Variant #0001004212 (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) -
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP8B1 NM_005603.4 -?/. - c.234C>G r.(?) p.(His78Gln)


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