Variant #0000798747 (NC_000001.10:g.1271606G>A, NM_004421.2:c.1929C>T (DVL1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1271606G>A
DNA change (hg38) -
Published as DVL1(NM_001330311.2):c.2004C>T (p.A668=)
ISCN -
DB-ID TAS1R3_000021
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) 9.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DVL1 NM_004421.2 -?/. - c.1929C>T r.(?) p.(Ala643=)
TAS1R3 NM_152228.1 -?/. - c.*1762G>A r.(=) p.(=)


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