Variant #0000621888 (NC_000007.13:g.43684847T>C, NC_000007.13(NM_018224.3):c.264+3A>G (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.43684847T>C
DNA change (hg38) g.43645248T>C
Published as COA1(NM_001350927.2):c.264+3A>G
ISCN -
DB-ID COA1_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) 0.00073 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK17A NM_004760.2 -?/. - c.*20406T>C r.(=) p.(=)
COA1 NM_018224.3 -?/. - c.264+3A>G r.spl? p.?


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