Variant #0000619910 (NC_000023.10:g.77301044G>C, NM_000052.5:c.4201G>C (ATP7A))

Chromosome X
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.77301044G>C
DNA change (hg38) g.78045547G>C
Published as ATP7A(NM_000052.5):c.4201G>C (p.(Val1401Leu)), ATP7A(NM_000052.6):c.4201G>C (p.V1401L), ATP7A(NM_000052.7):c.4201G>C (p.V1401L)
ISCN -
DB-ID PGAM4_000020 See all 3 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) 0.00123 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
ATP7A NM_000052.5 -?/. - c.4201G>C r.(?) p.(Val1401Leu) -
PGAM4 NM_001029891.2 -?/. - c.-75909C>G r.(?) p.(=) -


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