Sequence Name | Change(s) |
---|---|
GRCh38.p7 chr 6 | NC_000006.12:g.44834981T>C |
GRCh37.p13 chr 6 | NC_000006.11:g.44802718T>C |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
SUPT3H transcript variant 3 | NM_001261823.1:c. | N/A | Intron Variant |
SUPT3H transcript variant 1 | NM_003599.3:c. | N/A | Intron Variant |
SUPT3H transcript variant 2 | NM_181356.2:c. | N/A | Intron Variant |
SUPT3H transcript variant X4 | XM_011514949.2:c. | N/A | Intron Variant |
SUPT3H transcript variant X6 | XM_011514950.1:c. | N/A | Intron Variant |
SUPT3H transcript variant X7 | XM_011514951.2:c. | N/A | Intron Variant |
SUPT3H transcript variant X8 | XM_011514952.2:c. | N/A | Intron Variant |
SUPT3H transcript variant X8 | XM_011514953.2:c. | N/A | Intron Variant |
SUPT3H transcript variant X10 | XM_011514954.2:c. | N/A | Intron Variant |
SUPT3H transcript variant X3 | XM_017011369.1:c. | N/A | Intron Variant |
SUPT3H transcript variant X5 | XM_017011370.1:c. | N/A | Intron Variant |
SUPT3H transcript variant X11 | XM_017011371.1:c. | N/A | Intron Variant |
SUPT3H transcript variant X14 | XM_017011372.1:c. | N/A | Intron Variant |
SUPT3H transcript variant X16 | XM_017011373.1:c. | N/A | Intron Variant |
SUPT3H transcript variant X21 | XM_017011374.1:c. | N/A | Intron Variant |
SUPT3H transcript variant X2 | XR_001743685.1:n. | N/A | Intron Variant |
SUPT3H transcript variant X12 | XR_001743686.1:n. | N/A | Intron Variant |
SUPT3H transcript variant X15 | XR_001743687.1:n. | N/A | Intron Variant |
SUPT3H transcript variant X13 | XR_001743688.1:n. | N/A | Intron Variant |
SUPT3H transcript variant X19 | XR_001743689.1:n. | N/A | Intron Variant |
SUPT3H transcript variant X17 | XR_001743691.1:n. | N/A | Intron Variant |
SUPT3H transcript variant X1 | XR_926319.2:n. | N/A | Intron Variant |
SUPT3H transcript variant X20 | XR_001743690.1:n. | N/A | Genic Downstream Transcript Variant |
SUPT3H transcript variant X18 | XR_001743692.1:n. | N/A | Genic Downstream Transcript Variant |
SUPT3H transcript variant X10 | XR_926320.1:n. | N/A | Genic Downstream Transcript Variant |
SUPT3H transcript variant X14 | XR_926321.1:n. | N/A | Genic Downstream Transcript Variant |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
LOC107986600 transcript | XR_001744142.1:n....XR_001744142.1:n.3963T>C | T>C | Non Coding Transcript Variant |
Study | Population | Group | Sample # | Ref Allele | Alt Allele |
---|---|---|---|---|---|
1000Genomes | African | Sub | 1322 | T=0.754 | C=0.246 |
1000Genomes | American | Sub | 694 | T=0.920 | C=0.080 |
1000Genomes | East Asian | Sub | 1008 | T=0.996 | C=0.004 |
1000Genomes | Europe | Sub | 1006 | T=0.952 | C=0.048 |
1000Genomes | Global | Study-wide | 5008 | T=0.904 | C=0.096 |
1000Genomes | South Asian | Sub | 978 | T=0.950 | C=0.050 |
The Avon Longitudinal Study of Parents and Children | PARENT AND CHILD COHORT | Study-wide | 3854 | T=0.961 | C=0.039 |
The Genome Aggregation Database | African | Sub | 8702 | T=0.810 | C=0.190 |
The Genome Aggregation Database | American | Sub | 838 | T=0.890 | C=0.110 |
The Genome Aggregation Database | East Asian | Sub | 1616 | T=0.999 | C=0.001 |
The Genome Aggregation Database | Europe | Sub | 18484 | T=0.959 | C=0.040 |
The Genome Aggregation Database | Global | Study-wide | 29942 | T=0.916 | C=0.083 |
The Genome Aggregation Database | Other | Sub | 302 | T=0.970 | C=0.030 |
Trans-Omics for Precision Medicine | Global | Study-wide | 29118 | T=0.893 | C=0.107 |
UK 10K study - Twins | TWIN COHORT | Study-wide | 3708 | T=0.970 | C=0.030 |
PMID | Title | Author | Journal |
---|---|---|---|
23953852 | Genome-wide association studies of maximum number of drinks. | Pan Y | J Psychiatr Res |
SNP ID | p-value | Traits | Study |
---|---|---|---|
rs9463046 | 1.62E-05 | alcohol consumption | 23953852 |
Position (v37) | eGene | GeneID | Variant | p-value | TSS | Tissue | |
---|---|---|---|---|---|---|---|
There is no eQTL annotation for this SNP |
Probe ID | Position | Gene | beta | p-value | |||
---|---|---|---|---|---|---|---|
There is no meQTL annotation for this SNP |
There is no significant Hi-C chromatin interaction data for this SNP.
Chromosome | Start | End | Region | Distance ( -/+ : Up/Downstream ) |
---|---|---|---|---|
chr6 | 44810308 | 44811350 | E069 | 7590 |
chr6 | 44823596 | 44824311 | E070 | 20878 |
chr6 | 44824366 | 44824465 | E070 | 21648 |
chr6 | 44825639 | 44825910 | E070 | 22921 |
chr6 | 44825922 | 44826044 | E070 | 23204 |
chr6 | 44826727 | 44826785 | E070 | 24009 |
chr6 | 44826864 | 44827997 | E070 | 24146 |
chr6 | 44767847 | 44768497 | E071 | -34221 |
chr6 | 44823596 | 44824311 | E073 | 20878 |
chr6 | 44824366 | 44824465 | E073 | 21648 |
chr6 | 44810308 | 44811350 | E074 | 7590 |
chr6 | 44811613 | 44811657 | E074 | 8895 |
chr6 | 44811774 | 44811883 | E074 | 9056 |
chr6 | 44823596 | 44824311 | E081 | 20878 |
chr6 | 44824366 | 44824465 | E081 | 21648 |
chr6 | 44824366 | 44824465 | E082 | 21648 |
chr6 | 44825639 | 44825910 | E082 | 22921 |
chr6 | 44825922 | 44826044 | E082 | 23204 |
chr6 | 44826727 | 44826785 | E082 | 24009 |