Product Details

SNP ID

rs4552453

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:20252675 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTCTGCCGCGGAGCTGCGGCTTATC[C/T]GGGAGACGAGCGGGGTTGACACGCG

Phenotype

MIM: 603746

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLIT2 PubMed Links

Gene Details

Gene

SLIT2

Gene Name

slit guidance ligand 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001289135.2	771	UTR 5			NP_001276064.1
NM_001289136.2	771	UTR 5			NP_001276065.1
NM_004787.3	771	UTR 5			NP_004778.1
XM_005248211.3	771	UTR 5			XP_005248268.1
XM_006713986.3	771	UTR 5			XP_006714049.1
XM_011513909.2	771	Intron			XP_011512211.1
XM_011513910.2	771	Intron			XP_011512212.2
XM_017008845.1	771	Intron			XP_016864334.1

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