Transcript #00008001

Transcript name interferon induced with helicase C domain 1
Gene name IFIH1 (interferon induced with helicase C domain 1)
Chromosome 2
Transcript - NCBI ID NM_022168.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_071451.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

201 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.25G>A r.(?) p.(Glu9Lys)
?/? c.47C>T r.(?) p.(Ser16Leu)
?/? c.62G>T r.(?) p.(Arg21Met)
?/? c.97G>T r.(?) p.(Asp33Tyr)
?/? c.177T>C r.(=) p.(=)
?/? c.229C>T r.(?) p.(Arg77Trp)
?/? c.230G>A r.(?) p.(Arg77Gln)
?/? c.240G>A r.(=) p.(=)
?/? c.258C>G r.(=) p.(=)
?/? c.278G>A r.(?) p.(Arg93His)
?/? c.292G>C r.(?) p.(Glu98Gln)
?/? c.298A>G r.(?) p.(Thr100Ala)
?/? c.313C>G r.(?) p.(Pro105Ala)
?/? c.314C>A r.(?) p.(Pro105Gln)
?/? c.340T>A r.(?) p.(Tyr114Asn)
?/? c.373C>A r.(?) p.(Leu125Met)
?/? c.376G>A r.(?) p.(Val126Met)
?/? c.384G>C r.(?) p.(Lys128Asn)
?/? c.420G>A r.(=) p.(=)
?/? c.427C>T r.(=) p.(=)
?/? c.436A>G r.(?) p.(Ile146Val)
?/? c.445A>G r.(?) p.(Arg149Gly)
?/? c.453+17A>G r.(=) p.(=)
?/? c.453+37A>C r.(=) p.(=)
?/? c.453+38G>T r.(=) p.(=)
?/? c.454-40A>T r.(=) p.(=)
?/? c.454-25T>G r.(=) p.(=)
?/? c.454-1G>T r.spl? p.?
?/? c.460G>C r.(?) p.(Ala154Pro)
?/? c.461C>T r.(?) p.(Ala154Val)
?/? c.467A>C r.(?) p.(Glu156Ala)
?/? c.478A>G r.(?) p.(Asn160Asp)
?/? c.527A>G r.(?) p.(Asn176Ser)
?/? c.622+46G>A r.(=) p.(=)
?/? c.623-19C>G r.(=) p.(=)
?/? c.660G>C r.(=) p.(=)
?/? c.698T>C r.(?) p.(Leu233Pro)
?/? c.736G>T r.(?) p.(Glu246*)
?/? c.755C>A r.(?) p.(Ser252Tyr)
?/? c.766T>G r.(?) p.(Ser256Ala)
?/? c.769+11C>A r.(=) p.(=)
?/? c.769+28A>T r.(=) p.(=)
?/? c.769+37A>G r.(=) p.(=)
?/? c.770-42C>A r.(=) p.(=)
?/? c.874+25C>G r.(=) p.(=)
?/? c.874+37G>T r.(=) p.(=)
?/? c.874+46C>T r.(=) p.(=)
?/? c.875-40T>C r.(=) p.(=)
?/? c.875-34C>T r.(=) p.(=)
?/? c.891A>C r.(=) p.(=)
?/? c.936A>G r.(=) p.(=)
?/? c.937del r.(?) p.(Met313Trpfs*35)
?/? c.949C>T r.(?) p.(Gln317*)
?/? c.988C>T r.(?) p.(Pro330Ser)
?/? c.1046A>G r.(?) p.(Lys349Arg)
?/? c.1046del r.(?) p.(Lys349Argfs*12)
?/? c.1066C>A r.(?) p.(Pro356Thr)
?/? c.1095+1G>A r.spl? p.?
?/? c.1095+33T>C r.(=) p.(=)
?/? c.1095+43A>G r.(=) p.(=)
?/? c.1096-49G>A r.(=) p.(=)
?/? c.1096-43G>A r.(=) p.(=)
?/? c.1096-17C>G r.(=) p.(=)
?/? c.1096-13A>G r.(=) p.(=)
?/? c.1097T>A r.(?) p.(Val366Glu)
?/? c.1121G>A r.(?) p.(Arg374His)
?/? c.1222G>A r.(?) p.(Asp408Asn)
?/? c.1275A>G r.(=) p.(=)
?/? c.1306+17del r.(=) p.(=)
?/? c.1306+24_1306+25insT r.(=) p.(=)
?/? c.1306+25dup r.(=) p.(=)
?/? c.1306+31_1306+32insA r.(=) p.(=)
?/? c.1307-22A>G r.(=) p.(=)
?/? c.1357G>C r.(?) p.(Val453Leu)
?/? c.1379A>G r.(?) p.(His460Arg)
?/? c.1407T>C r.(=) p.(=)
?/? c.1457G>C r.(?) p.(Gly486Ala)
?/? c.1481G>T r.(?) p.(Gly494Val)
?/? c.1491G>C r.(=) p.(=)
?/? c.1515C>T r.(=) p.(=)
?/? c.1524+19T>C r.(=) p.(=)
?/? c.1524+24C>G r.(=) p.(=)
?/? c.1525-10T>C r.(=) p.(=)
?/? c.1535A>T r.(?) p.(Asn512Ile)
?/? c.1558A>G r.(?) p.(Thr520Ala)
?/? c.1583T>G r.(?) p.(Leu528Arg)
?/? c.1605A>G r.(=) p.(=)
?/? c.1609A>G r.(?) p.(Lys537Glu)
?/? c.1641+1G>C r.spl? p.?
?/? c.1642-23A>G r.(=) p.(=)
?/? c.1644T>C r.(=) p.(=)
?/? c.1692T>C r.(=) p.(=)
?/? c.1723A>G r.(?) p.(Thr575Ala)
?/? c.1744G>T r.(?) p.(Ala582Ser)
?/? c.1764_1765insA r.(?) p.(Ala589Serfs*21)
?/? c.1765G>A r.(?) p.(Ala589Thr)
?/? c.1765+9G>A r.(=) p.(=)
?/? c.1765+33T>A r.(=) p.(=)
?/? c.1765+39G>A r.(=) p.(=)
?/? c.1765+46C>T r.(=) p.(=)
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