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TTGTAGTTTTTCTGAATGTCTTTTT[A/C]CAAGCAGGAGAAAAAATATGAATGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608668 | ||||||||||||||||||||
Literature Links: |
ZMYND11 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ZMYND11 - zinc finger MYND-type containing 11 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001202464.1 | Intron | NP_001189393.1 | ||||
NM_001202465.1 | Intron | NP_001189394.1 | ||||
NM_001202466.1 | Intron | NP_001189395.1 | ||||
NM_001202467.1 | Intron | NP_001189396.1 | ||||
NM_001202468.1 | Intron | NP_001189397.1 | ||||
NM_006624.5 | Intron | NP_006615.2 | ||||
NM_212479.3 | Intron | NP_997644.2 | ||||
XM_005252359.4 | Intron | XP_005252416.1 | ||||
XM_005252361.3 | Intron | XP_005252418.1 | ||||
XM_005252362.2 | Intron | XP_005252419.1 | ||||
XM_006717376.2 | Intron | XP_006717439.1 | ||||
XM_017015587.1 | Intron | XP_016871076.1 | ||||
XM_017015588.1 | Intron | XP_016871077.1 | ||||
XM_017015589.1 | Intron | XP_016871078.1 | ||||
XM_017015590.1 | Intron | XP_016871079.1 | ||||
XM_017015591.1 | Intron | XP_016871080.1 | ||||
XM_017015592.1 | Intron | XP_016871081.1 | ||||
XM_017015593.1 | Intron | XP_016871082.1 | ||||
XM_017015594.1 | Intron | XP_016871083.1 |