Product Details

SNP ID: rs141117966
Assay Type: Functionally tested
NCBI dbSNP Submissions: 5
Location: Chr.1:26318024 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCACGAAGATCCTACCAAAATGAAG[C/T]GCTTCCTCTTCCTCCTACTCACCAT
Phenotype: MIM: 114280 MIM: 609151
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: AIM1L PubMed Links

Gene Details

Gene: AIM1L
Gene Name: absent in melanoma 1-like

There are no transcripts associated with this gene.

Gene: CD52
Gene Name: CD52 molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001803.2	105	Missense Mutation	CGC,TGC	R3C	NP_001794.2

Gene: UBXN11
Gene Name: UBX domain protein 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001077262.1	105	Intron			NP_001070730.1
NM_145345.2	105	Intron			NP_663320.2
NM_183008.2	105	Intron			NP_892120.2

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