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GTCTTGACTGTCGTGATGAAGAACT[G/A]GGAGCCGTTGGTGTCTTTGCCTGCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606274 MIM: 123841 | ||||||||||||||||||||
Literature Links: |
CSNK1G1 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 |
CSNK1G1 - casein kinase 1 gamma 1 | ||||||
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There are no transcripts associated with this gene. |
PPIB - peptidylprolyl isomerase B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000942.4 | 620 | Nonsense Mutation | CAG,TAG | Q,* 151 | NP_000933.1 |
SNX22 - sorting nexin 22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024798.2 | 620 | UTR 3 | NP_079074.2 | |||
XM_005254677.3 | 620 | Intron | XP_005254734.1 | |||
XM_017022581.1 | 620 | UTR 3 | XP_016878070.1 |