Variant #0000513898 (NC_000002.11:g.202093797C>T, NM_032977.3:c.*11333C>T (CASP10))

Chromosome 2
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.202093797C>T
DNA change (hg38) g.201229074C>T
Published as CASP10(NM_032974.4):c.1557C>T (p.S519=), CASP10(NM_032974.5):c.1557C>T (p.S519=)
ISCN -
DB-ID CASP8_000014 See all 2 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) 0.00047 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
CASP8 NM_001228.4 -?/. - c.-4672C>T r.(?) p.(=)
CASP10 NM_032977.3 -?/. - c.*11333C>T r.(=) p.(=)


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