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TGCGACTGTCCCCGCGGAAGGGGCT[A/G]TCAAGGGGCTCCCGGAGATGCTAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
13 submissions
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Phenotype: |
MIM: 602146 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LHX4 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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LHX4 - LIM homeobox 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033343.3 | 269 | Missense Mutation | ATC,GTC | I,V 13 | NP_203129.1 | |
XM_011510105.2 | 269 | Intron | XP_011508407.1 | |||
XM_011510106.2 | 269 | Intron | XP_011508408.1 | |||
XM_011510108.2 | 269 | Intron | XP_011508410.1 | |||
XM_017002755.1 | 269 | Intron | XP_016858244.1 |