Product Details

SNP ID
rs199667250
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:1483412 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGCGAGCGGATGGAGTTGTGGAG[A/G]CCGGCGCAGGCCGATACGTTTTCCC
Phenotype
MIM: 600487 MIM: 609346
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C19orf25 PubMed Links

Gene Details

Gene
C19orf25
Gene Name
chromosome 19 open reading frame 25
There are no transcripts associated with this gene.

Gene
PCSK4
Gene Name
proprotein convertase subtilisin/kexin type 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017573.4 1107 Silent Mutation GGC,GGT G481G NP_060043.2
XM_005259586.1 1107 Silent Mutation GGC,GGT G293G XP_005259643.1
XM_011528085.2 1107 Silent Mutation GGC,GGT G508G XP_011526387.1
XM_011528086.2 1107 Silent Mutation GGC,GGT G499G XP_011526388.1
XM_011528087.2 1107 Silent Mutation GGC,GGT G508G XP_011526389.1
XM_011528088.2 1107 Silent Mutation GGC,GGT G446G XP_011526390.1
XM_011528089.2 1107 Silent Mutation GGC,GGT G414G XP_011526391.1
XM_011528090.2 1107 Silent Mutation GGC,GGT G387G XP_011526392.1
XM_011528091.2 1107 Silent Mutation GGC,GGT G384G XP_011526393.1
XM_011528092.2 1107 Silent Mutation GGC,GGT G508G XP_011526394.1
XM_011528093.2 1107 Silent Mutation GGC,GGT G508G XP_011526395.1
XM_011528094.1 1107 Silent Mutation GGC,GGT G293G XP_011526396.1
XM_011528095.2 1107 Missense Mutation CCT,TCT P479S XP_011526397.1
XM_011528096.1 1107 Silent Mutation GGC,GGT G259G XP_011526398.1
XM_017026897.1 1107 Silent Mutation GGC,GGT G293G XP_016882386.1
Gene
REEP6
Gene Name
receptor accessory protein 6
There are no transcripts associated with this gene.

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