Product Details
- SNP ID
-
rs150924296
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:67074298 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ATTTATTGAAGAGCAAAAAGCCAGA[C/T]TGGCCGAAGACAAAGCAGAGTTGGA
- Phenotype
-
MIM: 611654
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CSPP1
PubMed Links
Gene Details
- Gene
- CSPP1
- Gene Name
- centrosome and spindle pole associated protein 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001291339.1 |
229 |
Intron |
|
|
NP_001278268.1 |
NM_024790.6 |
229 |
Silent Mutation |
CTG,TTG |
L52L |
NP_079066.5 |
XM_005251305.3 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_005251362.2 |
XM_006716474.2 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_006716537.2 |
XM_006716477.2 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_006716540.2 |
XM_011517598.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_011515900.1 |
XM_011517599.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_011515901.1 |
XM_011517600.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_011515902.1 |
XM_011517601.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_011515903.1 |
XM_011517602.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_011515904.1 |
XM_011517603.1 |
229 |
Silent Mutation |
CTG,TTG |
L16L |
XP_011515905.1 |
XM_011517607.1 |
229 |
Silent Mutation |
CTG,TTG |
L16L |
XP_011515909.1 |
XM_011517608.1 |
229 |
Silent Mutation |
CTG,TTG |
L16L |
XP_011515910.1 |
XM_011517609.1 |
229 |
Intron |
|
|
XP_011515911.1 |
XM_011517611.2 |
229 |
Intron |
|
|
XP_011515913.1 |
XM_017013847.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_016869336.1 |
XM_017013848.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_016869337.1 |
XM_017013849.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_016869338.1 |
XM_017013850.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_016869339.1 |
XM_017013851.1 |
229 |
Silent Mutation |
CTG,TTG |
L16L |
XP_016869340.1 |
XM_017013852.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_016869341.1 |
XM_017013853.1 |
229 |
Silent Mutation |
CTG,TTG |
L16L |
XP_016869342.1 |
XM_017013854.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_016869343.1 |
XM_017013855.1 |
229 |
Silent Mutation |
CTG,TTG |
L98L |
XP_016869344.1 |
XM_017013856.1 |
229 |
Silent Mutation |
CTG,TTG |
L16L |
XP_016869345.1 |
XM_017013857.1 |
229 |
Intron |
|
|
XP_016869346.1 |
XM_017013858.1 |
229 |
Intron |
|
|
XP_016869347.1 |
XM_017013859.1 |
229 |
Intron |
|
|
XP_016869348.1 |
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