Variant #0000574879 (NC_000023.10:g.153660248G>C, NM_001183.4:c.361G>C (ATP6AP1))

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.153660248G>C
DNA change (hg38) g.154431902G>C
Published as ATP6AP1(NM_001183.5):c.361G>C (p.E121Q, p.(Glu121Gln)), ATP6AP1(NM_001183.6):c.361G>C (p.E121Q)
ISCN -
DB-ID ATP6AP1_000021 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) 0.00099 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
ATP6AP1 NM_001183.4 -?/. - c.361G>C r.(?) p.(Glu121Gln)


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