Product Details

SNP ID
rs80338891
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:100620889 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGTTATCAATGTTCCAGACATCCC[T/C]GCTAAGCGCATTGGCTGCCCCTTGC
Phenotype
MIM: 609125 MIM: 604720
Polymorphism
T/C, 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 2415 Missense Mutation AGG,GGG R621G NP_001193784.1
NM_003227.3 2415 Missense Mutation AGG,GGG R792G NP_003218.2
XM_005250553.4 2415 Missense Mutation AGG,GGG R792G XP_005250610.1
XM_017012573.1 2415 Missense Mutation AGG,GGG R792G XP_016868062.1

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