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ACTGTCAATGGAAATATAACATGAG[C/T]CATACATGATAGCCATTTATGTAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611574 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SGMS2 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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SGMS2 - sphingomyelin synthase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136257.1 | Intron | NP_001129729.1 | ||||
NM_001136258.1 | Intron | NP_001129730.1 | ||||
NM_152621.5 | Intron | NP_689834.1 | ||||
XM_011531698.2 | Intron | XP_011530000.1 | ||||
XM_011531699.2 | Intron | XP_011530001.1 | ||||
XM_011531700.2 | Intron | XP_011530002.1 | ||||
XM_011531701.2 | Intron | XP_011530003.1 | ||||
XM_011531702.2 | Intron | XP_011530004.1 | ||||
XM_017007839.1 | Intron | XP_016863328.1 | ||||
XM_017007840.1 | Intron | XP_016863329.1 | ||||
XM_017007841.1 | Intron | XP_016863330.1 |