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TCTCATATCTGCCAAGATGCTATTA[C/T]TGGACAAATCACCAAAGCCCTCTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600810 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PLCB4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
PLCB4 - phospholipase C beta 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000933.3 | Intron | NP_000924.3 | ||||
NM_001172646.1 | Intron | NP_001166117.1 | ||||
NM_182797.2 | Intron | NP_877949.2 | ||||
XM_005260724.2 | Intron | XP_005260781.1 | ||||
XM_005260728.2 | Intron | XP_005260785.1 | ||||
XM_006723568.3 | Intron | XP_006723631.1 | ||||
XM_006723569.2 | Intron | XP_006723632.1 | ||||
XM_011529254.2 | Intron | XP_011527556.1 | ||||
XM_017027880.1 | Intron | XP_016883369.1 | ||||
XM_017027881.1 | Intron | XP_016883370.1 | ||||
XM_017027882.1 | Intron | XP_016883371.1 | ||||
XM_017027883.1 | Intron | XP_016883372.1 | ||||
XM_017027884.1 | Intron | XP_016883373.1 | ||||
XM_017027885.1 | Intron | XP_016883374.1 | ||||
XM_017027886.1 | Intron | XP_016883375.1 |