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TCACTGGCCAGTGGGTACCTCGCTC[A/G]CAATAGGGCACGCCCTCCTCCATGT
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 |
---|---|---|
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 |
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 | 1253 | Silent Mutation | TGC,TGT | C,C 388 | NP_005442.2 | |
NM_203352.2 | 1253 | Silent Mutation | TGC,TGT | C,C 354 | NP_976227.1 | |
NM_213636.2 | 1253 | Intron | NP_998801.1 | |||
XM_011534698.2 | 1253 | Silent Mutation | TGC,TGT | C,C 295 | XP_011533000.1 | |
XM_011534699.2 | 1253 | Silent Mutation | TGC,TGT | C,C 240 | XP_011533001.1 |