Transcript #00025392 (NM_001271223.2, OBSCN gene)

Transcript name transcript variant IC
Gene name OBSCN (obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF)
Chromosome 1
Transcript - NCBI ID NM_001271223.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001258152.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2019-03-19 20:49:30 +01:00 (CET)
Date last edited N/A


Variants

473 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-3C>G r.(?) p.(=)
?/. - c.35T>A r.(?) p.(Phe12Tyr)
-?/. - c.35T>A r.(?) p.(Phe12Tyr)
-?/. - c.35T>A r.(?) p.(Phe12Tyr)
?/. - c.35T>A r.(?) p.(Phe12Tyr)
?/. - c.88A>G r.(?) p.(Ser30Gly)
-/. - c.187G>A r.(?) p.(Asp63Asn)
-/. - c.282T>C r.(?) p.(Ala94=)
+/. - c.386_387delinsAA r.(?) p.(Phe129Ter)
?/. - c.436G>A r.(?) p.(Asp146Asn)
-?/. - c.496G>A r.(?) p.(Ala166Thr)
?/. - c.828G>T r.(?) p.(Gln276His)
?/. - c.1030G>C r.(?) p.(Val344Leu)
?/. - c.1204T>C r.(?) p.(Tyr402His)
-/. - c.1505A>G r.(?) p.(Gln502Arg)
-/. - c.1537C>T r.(?) p.(Leu513=)
?/. - c.1625C>T r.(?) p.(Pro542Leu)
?/. - c.1804G>A r.(?) p.(Glu602Lys)
-/. - c.1829-16G>T r.(=) p.(=)
-?/. - c.1829C>A r.(?) p.(Ala610Asp)
-?/. - c.1994G>A r.(?) p.(Arg665Gln)
?/. - c.2011C>T r.(?) p.(Arg671Trp)
./. - c.2096-225T>C r.(=) p.(=)
-?/. - c.2139C>T r.(?) p.(Ala713=)
-?/. - c.2143G>A r.(?) p.(Glu715Lys)
-?/. - c.2143G>A r.(?) p.(Glu715Lys)
-?/. - c.2163C>T r.(?) p.(His721=)
?/. - c.2186A>C r.(?) p.(Glu729Ala)
-?/. - c.2201C>G r.(?) p.(Ala734Gly)
-?/. - c.2230C>T r.(?) p.(Arg744Cys)
-?/. - c.2309G>A r.(?) p.(Arg770Gln)
-?/. - c.2342G>A r.(?) p.(Arg781His)
?/. - c.2351G>A r.(?) p.(Arg784His)
-?/. - c.2356G>A r.(?) p.(Ala786Thr)
-/. - c.2378-46T>C r.(=) p.(=)
-?/. - c.2441C>T r.(?) p.(Pro814Leu)
-?/. - c.2482G>T r.(?) p.(Val828Leu)
-?/. - c.2653+8C>T r.(=) p.(=)
-/. - c.2654-15C>T r.(=) p.(=)
-?/. - c.2661G>A r.(?) p.(Lys887=)
-?/. - c.2688G>T r.(?) p.(=)
-?/. - c.2746C>G r.(?) p.(Gln916Glu)
-/. - c.2894G>A r.(?) p.(Arg965Lys)
-?/. - c.2894G>A r.(?) p.(Arg965Lys)
-/. - c.2914C>T r.(?) p.(Arg972Cys)
-?/. - c.2938G>A r.(?) p.(Val980Met)
-?/. - c.2965C>T r.(?) p.(Arg989Cys)
-?/. - c.2965C>T r.(?) p.(Arg989Cys)
-/. - c.2997T>C r.(?) p.(Ser999=)
-/. - c.2998G>A r.(?) p.(Ala1000Thr)
-/. - c.3078G>A r.(?) p.(Ser1026=)
+?/. - c.3163G>A r.(?) p.(Glu1055Lys)
-?/. - c.3179G>A r.(?) p.(Arg1060Gln)
-?/. - c.3268dup r.(?) p.(Ala1090GlyfsTer85)
-/. - c.3269C>G r.(?) p.(Ala1090Gly)
-?/. - c.3308C>T r.(?) p.(Thr1103Met)
-/. - c.3417A>G r.(?) p.(Thr1139=)
?/. - c.3466C>T r.(?) p.(Arg1156Cys)
-?/. - c.3481+5G>T r.spl? p.?
-?/. - c.3482A>G r.(?) p.(Glu1161Gly)
-?/. - c.3545C>G r.(?) p.(Ala1182Gly)
-?/. - c.3546C>T r.(?) p.(=)
-?/. - c.3593C>A r.(?) p.(Thr1198Lys)
?/. - c.3598T>A r.(?) p.(Tyr1200Asn)
?/. - c.3667C>G r.(?) p.(Leu1223Val)
-?/. - c.3684G>A r.(?) p.(Ala1228=)
?/. - c.3704A>G r.(?) p.(Glu1235Gly)
-?/. - c.3805C>T r.(?) p.(Gln1269Ter)
-?/. - c.3815C>T r.(?) p.(Ala1272Val)
-/. - c.3861A>G r.(?) p.(Thr1287=)
-?/. - c.4082G>A r.(?) p.(Arg1361Gln)
-/. - c.4097C>G r.(?) p.(Ala1366Gly)
-?/. - c.4104C>A r.(?) p.(Ala1368=)
-/. - c.4200T>C r.(?) p.(Ala1400=)
-/. - c.4272T>C r.(?) p.(Ala1424=)
-?/. - c.4282C>T r.(?) p.(Arg1428Trp)
?/. - c.4361C>T r.(?) p.(Ala1454Val)
?/. - c.4361C>T r.(?) p.(Ala1454Val)
-?/. - c.4373C>G r.(?) p.(Ala1458Gly)
?/. - c.4393G>A r.(?) p.(Glu1465Lys)
?/. - c.4436G>A r.(?) p.(Gly1479Glu)
-/. - c.4586-34T>G r.(=) p.(=)
-/. - c.4619T>C r.(?) p.(Val1540Ala)
?/. - c.4624_4629dup r.(?) p.(Arg1542_Glu1543dup)
-?/. - c.4742G>A r.(?) p.(Arg1581His)
-?/. - c.4744A>G r.(?) p.(Met1582Val)
-/. - c.4797G>A r.(?) p.(Ala1599=)
?/. - c.4804G>A r.(?) p.(Gly1602Arg)
-?/. - c.4862-10C>G r.(=) p.(=)
?/. - c.4931C>T r.(?) p.(Ala1644Val)
-?/. - c.5122C>T r.(?) p.(Arg1708Cys)
-?/. - c.5122C>T r.(?) p.(Arg1708Cys)
-/. - c.5137+13G>A r.(=) p.(=)
-?/. - c.5148G>A r.(?) p.(Ala1716=)
-/. - c.5337G>C r.(?) p.(Glu1779Asp)
-?/. - c.5349G>A r.(?) p.(Ala1783=)
-?/. - c.5352C>T r.(?) p.(Asp1784=)
-?/. - c.5472G>A r.(?) p.(=)
-?/. - c.5565A>C r.(?) p.(Lys1855Asn)
?/. - c.5790C>G r.(?) p.(Ser1930Arg)
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