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Search Thermo Fisher Scientific
GGCTGCCAAACAATCCAATCCAAAA[A/G]GCAGCCCAGGACAACCGGAAGCAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 610563 MIM: 608676 | ||||||||||||||||||||
Literature Links: |
KPNA6 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 |
KPNA6 - karyopherin subunit alpha 6 | ||||||
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There are no transcripts associated with this gene. |
TXLNA - taxilin alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_175852.3 | 132 | Missense Mutation | AGC,GGC | S,G 18 | NP_787048.1 | |
XM_011540931.2 | 132 | UTR 5 | XP_011539233.1 | |||
XM_011540932.2 | 132 | Intron | XP_011539234.1 | |||
XM_017000561.1 | 132 | Missense Mutation | AGC,GGC | S,G 18 | XP_016856050.1 | |
XM_017000562.1 | 132 | Missense Mutation | AGC,GGC | S,G 18 | XP_016856051.1 | |
XM_017000563.1 | 132 | Missense Mutation | AGC,GGC | S,G 18 | XP_016856052.1 | |
XM_017000564.1 | 132 | Intron | XP_016856053.1 | |||
XM_017000565.1 | 132 | Intron | XP_016856054.1 |