Variant #0000607384 (NC_000002.11:g.202074098G>A, NM_032977.3:c.1228G>A (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.202074098G>A
DNA change (hg38) g.201209375G>A
Published as CASP10(NM_001206524.1):c.1027G>A (p.(Val343Ile)), CASP10(NM_032977.3):c.1228G>A (p.V410I)
ISCN -
DB-ID CASP10_000010 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) 0.04222 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASP10 NM_032977.3 -?/. - c.1228G>A r.(?) p.(Val410Ile)


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