Product Details
- SNP ID
-
rs34518648
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:23689297 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TAAACAACATAAAACTGACTTGGAA[A/G]CGATTCCTCAGCAGTGCCCCATTGA
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FAM221A
PubMed Links
Gene Details
- Gene
- FAM221A
- Gene Name
- family with sequence similarity 221 member A
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001127364.2 |
513 |
Missense Mutation |
ACG,GCG |
T90A |
NP_001120836.1 |
NM_001127365.2 |
513 |
Missense Mutation |
ACG,GCG |
T32A |
NP_001120837.1 |
NM_001300932.1 |
513 |
Missense Mutation |
ACG,GCG |
T32A |
NP_001287861.1 |
NM_199136.4 |
513 |
Missense Mutation |
ACG,GCG |
T90A |
NP_954587.2 |
XM_011515369.2 |
513 |
Missense Mutation |
ACG,GCG |
T90A |
XP_011513671.1 |
XM_011515370.2 |
513 |
Missense Mutation |
ACG,GCG |
T90A |
XP_011513672.1 |
XM_011515371.2 |
513 |
Missense Mutation |
ACG,GCG |
T90A |
XP_011513673.1 |
XM_011515372.2 |
513 |
Missense Mutation |
ACG,GCG |
T27A |
XP_011513674.1 |
XM_017012134.1 |
513 |
Missense Mutation |
ACG,GCG |
T90A |
XP_016867623.1 |
XM_017012135.1 |
513 |
Missense Mutation |
ACG,GCG |
T27A |
XP_016867624.1 |
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