Variant #0000911165 (NC_000002.11:g.100218010_100218018del, NM_002285.2:c.1258_1266del (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.100218010_100218018del
DNA change (hg38) -
Published as AFF3(NM_002285.3):c.1258_1266delGGCAGCAGC (p.G420_S422del)
ISCN -
DB-ID AFF3_000014
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.1333_1341del r.(?) p.(Gly445_Ser447del)
AFF3 NM_002285.2 ?/. - c.1258_1266del r.(?) p.(Gly420_Ser422del)


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