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TCAGCCGAGTCACCAGTTATGGCTG[C/G]TGCCTGAGTTAGGACCGGCAGAGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604500 | ||||||||||||||||||||
Literature Links: |
MYO19 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 |
MYO19 - myosin XIX | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033580.2 | 2817 | Intron | NP_001028752.1 | |||
NM_001163735.1 | 2817 | Missense Mutation | CCA,GCA | P,A 722 | NP_001157207.1 | |
NM_025109.5 | 2817 | Missense Mutation | CCA,GCA | P,A 522 | NP_079385.2 | |
XM_011525286.1 | 2817 | Missense Mutation | CCA,GCA | P,A 799 | XP_011523588.1 | |
XM_011525287.1 | 2817 | Missense Mutation | CCA,GCA | P,A 797 | XP_011523589.1 | |
XM_011525290.2 | 2817 | Missense Mutation | CCA,GCA | P,A 753 | XP_011523592.1 | |
XM_017025157.1 | 2817 | Missense Mutation | CCA,GCA | P,A 799 | XP_016880646.1 | |
XM_017025158.1 | 2817 | Missense Mutation | CCA,GCA | P,A 768 | XP_016880647.1 | |
XM_017025159.1 | 2817 | Missense Mutation | CCA,GCA | P,A 755 | XP_016880648.1 | |
XM_017025160.1 | 2817 | Missense Mutation | CCA,GCA | P,A 799 | XP_016880649.1 | |
XM_017025161.1 | 2817 | Missense Mutation | CCA,GCA | P,A 606 | XP_016880650.1 |
ZNHIT3 - zinc finger HIT-type containing 3 | ||||||
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There are no transcripts associated with this gene. |