Product Details

SNP ID
rs145744152
Assay Type
Functionally tested
NCBI dbSNP Submissions
15
Location
Chr.1:196902587 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGATTACATTCATTGCACACAAGA[C/T]GGTTGGTCACCAACGGTCCCATGCC
Phenotype
MIM: 605337
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CFHR4 PubMed Links

Gene Details

Gene
CFHR4
Gene Name
complement factor H related 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001201550.2 328 Silent Mutation GAC,GAT D76D NP_001188479.1
NM_001201551.1 328 Silent Mutation GAC,GAT D75D NP_001188480.1
NM_006684.4 328 Silent Mutation GAC,GAT D76D NP_006675.2
XM_006711129.3 328 Intron XP_006711192.1
XM_017000110.1 328 Intron XP_016855599.1
XM_017000111.1 328 Silent Mutation GAC,GAT D76D XP_016855600.1
XM_017000112.1 328 Intron XP_016855601.1
XM_017000113.1 328 Silent Mutation GAC,GAT D76D XP_016855602.1
XM_017000114.1 328 Intron XP_016855603.1

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