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GGCCCCGCGCCGCCCCTTAGACTGG[A/C]TGCGGCCGGAAGATTGCAGCCGCTT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 613893 | |||||||||||||||||||||||
Literature Links: |
DPY19L2 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)
|
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AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
DPY19L2 - dpy-19 like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173812.4 | Intron | NP_776173.3 | ||||
XM_006719352.2 | Intron | XP_006719415.1 | ||||
XM_011538215.2 | Intron | XP_011536517.1 | ||||
XM_011538218.2 | Intron | XP_011536520.1 | ||||
XM_017019188.1 | Intron | XP_016874677.1 | ||||
XM_017019189.1 | Intron | XP_016874678.1 | ||||
XM_017019190.1 | Intron | XP_016874679.1 | ||||
XM_017019191.1 | Intron | XP_016874680.1 | ||||
XM_017019192.1 | Intron | XP_016874681.1 | ||||
XM_017019193.1 | Intron | XP_016874682.1 | ||||
XM_017019194.1 | Intron | XP_016874683.1 | ||||
XM_017019195.1 | Intron | XP_016874684.1 | ||||
XM_017019196.1 | Intron | XP_016874685.1 | ||||
XM_017019197.1 | Intron | XP_016874686.1 | ||||
XM_017019198.1 | Intron | XP_016874687.1 | ||||
XM_017019199.1 | Intron | XP_016874688.1 | ||||
XM_017019200.1 | Intron | XP_016874689.1 | ||||
XM_017019201.1 | Intron | XP_016874690.1 | ||||
XM_017019202.1 | Intron | XP_016874691.1 | ||||
XM_017019203.1 | Intron | XP_016874692.1 | ||||
XM_017019204.1 | Intron | XP_016874693.1 | ||||
XM_017019205.1 | Intron | XP_016874694.1 |