Variant #0000571546 (NC_000022.10:g.24108450C>G, NM_213720.1:c.274G>C (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.24108450C>G
DNA change (hg38) g.23766263C>G
Published as CHCHD10(NM_001301339.2):c.295G>C (p.A99P)
ISCN -
DB-ID C22orf15_000002
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C22orf15 NM_182520.2 -?/. - c.*531C>G r.(=) p.(=)
CHCHD10 NM_213720.1 -?/. - c.274G>C r.(?) p.(Ala92Pro)


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