Product Details
- SNP ID
-
rs74140967
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
21
- Location
-
Chr.1:228107822 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGCTCGCCAGGAGGATGTGTGCAGG[C/T]GGCGGAGTGCAGGTCCGGTGGCCTT
- Phenotype
-
MIM: 103180
MIM: 611859
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
ARF1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs822730] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- ARF1
- Gene Name
- ADP ribosylation factor 1
There are no transcripts associated with this gene.
- Gene
- C1orf35
- Gene Name
- chromosome 1 open reading frame 35
There are no transcripts associated with this gene.
- Gene
- MRPL55
- Gene Name
- mitochondrial ribosomal protein L55
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001321284.1 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
NP_001308213.1 |
NM_181441.2 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
NP_852106.1 |
NM_181454.2 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
NP_852119.1 |
NM_181455.2 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
NP_852120.1 |
NM_181456.2 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
NP_852121.1 |
NM_181462.2 |
471 |
Missense Mutation |
CAC,CGC |
H61R |
NP_852127.2 |
NM_181463.2 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
NP_852128.1 |
NM_181464.2 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
NP_852129.1 |
NM_181465.2 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
NP_852130.1 |
XM_005273059.3 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
XP_005273116.1 |
XM_005273061.4 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
XP_005273118.1 |
XM_005273062.3 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
XP_005273119.1 |
XM_005273063.4 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
XP_005273120.1 |
XM_011544094.2 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
XP_011542396.1 |
XM_011544095.2 |
471 |
Missense Mutation |
CAC,CGC |
H25R |
XP_011542397.1 |
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