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CTTCCTGGCCTGCTCCCAGCCTCCC[A/C]GTCACAGTGGGGCTGCCCCTGAGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616864 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C17orf62 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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C17orf62 - chromosome 17 open reading frame 62 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033046.3 | Intron | NP_001028218.1 | ||||
NM_001100407.2 | Intron | NP_001093877.1 | ||||
NM_001100408.2 | Intron | NP_001093878.1 | ||||
NM_001193653.1 | Intron | NP_001180582.1 | ||||
NM_001193654.1 | Intron | NP_001180583.1 | ||||
NM_001193655.1 | Intron | NP_001180584.1 | ||||
NM_001193657.1 | Intron | NP_001180586.1 | ||||
XM_006722293.2 | Intron | XP_006722356.1 | ||||
XM_011523606.2 | Intron | XP_011521908.1 | ||||
XM_017025072.1 | Intron | XP_016880561.1 | ||||
XM_017025073.1 | Intron | XP_016880562.1 | ||||
XM_017025074.1 | Intron | XP_016880563.1 | ||||
XM_017025075.1 | Intron | XP_016880564.1 | ||||
XM_017025076.1 | Intron | XP_016880565.1 | ||||
XM_017025077.1 | Intron | XP_016880566.1 | ||||
XM_017025078.1 | Intron | XP_016880567.1 |
HEXDC - hexosaminidase D | ||||||
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There are no transcripts associated with this gene. |