Transcript #00025731 (NM_001042424.2, WHSC1 gene)

Transcript name transcript variant 10
Gene name WHSC1 (Wolf-Hirschhorn syndrome candidate 1)
Chromosome 4
Transcript - NCBI ID NM_001042424.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001035889.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2022-08-13 15:55:25 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_22_ c.-176_*3298{0} r.0 p.0
+/. _1_22_ c.-176_*3298{0} r.0? p.0?
+/. _1_18_ c.(?_-30+2016)_(3255+505_?)del r.? p.?
-?/. - c.-29-6414C>T r.(=) p.(=)
-?/. - c.-29-6378C>T r.(=) p.(=)
+/. - c.(?-1800852)_(*1230379_?)del r.0 p.0
+/. _10_22_ c.(?_1881+2806)_*3298{0} r.? p.?
+/. _1_6_ c.-176_(1556-1103_?){0} r.0? p.0?
-?/. - c.11G>A r.(?) p.(Ser4Asn)
?/. - c.293T>G r.(?) p.(Leu98Arg)
?/. - c.362C>G r.(?) p.(Ser121Cys)
?/. - c.383_385dup r.(?) p.(Ile128dup)
-?/. - c.393A>G r.(?) p.(=)
-?/. - c.452T>C r.(?) p.(Val151Ala)
?/. - c.541C>T r.(?) p.(Gln181Ter)
+/. - c.642dup r.(?) p.(Asp215Argfs*10)
+/. - c.660C>G r.(?) p.(Tyr220Ter)
+/. - c.708G>A r.(?) p.(Trp236*)
?/. - c.755T>A r.(?) p.(Leu252His)
+/. - c.793C>T r.(?) p.(Gln265*)
?/. - c.808G>A r.(?) p.(Ala270Thr)
?/. - c.884A>T r.(?) p.(Gln295Leu)
-?/. - c.884A>T r.(?) p.(Gln295Leu)
?/. - c.908C>T r.(?) p.(Thr303Met)
-?/. - c.928-6dup r.(=) p.(=)
+?/. - c.957G>T r.957g>u p.(Arg319Ser)
-?/. - c.1081A>C r.(?) p.(Lys361Gln)
+/. - c.1103_1104del r.(?) p.(Glu368ValfsTer13)
+?/. - c.1103_1104del r.(?) p.(Glu368Valfs*13)
-?/. - c.1210A>G r.(?) p.(Lys404Glu)
+?/. - c.1222_1226del r.(?) p.(Ser408ArgfsTer21)
-?/. - c.1249G>A r.(?) p.(Asp417Asn)
-?/. - c.1330A>G r.(?) p.(Thr444Ala)
+/. - c.1363_1364dup r.(?) p.(Asp455Glufs*19)
-?/. - c.1366G>C r.(?) p.(Ala456Pro)
-?/. - c.1411-4144T>G r.(=) p.(=)
-?/. - c.1411-6C>T r.(=) p.(=)
?/. - c.1423C>T r.(?) p.(His475Tyr)
+/. - c.1469dup r.(?) p.(Trp491Valfs*6)
-?/. - c.1555+1700G>T r.(=) p.(=)
+/. - c.1569dup r.(?) p.(Lys524GlufsTer17)
+/. - c.1569dup r.(?) p.(Lys524Glufs*17)
+/. - c.1577dup r.(?) p.(Asn527Lysfs*14)
+/. - c.1577dup r.(?) p.(Asn527Lysfs*14)
-?/. - c.1585A>C r.(?) p.(Thr529Pro)
+?/. - c.1588_1589dup r.(?) p.(Ile532GlyfsTer67)
?/. - c.1675-19_1675-10del r.(=) p.(=)
-?/. - c.1675-11_1675-10del r.(=) p.(=)
-?/. - c.1675-10T>A r.(=) p.(=)
+/. - c.1676_1679del r.(?) p.(Arg559Thrfs*38)
+/. - c.1676_1679del r.(?) p.(Arg559ThrfsTer38)
?/. - c.1757-1G>T r.spl? p.?
?/. - c.1780T>C r.(?) p.(Cys594Arg)
+/. - c.1798C>T r.(?) p.(Arg600Ter)
-?/. - c.1882-4C>G r.spl? p.?
?/. - c.1890_1913dup r.(?) p.(Asp630_Ser637dup)
-?/. - c.1902C>T r.(?) p.(=)
-?/. - c.1994A>G r.(?) p.(Lys665Arg)
?/. - c.2027C>T r.(?) p.(Pro676Leu)
?/. - c.2102C>T r.(?) p.(Pro701Leu)
?/. - c.2127G>C r.(?) p.(Glu709Asp)
+/. - c.2137+2C>G r.spl? p.?
-/. - c.2138-106A>G r.(=) p.(=)
+/. - c.2160T>A r.(?) p.(Cys720Ter)
?/. - c.2160T>A r.(?) p.(Cys720Ter)
-?/. - c.2179G>C r.(?) p.(Val727Leu)
+/. - c.2263C>T r.(?) p.(Arg755Ter)
+?/. - c.2263C>T r.(?) p.(Arg755Ter)
-?/. - c.2339-629dup r.(=) p.(=)
-?/. - c.2423C>G r.(?) p.(Ser808Cys)
+/. - c.2518+1G>A r.spl p.?
?/. - c.2543C>G r.(?) p.(Ser848Cys)
+?/. - c.2606G>A r.(?) p.(Cys869Tyr)
+?/. - c.2661del r.(?) p.(Lys887Asnfs*25)
+?/. - c.2684C>T r.(?) p.(Pro895Leu)
+?/. - c.2684C>T r.(?) p.(Pro895Leu)
?/. - c.2792C>T r.(?) p.(Thr931Met)
+/. - c.2803C>T r.(?) p.(Arg935*)
-/. - c.2814G>A r.(?) p.(=)
-?/. - c.2882-402G>A r.(=) p.(=)
?/. - c.2929G>C r.(?) p.(Glu977Gln)
?/. - c.2929G>C r.(?) p.(Glu977Gln)
+?/. - c.2935C>T r.(?) p.(Arg979*)
+/. - c.2973C>A r.(?) p.(Tyr991*)
?/. - c.3016T>C r.(?) p.(Tyr1006His)
+/. - c.3056A>G r.(?) p.(Lys1019Arg)
+?/. - c.3056A>G r.(?) p.(Lys1019Arg)
+/. - c.3223_3226dup r.(?) p.(Gly1076ValfsTer16)
+?/. - c.3271G>A r.(?) p.(Glu1091Lys)
+/. - c.3295G>A r.(?) p.(Glu1099Lys)
+/. - c.3295G>A r.(?) p.(Glu1099Lys)
-?/. - c.3351C>G r.(?) p.(Phe1117Leu)
-?/. - c.3372+10A>C r.(=) p.(=)
-?/. - c.3372+5306T>C r.(=) p.(=)
-?/. - c.3372+5315T>C r.(=) p.(=)
+/. - c.3410C>T r.(?) p.(Ser1137Phe)
+/. - c.3412C>T r.(?) p.(Arg1138*)
?/. - c.3442T>C r.(?) p.(Cys1148Arg)
+?/. - c.3472dup r.(?) p.(Asp1158GlyfsTer11)
+?/. - c.3472dup r.(?) p.(Asp1158GlyfsTer11)
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