Product Details

SNP ID
rs4238485
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:93045106 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTGCCTGGCAGGTCCCGAGTCCT[A/C]TCATACAGGTGCAGTTTGTCTTTGT
Phenotype
MIM: 607362
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
RGMA PubMed Links

Gene Details

Gene
RGMA
Gene Name
repulsive guidance molecule family member a
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166283.1 1500 Missense Mutation GAG,GAT E423D NP_001159755.1
NM_001166286.1 1500 Missense Mutation GAG,GAT E399D NP_001159758.1
NM_001166287.1 1500 Missense Mutation GAG,GAT E399D NP_001159759.1
NM_001166288.1 1500 Missense Mutation GAG,GAT E399D NP_001159760.1
NM_001166289.1 1500 Missense Mutation GAG,GAT E399D NP_001159761.1
NM_020211.2 1500 Missense Mutation GAG,GAT E415D NP_064596.2

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