Variant #0000984896 (NC_012920.1:m.14279G>A, NC_012920.1(ATP6_v001):c.*5072G>A (MT-ATP6))

Chromosome M
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) m.14279G>A
DNA change (hg38) -
Published as MT-ND6(ENST00000361681.2):c.395C>T (p.(Ser132Leu))
ISCN -
DB-ID MT-CO1_000008
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 2024-04-19 20:27:30 +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     
MT-ATP6 NC_012920.1(ATP6_v001) ?/. - c.*5072G>A r.(=) p.(=)
MT-CO1 NC_012920.1(COX1_v001) ?/. - c.*6834G>A r.(=) p.(=)
MT-CO2 NC_012920.1(COX2_v001) ?/. - c.*6010G>A r.(=) p.(=)
MT-CO3 NC_012920.1(COX3_v001) ?/. - c.*4289G>A r.(=) p.(=)
MT-CYB NC_012920.1(CYTB_v001) ?/. - c.-468G>A r.(?) p.(=)
MT-ND1 NC_012920.1(ND1_v001) ?/. - c.*10017G>A r.(=) p.(=)
MT-ND2 NC_012920.1(ND2_v001) ?/. - c.*8768G>A r.(=) p.(=)
MT-ND3 NC_012920.1(ND3_v001) ?/. - c.*3875G>A r.(=) p.(=)
MT-ND4 NC_012920.1(ND4_v001) ?/. - c.*2142G>A r.(=) p.(=)
MT-ND5 NC_012920.1(ND5_v001) ?/. - c.*131G>A r.(=) p.(=)


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