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TGGCCTCCTCGTGCTTCTTGCGGTG[A/G]GCCGTGATCTCCTGCACGCACGTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607074 MIM: 614767 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC107987269 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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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
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LOC107987269 - uncharacterized LOC107987269 | ||||||
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There are no transcripts associated with this gene. |
PRKD2 - protein kinase D2 | ||||||
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There are no transcripts associated with this gene. |
STRN4 - striatin 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039877.1 | 2247 | Silent Mutation | GCC,GCT | A,A 726 | NP_001034966.1 | |
NM_013403.2 | 2247 | Silent Mutation | GCC,GCT | A,A 719 | NP_037535.2 | |
XM_006723171.2 | 2247 | Silent Mutation | GCC,GCT | A,A 741 | XP_006723234.1 | |
XM_006723172.2 | 2247 | Silent Mutation | GCC,GCT | A,A 734 | XP_006723235.1 | |
XM_006723174.2 | 2247 | Silent Mutation | GCC,GCT | A,A 607 | XP_006723237.1 | |
XM_011526878.1 | 2247 | UTR 3 | XP_011525180.1 | |||
XM_011526879.1 | 2247 | Silent Mutation | GCC,GCT | A,A 331 | XP_011525181.1 | |
XM_017026716.1 | 2247 | Silent Mutation | GCC,GCT | A,A 622 | XP_016882205.1 | |
XM_017026717.1 | 2247 | Silent Mutation | GCC,GCT | A,A 607 | XP_016882206.1 | |
XM_017026718.1 | 2247 | Silent Mutation | GCC,GCT | A,A 505 | XP_016882207.1 | |
XM_017026719.1 | 2247 | UTR 3 | XP_016882208.1 |