Variant #0000434955 (NC_000009.11:g.136307563C>T, ADAMTS13(NM_139025.3):c.2012C>T)

Individual ID 00204540
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.136307563C>T
DNA change (hg38) g.133442442C>T
Published as -
ISCN -
DB-ID ADAMTS13_000019
Variant remarks submitted through SIB; ExPASy_067788
Reference PubMed: Schneppenheim et al (2006)
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner SIB - Livia Famiglietti
Database submission license No license selected
Created by SIB - Livia Famiglietti
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTS13 NM_139025.3 +/? ? c.2012C>T r.(?) p.(Pro671Leu)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000205569 DNA SEQ - - ADAMTS13 1 SIB - Livia Famiglietti