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CTTGTATTTCCACATATGTTCTAAA[G/T]ATAGTGAGAAAGATTTATGTTGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604112 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SCEL 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
|
SCEL - sciellin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001160706.1 | Intron | NP_001154178.1 | ||||
NM_003843.3 | Intron | NP_003834.3 | ||||
NM_144777.2 | Intron | NP_659001.2 | ||||
XM_005266578.1 | Intron | XP_005266635.1 | ||||
XM_006719882.1 | Intron | XP_006719945.1 | ||||
XM_006719884.1 | Intron | XP_006719947.1 | ||||
XM_006719885.1 | Intron | XP_006719948.1 | ||||
XM_011535281.1 | Intron | XP_011533583.1 | ||||
XM_011535282.1 | Intron | XP_011533584.1 | ||||
XM_011535283.1 | Intron | XP_011533585.1 | ||||
XM_011535284.1 | Intron | XP_011533586.1 | ||||
XM_011535285.1 | Intron | XP_011533587.1 | ||||
XM_011535286.1 | Intron | XP_011533588.1 | ||||
XM_011535287.1 | Intron | XP_011533589.1 | ||||
XM_011535288.1 | Intron | XP_011533590.1 | ||||
XM_011535289.1 | Intron | XP_011533591.1 | ||||
XM_011535290.1 | Intron | XP_011533592.1 | ||||
XM_011535291.1 | Intron | XP_011533593.1 | ||||
XM_017020805.1 | Intron | XP_016876294.1 |