Variant #0001036379 (NC_000007.13:g.43687110G>A, NC_000007.13(NM_018224.3):c.115+24C>T (COA1))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43687110G>A
DNA change (hg38) -
Published as COA1(NM_001321202.2):c.139C>T (p.(Arg47Trp))
ISCN -
DB-ID COA1_000003
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) 0.00307 View details
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     
STK17A NM_004760.2 -?/. - c.*22669G>A r.(=) p.(=)
COA1 NM_018224.3 -?/. - c.115+24C>T r.(=) p.(=)


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