Variant #0000548816 (NC_000012.11:g.58135794_58135795dup, NM_014770.3:c.60_61dup (AGAP2))

Chromosome 12
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.58135794_58135795dup
DNA change (hg38) g.57742011_57742012dup
Published as AGAP2(NM_014770.3):c.60_61dupGG (p.V21Gfs*7)
ISCN -
DB-ID AGAP2_000010
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-02 16:47:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDK4 NM_000075.3 ?/. - c.*6513_*6514dup r.(=) p.(=)
TSPAN31 NM_005981.3 ?/. - c.-3144_-3143dup r.(?) p.(=)
AGAP2 NM_014770.3 ?/. - c.60_61dup r.(?) p.(Val21GlyfsTer7)


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