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CCCTGCGCCATCTCCCGCTTCAGCA[G/A]CCCCAGCGAGATGCCTACGGGGATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 611354 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACAP3 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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ACAP3 - ArfGAP with coiled-coil, ankyrin repeat and PH domains 3 | ||||||
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There are no transcripts associated with this gene. |
CPSF3L - cleavage and polyadenylation specific factor 3-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256456.1 | 1612 | Silent Mutation | CTG,TTG | L,L 466 | NP_001243385.1 | |
NM_001256460.1 | 1612 | Silent Mutation | CTG,TTG | L,L 431 | NP_001243389.1 | |
NM_001256462.1 | 1612 | Silent Mutation | CTG,TTG | L,L 362 | NP_001243391.1 | |
NM_001256463.1 | 1612 | Silent Mutation | CTG,TTG | L,L 359 | NP_001243392.1 | |
NM_017871.5 | 1612 | Silent Mutation | CTG,TTG | L,L 460 | NP_060341.2 | |
XM_011541647.1 | 1612 | Silent Mutation | CTG,TTG | L,L 520 | XP_011539949.1 | |
XM_011541648.1 | 1612 | Silent Mutation | CTG,TTG | L,L 482 | XP_011539950.1 | |
XM_011541650.1 | 1612 | Silent Mutation | CTG,TTG | L,L 336 | XP_011539952.1 | |
XM_017001557.1 | 1612 | Silent Mutation | CTG,TTG | L,L 336 | XP_016857046.1 | |
XM_017001558.1 | 1612 | Silent Mutation | CTG,TTG | L,L 336 | XP_016857047.1 |
MIR6727 - microRNA 6727 | ||||||
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There are no transcripts associated with this gene. |
PUSL1 - pseudouridylate synthase-like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153339.1 | 1612 | Intron | NP_699170.1 | |||
XM_005244720.3 | 1612 | Intron | XP_005244777.1 |