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AACAGTAGTATAATTTGGGAATTAA[A/C]CGTAATTTATAGTGCAGTAATGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611395 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM110C 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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FAM110C - family with sequence similarity 110 member C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077710.2 | 1781 | UTR 3 | NP_001071178.2 | |||
XM_011510372.2 | 1781 | UTR 3 | XP_011508674.1 | |||
XM_017004689.1 | 1781 | Intron | XP_016860178.1 | |||
XM_017004690.1 | 1781 | Intron | XP_016860179.1 | |||
XM_017004691.1 | 1781 | UTR 3 | XP_016860180.1 | |||
XM_017004692.1 | 1781 | Intron | XP_016860181.1 |