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Search Thermo Fisher Scientific
CCATTCATCCAACTCACCTTGTTCC[G/T]TAGCAACCTCAGGTAAATATGTGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
AMMECR1L 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 |
AMMECR1L - AMMECR1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199140.1 | 1348 | Missense Mutation | AAG,ACG | K,T 239 | NP_001186069.1 | |
NM_031445.2 | 1348 | Intron | NP_113633.2 | |||
XM_005263804.4 | 1348 | Missense Mutation | AAG,ACG | K,T 239 | XP_005263861.1 | |
XM_005263806.4 | 1348 | Missense Mutation | AAG,ACG | K,T 202 | XP_005263863.1 | |
XM_005263807.4 | 1348 | Missense Mutation | AAG,ACG | K,T 202 | XP_005263864.1 | |
XM_011511952.2 | 1348 | Missense Mutation | AAG,ACG | K,T 239 | XP_011510254.1 | |
XM_011511954.2 | 1348 | Missense Mutation | AAG,ACG | K,T 111 | XP_011510256.1 | |
XM_011511955.2 | 1348 | Intron | XP_011510257.1 | |||
XM_011511956.2 | 1348 | Intron | XP_011510258.1 | |||
XM_017005063.1 | 1348 | UTR 3 | XP_016860552.1 |
LOC107985803 - uncharacterized LOC107985803 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017005446.1 | 1348 | Intron | XP_016860935.1 |