Variant #0000502856 (NC_000001.10:g.1269432C>A, NM_004421.2:c.*2090G>T (DVL1))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1269432C>A
DNA change (hg38) g.1334052C>A
Published as TAS1R3(NM_152228.1):c.2147C>A (p.(Thr716Lys))
ISCN -
DB-ID TAS1R3_000010
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) 0.00124 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DVL1 NM_004421.2 -/. - c.*2090G>T r.(=) p.(=)
TAS1R3 NM_152228.1 -/. - c.2147C>A r.(?) p.(Thr716Lys)


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