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GCACGTGCCAGGTCATCTTCAGGGC[A/G]TGCATGATCTCCTGGAAGGAGGTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 126660 MIM: 605903 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DBN1 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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DBN1 - drebrin 1 | ||||||
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There are no transcripts associated with this gene. |
PDLIM7 - PDZ and LIM domain 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005451.4 | 1151 | Silent Mutation | CAC,CAT | H,H 354 | NP_005442.2 | |
NM_203352.2 | 1151 | Silent Mutation | CAC,CAT | H,H 320 | NP_976227.1 | |
NM_213636.2 | 1151 | Intron | NP_998801.1 | |||
XM_011534698.2 | 1151 | Silent Mutation | CAC,CAT | H,H 261 | XP_011533000.1 | |
XM_011534699.2 | 1151 | Silent Mutation | CAC,CAT | H,H 206 | XP_011533001.1 |