Product Details
- SNP ID
-
rs138722161
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:48294743 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGGGGCTCTTCCTCCTCATACCAG[C/T]GCTGTTCACTGAAGTCAGGGAAGAA
- Phenotype
-
MIM: 608294
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FCF1P2
PubMed Links
Gene Details
- Gene
- FCF1P2
- Gene Name
- FCF1 pseudogene 2
There are no transcripts associated with this gene.
- Gene
- NME6
- Gene Name
- NME/NM23 nucleoside diphosphate kinase 6
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001308426.1 |
795 |
Missense Mutation |
CAC,CGC |
H152R |
NP_001295355.1 |
| NM_001308427.1 |
795 |
Missense Mutation |
CAC,CGC |
H152R |
NP_001295356.1 |
| NM_001308428.1 |
795 |
Missense Mutation |
CAC,CGC |
H152R |
NP_001295357.1 |
| NM_001308430.1 |
795 |
Missense Mutation |
ACT,GCT |
T147A |
NP_001295359.1 |
| NM_001308431.1 |
795 |
Missense Mutation |
ACT,GCT |
T139A |
NP_001295360.1 |
| NM_001308433.1 |
795 |
Missense Mutation |
ACT,GCT |
T139A |
NP_001295362.1 |
| NM_001308434.1 |
795 |
Missense Mutation |
CAC,CGC |
H107R |
NP_001295363.1 |
| NM_001308435.1 |
795 |
Missense Mutation |
CAC,CGC |
H85R |
NP_001295364.1 |
| NM_005793.4 |
795 |
Missense Mutation |
CAC,CGC |
H160R |
NP_005784.1 |
| XM_017005511.1 |
795 |
Intron |
|
|
XP_016861000.1 |
| XM_017005512.1 |
795 |
Intron |
|
|
XP_016861001.1 |
| XM_017005513.1 |
795 |
Missense Mutation |
CAC,CGC |
H156R |
XP_016861002.1 |
| XM_017005514.1 |
795 |
Missense Mutation |
CAC,CGC |
H152R |
XP_016861003.1 |
| XM_017005515.1 |
795 |
Missense Mutation |
ACT,GCT |
T139A |
XP_016861004.1 |
| XM_017005516.1 |
795 |
Intron |
|
|
XP_016861005.1 |
| XM_017005517.1 |
795 |
Missense Mutation |
CAC,CGC |
H80R |
XP_016861006.1 |
| XM_017005518.1 |
795 |
Missense Mutation |
CAC,CGC |
H77R |
XP_016861007.1 |
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