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SNP ID: rs9303142
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:17687422 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CACCCACTCCTTGGGCATGAGAAAC[C/T]AGGGACCCCGTGGAGACAGCTGATA
Phenotype: MIM: 607642
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: RAI1 PubMed Links

Gene Details

Gene: RAI1
Gene Name: retinoic acid induced 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030665.3		Intron			NP_109590.3
XM_017024025.1		Intron			XP_016879514.1
XM_017024026.1		Intron			XP_016879515.1
XM_017024027.1		Intron			XP_016879516.1
XM_017024028.1		Intron			XP_016879517.1

Gene: SMCR2
Gene Name: Smith-Magenis syndrome chromosome region, candidate 2 (non-protein coding)

There are no transcripts associated with this gene.

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