Variant #0000865038 (NC_000016.9:g.90097734G>T, NM_001481.2:c.118G>T (GAS8))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.90097734G>T
DNA change (hg38) -
Published as GAS8(NM_001286209.1):c.43G>T (p.E15*)
ISCN -
DB-ID C16orf3_000014
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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     
C16orf3 NM_001214.3 +/. - c.-1984C>A r.(?) p.(=)
GAS8 NM_001481.2 +/. - c.118G>T r.(?) p.(Glu40*)


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