Product Details

SNP ID

rs150994029

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:771397 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCACGAGCGGCAGGCGGGCGAAGCC[A/G]GGGGCCCTGACGAGCTCACACACAG

Phenotype

MIM: 602063

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LOC171391 PubMed Links

Gene Details

Gene

LOC171391

Gene Name

uncharacterized LOC171391

There are no transcripts associated with this gene.

Gene

PDDC1

Gene Name

Parkinson disease 7 domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318818.1	546	Silent Mutation	CCC,CCT	P110P	NP_001305747.1
NM_001318820.1	546	Silent Mutation	CCC,CCT	P124P	NP_001305749.1
NM_001318821.1	546	Silent Mutation	CCC,CCT	P160P	NP_001305750.1
NM_001318822.1	546	Silent Mutation	CCC,CCT	P74P	NP_001305751.1
NM_001318823.1	546	Silent Mutation	CCC,CCT	P110P	NP_001305752.1
NM_001318824.1	546	Silent Mutation	CCC,CCT	P124P	NP_001305753.1
NM_182612.3	546	Silent Mutation	CCC,CCT	P160P	NP_872418.1
XM_005252898.2	546	Missense Mutation	CCG,CTG	P174L	XP_005252955.1
XM_011520064.1	546	Silent Mutation	CCC,CCT	P160P	XP_011518366.1
XM_017017660.1	546	Silent Mutation	CCC,CCT	P160P	XP_016873149.1
XM_017017661.1	546	Silent Mutation	CCC,CCT	P160P	XP_016873150.1
XM_017017662.1	546	Intron			XP_016873151.1
XM_017017663.1	546	Silent Mutation	CCC,CCT	P124P	XP_016873152.1
XM_017017664.1	546	Missense Mutation	CCG,CTG	P174L	XP_016873153.1
XM_017017665.1	546	Missense Mutation	CCG,CTG	P174L	XP_016873154.1
XM_017017666.1	546	Silent Mutation	CCC,CCT	P110P	XP_016873155.1
XM_017017667.1	546	Missense Mutation	CCG,CTG	P138L	XP_016873156.1
XM_017017668.1	546	Silent Mutation	CCC,CCT	P110P	XP_016873157.1

Gene

TALDO1

Gene Name

transaldolase 1

There are no transcripts associated with this gene.

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