Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCTGCAGCCAGGCCTTGAGCGTGC[C/T]GGTGGTCTCGCGCGTGGCGTTCTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606199 | ||||||||||||||||||||
Literature Links: |
CTD-2194D22.4 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 |
CTD-2194D22.4 - uncharacterized LOC101929081 | ||||||
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There are no transcripts associated with this gene. |
IRX4 - iroquois homeobox 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278632.1 | 681 | Missense Mutation | AGC,GGC | S,G 155 | NP_001265561.1 | |
NM_001278633.1 | 681 | Missense Mutation | AGC,GGC | S,G 181 | NP_001265562.1 | |
NM_001278634.1 | 681 | Missense Mutation | AGC,GGC | S,G 155 | NP_001265563.1 | |
NM_001278635.1 | 681 | Missense Mutation | AGC,GGC | S,G 181 | NP_001265564.1 | |
NM_016358.2 | 681 | Missense Mutation | AGC,GGC | S,G 155 | NP_057442.1 |