Transcript #00012182 (NM_005535.1, IL12RB1 gene)

Transcript name transcript variant 1
Gene name IL12RB1 (interleukin 12 receptor, beta 1)
Chromosome 19
Transcript - NCBI ID NM_005535.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_005526.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

165 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.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.-2C>T -2 r.(=) p.(=) - utr-5 -
./. - c.139C>T 139 r.(?) p.(Pro47Ser) - missense -
./. - c.239+22C>T 239 r.(=) p.(=) - intron 22
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387G>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.409+21C>A 409 r.(=) p.(=) - intron 21
./. - c.409+21C>A 409 r.(=) p.(=) - intron 21
./. - c.467G>A 467 r.(?) p.(Arg156His) - missense -
./. - c.467G>A 467 r.(?) p.(Arg156His) - missense -
./. - c.467G>A 467 r.(?) p.(Arg156His) - missense -
./. - c.549+46G>T 549 r.(=) p.(=) - intron 46
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.641A>G 641 r.(?) p.(Gln214Arg) - missense -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.700+22G>A 700 r.(=) p.(=) - intron 22
./. - c.700+22G>A 700 r.(=) p.(=) - intron 22
./. - c.700+22G>A 700 r.(=) p.(=) - intron 22
./. - c.700+22G>A 700 r.(=) p.(=) - intron 22
./. - c.783+10C>T 783 r.(=) p.(=) - intron 10
./. - c.783+10C>T 783 r.(=) p.(=) - intron 10
./. - c.1021+24C>T 1021 r.(=) p.(=) - intron 24
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1094T>C 1094 r.(?) p.(Met365Thr) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1132G>C 1132 r.(?) p.(Gly378Arg) - missense -
./. - c.1573G>A 1573 r.(?) p.(Ala525Thr) - missense -
./. - c.1573G>A 1573 r.(?) p.(Ala525Thr) - missense -
./. - c.1573G>A 1573 r.(?) p.(Ala525Thr) - missense -
./. - c.1573G>A 1573 r.(?) p.(Ala525Thr) - missense -
./. - c.1791+46T>C 1791 r.(=) p.(=) - intron 46
./. - c.1791+46T>C 1791 r.(=) p.(=) - intron 46
./. - c.1791+46T>C 1791 r.(=) p.(=) - intron 46
./. - c.1791+46T>C 1791 r.(=) p.(=) - intron 46
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