Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCCCAATAATGCCGGCCACTATCA[A/G]TAAACACATTTCCAGCTACTCCATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300552 | ||||||||||||||||||||
Literature Links: |
MID1 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 |
MID1 - midline 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000381.3 | 1938 | Missense Mutation | ACT,ATT | T,I 536 | NP_000372.1 | |
NM_001098624.2 | 1938 | Missense Mutation | ACT,ATT | T,I 536 | NP_001092094.1 | |
NM_001193277.1 | 1938 | Missense Mutation | ACT,ATT | T,I 536 | NP_001180206.1 | |
NM_001193278.1 | 1938 | Intron | NP_001180207.1 | |||
NM_001193279.1 | 1938 | Intron | NP_001180208.1 | |||
NM_001193280.1 | 1938 | Intron | NP_001180209.1 | |||
NM_001193281.1 | 1938 | Intron | NP_001180210.1 | |||
NM_033289.1 | 1938 | Missense Mutation | ACT,ATT | T,I 498 | NP_150631.1 | |
NM_033290.3 | 1938 | Missense Mutation | ACT,ATT | T,I 536 | NP_150632.1 |