Product Details
- SNP ID
-
rs12407362
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
33
- Location
-
Chr.1:248850411 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TGTCTGGCTTCTCAAAGCGCTTGCC[A/G]CAGAATTCACAGGGGAAGCGCAAGG
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF672
PubMed Links
Gene Details
- Gene
- ZNF672
- Gene Name
- zinc finger protein 672
- Gene
- ZNF692
- Gene Name
- zinc finger protein 692
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001136036.2 |
1570 |
Silent Mutation |
TGC,TGT |
C458C |
NP_001129508.1 |
| NM_001193328.1 |
1570 |
Silent Mutation |
TGC,TGT |
C408C |
NP_001180257.1 |
| NM_017865.3 |
1570 |
Silent Mutation |
TGC,TGT |
C453C |
NP_060335.2 |
| XM_011544220.1 |
1570 |
Silent Mutation |
TGC,TGT |
C604C |
XP_011542522.1 |
| XM_011544221.1 |
1570 |
Silent Mutation |
TGC,TGT |
C603C |
XP_011542523.1 |
| XM_011544222.1 |
1570 |
Silent Mutation |
TGC,TGT |
C453C |
XP_011542524.1 |
| XM_011544223.2 |
1570 |
Silent Mutation |
TGC,TGT |
C559C |
XP_011542525.1 |
| XM_011544227.1 |
1570 |
Silent Mutation |
TGC,TGT |
C426C |
XP_011542529.1 |
| XM_017001698.1 |
1570 |
Silent Mutation |
TGC,TGT |
C452C |
XP_016857187.1 |
| XM_017001699.1 |
1570 |
Silent Mutation |
TGC,TGT |
C578C |
XP_016857188.1 |
| XM_017001700.1 |
1570 |
Silent Mutation |
TGC,TGT |
C427C |
XP_016857189.1 |
| XM_017001701.1 |
1570 |
Silent Mutation |
TGC,TGT |
C452C |
XP_016857190.1 |
| XM_017001702.1 |
1570 |
Silent Mutation |
TGC,TGT |
C427C |
XP_016857191.1 |
| XM_017001703.1 |
1570 |
Silent Mutation |
TGC,TGT |
C249C |
XP_016857192.1 |
| XM_017001704.1 |
1570 |
Silent Mutation |
TGC,TGT |
C249C |
XP_016857193.1 |
| XM_017001705.1 |
1570 |
Silent Mutation |
TGC,TGT |
C249C |
XP_016857194.1 |
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