Variant detail
mut_id 60 · c.1297T>G · p.Cys433Gly
Evidence at a glance
1
Linked patients
1
Patient-variant records
1
Linked references
1
Countries reported
cTTP (1)
Common phenotype
compound_heterozygous (1)
Common zygosity
Summary
Point missense_variant Residue 433 AlphaMissense key C433G
HGVS
c.1297T>G
Protein change
p.Cys433Gly
GRCh38 coordinate
133433693
Location
exon 11
Domain
TSP type-1 1
Gene
ADAMTS13
External links
References
Adult-onset congenital thrombotic thrombocytopenic purpura caused by a novel compound heterozygous mutation of the ADAMTS13 gene
Amino-acid property change
Residue substitution
C → G at 433
AlphaMissense score
0.8986
Likely pathogenic
CSV class: LPath
Hydrophobicity
hydrophilic → hydrophobic
Charge
neutral → neutral (unchanged)
Polarity
polar → polar (unchanged)
Size
medium → small
Residue type
Unknown → aliphatic
Typical protein position
buried → surface
Hydropathy index
2.5 → -0.4
Molecular weight
121.2 → 75.1
Original residue details
C
· cysteine
code: Cys
hydro: hydrophilic
charge: neutral
polarity: polar
size: medium
type:
code: Cys
hydro: hydrophilic
charge: neutral
polarity: polar
size: medium
type:
Variant residue details
G
· glycine
code: Gly
hydro: hydrophobic
charge: neutral
polarity: polar
size: small
type: aliphatic
code: Gly
hydro: hydrophobic
charge: neutral
polarity: polar
size: small
type: aliphatic
Interactive AlphaFold structure
Interactive local 3D view of the AlphaFold Q76LX8 ADAMTS13 structure.
Drag to rotate, shift-drag to move, and use the mouse wheel to zoom in and out. The default view shows the full ADAMTS13 structure, with residue 433 highlighted in red.
AlphaFold Q76LX8 ADAMTS13 structure
Domain: TSP type-1 1
Domain colours match the homepage domain viewer.
Patient summary
Countries represented
South Korea (1)
Phenotype
cTTP (1)
Zygosity
compound_heterozygous (1)
Sex
female (1)
Pregnancy-related
no (1)
Triggers
unknown (1)
Treatment
none (1)
ADAMTS13 activity
n=1; median=3; range=3–3
Age of onset
n=1; median=1; range=1–1
Age of diagnosis
n=1; median=5; range=5–5
Platelet count
n=1; median=13; range=13–13
Variant fields
mut_syn_HGVS
c.1297T>G
cdna_numb_HGVS
1297
cdna_numb_legacy
1297
nt_change
T>G
n_bp
1
nuc_numb
1297
g_numb
g16
aa_numb_HGVS
433
aa_numb_legacy
433
aa_first
Cys
aa_last
Gly
aa_syn
p.Cys433Gly
codon_first
TGC
codon_last
GGC
coordinate_GRCh38
133433693
g_id
g16
g_name
ADAMTS13
refState
complete
ref_id
102
Patients linked by mut_id
| patient_id | mut_id | compound_partner_mut_id | ref_id | phenotype | zygosity | country | sex | age_of_onset | age_of_diagnosis | ad13_activity | platelet_count | pregnancy_related | triggers | treatment |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 53 | 60 | 262 | 102 | cTTP | compound_heterozygous | South Korea | female | <1 | 5 | <3 | 13 | no | unknown | none |