Variant #0000477902 (NC_012920.1:m.8584G>A, NC_012920.1(ATP6_v001):c.58G>A (MT-ATP6))

Chromosome M
Allele Maternal (inferred)
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.8584G>A
DNA change (hg38) m.8584G>A
Published as -
ISCN -
DB-ID MT-ATP6_000003
Variant remarks Variant Error [EBUILDMISMATCH]: This variant seems to mismatch; the genomic variants on hg19 and hg38 seem to not belong together. Please fix this entry and then remove this message.
Reference PubMed: International HapMap 3 Consortium2010
ClinVar ID -
dbSNP ID rs3135028
Origin Somatic
Segregation -
Frequency 12/90 (0.120)
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Raúl Cuauhtémoc Baptista Rosas
Database submission license No license selected
Created by Raúl Cuauhtémoc Baptista Rosas
Date created 2019-05-05 18:32:57 +02:00 (CEST)
Date last edited 2019-05-22 19:49:56 +02:00 (CEST)
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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.58G>A r.(?) -



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