Variant #0000548811 (NC_000012.11:g.58114598G>A, NM_014770.3:c.*5737C>T (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.58114598G>A
DNA change (hg38) g.57720815G>A
Published as OS9(NM_006812.3):c.1910G>A (p.R637H)
ISCN -
DB-ID AGAP2_000005
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) 4.0E-5 View details
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OS9 NM_006812.3 ?/. - c.1910G>A r.(?) p.(Arg637His)
AGAP2 NM_014770.3 ?/. - c.*5737C>T r.(=) p.(=)


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