Variant #0001044554 (NC_012920.1:m.8010T>C, NC_012920.1(ATP6_v001):c.-517T>C (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.8010T>C
DNA change (hg38) -
Published as MT-CO2(ENST00000361739.1):c.425T>C (p.(Val142Ala))
ISCN -
DB-ID MT-CO1_000011
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     
MT-ATP6 NC_012920.1(ATP6_v001) ?/. - c.-517T>C r.(?) p.(=)
MT-CO1 NC_012920.1(COX1_v001) ?/. - c.*565T>C r.(=) p.(=)
MT-CO2 NC_012920.1(COX2_v001) ?/. - c.425T>C r.(?) p.(Val142Ala)
MT-CO3 NC_012920.1(COX3_v001) ?/. - c.-1197T>C r.(?) p.(=)
MT-CYB NC_012920.1(CYTB_v001) ?/. - c.-6737T>C r.(?) p.(=)
MT-ND1 NC_012920.1(ND1_v001) ?/. - c.*3748T>C r.(=) p.(=)
MT-ND2 NC_012920.1(ND2_v001) ?/. - c.*2499T>C r.(=) p.(=)
MT-ND3 NC_012920.1(ND3_v001) ?/. - c.-2049T>C r.(?) p.(=)
MT-ND4 NC_012920.1(ND4_v001) ?/. - c.-2750T>C r.(?) p.(=)
MT-ND5 NC_012920.1(ND5_v001) ?/. - c.-4327T>C r.(?) p.(=)


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