Variant #0000316219 (NC_000001.10:g.1268367G>A, NM_004421.2:c.*3155C>T (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.1268367G>A
DNA change (hg38) g.1332987G>A
Published as TAS1R3(NM_152228.3):c.1342G>A (p.G448R)
ISCN -
DB-ID TAS1R3_000005
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) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLTPD1 NM_001029885.1 ?/. - c.*5224G>A r.(=) p.(=)
DVL1 NM_004421.2 ?/. - c.*3155C>T r.(=) p.(=)
TAS1R3 NM_152228.1 ?/. - c.1342G>A r.(?) p.(Gly448Arg)


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