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TCCTCAGCAGGAACATGTTAGCAAG[T/C]TAAGATATCTGTACTTAGCTTCCTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
|
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Phenotype: |
MIM: 603831 | ||||||||||||||||||||
Literature Links: |
PDZK1 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 |
PDZK1 - PDZ domain containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001201325.1 | Intron | NP_001188254.1 | ||||
NM_001201326.1 | Intron | NP_001188255.1 | ||||
NM_002614.4 | Intron | NP_002605.2 | ||||
XM_011509616.2 | Intron | XP_011507918.1 | ||||
XM_011509618.2 | Intron | XP_011507920.1 | ||||
XM_011509619.2 | Intron | XP_011507921.2 | ||||
XM_017001464.1 | Intron | XP_016856953.1 | ||||
XM_017001465.1 | Intron | XP_016856954.1 | ||||
XM_017001466.1 | Intron | XP_016856955.1 | ||||
XM_017001467.1 | Intron | XP_016856956.1 |