Product Details

SNP ID

rs17371282

Assay Type

Functionally tested

NCBI dbSNP Submissions

19

Location

Chr.1:85019565 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATTGAGCTAGCCCCATCCCAAGTC[C/T]GAGAACCTCTGTCACTACTCTGCCC

Phenotype

MIM: 607400

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MCOLN3 PubMed Links

Gene Details

Gene

MCOLN3

Gene Name

mucolipin 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001253693.1		Intron			NP_001240622.1
NM_018298.10		Intron			NP_060768.8
XM_005271003.1		Intron			XP_005271060.1
XM_006710750.1		Intron			XP_006710813.1
XM_011541739.2		Intron			XP_011540041.2
XM_011541740.2		Intron			XP_011540042.1
XM_011541741.2		Intron			XP_011540043.1
XM_011541742.1		Intron			XP_011540044.1

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