Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AACAGTGACACGGCACCCTCCACAC[A/G]GCCTGTGGCTGCCAGTGCCACCACC
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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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267895.1 | 1353 | Intron | NP_001254824.1 | |||
NM_133455.3 | 1353 | Intron | NP_597712.2 | |||
XM_005261328.2 | 1353 | Intron | XP_005261385.1 | |||
XM_005261329.2 | 1353 | Intron | XP_005261386.1 | |||
XM_011529868.2 | 1353 | Intron | XP_011528170.1 | |||
XM_011529869.2 | 1353 | Intron | XP_011528171.1 | |||
XM_011529870.2 | 1353 | Intron | XP_011528172.1 | |||
XM_011529871.2 | 1353 | Intron | XP_011528173.1 | |||
XM_011529872.2 | 1353 | Intron | XP_011528174.1 | |||
XM_011529873.2 | 1353 | Intron | XP_011528175.1 | |||
XM_011529874.2 | 1353 | Intron | XP_011528176.1 | |||
XM_011529875.2 | 1353 | Intron | XP_011528177.1 | |||
XM_011529876.1 | 1353 | Intron | XP_011528178.1 | |||
XM_017028589.1 | 1353 | Intron | XP_016884078.1 |
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 | 1353 | Missense Mutation | CGT,TGT | R,C 223 | XP_006724287.1 | |
XM_011530107.2 | 1353 | Missense Mutation | CGT,TGT | R,C 351 | XP_011528409.1 | |
XM_017028749.1 | 1353 | Missense Mutation | CGT,TGT | R,C 354 | XP_016884238.1 | |
XM_017028750.1 | 1353 | Missense Mutation | CGT,TGT | R,C 218 | XP_016884239.1 |