Variant #0001031152 (NC_000001.10:g.1271648dup, NM_004421.2:c.1893dup (DVL1))

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.1271648dup
DNA change (hg38) -
Published as DVL1(NM_001330311.2):c.1968dup (p.(Pro657Alafs*50))
ISCN -
DB-ID TAS1R3_000042
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DVL1 NM_004421.2 ?/. - c.1893dup r.(?) p.(Pro632Alafs*50)
TAS1R3 NM_152228.1 ?/. - c.*1804dup r.(?) p.(=)


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