Variant detail

mut_id 86 · c.1867G>A · p.Asp623Asn

Evidence at a glance

0
Linked patients
0
Patient-variant records
0
Linked references
0
Countries reported
—
Common phenotype
—
Common zygosity

Summary

Point missense_variant Residue 623 AlphaMissense key D623N
HGVS
c.1867G>A
Protein change
p.Asp623Asn
rsID
rs1841581998
GRCh38 coordinate
133440424
Location
exon 16
gnomAD AF
0.00000247
Domain
Spacer
Gene
ADAMTS13

External links

References

No references linked via ref_id / all_references / reference.

Amino-acid property change

Residue substitution
D → N at 623
AlphaMissense score
0.1841
Likely benign
CSV class: LBen
Hydrophobicity
hydrophilic → hydrophilic (unchanged)
Charge
negative → neutral
Polarity
polar → polar (unchanged)
Size
medium → medium (unchanged)
Residue type
acidic → Unknown
Typical protein position
surface → surface (unchanged)
Hydropathy index
-3.5 → -3.5 (unchanged)
Molecular weight
133.1 → 132.1
Original residue details
D · aspartic acid
code: Asp
hydro: hydrophilic
charge: negative
polarity: polar
size: medium
type: acidic
Variant residue details
N · asparagine
code: Asn
hydro: hydrophilic
charge: neutral
polarity: polar
size: medium
type:

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 623 highlighted in red.
AlphaFold Q76LX8 ADAMTS13 structure
Domain: Spacer
Domain colours match the homepage domain viewer.

Patient summary

No linked patients found for this variant.

Variant fields

mut_syn_HGVS
c.1867G>A
cdna_numb_HGVS
1867
cdna_numb_legacy
1867
nt_change
G>A
n_bp
1
nuc_numb
1867
g_numb
g16
aa_numb_HGVS
623
aa_numb_legacy
623
aa_first
Asp
aa_last
Asn
aa_syn
p.Asp623Asn
codon_first
GAT
codon_last
AAT
coordinate_GRCh38
133440424
gnomAD_AC
4
gnomAD_AN
1613902
gnomAD_AF
0.00000247
g_id
g16
g_name
ADAMTS13
refState
complete
ref_id
332

Patients linked by mut_id

No linked patients found.