Transcript #00017937 (NM_001256071.1, RNF213 gene)

Transcript name transcript variant 3
Gene name RNF213 (ring finger protein 213)
Chromosome 17
Transcript - NCBI ID NM_001256071.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001243000.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.128C>T r.(?) p.(Ser43Leu)
-?/. - c.161A>C r.(?) p.(Glu54Ala)
-?/. - c.182C>T r.(?) p.(Pro61Leu)
-?/. - c.222C>T r.(?) p.(=)
-?/. - c.355C>T r.(?) p.(His119Tyr)
-/. - c.378G>A r.(?) p.(Pro126=)
-?/. - c.397C>A r.(?) p.(Leu133Met)
-/. - c.453A>G r.(?) p.(Pro151=)
-?/. - c.502G>A r.(?) p.(Glu168Lys)
-?/. - c.609G>C r.(?) p.(Glu203Asp)
-?/. - c.626T>A r.(?) p.(Ile209Asn)
-/. - c.809T>C r.(?) p.(Met270Thr)
-/. - c.962T>C r.(?) p.(Met321Thr)
-/. - c.990G>A r.(?) p.(Lys330=)
?/. - c.1027G>C r.(?) p.(Glu343Gln)
-?/. - c.1116G>T r.(?) p.(=)
?/. - c.1149C>G r.(?) p.(Phe383Leu)
-?/. - c.1198G>C r.(?) p.(Val400Leu)
?/. - c.1214_1216del r.(?) p.(Gly405del)
-?/. - c.1214_1216del r.(?) p.(Gly405del)
?/. - c.1939C>T r.(?) p.(Leu647Phe)
-?/. - c.2122C>G r.(?) p.(His708Asp)
?/. - c.2131G>A r.(?) p.(Ala711Thr)
?/. - c.2796C>T r.(?) p.(=)
-/. - c.2811+19G>C r.(=) p.(=)
-?/. - c.2838A>G r.(?) p.(=)
-?/. - c.2846C>T r.(?) p.(Ala949Val)
-?/. - c.3024+33G>A r.(=) p.(=)
-/. - c.3024+77A>T r.(=) p.(=)
-/. - c.3121G>A r.(?) p.(Ala1041Thr)
-/. - c.3133A>G r.(?) p.(Asn1045Asp)
-?/. - c.3391G>A r.(?) p.(Asp1131Asn)
-/. - c.3397C>A r.(?) p.(Gln1133Lys)
-?/. - c.3518-9C>T r.(=) p.(=)
-?/. - c.3672A>G r.(?) p.(Ile1224Met)
-?/. - c.3681C>T r.(?) p.(Leu1227=)
-?/. - c.3729G>A r.(?) p.(=)
-?/. - c.3774T>G r.(?) p.(Ser1258Arg)
-/. - c.3992A>G r.(?) p.(Asp1331Gly)
-?/. - c.4156G>A r.(?) p.(Asp1386Asn)
-?/. - c.4405G>C r.(?) p.(Val1469Leu)
?/. - c.4527+7C>G r.(=) p.(=)
-?/. - c.4593C>T r.(?) p.(Arg1531=)
-?/. - c.4645C>A r.(?) p.(Gln1549Lys)
-/. - c.4650G>A r.(?) p.(Ala1550=)
-?/. - c.4951C>T r.(?) p.(Leu1651Phe)
?/. - c.5114C>A r.(?) p.(Thr1705Lys)
-?/. - c.5162C>T r.(?) p.(Pro1721Leu)
?/. - c.5266C>T r.(?) p.(Arg1756Cys)
-?/. - c.5716C>T r.(?) p.(Arg1906Cys)
?/. - c.5947C>T r.(?) p.(Arg1983Trp)
-?/. - c.6032T>C r.(?) p.(Met2011Thr)
-?/. - c.6112G>A r.(?) p.(Ala2038Thr)
?/. - c.6290T>C r.(?) p.(Val2097Ala)
-?/. - c.6490T>G r.(?) p.(Phe2164Val)
-/. - c.7001G>A r.(?) p.(Ser2334Asn)
-?/. - c.7335C>G r.(?) p.(=)
?/. - c.7547C>T r.(?) p.(Ser2516Phe)
?/. - c.7660G>A r.(?) p.(Asp2554Asn)
-?/. - c.7830C>T r.(?) p.(=)
-?/. - c.8067C>T r.(?) p.(Ile2689=)
-?/. - c.8149G>A r.(?) p.(Asp2717Asn)
-?/. - c.8262G>T r.(?) p.(Met2754Ile)
-?/. - c.8790G>A r.(?) p.(=)
-?/. - c.8790G>A r.(?) p.(=)
?/. - c.8936T>C r.(?) p.(Ile2979Thr)
?/. - c.8968A>C r.(?) p.(Lys2990Gln)
?/. - c.9201G>T r.(?) p.(Glu3067Asp)
-?/. - c.9530A>G r.(?) p.(Asn3177Ser)
-?/. - c.9727A>G r.(?) p.(Thr3243Ala)
-?/. - c.9852G>A r.(?) p.(=)
-?/. - c.9951+3G>T r.spl? p.?
?/. - c.9951+3G>T r.spl? p.?
-?/. - c.9952A>G r.(?) p.(Ile3318Val)
?/. - c.10265G>A r.(?) p.(Arg3422Gln)
?/. - c.10268T>C r.(?) p.(Val3423Ala)
?/. - c.10300G>A r.(?) p.(Gly3434Arg)
-?/. - c.10443G>A r.(?) p.(=)
-/. - c.10470G>A r.(?) p.(Glu3490=)
?/. - c.10666C>T r.(?) p.(Arg3556Cys)
-?/. - c.10717G>A r.(?) p.(Ala3573Thr)
-?/. - c.10727-4A>G r.spl? p.?
?/. - c.10754G>A r.(?) p.(Arg3585His)
-?/. - c.11201-6C>A r.(=) p.(=)
-/. - c.11277G>A r.(?) p.(=)
?/. - c.11717G>A r.(?) p.(Gly3906Glu)
-?/. - c.11886C>T r.(?) p.(Asn3962=)
-?/. - c.11972+8C>T r.(=) p.(=)
-?/. - c.12013A>G r.(?) p.(Lys4005Glu)
+?/. - c.12059G>T r.(?) p.(Cys4020Phe)
-?/. - c.12243C>T r.(?) p.(=)
-?/. - c.12247C>A r.(?) p.(Pro4083Thr)
?/. - c.12286_12288del r.(?) p.(Leu4096del)
+?/. - c.12345A>C r.(?) p.(Lys4115Asn)
+/. - c.12365A>C r.(?) p.(Asp4122Ala)
?/. - c.12417G>T r.(?) p.(Leu4139Phe)
-/. - c.12807G>A r.(?) p.(=)
-?/. - c.12817G>A r.(?) p.(Asp4273Asn)
-?/. - c.12817G>A r.(?) p.(Asp4273Asn)
-/. - c.12847C>A r.(?) p.(Leu4283Ile)
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