Product Details

SNP ID
rs200825852
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:65376994 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGCACGGGCCCCTGGTACCGGGGT[G/T]GGGGGCTCCCTGGCTGGGCCCTTGG
Phenotype
MIM: 610825
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
FRMD8 PubMed Links

Gene Details

Gene
FRMD8
Gene Name
FERM domain containing 8
There are no transcripts associated with this gene.

Gene
SLC25A45
Gene Name
solute carrier family 25 member 45
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001077241.2 1431 Missense Mutation NP_001070709.2
NM_001278250.2 1431 Missense Mutation NP_001265179.2
NM_001278251.2 1431 Missense Mutation NP_001265180.2
NM_001300820.1 1431 Missense Mutation NP_001287749.1
NM_182556.3 1431 Missense Mutation NP_872362.3
XM_006718509.3 1431 Missense Mutation XP_006718572.1
XM_006718510.3 1431 Missense Mutation XP_006718573.1
XM_011544943.2 1431 Missense Mutation XP_011543245.1
XM_011544944.2 1431 Missense Mutation XP_011543246.1
XM_011544947.2 1431 Missense Mutation XP_011543249.1
XM_011544949.2 1431 Missense Mutation XP_011543251.1
XM_017017562.1 1431 Missense Mutation XP_016873051.1
XM_017017563.1 1431 Missense Mutation XP_016873052.1
XM_017017564.1 1431 Missense Mutation XP_016873053.1
XM_017017565.1 1431 Missense Mutation XP_016873054.1
XM_017017566.1 1431 Missense Mutation XP_016873055.1
XM_017017567.1 1431 Missense Mutation XP_016873056.1
XM_017017568.1 1431 Missense Mutation XP_016873057.1
XM_017017569.1 1431 Missense Mutation XP_016873058.1
XM_017017570.1 1431 Missense Mutation XP_016873059.1
XM_017017571.1 1431 Missense Mutation XP_016873060.1

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