Variant #0000850187 (NC_000003.11:g.183888535G>A, NM_004423.3:c.2143G>A (DVL3))

Chromosome 3
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.183888535G>A
DNA change (hg38) -
Published as DVL3(NM_004423.4):c.2143G>A (p.V715M)
ISCN -
DB-ID AP2M1_000006
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP2M1 NM_004068.3 ?/. - c.-4256G>A r.(?) p.(=)
DVL3 NM_004423.3 ?/. - c.2143G>A r.(?) p.(Val715Met)


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