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GGTCAGGTCTCGGGGGACACCTCGC[C/T]GGACAGCCCTGACCTCACTTTCTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607755 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CHKB-AS1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CHKB-AS1 - CHKB antisense RNA 1 (head to head) | ||||||
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There are no transcripts associated with this gene. |
MAPK8IP2 - mitogen-activated protein kinase 8 interacting protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012324.4 | 1720 | Missense Mutation | CCG,CTG | P,L 565 | NP_036456.1 | |
XM_011530679.2 | 1720 | Missense Mutation | CCG,CTG | P,L 566 | XP_011528981.1 | |
XM_011530680.2 | 1720 | Missense Mutation | CCG,CTG | P,L 528 | XP_011528982.1 | |
XM_011530681.2 | 1720 | Missense Mutation | CCG,CTG | P,L 521 | XP_011528983.1 |