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SNP ID: rs11160
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:17116407 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGTGCCACTTCCCTCCTTCTTCCAG[A/G]CTCTAACCGCCAGCTAGCTCTCTTT
Phenotype: MIM: 605461
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CECR6 PubMed Links

Gene Details

Gene: CECR6
Gene Name: cat eye syndrome chromosome region, candidate 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001163079.1	3853	UTR 3			NP_001156551.1
NM_031890.3	3853	UTR 3			NP_114096.1
XM_011546124.2	3853	UTR 3			XP_011544426.1
XM_011546125.2	3853	UTR 3			XP_011544427.1

Gene: IL17RA
Gene Name: interleukin 17 receptor A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001289905.1	3853	Intron			NP_001276834.1
NM_014339.6	3853	Intron			NP_055154.3

Gene: LOC100996342
Gene Name: uncharacterized LOC100996342

There are no transcripts associated with this gene.

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