Variant #0001049852 (NC_000001.10:g.1267644_1267656del, NM_004421.2:c.*3872_*3884del (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.1267644_1267656del
DNA change (hg38) -
Published as TAS1R3(NM_152228.3):c.733_745del (p.(Leu245Metfs*15))
ISCN -
DB-ID TAS1R3_000048
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 2025-11-01 13:22:20 +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     
GLTPD1 NM_001029885.1 ?/. - c.*4501_*4513del r.(=) p.(=)
DVL1 NM_004421.2 ?/. - c.*3872_*3884del r.(=) p.(=)
TAS1R3 NM_152228.1 ?/. - c.733_745del r.(?) p.(Leu245Metfs*15)


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