Product Details

SNP ID

rs10070137

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:65736700 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGTGTTTCTTTGCCATTTGTATTTT[C/G]TGCCTGTTTATGTCTTTTGCCCATT

Phenotype

MIM: 611530

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NLN PubMed Links

Gene Details

Gene

NLN

Gene Name

neurolysin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020726.4		Intron			NP_065777.1
XM_005248559.2		Intron			XP_005248616.1
XM_006714661.2		Intron			XP_006714724.1
XM_017009673.1		Intron			XP_016865162.1

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