Transcript #00020835 (NM_005993.4, TBCD gene)

Transcript name tubulin folding cofactor D
Gene name TBCD (tubulin folding cofactor D)
Chromosome 17
Transcript - NCBI ID NM_005993.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005984.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

81 entries on 1 page. Showing entries 1 - 81.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.112G>T r.(?) p.(Ala38Ser)
-?/. - c.184+8_184+21del r.(=) p.(=)
?/. - c.230A>G r.(?) p.(His77Arg)
+/. - c.230A>G r.(?) p.(His77Arg)
+?/. - c.771+1_771+10del r.spl? p.?
-?/. - c.772-2_778del r.spl? p.?
-?/. - c.1044C>T r.(?) p.(Asp348=)
-?/. - c.1047C>T r.(?) p.(Asp349=)
-?/. - c.1087+4C>T r.spl? p.?
?/. - c.1115_1120del r.(?) p.(Lys372_Asp373del)
?/. - c.1121C>T r.(?) p.(Thr374Met)
+?/. - c.1126G>A r.(?) p.(Val376Met)
?/. - c.1130G>A r.(?) p.(Arg377Gln)
+?/. - c.1306C>T r.(?) p.(Arg436*)
-?/. - c.1318+15363T>C r.(=) p.(=)
-?/. - c.1318+15389C>T r.(=) p.(=)
?/. - c.1318+15427C>T r.(=) p.(=)
?/. - c.1318+15432G>A r.(=) p.(=)
-/. - c.1318+15655T>C r.(=) p.(=)
-/. - c.1318+15682A>G r.(=) p.(=)
-?/. - c.1318+15736G>A r.(=) p.(=)
?/. - c.1318+15900C>T r.(=) p.(=)
?/. - c.1318+16470C>G r.(=) p.(=)
?/. - c.1318+16652G>A r.(=) p.(=)
-?/. - c.1318+16838A>G r.(=) p.(=)
-?/. - c.1318+16992C>T r.(=) p.(=)
?/. - c.1318+17373del r.(=) p.(=)
-?/. - c.1323C>T r.(?) p.(Val441=)
?/. - c.1414T>G r.(?) p.(Trp472Gly)
+?/. 14 c.1423G>A r.(?) p.(Ala475Thr)
+?/. 14 c.1423G>A r.(?) p.(Ala475Thr)
-?/. - c.1467A>G r.(?) p.(Ala489=)
-?/. - c.1534-4G>A r.spl? p.?
-?/. - c.1578T>C r.(?) p.(His526=)
?/. - c.1650-9C>G r.(=) p.(=)
-?/. - c.1650-3C>T r.spl? p.?
+?/. - c.1661C>A r.(?) p.(Ala554Asp)
?/. - c.1699C>G r.(?) p.(Leu567Val)
+/. - c.1712A>G r.(?) p.(Lys571Arg)
-?/. - c.1795G>A r.(?) p.(Ala599Thr)
?/. - c.1842T>G r.(?) p.(Asp614Glu)
?/. - c.1876G>A r.(?) p.(Ala626Thr)
?/. - c.1876G>T r.(?) p.(Ala626Ser)
+?/. - c.1922G>C r.1805_2006del p.Val602GlyfsTer8
-?/. - c.2040G>T r.(?) p.(Val680=)
-?/. - c.2042G>T r.(?) p.(Cys681Phe)
-?/. - c.2044G>T r.(?) p.(Val682Phe)
?/. - c.2061G>T r.(?) p.(Leu687Phe)
-?/. - c.2239G>A r.(?) p.(Glu747Lys)
-?/. - c.2253A>G r.(?) p.(Ala751=)
-?/. - c.2419G>A r.(?) p.(Glu807Lys)
-?/. - c.2566A>G r.(?) p.(Met856Val)
?/. - c.2609+4C>T r.spl? p.?
-?/. - c.2610-5A>G r.spl? p.?
?/. - c.2852+3A>G r.spl? p.?
-?/. - c.2852+3A>G r.spl? p.?
-?/. - c.2852+8C>T r.(=) p.(=)
?/. - c.2914C>T r.(?) p.(Leu972Phe)
?/. - c.2974G>A r.(?) p.(Gly992Ser)
-?/. - c.2991+8G>A r.(=) p.(=)
-?/. - c.3069C>T r.(?) p.(Ser1023=)
+?/. 33 c.3099C>G r.(?) p.(Asn1033Lys)
+?/. - c.3099C>G r.(?) p.(Asn1033Lys)
+?/. - c.3099C>G r.(?) p.(Asn1033Lys)
+?/. - c.3099C>G r.(?) p.(Asn1033Lys)
+?/. - c.3099C>G r.(?) p.(Asn1033Lys)
+?/. 33 c.3099C>G r.(?) p.(Asn1033Lys)
+?/. 33 c.3099C>G r.(?) p.(Asn1033Lys)
+?/. 33 c.3099C>G r.(?) p.(Asn1033Lys)
?/. - c.3307G>A r.(?) p.(Gly1103Ser)
?/. - c.3372C>G r.(?) p.(Ile1124Met)
-?/. - c.3426C>T r.(?) p.(Val1142=)
-?/. - c.3447C>T r.(?) p.(Asp1149=)
-?/. - c.3518G>A r.(?) p.(Arg1173His)
?/. - c.3520C>G r.(?) p.(Leu1174Val)
-?/. - c.3554T>C r.(?) p.(Leu1185Pro)
?/. - c.3565-13_3565-9del r.(=) p.(=)
?/. - c.*14957C>T r.(=) p.(=)
-?/. - c.*15009C>T r.(=) p.(=)
-?/. - c.*18655C>T r.(=) p.(=)
?/. - c.*106289A>G r.(=) p.(=)
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