Variant #0001013187 (NC_000001.10:g.110091339C>T, NM_006496.3:c.-4C>T (GNAI3))

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.110091339C>T
DNA change (hg38) -
Published as GNAI3(NM_006496.4):c.-4C>T
ISCN -
DB-ID GNAI3_000022
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) 0.00267 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 20:49:11 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAI3 NM_006496.3 -?/. - c.-4C>T r.(?) p.(=)
GPR61 NM_031936.4 -?/. - c.*3668C>T r.(=) p.(=)


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