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TCTGTGCTGACATAGTCATTCCAGG[G/T]TGGGTAGGGGGTCCTCCGTGCATCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601740 | ||||||||||||||||||||
Literature Links: |
LOC145845 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 |
LOC145845 - uncharacterized LOC145845 | ||||||
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There are no transcripts associated with this gene. |
MEIS2 - Meis homeobox 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001220482.1 | 1861 | Missense Mutation | CAA,CAC | Q,H 440 | NP_001207411.1 | |
NM_002399.3 | 1861 | UTR 3 | NP_002390.1 | |||
NM_170674.4 | 1861 | UTR 3 | NP_733774.1 | |||
NM_170675.4 | 1861 | Missense Mutation | CAA,CAC | Q,H 447 | NP_733775.1 | |
NM_170676.4 | 1861 | Missense Mutation | CAA,CAC | Q,H 440 | NP_733776.1 | |
NM_170677.4 | 1861 | UTR 3 | NP_733777.1 | |||
NM_172315.2 | 1861 | UTR 3 | NP_758526.1 | |||
NM_172316.2 | 1861 | UTR 3 | NP_758527.1 | |||
XM_006720523.1 | 1861 | Missense Mutation | CAA,CAC | Q,H 446 | XP_006720586.1 | |
XM_006720524.1 | 1861 | UTR 3 | XP_006720587.1 | |||
XM_006720525.1 | 1861 | UTR 3 | XP_006720588.1 | |||
XM_006720526.2 | 1861 | Missense Mutation | CAA,CAC | Q,H 359 | XP_006720589.1 | |
XM_006720527.2 | 1861 | Missense Mutation | CAA,CAC | Q,H 301 | XP_006720590.1 | |
XM_006720529.2 | 1861 | UTR 3 | XP_006720592.1 | |||
XM_011521591.2 | 1861 | Missense Mutation | CAA,CAC | Q,H 301 | XP_011519893.1 | |
XM_017022205.1 | 1861 | UTR 3 | XP_016877694.1 |