Product Details

SNP ID

rs16857898

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:170178804 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTTCCTCATGCTTTGGTGGGGAAA[C/T]GAAAAATCTGATCATTTAGTTAATC

Phenotype

MIM: 610040

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYO3B PubMed Links

Gene Details

Gene

MYO3B

Gene Name

myosin IIIB

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001083615.3		Intron			NP_001077084.2
NM_138995.4		Intron			NP_620482.3
XM_006712299.3		Intron			XP_006712362.1
XM_011510654.2		Intron			XP_011508956.1
XM_011510655.2		Intron			XP_011508957.1
XM_011510656.2		Intron			XP_011508958.1
XM_011510657.2		Intron			XP_011508959.1
XM_011510658.2		Intron			XP_011508960.1

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