Variant #0000991401 (NC_000001.10:g.68512954C>G, NM_004675.2:c.27G>C (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.68512954C>G
DNA change (hg38) -
Published as DIRAS3(NM_004675.2):c.27G>C (p.(Lys9Asn))
ISCN -
DB-ID DIRAS3_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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     
DIRAS3 NM_004675.2 ?/. - c.27G>C r.(?) p.(Lys9Asn)
GNG12 NM_018841.5 ?/. - c.-214004G>C r.(?) p.(=)
WLS NM_024911.6 ?/. - c.*78955G>C r.(=) p.(=)
GNG12-AS1 NR_040077.1 ?/. - n.266+12508C>G r.(?) -


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