Search Thermo Fisher Scientific
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GTGAAAGAGTGACGACTTTTCAGGT[A/G]CATCTGTGGAAGCATCCCAGTGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608141 | ||||||||||||||||||||
Literature Links: |
NUP43 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 |
NUP43 - nucleoporin 43 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198887.2 | 961 | Missense Mutation | NP_942590.1 | |||
XM_005266960.4 | 961 | Missense Mutation | XP_005267017.1 | |||
XM_005266961.3 | 961 | Missense Mutation | XP_005267018.1 | |||
XM_005266962.3 | 961 | Missense Mutation | XP_005267019.1 | |||
XM_011535798.2 | 961 | Missense Mutation | XP_011534100.1 | |||
XM_011535799.2 | 961 | Missense Mutation | XP_011534101.1 |