Variant #0001044552 (NC_012920.1:m.1494C>T, NC_012920.1(ATP6_v001):c.-7033C>T (MT-ATP6))

Chromosome M
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) m.1494C>T
DNA change (hg38) -
Published as MT-RNR1(NC_012920.1):m.1494C>T
ISCN -
DB-ID MT-CO1_000009
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 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.-7033C>T r.(?) p.(=)
MT-CO1 NC_012920.1(COX1_v001) +/. - c.-4410C>T r.(?) p.(=)
MT-CO2 NC_012920.1(COX2_v001) +/. - c.-6092C>T r.(?) p.(=)
MT-CO3 NC_012920.1(COX3_v001) +/. - c.-7713C>T r.(?) p.(=)
MT-CYB NC_012920.1(CYTB_v001) +/. - c.-13253C>T r.(?) p.(=)
MT-ND1 NC_012920.1(ND1_v001) +/. - c.-1813C>T r.(?) p.(=)
MT-ND2 NC_012920.1(ND2_v001) +/. - c.-2976C>T r.(?) p.(=)
MT-ND3 NC_012920.1(ND3_v001) +/. - c.-8565C>T r.(?) p.(=)
MT-ND4 NC_012920.1(ND4_v001) +/. - c.-9266C>T r.(?) p.(=)
MT-ND5 NC_012920.1(ND5_v001) +/. - c.-10843C>T r.(?) p.(=)


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