Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGATCCTTTGTCCTGGATGGAGCCC[A/G]AGACACCCTGCGCGATCTTCACTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 146690 | ||||||||||||||||||||
Literature Links: |
IMPDH1 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 |
IMPDH1 - inosine monophosphate dehydrogenase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000883.3 | 1637 | Missense Mutation | TCG,TTG | S,L 529 | NP_000874.2 | |
NM_001102605.1 | 1637 | Missense Mutation | TCG,TTG | S,L 519 | NP_001096075.1 | |
NM_001142573.1 | 1637 | Intron | NP_001136045.1 | |||
NM_001142574.1 | 1637 | Intron | NP_001136046.1 | |||
NM_001142575.1 | 1637 | Intron | NP_001136047.1 | |||
NM_001142576.1 | 1637 | Missense Mutation | TCG,TTG | S,L 496 | NP_001136048.1 | |
NM_001304521.1 | 1637 | Missense Mutation | TCG,TTG | S,L 460 | NP_001291450.1 | |
NM_183243.2 | 1637 | Intron | NP_899066.1 | |||
XM_017012168.1 | 1637 | Missense Mutation | TCG,TTG | S,L 519 | XP_016867657.1 | |
XM_017012169.1 | 1637 | Missense Mutation | TCG,TTG | S,L 493 | XP_016867658.1 | |
XM_017012170.1 | 1637 | Missense Mutation | TCG,TTG | S,L 460 | XP_016867659.1 | |
XM_017012171.1 | 1637 | Missense Mutation | TCG,TTG | S,L 452 | XP_016867660.1 | |
XM_017012172.1 | 1637 | Missense Mutation | TCG,TTG | S,L 452 | XP_016867661.1 | |
XM_017012173.1 | 1637 | Intron | XP_016867662.1 |