Product Details

SNP ID
rs200305092
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:8288815 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGAGCCCACGAGAGACTGCCCGCT[C/G]TTCGGGGGCGCCTTTTCCGCCATCC
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_001177801.1 165 Silent Mutation CTC,CTG L9L NP_001171272.1
NM_001177802.1 165 Silent Mutation CTC,CTG L9L NP_001171273.1
NM_016492.4 165 Silent Mutation CTC,CTG L9L NP_057576.2
XM_005256618.4 165 Silent Mutation CTC,CTG L9L 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_001320870.1 165 Intron NP_001307799.1
NM_001320871.1 165 Intron NP_001307800.1
NM_001320872.1 165 Intron NP_001307801.1
NM_001320877.1 165 Intron NP_001307806.1
NM_201520.2 165 UTR 3 NP_958928.1
XM_005256641.2 165 Intron XP_005256698.1
XM_011523846.1 165 Intron XP_011522148.1
XM_017024633.1 165 Intron XP_016880122.1
XM_017024634.1 165 Intron XP_016880123.1

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