Product Details

SNP ID
rs141560628
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:120952628 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCACTAATTCTAAGTAAAGTGAGC[G/T]TTACAAATAAGACCAGCTATGAATG
Phenotype
MIM: 120900
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
C5 PubMed Links

Gene Details

Gene
C5
Gene Name
complement component 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001317163.1 5326 UTR 3 NP_001304092.1
NM_001317164.1 5326 Intron NP_001304093.1
NM_001735.2 5326 UTR 3 NP_001726.2
XM_011518980.2 5326 UTR 3 XP_011517282.1
XM_017015102.1 5326 UTR 3 XP_016870591.1
XM_017015103.1 5326 UTR 3 XP_016870592.1
XM_017015104.1 5326 Intron XP_016870593.1

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