Genomic variant #0000238542

Individual ID 00145091
Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.148406653T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID SH3TC2_000013 See all 3 reported entries
Variant remarks -
Reference PubMed: Azzedine 2006
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
SH3TC2 NM_024577.3 +/. 11 c.2642A>G - r.(?) p.(Asn881Ser)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000145948 DNA SEQ - - SH3TC2 1 Johan den Dunnen