Transcript #00014618 (NM_021209.4, NLRC4 gene)

Transcript name transcript variant 1
Gene name NLRC4 (NLR family, CARD domain containing 4)
Chromosome 2
Transcript - NCBI ID NM_021209.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_067032.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

67 entries on 1 page. Showing entries 1 - 67.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-29590644_*4849134dup r.0? p.0?
-?/. - c.26G>A r.(?) p.(Arg9Gln)
?/. - c.88del r.(?) p.(Trp30Glyfs*4)
?/. - c.122T>C r.(?) p.(Ile41Thr)
-?/. - c.129C>T r.(?) p.(Cys43=)
-?/. - c.191A>C r.(?) p.(Glu64Ala)
-?/. - c.207T>C r.(?) p.(Phe69=)
?/. - c.208C>T r.(?) p.(Leu70Phe)
?/. - c.208C>T r.(?) p.(Leu70Phe)
?/. - c.208C>T r.(?) p.(Leu70Phe)
-?/. - c.252G>A r.(?) p.(Leu84=)
-?/. - c.262+15G>A r.(=) p.(=)
-/. - c.262+100A>G r.(=) p.(=)
-?/. - c.263-19A>G r.(=) p.(=)
-?/. - c.411T>G r.(?) p.(Pro137=)
-?/. - c.433C>T r.(?) p.(His145Tyr)
-?/. - c.478G>A r.(?) p.(Ala160Thr)
-?/. - c.478G>A r.(?) p.(Ala160Thr)
-?/. - c.480T>C r.(?) p.(Ala160=)
?/. - c.493T>C r.(?) p.(Cys165Arg)
+?/. - c.515G>A r.(?) p.(Gly172Asp)
?/. - c.517A>G r.(?) p.(Lys173Glu)
-/. - c.543A>C r.(?) p.(Arg181=)
-/. - c.543A>C r.(?) p.(Arg181=)
-?/. - c.704T>C r.(?) p.(Met235Thr)
-?/. - c.822G>C r.(?) p.(Met274Ile)
?/. - c.928C>T r.(?) p.(Arg310*)
-?/. - c.1083G>A r.(?) p.(Thr361=)
-?/. - c.1224C>T r.(?) p.(Phe408=)
-?/. - c.1248G>A r.(?) p.(Val416=)
+/. - c.1333T>C r.(?) p.(Ser445Pro)
?/. - c.1357C>T r.(?) p.(Arg453*)
-/. - c.1542A>G r.(?) p.(Gln514=)
-?/. - c.1570G>A r.(?) p.(Ala524Thr)
-?/. - c.1804T>C r.(?) p.(Leu602=)
-/. - c.1824C>T r.(?) p.(Ala608=)
-?/. - c.1893A>G r.(?) p.(Thr631=)
-?/. - c.2217A>G r.(?) p.(Lys739=)
-?/. - c.2350+9del r.(=) p.(=)
-?/. - c.2357G>T r.(?) p.(Gly786Val)
-?/. - c.2357G>T r.(?) p.(Gly786Val)
-?/. - c.2380T>C r.(?) p.(Cys794Arg)
-/. - c.2522-86_2522-85insG r.(=) p.(=)
-?/. - c.2614+12A>T r.(=) p.(=)
-?/. - c.2614+12A>T r.(=) p.(=)
-?/. - c.2628C>T r.(?) p.(Asn876=)
-?/. - c.2629G>A r.(?) p.(Val877Met)
-?/. - c.2629G>A r.(?) p.(Val877Met)
-?/. - c.2647G>A r.(?) p.(Ala883Thr)
-?/. - c.2668T>C r.(?) p.(Cys890Arg)
-/. - c.2668T>C r.(?) p.(Cys890Arg)
-?/. - c.2727C>T r.(?) p.(Leu909=)
-?/. - c.2740T>C r.(?) p.(Leu914=)
-/. - c.2740T>C r.(?) p.(Leu914=)
-/. - c.2782+77C>T r.(=) p.(=)
-/. - c.2782+122T>C r.(=) p.(=)
-/. - c.2783-46del r.(=) p.(=)
-?/. - c.2783-41_2783-38del r.(=) p.(=)
-/. - c.2785G>T r.(?) p.(Ala929Ser)
-/. - c.2785G>T r.(?) p.(Ala929Ser)
?/. - c.2828A>T r.(?) p.(Asn943Ile)
?/. - c.2834C>T r.(?) p.(Ala945Val)
?/. - c.2834C>T r.(?) p.(Ala945Val)
-?/. - c.2883T>C r.(?) p.(Phe961=)
-?/. - c.2945C>G r.(?) p.(Ala982Gly)
?/. - c.2992C>A r.(?) p.(Gln998Lys)
?/. - c.3052G>A r.(?) p.(Ala1018Thr)
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