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AGCCTTAGAGATTCATAGGTTCTTC[A/C]TCCTCCACCAGCTGCTCCGAGGGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 606542 MIM: 612187 | ||||||||||||||||||||
Literature Links: |
HDAC7 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 |
HDAC7 - histone deacetylase 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098416.3 | 3051 | Silent Mutation | NP_001091886.1 | |||
NM_001308090.1 | 3051 | Silent Mutation | NP_001295019.1 | |||
NM_015401.4 | 3051 | Silent Mutation | NP_056216.2 | |||
XM_011538478.1 | 3051 | Missense Mutation | XP_011536780.1 | |||
XM_011538479.1 | 3051 | Silent Mutation | XP_011536781.1 | |||
XM_011538480.1 | 3051 | Missense Mutation | XP_011536782.1 | |||
XM_011538481.1 | 3051 | Missense Mutation | XP_011536783.1 | |||
XM_011538482.1 | 3051 | Missense Mutation | XP_011536784.1 | |||
XM_011538483.1 | 3051 | Intron | XP_011536785.1 | |||
XM_017019455.1 | 3051 | Missense Mutation | XP_016874944.1 | |||
XM_017019456.1 | 3051 | Intron | XP_016874945.1 |
SLC48A1 - solute carrier family 48 member 1 | ||||||
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There are no transcripts associated with this gene. |