Product Details

SNP ID

rs200250903

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:51288871 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTCCAAAAGTTTGATGGCCTCTTC[A/G]TTTCTGTCTTGCTCCATAAGCAGCA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TTC39A PubMed Links

Gene Details

Gene

TTC39A

Gene Name

tetratricopeptide repeat domain 39A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080494.3	1785	Silent Mutation	AAC,AAT	N527N	NP_001073963.1
NM_001144832.2	1785	Silent Mutation	AAC,AAT	N530N	NP_001138304.1
NM_001297662.1	1785	Intron			NP_001284591.1
NM_001297663.1	1785	Silent Mutation	AAC,AAT	N526N	NP_001284592.1
NM_001297664.1	1785	Silent Mutation	AAC,AAT	N499N	NP_001284593.1
NM_001297665.1	1785	Silent Mutation	AAC,AAT	N562N	NP_001284594.1
NM_001297666.1	1785	Silent Mutation	AAC,AAT	N170N	NP_001284595.1
NM_001297667.1	1785	Silent Mutation	AAC,AAT	N103N	NP_001284596.1
XM_005270644.2	1785	Silent Mutation	AAC,AAT	N523N	XP_005270701.1
XM_006710471.2	1785	Silent Mutation	AAC,AAT	N558N	XP_006710534.1
XM_011541048.2	1785	Silent Mutation	AAC,AAT	N565N	XP_011539350.1
XM_011541049.2	1785	Silent Mutation	AAC,AAT	N563N	XP_011539351.1
XM_011541050.2	1785	Silent Mutation	AAC,AAT	N561N	XP_011539352.1
XM_011541051.2	1785	Silent Mutation	AAC,AAT	N534N	XP_011539353.1
XM_011541052.2	1785	Silent Mutation	AAC,AAT	N534N	XP_011539354.1
XM_011541053.2	1785	Silent Mutation	AAC,AAT	N534N	XP_011539355.1
XM_011541054.2	1785	Silent Mutation	AAC,AAT	N499N	XP_011539356.1
XM_017000715.1	1785	Silent Mutation	AAC,AAT	N499N	XP_016856204.1

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