Variant #0000619100 (NC_000023.10:g.148044334G>A, NM_002025.3:c.2780G>A (AFF2))

Chromosome X
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.148044334G>A
DNA change (hg38) g.148962804G>A
Published as AFF2(NM_001169122.1):c.2681G>A (p.(Arg894His)), AFF2(NM_002025.3):c.2780G>A (p.R927H), AFF2(NM_002025.4):c.2780G>A (p.R927H)
ISCN -
DB-ID AFF2_000080 See all 4 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) 0.00165 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 15:24:38 +01:00 (CET)
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     
AFF2 NM_002025.3 -?/. - c.2780G>A r.(?) p.(Arg927His)


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