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TGATCGAATCCGGGGCAACGGTATG[A/G]AGCCCGACAGCTTAGACGAGGAGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C11orf63 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 |
C11orf63 - chromosome 11 open reading frame 63 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024806.3 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | NP_079082.2 | |
NM_199124.2 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | NP_954575.1 | |
XM_005271680.4 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | XP_005271737.1 | |
XM_006718915.2 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | XP_006718978.1 | |
XM_011543009.2 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | XP_011541311.1 | |
XM_017018338.1 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | XP_016873827.1 | |
XM_017018339.1 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | XP_016873828.1 | |
XM_017018340.1 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | XP_016873829.1 | |
XM_017018341.1 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | XP_016873830.1 | |
XM_017018342.1 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | XP_016873831.1 | |
XM_017018343.1 | 1092 | Missense Mutation | AAG,GAG | K,E 70 | XP_016873832.1 | |
XM_017018344.1 | 1092 | Intron | XP_016873833.1 |