Genomic variant #0000163873

Individual ID 00100928
Chromosome 6
Allele Parent #2
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.158532439G>A
DNA change (hg38) g.158111407G>A
Published as -
ISCN -
DB-ID SERAC1_000012
Variant remarks -
Reference PubMed: Wortmann 2012, Journal: Wortmann 2012
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




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
SERAC1 NM_032861.3 +/. 17 c.1924C>T - r.(?) p.(Gln642*)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000101350 DNA SEQ - - SERAC1 2 Johan den Dunnen