Product Details
- SNP ID
-
rs34326649
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:83903186 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGCCTTCCTGACCTCTTGGATCAT[A/G]TTAAACCACTCCTGCAGTTTGTGTT
- Phenotype
-
MIM: 611253
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
KIF27
PubMed Links
Gene Details
- Gene
- KIF27
- Gene Name
- kinesin family member 27
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001271927.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
NP_001258856.1 |
| NM_001271928.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
NP_001258857.1 |
| NM_017576.2 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
NP_060046.1 |
| XM_011518848.2 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_011517150.1 |
| XM_011518849.2 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_011517151.1 |
| XM_011518850.2 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_011517152.1 |
| XM_011518854.2 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_011517156.1 |
| XM_011518856.2 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_011517158.1 |
| XM_011518857.2 |
1665 |
Silent Mutation |
AAC,AAT |
N86N |
XP_011517159.1 |
| XM_011518858.2 |
1665 |
Intron |
|
|
XP_011517160.1 |
| XM_017014900.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870389.1 |
| XM_017014901.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870390.1 |
| XM_017014902.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870391.1 |
| XM_017014903.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870392.1 |
| XM_017014904.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870393.1 |
| XM_017014905.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870394.1 |
| XM_017014906.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870395.1 |
| XM_017014907.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870396.1 |
| XM_017014908.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870397.1 |
| XM_017014909.1 |
1665 |
Silent Mutation |
AAC,AAT |
N292N |
XP_016870398.1 |
| XM_017014910.1 |
1665 |
Silent Mutation |
AAC,AAT |
N444N |
XP_016870399.1 |
| XM_017014911.1 |
1665 |
Silent Mutation |
AAC,AAT |
N86N |
XP_016870400.1 |
| XM_017014912.1 |
1665 |
Intron |
|
|
XP_016870401.1 |
| XM_017014913.1 |
1665 |
Intron |
|
|
XP_016870402.1 |
| XM_017014914.1 |
1665 |
Intron |
|
|
XP_016870403.1 |
| XM_017014915.1 |
1665 |
Intron |
|
|
XP_016870404.1 |
| XM_017014916.1 |
1665 |
UTR 5 |
|
|
XP_016870405.1 |
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