Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTGCTTTCTTCATCTAAACCTGTC[C/T]CAAAAACCTATGTACCAAAACTTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 613121 | ||||||||||||||||||||
Literature Links: |
NEXN 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 |
NEXN - nexilin F-actin binding protein | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172309.1 | 352 | Intron | NP_001165780.1 | |||
NM_144573.3 | 352 | Missense Mutation | CCA,TCA | P,S 19 | NP_653174.3 | |
XM_005271322.3 | 352 | Missense Mutation | CCA,TCA | P,S 19 | XP_005271379.1 | |
XM_005271323.3 | 352 | Missense Mutation | CCA,TCA | P,S 19 | XP_005271380.1 | |
XM_005271324.4 | 352 | Intron | XP_005271381.1 | |||
XM_005271325.3 | 352 | Missense Mutation | CCA,TCA | P,S 19 | XP_005271382.1 | |
XM_005271326.3 | 352 | Intron | XP_005271383.1 | |||
XM_005271327.3 | 352 | Missense Mutation | CCA,TCA | P,S 19 | XP_005271384.1 |