Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATCGCAGAGGGAAGGCGAATCCCCA[G/T]AAGTAAGGTAAGCAAGATGGCTGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 182175 | ||||||||||||||||||||
Literature Links: |
SRP19 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 |
SRP19 - signal recognition particle 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204193.1 | 299 | Missense Mutation | AGA,ATA | R,I 37 | NP_001191122.1 | |
NM_001204194.1 | 299 | Missense Mutation | AGA,ATA | R,I 37 | NP_001191123.1 | |
NM_001204196.1 | 299 | Intron | NP_001191125.1 | |||
NM_001204199.1 | 299 | Missense Mutation | AGA,ATA | R,I 37 | NP_001191128.1 | |
NM_003135.2 | 299 | Missense Mutation | AGA,ATA | R,I 37 | NP_003126.1 |