Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCAAGCAATTCTTCACTTTGCTGAG[A/G]ATTTTCTTCTGGAAAAGAACACGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602944 | ||||||||||||||||||||
Literature Links: |
E2F6 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 |
E2F6 - E2F transcription factor 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278275.1 | 1239 | Missense Mutation | CCT,TCT | P,S 238 | NP_001265204.1 | |
NM_001278276.1 | 1239 | Missense Mutation | CCT,TCT | P,S 195 | NP_001265205.1 | |
NM_001278277.1 | 1239 | Missense Mutation | CCT,TCT | P,S 195 | NP_001265206.1 | |
NM_001278278.1 | 1239 | Missense Mutation | CCT,TCT | P,S 195 | NP_001265207.1 | |
NM_198256.3 | 1239 | Missense Mutation | CCT,TCT | P,S 270 | NP_937987.2 | |
NM_212540.2 | 1239 | Missense Mutation | CCT,TCT | P,S 118 | NP_997705.1 | |
XM_017003547.1 | 1239 | Intron | XP_016859036.1 | |||
XM_017003548.1 | 1239 | Intron | XP_016859037.1 | |||
XM_017003549.1 | 1239 | Intron | XP_016859038.1 |