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SNP ID: rs148863517
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:67451625 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGTGGCTGAGCTGTGGGATCCGAT[C/T]GTGGCTGGAGTGTGGGGTTCACCTG
Phenotype: MIM: 608965 MIM: 609849
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CABP4 PubMed Links

Gene Details

Gene: CABP4
Gene Name: calcium binding protein 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300895.1	1105	Intron			NP_001287824.1
NM_001300896.1	1105	Intron			NP_001287825.1
NM_145200.3	1105	Intron			NP_660201.1
XM_005274114.3	1105	Intron			XP_005274171.2
XM_011545181.2	1105	Intron			XP_011543483.1
XM_011545182.2	1105	Intron			XP_011543484.1
XM_011545183.2	1105	Intron			XP_011543485.1
XM_017018025.1	1105	Intron			XP_016873514.1

Gene: CORO1B
Gene Name: coronin 1B

There are no transcripts associated with this gene.

Gene: GPR152
Gene Name: G protein-coupled receptor 152

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_206997.1	1105	Missense Mutation	CAA,CGA	Q367R	NP_996880.1

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