Variant #0001035669 (NC_000006.11:g.31513212G>T, NM_130463.3:c.330C>A (ATP6V1G2))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31513212G>T
DNA change (hg38) -
Published as ATP6V1G2(NM_130463.4):c.330C>A (p.(Val110=))
ISCN -
DB-ID ATP6V1G2_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCCD1 NM_001011700.2 ?/. - c.*15500G>T r.(=) p.(=)
DDX39B NM_004640.6 ?/. - c.-3618C>A r.(?) p.(=)
NFKBIL1 NM_005007.3 ?/. - c.-2260G>T r.(?) p.(=)
ATP6V1G2 NM_130463.3 ?/. - c.330C>A r.(?) p.(=)
ATP6V1G2-DDX39B NR_037853.1 ?/. - n.472+674C>A r.(?) -


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