Product Details
- SNP ID
-
rs151025137
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:6667856 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTTGGGATTGCTGTCCCCACCACCC[C/G]CACCCTGGGGGGCTGCCCCAGGAGA
- Phenotype
-
MIM: 608524
MIM: 609951
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ING4
PubMed Links
Gene Details
- Gene
- ING4
- Gene Name
- inhibitor of growth family member 4
There are no transcripts associated with this gene.
- Gene
- ZNF384
- Gene Name
- zinc finger protein 384
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001039920.2 |
1932 |
Missense Mutation |
GCG,GGG |
A415G |
NP_001035009.1 |
NM_001135734.2 |
1932 |
Missense Mutation |
GCG,GGG |
A531G |
NP_001129206.1 |
NM_133476.4 |
1932 |
Missense Mutation |
GCG,GGG |
A470G |
NP_597733.2 |
XM_006718969.3 |
1932 |
Missense Mutation |
GCG,GGG |
A300G |
XP_006719032.1 |
XM_011520917.1 |
1932 |
Missense Mutation |
GCG,GGG |
A562G |
XP_011519219.1 |
XM_011520918.1 |
1932 |
Missense Mutation |
GCG,GGG |
A562G |
XP_011519220.1 |
XM_011520919.1 |
1932 |
Missense Mutation |
GCG,GGG |
A562G |
XP_011519221.1 |
XM_011520920.1 |
1932 |
Missense Mutation |
GCG,GGG |
A562G |
XP_011519222.1 |
XM_011520921.2 |
1932 |
Missense Mutation |
GCG,GGG |
A562G |
XP_011519223.1 |
XM_011520922.1 |
1932 |
Missense Mutation |
GCG,GGG |
A546G |
XP_011519224.1 |
XM_011520923.1 |
1932 |
Missense Mutation |
GCG,GGG |
A546G |
XP_011519225.1 |
XM_017018941.1 |
1932 |
Missense Mutation |
GCG,GGG |
A531G |
XP_016874430.1 |
XM_017018942.1 |
1932 |
Missense Mutation |
GCG,GGG |
A531G |
XP_016874431.1 |
XM_017018943.1 |
1932 |
Missense Mutation |
GCG,GGG |
A531G |
XP_016874432.1 |
XM_017018944.1 |
1932 |
Missense Mutation |
GCG,GGG |
A515G |
XP_016874433.1 |
XM_017018945.1 |
1932 |
Missense Mutation |
GCG,GGG |
A515G |
XP_016874434.1 |
XM_017018946.1 |
1932 |
Missense Mutation |
GCG,GGG |
A501G |
XP_016874435.1 |
XM_017018947.1 |
1932 |
Missense Mutation |
GCG,GGG |
A501G |
XP_016874436.1 |
XM_017018948.1 |
1932 |
Missense Mutation |
GCG,GGG |
A485G |
XP_016874437.1 |
XM_017018949.1 |
1932 |
Missense Mutation |
GCG,GGG |
A470G |
XP_016874438.1 |
XM_017018950.1 |
1932 |
Missense Mutation |
GCG,GGG |
A470G |
XP_016874439.1 |
XM_017018951.1 |
1932 |
Missense Mutation |
GCG,GGG |
A454G |
XP_016874440.1 |
XM_017018952.1 |
1932 |
Missense Mutation |
GCG,GGG |
A454G |
XP_016874441.1 |
XM_017018953.1 |
1932 |
Missense Mutation |
GCG,GGG |
A454G |
XP_016874442.1 |
XM_017018954.1 |
1932 |
Missense Mutation |
GCG,GGG |
A386G |
XP_016874443.1 |
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