Variant #0000434931 (NC_000009.11:g.136291366C>T, ADAMTS13(NM_139025.3):c.587C>T)

Individual ID 00204516
Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.136291366C>T
DNA change (hg38) g.133426246C>T
Published as -
ISCN -
DB-ID ADAMTS13_000021 See all 2 reported entries
Variant remarks submitted through SIB; ExPASy_027114; Corresponds to rs121908470 in dbSNP
Reference PubMed: Levy et al (2001)
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner SIB - Livia Famiglietti
Database submission license No license selected
Created by SIB - Livia Famiglietti
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTS13 NM_139025.3 +/? ? c.587C>T r.(?) p.(Thr196Ile)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000205545 DNA SEQ - - ADAMTS13 1 SIB - Livia Famiglietti