Variant #0000605916 (NC_000001.10:g.68512460T>G, NM_004675.2:c.521A>C (DIRAS3))

Chromosome 1
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.68512460T>G
DNA change (hg38) g.68046777T>G
Published as DIRAS3(NM_004675.2):c.521A>C (p.(Asn174Thr))
ISCN -
DB-ID DIRAS3_000006
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-04 16:17:29 +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.521A>C r.(?) p.(Asn174Thr)
GNG12 NM_018841.5 -?/. - c.-213510A>C r.(?) p.(=)
WLS NM_024911.6 -?/. - c.*79449A>C r.(=) p.(=)
GNG12-AS1 NR_040077.1 -?/. - n.266+12014T>G r.(?) -


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