Product Details

SNP ID

rs35755655

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:139561386 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCCCACAGAGAAGCTTCAGCTCA[A/G]GCACAGCTGCAAAAACAAGGATGGA

Phenotype

MIM: 608702

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LOC100507291 PubMed Links

Gene Details

Gene

LOC100507291

Gene Name

uncharacterized LOC100507291

There are no transcripts associated with this gene.

Gene

NMNAT3

Gene Name

nicotinamide nucleotide adenylyltransferase 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001200047.2	880	Missense Mutation	CCT,CTT	P39L	NP_001186976.1
NM_001320510.1	880	Missense Mutation	CCT,CTT	P222L	NP_001307439.1
NM_001320511.1	880	Missense Mutation	CCT,CTT	P128L	NP_001307440.1
NM_001320512.1	880	Missense Mutation	CCT,CTT	P128L	NP_001307441.1
NM_001320513.1	880	Missense Mutation	CCT,CTT	P18L	NP_001307442.1
NM_178177.4	880	Missense Mutation	CCT,CTT	P91L	NP_835471.1
XM_011512790.1	880	Missense Mutation	CCT,CTT	P91L	XP_011511092.1
XM_011512791.2	880	Missense Mutation	CCT,CTT	P91L	XP_011511093.1
XM_017006328.1	880	Missense Mutation	CCT,CTT	P222L	XP_016861817.1
XM_017006329.1	880	Missense Mutation	CCT,CTT	P222L	XP_016861818.1
XM_017006330.1	880	Missense Mutation	CCT,CTT	P222L	XP_016861819.1
XM_017006331.1	880	Missense Mutation	CCT,CTT	P222L	XP_016861820.1
XM_017006332.1	880	Missense Mutation	CCT,CTT	P222L	XP_016861821.1
XM_017006333.1	880	Missense Mutation	CCT,CTT	P222L	XP_016861822.1
XM_017006334.1	880	Missense Mutation	CCT,CTT	P222L	XP_016861823.1
XM_017006335.1	880	Missense Mutation	CCT,CTT	P128L	XP_016861824.1
XM_017006336.1	880	Missense Mutation	CCT,CTT	P128L	XP_016861825.1
XM_017006337.1	880	Missense Mutation	CCT,CTT	P128L	XP_016861826.1
XM_017006338.1	880	Missense Mutation	CCT,CTT	P91L	XP_016861827.1
XM_017006339.1	880	Silent Mutation	GCC,GCT	A194A	XP_016861828.1
XM_017006340.1	880	Silent Mutation	GCC,GCT	A194A	XP_016861829.1
XM_017006341.1	880	Silent Mutation	GCC,GCT	A170A	XP_016861830.1
XM_017006342.1	880	Silent Mutation	GCC,GCT	A170A	XP_016861831.1
XM_017006343.1	880	Silent Mutation	GCC,GCT	A170A	XP_016861832.1
XM_017006344.1	880	Silent Mutation	GCC,GCT	A170A	XP_016861833.1

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