Variant #0000323823 (NC_000014.8:g.93398849G>A, NM_014216.4:c.*9057C>T (ITPK1))

Chromosome 14
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.93398849G>A
DNA change (hg38) g.92932504G>A
Published as CHGA(NM_001275.3):c.943G>A (p.(Gly315Ser))
ISCN -
DB-ID CHGA_000001
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) 0.01899 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHGA NM_001275.3 -?/. - c.943G>A r.(?) p.(Gly315Ser)
ITPK1 NM_014216.4 -?/. - c.*9057C>T r.(=) p.(=)


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