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TTCCATTTTAGCTGTGTTGCTTGGT[A/C]AGGGAACTATTTTGAGGGGGAAAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300182 | ||||||||||||||||||||
Literature Links: |
CXorf38 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 |
CXorf38 - chromosome X open reading frame 38 | ||||||
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There are no transcripts associated with this gene. |
MED14 - mediator complex subunit 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004229.3 | 4029 | Missense Mutation | GAC,TAC | D,Y 1327 | NP_004220.2 | |
XM_005272701.2 | 4029 | Missense Mutation | GAC,TAC | D,Y 1211 | XP_005272758.1 | |
XM_011544000.2 | 4029 | Missense Mutation | GAC,TAC | D,Y 1211 | XP_011542302.1 | |
XM_017029962.1 | 4029 | Missense Mutation | GAC,TAC | D,Y 1211 | XP_016885451.1 |