Product Details

SNP ID

rs9574083

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.13:77538505 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AAACTGTGATTTTTTTCCATGAACT[G/T]GTGATTTTGAAGCTCGGGAGAAGCT

Phenotype

MIM: 604112

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SCEL PubMed Links

Gene Details

Gene

SCEL

Gene Name

sciellin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001160706.1		Intron			NP_001154178.1
NM_003843.3		Intron			NP_003834.3
NM_144777.2		Intron			NP_659001.2
XM_005266578.1		Intron			XP_005266635.1
XM_006719882.1		Intron			XP_006719945.1
XM_006719884.1		Intron			XP_006719947.1
XM_006719885.1		Intron			XP_006719948.1
XM_011535281.1		Intron			XP_011533583.1
XM_011535282.1		Intron			XP_011533584.1
XM_011535283.1		Intron			XP_011533585.1
XM_011535284.1		Intron			XP_011533586.1
XM_011535285.1		Intron			XP_011533587.1
XM_011535286.1		Intron			XP_011533588.1
XM_011535287.1		Intron			XP_011533589.1
XM_011535288.1		Intron			XP_011533590.1
XM_011535289.1		Intron			XP_011533591.1
XM_011535290.1		Intron			XP_011533592.1
XM_011535291.1		Intron			XP_011533593.1
XM_017020805.1		Intron			XP_016876294.1

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