Search Thermo Fisher Scientific
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CTGAACTTAAACTTACCAGATTACA[G/T]TATAATGCATTTTTTAATTTTCACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 190070 | ||||||||||||||||||||
Literature Links: |
KRAS 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 |
KRAS - KRAS proto-oncogene, GTPase | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004985.4 | 763 | Intron | NP_004976.2 | |||
NM_033360.3 | 763 | Missense Mutation | ATG,CTG | M,L 189 | NP_203524.1 | |
XM_006719069.3 | 763 | Missense Mutation | ATG,CTG | M,L 189 | XP_006719132.1 | |
XM_011520653.2 | 763 | Intron | XP_011518955.1 | |||
XM_017019292.1 | 763 | Intron | XP_016874781.1 | |||
XM_017019293.1 | 763 | Missense Mutation | ATG,CTG | M,L 189 | XP_016874782.1 |