Product Details

SNP ID

rs75813706

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:35610652 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCCTTTCCTCTTTGGTAATAAGA[C/T]GTGAATTTGGCATACTAAATTAAAA

Phenotype

MIM: 160000

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MB PubMed Links

Gene Details

Gene

MB

Gene Name

myoglobin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005368.2		Intron			NP_005359.1
NM_203377.1		Intron			NP_976311.1
NM_203378.1		Intron			NP_976312.1
XM_005261605.2		Intron			XP_005261662.1

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