Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGTCCAGCACCTCCTGGTTGGTGC[A/G]CCCAGGATAGGGCATGTAGCCCAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147521 MIM: 151520 | ||||||||||||||||||||
Literature Links: |
ITPKA 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 |
ITPKA - inositol-trisphosphate 3-kinase A | ||||||
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There are no transcripts associated with this gene. |
LTK - leukocyte receptor tyrosine kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135685.1 | 2276 | Missense Mutation | CGC,TGC | R,C 597 | NP_001129157.1 | |
NM_002344.5 | 2276 | Missense Mutation | CGC,TGC | R,C 727 | NP_002335.2 | |
NM_206961.3 | 2276 | Missense Mutation | CGC,TGC | R,C 666 | NP_996844.1 | |
XM_011521556.2 | 2276 | Missense Mutation | CGC,TGC | R,C 743 | XP_011519858.1 | |
XM_011521557.2 | 2276 | Missense Mutation | CGC,TGC | R,C 687 | XP_011519859.1 | |
XM_017022181.1 | 2276 | Missense Mutation | CGC,TGC | R,C 748 | XP_016877670.1 | |
XM_017022182.1 | 2276 | Missense Mutation | CGC,TGC | R,C 700 | XP_016877671.1 | |
XM_017022183.1 | 2276 | Missense Mutation | CGC,TGC | R,C 663 | XP_016877672.1 |