Product Details

SNP ID
rs138002949
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:83961490 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGTATGTCCTGGCCTTTGCCGAC[A/G]TTGTTTTCGGTCCCTTTTCCAAACT
Phenotype
MIM: 603961
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SEMA3A PubMed Links

Gene Details

Gene
SEMA3A
Gene Name
semaphorin 3A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006080.2 2547 Missense Mutation CGT,TGT R733C NP_006071.1
XM_005250110.3 2547 Missense Mutation CGT,TGT R733C XP_005250167.1
XM_005250111.4 2547 Missense Mutation CGT,TGT R733C XP_005250168.1
XM_006715839.3 2547 Missense Mutation CGT,TGT R733C XP_006715902.1
XM_011515734.2 2547 Missense Mutation CGT,TGT R733C XP_011514036.1
XM_017011673.1 2547 Missense Mutation CGT,TGT R733C XP_016867162.1

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