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SNP ID: rs145498713
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:66928071 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCCGACGTTTAAGCCCAAGCTCCC[C/G]AGGCCGAAGCATGAGAGCAAACCCC
Phenotype: MIM: 607667 MIM: 610869
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: CTNNA3 PubMed Links

Gene Details

Gene: CTNNA3
Gene Name: catenin alpha 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127384.2	1705	Intron			NP_001120856.1
NM_001291133.1	1705	Intron			NP_001278062.1
NM_013266.3	1705	Intron			NP_037398.2
XM_017016151.1	1705	Intron			XP_016871640.1
XM_017016152.1	1705	Intron			XP_016871641.1
XM_017016153.1	1705	Intron			XP_016871642.1
XM_017016154.1	1705	Intron			XP_016871643.1
XM_017016155.1	1705	Intron			XP_016871644.1
XM_017016156.1	1705	Intron			XP_016871645.1
XM_017016157.1	1705	Intron			XP_016871646.1
XM_017016158.1	1705	Intron			XP_016871647.1

Gene: LOC101928961
Gene Name: uncharacterized LOC101928961

There are no transcripts associated with this gene.

Gene: LRRTM3
Gene Name: leucine rich repeat transmembrane neuronal 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_178011.4	1705	Silent Mutation	CCC,CCG	P385P	NP_821079.3

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