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CTGGGTTATACCTTGTTGTTTGCTC[C/G]CCAGGTGTAACAATGATTTTTAAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610436 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RTTN PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
RTTN - rotatin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318520.1 | Intron | NP_001305449.1 | ||||
NM_173630.3 | Intron | NP_775901.3 | ||||
XM_006722434.3 | Intron | XP_006722497.1 | ||||
XM_006722435.3 | Intron | XP_006722498.1 | ||||
XM_011525902.2 | Intron | XP_011524204.1 | ||||
XM_011525903.2 | Intron | XP_011524205.1 | ||||
XM_011525904.2 | Intron | XP_011524206.1 | ||||
XM_011525905.2 | Intron | XP_011524207.1 | ||||
XM_011525906.2 | Intron | XP_011524208.1 | ||||
XM_011525907.2 | Intron | XP_011524209.1 | ||||
XM_011525908.2 | Intron | XP_011524210.1 | ||||
XM_017025693.1 | Intron | XP_016881182.1 | ||||
XM_017025694.1 | Intron | XP_016881183.1 | ||||
XM_017025695.1 | Intron | XP_016881184.1 | ||||
XM_017025696.1 | Intron | XP_016881185.1 |