Product Details
- SNP ID
-
rs34762693
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:207081251 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCATGTGGAGGGCAAGATGGTCAG[A/C]CCTGGAAAAACACCTAGGAGATATA
- Phenotype
-
MIM: 604865
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
KLF7
PubMed Links
Gene Details
- Gene
- KLF7
- Gene Name
- Kruppel like factor 7
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001270942.1 |
1105 |
Silent Mutation |
GGG,GGT |
G223G |
NP_001257871.1 |
NM_001270943.1 |
1105 |
Missense Mutation |
GCT,TCT |
A258S |
NP_001257872.1 |
NM_001270944.1 |
1105 |
Missense Mutation |
GCT,TCT |
A263S |
NP_001257873.1 |
NM_003709.3 |
1105 |
Missense Mutation |
GCT,TCT |
A291S |
NP_003700.1 |
XM_005246926.3 |
1105 |
Missense Mutation |
GCT,TCT |
A292S |
XP_005246983.1 |
XM_006712815.3 |
1105 |
Missense Mutation |
GCT,TCT |
A292S |
XP_006712878.1 |
XM_011512072.2 |
1105 |
Missense Mutation |
GCT,TCT |
A292S |
XP_011510374.1 |
XM_011512073.2 |
1105 |
Missense Mutation |
GCT,TCT |
A261S |
XP_011510375.1 |
XM_011512074.2 |
1105 |
Missense Mutation |
GCT,TCT |
A259S |
XP_011510376.1 |
XM_011512075.1 |
1105 |
Intron |
|
|
XP_011510377.1 |
XM_017005161.1 |
1105 |
Missense Mutation |
GCT,TCT |
A291S |
XP_016860650.1 |
XM_017005162.1 |
1105 |
Missense Mutation |
GCT,TCT |
A264S |
XP_016860651.1 |
XM_017005163.1 |
1105 |
Intron |
|
|
XP_016860652.1 |
XM_017005164.1 |
1105 |
Silent Mutation |
GGG,GGT |
G223G |
XP_016860653.1 |
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