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GGCACGGCTGCCTGTCCTAATGGCA[A/G]CTTCCACTGCACCAACACTGGCTAT
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615956 MIM: 177060 | ||||||||||||||||||||||||||
Literature Links: |
CCDC151 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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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)
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EUR - Not Available | |||||
AMR - Not Available |
CCDC151 - coiled-coil domain containing 151 | ||||||
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There are no transcripts associated with this gene. |
PRKCSH - protein kinase C substrate 80K-H | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001001329.2 | 599 | Missense Mutation | AAC,AGC | N,S 74 | NP_001001329.1 | |
NM_001289102.1 | 599 | Missense Mutation | AAC,AGC | N,S 74 | NP_001276031.1 | |
NM_001289103.1 | 599 | Missense Mutation | AAC,AGC | N,S 74 | NP_001276032.1 | |
NM_001289104.1 | 599 | Missense Mutation | AAC,AGC | N,S 74 | NP_001276033.1 | |
NM_002743.3 | 599 | Missense Mutation | AAC,AGC | N,S 74 | NP_002734.2 | |
XM_011528130.1 | 599 | Missense Mutation | AAC,AGC | N,S 74 | XP_011526432.1 | |
XM_011528131.1 | 599 | Missense Mutation | AAC,AGC | N,S 74 | XP_011526433.1 | |
XM_011528132.1 | 599 | Missense Mutation | AAC,AGC | N,S 74 | XP_011526434.1 | |
XM_017026977.1 | 599 | Missense Mutation | AAC,AGC | N,S 74 | XP_016882466.1 |
Set Membership: |
HapMap |