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AAATTAAAAAAGACAATGCAGTGAG[A/G]ACACTTCAAAAAGATTAATTACATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607327 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MBNL2 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
|
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
|
MBNL2 - muscleblind like splicing regulator 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306070.1 | Intron | NP_001292999.1 | ||||
NM_144778.3 | Intron | NP_659002.1 | ||||
NM_207304.2 | Intron | NP_997187.1 | ||||
XM_005254018.2 | Intron | XP_005254075.1 | ||||
XM_005254019.2 | Intron | XP_005254076.1 | ||||
XM_005254021.2 | Intron | XP_005254078.1 | ||||
XM_005254022.2 | Intron | XP_005254079.1 | ||||
XM_006719912.2 | Intron | XP_006719975.1 | ||||
XM_011521045.2 | Intron | XP_011519347.1 | ||||
XM_017020308.1 | Intron | XP_016875797.1 | ||||
XM_017020309.1 | Intron | XP_016875798.1 | ||||
XM_017020310.1 | Intron | XP_016875799.1 | ||||
XM_017020311.1 | Intron | XP_016875800.1 |