Search Thermo Fisher Scientific
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GCTGGCTTTGGCCTGAAGGTGCTGA[A/G]CTGGCTGCCCGGCTCCTGCTTCGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610109 | ||||||||||||||||||||
Literature Links: |
ANO2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ANO2 - anoctamin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278596.1 | 3260 | Silent Mutation | AGC,AGT | S,S 981 | NP_001265525.1 | |
NM_001278597.1 | 3260 | Silent Mutation | AGC,AGT | S,S 977 | NP_001265526.1 | |
XM_006718988.3 | 3260 | Silent Mutation | AGC,AGT | S,S 976 | XP_006719051.1 | |
XM_011520975.2 | 3260 | Silent Mutation | AGC,AGT | S,S 972 | XP_011519277.1 | |
XM_011520978.2 | 3260 | Silent Mutation | AGC,AGT | S,S 765 | XP_011519280.1 | |
XM_017019672.1 | 3260 | Intron | XP_016875161.1 |