Product Details

SNP ID
rs80148714
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:241327105 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGGCATTTACAGTGTAACATTCA[C/T]AATGTCTAATGTCTAATAGAAAATT
Phenotype
MIM: 601506
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SEPT2 PubMed Links

Gene Details

Gene
SEPT2
Gene Name
septin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001008491.2 Intron NP_001008491.1
NM_001008492.2 Intron NP_001008492.1
NM_001282972.1 Intron NP_001269901.1
NM_001282973.1 Intron NP_001269902.1
NM_001321029.1 Intron NP_001307958.1
NM_001321030.1 Intron NP_001307959.1
NM_001321031.1 Intron NP_001307960.1
NM_001321032.1 Intron NP_001307961.1
NM_001321033.1 Intron NP_001307962.1
NM_001321034.1 Intron NP_001307963.1
NM_001321035.1 Intron NP_001307964.1
NM_004404.4 Intron NP_004395.1
NM_006155.2 Intron NP_006146.1
XM_011511237.1 Intron XP_011509539.1
XM_011511238.1 Intron XP_011509540.1
XM_011511240.1 Intron XP_011509542.1
XM_017004189.1 Intron XP_016859678.1
XM_017004190.1 Intron XP_016859679.1
XM_017004191.1 Intron XP_016859680.1
XM_017004192.1 Intron XP_016859681.1
XM_017004193.1 Intron XP_016859682.1
XM_017004194.1 Intron XP_016859683.1
XM_017004195.1 Intron XP_016859684.1
XM_017004196.1 Intron XP_016859685.1
XM_017004197.1 Intron XP_016859686.1
XM_017004198.1 Intron XP_016859687.1
XM_017004199.1 Intron XP_016859688.1
XM_017004200.1 Intron XP_016859689.1
XM_017004201.1 Intron XP_016859690.1
XM_017004202.1 Intron XP_016859691.1
XM_017004203.1 Intron XP_016859692.1
XM_017004204.1 Intron XP_016859693.1
XM_017004205.1 Intron XP_016859694.1
XM_017004206.1 Intron XP_016859695.1
XM_017004207.1 Intron XP_016859696.1
XM_017004208.1 Intron XP_016859697.1
XM_017004209.1 Intron XP_016859698.1
XM_017004210.1 Intron XP_016859699.1
XM_017004211.1 Intron XP_016859700.1
XM_017004212.1 Intron XP_016859701.1
XM_017004213.1 Intron XP_016859702.1

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