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ATTTTAGACTTTTTTCTTCTCGGAT[C/T]ACCTCATCTGGTCTCTGTCTTCTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615117 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C2orf88 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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C2orf88 - chromosome 2 open reading frame 88 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042519.1 | Intron | NP_001035984.1 | ||||
NM_001042520.1 | Intron | NP_001035985.1 | ||||
NM_001042521.1 | Intron | NP_001035986.1 | ||||
NM_032321.2 | Intron | NP_115697.2 | ||||
XM_005246905.1 | Intron | XP_005246962.1 | ||||
XM_006712795.2 | Intron | XP_006712858.1 | ||||
XM_011511982.1 | Intron | XP_011510284.1 | ||||
XM_011511983.1 | Intron | XP_011510285.1 | ||||
XM_011511984.2 | Intron | XP_011510286.1 | ||||
XM_011511985.2 | Intron | XP_011510287.1 | ||||
XM_011511986.2 | Intron | XP_011510288.1 | ||||
XM_017005096.1 | Intron | XP_016860585.1 |