Variant #0000991512 (NC_000002.11:g.100210283G>C, NM_002285.2:c.1840C>G (AFF3))

Chromosome 2
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.100210283G>C
DNA change (hg38) -
Published as AFF3(NM_002285.2):c.1840C>G (p.(Leu614Val))
ISCN -
DB-ID AFF3_000024
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AFF3 NM_001025108.1 ?/. - c.1915C>G r.(?) p.(Leu639Val)
AFF3 NM_002285.2 ?/. - c.1840C>G r.(?) p.(Leu614Val)


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