Variant #0000261289 (NC_000018.9:g.55373767G>C, NM_005603.4:c.234C>G (ATP8B1))
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.55373767G>C |
DNA change (hg38) |
g.57706535G>C |
Published as |
ATP8B1(NM_001374385.1):c.234C>G (p.(His78Gln)), ATP8B1(NM_005603.6):c.234C>G (p.H78Q) |
ISCN |
- |
DB-ID |
ATP8B1_000022 See all 2 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) |
0.00422 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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