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CCTCCTATAACTCTTGGTCTTTAAC[A/T]TGGGAGTTGGATGGTGGCTGGGTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603215 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NAPA 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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NAPA - NSF attachment protein alpha | ||||||
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There are no transcripts associated with this gene. |
ZNF541 - zinc finger protein 541 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277075.1 | 4055 | Missense Mutation | AAG,ATG | K,M 1253 | NP_001264004.1 | |
XM_005259311.4 | 4055 | Missense Mutation | AAG,ATG | K,M 1253 | XP_005259368.1 | |
XM_005259314.3 | 4055 | Missense Mutation | AAG,ATG | K,M 615 | XP_005259371.1 | |
XM_011527367.2 | 4055 | Missense Mutation | AAG,ATG | K,M 1258 | XP_011525669.1 | |
XM_011527368.2 | 4055 | Missense Mutation | AAG,ATG | K,M 1258 | XP_011525670.1 | |
XM_011527369.2 | 4055 | Missense Mutation | AAG,ATG | K,M 1258 | XP_011525671.1 | |
XM_011527370.2 | 4055 | Missense Mutation | AAG,ATG | K,M 1258 | XP_011525672.1 | |
XM_011527371.2 | 4055 | Missense Mutation | AAG,ATG | K,M 1258 | XP_011525673.1 | |
XM_011527372.2 | 4055 | Missense Mutation | AAG,ATG | K,M 1203 | XP_011525674.1 | |
XM_011527373.2 | 4055 | Missense Mutation | AAG,ATG | K,M 1200 | XP_011525675.1 | |
XM_011527374.2 | 4055 | Missense Mutation | AAG,ATG | K,M 1196 | XP_011525676.1 | |
XM_011527375.1 | 4055 | Intron | XP_011525677.1 | |||
XM_017027351.1 | 4055 | Missense Mutation | AAG,ATG | K,M 1211 | XP_016882840.1 |