Variant #0000264642 (NC_000022.10:g.24109550T>C, CHCHD10(NM_213720.1):c.261+11A>G)

Chromosome 22
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) g.24109550T>C
DNA change (hg38) g.23767363T>C
Published as CHCHD10(NM_001301339.2):c.261+11A>G
ISCN -
DB-ID CHCHD10_000003 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.87759 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C22orf15 NM_182520.2 -/. - c.*1631T>C r.(=) p.(=)
CHCHD10 NM_213720.1 -/. - c.261+11A>G r.(=) p.(=)