GRCh37/hg19 position | 12:103234192 |
GRCh38/hg38 position | 12:102840414 |
Alleles (ref/alt) | G/T |
dbSNP rsid | rs199475659 |
Gene symbol |
PAH |
Most severe consequence | missense_variant |
Flanking sequence | AGGTGTAAATTACTTACTGTTAATGGAATCA[G/T]CCAAAATCTTAAGCTGCTGGGTATTGTCCAA |
HGVS |
NM_000277.3:c.1301C>A NM_001354304.2:c.1301C>A NP_000268.1:p.Ala434Asp |
Transcript | Gene | Exon number | Consequence | HGVS cDNA | HGVS protein | Location | Protein location | ||||
NM_000277.3 | PAH | 13 | missense_variant | c.1301C>A | p.Ala434Asp | Exon 12 |
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NM_001354304.2 | PAH | 14 | missense_variant | c.1301C>A | p.Ala434Asp | Exon 13 |
|
Database | Population | AC | AN | Hom | AF |
Tool | Score | Prediction |
---|---|---|
SIFT | 0.005 | damaging |
Polyphen2 HDIV | 0.999 | probably damaging |
Polyphen2 HVAR | 0.998 | probably damaging |
LRT | 0.000000 | deleterious |
MutationTaster | 1 | disease_causing |
MutationAssessor | 3.2 | medium |
FATHMM | -6.15 | damaging |
MetaSVM | 1.0435 | damaging |
MetaLR | 0.986 | damaging |
PROVEAN | -3.68 | damaging |
M-CAP | 0.690996 | damaging |
CADD | 5.06978 | - |
REVEL | 0.966 | - |
Method | Score | Level |
GERP++ | 5.33 | Conserved |
phastCons46way primates | 0.904 | Highly conserved |
phastCons46way placental | 1.000 | Highly conserved |
phastCons100way vertebrates | 1.000 | Highly conserved |
phyloP46way primates | 0.561 | Conserved |
phyloP46way placental | 2.664 | Conserved |
phyloP100way vertebrates | 8.898 | Conserved |
Accession | Clinical significance | Date last evaluated | Review status | Method | Disease name | Disease symbol | Disease inheritance | Pubmed |
---|---|---|---|---|---|---|---|---|
RCV000088825 | not provided | . | no assertion provided | literature only | not provided | - | - | - |
RCV000169393 | Pathogenic/Likely pathogenic | 2021-08-31 | criteria provided, multiple submitters, no conflicts | literature only | Phenylketonuria | PKU | Autosomal recessive inheritance |
InterVar is a software tool for clinical interpretation of genetic variants by the ACMG/AMP 2015 guideline. The eveidence tags that variant met are highlighted. Please note that evidence tags with need to be evaluated manually.
Benign | Pathogenic | |||||
---|---|---|---|---|---|---|
Strong | Supporting | Supporting | Moderate | Strong | Very Strong | |
Population data | BA1 BS1 BS2 |
PM2 | PS4 | |||
Computational and predictive data | BP1 BP3 BP4 BP7 |
PP3 | PM4 PM5 |
PS1 | PVS1 | |
Functional data | BS3 | PP2 | PM1 | PS3 | ||
Segregation data | BS4 | PP1 | PP1 | PP1 | ||
De novo data | PM6 | PS2 | ||||
Allelic data | BP2 | PM3 | ||||
Other database | BP6 | PP5 | ||||
Other data | BP5 | PP4 |
The physichemical property of amino acid change.
Trait | Ala (A) | Asp (D) |
Amino acid name | Alanine | Aspartic acid |
Side chain class | aliphatic | acid |
Polarity | nonpolar | acidic polar |
Charge (pH=7.4) | neutrally charged | negatively charged |
Hydropathy | hydrophobic | hydrophilic |
Molecular weight | 89.094 | 133.104 |