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AACTGCAGTGCTGTGCTTGAGGATG[C/G]CTCCTCCTGAGCCGGCAGGCTCCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610522 MIM: 606198 | ||||||||||||||||||||
Literature Links: |
C5orf38 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 |
C5orf38 - chromosome 5 open reading frame 38 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001294337.1 | 513 | Intron | NP_001281266.1 | |||
NM_001306149.1 | 513 | Missense Mutation | CCT,GCT | P,A 127 | NP_001293078.1 | |
NM_001306150.1 | 513 | Missense Mutation | CCT,GCT | P,A 127 | NP_001293079.1 | |
NM_178569.3 | 513 | Missense Mutation | CCT,GCT | P,A 127 | NP_848664.1 | |
XM_005248256.3 | 513 | Intron | XP_005248313.1 | |||
XM_005248257.3 | 513 | UTR 3 | XP_005248314.1 | |||
XM_011513975.2 | 513 | UTR 3 | XP_011512277.1 | |||
XM_011513977.2 | 513 | Intron | XP_011512279.1 |
IRX2 - iroquois homeobox 2 | ||||||
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There are no transcripts associated with this gene. |