Variant #0000980407 (NC_000012.11:g.58135836A>T, NM_014770.3:c.19T>A (AGAP2))

Chromosome 12
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.58135836A>T
DNA change (hg38) -
Published as AGAP2(NM_014770.4):c.19T>A (p.(Phe7Ile))
ISCN -
DB-ID AGAP2_000025
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) 0.00043 View details
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 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDK4 NM_000075.3 -?/. - c.*6472T>A r.(=) p.(=)
TSPAN31 NM_005981.3 -?/. - c.-3102A>T r.(?) p.(=)
AGAP2 NM_014770.3 -?/. - c.19T>A r.(?) p.(Phe7Ile)


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