Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAAGTCCTTGTCACCCTCATCATCA[A/G]CATGGACTCGCTGATGAATGATAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 194554 | ||||||||||||||||||||
Literature Links: |
ZNF45 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 |
ZNF45 - zinc finger protein 45 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003425.3 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | NP_003416.1 | |
XM_011527267.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_011525569.1 | |
XM_011527269.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_011525571.1 | |
XM_011527271.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_011525573.1 | |
XM_011527273.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_011525575.1 | |
XM_017027217.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882706.1 | |
XM_017027218.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882707.1 | |
XM_017027219.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882708.1 | |
XM_017027220.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882709.1 | |
XM_017027221.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882710.1 | |
XM_017027222.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882711.1 | |
XM_017027223.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882712.1 | |
XM_017027224.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882713.1 | |
XM_017027225.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882714.1 | |
XM_017027226.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882715.1 | |
XM_017027227.1 | 3142 | Missense Mutation | GCT,GTT | A,V 663 | XP_016882716.1 | |
XM_017027228.1 | 3142 | Missense Mutation | GCT,GTT | A,V 627 | XP_016882717.1 | |
XM_017027229.1 | 3142 | Missense Mutation | GCT,GTT | A,V 627 | XP_016882718.1 | |
XM_017027230.1 | 3142 | Missense Mutation | GCT,GTT | A,V 627 | XP_016882719.1 |