Product Details

SNP ID

rs184693277

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:168666590 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGCACTGGGGCCCACAGCCCCCA[C/T]GACATTCCATGATGGGCACCTTGGA

Phenotype

MIM: 603745

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLIT3 PubMed Links

Gene Details

Gene

SLIT3

Gene Name

slit guidance ligand 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271946.1	4856	Missense Mutation			NP_001258875.1
NM_003062.3	4856	Missense Mutation			NP_003053.1
XM_017009779.1	4856	Missense Mutation			XP_016865268.1

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