Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611202 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASAH2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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ASAH2 - N-acylsphingosine amidohydrolase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143974.1 | 492 | Silent Mutation | TCA,TCC | S,S 164 | NP_001137446.1 | |
NM_019893.2 | 492 | Silent Mutation | TCA,TCC | S,S 164 | NP_063946.2 | |
XM_011539970.2 | 492 | Silent Mutation | TCA,TCC | S,S 164 | XP_011538272.1 | |
XM_011539971.2 | 492 | Silent Mutation | TCA,TCC | S,S 164 | XP_011538273.1 | |
XM_011539972.2 | 492 | Silent Mutation | TCA,TCC | S,S 164 | XP_011538274.1 | |
XM_011539973.2 | 492 | Silent Mutation | TCA,TCC | S,S 164 | XP_011538275.1 | |
XM_017016435.1 | 492 | Silent Mutation | TCA,TCC | S,S 164 | XP_016871924.1 | |
XM_017016436.1 | 492 | Intron | XP_016871925.1 |