Product Details

SNP ID

rs2046364

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:52877051 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCCCATGGGTGCTAAGTCTTCTCA[G/T]CAGGTTTGAGGAACTTGGAGTGAAA

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SCFD2 PubMed Links

Gene Details

Gene

SCFD2

Gene Name

sec1 family domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152540.3		Intron			NP_689753.2
XM_011534375.2		Intron			XP_011532677.1
XM_011534376.2		Intron			XP_011532678.1
XM_011534378.2		Intron			XP_011532680.1
XM_017007786.1		Intron			XP_016863275.1
XM_017007787.1		Intron			XP_016863276.1

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