Genomic variant #0000393182

Individual ID 00172442
Chromosome X
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.148035200G>A
DNA change (hg38) -
Published as S496S
ISCN -
DB-ID AFF2_000090
Variant remarks recurrent, found 7 times
Reference PubMed: Tarpey 2009
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 7/208 cases
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.17211 View details
Owner Lucy Raymond




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
AFF2 NM_002025.3 -?/. - c.1488G>A - r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000173325 DNA SEQ - - AFF2 1 Lucy Raymond