Transcript #00001750 (NM_000213.3, ITGB4 gene)

Transcript name transcript variant 1
Gene name ITGB4 (integrin, beta 4)
Chromosome 17
Transcript - NCBI ID NM_000213.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000204.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-11-14 17:24:25 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.162+9C>T r.(=) p.(=)
-?/. - c.163-4C>G r.spl? p.?
-?/. - c.189C>T r.(?) p.(Thr63=)
-?/. - c.231C>T r.(?) p.(=)
+/. 4i c.264+2T>A r.[264_265insgagccug, 264_265ins[ga;264+3_265-1]] p.Glu89fs
-?/. - c.290G>A r.(?) p.(Arg97Gln)
-?/. - c.332G>A r.(?) p.(Arg111Gln)
-?/. - c.387C>T r.(?) p.(Pro129=)
-?/. - c.469+4C>T r.spl? p.?
?/. - c.499T>A r.(?) p.(Tyr167Asn)
-/. - c.567-22_567-19del r.(=) p.(=)
?/. - c.599C>T r.(?) p.(Pro200Leu)
?/. - c.599C>T r.(?) p.(Pro200Leu)
?/. - c.665del r.(?) p.(Gly222Glufs*60)
?/. - c.848G>A r.(?) p.(Arg283His)
-?/. - c.860G>A r.(?) p.(Arg287Gln)
-?/. - c.867C>T r.(?) p.(His289=)
?/. - c.1002+5G>A r.spl? p.?
-?/. - c.1002+20C>G r.(=) p.(=)
-?/. - c.1003-16G>A r.(=) p.(=)
-?/. - c.1056G>A r.(?) p.(Ser352=)
?/. - c.1118G>C r.(?) p.(Arg373Pro)
-?/. - c.1215+19A>G r.(=) p.(=)
-?/. - c.1266C>T r.(?) p.(His422=)
-?/. - c.1266C>T r.(?) p.(His422=)
-?/. - c.1299C>G r.(?) p.(Asn433Lys)
-?/. - c.1345G>A r.(?) p.(Gly449Ser)
-?/. - c.1377+7C>T r.(=) p.(=)
-?/. - c.1377+15C>T r.(=) p.(=)
-?/. - c.1377+18A>T r.(=) p.(=)
-?/. - c.1428C>T r.(?) p.(Cys476=)
-?/. - c.1428C>T r.(?) p.(Cys476=)
-?/. - c.1434G>T r.(?) p.(Gln478His)
-?/. - c.1522G>A r.(?) p.(Glu508Lys)
-?/. - c.1533G>A r.(?) p.(Pro511=)
-/. - c.1544G>A r.(?) p.(Arg515His)
+?/. - c.1642G>A r.(?) p.(Gly548Arg)
-?/. - c.1657+6C>T r.(=) p.(=)
-?/. - c.1657+330G>A r.(=) p.(=)
-/. 13i c.1658-107C>T r.= p.=
-/. - c.1667G>A r.(?) p.(Arg556His)
-?/. - c.1749C>T r.(?) p.(Ile583=)
-?/. - c.1749C>T r.(?) p.(Ile583=)
+/. 14i c.1762-25T>A r.[1761_1762ins[1761+1762-26;a;1762-24_1762-1];1860_1861ins[1860+1_1860+54;g;1860+56_1861-1], 1761_1762ins[1761+1762-26;a;1762-24_1762-1]] p.Gly885fs
-?/. - c.1805A>T r.(?) p.(His602Leu)
-?/. - c.1806C>T r.(?) p.(His602=)
-?/. 15 c.1821G>A r.1821g>a p.Ser607=
?/. 15 c.1843G>A r.(?) p.(Glu615Lys)
-/. - c.1860+17C>T r.(=) p.(=)
-?/. 15i c.1860+55T>G r.(=) p.(=)
-?/. - c.1893C>G r.(?) p.(Ser631=)
-?/. - c.1911G>A r.(?) p.(Ala637=)
-?/. - c.1911G>A r.(?) p.(Ala637=)
+?/. - c.1940C>T r.(?) p.(Thr647Met)
?/. - c.1955A>G r.(?) p.(Asn652Ser)
-?/. - c.2009G>A r.(?) p.(Arg670His)
-?/. - c.2009G>A r.(?) p.(Arg670His)
-?/. - c.2115C>A r.(?) p.(Asp705Glu)
-?/. - c.2145C>T r.(?) p.(=)
-?/. - c.2207G>T r.(?) p.(Cys736Phe)
?/. - c.2359C>T r.(?) p.(Arg787Cys)
?/. - c.2371C>T r.(?) p.(Arg791Cys)
?/. - c.2405G>A r.(?) p.(Gly802Asp)
-?/. - c.2422G>A r.(?) p.(Ala808Thr)
-?/. - c.2446+19G>A r.(=) p.(=)
?/. - c.2510C>T r.(?) p.(Thr837Ile)
-?/. - c.2550+7A>T r.(=) p.(=)
-?/. - c.2551-16_2551-12del r.(=) p.(=)
?/. - c.2596C>T r.(?) p.(Gln866*)
?/. - c.2631A>C r.(?) p.(Lys877Asn)
-?/. - c.2638G>A r.(?) p.(Asp880Asn)
?/. - c.2675G>A r.(?) p.(Arg892His)
-/. - c.2730C>T r.(?) p.(Ala910=)
-/. - c.2730C>T r.(?) p.(Ala910=)
-?/. - c.2782+17G>A r.(=) p.(=)
-?/. - c.2784C>T r.(?) p.(=)
?/. - c.2834G>A r.(?) p.(Arg945Gln)
-?/. - c.2918C>A r.(?) p.(Thr973Asn)
-?/. - c.2922C>T r.(?) p.(Leu974=)
-/. - c.2929C>T r.(?) p.(Arg977Cys)
?/. - c.2929C>T r.(?) p.(Arg977Cys)
-?/. - c.2929C>T r.(?) p.(Arg977Cys)
-?/. - c.3017A>T r.(?) p.(Gln1006Leu)
?/. - c.3080G>A r.(?) p.(Arg1027His)
-?/. - c.3112-3C>T r.spl? p.?
?/. - c.3221G>A r.(?) p.(Arg1074His)
?/. - c.3224A>C r.(?) p.(Gln1075Pro)
?/. - c.3304A>C r.(?) p.(Ile1102Leu)
-?/. - c.3384C>T r.(?) p.(=)
?/. - c.3392A>G r.(?) p.(Gln1131Arg)
-?/. - c.3442C>G r.(?) p.(Leu1148Val)
-?/. - c.3474+7C>T r.(=) p.(=)
?/. - c.3508G>A r.(?) p.(Glu1170Lys)
-?/. - c.3519G>A r.(?) p.(Leu1173=)
-?/. - c.3598G>A r.(?) p.(Gly1200Arg)
-?/. - c.3598G>A r.(?) p.(Gly1200Arg)
?/. - c.3702G>A r.(?) p.(=)
?/. - c.3707C>T r.(?) p.(Thr1236Ile)
-?/. - c.3729G>A r.(=) p.(=)
-?/. - c.3729G>A r.(=) p.(=)
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