Product Details
- SNP ID
-
rs143600797
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:59863805 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTTCCACACGTTGAAAGCATTAACA[A/G]GCTTCAACCAGGAAGTATACAGAGC
- Phenotype
-
MIM: 607344
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TUBD1
PubMed Links
Gene Details
- Gene
- TUBD1
- Gene Name
- tubulin delta 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001193609.1 |
1406 |
Missense Mutation |
CCT,CTT |
P318L |
NP_001180538.1 |
NM_001193610.1 |
1406 |
Intron |
|
|
NP_001180539.1 |
NM_001193611.1 |
1406 |
Missense Mutation |
CCT,CTT |
P271L |
NP_001180540.1 |
NM_001193612.1 |
1406 |
Missense Mutation |
CCT,CTT |
P199L |
NP_001180541.1 |
NM_001193613.1 |
1406 |
Missense Mutation |
CCT,CTT |
P157L |
NP_001180542.1 |
NM_016261.3 |
1406 |
Missense Mutation |
CCT,CTT |
P373L |
NP_057345.2 |
XM_005257425.1 |
1406 |
Missense Mutation |
CCT,CTT |
P306L |
XP_005257482.1 |
XM_011524871.2 |
1406 |
Missense Mutation |
CCT,CTT |
P326L |
XP_011523173.1 |
XM_017024716.1 |
1406 |
Intron |
|
|
XP_016880205.1 |
XM_017024717.1 |
1406 |
Missense Mutation |
CCT,CTT |
P169L |
XP_016880206.1 |
XM_017024718.1 |
1406 |
Missense Mutation |
CCT,CTT |
P169L |
XP_016880207.1 |
XM_017024719.1 |
1406 |
Missense Mutation |
CCT,CTT |
P161L |
XP_016880208.1 |
XM_017024720.1 |
1406 |
Missense Mutation |
CCT,CTT |
P161L |
XP_016880209.1 |
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