Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCTTTGGTGCATTAACCACAGGAT[C/T]TGCCTCGTGCAAGTATCTCCTCCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
ZFAND4 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
ZFAND4 - zinc finger AN1-type containing 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128324.2 | 2848 | Missense Mutation | AAT,GAT | N,D 716 | NP_001121796.1 | |
NM_001282905.1 | 2848 | Missense Mutation | AAT,GAT | N,D 642 | NP_001269834.1 | |
NM_001282906.1 | 2848 | Missense Mutation | AAT,GAT | N,D 642 | NP_001269835.1 | |
NM_174890.3 | 2848 | Missense Mutation | AAT,GAT | N,D 716 | NP_777550.2 | |
XM_005271842.2 | 2848 | Missense Mutation | AAT,GAT | N,D 617 | XP_005271899.1 | |
XM_005271843.2 | 2848 | Missense Mutation | AAT,GAT | N,D 617 | XP_005271900.1 | |
XM_005271844.3 | 2848 | Missense Mutation | AAT,GAT | N,D 598 | XP_005271901.1 | |
XM_011540366.2 | 2848 | Missense Mutation | AAT,GAT | N,D 724 | XP_011538668.1 | |
XM_011540368.1 | 2848 | Missense Mutation | AAT,GAT | N,D 544 | XP_011538670.1 | |
XM_017016931.1 | 2848 | Missense Mutation | AAT,GAT | N,D 730 | XP_016872420.1 | |
XM_017016932.1 | 2848 | Missense Mutation | AAT,GAT | N,D 722 | XP_016872421.1 | |
XM_017016933.1 | 2848 | Missense Mutation | AAT,GAT | N,D 722 | XP_016872422.1 | |
XM_017016934.1 | 2848 | Missense Mutation | AAT,GAT | N,D 722 | XP_016872423.1 | |
XM_017016935.1 | 2848 | Intron | XP_016872424.1 | |||
XM_017016936.1 | 2848 | Missense Mutation | AAT,GAT | N,D 674 | XP_016872425.1 | |
XM_017016937.1 | 2848 | Missense Mutation | AAT,GAT | N,D 674 | XP_016872426.1 | |
XM_017016938.1 | 2848 | Missense Mutation | AAT,GAT | N,D 668 | XP_016872427.1 | |
XM_017016939.1 | 2848 | Missense Mutation | AAT,GAT | N,D 668 | XP_016872428.1 | |
XM_017016940.1 | 2848 | Missense Mutation | AAT,GAT | N,D 648 | XP_016872429.1 | |
XM_017016941.1 | 2848 | Missense Mutation | AAT,GAT | N,D 648 | XP_016872430.1 | |
XM_017016942.1 | 2848 | Missense Mutation | AAT,GAT | N,D 623 | XP_016872431.1 | |
XM_017016943.1 | 2848 | Missense Mutation | AAT,GAT | N,D 623 | XP_016872432.1 | |
XM_017016944.1 | 2848 | Missense Mutation | AAT,GAT | N,D 623 | XP_016872433.1 | |
XM_017016945.1 | 2848 | Missense Mutation | AAT,GAT | N,D 604 | XP_016872434.1 | |
XM_017016946.1 | 2848 | Missense Mutation | AAT,GAT | N,D 523 | XP_016872435.1 |