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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.

rs761607951

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr3:101561335-101561361 (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(T)16 / del(T)15 / del(T)14 / d…

del(T)16 / del(T)15 / del(T)14 / del(T)13 / del(T)12 / del(T)11 / del(T)10 / del(T)9 / del(T)8 / del(T)7 / del(T)6 / del(T)5 / del(T)4 / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)4 / dup(T)5 / dup(T)6 / dup(T)7 / dup(T)8 / dup(T)9 / dup(T)10 / dup(T)11 / dup(T)12 / dup(T)13 / dup(T)14 / dup(T)15 / dup(T)16 / dup(T)18 / dup(T)19 / dup(T)20 / dup(T)21 / dup(T)22 / dup(T)23 / dup(T)24 / dup(T)25 / dup(T)27 / ins(T)28 / ins(T)29 / ins(T)30 / ins(T)31 / ins(T)33 / ins(T)34 / ins(T)35 / ins(T)36 / ins(T)37 / ins(T)38 / ins(T)39

Variation Type
Indel Insertion and Deletion
Frequency
dupTT=0.1425 (765/5368, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TRMT10C : 2KB Upstream 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 5368 TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.6855 TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0067, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.1425, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0073, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0503, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.1023, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0054, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000 0.838784 0.154307 0.006909 32
European Sub 4804 TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.6499 TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0071, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.1592, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0081, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0560, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.1137, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0060, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000 0.815011 0.177061 0.007928 32
African Sub 468 TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000 TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A
African Others Sub 20 TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
African American Sub 448 TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000 TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A
Asian Sub 0 TTTTTTTTTTTTTTTTTTTTTTTTTTT=0 TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0 0 0 0 N/A
East Asian Sub 0 TTTTTTTTTTTTTTTTTTTTTTTTTTT=0 TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0 0 0 0 N/A
Other Asian Sub 0 TTTTTTTTTTTTTTTTTTTTTTTTTTT=0 TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0 0 0 0 N/A
Latin American 1 Sub 10 TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0 TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0 1.0 0.0 0.0 N/A
Latin American 2 Sub 28 TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
South Asian Sub 4 TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0 TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0 1.0 0.0 0.0 N/A
Other Sub 54 TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.89 TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.06, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A


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 5368 (T)27=0.6855 del(T)16=0.0000, del(T)15=0.0000, del(T)14=0.0000, del(T)13=0.0000, del(T)12=0.0000, del(T)11=0.0000, del(T)10=0.0000, del(T)9=0.0000, del(T)8=0.0000, del(T)7=0.0000, del(T)6=0.0000, del(T)5=0.0000, del(T)4=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0067, dupTT=0.1425, dupTTT=0.0503, dup(T)4=0.1023, dup(T)5=0.0054, dup(T)6=0.0000, dup(T)7=0.0000, dup(T)9=0.0000, dup(T)16=0.0073
Allele Frequency Aggregator European Sub 4804 (T)27=0.6499 del(T)16=0.0000, del(T)15=0.0000, del(T)14=0.0000, del(T)13=0.0000, del(T)12=0.0000, del(T)11=0.0000, del(T)10=0.0000, del(T)9=0.0000, del(T)8=0.0000, del(T)7=0.0000, del(T)6=0.0000, del(T)5=0.0000, del(T)4=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0071, dupTT=0.1592, dupTTT=0.0560, dup(T)4=0.1137, dup(T)5=0.0060, dup(T)6=0.0000, dup(T)7=0.0000, dup(T)9=0.0000, dup(T)16=0.0081
Allele Frequency Aggregator African Sub 468 (T)27=1.000 del(T)16=0.000, del(T)15=0.000, del(T)14=0.000, del(T)13=0.000, del(T)12=0.000, del(T)11=0.000, del(T)10=0.000, del(T)9=0.000, del(T)8=0.000, del(T)7=0.000, del(T)6=0.000, del(T)5=0.000, del(T)4=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)4=0.000, dup(T)5=0.000, dup(T)6=0.000, dup(T)7=0.000, dup(T)9=0.000, dup(T)16=0.000
Allele Frequency Aggregator Other Sub 54 (T)27=0.89 del(T)16=0.00, del(T)15=0.00, del(T)14=0.00, del(T)13=0.00, del(T)12=0.00, del(T)11=0.00, del(T)10=0.00, del(T)9=0.00, del(T)8=0.00, del(T)7=0.00, del(T)6=0.00, del(T)5=0.00, del(T)4=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.04, dupTT=0.00, dupTTT=0.02, dup(T)4=0.06, dup(T)5=0.00, dup(T)6=0.00, dup(T)7=0.00, dup(T)9=0.00, dup(T)16=0.00
Allele Frequency Aggregator Latin American 2 Sub 28 (T)27=1.00 del(T)16=0.00, del(T)15=0.00, del(T)14=0.00, del(T)13=0.00, del(T)12=0.00, del(T)11=0.00, del(T)10=0.00, del(T)9=0.00, del(T)8=0.00, del(T)7=0.00, del(T)6=0.00, del(T)5=0.00, del(T)4=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)4=0.00, dup(T)5=0.00, dup(T)6=0.00, dup(T)7=0.00, dup(T)9=0.00, dup(T)16=0.00
Allele Frequency Aggregator Latin American 1 Sub 10 (T)27=1.0 del(T)16=0.0, del(T)15=0.0, del(T)14=0.0, del(T)13=0.0, del(T)12=0.0, del(T)11=0.0, del(T)10=0.0, del(T)9=0.0, del(T)8=0.0, del(T)7=0.0, del(T)6=0.0, del(T)5=0.0, del(T)4=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)4=0.0, dup(T)5=0.0, dup(T)6=0.0, dup(T)7=0.0, dup(T)9=0.0, dup(T)16=0.0
Allele Frequency Aggregator South Asian Sub 4 (T)27=1.0 del(T)16=0.0, del(T)15=0.0, del(T)14=0.0, del(T)13=0.0, del(T)12=0.0, del(T)11=0.0, del(T)10=0.0, del(T)9=0.0, del(T)8=0.0, del(T)7=0.0, del(T)6=0.0, del(T)5=0.0, del(T)4=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)4=0.0, dup(T)5=0.0, dup(T)6=0.0, dup(T)7=0.0, dup(T)9=0.0, dup(T)16=0.0
Allele Frequency Aggregator Asian Sub 0 (T)27=0 del(T)16=0, del(T)15=0, del(T)14=0, del(T)13=0, del(T)12=0, del(T)11=0, del(T)10=0, del(T)9=0, del(T)8=0, del(T)7=0, del(T)6=0, del(T)5=0, del(T)4=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)4=0, dup(T)5=0, dup(T)6=0, dup(T)7=0, dup(T)9=0, dup(T)16=0
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 3 NC_000003.12:g.101561346_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561347_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561348_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561349_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561350_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561351_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561352_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561353_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561354_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561355_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561356_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561357_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561358_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561359_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561360_101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561361del
GRCh38.p14 chr 3 NC_000003.12:g.101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561360_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561359_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561358_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561357_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561356_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561355_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561354_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561353_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561352_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561351_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561350_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561349_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561348_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561347_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561346_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561344_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561343_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561342_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561341_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561340_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561339_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561338_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561337_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561335_101561361dup
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3 NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280190_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280191_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280192_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280193_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280194_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280195_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280196_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280197_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280198_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280199_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280200_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280201_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280202_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280203_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280204_101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280205del
GRCh37.p13 chr 3 NC_000003.11:g.101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280204_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280203_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280202_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280201_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280200_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280199_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280198_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280197_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280196_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280195_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280194_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280193_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280192_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280191_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280190_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280188_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280187_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280186_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280185_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280184_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280183_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280182_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280181_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280179_101280205dup
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4511_4526del
TRMT10C RefSeqGene NG_050898.1:g.4512_4526del
TRMT10C RefSeqGene NG_050898.1:g.4513_4526del
TRMT10C RefSeqGene NG_050898.1:g.4514_4526del
TRMT10C RefSeqGene NG_050898.1:g.4515_4526del
TRMT10C RefSeqGene NG_050898.1:g.4516_4526del
TRMT10C RefSeqGene NG_050898.1:g.4517_4526del
TRMT10C RefSeqGene NG_050898.1:g.4518_4526del
TRMT10C RefSeqGene NG_050898.1:g.4519_4526del
TRMT10C RefSeqGene NG_050898.1:g.4520_4526del
TRMT10C RefSeqGene NG_050898.1:g.4521_4526del
TRMT10C RefSeqGene NG_050898.1:g.4522_4526del
TRMT10C RefSeqGene NG_050898.1:g.4523_4526del
TRMT10C RefSeqGene NG_050898.1:g.4524_4526del
TRMT10C RefSeqGene NG_050898.1:g.4525_4526del
TRMT10C RefSeqGene NG_050898.1:g.4526del
TRMT10C RefSeqGene NG_050898.1:g.4526dup
TRMT10C RefSeqGene NG_050898.1:g.4525_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4524_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4523_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4522_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4521_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4520_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4519_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4518_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4517_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4516_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4515_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4514_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4513_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4512_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4511_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4509_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4508_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4507_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4506_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4505_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4504_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4503_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4502_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4500_4526dup
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene: TRMT10C, tRNA methyltransferase 10C, mitochondrial RNase P subunit (plus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
TRMT10C transcript NM_017819.4:c. N/A Upstream Transcript Variant
Help

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

Not Reported in ClinVar
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)27= del(T)16 del(T)15 del(T)14 del(T)13 del(T)12 del(T)11 del(T)10 del(T)9 del(T)8 del(T)7 del(T)6 del(T)5 del(T)4 delTTT delTT delT dupT dupTT dupTTT dup(T)4 dup(T)5 dup(T)6 dup(T)7 dup(T)8 dup(T)9 dup(T)10 dup(T)11 dup(T)12 dup(T)13 dup(T)14 dup(T)15 dup(T)16 dup(T)18 dup(T)19 dup(T)20 dup(T)21 dup(T)22 dup(T)23 dup(T)24 dup(T)25 dup(T)27 ins(T)28 ins(T)29 ins(T)30 ins(T)31 ins(T)33 ins(T)34 ins(T)35 ins(T)36 ins(T)37 ins(T)38 ins(T)39
GRCh38.p14 chr 3 NC_000003.12:g.101561335_101561361= NC_000003.12:g.101561346_101561361del NC_000003.12:g.101561347_101561361del NC_000003.12:g.101561348_101561361del NC_000003.12:g.101561349_101561361del NC_000003.12:g.101561350_101561361del NC_000003.12:g.101561351_101561361del NC_000003.12:g.101561352_101561361del NC_000003.12:g.101561353_101561361del NC_000003.12:g.101561354_101561361del NC_000003.12:g.101561355_101561361del NC_000003.12:g.101561356_101561361del NC_000003.12:g.101561357_101561361del NC_000003.12:g.101561358_101561361del NC_000003.12:g.101561359_101561361del NC_000003.12:g.101561360_101561361del NC_000003.12:g.101561361del NC_000003.12:g.101561361dup NC_000003.12:g.101561360_101561361dup NC_000003.12:g.101561359_101561361dup NC_000003.12:g.101561358_101561361dup NC_000003.12:g.101561357_101561361dup NC_000003.12:g.101561356_101561361dup NC_000003.12:g.101561355_101561361dup NC_000003.12:g.101561354_101561361dup NC_000003.12:g.101561353_101561361dup NC_000003.12:g.101561352_101561361dup NC_000003.12:g.101561351_101561361dup NC_000003.12:g.101561350_101561361dup NC_000003.12:g.101561349_101561361dup NC_000003.12:g.101561348_101561361dup NC_000003.12:g.101561347_101561361dup NC_000003.12:g.101561346_101561361dup NC_000003.12:g.101561344_101561361dup NC_000003.12:g.101561343_101561361dup NC_000003.12:g.101561342_101561361dup NC_000003.12:g.101561341_101561361dup NC_000003.12:g.101561340_101561361dup NC_000003.12:g.101561339_101561361dup NC_000003.12:g.101561338_101561361dup NC_000003.12:g.101561337_101561361dup NC_000003.12:g.101561335_101561361dup NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3 NC_000003.11:g.101280179_101280205= NC_000003.11:g.101280190_101280205del NC_000003.11:g.101280191_101280205del NC_000003.11:g.101280192_101280205del NC_000003.11:g.101280193_101280205del NC_000003.11:g.101280194_101280205del NC_000003.11:g.101280195_101280205del NC_000003.11:g.101280196_101280205del NC_000003.11:g.101280197_101280205del NC_000003.11:g.101280198_101280205del NC_000003.11:g.101280199_101280205del NC_000003.11:g.101280200_101280205del NC_000003.11:g.101280201_101280205del NC_000003.11:g.101280202_101280205del NC_000003.11:g.101280203_101280205del NC_000003.11:g.101280204_101280205del NC_000003.11:g.101280205del NC_000003.11:g.101280205dup NC_000003.11:g.101280204_101280205dup NC_000003.11:g.101280203_101280205dup NC_000003.11:g.101280202_101280205dup NC_000003.11:g.101280201_101280205dup NC_000003.11:g.101280200_101280205dup NC_000003.11:g.101280199_101280205dup NC_000003.11:g.101280198_101280205dup NC_000003.11:g.101280197_101280205dup NC_000003.11:g.101280196_101280205dup NC_000003.11:g.101280195_101280205dup NC_000003.11:g.101280194_101280205dup NC_000003.11:g.101280193_101280205dup NC_000003.11:g.101280192_101280205dup NC_000003.11:g.101280191_101280205dup NC_000003.11:g.101280190_101280205dup NC_000003.11:g.101280188_101280205dup NC_000003.11:g.101280187_101280205dup NC_000003.11:g.101280186_101280205dup NC_000003.11:g.101280185_101280205dup NC_000003.11:g.101280184_101280205dup NC_000003.11:g.101280183_101280205dup NC_000003.11:g.101280182_101280205dup NC_000003.11:g.101280181_101280205dup NC_000003.11:g.101280179_101280205dup NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TRMT10C RefSeqGene NG_050898.1:g.4500_4526= NG_050898.1:g.4511_4526del NG_050898.1:g.4512_4526del NG_050898.1:g.4513_4526del NG_050898.1:g.4514_4526del NG_050898.1:g.4515_4526del NG_050898.1:g.4516_4526del NG_050898.1:g.4517_4526del NG_050898.1:g.4518_4526del NG_050898.1:g.4519_4526del NG_050898.1:g.4520_4526del NG_050898.1:g.4521_4526del NG_050898.1:g.4522_4526del NG_050898.1:g.4523_4526del NG_050898.1:g.4524_4526del NG_050898.1:g.4525_4526del NG_050898.1:g.4526del NG_050898.1:g.4526dup NG_050898.1:g.4525_4526dup NG_050898.1:g.4524_4526dup NG_050898.1:g.4523_4526dup NG_050898.1:g.4522_4526dup NG_050898.1:g.4521_4526dup NG_050898.1:g.4520_4526dup NG_050898.1:g.4519_4526dup NG_050898.1:g.4518_4526dup NG_050898.1:g.4517_4526dup NG_050898.1:g.4516_4526dup NG_050898.1:g.4515_4526dup NG_050898.1:g.4514_4526dup NG_050898.1:g.4513_4526dup NG_050898.1:g.4512_4526dup NG_050898.1:g.4511_4526dup NG_050898.1:g.4509_4526dup NG_050898.1:g.4508_4526dup NG_050898.1:g.4507_4526dup NG_050898.1:g.4506_4526dup NG_050898.1:g.4505_4526dup NG_050898.1:g.4504_4526dup NG_050898.1:g.4503_4526dup NG_050898.1:g.4502_4526dup NG_050898.1:g.4500_4526dup NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
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#.

80 SubSNP, 57 Frequency submissions
No Submitter Submission ID Date (Build)
1 ABI ss41881273 Oct 12, 2018 (152)
2 HUMANGENOME_JCVI ss95326061 Oct 12, 2018 (152)
3 SSMP ss663338767 Apr 01, 2015 (144)
4 SWEGEN ss2992860794 Nov 08, 2017 (151)
5 SWEGEN ss2992860795 Nov 08, 2017 (151)
6 SWEGEN ss2992860796 Nov 08, 2017 (151)
7 SWEGEN ss2992860797 Nov 08, 2017 (151)
8 SWEGEN ss2992860798 Nov 08, 2017 (151)
9 SWEGEN ss2992860799 Nov 08, 2017 (151)
10 MCHAISSO ss3065895718 Nov 08, 2017 (151)
11 EVA_DECODE ss3709885498 Jul 13, 2019 (153)
12 EVA_DECODE ss3709885499 Jul 13, 2019 (153)
13 EVA_DECODE ss3709885500 Jul 13, 2019 (153)
14 EVA_DECODE ss3709885501 Jul 13, 2019 (153)
15 EVA_DECODE ss3709885502 Jul 13, 2019 (153)
16 PACBIO ss3784404954 Jul 13, 2019 (153)
17 EVA ss3827967694 Apr 25, 2020 (154)
18 GNOMAD ss4077231117 Apr 26, 2021 (155)
19 GNOMAD ss4077231119 Apr 26, 2021 (155)
20 GNOMAD ss4077231121 Apr 26, 2021 (155)
21 GNOMAD ss4077231124 Apr 26, 2021 (155)
22 GNOMAD ss4077231126 Apr 26, 2021 (155)
23 GNOMAD ss4077231127 Apr 26, 2021 (155)
24 GNOMAD ss4077231129 Apr 26, 2021 (155)
25 GNOMAD ss4077231132 Apr 26, 2021 (155)
26 GNOMAD ss4077231133 Apr 26, 2021 (155)
27 GNOMAD ss4077231134 Apr 26, 2021 (155)
28 GNOMAD ss4077231135 Apr 26, 2021 (155)
29 GNOMAD ss4077231150 Apr 26, 2021 (155)
30 GNOMAD ss4077231154 Apr 26, 2021 (155)
31 GNOMAD ss4077231159 Apr 26, 2021 (155)
32 GNOMAD ss4077231161 Apr 26, 2021 (155)
33 GNOMAD ss4077231170 Apr 26, 2021 (155)
34 GNOMAD ss4077231172 Apr 26, 2021 (155)
35 GNOMAD ss4077231173 Apr 26, 2021 (155)
36 GNOMAD ss4077231174 Apr 26, 2021 (155)
37 GNOMAD ss4077231175 Apr 26, 2021 (155)
38 GNOMAD ss4077231176 Apr 26, 2021 (155)
39 GNOMAD ss4077231177 Apr 26, 2021 (155)
40 GNOMAD ss4077231178 Apr 26, 2021 (155)
41 GNOMAD ss4077231179 Apr 26, 2021 (155)
42 GNOMAD ss4077231180 Apr 26, 2021 (155)
43 GNOMAD ss4077231181 Apr 26, 2021 (155)
44 GNOMAD ss4077231182 Apr 26, 2021 (155)
45 GNOMAD ss4077231183 Apr 26, 2021 (155)
46 GNOMAD ss4077231184 Apr 26, 2021 (155)
47 GNOMAD ss4077231185 Apr 26, 2021 (155)
48 GNOMAD ss4077231186 Apr 26, 2021 (155)
49 GNOMAD ss4077231187 Apr 26, 2021 (155)
50 GNOMAD ss4077231188 Apr 26, 2021 (155)
51 GNOMAD ss4077231189 Apr 26, 2021 (155)
52 GNOMAD ss4077231190 Apr 26, 2021 (155)
53 GNOMAD ss4077231192 Apr 26, 2021 (155)
54 GNOMAD ss4077231193 Apr 26, 2021 (155)
55 GNOMAD ss4077231194 Apr 26, 2021 (155)
56 GNOMAD ss4077231195 Apr 26, 2021 (155)
57 GNOMAD ss4077231196 Apr 26, 2021 (155)
58 GNOMAD ss4077231197 Apr 26, 2021 (155)
59 GNOMAD ss4077231198 Apr 26, 2021 (155)
60 GNOMAD ss4077231199 Apr 26, 2021 (155)
61 GNOMAD ss4077231200 Apr 26, 2021 (155)
62 GNOMAD ss4077231201 Apr 26, 2021 (155)
63 GNOMAD ss4077231202 Apr 26, 2021 (155)
64 GNOMAD ss4077231203 Apr 26, 2021 (155)
65 GNOMAD ss4077231204 Apr 26, 2021 (155)
66 GNOMAD ss4077231205 Apr 26, 2021 (155)
67 GNOMAD ss4077231206 Apr 26, 2021 (155)
68 GNOMAD ss4077231207 Apr 26, 2021 (155)
69 HUGCELL_USP ss5454530546 Oct 12, 2022 (156)
70 HUGCELL_USP ss5454530547 Oct 12, 2022 (156)
71 HUGCELL_USP ss5454530548 Oct 12, 2022 (156)
72 HUGCELL_USP ss5454530549 Oct 12, 2022 (156)
73 TOMMO_GENOMICS ss5693269476 Oct 12, 2022 (156)
74 TOMMO_GENOMICS ss5693269477 Oct 12, 2022 (156)
75 TOMMO_GENOMICS ss5693269478 Oct 12, 2022 (156)
76 TOMMO_GENOMICS ss5693269479 Oct 12, 2022 (156)
77 TOMMO_GENOMICS ss5693269480 Oct 12, 2022 (156)
78 EVA ss5826202662 Oct 12, 2022 (156)
79 EVA ss5826202663 Oct 12, 2022 (156)
80 EVA ss5826202664 Oct 12, 2022 (156)
81 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

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

Submission ignored due to conflicting rows:
Row 117823339 (NC_000003.12:101561334::T 2478/63310)
Row 117823341 (NC_000003.12:101561334::TT 19422/62830)
Row 117823343 (NC_000003.12:101561334::TTT 9148/63470)...

- Apr 26, 2021 (155)
132 14KJPN

Submission ignored due to conflicting rows:
Row 27106580 (NC_000003.12:101561334::TT 7522/27580)
Row 27106581 (NC_000003.12:101561334::TTT 1543/27580)
Row 27106582 (NC_000003.12:101561334:TTTTTTTTTT: 136/27580)...

- Oct 12, 2022 (156)
133 14KJPN

Submission ignored due to conflicting rows:
Row 27106580 (NC_000003.12:101561334::TT 7522/27580)
Row 27106581 (NC_000003.12:101561334::TTT 1543/27580)
Row 27106582 (NC_000003.12:101561334:TTTTTTTTTT: 136/27580)...

- Oct 12, 2022 (156)
134 14KJPN

Submission ignored due to conflicting rows:
Row 27106580 (NC_000003.12:101561334::TT 7522/27580)
Row 27106581 (NC_000003.12:101561334::TTT 1543/27580)
Row 27106582 (NC_000003.12:101561334:TTTTTTTTTT: 136/27580)...

- Oct 12, 2022 (156)
135 14KJPN

Submission ignored due to conflicting rows:
Row 27106580 (NC_000003.12:101561334::TT 7522/27580)
Row 27106581 (NC_000003.12:101561334::TTT 1543/27580)
Row 27106582 (NC_000003.12:101561334:TTTTTTTTTT: 136/27580)...

- Oct 12, 2022 (156)
136 14KJPN

Submission ignored due to conflicting rows:
Row 27106580 (NC_000003.12:101561334::TT 7522/27580)
Row 27106581 (NC_000003.12:101561334::TTT 1543/27580)
Row 27106582 (NC_000003.12:101561334:TTTTTTTTTT: 136/27580)...

- Oct 12, 2022 (156)
137 ALFA NC_000003.12 - 101561335 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss4077231207 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTT:

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

(self)
ss4077231206 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTT:

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT

(self)
ss4077231205 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTT:

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT

(self)
ss4077231204 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTT:

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

(self)
ss4077231203 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTT:

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
ss4077231202 NC_000003.12:101561334:TTTTTTTTTTT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

(self)
ss4077231201, ss5693269478 NC_000003.12:101561334:TTTTTTTTTT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss4077231200 NC_000003.12:101561334:TTTTTTTTT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

(self)
ss4077231199 NC_000003.12:101561334:TTTTTTTT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
ss4077231198 NC_000003.12:101561334:TTTTTTT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
ss4077231197 NC_000003.12:101561334:TTTTTT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231196 NC_000003.12:101561334:TTTTT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231195 NC_000003.12:101561334:TTTT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231194 NC_000003.12:101561334:TTT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231193 NC_000003.12:101561334:TT: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231192 NC_000003.12:101561334:T: NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss2992860798 NC_000003.11:101280178::T NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3709885498, ss4077231117, ss5454530547 NC_000003.12:101561334::T NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss95326061 NT_005612.16:7775351::T NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss2992860794, ss5826202662 NC_000003.11:101280178::TT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3065895718, ss3709885499, ss4077231119, ss5454530548, ss5693269476 NC_000003.12:101561334::TT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss41881273 NT_005612.16:7775351::TT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss2992860796, ss5826202663 NC_000003.11:101280178::TTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3709885500, ss4077231121, ss5454530549, ss5693269477 NC_000003.12:101561334::TTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss2992860797, ss3827967694, ss5826202664 NC_000003.11:101280178::TTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3709885501, ss4077231124, ss5454530546, ss5693269479 NC_000003.12:101561334::TTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss2992860799 NC_000003.11:101280178::TTTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3709885502, ss4077231126, ss5693269480 NC_000003.12:101561334::TTTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231127 NC_000003.12:101561334::TTTTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231129 NC_000003.12:101561334::TTTTTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231132 NC_000003.12:101561334::TTTTTTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231133 NC_000003.12:101561334::TTTTTTTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231134 NC_000003.12:101561334::TTTTTTTTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231135 NC_000003.12:101561334::TTTTTTTTTTT NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231150 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231154 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231159 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss663338767 NC_000003.11:101280178::TTTTTTTTTT…

NC_000003.11:101280178::TTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231161 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss2992860795 NC_000003.11:101280178::TTTTTTTTTT…

NC_000003.11:101280178::TTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
10258149770 NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231170 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231172 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3784404954 NC_000003.11:101280178::TTTTTTTTTT…

NC_000003.11:101280178::TTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231173 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231174 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231175 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231176 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231177 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231178 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231179 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231180 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231181 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231182 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231183 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231184 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231185 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231186 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231187 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231188 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231189 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4077231190 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
Removed from this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Destination RSIDs
ss3400143845 NC_000003.12:101561334::TTTTTTTTTT…

NC_000003.12:101561334::TTTTTTTTTTTTTTTT

NC_000003.12:101561334:TTTTTTTTTTT…

NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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 rs761607951

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