Variant #0000622842 (NC_000012.11:g.21331398_21331403del, NC_000012.11(NM_006446.4):c.482-112_482-107del (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.21331398_21331403del |
DNA change (hg38) |
g.21178464_21178469del |
Published as |
SLCO1B1(NM_006446.5):c.482-112_482-107delCTTGTA |
ISCN |
- |
DB-ID |
SLCO1B1_000168 |
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) |
Retrieve |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-12-06 12:43:26 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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