Product Details

SNP ID

rs1703973

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:48351669 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTATGTGAGGTGTAATAATCTAGTT[A/T]TATCTTAATTCATCTTCACATTTCT

Phenotype

MIM: 610492

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

SLAIN2 PubMed Links

Gene Details

Gene

SLAIN2

Gene Name

SLAIN motif family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020846.1		Intron			NP_065897.1
XM_005248121.2		Intron			XP_005248178.1

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