Variant #0000259558 (NC_000013.10:g.52585445G>A, NM_000053.3:c.29C>T (ATP7B))

Chromosome 13
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.52585445G>A
DNA change (hg38) g.52011309G>A
Published as ATP7B(NM_000053.4):c.29C>T (p.A10V)
ISCN -
DB-ID ATP7B_000126
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP7B NM_000053.3 -?/. - c.29C>T r.(?) p.(Ala10Val)
ALG11 NM_001004127.2 -?/. - c.-1110G>A r.(?) p.(=)
UTP14C NM_021645.5 -?/. - c.-14115G>A r.(?) p.(=)


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