Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCCAACTCTCTGCTCTTTGTAGAC[A/C]TTCCTGCAAAAAAGGTTTGCCGGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 300212 | ||||||||||||||||||||
Literature Links: |
RGN PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
RGN - regucalcin | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282848.1 | 1090 | UTR 5 | NP_001269777.1 | |||
NM_001282849.1 | 1090 | Missense Mutation | ATT,CTT | I,L 34 | NP_001269778.1 | |
NM_004683.5 | 1090 | Missense Mutation | ATT,CTT | I,L 34 | NP_004674.1 | |
NM_152869.3 | 1090 | Missense Mutation | ATT,CTT | I,L 34 | NP_690608.1 | |
XM_006724567.2 | 1090 | Missense Mutation | ATT,CTT | I,L 34 | XP_006724630.1 | |
XM_006724568.2 | 1090 | Missense Mutation | ATT,CTT | I,L 34 | XP_006724631.1 | |
XM_017029954.1 | 1090 | Missense Mutation | ATT,CTT | I,L 34 | XP_016885443.1 |