Transcript #00012178 (NM_001257407.1, IL4R gene)

Transcript name transcript variant 4
Gene name IL4R (interleukin 4 receptor)
Chromosome 16
Transcript - NCBI ID NM_001257407.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001244336.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

173 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-220+9C>T -220 r.(=) p.(=) - intron 9
./. - c.-219-150C>T -219 r.(=) p.(=) - intron 150
./. - c.-219-143G>T -219 r.(=) p.(=) - intron 143
./. - c.-219-143G>T -219 r.(=) p.(=) - intron 143
./. - c.26-45G>A 26 r.(=) p.(=) - intron 45
./. - c.26-27G>T 26 r.(=) p.(=) - intron 27
./. - c.164+9G>C 164 r.(=) p.(=) - intron 9
./. - c.164+9G>C 164 r.(=) p.(=) - intron 9
./. - c.164+9G>C 164 r.(=) p.(=) - intron 9
./. - c.164+9G>C 164 r.(=) p.(=) - intron 9
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.178A>G 178 r.(?) p.(Ile60Val) - missense -
./. - c.199G>A 199 r.(?) p.(Ala67Thr) - missense -
./. - c.199G>A 199 r.(?) p.(Ala67Thr) - missense -
./. - c.208G>A 208 r.(?) p.(Val70Met) - missense -
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.316+18C>T 316 r.(=) p.(=) - intron 18
./. - c.456C>T 456 r.(?) p.(=) - coding-synonymous -
./. - c.456C>T 456 r.(?) p.(=) - coding-synonymous -
./. - c.456C>T 456 r.(?) p.(=) - coding-synonymous -
./. - c.456C>T 456 r.(?) p.(=) - coding-synonymous -
./. - c.456C>T 456 r.(?) p.(=) - coding-synonymous -
./. - c.723C>G 723 r.(?) p.(=) - coding-synonymous-near-splice -
./. - c.723C>G 723 r.(?) p.(=) - coding-synonymous-near-splice -
./. - c.725+32C>T 725 r.(=) p.(=) - intron 32
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.855-15C>A 855 r.(=) p.(=) - intron 15
./. - c.963T>C 963 r.(?) p.(=) - coding-synonymous -
./. - c.1154A>C 1154 r.(?) p.(Glu385Ala) - missense -
./. - c.1154A>C 1154 r.(?) p.(Glu385Ala) - missense -
./. - c.1154A>C 1154 r.(?) p.(Glu385Ala) - missense -
./. - c.1154A>C 1154 r.(?) p.(Glu385Ala) - missense -
./. - c.1154A>C 1154 r.(?) p.(Glu385Ala) - missense -
./. - c.1154A>C 1154 r.(?) p.(Glu385Ala) - missense -
./. - c.1154A>C 1154 r.(?) p.(Glu385Ala) - missense -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197G>T 1197 r.(?) p.(=) - coding-synonymous -
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