Product Details
- SNP ID
-
rs34989098
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.18:70006461 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTTTGATTCTCACTTTCCAGACAGG[C/T]AGCAAGCACAGTAATGACTTTTTCT
- Phenotype
-
MIM: 610436
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
RTTN
PubMed Links
Gene Details
- Gene
- RTTN
- Gene Name
- rotatin
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001318520.1 |
6276 |
Missense Mutation |
ACC,GCC |
T1237A |
NP_001305449.1 |
NM_173630.3 |
6276 |
Missense Mutation |
ACC,GCC |
T2149A |
NP_775901.3 |
XM_006722434.3 |
6276 |
Missense Mutation |
ACC,GCC |
T2150A |
XP_006722497.1 |
XM_006722435.3 |
6276 |
Intron |
|
|
XP_006722498.1 |
XM_011525902.2 |
6276 |
Missense Mutation |
ACC,GCC |
T2070A |
XP_011524204.1 |
XM_011525903.2 |
6276 |
Missense Mutation |
ACC,GCC |
T2007A |
XP_011524205.1 |
XM_011525904.2 |
6276 |
Intron |
|
|
XP_011524206.1 |
XM_011525905.2 |
6276 |
Intron |
|
|
XP_011524207.1 |
XM_011525906.2 |
6276 |
Missense Mutation |
ACC,GCC |
T1650A |
XP_011524208.1 |
XM_011525907.2 |
6276 |
Intron |
|
|
XP_011524209.1 |
XM_011525908.2 |
6276 |
Intron |
|
|
XP_011524210.1 |
XM_017025693.1 |
6276 |
Missense Mutation |
ACC,GCC |
T2069A |
XP_016881182.1 |
XM_017025694.1 |
6276 |
Missense Mutation |
ACC,GCC |
T1936A |
XP_016881183.1 |
XM_017025695.1 |
6276 |
Missense Mutation |
ACC,GCC |
T1795A |
XP_016881184.1 |
XM_017025696.1 |
6276 |
Missense Mutation |
ACC,GCC |
T1447A |
XP_016881185.1 |
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