Product Details

SNP ID
rs11650333
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:77297956 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGGAGCCAGCAGTGCAAGGACTA[A/G]GCTGGAAGCAAGCTTGGTGCATTCC
Phenotype
MIM: 604061
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SEPT9 PubMed Links

Gene Details

Gene
SEPT9
Gene Name
septin 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001113491.1 Intron NP_001106963.1
NM_001113492.1 Intron NP_001106964.1
NM_001113493.1 Intron NP_001106965.1
NM_001113494.1 Intron NP_001106966.1
NM_001113495.1 Intron NP_001106967.1
NM_001113496.1 Intron NP_001106968.1
NM_001293695.1 Intron NP_001280624.1
NM_001293696.1 Intron NP_001280625.1
NM_001293697.1 Intron NP_001280626.1
NM_001293698.1 Intron NP_001280627.1
NM_006640.4 Intron NP_006631.2
XM_005256962.1 Intron XP_005257019.1
XM_006721643.2 Intron XP_006721706.1
XM_006721644.1 Intron XP_006721707.1
XM_011524204.1 Intron XP_011522506.1
XM_011524206.1 Intron XP_011522508.1
XM_011524207.1 Intron XP_011522509.1
XM_011524208.2 Intron XP_011522510.1
XM_017024031.1 Intron XP_016879520.1
XM_017024032.1 Intron XP_016879521.1

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