Variant #0000927439 (NC_012920.1:m.14905G>A, NC_012920.1(ATP6_v001):c.*5698G>A (MT-ATP6))

Chromosome M
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) m.14905G>A
DNA change (hg38) -
Published as MT-CYB(NC_012920.1):m.14905G>A (p.M53=)
ISCN -
DB-ID MT-CO1_000007
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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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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.*5698G>A r.(=) p.(=)
MT-CO1 NC_012920.1(COX1_v001) -/. - c.*7460G>A r.(=) p.(=)
MT-CO2 NC_012920.1(COX2_v001) -/. - c.*6636G>A r.(=) p.(=)
MT-CO3 NC_012920.1(COX3_v001) -/. - c.*4915G>A r.(=) p.(=)
MT-CYB NC_012920.1(CYTB_v001) -/. - c.159G>A r.(?) p.?
MT-ND1 NC_012920.1(ND1_v001) -/. - c.*10643G>A r.(=) p.(=)
MT-ND2 NC_012920.1(ND2_v001) -/. - c.*9394G>A r.(=) p.(=)
MT-ND3 NC_012920.1(ND3_v001) -/. - c.*4501G>A r.(=) p.(=)
MT-ND4 NC_012920.1(ND4_v001) -/. - c.*2768G>A r.(=) p.(=)
MT-ND5 NC_012920.1(ND5_v001) -/. - c.*757G>A r.(=) p.(=)


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