Variant #0000320858 (NC_000001.10:g.68512625G>C, NM_004675.2:c.356C>G (DIRAS3))

Chromosome 1
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.68512625G>C
DNA change (hg38) g.68046942G>C
Published as DIRAS3(NM_004675.2):c.356C>G (p.(Thr119Ser))
ISCN -
DB-ID DIRAS3_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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-04 16:17:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DIRAS3 NM_004675.2 ?/. - c.356C>G r.(?) p.(Thr119Ser)
GNG12 NM_018841.5 ?/. - c.-213675C>G r.(?) p.(=)
WLS NM_024911.6 ?/. - c.*79284C>G r.(=) p.(=)
GNG12-AS1 NR_040077.1 ?/. - n.266+12179G>C r.(?) -


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