Product Details

SNP ID

rs143873124

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:85514095 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTGAGAAGTGTTATGAGTGAGAC[C/T]AAACGGTGCTCCTGAAATAGCTGTT

Phenotype

MIM: 616105

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SNX14 PubMed Links

Gene Details

Gene

SNX14

Gene Name

sorting nexin 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001297614.2	2681	Silent Mutation	TTA,TTG	L835L	NP_001284543.1
NM_001304479.1	2681	Silent Mutation	TTA,TTG	L792L	NP_001291408.1
NM_020468.5	2681	Silent Mutation	TTA,TTG	L791L	NP_065201.1
NM_153816.5	2681	Silent Mutation	TTA,TTG	L844L	NP_722523.1
XM_005248738.3	2681	Silent Mutation	TTA,TTG	L843L	XP_005248795.1
XM_005248740.3	2681	Silent Mutation	TTA,TTG	L800L	XP_005248797.1
XM_011535977.2	2681	Silent Mutation	TTA,TTG	L792L	XP_011534279.1
XM_011535979.1	2681	Silent Mutation	TTA,TTG	L748L	XP_011534281.1
XM_017011090.1	2681	Silent Mutation	TTA,TTG	L791L	XP_016866579.1
XM_017011091.1	2681	Silent Mutation	TTA,TTG	L834L	XP_016866580.1
XM_017011092.1	2681	Silent Mutation	TTA,TTG	L799L	XP_016866581.1
XM_017011093.1	2681	Silent Mutation	TTA,TTG	L791L	XP_016866582.1
XM_017011094.1	2681	Silent Mutation	TTA,TTG	L747L	XP_016866583.1
XM_017011095.1	2681	Silent Mutation	TTA,TTG	L494L	XP_016866584.1
XM_017011096.1	2681	Silent Mutation	TTA,TTG	L459L	XP_016866585.1
XM_017011097.1	2681	Silent Mutation	TTA,TTG	L459L	XP_016866586.1
XM_017011098.1	2681	Silent Mutation	TTA,TTG	L459L	XP_016866587.1
XM_017011099.1	2681	Silent Mutation	TTA,TTG	L459L	XP_016866588.1
XM_017011100.1	2681	Silent Mutation	TTA,TTG	L459L	XP_016866589.1
XM_017011101.1	2681	Silent Mutation	TTA,TTG	L450L	XP_016866590.1

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