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GCCAGTCAGCTTCGCTCTCGCACCG[A/G]GCCCGGCCATGGAAGAAGTGCCTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603781 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYO15B 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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RECQL5 - RecQ like helicase 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003715.3 | 2029 | Intron | NP_001003715.1 | |||
NM_001003716.3 | 2029 | Intron | NP_001003716.1 | |||
NM_004259.6 | 2029 | Silent Mutation | GCC,GCT | A,A 975 | NP_004250.4 | |
XM_005257818.3 | 2029 | Silent Mutation | GCC,GCT | A,A 996 | XP_005257875.1 | |
XM_005257822.3 | 2029 | Silent Mutation | GCC,GCT | A,A 570 | XP_005257879.1 | |
XM_005257823.3 | 2029 | Intron | XP_005257880.1 | |||
XM_006722186.2 | 2029 | Silent Mutation | GCC,GCT | A,A 591 | XP_006722249.1 | |
XM_011525482.2 | 2029 | Silent Mutation | GCC,GCT | A,A 996 | XP_011523784.1 | |
XM_011525484.1 | 2029 | Silent Mutation | GCC,GCT | A,A 602 | XP_011523786.1 | |
XM_011525485.2 | 2029 | Silent Mutation | GCC,GCT | A,A 596 | XP_011523787.1 | |
XM_011525486.2 | 2029 | Silent Mutation | GCC,GCT | A,A 485 | XP_011523788.1 | |
XM_017025343.1 | 2029 | Silent Mutation | GCC,GCT | A,A 975 | XP_016880832.1 | |
XM_017025344.1 | 2029 | Intron | XP_016880833.1 |
SMIM5 - small integral membrane protein 5 | ||||||
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There are no transcripts associated with this gene. |