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GTTCTACCCTTTATATACCGGGCCA[C/T]AGGCTCAAAGCATCTTCCTGCCAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608828 | ||||||||||||||||||||
Literature Links: |
C5orf22 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 |
C5orf22 - chromosome 5 open reading frame 22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018356.2 | 414 | Missense Mutation | ACA,ATA | T,I 36 | NP_060826.2 | |
XM_006714479.2 | 414 | UTR 5 | XP_006714542.1 | |||
XM_006714480.3 | 414 | UTR 5 | XP_006714543.1 | |||
XM_011514062.2 | 414 | Missense Mutation | ACA,ATA | T,I 36 | XP_011512364.1 | |
XM_017009607.1 | 414 | Missense Mutation | ACA,ATA | T,I 36 | XP_016865096.1 | |
XM_017009608.1 | 414 | Missense Mutation | ACA,ATA | T,I 36 | XP_016865097.1 | |
XM_017009609.1 | 414 | UTR 5 | XP_016865098.1 | |||
XM_017009610.1 | 414 | UTR 5 | XP_016865099.1 | |||
XM_017009611.1 | 414 | UTR 5 | XP_016865100.1 | |||
XM_017009612.1 | 414 | UTR 5 | XP_016865101.1 | |||
XM_017009613.1 | 414 | UTR 5 | XP_016865102.1 | |||
XM_017009614.1 | 414 | UTR 5 | XP_016865103.1 | |||
XM_017009615.1 | 414 | UTR 5 | XP_016865104.1 | |||
XM_017009616.1 | 414 | UTR 5 | XP_016865105.1 |
DROSHA - drosha ribonuclease III | ||||||
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There are no transcripts associated with this gene. |