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CCTTCGGCACCACCAGAGCAGAGAT[A/C]CAGCCACTGTAAAGGGAAGGATGTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 602989 MIM: 606913 | ||||||||||||||||||||
Literature Links: |
CLK2 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 |
CLK2 - CDC like kinase 2 | ||||||
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There are no transcripts associated with this gene. |
FAM189B - family with sequence similarity 189 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267608.1 | 942 | Intron | NP_001254537.1 | |||
NM_006589.2 | 942 | Intron | NP_006580.2 | |||
NM_198264.1 | 942 | Intron | NP_937995.1 |
SCAMP3 - secretory carrier membrane protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005698.3 | 942 | Missense Mutation | TGG,TGT | W,C 262 | NP_005689.2 | |
NM_052837.2 | 942 | Missense Mutation | TGG,TGT | W,C 236 | NP_443069.1 | |
XM_006711105.3 | 942 | Missense Mutation | TGG,TGT | W,C 248 | XP_006711168.1 | |
XM_006711106.3 | 942 | Missense Mutation | TGG,TGT | W,C 195 | XP_006711169.1 | |
XM_016999991.1 | 942 | Missense Mutation | GGA,GTA | G,V 175 | XP_016855480.1 |