Variant #0000256288 (NC_000010.10:g.7830171A>G, NM_005174.2:c.1A>G (ATP5C1))

Chromosome 10
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) g.7830171A>G
DNA change (hg38) g.7788208A>G
Published as ATP5F1C(NM_001001973.3):c.1A>G (p.M1?)
ISCN -
DB-ID ATP5C1_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-26 13:28:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP5C1 NM_005174.2 ?/. - c.1A>G r.(?) p.(Met1?)
KIN NM_012311.3 ?/. - c.-275T>C r.(?) p.(=)


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