Variant #0000337188 (NC_000007.13:g.138447631C>G, NC_000007.13(NM_020632.2):c.417+14G>C (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.138447631C>G
DNA change (hg38) g.138762886C>G
Published as ATP6V0A4(NM_020632.3):c.417+14G>C
ISCN -
DB-ID ATP6V0A4_000019 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) 0.01171 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
TMEM213 NM_001085429.1 -/. - c.-35219C>G r.(?) p.(=)
ATP6V0A4 NM_020632.2 -/. - c.417+14G>C r.(=) p.(=)


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