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CAATTGCATTAAAATTACTTTCCTG[C/T]TTGTAGAGTTTTTGTAAGGATGGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611870 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CNTLN 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
|
CNTLN - centlein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114395.2 | Intron | NP_001107867.1 | ||||
NM_001286984.1 | Intron | NP_001273913.1 | ||||
NM_001286985.1 | Intron | NP_001273914.1 | ||||
NM_017738.3 | Intron | NP_060208.2 | ||||
XM_005251492.1 | Intron | XP_005251549.1 | ||||
XM_006716793.3 | Intron | XP_006716856.1 | ||||
XM_011517941.2 | Intron | XP_011516243.1 | ||||
XM_017014839.1 | Intron | XP_016870328.1 | ||||
XM_017014840.1 | Intron | XP_016870329.1 | ||||
XM_017014841.1 | Intron | XP_016870330.1 | ||||
XM_017014842.1 | Intron | XP_016870331.1 | ||||
XM_017014843.1 | Intron | XP_016870332.1 | ||||
XM_017014844.1 | Intron | XP_016870333.1 | ||||
XM_017014845.1 | Intron | XP_016870334.1 | ||||
XM_017014846.1 | Intron | XP_016870335.1 | ||||
XM_017014847.1 | Intron | XP_016870336.1 |