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CGGGGCATGAAGAGTGCCGTTCTGG[A/G]AACAGTGCTGTCGGGAAGCAATATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606017 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AMMECR1L 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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AMMECR1L - AMMECR1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199140.1 | 1743 | Missense Mutation | NP_001186069.1 | |||
NM_031445.2 | 1743 | Intron | NP_113633.2 | |||
XM_005263804.4 | 1743 | Missense Mutation | XP_005263861.1 | |||
XM_005263806.4 | 1743 | Missense Mutation | XP_005263863.1 | |||
XM_005263807.4 | 1743 | Missense Mutation | XP_005263864.1 | |||
XM_011511952.2 | 1743 | Missense Mutation | XP_011510254.1 | |||
XM_011511954.2 | 1743 | Missense Mutation | XP_011510256.1 | |||
XM_011511955.2 | 1743 | Intron | XP_011510257.1 | |||
XM_011511956.2 | 1743 | Intron | XP_011510258.1 | |||
XM_017005063.1 | 1743 | Intron | 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 | 1743 | Intron | XP_016860935.1 |
POLR2D - RNA polymerase II subunit D | ||||||
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There are no transcripts associated with this gene. |