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CTCATGTAACCCTGTTCCTTGTTCC[C/T]GGAGAAGGGTTGGCAGCAGCGCCAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 180466 | ||||||||||||||||||||
Literature Links: |
RPL19 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 |
RPL19 - ribosomal protein L19 | ||||||
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There are no transcripts associated with this gene. |
STAC2 - SH3 and cysteine rich domain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198993.3 | 1323 | Missense Mutation | AGG,GGG | R,G 364 | NP_945344.1 | |
XM_017024580.1 | 1323 | Missense Mutation | AGG,GGG | R,G 369 | XP_016880069.1 | |
XM_017024581.1 | 1323 | Missense Mutation | AGG,GGG | R,G 314 | XP_016880070.1 | |
XM_017024582.1 | 1323 | UTR 3 | XP_016880071.1 | |||
XM_017024583.1 | 1323 | Intron | XP_016880072.1 |