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SNP ID: rs2231423
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:73234216 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAGCCTCAGGTCCTTCTAGCCGCAC[C/G]GAGTCGGTGGTAACGAACCATAGAG
Phenotype: MIM: 605140
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: CCT7 PubMed Links

Gene Details

Gene: CCT7
Gene Name: chaperonin containing TCP1 subunit 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001009570.2		Intron			NP_001009570.1
NM_001166284.1		Intron			NP_001159756.1
NM_001166285.1		Intron			NP_001159757.1
NM_006429.3		Intron			NP_006420.1
XM_011532478.2		Intron			XP_011530780.1
XM_011532479.1		Intron			XP_011530781.1

Gene: PRADC1
Gene Name: protease associated domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032319.1		Intron			NP_115695.1

Gene: SMYD5
Gene Name: SMYD family member 5

There are no transcripts associated with this gene.

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