Variant #0000508378 (NC_000001.10:g.7724697C>T, NM_015215.2:c.2090C>T (CAMTA1))

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.7724697C>T
DNA change (hg38) g.7664637C>T
Published as CAMTA1(NM_015215.3):c.2090C>T (p.A697V), CAMTA1(NM_015215.4):c.2090C>T (p.A697V)
ISCN -
DB-ID CAMTA1_000014 See all 2 reported entries
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) 0.00099 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAMTA1 NM_015215.2 -?/. - c.2090C>T r.(?) p.(Ala697Val)


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