Transcript #00025753 (NM_015311.2, OBSL1 gene)

Transcript name transcript variant 1
Gene name OBSL1 (obscurin-like 1)
Chromosome 2
Transcript - NCBI ID NM_015311.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_056126.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2022-10-27 09:01:01 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-4229C>G r.(?) p.(=)
-?/. - c.-4025G>A r.(?) p.(=)
?/. - c.-3959G>A r.(?) p.(=)
-?/. - c.-3680C>T r.(?) p.(=)
-?/. - c.-1349G>A r.(?) p.(=)
+?/. - c.-1320G>A r.(?) p.(=)
+/. - c.71dup r.(?) p.(Ser25Lysfs*229)
-?/. - c.119C>G r.(?) p.(Pro40Arg)
-?/. - c.202G>A r.(?) p.(Gly68Ser)
+/. - c.255_629del r.(?) p.(Ala90_Ala214del)
?/. - c.458G>A r.(?) p.(Gly153Asp)
?/. - c.518del r.(?) p.(Asp173AlafsTer85)
-?/. - c.569C>G r.(?) p.(Ala190Gly)
-/. - c.580C>T r.(?) p.(Leu194=)
-/. - c.580C>T r.(?) p.(Leu194=)
-?/. - c.593C>A r.(?) p.(Ala198Glu)
-?/. - c.622G>A r.(?) p.(Val208Met)
?/. - c.690del r.(?) p.(Glu231Argfs*27)
+/. - c.707del r.(?) p.(Asp236Thrfs*22)
-?/. - c.751G>T r.(?) p.(Ala251Ser)
?/. - c.752C>T r.(?) p.(Ala251Val)
-?/. - c.851G>A r.(?) p.(Arg284His)
?/. - c.854C>A r.(?) p.(Pro285Gln)
?/. - c.892C>T r.(?) p.(Arg298Cys)
-/. - c.921T>C r.(?) p.(Leu307=)
-/. - c.921T>C r.(?) p.(Leu307=)
+/. - c.951C>A r.(?) p.(Tyr317*)
-?/. - c.955T>G r.(?) p.(Cys319Gly)
?/. - c.962C>T r.(?) p.(Ala321Val)
-?/. - c.984G>T r.(?) p.(Thr328=)
?/. - c.992C>A r.(?) p.(Ala331Asp)
?/. - c.1001T>C r.(?) p.(Leu334Pro)
-?/. - c.1065C>T r.(?) p.(His355=)
-?/. - c.1102C>T r.(?) p.(Arg368Cys)
-/. - c.1102C>T r.(?) p.(Arg368Cys)
-?/. - c.1102C>T r.(?) p.(Arg368Cys)
?/. - c.1109C>T r.(?) p.(Pro370Leu)
?/. - c.1168G>A r.(?) p.(Glu390Lys)
?/. - c.1228T>C r.(?) p.(Tyr410His)
+/. - c.1255C>T r.(?) p.(Arg419Cys)
?/. - c.1255C>T r.(?) p.(Arg419Cys)
?/. - c.1255C>T r.(?) p.(Arg419Cys)
+/. - c.1273dup r.(?) p.(Thr425Asnfs*40)
+/. - c.1273dup r.(?) p.(Thr425Asnfs*40)
+/. - c.1273dup r.(?) p.(Thr425Asnfs*40)
+/. - c.1273dup r.(?) p.(Thr425Asnfs*40)
-/. - c.1283-18T>A r.(=) p.(=)
-/. - c.1283-18T>A r.(=) p.(=)
+/. - c.1303del r.(?) p.(Arg436Glyfs*14)
+/. - c.1303del r.(?) p.(Arg436Glyfs*14)
+/. - c.1303del r.(?) p.(Arg436Glyfs*14)
+/. - c.1306del r.(?) p.(Arg436GlyfsTer14)
?/. - c.1318G>A r.(?) p.(Val440Ile)
?/. - c.1390G>T r.(?) p.(Asp464Tyr)
?/. - c.1486A>G r.(?) p.(Thr496Ala)
-?/. - c.1734G>A r.(?) p.(Pro578=)
-?/. - c.1737C>A r.(?) p.(Gly579=)
?/. - c.1738G>A r.(?) p.(Asp580Asn)
?/. - c.1742G>A r.(?) p.(Cys581Tyr)
-/. - c.1818C>T r.(?) p.(Phe606=)
-?/. - c.1820A>G r.(?) p.(His607Arg)
-?/. - c.1912G>A r.(?) p.(Asp638Asn)
-?/. - c.1950T>C r.(?) p.(Asn650=)
?/. - c.1976C>T r.(?) p.(Pro659Leu)
-?/. - c.1999G>A r.(?) p.(Ala667Thr)
-/. - c.2055C>A r.(?) p.(Ala685=)
-?/. - c.2056G>A r.(?) p.(Val686Ile)
+/. - c.2077G>C r.(?) p.(Ala693Pro)
?/. - c.2104G>A r.(?) p.(Val702Met)
?/. - c.2104G>A r.(?) p.(Val702Met)
-/. - c.2168G>A r.(?) p.(Arg723Lys)
-/. - c.2168G>A r.(?) p.(Arg723Lys)
-?/. - c.2238G>A r.(?) p.(Pro746=)
-?/. - c.2392G>A r.(?) p.(Gly798Ser)
-?/. - c.2392G>A r.(?) p.(Gly798Ser)
-?/. - c.2470T>A r.(?) p.(Cys824Ser)
+?/. - c.2497C>T r.(?) p.(Arg833*)
?/. - c.2608C>G r.(?) p.(Gln870Glu)
-?/. - c.2661C>T r.(?) p.(Tyr887=)
?/. - c.2680+8G>A r.(=) p.(=)
-/. - c.2682C>T r.(?) p.(Asp894=)
-/. - c.2682C>T r.(?) p.(Asp894=)
-/. - c.2730C>A r.(?) p.(Ala910=)
-/. - c.2730C>A r.(?) p.(Ala910=)
?/. - c.2803G>A r.(?) p.(Gly935Arg)
?/. - c.2863C>A r.(?) p.(Leu955Met)
-?/. - c.2887G>A r.(?) p.(Glu963Lys)
-?/. - c.2938A>G r.(?) p.(Thr980Ala)
?/. - c.2947G>A r.(?) p.(Val983Ile)
-?/. - c.2947G>A r.(?) p.(Val983Ile)
-?/. - c.2953+457C>T r.(=) p.(=)
?/. - c.2998_3012del r.(?) p.(Ile1000_Leu1004del)
?/. - c.3077G>A r.(?) p.(Gly1026Glu)
?/. - c.3118G>A r.(?) p.(Asp1040Asn)
?/. - c.3236A>T r.(?) p.(Glu1079Val)
-?/. - c.3252G>A r.(?) p.(Pro1084=)
-?/. - c.3259C>T r.(?) p.(Arg1087Cys)
-?/. - c.3283G>A r.(?) p.(Ala1095Thr)
?/. - c.3292C>T r.(?) p.(Arg1098Cys)
-?/. - c.3304C>T r.(?) p.(Arg1102Cys)
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