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SNP ID: rs11853992
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.15:92469121 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTGGGAGGTGGAGTTATAGGACCCC[A/G]TCAGTCATTCCCACTGCTGTTGTTG
Phenotype: MIM: 602546
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C15orf32 PubMed Links

Gene Details

Gene: C15orf32
Gene Name: chromosome 15 open reading frame 32

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301106.1	3360	Intron			NP_001288035.1
NM_153040.2	3360	Intron			NP_694585.1
XM_011521257.2	3360	UTR 5			XP_011519559.1

Gene: LOC104613533
Gene Name: uncharacterized LOC104613533

There are no transcripts associated with this gene.

Gene: ST8SIA2
Gene Name: ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006011.3	3360	Intron			NP_006002.1
XM_017022642.1	3360	Intron			XP_016878131.1
XM_017022643.1	3360	Intron			XP_016878132.1

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