Variant #0000296012 (NC_000012.11:g.21331549T>C, NM_006446.4:c.521T>C (SLCO1B1))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.21331549T>C |
DNA change (hg38) |
g.21178615T>C |
Published as |
SLCO1B1(NM_006446.4):c.521T>C (p.V174A), SLCO1B1(NM_006446.5):c.521T>C (p.V174A) |
ISCN |
- |
DB-ID |
SLCO1B1_000001 See all 58 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.13262 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|