Product Details
- SNP ID
-
rs111871930
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:34111277 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCGGAAGGGCCCCTTGGGAGGGGC[A/G]TAACTGGGGTCCTGGACTTTCTTAT
- Phenotype
-
MIM: 606745
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
PARD3
PubMed Links
Gene Details
- Gene
- PARD3
- Gene Name
- par-3 family cell polarity regulator
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001184785.1 |
4116 |
Silent Mutation |
TAC,TAT |
Y1318Y |
NP_001171714.1 |
| NM_001184786.1 |
4116 |
Silent Mutation |
TAC,TAT |
Y1305Y |
NP_001171715.1 |
| NM_001184787.1 |
4116 |
Silent Mutation |
TAC,TAT |
Y1284Y |
NP_001171716.1 |
| NM_001184788.1 |
4116 |
Silent Mutation |
TAC,TAT |
Y1275Y |
NP_001171717.1 |
| NM_001184789.1 |
4116 |
Silent Mutation |
TAC,TAT |
Y1238Y |
NP_001171718.1 |
| NM_001184790.1 |
4116 |
Silent Mutation |
TAC,TAT |
Y1231Y |
NP_001171719.1 |
| NM_001184791.1 |
4116 |
Silent Mutation |
TAC,TAT |
Y1209Y |
NP_001171720.1 |
| NM_001184792.1 |
4116 |
Intron |
|
|
NP_001171721.1 |
| NM_001184793.1 |
4116 |
Intron |
|
|
NP_001171722.1 |
| NM_001184794.1 |
4116 |
Intron |
|
|
NP_001171723.1 |
| NM_019619.3 |
4116 |
Silent Mutation |
TAC,TAT |
Y1321Y |
NP_062565.2 |
| XM_005252528.4 |
4116 |
Silent Mutation |
TAC,TAT |
Y1317Y |
XP_005252585.1 |
| XM_005252530.4 |
4116 |
Silent Mutation |
TAC,TAT |
Y1303Y |
XP_005252587.1 |
| XM_005252531.4 |
4116 |
Silent Mutation |
TAC,TAT |
Y1288Y |
XP_005252588.1 |
| XM_005252532.4 |
4116 |
Silent Mutation |
TAC,TAT |
Y1274Y |
XP_005252589.1 |
| XM_005252534.4 |
4116 |
Intron |
|
|
XP_005252591.1 |
| XM_005252535.4 |
4116 |
Intron |
|
|
XP_005252592.1 |
| XM_005252536.4 |
4116 |
Intron |
|
|
XP_005252593.1 |
| XM_011519569.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1320Y |
XP_011517871.1 |
| XM_011519570.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1308Y |
XP_011517872.1 |
| XM_011519571.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1306Y |
XP_011517873.1 |
| XM_011519572.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1305Y |
XP_011517874.1 |
| XM_011519573.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1291Y |
XP_011517875.1 |
| XM_011519575.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1287Y |
XP_011517877.1 |
| XM_011519576.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1277Y |
XP_011517878.1 |
| XM_011519577.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1265Y |
XP_011517879.1 |
| XM_011519578.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1263Y |
XP_011517880.1 |
| XM_011519579.2 |
4116 |
Silent Mutation |
TAC,TAT |
Y1243Y |
XP_011517881.1 |
| XM_011519581.2 |
4116 |
Intron |
|
|
XP_011517883.1 |
| XM_011519583.2 |
4116 |
Intron |
|
|
XP_011517885.1 |
| XM_011519584.2 |
4116 |
Intron |
|
|
XP_011517886.1 |
| XM_017016430.1 |
4116 |
Intron |
|
|
XP_016871919.1 |
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