Product Details

SNP ID

rs146487447

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:100620943 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCCAGGTGAGCAGGGCTAGCTGAC[A/G]CCGGAAACGGCTCTCCTGGAAGCCA

Phenotype

MIM: 609125 MIM: 604720

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MOSPD3 PubMed Links

Gene Details

Gene

MOSPD3

Gene Name

motile sperm domain containing 3

There are no transcripts associated with this gene.

Gene

TFR2

Gene Name

transferrin receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206855.1	2361	Missense Mutation	CGT,TGT	R603C	NP_001193784.1
NM_003227.3	2361	Missense Mutation	CGT,TGT	R774C	NP_003218.2
XM_005250553.4	2361	Missense Mutation	CGT,TGT	R774C	XP_005250610.1
XM_017012573.1	2361	Missense Mutation	CGT,TGT	R774C	XP_016868062.1

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