Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 314995 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF41 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)
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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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ZNF41 - zinc finger protein 41 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324139.1 | 1712 | Missense Mutation | GAG,GAT | E,D 229 | NP_001311068.1 | |
NM_001324140.1 | 1712 | Missense Mutation | GAG,GAT | E,D 315 | NP_001311069.1 | |
NM_001324141.1 | 1712 | Missense Mutation | GAG,GAT | E,D 229 | NP_001311070.1 | |
NM_001324142.1 | 1712 | Missense Mutation | GAG,GAT | E,D 317 | NP_001311071.1 | |
NM_001324143.1 | 1712 | Missense Mutation | GAG,GAT | E,D 229 | NP_001311072.1 | |
NM_001324144.1 | 1712 | Missense Mutation | GAG,GAT | E,D 315 | NP_001311073.1 | |
NM_001324145.1 | 1712 | Missense Mutation | GAG,GAT | E,D 229 | NP_001311074.1 | |
NM_001324147.1 | 1712 | Missense Mutation | GAG,GAT | E,D 315 | NP_001311076.1 | |
NM_001324148.1 | 1712 | Missense Mutation | GAG,GAT | E,D 317 | NP_001311077.1 | |
NM_001324149.1 | 1712 | Missense Mutation | GAG,GAT | E,D 229 | NP_001311078.1 | |
NM_001324150.1 | 1712 | Missense Mutation | GAG,GAT | E,D 315 | NP_001311079.1 | |
NM_001324151.1 | 1712 | Missense Mutation | GAG,GAT | E,D 325 | NP_001311080.1 | |
NM_001324152.1 | 1712 | Missense Mutation | GAG,GAT | E,D 229 | NP_001311081.1 | |
NM_001324153.1 | 1712 | Missense Mutation | GAG,GAT | E,D 325 | NP_001311082.1 | |
NM_001324154.1 | 1712 | Missense Mutation | GAG,GAT | E,D 349 | NP_001311083.1 | |
NM_001324155.1 | 1712 | Missense Mutation | GAG,GAT | E,D 357 | NP_001311084.1 | |
NM_001324156.1 | 1712 | Missense Mutation | GAG,GAT | E,D 281 | NP_001311085.1 | |
NM_001324157.1 | 1712 | Missense Mutation | GAG,GAT | E,D 279 | NP_001311086.1 | |
NM_007130.3 | 1712 | Missense Mutation | GAG,GAT | E,D 315 | NP_009061.1 | |
NM_153380.3 | 1712 | Missense Mutation | GAG,GAT | E,D 315 | NP_700359.1 | |
XM_006724550.3 | 1712 | Missense Mutation | GAG,GAT | E,D 349 | XP_006724613.1 | |
XM_006724555.3 | 1712 | Missense Mutation | GAG,GAT | E,D 325 | XP_006724618.1 | |
XM_017029810.1 | 1712 | Missense Mutation | GAG,GAT | E,D 349 | XP_016885299.1 | |
XM_017029811.1 | 1712 | Missense Mutation | GAG,GAT | E,D 349 | XP_016885300.1 | |
XM_017029812.1 | 1712 | Missense Mutation | GAG,GAT | E,D 349 | XP_016885301.1 | |
XM_017029813.1 | 1712 | Missense Mutation | GAG,GAT | E,D 349 | XP_016885302.1 | |
XM_017029814.1 | 1712 | Missense Mutation | GAG,GAT | E,D 349 | XP_016885303.1 | |
XM_017029815.1 | 1712 | Missense Mutation | GAG,GAT | E,D 349 | XP_016885304.1 | |
XM_017029816.1 | 1712 | Missense Mutation | GAG,GAT | E,D 325 | XP_016885305.1 | |
XM_017029817.1 | 1712 | Missense Mutation | GAG,GAT | E,D 315 | XP_016885306.1 |
Set Membership: |
HapMap |