Product Details

SNP ID

rs147550639

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:85507977 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTAATGAGCTTTACCTGCTTGTT[A/G]AGTACTGGTTGCTGTAAGCCATCAA

Phenotype

MIM: 616105

Polymorphism

A/G, 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	2885	Silent Mutation	CTC,CTT	L903L	NP_001284543.1
NM_001304479.1	2885	Silent Mutation	CTC,CTT	L860L	NP_001291408.1
NM_020468.5	2885	Silent Mutation	CTC,CTT	L859L	NP_065201.1
NM_153816.5	2885	Silent Mutation	CTC,CTT	L912L	NP_722523.1
XM_005248738.3	2885	Silent Mutation	CTC,CTT	L911L	XP_005248795.1
XM_005248740.3	2885	Silent Mutation	CTC,CTT	L868L	XP_005248797.1
XM_011535977.2	2885	Intron			XP_011534279.1
XM_011535979.1	2885	Silent Mutation	CTC,CTT	L816L	XP_011534281.1
XM_017011090.1	2885	Silent Mutation	CTC,CTT	L859L	XP_016866579.1
XM_017011091.1	2885	Silent Mutation	CTC,CTT	L902L	XP_016866580.1
XM_017011092.1	2885	Silent Mutation	CTC,CTT	L867L	XP_016866581.1
XM_017011093.1	2885	Silent Mutation	CTC,CTT	L859L	XP_016866582.1
XM_017011094.1	2885	Silent Mutation	CTC,CTT	L815L	XP_016866583.1
XM_017011095.1	2885	Silent Mutation	CTC,CTT	L562L	XP_016866584.1
XM_017011096.1	2885	Silent Mutation	CTC,CTT	L527L	XP_016866585.1
XM_017011097.1	2885	Silent Mutation	CTC,CTT	L527L	XP_016866586.1
XM_017011098.1	2885	Silent Mutation	CTC,CTT	L527L	XP_016866587.1
XM_017011099.1	2885	Silent Mutation	CTC,CTT	L527L	XP_016866588.1
XM_017011100.1	2885	Silent Mutation	CTC,CTT	L527L	XP_016866589.1
XM_017011101.1	2885	Silent Mutation	CTC,CTT	L518L	XP_016866590.1

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