Product Details
- SNP ID
-
rs112442492
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:145765586 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCCTCACTGTTCAGTGAGGGCTGGC[C/T]CCCAGGCATGACAGAGATGACCAGC
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
C4orf51
PubMed Links
Gene Details
- Gene
- C4orf51
- Gene Name
- chromosome 4 open reading frame 51
- Gene
- ZNF827
- Gene Name
- zinc finger protein 827
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001306215.1 |
3612 |
Missense Mutation |
AGC,GGC |
S1005G |
NP_001293144.1 |
NM_178835.4 |
3612 |
Missense Mutation |
AGC,GGC |
S1005G |
NP_849157.2 |
XM_011531634.2 |
3612 |
Missense Mutation |
AGC,GGC |
S1005G |
XP_011529936.1 |
XM_011531635.2 |
3612 |
Missense Mutation |
AGC,GGC |
S993G |
XP_011529937.1 |
XM_011531645.2 |
3612 |
Missense Mutation |
AGC,GGC |
S337G |
XP_011529947.1 |
XM_017007768.1 |
3612 |
Missense Mutation |
AGC,GGC |
S1003G |
XP_016863257.1 |
XM_017007769.1 |
3612 |
Missense Mutation |
AGC,GGC |
S993G |
XP_016863258.1 |
XM_017007770.1 |
3612 |
Missense Mutation |
AGC,GGC |
S927G |
XP_016863259.1 |
XM_017007771.1 |
3612 |
Missense Mutation |
AGC,GGC |
S1005G |
XP_016863260.1 |
XM_017007772.1 |
3612 |
Missense Mutation |
AGC,GGC |
S1005G |
XP_016863261.1 |
XM_017007773.1 |
3612 |
Missense Mutation |
AGC,GGC |
S1005G |
XP_016863262.1 |
XM_017007774.1 |
3612 |
Missense Mutation |
AGC,GGC |
S1005G |
XP_016863263.1 |
XM_017007775.1 |
3612 |
Missense Mutation |
AGC,GGC |
S1005G |
XP_016863264.1 |
XM_017007776.1 |
3612 |
Intron |
|
|
XP_016863265.1 |
XM_017007777.1 |
3612 |
Missense Mutation |
AGC,GGC |
S416G |
XP_016863266.1 |
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