Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCTTCTTCATCTGCTGCTCCTTCC[A/G]CCTCTGTTCCTGGCGAAGGAGCTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606745 | ||||||||||||||||||||
Literature Links: |
PARD3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
PARD3 - par-3 family cell polarity regulator | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184785.1 | 4030 | Missense Mutation | CGG,TGG | R,W 1290 | NP_001171714.1 | |
NM_001184786.1 | 4030 | Missense Mutation | CGG,TGG | R,W 1277 | NP_001171715.1 | |
NM_001184787.1 | 4030 | Missense Mutation | CGG,TGG | R,W 1256 | NP_001171716.1 | |
NM_001184788.1 | 4030 | Missense Mutation | CGG,TGG | R,W 1247 | NP_001171717.1 | |
NM_001184789.1 | 4030 | Missense Mutation | CGG,TGG | R,W 1210 | NP_001171718.1 | |
NM_001184790.1 | 4030 | Missense Mutation | CGG,TGG | R,W 1203 | NP_001171719.1 | |
NM_001184791.1 | 4030 | Missense Mutation | CGG,TGG | R,W 1181 | NP_001171720.1 | |
NM_001184792.1 | 4030 | Intron | NP_001171721.1 | |||
NM_001184793.1 | 4030 | Intron | NP_001171722.1 | |||
NM_001184794.1 | 4030 | Intron | NP_001171723.1 | |||
NM_019619.3 | 4030 | Missense Mutation | CGG,TGG | R,W 1293 | NP_062565.2 | |
XM_005252528.4 | 4030 | Missense Mutation | CGG,TGG | R,W 1289 | XP_005252585.1 | |
XM_005252530.4 | 4030 | Missense Mutation | CGG,TGG | R,W 1275 | XP_005252587.1 | |
XM_005252531.4 | 4030 | Missense Mutation | CGG,TGG | R,W 1260 | XP_005252588.1 | |
XM_005252532.4 | 4030 | Missense Mutation | CGG,TGG | R,W 1246 | XP_005252589.1 | |
XM_005252534.4 | 4030 | Intron | XP_005252591.1 | |||
XM_005252535.4 | 4030 | Intron | XP_005252592.1 | |||
XM_005252536.4 | 4030 | Intron | XP_005252593.1 | |||
XM_011519569.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1292 | XP_011517871.1 | |
XM_011519570.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1280 | XP_011517872.1 | |
XM_011519571.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1278 | XP_011517873.1 | |
XM_011519572.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1277 | XP_011517874.1 | |
XM_011519573.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1263 | XP_011517875.1 | |
XM_011519575.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1259 | XP_011517877.1 | |
XM_011519576.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1249 | XP_011517878.1 | |
XM_011519577.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1237 | XP_011517879.1 | |
XM_011519578.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1235 | XP_011517880.1 | |
XM_011519579.2 | 4030 | Missense Mutation | CGG,TGG | R,W 1215 | XP_011517881.1 | |
XM_011519581.2 | 4030 | Intron | XP_011517883.1 | |||
XM_011519583.2 | 4030 | Intron | XP_011517885.1 | |||
XM_011519584.2 | 4030 | Intron | XP_011517886.1 | |||
XM_017016430.1 | 4030 | Intron | XP_016871919.1 |