Variant #0000614327 (NC_000012.11:g.58120438_58120455del, NM_014770.3:c.2413_2430del (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.58120438_58120455del
DNA change (hg38) g.57726655_57726672del
Published as AGAP2(NM_001122772.2):c.3481_3498delGCGGCCACCACGCCCAGC (p.A1161_S1166del)
ISCN -
DB-ID AGAP2_000012
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGAP2 NM_014770.3 ?/. - c.2413_2430del r.(?) p.(Ala805_Ser810del)


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