Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTCGCCCCTGTCCCGTCGGTAGCG[G/T]CTGCCTACCCGCTTGGCTTGTCCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 601911 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DLX4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
DLX4 - distal-less homeobox 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001934.3 | 356 | Intron | NP_001925.2 | |||
NM_138281.2 | 356 | Missense Mutation | GCT,TCT | A,S 29 | NP_612138.1 | |
XM_017024291.1 | 356 | Intron | XP_016879780.1 |