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TGACCCAGTGGCAATGGGAAAAGCT[C/T]TTCTGCTCTTAGACATATCTGAAGC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 146691 | |||||||||||||||||||||||
Literature Links: |
IMPDH2 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
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 |
IMPDH2 - inosine monophosphate dehydrogenase 2 | ||||||
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There are no transcripts associated with this gene. |
QRICH1 - glutamine rich 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320580.1 | Intron | NP_001307509.1 | ||||
NM_001320581.1 | Intron | NP_001307510.1 | ||||
NM_001320582.1 | Intron | NP_001307511.1 | ||||
NM_001320583.1 | Intron | NP_001307512.1 | ||||
NM_001320584.1 | Intron | NP_001307513.1 | ||||
NM_001320585.1 | Intron | NP_001307514.1 | ||||
NM_017730.3 | Intron | NP_060200.2 | ||||
NM_198880.2 | Intron | NP_942581.1 | ||||
XM_011533863.1 | Intron | XP_011532165.1 |