Product Details

SNP ID
rs149356662
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:122910281 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAAGTTGGCTCTGTCATCAGGGAT[C/T]AAGTTATTCTTGTTCAGGGTCTGTG
Phenotype
MIM: 609298
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SEMA5B PubMed Links

Gene Details

Gene
SEMA5B
Gene Name
semaphorin 5B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001031702.3 3755 Silent Mutation TTA,TTG L1106L NP_001026872.2
NM_001256346.1 3755 Silent Mutation TTA,TTG L1106L NP_001243275.1
NM_001256347.1 3755 Silent Mutation TTA,TTG L1160L NP_001243276.1
NM_001256348.1 3755 Silent Mutation TTA,TTG L1012L NP_001243277.1
XM_017006638.1 3755 Silent Mutation TTA,TTG L1072L XP_016862127.1
XM_017006639.1 3755 Intron XP_016862128.1

View Full Product Details