Variant #0000974114 (NC_000001.10:g.7826544G>A, NM_015215.2:c.5015G>A (CAMTA1))

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.7826544G>A
DNA change (hg38) -
Published as CAMTA1(NM_015215.4):c.5015G>A (p.(Gly1672Glu))
ISCN -
DB-ID CAMTA1_000121
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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VAMP3 NM_004781.3 ?/. - c.-4900G>A r.(?) p.(=)
CAMTA1 NM_015215.2 ?/. - c.5015G>A r.(?) p.(Gly1672Glu)


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