Product Details
- SNP ID
-
rs34265970
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:14521300 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCTTCTTGCAATTTCTGCTTCTCAA[C/G]TTCAAGCTAAATGACATTCAGAAAA
- Phenotype
-
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
FAM107B
PubMed Links
Gene Details
- Gene
- FAM107B
- Gene Name
- family with sequence similarity 107 member B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001282695.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001269624.1 |
NM_001282696.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001269625.1 |
NM_001282697.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001269626.1 |
NM_001282698.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001269627.1 |
NM_001282699.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001269628.1 |
NM_001282700.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001269629.1 |
NM_001282701.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001269630.1 |
NM_001282702.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001269631.1 |
NM_001282703.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001269632.1 |
NM_001320735.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001307664.1 |
NM_001320736.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001307665.1 |
NM_001320737.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001307666.1 |
NM_001320738.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001307667.1 |
NM_001320739.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001307668.1 |
NM_001320740.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
NP_001307669.1 |
NM_001320741.1 |
442 |
Missense Mutation |
CTT,GTT |
L135V |
NP_001307670.1 |
NM_031453.3 |
442 |
Missense Mutation |
CTT,GTT |
L271V |
NP_113641.2 |
XM_005252616.3 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
XP_005252673.1 |
XM_011519735.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
XP_011518037.1 |
XM_017016746.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
XP_016872235.1 |
XM_017016747.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
XP_016872236.1 |
XM_017016748.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
XP_016872237.1 |
XM_017016749.1 |
442 |
Missense Mutation |
CTT,GTT |
L96V |
XP_016872238.1 |
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