Product Details

SNP ID

rs148906362

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:97001275 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGGCACTCCACCCATGACAGGGGG[C/T]GCGTGGTCTGGCAGATGGCATAGCC

Phenotype

MIM: 603742

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLIT1 PubMed Links

Gene Details

Gene

SLIT1

Gene Name

slit guidance ligand 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003061.2	4694	Missense Mutation	CAC,CGC	H1481R	NP_003052.2

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