Variant #0000250709 (NC_000007.13:g.138434080del, NC_000007.13(NM_020632.2):c.1030-5del (ATP6V0A4))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.138434080del
DNA change (hg38) g.138749335del
Published as ATP6V0A4(NM_020632.2):c.1030-5del (p.?), ATP6V0A4(NM_020632.2):c.1030-5delT, ATP6V0A4(NM_020632.3):c.1030-5delT
ISCN -
DB-ID ATP6V0A4_000017 See all 4 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM213 NM_001085429.1 -/. - c.-48770del r.(?) p.(=)
ATP6V0A4 NM_020632.2 -/. - c.1030-5del r.spl? p.?


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