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ATTTTCTTAAGCTTCTAGAATTCAT[C/T]TTGTTATGTATATATATTTGGAAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCSER2 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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CCSER2 - coiled-coil serine rich protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284240.1 | Intron | NP_001271169.1 | ||||
NM_001284241.1 | Intron | NP_001271170.1 | ||||
NM_001284242.1 | Intron | NP_001271171.1 | ||||
NM_001284243.1 | Intron | NP_001271172.1 | ||||
NM_018999.3 | Intron | NP_061872.2 | ||||
XM_005269905.3 | Intron | XP_005269962.1 | ||||
XM_005269906.3 | Intron | XP_005269963.1 | ||||
XM_005269908.3 | Intron | XP_005269965.1 | ||||
XM_006717894.1 | Intron | XP_006717957.1 | ||||
XM_006717895.1 | Intron | XP_006717958.1 | ||||
XM_011539870.2 | Intron | XP_011538172.1 | ||||
XM_011539871.2 | Intron | XP_011538173.1 | ||||
XM_011539872.2 | Intron | XP_011538174.1 | ||||
XM_011539873.1 | Intron | XP_011538175.1 | ||||
XM_017016340.1 | Intron | XP_016871829.1 | ||||
XM_017016341.1 | Intron | XP_016871830.1 | ||||
XM_017016342.1 | Intron | XP_016871831.1 | ||||
XM_017016343.1 | Intron | XP_016871832.1 |