Product Details
- SNP ID
-
rs201253732
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:171692859 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAAAGGAGAGAAGCTGAAGCATTGC[C/T]TCAAAGCATGGGGCTAACTCCAGAA
- Phenotype
-
MIM: 603331
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
DYNC1I2
PubMed Links
Gene Details
- Gene
- DYNC1I2
- Gene Name
- dynein cytoplasmic 1 intermediate chain 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001271785.1 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001258714.1 |
NM_001271786.1 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001258715.1 |
NM_001271787.1 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001258716.1 |
NM_001271788.1 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001258717.1 |
NM_001271789.1 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001258718.1 |
NM_001271790.1 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001258719.1 |
NM_001320882.1 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001307811.1 |
NM_001320883.1 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001307812.1 |
NM_001320884.1 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001307813.1 |
NM_001378.2 |
419 |
Missense Mutation |
CCT,CTT |
P64L |
NP_001369.1 |
XM_006712347.3 |
419 |
Intron |
|
|
XP_006712410.1 |
XM_017003525.1 |
419 |
Intron |
|
|
XP_016859014.1 |
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