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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.

rs35224672

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr20:13247518-13247559 (GRCh38.p14) 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
del(GT)13 / del(GT)11 / del(GT)10

del(GT)13 / del(GT)11 / del(GT)10 / del(GT)9 / del(GT)8 / del(GT)7 / del(GT)6 / del(GT)5 / del(GT)4 / del(GT)3 / delGTGT / delGT / dupGT / dupGTGT / dup(GT)3 / dup(GT)4 / dup(GT)5 / dup(GT)6 / dup(GT)7 / dup(GT)9

Variation Type
Indel Insertion and Deletion
Frequency
del(GT)3=0.0614 (588/9570, ALFA)
del(GT)3=0.1443 (556/3854, ALSPAC)
del(GT)3=0.1427 (529/3708, TWINSUK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TASP1 : Non Coding Transcript Variant
ISM1 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome

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: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 9570 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.8564 GTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0614, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0383, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0320, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0070, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0048, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000 0.898468 0.009881 0.09165 N/A
European Sub 8193 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.8325 GTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0716, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0448, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0373, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0082, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0055, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000 0.878012 0.011901 0.110086 25
African Sub 840 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000 GTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000 1.0 0.0 0.0 N/A
African Others Sub 28 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00 GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00 1.0 0.0 0.0 N/A
African American Sub 812 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000 GTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000 1.0 0.0 0.0 N/A
Asian Sub 14 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00 GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00 1.0 0.0 0.0 N/A
East Asian Sub 10 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0 GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0 1.0 0.0 0.0 N/A
Other Asian Sub 4 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0 GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0 1.0 0.0 0.0 N/A
Latin American 1 Sub 66 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00 GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00 1.0 0.0 0.0 N/A
Latin American 2 Sub 226 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000 GTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000 1.0 0.0 0.0 N/A
South Asian Sub 40 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00 GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00 1.0 0.0 0.0 N/A
Other Sub 191 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.990 GTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.005, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.005, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000 0.989362 0.0 0.010638 0


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
Allele Frequency Aggregator Total Global 9570 (GT)21=0.8564 del(GT)13=0.0000, del(GT)11=0.0000, del(GT)10=0.0000, del(GT)9=0.0000, del(GT)8=0.0000, del(GT)7=0.0000, del(GT)6=0.0000, del(GT)5=0.0000, del(GT)4=0.0000, del(GT)3=0.0614, delGTGT=0.0000, delGT=0.0383, dupGT=0.0320, dupGTGT=0.0048, dup(GT)3=0.0070, dup(GT)4=0.0000, dup(GT)5=0.0000, dup(GT)6=0.0000, dup(GT)7=0.0000
Allele Frequency Aggregator European Sub 8193 (GT)21=0.8325 del(GT)13=0.0000, del(GT)11=0.0000, del(GT)10=0.0000, del(GT)9=0.0000, del(GT)8=0.0000, del(GT)7=0.0000, del(GT)6=0.0000, del(GT)5=0.0000, del(GT)4=0.0000, del(GT)3=0.0716, delGTGT=0.0000, delGT=0.0448, dupGT=0.0373, dupGTGT=0.0055, dup(GT)3=0.0082, dup(GT)4=0.0000, dup(GT)5=0.0000, dup(GT)6=0.0000, dup(GT)7=0.0000
Allele Frequency Aggregator African Sub 840 (GT)21=1.000 del(GT)13=0.000, del(GT)11=0.000, del(GT)10=0.000, del(GT)9=0.000, del(GT)8=0.000, del(GT)7=0.000, del(GT)6=0.000, del(GT)5=0.000, del(GT)4=0.000, del(GT)3=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)3=0.000, dup(GT)4=0.000, dup(GT)5=0.000, dup(GT)6=0.000, dup(GT)7=0.000
Allele Frequency Aggregator Latin American 2 Sub 226 (GT)21=1.000 del(GT)13=0.000, del(GT)11=0.000, del(GT)10=0.000, del(GT)9=0.000, del(GT)8=0.000, del(GT)7=0.000, del(GT)6=0.000, del(GT)5=0.000, del(GT)4=0.000, del(GT)3=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)3=0.000, dup(GT)4=0.000, dup(GT)5=0.000, dup(GT)6=0.000, dup(GT)7=0.000
Allele Frequency Aggregator Other Sub 191 (GT)21=0.990 del(GT)13=0.000, del(GT)11=0.000, del(GT)10=0.000, del(GT)9=0.000, del(GT)8=0.000, del(GT)7=0.000, del(GT)6=0.000, del(GT)5=0.000, del(GT)4=0.000, del(GT)3=0.005, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.005, dup(GT)3=0.000, dup(GT)4=0.000, dup(GT)5=0.000, dup(GT)6=0.000, dup(GT)7=0.000
Allele Frequency Aggregator Latin American 1 Sub 66 (GT)21=1.00 del(GT)13=0.00, del(GT)11=0.00, del(GT)10=0.00, del(GT)9=0.00, del(GT)8=0.00, del(GT)7=0.00, del(GT)6=0.00, del(GT)5=0.00, del(GT)4=0.00, del(GT)3=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)3=0.00, dup(GT)4=0.00, dup(GT)5=0.00, dup(GT)6=0.00, dup(GT)7=0.00
Allele Frequency Aggregator South Asian Sub 40 (GT)21=1.00 del(GT)13=0.00, del(GT)11=0.00, del(GT)10=0.00, del(GT)9=0.00, del(GT)8=0.00, del(GT)7=0.00, del(GT)6=0.00, del(GT)5=0.00, del(GT)4=0.00, del(GT)3=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)3=0.00, dup(GT)4=0.00, dup(GT)5=0.00, dup(GT)6=0.00, dup(GT)7=0.00
Allele Frequency Aggregator Asian Sub 14 (GT)21=1.00 del(GT)13=0.00, del(GT)11=0.00, del(GT)10=0.00, del(GT)9=0.00, del(GT)8=0.00, del(GT)7=0.00, del(GT)6=0.00, del(GT)5=0.00, del(GT)4=0.00, del(GT)3=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)3=0.00, dup(GT)4=0.00, dup(GT)5=0.00, dup(GT)6=0.00, dup(GT)7=0.00
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 (GT)21=0.8557 del(GT)3=0.1443
UK 10K study - Twins TWIN COHORT Study-wide 3708 (GT)21=0.8573 del(GT)3=0.1427
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.p14 chr 20 NC_000020.11:g.13247518GT[8]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[10]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[11]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[12]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[13]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[14]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[15]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[16]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[17]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[18]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[19]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[20]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[22]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[23]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[24]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[25]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[26]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[27]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[28]
GRCh38.p14 chr 20 NC_000020.11:g.13247518GT[30]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[8]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[10]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[11]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[12]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[13]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[14]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[15]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[16]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[17]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[18]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[19]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[20]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[22]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[23]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[24]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[25]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[26]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[27]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[28]
GRCh37.p13 chr 20 NC_000020.10:g.13228165GT[30]
LOC112694689 genomic region NG_060719.1:g.277GT[8]
LOC112694689 genomic region NG_060719.1:g.277GT[10]
LOC112694689 genomic region NG_060719.1:g.277GT[11]
LOC112694689 genomic region NG_060719.1:g.277GT[12]
LOC112694689 genomic region NG_060719.1:g.277GT[13]
LOC112694689 genomic region NG_060719.1:g.277GT[14]
LOC112694689 genomic region NG_060719.1:g.277GT[15]
LOC112694689 genomic region NG_060719.1:g.277GT[16]
LOC112694689 genomic region NG_060719.1:g.277GT[17]
LOC112694689 genomic region NG_060719.1:g.277GT[18]
LOC112694689 genomic region NG_060719.1:g.277GT[19]
LOC112694689 genomic region NG_060719.1:g.277GT[20]
LOC112694689 genomic region NG_060719.1:g.277GT[22]
LOC112694689 genomic region NG_060719.1:g.277GT[23]
LOC112694689 genomic region NG_060719.1:g.277GT[24]
LOC112694689 genomic region NG_060719.1:g.277GT[25]
LOC112694689 genomic region NG_060719.1:g.277GT[26]
LOC112694689 genomic region NG_060719.1:g.277GT[27]
LOC112694689 genomic region NG_060719.1:g.277GT[28]
LOC112694689 genomic region NG_060719.1:g.277GT[30]
Gene: ISM1, isthmin 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ISM1 transcript NM_080826.2:c.139-22986GT…

NM_080826.2:c.139-22986GT[8]

N/A Intron Variant
ISM1 transcript variant X1 XM_017027680.2:c.139-2298…

XM_017027680.2:c.139-22986GT[8]

N/A Intron Variant
Gene: TASP1, taspase 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
TASP1 transcript variant 2 NM_001323602.2:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant 3 NM_001323603.2:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant 4 NM_001323604.2:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant 1 NM_017714.3:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant 5 NR_136628.2:n. N/A Genic Downstream Transcript Variant
TASP1 transcript variant 6 NR_136629.2:n. N/A Genic Downstream Transcript Variant
TASP1 transcript variant 7 NR_136630.2:n. N/A Genic Downstream Transcript Variant
TASP1 transcript variant 8 NR_136631.2:n. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X12 XM_017027929.3:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X14 XM_017027931.3:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X1 XM_047440267.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X2 XM_047440268.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X4 XM_047440269.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X6 XM_047440270.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X7 XM_047440271.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X8 XM_047440272.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X9 XM_047440273.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X10 XM_047440274.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X11 XM_047440275.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X13 XM_047440276.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X15 XM_047440277.1:c. N/A Genic Downstream Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[8]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[10]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[11]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[12]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[13]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[14]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[15]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[16]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[17]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[18]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[19]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[20]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[22]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[23]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[24]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[25]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[26]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[27]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[28]

N/A Non Coding Transcript Variant
TASP1 transcript variant X3 XR_007067463.1:n.19993AC[…

XR_007067463.1:n.19993AC[30]

N/A Non Coding Transcript Variant
TASP1 transcript variant X5 XR_001754319.3:n. N/A Intron 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
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 (GT)21= del(GT)13 del(GT)11 del(GT)10 del(GT)9 del(GT)8 del(GT)7 del(GT)6 del(GT)5 del(GT)4 del(GT)3 delGTGT delGT dupGT dupGTGT dup(GT)3 dup(GT)4 dup(GT)5 dup(GT)6 dup(GT)7 dup(GT)9
GRCh38.p14 chr 20 NC_000020.11:g.13247518_13247559= NC_000020.11:g.13247518GT[8] NC_000020.11:g.13247518GT[10] NC_000020.11:g.13247518GT[11] NC_000020.11:g.13247518GT[12] NC_000020.11:g.13247518GT[13] NC_000020.11:g.13247518GT[14] NC_000020.11:g.13247518GT[15] NC_000020.11:g.13247518GT[16] NC_000020.11:g.13247518GT[17] NC_000020.11:g.13247518GT[18] NC_000020.11:g.13247518GT[19] NC_000020.11:g.13247518GT[20] NC_000020.11:g.13247518GT[22] NC_000020.11:g.13247518GT[23] NC_000020.11:g.13247518GT[24] NC_000020.11:g.13247518GT[25] NC_000020.11:g.13247518GT[26] NC_000020.11:g.13247518GT[27] NC_000020.11:g.13247518GT[28] NC_000020.11:g.13247518GT[30]
GRCh37.p13 chr 20 NC_000020.10:g.13228165_13228206= NC_000020.10:g.13228165GT[8] NC_000020.10:g.13228165GT[10] NC_000020.10:g.13228165GT[11] NC_000020.10:g.13228165GT[12] NC_000020.10:g.13228165GT[13] NC_000020.10:g.13228165GT[14] NC_000020.10:g.13228165GT[15] NC_000020.10:g.13228165GT[16] NC_000020.10:g.13228165GT[17] NC_000020.10:g.13228165GT[18] NC_000020.10:g.13228165GT[19] NC_000020.10:g.13228165GT[20] NC_000020.10:g.13228165GT[22] NC_000020.10:g.13228165GT[23] NC_000020.10:g.13228165GT[24] NC_000020.10:g.13228165GT[25] NC_000020.10:g.13228165GT[26] NC_000020.10:g.13228165GT[27] NC_000020.10:g.13228165GT[28] NC_000020.10:g.13228165GT[30]
LOC112694689 genomic region NG_060719.1:g.277_318= NG_060719.1:g.277GT[8] NG_060719.1:g.277GT[10] NG_060719.1:g.277GT[11] NG_060719.1:g.277GT[12] NG_060719.1:g.277GT[13] NG_060719.1:g.277GT[14] NG_060719.1:g.277GT[15] NG_060719.1:g.277GT[16] NG_060719.1:g.277GT[17] NG_060719.1:g.277GT[18] NG_060719.1:g.277GT[19] NG_060719.1:g.277GT[20] NG_060719.1:g.277GT[22] NG_060719.1:g.277GT[23] NG_060719.1:g.277GT[24] NG_060719.1:g.277GT[25] NG_060719.1:g.277GT[26] NG_060719.1:g.277GT[27] NG_060719.1:g.277GT[28] NG_060719.1:g.277GT[30]
TASP1 transcript variant X3 XR_007067463.1:n.19993_20034= XR_007067463.1:n.19993AC[8] XR_007067463.1:n.19993AC[10] XR_007067463.1:n.19993AC[11] XR_007067463.1:n.19993AC[12] XR_007067463.1:n.19993AC[13] XR_007067463.1:n.19993AC[14] XR_007067463.1:n.19993AC[15] XR_007067463.1:n.19993AC[16] XR_007067463.1:n.19993AC[17] XR_007067463.1:n.19993AC[18] XR_007067463.1:n.19993AC[19] XR_007067463.1:n.19993AC[20] XR_007067463.1:n.19993AC[22] XR_007067463.1:n.19993AC[23] XR_007067463.1:n.19993AC[24] XR_007067463.1:n.19993AC[25] XR_007067463.1:n.19993AC[26] XR_007067463.1:n.19993AC[27] XR_007067463.1:n.19993AC[28] XR_007067463.1:n.19993AC[30]
ISM1 transcript NM_080826.1:c.139-22986= NM_080826.1:c.139-22986GT[8] NM_080826.1:c.139-22986GT[10] NM_080826.1:c.139-22986GT[11] NM_080826.1:c.139-22986GT[12] NM_080826.1:c.139-22986GT[13] NM_080826.1:c.139-22986GT[14] NM_080826.1:c.139-22986GT[15] NM_080826.1:c.139-22986GT[16] NM_080826.1:c.139-22986GT[17] NM_080826.1:c.139-22986GT[18] NM_080826.1:c.139-22986GT[19] NM_080826.1:c.139-22986GT[20] NM_080826.1:c.139-22986GT[22] NM_080826.1:c.139-22986GT[23] NM_080826.1:c.139-22986GT[24] NM_080826.1:c.139-22986GT[25] NM_080826.1:c.139-22986GT[26] NM_080826.1:c.139-22986GT[27] NM_080826.1:c.139-22986GT[28] NM_080826.1:c.139-22986GT[30]
ISM1 transcript NM_080826.2:c.139-22986= NM_080826.2:c.139-22986GT[8] NM_080826.2:c.139-22986GT[10] NM_080826.2:c.139-22986GT[11] NM_080826.2:c.139-22986GT[12] NM_080826.2:c.139-22986GT[13] NM_080826.2:c.139-22986GT[14] NM_080826.2:c.139-22986GT[15] NM_080826.2:c.139-22986GT[16] NM_080826.2:c.139-22986GT[17] NM_080826.2:c.139-22986GT[18] NM_080826.2:c.139-22986GT[19] NM_080826.2:c.139-22986GT[20] NM_080826.2:c.139-22986GT[22] NM_080826.2:c.139-22986GT[23] NM_080826.2:c.139-22986GT[24] NM_080826.2:c.139-22986GT[25] NM_080826.2:c.139-22986GT[26] NM_080826.2:c.139-22986GT[27] NM_080826.2:c.139-22986GT[28] NM_080826.2:c.139-22986GT[30]
ISM1 transcript variant X1 XM_017027680.2:c.139-22986= XM_017027680.2:c.139-22986GT[8] XM_017027680.2:c.139-22986GT[10] XM_017027680.2:c.139-22986GT[11] XM_017027680.2:c.139-22986GT[12] XM_017027680.2:c.139-22986GT[13] XM_017027680.2:c.139-22986GT[14] XM_017027680.2:c.139-22986GT[15] XM_017027680.2:c.139-22986GT[16] XM_017027680.2:c.139-22986GT[17] XM_017027680.2:c.139-22986GT[18] XM_017027680.2:c.139-22986GT[19] XM_017027680.2:c.139-22986GT[20] XM_017027680.2:c.139-22986GT[22] XM_017027680.2:c.139-22986GT[23] XM_017027680.2:c.139-22986GT[24] XM_017027680.2:c.139-22986GT[25] XM_017027680.2:c.139-22986GT[26] XM_017027680.2:c.139-22986GT[27] XM_017027680.2:c.139-22986GT[28] XM_017027680.2:c.139-22986GT[30]
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#.

57 SubSNP, 41 Frequency submissions
No Submitter Submission ID Date (Build)
1 HGSV ss81983829 Dec 16, 2007 (130)
2 HGSV ss82114555 Dec 16, 2007 (130)
3 HGSV ss82150866 Dec 15, 2007 (129)
4 HGSV ss82236428 Dec 15, 2007 (129)
5 HUMANGENOME_JCVI ss95736338 Feb 06, 2009 (130)
6 PJP ss295040030 May 09, 2011 (135)
7 SSMP ss664462300 Apr 01, 2015 (144)
8 EVA_UK10K_ALSPAC ss1709302365 Apr 01, 2015 (144)
9 EVA_UK10K_TWINSUK ss1709304053 Apr 01, 2015 (144)
10 SWEGEN ss3017901999 Nov 08, 2017 (151)
11 MCHAISSO ss3063990882 Nov 08, 2017 (151)
12 URBANLAB ss3650976194 Oct 12, 2018 (152)
13 ACPOP ss3743268073 Jul 13, 2019 (153)
14 ACPOP ss3743268075 Jul 13, 2019 (153)
15 ACPOP ss3743268077 Jul 13, 2019 (153)
16 EVA ss3835599543 Apr 27, 2020 (154)
17 KOGIC ss3981861467 Apr 27, 2020 (154)
18 KOGIC ss3981861468 Apr 27, 2020 (154)
19 KOGIC ss3981861469 Apr 27, 2020 (154)
20 KOGIC ss3981861470 Apr 27, 2020 (154)
21 KOGIC ss3981861471 Apr 27, 2020 (154)
22 KOGIC ss3981861472 Apr 27, 2020 (154)
23 GNOMAD ss4335427844 Apr 26, 2021 (155)
24 GNOMAD ss4335427845 Apr 26, 2021 (155)
25 GNOMAD ss4335427846 Apr 26, 2021 (155)
26 GNOMAD ss4335427847 Apr 26, 2021 (155)
27 GNOMAD ss4335427848 Apr 26, 2021 (155)
28 GNOMAD ss4335427849 Apr 26, 2021 (155)
29 GNOMAD ss4335427858 Apr 26, 2021 (155)
30 GNOMAD ss4335427864 Apr 26, 2021 (155)
31 GNOMAD ss4335427865 Apr 26, 2021 (155)
32 GNOMAD ss4335427866 Apr 26, 2021 (155)
33 GNOMAD ss4335427867 Apr 26, 2021 (155)
34 GNOMAD ss4335427868 Apr 26, 2021 (155)
35 GNOMAD ss4335427869 Apr 26, 2021 (155)
36 GNOMAD ss4335427870 Apr 26, 2021 (155)
37 GNOMAD ss4335427871 Apr 26, 2021 (155)
38 GNOMAD ss4335427872 Apr 26, 2021 (155)
39 GNOMAD ss4335427873 Apr 26, 2021 (155)
40 TOMMO_GENOMICS ss5228933080 Apr 26, 2021 (155)
41 TOMMO_GENOMICS ss5228933081 Apr 26, 2021 (155)
42 TOMMO_GENOMICS ss5228933082 Apr 26, 2021 (155)
43 TOMMO_GENOMICS ss5228933083 Apr 26, 2021 (155)
44 TOMMO_GENOMICS ss5228933084 Apr 26, 2021 (155)
45 TOMMO_GENOMICS ss5228933085 Apr 26, 2021 (155)
46 1000G_HIGH_COVERAGE ss5308158873 Oct 13, 2022 (156)
47 HUGCELL_USP ss5500552167 Oct 13, 2022 (156)
48 HUGCELL_USP ss5500552168 Oct 13, 2022 (156)
49 HUGCELL_USP ss5500552169 Oct 13, 2022 (156)
50 HUGCELL_USP ss5500552170 Oct 13, 2022 (156)
51 HUGCELL_USP ss5500552171 Oct 13, 2022 (156)
52 TOMMO_GENOMICS ss5787945897 Oct 13, 2022 (156)
53 TOMMO_GENOMICS ss5787945898 Oct 13, 2022 (156)
54 TOMMO_GENOMICS ss5787945899 Oct 13, 2022 (156)
55 TOMMO_GENOMICS ss5787945900 Oct 13, 2022 (156)
56 TOMMO_GENOMICS ss5787945901 Oct 13, 2022 (156)
57 TOMMO_GENOMICS ss5787945902 Oct 13, 2022 (156)
58 The Avon Longitudinal Study of Parents and Children NC_000020.10 - 13228165 Oct 12, 2018 (152)
59 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

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

Submission ignored due to conflicting rows:
Row 547086295 (NC_000020.11:13247517::GT 7543/128546)
Row 547086296 (NC_000020.11:13247517::GTGT 1602/128654)
Row 547086297 (NC_000020.11:13247517::GTGTGT 1680/128648)...

- Apr 26, 2021 (155)
76 Korean Genome Project

Submission ignored due to conflicting rows:
Row 38239468 (NC_000020.11:13247521:GTGT: 116/1828)
Row 38239469 (NC_000020.11:13247523:GT: 442/1828)
Row 38239470 (NC_000020.11:13247519:GTGTGT: 353/1828)...

- Apr 27, 2020 (154)
77 Korean Genome Project

Submission ignored due to conflicting rows:
Row 38239468 (NC_000020.11:13247521:GTGT: 116/1828)
Row 38239469 (NC_000020.11:13247523:GT: 442/1828)
Row 38239470 (NC_000020.11:13247519:GTGTGT: 353/1828)...

- Apr 27, 2020 (154)
78 Korean Genome Project

Submission ignored due to conflicting rows:
Row 38239468 (NC_000020.11:13247521:GTGT: 116/1828)
Row 38239469 (NC_000020.11:13247523:GT: 442/1828)
Row 38239470 (NC_000020.11:13247519:GTGTGT: 353/1828)...

- Apr 27, 2020 (154)
79 Korean Genome Project

Submission ignored due to conflicting rows:
Row 38239468 (NC_000020.11:13247521:GTGT: 116/1828)
Row 38239469 (NC_000020.11:13247523:GT: 442/1828)
Row 38239470 (NC_000020.11:13247519:GTGTGT: 353/1828)...

- Apr 27, 2020 (154)
80 Korean Genome Project

Submission ignored due to conflicting rows:
Row 38239468 (NC_000020.11:13247521:GTGT: 116/1828)
Row 38239469 (NC_000020.11:13247523:GT: 442/1828)
Row 38239470 (NC_000020.11:13247519:GTGTGT: 353/1828)...

- Apr 27, 2020 (154)
81 Korean Genome Project

Submission ignored due to conflicting rows:
Row 38239468 (NC_000020.11:13247521:GTGT: 116/1828)
Row 38239469 (NC_000020.11:13247523:GT: 442/1828)
Row 38239470 (NC_000020.11:13247519:GTGTGT: 353/1828)...

- Apr 27, 2020 (154)
82 Northern Sweden

Submission ignored due to conflicting rows:
Row 16552938 (NC_000020.10:13228164:GTGTGT: 59/598)
Row 16552940 (NC_000020.10:13228164::GT 17/598)
Row 16552942 (NC_000020.10:13228164:GT: 27/598)

- Jul 13, 2019 (153)
83 Northern Sweden

Submission ignored due to conflicting rows:
Row 16552938 (NC_000020.10:13228164:GTGTGT: 59/598)
Row 16552940 (NC_000020.10:13228164::GT 17/598)
Row 16552942 (NC_000020.10:13228164:GT: 27/598)

- Jul 13, 2019 (153)
84 Northern Sweden

Submission ignored due to conflicting rows:
Row 16552938 (NC_000020.10:13228164:GTGTGT: 59/598)
Row 16552940 (NC_000020.10:13228164::GT 17/598)
Row 16552942 (NC_000020.10:13228164:GT: 27/598)

- Jul 13, 2019 (153)
85 8.3KJPN

Submission ignored due to conflicting rows:
Row 86902387 (NC_000020.10:13228164:GTGT: 624/16732)
Row 86902388 (NC_000020.10:13228164:GT: 3598/16732)
Row 86902389 (NC_000020.10:13228164:GTGTGT: 3413/16732)...

- Apr 26, 2021 (155)
86 8.3KJPN

Submission ignored due to conflicting rows:
Row 86902387 (NC_000020.10:13228164:GTGT: 624/16732)
Row 86902388 (NC_000020.10:13228164:GT: 3598/16732)
Row 86902389 (NC_000020.10:13228164:GTGTGT: 3413/16732)...

- Apr 26, 2021 (155)
87 8.3KJPN

Submission ignored due to conflicting rows:
Row 86902387 (NC_000020.10:13228164:GTGT: 624/16732)
Row 86902388 (NC_000020.10:13228164:GT: 3598/16732)
Row 86902389 (NC_000020.10:13228164:GTGTGT: 3413/16732)...

- Apr 26, 2021 (155)
88 8.3KJPN

Submission ignored due to conflicting rows:
Row 86902387 (NC_000020.10:13228164:GTGT: 624/16732)
Row 86902388 (NC_000020.10:13228164:GT: 3598/16732)
Row 86902389 (NC_000020.10:13228164:GTGTGT: 3413/16732)...

- Apr 26, 2021 (155)
89 8.3KJPN

Submission ignored due to conflicting rows:
Row 86902387 (NC_000020.10:13228164:GTGT: 624/16732)
Row 86902388 (NC_000020.10:13228164:GT: 3598/16732)
Row 86902389 (NC_000020.10:13228164:GTGTGT: 3413/16732)...

- Apr 26, 2021 (155)
90 8.3KJPN

Submission ignored due to conflicting rows:
Row 86902387 (NC_000020.10:13228164:GTGT: 624/16732)
Row 86902388 (NC_000020.10:13228164:GT: 3598/16732)
Row 86902389 (NC_000020.10:13228164:GTGTGT: 3413/16732)...

- Apr 26, 2021 (155)
91 14KJPN

Submission ignored due to conflicting rows:
Row 121783001 (NC_000020.11:13247517:GT: 5929/28252)
Row 121783002 (NC_000020.11:13247517:GTGTGT: 5830/28252)
Row 121783003 (NC_000020.11:13247517:GTGT: 1018/28252)...

- Oct 13, 2022 (156)
92 14KJPN

Submission ignored due to conflicting rows:
Row 121783001 (NC_000020.11:13247517:GT: 5929/28252)
Row 121783002 (NC_000020.11:13247517:GTGTGT: 5830/28252)
Row 121783003 (NC_000020.11:13247517:GTGT: 1018/28252)...

- Oct 13, 2022 (156)
93 14KJPN

Submission ignored due to conflicting rows:
Row 121783001 (NC_000020.11:13247517:GT: 5929/28252)
Row 121783002 (NC_000020.11:13247517:GTGTGT: 5830/28252)
Row 121783003 (NC_000020.11:13247517:GTGT: 1018/28252)...

- Oct 13, 2022 (156)
94 14KJPN

Submission ignored due to conflicting rows:
Row 121783001 (NC_000020.11:13247517:GT: 5929/28252)
Row 121783002 (NC_000020.11:13247517:GTGTGT: 5830/28252)
Row 121783003 (NC_000020.11:13247517:GTGT: 1018/28252)...

- Oct 13, 2022 (156)
95 14KJPN

Submission ignored due to conflicting rows:
Row 121783001 (NC_000020.11:13247517:GT: 5929/28252)
Row 121783002 (NC_000020.11:13247517:GTGTGT: 5830/28252)
Row 121783003 (NC_000020.11:13247517:GTGT: 1018/28252)...

- Oct 13, 2022 (156)
96 14KJPN

Submission ignored due to conflicting rows:
Row 121783001 (NC_000020.11:13247517:GT: 5929/28252)
Row 121783002 (NC_000020.11:13247517:GTGTGT: 5830/28252)
Row 121783003 (NC_000020.11:13247517:GTGT: 1018/28252)...

- Oct 13, 2022 (156)
97 UK 10K study - Twins NC_000020.10 - 13228165 Oct 12, 2018 (152)
98 ALFA NC_000020.11 - 13247518 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)
rs58565199 May 13, 2013 (138)
rs61465076 May 26, 2008 (130)
rs71824327 May 11, 2012 (137)
rs71901068 May 11, 2012 (137)
rs139984275 Sep 17, 2011 (135)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT

(self)
ss4335427873 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGT:

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427872 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGT:

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427871 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGT:

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427870 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGT:

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427869 NC_000020.11:13247517:GTGTGTGTGTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427868 NC_000020.11:13247517:GTGTGTGTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3981861472, ss4335427867, ss5500552169 NC_000020.11:13247517:GTGTGTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss82150866, ss82236428 NC_000020.9:13176200:GTGTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
42955653, 42955653, ss664462300, ss1709302365, ss1709304053, ss3017901999, ss3743268073, ss3835599543, ss5228933082 NC_000020.10:13228164:GTGTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427866, ss5500552170, ss5787945898 NC_000020.11:13247517:GTGTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3981861469 NC_000020.11:13247519:GTGTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3650976194 NC_000020.11:13247529:GTGTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss95736338 NT_011387.8:13168200:GTGTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss5228933080 NC_000020.10:13228164:GTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3063990882, ss4335427865, ss5500552171, ss5787945899 NC_000020.11:13247517:GTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3981861467 NC_000020.11:13247521:GTGT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss81983829, ss82114555, ss295040030 NC_000020.9:13176204:GT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3743268077, ss5228933081 NC_000020.10:13228164:GT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427864, ss5500552167, ss5787945897 NC_000020.11:13247517:GT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3981861468 NC_000020.11:13247523:GT: NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3743268075, ss5228933083 NC_000020.10:13228164::GT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427844, ss5308158873, ss5500552168, ss5787945900 NC_000020.11:13247517::GT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3981861470 NC_000020.11:13247525::GT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss5228933084 NC_000020.10:13228164::GTGT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427845, ss5787945902 NC_000020.11:13247517::GTGT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss3981861471 NC_000020.11:13247525::GTGT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss5228933085 NC_000020.10:13228164::GTGTGT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427846, ss5787945901 NC_000020.11:13247517::GTGTGT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427847 NC_000020.11:13247517::GTGTGTGT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427848 NC_000020.11:13247517::GTGTGTGTGT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427849 NC_000020.11:13247517::GTGTGTGTGTGT NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
5907173703 NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
ss4335427858 NC_000020.11:13247517::GTGTGTGTGTG…

NC_000020.11:13247517::GTGTGTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

(self)
Removed from this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Destination RSIDs
ss3355469156 NC_000020.11:13247517::GTGTGTGTGTG…

NC_000020.11:13247517::GTGTGTGTGTGTGT

NC_000020.11:13247517:GTGTGTGTGTGT…

NC_000020.11:13247517:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

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 rs35224672

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.post820+afb47a3d