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GGCAAAAGGGTTAGGTGGCCATCTT[A/G]CCTTCTCCCAAACACAAAACGATTG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 176977 | |||||||||||||||||||||||
Literature Links: |
PRKCD PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
PRKCD - protein kinase C delta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001316327.1 | Intron | NP_001303256.1 | ||||
NM_006254.3 | Intron | NP_006245.2 | ||||
NM_212539.1 | Intron | NP_997704.1 | ||||
XM_006713257.3 | Intron | XP_006713320.1 | ||||
XM_006713259.2 | Intron | XP_006713322.1 | ||||
XM_017006855.1 | Intron | XP_016862344.1 | ||||
XM_017006856.1 | Intron | XP_016862345.1 |