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AATCGCTTCATGGTGCTTATTCATA[A/C]CAGCCACGGTTATGACGGGTCGATT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DZANK1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
DZANK1 - double zinc ribbon and ankyrin repeat domains 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099407.1 | 2242 | Missense Mutation | GGT,GTT | G,V 649 | NP_001092877.1 | |
XM_005260742.3 | 2242 | Missense Mutation | GGT,GTT | G,V 668 | XP_005260799.1 | |
XM_005260743.3 | 2242 | Missense Mutation | GGT,GTT | G,V 482 | XP_005260800.1 | |
XM_006723584.2 | 2242 | Missense Mutation | GGT,GTT | G,V 593 | XP_006723647.1 | |
XM_011529268.2 | 2242 | Missense Mutation | GGT,GTT | G,V 683 | XP_011527570.1 | |
XM_011529271.2 | 2242 | Missense Mutation | GGT,GTT | G,V 674 | XP_011527573.1 | |
XM_011529272.2 | 2242 | Missense Mutation | GGT,GTT | G,V 674 | XP_011527574.1 | |
XM_011529275.2 | 2242 | Missense Mutation | GGT,GTT | G,V 482 | XP_011527577.1 | |
XM_011529277.2 | 2242 | Missense Mutation | GGT,GTT | G,V 336 | XP_011527579.1 | |
XM_017027909.1 | 2242 | Missense Mutation | GGT,GTT | G,V 677 | XP_016883398.1 | |
XM_017027910.1 | 2242 | Missense Mutation | GGT,GTT | G,V 674 | XP_016883399.1 | |
XM_017027911.1 | 2242 | Missense Mutation | GGT,GTT | G,V 674 | XP_016883400.1 | |
XM_017027912.1 | 2242 | Missense Mutation | GGT,GTT | G,V 672 | XP_016883401.1 | |
XM_017027913.1 | 2242 | Missense Mutation | GGT,GTT | G,V 667 | XP_016883402.1 | |
XM_017027914.1 | 2242 | Missense Mutation | GGT,GTT | G,V 655 | XP_016883403.1 | |
XM_017027915.1 | 2242 | Missense Mutation | GGT,GTT | G,V 655 | XP_016883404.1 | |
XM_017027916.1 | 2242 | Missense Mutation | GGT,GTT | G,V 605 | XP_016883405.1 | |
XM_017027917.1 | 2242 | Missense Mutation | GGT,GTT | G,V 541 | XP_016883406.1 | |
XM_017027918.1 | 2242 | Missense Mutation | GGT,GTT | G,V 541 | XP_016883407.1 | |
XM_017027919.1 | 2242 | Missense Mutation | GGT,GTT | G,V 541 | XP_016883408.1 | |
XM_017027920.1 | 2242 | Missense Mutation | GGT,GTT | G,V 482 | XP_016883409.1 | |
XM_017027921.1 | 2242 | Missense Mutation | GGT,GTT | G,V 410 | XP_016883410.1 |
LINC00851 - long intergenic non-protein coding RNA 851 | ||||||
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There are no transcripts associated with this gene. |