Product Details

SNP ID: rs199873362
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:136941363 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCACCTCCCGCATGGTCTTGAGGT[C/T]GAACACCAGCAGGTCAATCTCCTCC
Phenotype: MIM: 120930 MIM: 609072 MIM: 612905
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: C8G PubMed Links

Gene Details

Gene: C8G
Gene Name: complement component 8, gamma polypeptide

There are no transcripts associated with this gene.

Gene: FBXW5
Gene Name: F-box and WD repeat domain containing 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018998.3	1525	Missense Mutation			NP_061871.1
XM_005266089.2	1525	Missense Mutation			XP_005266146.2
XM_011518789.1	1525	Missense Mutation			XP_011517091.1
XM_017014812.1	1525	Missense Mutation			XP_016870301.1

Gene: LCN12
Gene Name: lipocalin 12

There are no transcripts associated with this gene.

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