Product Details

SNP ID
rs149089464
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:8289375 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGCCGCTGTCAAGAAGCCTGGGT[C/G]CTCTCTGGCAAGCAGCAGATAGCTA
Phenotype
MIM: 607954 MIM: 610818
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
RANGRF PubMed Links

Gene Details

Gene
RANGRF
Gene Name
RAN guanine nucleotide release factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001177801.1 450 Silent Mutation GTC,GTG V104V NP_001171272.1
NM_001177802.1 450 Silent Mutation GTC,GTG V104V NP_001171273.1
NM_016492.4 450 Silent Mutation GTC,GTG V104V NP_057576.2
XM_005256618.4 450 Silent Mutation GTC,GTG V104V XP_005256675.1
Gene
SLC25A35
Gene Name
solute carrier family 25 member 35
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320870.1 450 Intron NP_001307799.1
NM_001320871.1 450 Intron NP_001307800.1
NM_001320872.1 450 UTR 3 NP_001307801.1
NM_001320877.1 450 Intron NP_001307806.1
NM_201520.2 450 UTR 3 NP_958928.1
XM_005256641.2 450 Intron XP_005256698.1
XM_011523846.1 450 Intron XP_011522148.1
XM_017024633.1 450 Intron XP_016880122.1
XM_017024634.1 450 Intron XP_016880123.1

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