Product Details
- SNP ID
-
rs75057934
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.22:17790794 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCAGCCTCCAGGTCCTTGTCCTCCT[C/G]TCTCTCCCGGAGCCGCTGCTCCTCC
- Phenotype
-
MIM: 608882
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
MICAL3
PubMed Links
Gene Details
- Gene
- MICAL3
- Gene Name
- microtubule associated monooxygenase, calponin and LIM domain containing 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001122731.2 |
6666 |
Intron |
|
|
NP_001116203.1 |
NM_001136004.3 |
6666 |
Intron |
|
|
NP_001129476.1 |
NM_015241.2 |
6666 |
Missense Mutation |
CAG,GAG |
Q1983E |
NP_056056.2 |
XM_005261262.3 |
6666 |
Missense Mutation |
CAG,GAG |
Q1983E |
XP_005261319.1 |
XM_011546137.2 |
6666 |
Missense Mutation |
CAG,GAG |
Q2190E |
XP_011544439.1 |
XM_011546139.2 |
6666 |
Missense Mutation |
CAG,GAG |
Q2173E |
XP_011544441.1 |
XM_011546142.2 |
6666 |
Missense Mutation |
CAG,GAG |
Q2156E |
XP_011544444.1 |
XM_011546146.2 |
6666 |
Intron |
|
|
XP_011544448.1 |
XM_017028865.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2190E |
XP_016884354.1 |
XM_017028866.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2190E |
XP_016884355.1 |
XM_017028867.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2190E |
XP_016884356.1 |
XM_017028868.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2190E |
XP_016884357.1 |
XM_017028869.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2190E |
XP_016884358.1 |
XM_017028870.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2190E |
XP_016884359.1 |
XM_017028871.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2189E |
XP_016884360.1 |
XM_017028872.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2173E |
XP_016884361.1 |
XM_017028873.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2169E |
XP_016884362.1 |
XM_017028874.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2162E |
XP_016884363.1 |
XM_017028875.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2154E |
XP_016884364.1 |
XM_017028876.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2144E |
XP_016884365.1 |
XM_017028877.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2123E |
XP_016884366.1 |
XM_017028878.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2085E |
XP_016884367.1 |
XM_017028879.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2038E |
XP_016884368.1 |
XM_017028880.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2038E |
XP_016884369.1 |
XM_017028881.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2038E |
XP_016884370.1 |
XM_017028882.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q2017E |
XP_016884371.1 |
XM_017028883.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q1890E |
XP_016884372.1 |
XM_017028884.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q1738E |
XP_016884373.1 |
XM_017028885.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q1289E |
XP_016884374.1 |
XM_017028886.1 |
6666 |
Missense Mutation |
CAG,GAG |
Q1289E |
XP_016884375.1 |
XM_017028887.1 |
6666 |
Intron |
|
|
XP_016884376.1 |
View Full Product Details