Product Details

SNP ID

rs143268395

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:74863963 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAGCTTGGAGTCAAAGGGCACGCT[A/T]GGGTCGACAGGGCGGCTCTTATACC

Phenotype

MIM: 103270 MIM: 138254

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

FDXR PubMed Links

Gene Details

Gene

FDXR

Gene Name

ferredoxin reductase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001258012.3	1252	Silent Mutation	CCA,CCT	P412P	NP_001244941.2
NM_001258013.3	1252	Silent Mutation	CCA,CCT	P400P	NP_001244942.2
NM_001258014.3	1252	Silent Mutation	CCA,CCT	P361P	NP_001244943.2
NM_001258015.2	1252	Silent Mutation	CCA,CCT	P329P	NP_001244944.1
NM_001258016.3	1252	Silent Mutation	CCA,CCT	P317P	NP_001244945.2
NM_004110.5	1252	Silent Mutation	CCA,CCT	P375P	NP_004101.3
NM_024417.4	1252	Silent Mutation	CCA,CCT	P369P	NP_077728.3
XM_006721772.1	1252	Silent Mutation	CCA,CCT	P370P	XP_006721835.1
XM_011524527.1	1252	Silent Mutation	CCA,CCT	P376P	XP_011522829.1
XM_011524528.1	1252	Silent Mutation	CCA,CCT	P373P	XP_011522830.1
XM_011524529.1	1252	Silent Mutation	CCA,CCT	P372P	XP_011522831.1
XM_011524531.2	1252	Silent Mutation	CCA,CCT	P324P	XP_011522833.1
XM_011524532.2	1252	Silent Mutation	CCA,CCT	P323P	XP_011522834.1
XM_011524533.2	1252	Silent Mutation	CCA,CCT	P318P	XP_011522835.1

Gene

GRIN2C

Gene Name

glutamate ionotropic receptor NMDA type subunit 2C

There are no transcripts associated with this gene.

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