Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGTAGAGGAAGAGTTAGATTTTTG[A/G]AAGCTTTGGTGCATTAACCACAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZFAND4 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
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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
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ZFAND4 - zinc finger AN1-type containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128324.2 | 2875 | Missense Mutation | CCA,TCA | P,S 725 | NP_001121796.1 | |
NM_001282905.1 | 2875 | Missense Mutation | CCA,TCA | P,S 651 | NP_001269834.1 | |
NM_001282906.1 | 2875 | Missense Mutation | CCA,TCA | P,S 651 | NP_001269835.1 | |
NM_174890.3 | 2875 | Missense Mutation | CCA,TCA | P,S 725 | NP_777550.2 | |
XM_005271842.2 | 2875 | Missense Mutation | CCA,TCA | P,S 626 | XP_005271899.1 | |
XM_005271843.2 | 2875 | Missense Mutation | CCA,TCA | P,S 626 | XP_005271900.1 | |
XM_005271844.3 | 2875 | Missense Mutation | CCA,TCA | P,S 607 | XP_005271901.1 | |
XM_011540366.2 | 2875 | Missense Mutation | CCA,TCA | P,S 733 | XP_011538668.1 | |
XM_011540368.1 | 2875 | Missense Mutation | CCA,TCA | P,S 553 | XP_011538670.1 | |
XM_017016931.1 | 2875 | Missense Mutation | CCA,TCA | P,S 739 | XP_016872420.1 | |
XM_017016932.1 | 2875 | Missense Mutation | CCA,TCA | P,S 731 | XP_016872421.1 | |
XM_017016933.1 | 2875 | Missense Mutation | CCA,TCA | P,S 731 | XP_016872422.1 | |
XM_017016934.1 | 2875 | Missense Mutation | CCA,TCA | P,S 731 | XP_016872423.1 | |
XM_017016935.1 | 2875 | Intron | XP_016872424.1 | |||
XM_017016936.1 | 2875 | Missense Mutation | CCA,TCA | P,S 683 | XP_016872425.1 | |
XM_017016937.1 | 2875 | Missense Mutation | CCA,TCA | P,S 683 | XP_016872426.1 | |
XM_017016938.1 | 2875 | Missense Mutation | CCA,TCA | P,S 677 | XP_016872427.1 | |
XM_017016939.1 | 2875 | Missense Mutation | CCA,TCA | P,S 677 | XP_016872428.1 | |
XM_017016940.1 | 2875 | Missense Mutation | CCA,TCA | P,S 657 | XP_016872429.1 | |
XM_017016941.1 | 2875 | Missense Mutation | CCA,TCA | P,S 657 | XP_016872430.1 | |
XM_017016942.1 | 2875 | Missense Mutation | CCA,TCA | P,S 632 | XP_016872431.1 | |
XM_017016943.1 | 2875 | Missense Mutation | CCA,TCA | P,S 632 | XP_016872432.1 | |
XM_017016944.1 | 2875 | Missense Mutation | CCA,TCA | P,S 632 | XP_016872433.1 | |
XM_017016945.1 | 2875 | Missense Mutation | CCA,TCA | P,S 613 | XP_016872434.1 | |
XM_017016946.1 | 2875 | Missense Mutation | CCA,TCA | P,S 532 | XP_016872435.1 |