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SNP ID: rs3814721
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:71998226 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCTCAGAAACCCCAGGCAGCCTTGC[C/T]TCCTGACCTAACTCCTGGAGATGCT
Phenotype: MIM: 604113 MIM: 164009
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: IL18BP PubMed Links

Gene Details

Gene: IL18BP
Gene Name: interleukin 18 binding protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039659.1	283	Intron			NP_001034748.1
NM_001039660.1	283	Intron			NP_001034749.1
NM_001145055.1	283	Intron			NP_001138527.1
NM_001145057.1	283	Intron			NP_001138529.1
NM_005699.3	283	Intron			NP_005690.2
NM_173042.2	283	Intron			NP_766630.2
NM_173044.2	283	Intron			NP_766632.2
XM_017017059.1	283	Intron			XP_016872548.1
XM_017017060.1	283	Intron			XP_016872549.1
XM_017017061.1	283	Intron			XP_016872550.1
XM_017017062.1	283	Intron			XP_016872551.1
XM_017017063.1	283	UTR 5			XP_016872552.1

Gene: NUMA1
Gene Name: nuclear mitotic apparatus protein 1

There are no transcripts associated with this gene.

Gene: RNF121
Gene Name: ring finger protein 121

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300926.1	283	Intron			NP_001287855.1
NM_018320.4	283	Intron			NP_060790.2
XM_006718629.1	283	Intron			XP_006718692.1
XM_006718630.1	283	Intron			XP_006718693.1
XM_006718632.1	283	Intron			XP_006718695.1
XM_011545150.1	283	Intron			XP_011543452.1

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