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CTGCCCTTCAGCGTGGAGGCGCTCA[A/T]GGCCGACCACAGGAAGCCGGGGGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 142983 | ||||||||||||||||||||
Literature Links: |
LINC01396 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 |
LINC01396 - long intergenic non-protein coding RNA 1396 | ||||||
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There are no transcripts associated with this gene. |
MSX1 - msh homeobox 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002448.3 | 435 | Missense Mutation | AAG,ATG | K,M 67 | NP_002439.2 |