Variant #0000895611 (NC_000022.10:g.24109722G>A, NM_213720.1:c.100C>T (CHCHD10))

Chromosome 22
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.24109722G>A
DNA change (hg38) -
Published as CHCHD10(NM_001301339.1):c.100C>T (p.(Pro34Ser)), CHCHD10(NM_001301339.2):c.100C>T (p.P34S)
ISCN -
DB-ID CHCHD10_000008 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 -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00277 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C22orf15 NM_182520.2 -?/. - c.*1803G>A r.(=) p.(=)
CHCHD10 NM_213720.1 -?/. - c.100C>T r.(?) p.(Pro34Ser)


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