Product Details
- SNP ID
-
rs77992199
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:15103337 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAAATGGCTGCAGCTCCTCAAGCAC[C/T]GGGGCGGGGATCTCTCCGTAAGACG
- Phenotype
-
MIM: 603801
MIM: 606116
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
C10orf111
PubMed Links
Gene Details
- Gene
- C10orf111
- Gene Name
- chromosome 10 open reading frame 111
There are no transcripts associated with this gene.
- Gene
- NMT2
- Gene Name
- N-myristoyltransferase 2
There are no transcripts associated with this gene.
- Gene
- RPP38
- Gene Name
- ribonuclease P/MRP subunit p38
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001097590.2 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
NP_001091059.1 |
| NM_001265601.1 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
NP_001252530.1 |
| NM_006414.4 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
NP_006405.2 |
| NM_183005.4 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
NP_892117.1 |
| XM_006717363.1 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
XP_006717426.1 |
| XM_006717364.3 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
XP_006717427.1 |
| XM_011519293.1 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
XP_011517595.1 |
| XM_017015479.1 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
XP_016870968.1 |
| XM_017015480.1 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
XP_016870969.1 |
| XM_017015481.1 |
263 |
Missense Mutation |
CCG,CTG |
P8L |
XP_016870970.1 |
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