Product Details

SNP ID
rs145133730
Assay Type
Functionally tested
NCBI dbSNP Submissions
9
Location
Chr.1:156154598 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGAGCATGGCCCTCCCAGCCCTGG[A/G]CCTGGACCCCTGGAGCCTCCTGGGC
Phenotype
MIM: 607292
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SEMA4A PubMed Links

Gene Details

Gene
SEMA4A
Gene Name
semaphorin 4A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001193300.1 318 Missense Mutation GAC,GGC D7G NP_001180229.1
NM_001193301.1 318 Missense Mutation GAC,GGC D7G NP_001180230.1
NM_001193302.1 318 Intron NP_001180231.1
NM_022367.3 318 Missense Mutation GAC,GGC D7G NP_071762.2
XM_011509871.2 318 Intron XP_011508173.1
XM_011509872.2 318 Missense Mutation GAC,GGC D7G XP_011508174.1
XM_011509873.2 318 Missense Mutation GAC,GGC D7G XP_011508175.1
XM_011509874.2 318 Intron XP_011508176.1
XM_011509875.2 318 Intron XP_011508177.1
XM_011509876.2 318 Intron XP_011508178.1
XM_011509878.2 318 Intron XP_011508180.1
XM_011509879.2 318 Intron XP_011508181.1
XM_017002056.1 318 Missense Mutation GAC,GGC D7G XP_016857545.1
XM_017002057.1 318 UTR 5 XP_016857546.1

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