Product Details
- SNP ID
-
rs141911278
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:75339340 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGAAGCACTTGCGGGTCTGCAGCCT[A/G]CGCAGTAAGTATGAGGCCAGCCAGG
- Phenotype
-
MIM: 616701
MIM: 608844
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
COMMD4
PubMed Links
Gene Details
- Gene
- COMMD4
- Gene Name
- COMM domain containing 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001284377.1 |
450 |
Silent Mutation |
CTA,CTG |
L126L |
NP_001271306.1 |
NM_001284378.1 |
450 |
Intron |
|
|
NP_001271307.1 |
NM_001284379.1 |
450 |
Silent Mutation |
CTA,CTG |
L132L |
NP_001271308.1 |
NM_001321844.1 |
450 |
Silent Mutation |
CTA,CTG |
L102L |
NP_001308773.1 |
NM_001321845.1 |
450 |
Silent Mutation |
CTA,CTG |
L80L |
NP_001308774.1 |
NM_001321846.1 |
450 |
Silent Mutation |
CTA,CTG |
L104L |
NP_001308775.1 |
NM_001321847.1 |
450 |
Silent Mutation |
CTA,CTG |
L104L |
NP_001308776.1 |
NM_001321848.1 |
450 |
Silent Mutation |
CTA,CTG |
L132L |
NP_001308777.1 |
NM_017828.4 |
450 |
Silent Mutation |
CTA,CTG |
L126L |
NP_060298.2 |
XM_005254509.3 |
450 |
Silent Mutation |
CTA,CTG |
L153L |
XP_005254566.1 |
XM_005254510.3 |
450 |
Silent Mutation |
CTA,CTG |
L131L |
XP_005254567.1 |
XM_011521739.1 |
450 |
Silent Mutation |
CTA,CTG |
L156L |
XP_011520041.1 |
XM_011521740.1 |
450 |
Silent Mutation |
CTA,CTG |
L134L |
XP_011520042.1 |
XM_011521741.1 |
450 |
Silent Mutation |
CTA,CTG |
L156L |
XP_011520043.1 |
XM_017022385.1 |
450 |
Silent Mutation |
CTA,CTG |
L134L |
XP_016877874.1 |
- Gene
- NEIL1
- Gene Name
- nei like DNA glycosylase 1
There are no transcripts associated with this gene.
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