Full data view for gene PGAP2

Information The variants shown are described using the NM_001256240.1 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.554G>A r.(?) p.(Arg185Gln) Both (homozygous) - pathogenic g.3846278G>A g.3825048G>A NM_001256240.1:c.554G>A, p.(Arg185Gln) - PGAP2_000013 The mutation replaces a highly conserved arginine residue with glutamine within the Frag1 (FGF receptor activating) domain of PGAP2. The mutation was also found to be possibly damaging by Polyphen-2 predictions with a score of 0.942. - - rs745521288 Germline - 0.00000824 in dbSNP. In ExAC database: allele frequency of 0.000008122 - - - DNA PCRq, SEQ, SEQ-NG - WES, Homozygosity mapping HPMRS3;GPIBD8 IV-3 PubMed: Perez et al., 2017 Consanguineous Bedouin kindred presenting with an autosomal recessive syndrome of intellectual disability and elevated serum alkaline phosphatase.  M yes Saudi Arabia Bedouin >25y - - - 1 Philippe Campeau
+/. - c.554G>A r.(?) p.(Arg185Gln) Both (homozygous) - pathogenic g.3846278G>A g.3825048G>A NM_001256240.1:c.554G>A, p.(Arg185Gln) - PGAP2_000013 The mutation replaces a highly conserved arginine residue with glutamine within the Frag1 (FGF receptor activating) domain of PGAP2. The mutation was also found to be possibly damaging by Polyphen-2 predictions with a score of 0.942. - - rs745521288 Germline - 0.00000824 in dbSNP. In ExAC database: allele frequency of 0.000008122 - - - DNA PCRq, SEQ, SEQ-NG - WES, Homozygosity mapping HPMRS3;GPIBD8 IV-5 PubMed: Perez et al., 2017 consanguineous Bedouin kindred presenting with an autosomal recessive syndrome of intellectual disability and elevated serum alkaline phosphatase.  M yes Saudi Arabia Bedouin >18y - - - 1 Philippe Campeau
+/. - c.554G>A r.(?) p.(Arg185Gln) Both (homozygous) - pathogenic g.3846278G>A g.3825048G>A NM_001256240.1:c.554G>A, p.(Arg185Gln) - PGAP2_000013 The mutation replaces a highly conserved arginine residue with glutamine within the Frag1 (FGF receptor activating) domain of PGAP2. The mutation was also found to be possibly damaging by Polyphen-2 predictions with a score of 0.942. - - rs745521288 Germline - 0.00000824 in dbSNP. In ExAC database: allele frequency of 0.000008122 - - - DNA PCRq, SEQ, SEQ-NG - - HPMRS3;GPIBD8 IV-6 PubMed: Perez et al., 2017 consanguineous Bedouin kindred presenting with an autosomal recessive syndrome of intellectual disability and elevated serum alkaline phosphatase.  F yes Saudi Arabia Bedouin >15y - - - 1 Philippe Campeau
+/. - c.554G>A r.(?) p.(Arg185Gln) Both (homozygous) - pathogenic g.3846278G>A g.3825048G>A NM_001256240.1:c.554G>A, p.(Arg185Gln) - PGAP2_000013 The mutation replaces a highly conserved arginine residue with glutamine within the Frag1 (FGF receptor activating) domain of PGAP2. The mutation was also found to be possibly damaging by Polyphen-2 predictions with a score of 0.942. - - rs745521288 Germline - 0.00000824 in dbSNP. In ExAC database: allele frequency of 0.000008122 - - - DNA PCRq, SEQ, SEQ-NG - WES, Homozygosity mapping HPMRS3;GPIBD8 IV-7 PubMed: Perez et al., 2017 consanguineous Bedouin kindred presenting with an autosomal recessive syndrome of intellectual disability and elevated serum alkaline phosphatase.  F yes Saudi Arabia Bedouin >11y - - - 1 Philippe Campeau
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