Variant #0000288216 (NC_000013.10:g.114542724del, NM_000820.2:c.449del (GAS6))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.114542724del
DNA change (hg38) g.113839751del
Published as GAS6(NM_000820.3):c.449delG (p.G150Afs*49)
ISCN -
DB-ID GAS6_000003
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 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     
GAS6 NM_000820.2 ?/. - c.449del r.(?) p.(Gly150AlafsTer49)
GAS6-AS1 NR_044995.2 ?/. - n.422+1504del r.(?) -


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