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TATGAGGCTGGGTCGGCCAGGGCTG[A/G]GGGCCGATGGGACAGGGGTACAGCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LOC101929060 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 |
LOC101929060 - uncharacterized LOC101929060 | ||||||
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There are no transcripts associated with this gene. |
MIER2 - MIER family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005259582.4 | 1932 | Missense Mutation | CCA,TCA | P,S 449 | XP_005259639.1 | |
XM_006722769.3 | 1932 | Missense Mutation | CCA,TCA | P,S 442 | XP_006722832.1 | |
XM_011528072.2 | 1932 | Missense Mutation | CCA,TCA | P,S 449 | XP_011526374.1 | |
XM_011528073.1 | 1932 | Missense Mutation | CCA,TCA | P,S 447 | XP_011526375.1 | |
XM_011528074.2 | 1932 | Missense Mutation | CCA,TCA | P,S 442 | XP_011526376.1 | |
XM_011528075.2 | 1932 | Missense Mutation | CCA,TCA | P,S 411 | XP_011526377.1 | |
XM_011528077.2 | 1932 | Missense Mutation | CCA,TCA | P,S 411 | XP_011526379.1 | |
XM_011528081.2 | 1932 | Missense Mutation | CCA,TCA | P,S 371 | XP_011526383.1 | |
XM_011528082.2 | 1932 | Missense Mutation | CCA,TCA | P,S 363 | XP_011526384.1 |