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CCCATGCTGAGTACCTTCCTGCTTG[A/T]CGATGACGCCCACTGCACTGGCATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300959 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CXorf36 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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CXorf36 - chromosome X open reading frame 36 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024689.2 | 826 | Intron | NP_078965.2 | |||
NM_176819.3 | 826 | Missense Mutation | GAC,GTC | D,V 317 | NP_789789.2 | |
XM_005272670.1 | 826 | Missense Mutation | GAC,GTC | D,V 259 | XP_005272727.1 | |
XM_006724559.1 | 826 | Intron | XP_006724622.1 |