GRCh37/hg19 position | 12:103234224 |
GRCh38/hg38 position | 12:102840446 |
Alleles (ref/alt) | G/- |
dbSNP rsid | - |
Gene symbol |
PAH |
Most severe consequence | frameshift_variant |
Flanking sequence | CCAAAATCTTAAGCTGCTGGGTATTGTCCAA[G/-]ACCTCAATCCTTTGGGTGTATGGGTCGTAGC |
HGVS |
NM_000277.3:c.1269del NM_001354304.2:c.1269del NP_000268.1:p.Leu424TrpfsTer28 |
Transcript | Gene | Exon number | Consequence | HGVS cDNA | HGVS protein | Location | Protein location | ||||
NM_000277.3 | PAH | 13 | frameshift_variant | c.1269del | p.Leu424TrpfsTer28 | Exon 12 |
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NM_001354304.2 | PAH | 14 | frameshift_variant | c.1269del | p.Leu424TrpfsTer28 | Exon 13 |
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Database | Population | AC | AN | Hom | AF |
Method | Score | Level |
GERP++ | 2 | Conserved |
phastCons46way primates | 0.993 | Highly conserved |
phastCons46way placental | 0.993 | Highly conserved |
phastCons100way vertebrates | 1 | Highly conserved |
phyloP46way primates | 0.561 | Conserved |
phyloP46way placental | 0.524 | Not conserved |
phyloP100way vertebrates | 1.032 | Not conserved |
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 | Leu (L) | TrpfsTer |
Amino acid name | Leucine | - |
Side chain class | aliphatic | - |
Polarity | nonpolar | - |
Charge (pH=7.4) | neutrally charged | - |
Hydropathy | hydrophobic | - |
Molecular weight | 131.175 | - |