Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGGCTTTCAGGAGGGTCTGAGATA[C/G]AGGTCCGGTCTGATATTGAATATCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 182530 | ||||||||||||||||||||
Literature Links: |
SOS1 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 |
SOS1 - SOS Ras/Rac guanine nucleotide exchange factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005633.3 | 3817 | Missense Mutation | TCT,TGT | S,C 1203 | NP_005624.2 | |
XM_005264515.4 | 3817 | Missense Mutation | TCT,TGT | S,C 1188 | XP_005264572.1 | |
XM_011533062.2 | 3817 | Missense Mutation | TCT,TGT | S,C 1196 | XP_011531364.1 | |
XM_011533064.2 | 3817 | Missense Mutation | TCT,TGT | S,C 1146 | XP_011531366.1 | |
XM_011533066.2 | 3817 | Missense Mutation | TCT,TGT | S,C 848 | XP_011531368.1 |