Product Details

SNP ID

rs11049127

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:27769141 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAGAAAGAATAAGACAAAAATTAG[C/T]TAATAATACATTGCTAATACATTAC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MANSC4 PubMed Links

Gene Details

Gene

MANSC4

Gene Name

MANSC domain containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146221.1		Intron			NP_001139693.1
XM_006719024.3		Intron			XP_006719087.1
XM_011520542.2		Intron			XP_011518844.1

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