Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATTTTGAAGACATTTCAGTATAATC[A/G]CCTTTTCTTTATTGAATCTGAAAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612620 | ||||||||||||||||||||
Literature Links: |
RASSF6 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 |
RASSF6 - Ras association domain family member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270391.1 | 3809 | Missense Mutation | GCG,GTG | A,V 285 | NP_001257320.1 | |
NM_001270392.1 | 3809 | Missense Mutation | GCG,GTG | A,V 307 | NP_001257321.1 | |
NM_177532.4 | 3809 | Missense Mutation | GCG,GTG | A,V 319 | NP_803876.1 | |
NM_201431.2 | 3809 | Missense Mutation | GCG,GTG | A,V 351 | NP_958834.1 | |
XM_011531687.2 | 3809 | UTR 3 | XP_011529989.1 | |||
XM_011531688.1 | 3809 | Missense Mutation | GCG,GTG | A,V 319 | XP_011529990.1 | |
XM_011531689.2 | 3809 | Missense Mutation | GCG,GTG | A,V 317 | XP_011529991.1 | |
XM_011531690.2 | 3809 | Missense Mutation | GCG,GTG | A,V 261 | XP_011529992.1 | |
XM_011531691.1 | 3809 | Missense Mutation | GCG,GTG | A,V 261 | XP_011529993.1 | |
XM_017007837.1 | 3809 | Missense Mutation | GCG,GTG | A,V 223 | XP_016863326.1 | |
XM_017007838.1 | 3809 | Intron | XP_016863327.1 |