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CCCCAAAGTCACAGCAGGACTCTCA[C/T]TGGTGCCCCATTAGTTGCTGAGATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 142991 MIM: 142988 MIM: 142989 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EVX2 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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EVX2 - even-skipped homeobox 2 | ||||||
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There are no transcripts associated with this gene. |
HOXD12 - homeobox D12 | ||||||
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There are no transcripts associated with this gene. |
HOXD13 - homeobox D13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000523.3 | 2999 | Intron | NP_000514.2 | |||
XM_011511068.2 | 2999 | Intron | XP_011509370.1 | |||
XM_011511069.2 | 2999 | UTR 3 | XP_011509371.1 |