Product Details
- SNP ID
-
rs191606676
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:96661360 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTAAGGAAATGGCTAGGCCTCTGC[A/C]AGCCAAATAACCCTGGCAGTGGTGT
- Phenotype
-
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
FER1L5
PubMed Links
Gene Details
- Gene
- FER1L5
- Gene Name
- fer-1 like family member 5
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001293083.1 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
NP_001280012.1 |
XM_011512110.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510412.1 |
XM_011512111.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510413.1 |
XM_011512113.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510415.1 |
XM_011512114.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510416.1 |
XM_011512115.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510417.1 |
XM_011512116.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510418.1 |
XM_011512117.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510419.1 |
XM_011512118.2 |
932 |
Intron |
|
|
XP_011510420.1 |
XM_011512119.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510421.1 |
XM_011512120.2 |
932 |
Missense Mutation |
AAG,CAG |
K202Q |
XP_011510422.1 |
XM_011512122.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510424.1 |
XM_011512124.2 |
932 |
Intron |
|
|
XP_011510426.1 |
XM_011512125.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510427.1 |
XM_011512126.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510428.1 |
XM_011512127.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510429.1 |
XM_011512128.2 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_011510430.1 |
XM_017005222.1 |
932 |
Missense Mutation |
AAG,CAG |
K272Q |
XP_016860711.1 |
XM_017005223.1 |
932 |
Intron |
|
|
XP_016860712.1 |
XM_017005224.1 |
932 |
Intron |
|
|
XP_016860713.1 |
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