Product Details

SNP ID
rs79617622
Assay Type
Functionally tested
NCBI dbSNP Submissions
10
Location
Chr.1:246569776 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTAACGTTGAGCCCCATGCTTGTTT[A/C]ATGAGGCTCATAAGATGAATAGTGT
Phenotype
MIM: 613439 MIM: 607055
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CNST PubMed Links

Gene Details

Gene
CNST
Gene Name
consortin, connexin sorting protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001139459.1 Intron NP_001132931.1
NM_152609.2 Intron NP_689822.2
XM_005273081.3 Intron XP_005273138.2
XM_005273083.4 Intron XP_005273140.1
XM_011544110.2 Intron XP_011542412.1
XM_011544111.1 Intron XP_011542413.1
XM_011544112.1 Intron XP_011542414.1
XM_011544113.1 Intron XP_011542415.1
XM_011544114.2 Intron XP_011542416.1
XM_017000487.1 Intron XP_016855976.1
XM_017000488.1 Intron XP_016855977.1
XM_017000489.1 Intron XP_016855978.1
Gene
TFB2M
Gene Name
transcription factor B2, mitochondrial
There are no transcripts associated with this gene.

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