Product Details
- SNP ID
-
rs113903111
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:49550799 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCGGTCAAAGAAGGAACGAATGAAT[A/G]ACCCTTTTGCCAGGATGGAGACCCG
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
C6orf141
PubMed Links
Gene Details
- Gene
- C6orf141
- Gene Name
- chromosome 6 open reading frame 141
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001145652.1 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
NP_001139124.1 |
XM_005248850.3 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_005248907.1 |
XM_005248852.2 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_005248909.1 |
XM_005248853.2 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_005248910.1 |
XM_006714997.2 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_006715060.1 |
XM_011514303.2 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_011512605.1 |
XM_017010294.1 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_016865783.1 |
XM_017010295.1 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_016865784.1 |
XM_017010296.1 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_016865785.1 |
XM_017010297.1 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_016865786.1 |
XM_017010298.1 |
156 |
Missense Mutation |
AAC,GAC |
N3D |
XP_016865787.1 |
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