Product Details

SNP ID

rs145437840

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:16130652 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTTATGGCTAAACCTGAGAAACCG[C/G]ATCTCCCAGCAGATGGATGGGCTAG

Phenotype

MIM: 610082

Polymorphism

C/G, Transversion 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	420	Silent Mutation	CGC,CGG	R61R	NP_037394.2
XM_005249032.2	420	Silent Mutation	CGC,CGG	R61R	XP_005249089.1
XM_005249033.2	420	Intron			XP_005249090.1
XM_017010789.1	420	Silent Mutation	CGC,CGG	R61R	XP_016866278.1

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