 C=1.0000 G=0.0000
1000Genomes Europe Sub 1006 C=0.9761 G=0.0239
1000Genomes South Asian Sub 978 C=0.990 G=0.010
1000Genomes American Sub 694 C=0.991 G=0.009
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.9467 G=0.0533
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.9603 G=0.0397
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.9631 G=0.0369
KOREAN population from KRGDB KOREAN Study-wide 2922 C=0.9997 G=0.0003
Korean Genome Project KOREAN Study-wide 1832 C=0.9995 G=0.0005
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.965 G=0.035
Northern Sweden ACPOP Study-wide 600 C=0.962 G=0.038
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 C=0.968 G=0.032
FINRISK Finnish from FINRISK project Study-wide 304 C=0.967 G=0.033
Qatari Global Study-wide 216 C=0.935 G=0.065
The Danish reference pan genome Danish Study-wide 40 C=0.93 G=0.07
SGDP_PRJ Global Study-wide 36 C=0.50 G=0.50
Siberian Global Study-wide 2 C=0.5 G=0.5
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= G
GRCh38.p13 chr 4 NC_000004.12:g.99591762= NC_000004.12:g.99591762C>G
GRCh37.p13 chr 4 NC_000004.11:g.100512919= NC_000004.11:g.100512919C>G
MTTP RefSeqGene NG_011469.1:g.32680= NG_011469.1:g.32680C>G
MTTP transcript variant 1 NM_000253.4:c.730= NM_000253.4:c.730C>G
MTTP transcript variant 1 NM_000253.3:c.730= NM_000253.3:c.730C>G
MTTP transcript NM_000253.2:c.730= NM_000253.2:c.730C>G
MTTP transcript variant 2 NM_001300785.2:c.481= NM_001300785.2:c.481C>G
MTTP transcript variant 2 NM_001300785.1:c.811= NM_001300785.1:c.811C>G
MTTP transcript variant 3 NM_001386140.1:c.730= NM_001386140.1:c.730C>G
microsomal triglyceride transfer protein large subunit isoform 1 precursor NP_000244.2:p.Gln244= NP_000244.2:p.Gln244Glu
microsomal triglyceride transfer protein large subunit isoform 2 NP_001287714.2:p.Gln161= NP_001287714.2:p.Gln161Glu
microsomal triglyceride transfer protein large subunit isoform 1 precursor NP_001373069.1:p.Gln244= NP_001373069.1:p.Gln244Glu
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#.

93 SubSNP, 21 Frequency, 2 ClinVar submissions
No Submitter Submission ID Date (Build)
1 PERLEGEN ss24366006 Sep 20, 2004 (123)
2 PERLEGEN ss68906301 May 17, 2007 (127)
3 AFFY ss74821715 Aug 16, 2007 (128)
4 ILLUMINA ss74884311 Dec 07, 2007 (129)
5 KRIBB_YJKIM ss119890091 Dec 01, 2009 (131)
6 ILLUMINA ss160449189 Dec 01, 2009 (131)
7 ILLUMINA ss172857326 Jul 04, 2010 (132)
8 BUSHMAN ss198924239 Jul 04, 2010 (132)
9 1000GENOMES ss221099991 Jul 14, 2010 (132)
10 1000GENOMES ss232516222 Jul 14, 2010 (132)
11 ILLUMINA ss244283987 Jul 04, 2010 (132)
12 NHLBI-ESP ss342168428 May 09, 2011 (134)
13 ILLUMINA ss480257998 May 04, 2012 (137)
14 ILLUMINA ss480268850 May 04, 2012 (137)
15 ILLUMINA ss481012750 Sep 08, 2015 (146)
16 ILLUMINA ss484069238 May 04, 2012 (137)
17 ILLUMINA ss484659666 May 04, 2012 (137)
18 ILLUMINA ss484926912 May 04, 2012 (137)
19 1000GENOMES ss490892026 May 04, 2012 (137)
20 EXOME_CHIP ss491358953 May 04, 2012 (137)
21 CLINSEQ_SNP ss491857860 May 04, 2012 (137)
22 ILLUMINA ss536975753 Sep 08, 2015 (146)
23 TISHKOFF ss557722964 Apr 25, 2013 (138)
24 ILLUMINA ss778342317 Aug 21, 2014 (142)
25 ILLUMINA ss782479440 Aug 21, 2014 (142)
26 ILLUMINA ss782909776 Aug 21, 2014 (142)
27 ILLUMINA ss783873004 Aug 21, 2014 (142)
28 ILLUMINA ss832164702 Apr 01, 2015 (144)
29 ILLUMINA ss833796927 Aug 21, 2014 (142)
30 JMKIDD_LAB ss974453482 Aug 21, 2014 (142)
31 EVA-GONL ss980453116 Aug 21, 2014 (142)
32 JMKIDD_LAB ss1067463184 Aug 21, 2014 (142)
33 JMKIDD_LAB ss1071789228 Aug 21, 2014 (142)
34 1000GENOMES ss1310989010 Aug 21, 2014 (142)
35 DDI ss1429983785 Apr 01, 2015 (144)
36 CLINVAR ss1457614644 Nov 23, 2014 (142)
37 EVA_GENOME_DK ss1580688773 Apr 01, 2015 (144)
38 EVA_FINRISK ss1584035552 Apr 01, 2015 (144)
39 EVA_DECODE ss1589957243 Apr 01, 2015 (144)
40 EVA_UK10K_ALSPAC ss1610741892 Apr 01, 2015 (144)
41 EVA_UK10K_TWINSUK ss1653735925 Apr 01, 2015 (144)
42 EVA_EXAC ss1687585716 Apr 01, 2015 (144)
43 EVA_MGP ss1711067345 Apr 01, 2015 (144)
44 ILLUMINA ss1752489394 Sep 08, 2015 (146)
45 HAMMER_LAB ss1801913100 Sep 08, 2015 (146)
46 WEILL_CORNELL_DGM ss1923692951 Feb 12, 2016 (147)
47 ILLUMINA ss1958707225 Feb 12, 2016 (147)
48 JJLAB ss2022432673 Sep 14, 2016 (149)
49 USC_VALOUEV ss2150561880 Dec 20, 2016 (150)
50 HUMAN_LONGEVITY ss2265445348 Dec 20, 2016 (150)
51 TOPMED ss2433264324 Dec 20, 2016 (150)
52 ILLUMINA ss2634154864 Nov 08, 2017 (151)
53 ILLUMINA ss2711011854 Nov 08, 2017 (151)
54 GNOMAD ss2734651894 Nov 08, 2017 (151)
55 GNOMAD ss2747279441 Nov 08, 2017 (151)
56 GNOMAD ss2812881610 Nov 08, 2017 (151)
57 AFFY ss2985298982 Nov 08, 2017 (151)
58 AFFY ss2985927027 Nov 08, 2017 (151)
59 SWEGEN ss2995214690 Nov 08, 2017 (151)
60 ILLUMINA ss3022398885 Nov 08, 2017 (151)
61 CSHL ss3345863204 Nov 08, 2017 (151)
62 TOPMED ss3437302871 Nov 08, 2017 (151)
63 ILLUMINA ss3629026110 Oct 12, 2018 (152)
64 ILLUMINA ss3632089173 Oct 12, 2018 (152)
65 ILLUMINA ss3633343463 Oct 12, 2018 (152)
66 ILLUMINA ss3634062769 Oct 12, 2018 (152)
67 ILLUMINA ss3634963635 Oct 12, 2018 (152)
68 ILLUMINA ss3635745494 Oct 12, 2018 (152)
69 ILLUMINA ss3636667936 Oct 12, 2018 (152)
70 ILLUMINA ss3637498032 Oct 12, 2018 (152)
71 ILLUMINA ss3638501945 Oct 12, 2018 (152)
72 ILLUMINA ss3640670928 Oct 12, 2018 (152)
73 ILLUMINA ss3643452090 Oct 12, 2018 (152)
74 OMUKHERJEE_ADBS ss3646310758 Oct 12, 2018 (152)
75 ILLUMINA ss3652885150 Oct 12, 2018 (152)
76 ILLUMINA ss3654070855 Oct 12, 2018 (152)
77 EGCUT_WGS ss3663110855 Jul 13, 2019 (153)
78 EVA_DECODE ss3712661790 Jul 13, 2019 (153)
79 ILLUMINA ss3726155954 Jul 13, 2019 (153)
80 ACPOP ss3731424298 Jul 13, 2019 (153)
81 ILLUMINA ss3745263891 Jul 13, 2019 (153)
82 PAGE_CC ss3771142782 Jul 13, 2019 (153)
83 ILLUMINA ss3772758429 Jul 13, 2019 (153)
84 EVA ss3824035461 Apr 26, 2020 (154)
85 EVA ss3825661769 Apr 26, 2020 (154)
86 SGDP_PRJ ss3859615673 Apr 26, 2020 (154)
87 KRGDB ss3905893016 Apr 26, 2020 (154)
88 KOGIC ss3954746312 Apr 26, 2020 (154)
89 FSA-LAB ss3984290152 Apr 26, 2021 (155)
90 EVA ss3986287455 Apr 26, 2021 (155)
91 EVA ss4017159720 Apr 26, 2021 (155)
92 TOPMED ss4624726182 Apr 26, 2021 (155)
93 EVA ss5237008040 Apr 26, 2021 (155)
94 1000Genomes NC_000004.11 - 100512919 Oct 12, 2018 (152)
95 The Avon Longitudinal Study of Parents and Children NC_000004.11 - 100512919 Oct 12, 2018 (152)
96 Genetic variation in the Estonian population NC_000004.11 - 100512919 Oct 12, 2018 (152)
97 ExAC NC_000004.11 - 100512919 Oct 12, 2018 (152)
98 FINRISK NC_000004.11 - 100512919 Apr 26, 2020 (154)
99 The Danish reference pan genome NC_000004.11 - 100512919 Apr 26, 2020 (154)
100 gnomAD - Genomes NC_000004.12 - 99591762 Apr 26, 2021 (155)
101 gnomAD - Exomes NC_000004.11 - 100512919 Jul 13, 2019 (153)
102 GO Exome Sequencing Project NC_000004.11 - 100512919 Oct 12, 2018 (152)
103 Genome of the Netherlands Release 5 NC_000004.11 - 100512919 Apr 26, 2020 (154)
104 KOREAN population from KRGDB NC_000004.11 - 100512919 Apr 26, 2020 (154)
105 Korean Genome Project NC_000004.12 - 99591762 Apr 26, 2020 (154)
106 Medical Genome Project healthy controls from Spanish population NC_000004.11 - 100512919 Apr 26, 2020 (154)
107 Northern Sweden NC_000004.11 - 100512919 Jul 13, 2019 (153)
108 The PAGE Study NC_000004.12 - 99591762 Jul 13, 2019 (153)
109 Qatari NC_000004.11 - 100512919 Apr 26, 2020 (154)
110 SGDP_PRJ NC_000004.11 - 100512919 Apr 26, 2020 (154)
111 Siberian NC_000004.11 - 100512919 Apr 26, 2020 (154)
112 TopMed NC_000004.12 - 99591762 Apr 26, 2021 (155)
113 UK 10K study - Twins NC_000004.11 - 100512919 Oct 12, 2018 (152)
114 ALFA NC_000004.12 - 99591762 Apr 26, 2021 (155)
115 ClinVar RCV000117639.2 Oct 12, 2018 (152)
116 ClinVar RCV000625114.3 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)
rs52789259 Sep 21, 2007 (128)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss198924239, ss480257998, ss484659666, ss491857860, ss1589957243, ss3643452090 NC_000004.10:100731941:C:G NC_000004.12:99591761:C:G (self)
22431547, 12478621, 8849103, 7557922, 32013, 6853712, 3759931, 493658, 5516537, 13070410, 183105, 4709163, 5734881, 11632653, 3078234, 12478621, ss221099991, ss232516222, ss342168428, ss480268850, ss481012750, ss484069238, ss484926912, ss490892026, ss491358953, ss536975753, ss557722964, ss778342317, ss782479440, ss782909776, ss783873004, ss832164702, ss833796927, ss974453482, ss980453116, ss1067463184, ss1071789228, ss1310989010, ss1429983785, ss1580688773, ss1584035552, ss1610741892, ss1653735925, ss1687585716, ss1711067345, ss1752489394, ss1801913100, ss1923692951, ss1958707225, ss2022432673, ss2150561880, ss2433264324, ss2634154864, ss2711011854, ss2734651894, ss2747279441, ss2812881610, ss2985298982, ss2985927027, ss2995214690, ss3022398885, ss3345863204, ss3629026110, ss3632089173, ss3633343463, ss3634062769, ss3634963635, ss3635745494, ss3636667936, ss3637498032, ss3638501945, ss3640670928, ss3646310758, ss3652885150, ss3654070855, ss3663110855, ss3731424298, ss3745263891, ss3772758429, ss3824035461, ss3825661769, ss3859615673, ss3905893016, ss3984290152, ss3986287455, ss4017159720 NC_000004.11:100512918:C:G NC_000004.12:99591761:C:G (self)
RCV000117639.2, RCV000625114.3, 158903760, 11124313, 364251, 288860410, 462103738, 11649252210, ss1457614644, ss2265445348, ss3437302871, ss3712661790, ss3726155954, ss3771142782, ss3954746312, ss4624726182, ss5237008040 NC_000004.12:99591761:C:G NC_000004.12:99591761:C:G (self)
ss24366006, ss68906301, ss74821715, ss74884311, ss119890091, ss160449189, ss172857326, ss244283987 NT_016354.19:25060639:C:G NC_000004.12:99591761: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.

No publications for rs17599091

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