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GTTCAGGTGTGTGACTCTTCTTGGA[C/T]GATGACTCATCACGTTCTACTGTCA
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 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000381.3 | 2050 | Silent Mutation | TCA,TCG | S,S 512 | NP_000372.1 | |
NM_001098624.2 | 2050 | Silent Mutation | TCA,TCG | S,S 512 | NP_001092094.1 | |
NM_001193277.1 | 2050 | Silent Mutation | TCA,TCG | S,S 512 | NP_001180206.1 | |
NM_001193278.1 | 2050 | Intron | NP_001180207.1 | |||
NM_001193279.1 | 2050 | Intron | NP_001180208.1 | |||
NM_001193280.1 | 2050 | Intron | NP_001180209.1 | |||
NM_001193281.1 | 2050 | Intron | NP_001180210.1 | |||
NM_033289.1 | 2050 | Silent Mutation | TCA,TCG | S,S 474 | NP_150631.1 | |
NM_033290.3 | 2050 | Silent Mutation | TCA,TCG | S,S 512 | NP_150632.1 | |
XM_005274536.1 | 2050 | Silent Mutation | TCA,TCG | S,S 563 | XP_005274593.1 | |
XM_005274537.1 | 2050 | Silent Mutation | TCA,TCG | S,S 563 | XP_005274594.1 | |
XM_006724492.3 | 2050 | Silent Mutation | TCA,TCG | S,S 563 | XP_006724555.1 | |
XM_011545525.2 | 2050 | Silent Mutation | TCA,TCG | S,S 563 | XP_011543827.1 | |
XM_011545526.2 | 2050 | Silent Mutation | TCA,TCG | S,S 563 | XP_011543828.1 | |
XM_011545527.2 | 2050 | Silent Mutation | TCA,TCG | S,S 563 | XP_011543829.1 | |
XM_017029534.1 | 2050 | Silent Mutation | TCA,TCG | S,S 563 | XP_016885023.1 | |
XM_017029535.1 | 2050 | Silent Mutation | TCA,TCG | S,S 525 | XP_016885024.1 | |
XM_017029536.1 | 2050 | Silent Mutation | TCA,TCG | S,S 512 | XP_016885025.1 | |
XM_017029537.1 | 2050 | Silent Mutation | TCA,TCG | S,S 474 | XP_016885026.1 | |
XM_017029538.1 | 2050 | Silent Mutation | TCA,TCG | S,S 474 | XP_016885027.1 | |
XM_017029539.1 | 2050 | Silent Mutation | TCA,TCG | S,S 474 | XP_016885028.1 | |
XM_017029540.1 | 2050 | Silent Mutation | TCA,TCG | S,S 512 | XP_016885029.1 | |
XM_017029541.1 | 2050 | Intron | XP_016885030.1 | |||
XM_017029542.1 | 2050 | Intron | XP_016885031.1 |