Variant #0000288215 (NC_000013.10:g.114524966C>T, NM_000820.2:c.1847G>A (GAS6))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.114524966C>T
DNA change (hg38) g.113821993C>T
Published as GAS6(NM_000820.3):c.1847G>A (p.R616Q)
ISCN -
DB-ID GAS6_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) 0.0016 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 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.1847G>A r.(?) p.(Arg616Gln)
GAS6-AS1 NR_044995.2 -/. - n.82+6302C>T r.(?) -


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