Transcript #00025324 (NM_000192.3, TBX5 gene)

Transcript name transcript variant 1
Gene name TBX5 (T-box 5)
Chromosome 12
Transcript - NCBI ID NM_000192.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000183.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2018-10-11 15:31:23 +02:00 (CEST)
Date last edited N/A


Variants

78 entries on 1 page. Showing entries 1 - 78.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.16G>A r.(?) p.(Glu6Lys)
?/. - c.16G>A r.(?) p.(Glu6Lys)
-?/. - c.55G>T r.(?) p.(Ala19Ser)
?/. - c.55G>T r.(?) p.(Ala19Ser)
-?/. - c.147+4A>G r.spl? p.?
-?/. - c.147+13C>A r.(=) p.(=)
-/. - c.148-19T>A r.(=) p.(=)
+/. 3 c.192G>A r.(?) p.(Trp64*)
?/. - c.271G>A r.(?) p.(Val91Met)
?/. - c.278G>A r.(?) p.(Gly93Asp)
-?/. - c.309C>T r.(?) p.(Leu103=)
-/. - c.309C>T r.(?) p.(Leu103=)
-/. - c.316A>G r.(?) p.(Ile106Val)
-?/. - c.316A>G r.(?) p.(Ile106Val)
-?/. - c.331G>T r.(?) p.(Asp111Tyr)
-?/. - c.331G>T r.(?) p.(Asp111Tyr)
-/. - c.331G>T r.(?) p.(Asp111Tyr)
-?/. - c.354T>C r.(?) p.(Asp118=)
-?/. - c.354T>C r.(?) p.(Asp118=)
-?/. - c.363-6A>G r.(=) p.(=)
-?/. - c.372G>A r.(?) p.(Thr124=)
+/. 5 c.373G>C r.(?) p.(Gly125Arg)
+?/. - c.394C>A r.(?) p.(Pro132Thr)
+/. - c.408C>A r.(?) p.(Tyr136Ter)
+/. - c.408C>G r.(?) p.(Tyr136Ter)
-?/. - c.420C>T r.(=) p.(=)
+/. - c.451C>A r.(?) p.(Gln151Lys)
+/. - c.451C>T r.(?) p.(Gln151*)
+/. - c.510+2dup r.spl? p.?
?/. - c.510+3G>A r.spl? p.?
-/. - c.511-56T>C r.(=) p.(=)
+/. - c.521del r.(?) p.(Asn174IlefsTer13)
?/. - c.556G>A r.(?) p.(Val186Met)
?/. - c.563C>T r.(?) p.(Ala188Val)
+/. - c.587C>A r.(?) p.(Ser196Ter)
+/. - c.643dup r.(?) p.(Thr215Asnfs*14)
+?/. - c.652C>G r.(?) p.(Gln218Glu)
+?/. - c.663+1G>A r.spl? p.?
-/. - c.663+36G>T r.(=) p.(=)
-/. - c.663+186A>G r.(=) p.(=)
+/. - c.668C>T r.(?) p.(Thr223Met)
+/. - c.710G>A r.(?) p.(Arg237Gln)
?/. - c.716G>A r.(?) p.(Ser239Asn)
-?/. - c.755+35A>G r.(=) p.(=)
-/. - c.755+94C>A r.(=) p.(=)
-?/. - c.768C>T r.(?) p.(Pro256=)
?/. - c.775C>T r.(?) p.(Pro259Ser)
-/. - c.786C>T r.(?) p.(Thr262=)
-/. - c.786C>T r.(?) p.(Thr262=)
-?/. - c.787G>A r.(?) p.(Val263Met)
-?/. - c.827G>A r.(?) p.(Ser276Asn)
-?/. - c.827G>A r.(?) p.(Ser276Asn)
-?/. - c.827G>A r.(?) p.(Ser276Asn)
+/. - c.835C>T r.(?) p.(Arg279Ter)
+/. - c.835C>T r.(?) p.(Arg279Ter)
-?/. - c.836G>A r.(?) p.(Arg279Gln)
-?/. - c.836G>A r.(?) p.(Arg279Gln)
+?/. - c.874C>T r.(?) p.(Gln292*)
+/. - c.958del r.(?) p.(Ile320PhefsTer74)
+/. - c.982+1G>C r.spl? p.?
-/. - c.982+16C>T r.(=) p.(=)
-?/. - c.982+16C>T r.(=) p.(=)
-?/. - c.982+321_982+322insGA r.(=) p.(=)
-?/. - c.1115C>T r.(?) p.(Ser372Leu)
?/. - c.1169T>G r.(?) p.(Val390Gly)
-?/. - c.1234G>A r.(?) p.(Val412Ile)
?/. - c.1273C>A r.(?) p.(His425Asn)
-/. - c.1281C>T r.(?) p.(Ser427=)
-?/. - c.1282G>A r.(?) p.(Ala428Thr)
?/. - c.1292C>T r.(?) p.(Thr431Ile)
-?/. - c.1313G>A r.(?) p.(Arg438Gln)
?/. - c.1502A>G r.(?) p.(Gln501Arg)
-/. - c.*40A>G r.(=) p.(=)
-/. - c.*40A>G r.(=) p.(=)
-/. - c.*77A>G r.(=) p.(=)
-/. - c.*97G>A r.(=) p.(=)
-/. - c.*97G>A r.(=) p.(=)
-?/. - c.*384T>C r.(=) p.(=)
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