Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACACTTGTTCCCCACCAGCACCAT[A/G]GGCACGTCATCCGAGTCCTTCACCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 190020 | ||||||||||||||||||||
Literature Links: |
HRAS 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 |
HRAS - HRas proto-oncogene, GTPase | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130442.2 | 535 | Silent Mutation | CCC,CCT | P,P 110 | NP_001123914.1 | |
NM_001318054.1 | 535 | Missense Mutation | CCA,CTA | P,L 4 | NP_001304983.1 | |
NM_005343.3 | 535 | Silent Mutation | CCC,CCT | P,P 110 | NP_005334.1 | |
NM_176795.4 | 535 | Silent Mutation | CCC,CCT | P,P 110 | NP_789765.1 |
LOC101059906 - collagen alpha-2(IV) chain-like | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
LRRC56 - leucine rich repeat containing 56 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198075.3 | 535 | Intron | NP_932341.1 | |||
XM_005252775.2 | 535 | Intron | XP_005252832.1 | |||
XM_005252776.2 | 535 | Intron | XP_005252833.1 | |||
XM_006718132.2 | 535 | Intron | XP_006718195.1 | |||
XM_006718133.2 | 535 | Intron | XP_006718196.1 | |||
XM_011519875.2 | 535 | Intron | XP_011518177.1 | |||
XM_011519876.1 | 535 | Intron | XP_011518178.1 | |||
XM_011519877.2 | 535 | Intron | XP_011518179.1 | |||
XM_017017167.1 | 535 | Intron | XP_016872656.1 | |||
XM_017017168.1 | 535 | Intron | XP_016872657.1 |