Product Details

SNP ID
rs147761775
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:10250388 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTCGATGAATATGGGCGCCCTTT[C/T]CTCATCATCAAGGATCAGGACCGCA
Phenotype
MIM: 610150
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CCT5 PubMed Links

Gene Details

Gene
CCT5
Gene Name
chaperonin containing TCP1 subunit 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001306153.1 468 Intron NP_001293082.1
NM_001306154.1 468 Silent Mutation TTC,TTT F16F NP_001293083.1
NM_001306155.1 468 Intron NP_001293084.1
NM_001306156.1 468 Intron NP_001293085.1
NM_012073.4 468 Silent Mutation TTC,TTT F16F NP_036205.1
Gene
FAM173B
Gene Name
family with sequence similarity 173 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001258388.1 468 Intron NP_001245317.1
NM_001258389.1 468 Intron NP_001245318.1
NM_199133.3 468 Intron NP_954584.2
XM_011513964.1 468 Intron XP_011512266.1

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