Variant #0001049853 (NC_000001.10:g.1273609_1273610insGG, NC_000001.10(NM_004421.2):c.1432+39_1432+40insCC (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.1273609_1273610insGG
DNA change (hg38) -
Published as DVL1(NM_001330311.2):c.1507+39_1507+40insCC
ISCN -
DB-ID TAS1R3_000049
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DVL1 NM_004421.2 ?/. - c.1432+39_1432+40insCC r.(=) p.(=)
TAS1R3 NM_152228.1 ?/. - c.*3765_*3766insGG r.(=) p.(=)


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