Product Details

SNP ID

rs909562

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:16130102 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACCCCTCTAGCTCTGAGATGTTTGG[A/G]AAACCGCTTGTGAAGCTTAGCTGAC

Phenotype

MIM: 610082

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MYLIP PubMed Links

Gene Details

Gene

MYLIP

Gene Name

myosin regulatory light chain interacting protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_013262.3		Intron			NP_037394.2
XM_005249032.2		Intron			XP_005249089.1
XM_005249033.2		Intron			XP_005249090.1
XM_017010789.1		Intron			XP_016866278.1

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