Product Details

SNP ID
rs151088367
Assay Type
Functionally tested
NCBI dbSNP Submissions
16
Location
Chr.1:186300199 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGGAGTGCTGCCCTGATTTCAAGA[A/G]AGTCTGCACTGCGGGTAAGTCCTGA
Phenotype
MIM: 604283
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PRG4 PubMed Links

Gene Details

Gene
PRG4
Gene Name
proteoglycan 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127708.2 236 Intron NP_001121180.2
NM_001127709.2 236 Missense Mutation AAA,AGA K62R NP_001121181.2
NM_001127710.2 236 Intron NP_001121182.2
NM_001303232.1 236 Missense Mutation AAA,AGA K62R NP_001290161.1
NM_005807.4 236 Missense Mutation AAA,AGA K62R NP_005798.3
XM_017000002.1 236 Missense Mutation AAA,AGA K62R XP_016855491.1
XM_017000003.1 236 Intron XP_016855492.1

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