Genomic variant #0000156724

Individual ID 00095869
Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.49458984G>A
DNA change (hg38) g.49421551G>A
Published as -
ISCN -
DB-ID AMT_000072 See all 10 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Pilar Rodriguez Pombo




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
AMT NM_000481.3 +?/. 3 c.280C>T - r.280c>u p.Arg94Trp



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000096269 DNA;RNA SEQ - - AMT 1 Pilar Rodriguez Pombo