Variant #0000990093 (NC_000001.10:g.110091380T>C, NM_006496.3:c.38T>C (GNAI3))

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.110091380T>C
DNA change (hg38) -
Published as GNAI3(NM_006496.3):c.38T>C (p.(Val13Ala))
ISCN -
DB-ID GNAI3_000020
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAI3 NM_006496.3 ?/. - c.38T>C r.(?) p.(Val13Ala)
GPR61 NM_031936.4 ?/. - c.*3709T>C r.(=) p.(=)


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