Product Details

SNP ID

rs17036114

Assay Type

Functionally tested

NCBI dbSNP Submissions

23

Location

Chr.1:109294170 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAACAACACTAGCCATAAACAGGAA[C/G]TAATCCAGTGAGACATCTTGCCTCT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

MYBPHL PubMed Links

Gene Details

Gene

MYBPHL

Gene Name

myosin binding protein H like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010985.2		Intron			NP_001010985.2
NM_001265613.1		Intron			NP_001252542.1
XM_017001173.1		Intron			XP_016856662.1
XM_017001174.1		Intron			XP_016856663.1
XM_017001175.1		Intron			XP_016856664.1

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