Search
LOADING 
- SNP ID:
- rs199557562
- Gene
-
FAM135B - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.8: 138132625 - 138132625 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
AAGTAGTTGAGTCCTGCCACCAAGA[A/G]AAACTTCTCCAGGAAGAGTTCTGAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM135B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
| FAM135B - family with sequence similarity 135 member B | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_015912.3 | 5033 | Missense Mutation | CTC,TTC | L,F 1397 | NP_056996.2 | |
| XM_011517056.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1401 | XP_011515358.1 | |
| XM_011517058.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1401 | XP_011515360.1 | |
| XM_011517059.1 | 5033 | Missense Mutation | CTC,TTC | L,F 1401 | XP_011515361.1 | |
| XM_011517060.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1401 | XP_011515362.1 | |
| XM_011517061.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1401 | XP_011515363.1 | |
| XM_011517062.1 | 5033 | Missense Mutation | CTC,TTC | L,F 1401 | XP_011515364.1 | |
| XM_011517063.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1401 | XP_011515365.1 | |
| XM_011517064.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1397 | XP_011515366.1 | |
| XM_011517065.1 | 5033 | Missense Mutation | CTC,TTC | L,F 1385 | XP_011515367.1 | |
| XM_011517068.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1298 | XP_011515370.1 | |
| XM_011517069.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1279 | XP_011515371.1 | |
| XM_011517070.2 | 5033 | Intron | XP_011515372.1 | |||
| XM_011517072.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1200 | XP_011515374.1 | |
| XM_011517073.2 | 5033 | Missense Mutation | CTC,TTC | L,F 1168 | XP_011515375.1 | |
| XM_011517074.1 | 5033 | Missense Mutation | CTC,TTC | L,F 1152 | XP_011515376.1 | |
| XM_017013470.1 | 5033 | Missense Mutation | CTC,TTC | L,F 1397 | XP_016868959.1 | |
| XM_017013471.1 | 5033 | Missense Mutation | CTC,TTC | L,F 1382 | XP_016868960.1 | |
Back To Top