Variant #0000320503 (NC_000001.10:g.6639166_6639167del, NM_138697.3:c.2048_2049del (TAS1R1))

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.6639166_6639167del
DNA change (hg38) g.6579106_6579107del
Published as TAS1R1(NM_138697.3):c.2046_2047del (p.(Val683AspfsTer24))
ISCN -
DB-ID TAS1R1_000004
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB48 NM_005341.2 ?/. - c.-1100_-1099del r.(?) p.(=)
TAS1R1 NM_138697.3 ?/. - c.2048_2049del r.(?) p.(Val683AspfsTer24)


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