Variant #0000853585 (NC_000013.10:g.114535404G>A, NM_000820.2:c.1011C>T (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.114535404G>A
DNA change (hg38) -
Published as GAS6(NM_000820.3):c.1011C>T (p.A337=)
ISCN -
DB-ID GAS6_000013
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) 0.00015 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 2022-05-09 15:40:45 +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     
GAS6 NM_000820.2 -?/. - c.1011C>T r.(?) p.(Ala337=)
GAS6-AS1 NR_044995.2 -?/. - n.83-1061G>A r.(?) -


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