Variant #0000977555 (NC_000007.13:g.142989563A>G, NC_000007.13(NM_032982.3):c.393+3A>G (CASP2))

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.142989563A>G
DNA change (hg38) -
Published as CASP2(NM_032982.4):c.393+3A>G
ISCN -
DB-ID CASP2_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
CASP2 NM_032982.3 -?/. - c.393+3A>G r.spl? p.?
TMEM139 NM_153345.2 -?/. - c.*5641A>G r.(=) p.(=)


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