Product Details

SNP ID
rs199723015
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:156244032 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCAGCCCCTGTTGGTTCCAGGCT[G/T]AGATGCGTCCCCACCTGATTAGGCC
Phenotype
MIM: 112260 MIM: 614579 MIM: 609176 MIM: 610962
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
BGLAP PubMed Links

Gene Details

Gene
BGLAP
Gene Name
bone gamma-carboxyglutamate protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_199173.5 1360 Intron NP_954642.1
Gene
PAQR6
Gene Name
progestin and adipoQ receptor family member 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001272104.1 1360 UTR 3 NP_001259033.1
NM_001272105.1 1360 UTR 3 NP_001259034.1
NM_001272106.1 1360 Silent Mutation CTA,CTC L227L NP_001259035.1
NM_001272107.1 1360 UTR 3 NP_001259036.1
NM_001272108.1 1360 UTR 3 NP_001259037.1
NM_001272109.1 1360 Silent Mutation CTA,CTC L155L NP_001259038.1
NM_001272110.1 1360 Silent Mutation CTA,CTC L155L NP_001259039.1
NM_001272111.1 1360 Silent Mutation CTA,CTC L155L NP_001259040.1
NM_001272112.1 1360 Silent Mutation CTA,CTC L155L NP_001259041.1
NM_001272113.1 1360 Silent Mutation CTA,CTC L155L NP_001259042.1
NM_024897.3 1360 Silent Mutation CTA,CTC L295L NP_079173.2
NM_198406.2 1360 UTR 3 NP_940798.1
XM_005245494.3 1360 Silent Mutation CTA,CTC L155L XP_005245551.1
XM_006711546.2 1360 Silent Mutation CTA,CTC L401L XP_006711609.1
XM_006711547.3 1360 Silent Mutation CTA,CTC L401L XP_006711610.1
XM_006711548.3 1360 Silent Mutation CTA,CTC L377L XP_006711611.1
XM_006711552.2 1360 Silent Mutation CTA,CTC L290L XP_006711615.1
XM_006711553.3 1360 Silent Mutation CTA,CTC L290L XP_006711616.1
XM_011510000.2 1360 Silent Mutation CTA,CTC L155L XP_011508302.1
XM_017002385.1 1360 Silent Mutation CTA,CTC L401L XP_016857874.1
Gene
PMF1
Gene Name
polyamine-modulated factor 1
There are no transcripts associated with this gene.

Gene
PMF1-BGLAP
Gene Name
PMF1-BGLAP readthrough
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199661.1 1360 Intron NP_001186590.1
NM_001199662.1 1360 Intron NP_001186591.1
NM_001199663.1 1360 Intron NP_001186592.1
NM_001199664.1 1360 Intron NP_001186593.1
Gene
SMG5
Gene Name
SMG5, nonsense mediated mRNA decay factor
There are no transcripts associated with this gene.

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