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SNP ID: rs148496514
Assay Type: Functionally tested
NCBI dbSNP Submissions: 2
Location: Chr.1:247531584 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCCAGCTTGCCTGCAGAGCCACAGC[A/G]GTTCTCTAATACCATGTGCCGGAGG
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: GCSAML PubMed Links

Gene Details

Gene: GCSAML
Gene Name: germinal center associated signaling and motility like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001281834.1	1290	Intron			NP_001268763.1
NM_001281835.1	1290	Intron			NP_001268764.1
NM_001281836.1	1290	Intron			NP_001268765.1
NM_001281837.1	1290	Intron			NP_001268766.1
NM_001281838.1	1290	Intron			NP_001268767.1
NM_001281853.1	1290	Intron			NP_001268782.1
NM_145278.4	1290	Intron			NP_660321.1
XM_017000399.1	1290	Intron			XP_016855888.1

Gene: GCSAML-AS1
Gene Name: GCSAML antisense RNA 1

There are no transcripts associated with this gene.

Gene: OR2C3
Gene Name: olfactory receptor family 2 subfamily C member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198074.4	1290	Missense Mutation	CGC,TGC	R310C	NP_932340.3

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