Product Details
- SNP ID
-
rs56341011
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:38413948 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGGAGGTCAAGGCCACGATGCGGTC[C/T]AGGTCTTCCACCAGCTGCTTGAAGG
- Phenotype
-
MIM: 136350
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FGFR1
PubMed Links
Gene Details
- Gene
- FGFR1
- Gene Name
- fibroblast growth factor receptor 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001174063.1 |
2097 |
Silent Mutation |
CTA,CTG |
L752L |
NP_001167534.1 |
| NM_001174064.1 |
2097 |
Silent Mutation |
CTA,CTG |
L744L |
NP_001167535.1 |
| NM_001174065.1 |
2097 |
Silent Mutation |
CTA,CTG |
L752L |
NP_001167536.1 |
| NM_001174066.1 |
2097 |
Silent Mutation |
CTA,CTG |
L665L |
NP_001167537.1 |
| NM_001174067.1 |
2097 |
Silent Mutation |
CTA,CTG |
L785L |
NP_001167538.1 |
| NM_015850.3 |
2097 |
Silent Mutation |
CTA,CTG |
L752L |
NP_056934.2 |
| NM_023105.2 |
2097 |
Silent Mutation |
CTA,CTG |
L665L |
NP_075593.1 |
| NM_023106.2 |
2097 |
Silent Mutation |
CTA,CTG |
L663L |
NP_075594.1 |
| NM_023110.2 |
2097 |
Silent Mutation |
CTA,CTG |
L754L |
NP_075598.2 |
| XM_006716303.2 |
2097 |
Silent Mutation |
CTA,CTG |
L754L |
XP_006716366.1 |
| XM_006716304.1 |
2097 |
Silent Mutation |
CTA,CTG |
L754L |
XP_006716367.1 |
| XM_006716306.2 |
2097 |
Silent Mutation |
CTA,CTG |
L752L |
XP_006716369.1 |
| XM_006716307.1 |
2097 |
Silent Mutation |
CTA,CTG |
L752L |
XP_006716370.1 |
| XM_006716309.3 |
2097 |
Silent Mutation |
CTA,CTG |
L746L |
XP_006716372.1 |
| XM_006716310.2 |
2097 |
Silent Mutation |
CTA,CTG |
L665L |
XP_006716373.1 |
| XM_006716311.1 |
2097 |
Silent Mutation |
CTA,CTG |
L665L |
XP_006716374.1 |
| XM_006716312.1 |
2097 |
Silent Mutation |
CTA,CTG |
L665L |
XP_006716375.1 |
| XM_006716313.2 |
2097 |
Silent Mutation |
CTA,CTG |
L663L |
XP_006716376.1 |
| XM_006716314.1 |
2097 |
Silent Mutation |
CTA,CTG |
L663L |
XP_006716377.1 |
| XM_011544443.2 |
2097 |
Silent Mutation |
CTA,CTG |
L787L |
XP_011542745.1 |
| XM_011544444.1 |
2097 |
Silent Mutation |
CTA,CTG |
L785L |
XP_011542746.1 |
| XM_011544445.2 |
2097 |
Silent Mutation |
CTA,CTG |
L785L |
XP_011542747.1 |
| XM_011544446.2 |
2097 |
Silent Mutation |
CTA,CTG |
L787L |
XP_011542748.1 |
| XM_011544447.2 |
2097 |
Silent Mutation |
CTA,CTG |
L785L |
XP_011542749.1 |
| XM_011544448.1 |
2097 |
Silent Mutation |
CTA,CTG |
L698L |
XP_011542750.1 |
| XM_011544449.1 |
2097 |
Silent Mutation |
CTA,CTG |
L696L |
XP_011542751.1 |
| XM_011544450.2 |
2097 |
Silent Mutation |
CTA,CTG |
L696L |
XP_011542752.1 |
| XM_011544451.1 |
2097 |
Silent Mutation |
CTA,CTG |
L657L |
XP_011542753.1 |
| XM_011544452.2 |
2097 |
Intron |
|
|
XP_011542754.1 |
| XM_017013219.1 |
2097 |
Silent Mutation |
CTA,CTG |
L783L |
XP_016868708.1 |
| XM_017013220.1 |
2097 |
Silent Mutation |
CTA,CTG |
L783L |
XP_016868709.1 |
| XM_017013221.1 |
2097 |
Silent Mutation |
CTA,CTG |
L754L |
XP_016868710.1 |
| XM_017013222.1 |
2097 |
Silent Mutation |
CTA,CTG |
L752L |
XP_016868711.1 |
| XM_017013223.1 |
2097 |
Silent Mutation |
CTA,CTG |
L750L |
XP_016868712.1 |
| XM_017013224.1 |
2097 |
Silent Mutation |
CTA,CTG |
L750L |
XP_016868713.1 |
| XM_017013225.1 |
2097 |
Silent Mutation |
CTA,CTG |
L750L |
XP_016868714.1 |
| XM_017013226.1 |
2097 |
Silent Mutation |
CTA,CTG |
L696L |
XP_016868715.1 |
| XM_017013227.1 |
2097 |
Silent Mutation |
CTA,CTG |
L694L |
XP_016868716.1 |
| XM_017013228.1 |
2097 |
Silent Mutation |
CTA,CTG |
L661L |
XP_016868717.1 |
| XM_017013229.1 |
2097 |
Silent Mutation |
CTA,CTG |
L430L |
XP_016868718.1 |
| XM_017013230.1 |
2097 |
Silent Mutation |
CTA,CTG |
L430L |
XP_016868719.1 |
| XM_017013231.1 |
2097 |
Intron |
|
|
XP_016868720.1 |
- Gene
- LETM2
- Gene Name
- leucine zipper and EF-hand containing transmembrane protein 2
There are no transcripts associated with this gene.
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