Product Details

SNP ID
rs199506671
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:11450096 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGTTCATGGAAGGCCTGAATGCT[A/G]TGAATGTCTTGATAGGTCACATATG
Phenotype
MIM: 602944
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
E2F6 PubMed Links

Gene Details

Gene
E2F6
Gene Name
E2F transcription factor 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001278275.1 998 Silent Mutation CAC,CAT H157H NP_001265204.1
NM_001278276.1 998 Silent Mutation CAC,CAT H114H NP_001265205.1
NM_001278277.1 998 Silent Mutation CAC,CAT H114H NP_001265206.1
NM_001278278.1 998 Silent Mutation CAC,CAT H114H NP_001265207.1
NM_198256.3 998 Silent Mutation CAC,CAT H189H NP_937987.2
NM_212540.2 998 Silent Mutation CAC,CAT H37H NP_997705.1
XM_017003547.1 998 Silent Mutation CAC,CAT H189H XP_016859036.1
XM_017003548.1 998 Silent Mutation CAC,CAT H157H XP_016859037.1
XM_017003549.1 998 Silent Mutation CAC,CAT H114H XP_016859038.1

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