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TCCCCCCCATCACCCTCACCTCACT[A/C]CGGCAGGATGGGTGACAGGCAGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608926 MIM: 133450 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EMID1 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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EMID1 - EMI domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
EWSR1 - EWS RNA binding protein 1 | ||||||
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There are no transcripts associated with this gene. |
RHBDD3 - rhomboid domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_006724224.3 | 991 | Missense Mutation | XP_006724287.1 | |||
XM_011530107.2 | 991 | Missense Mutation | XP_011528409.1 | |||
XM_017028749.1 | 991 | Missense Mutation | XP_016884238.1 | |||
XM_017028750.1 | 991 | Missense Mutation | XP_016884239.1 |