Variant #0000973262 (NC_000001.10:g.1262302G>A, NM_004421.2:c.*9220C>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.1262302G>A
DNA change (hg38) -
Published as CPTP(NM_001029885.2):c.12G>A (p.(Ser4=))
ISCN -
DB-ID TAS1R3_000031
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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +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     
GLTPD1 NM_001029885.1 ?/. - c.12G>A r.(?) p.(=)
CPSF3L NM_001256456.1 ?/. - c.-2769C>T r.(?) p.(=)
DVL1 NM_004421.2 ?/. - c.*9220C>T r.(=) p.(=)
TAS1R3 NM_152228.1 ?/. - c.-4424G>A r.(?) p.(=)
PUSL1 NM_153339.1 ?/. - c.*15543G>A r.(=) p.(=)


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