Variant #0000508805 (NC_000002.11:g.100210336del, NM_002285.2:c.1788del (AFF3))

Chromosome 2
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.100210336del
DNA change (hg38) g.99593874del
Published as AFF3(NM_001386135.1):c.1788del (p.(Asp598Thrfs*48))
ISCN -
DB-ID AFF3_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AFF3 NM_001025108.1 -?/. - c.1863del r.(?) p.(Asp623ThrfsTer48)
AFF3 NM_002285.2 -?/. - c.1788del r.(?) p.(Asp598ThrfsTer48)


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