Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGCATTTTTTAATTTTCACACAGC[C/T]AGGAGTCTTTTCTTCTTTGCTGATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 190070 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KRAS PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
KRAS - KRAS proto-oncogene, GTPase | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004985.4 | 733 | Intron | NP_004976.2 | |||
NM_033360.3 | 733 | Missense Mutation | AGC,GGC | S,G 179 | NP_203524.1 | |
XM_006719069.3 | 733 | Missense Mutation | AGC,GGC | S,G 179 | XP_006719132.1 | |
XM_011520653.2 | 733 | Intron | XP_011518955.1 | |||
XM_017019292.1 | 733 | Intron | XP_016874781.1 | |||
XM_017019293.1 | 733 | Missense Mutation | AGC,GGC | S,G 179 | XP_016874782.1 |