Product Details
- SNP ID
-
rs201744533
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:138132743 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGTTGTGTCGGATTAAAGTGCAGTC[C/G]TTGGCTTCAACCAGAGGGCCCAGGA
- Phenotype
-
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
FAM135B
PubMed Links
Gene Details
- Gene
- FAM135B
- Gene Name
- family with sequence similarity 135 member B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_015912.3 |
4915 |
Missense Mutation |
AAC,AAG |
N1357K |
NP_056996.2 |
XM_011517056.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1361K |
XP_011515358.1 |
XM_011517058.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1361K |
XP_011515360.1 |
XM_011517059.1 |
4915 |
Missense Mutation |
AAC,AAG |
N1361K |
XP_011515361.1 |
XM_011517060.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1361K |
XP_011515362.1 |
XM_011517061.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1361K |
XP_011515363.1 |
XM_011517062.1 |
4915 |
Missense Mutation |
AAC,AAG |
N1361K |
XP_011515364.1 |
XM_011517063.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1361K |
XP_011515365.1 |
XM_011517064.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1357K |
XP_011515366.1 |
XM_011517065.1 |
4915 |
Missense Mutation |
AAC,AAG |
N1345K |
XP_011515367.1 |
XM_011517068.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1258K |
XP_011515370.1 |
XM_011517069.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1239K |
XP_011515371.1 |
XM_011517070.2 |
4915 |
Intron |
|
|
XP_011515372.1 |
XM_011517072.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1160K |
XP_011515374.1 |
XM_011517073.2 |
4915 |
Missense Mutation |
AAC,AAG |
N1128K |
XP_011515375.1 |
XM_011517074.1 |
4915 |
Missense Mutation |
AAC,AAG |
N1112K |
XP_011515376.1 |
XM_017013470.1 |
4915 |
Missense Mutation |
AAC,AAG |
N1357K |
XP_016868959.1 |
XM_017013471.1 |
4915 |
Missense Mutation |
AAC,AAG |
N1342K |
XP_016868960.1 |
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