Variant #0000549891 (NC_000013.10:g.114538594C>T, NM_000820.2:c.604G>A (GAS6))

Chromosome 13
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.114538594C>T
DNA change (hg38) g.113835621C>T
Published as GAS6(NM_000820.2):c.604G>A (p.(Ala202Thr))
ISCN -
DB-ID GAS6_000008
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) 7.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
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.604G>A r.(?) p.(Ala202Thr)
GAS6-AS1 NR_044995.2 -?/. - n.251+857C>T r.(?) -


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