Transcript #00018748 (NM_014159.6, SETD2 gene)

Transcript name SET domain containing 2
Gene name SETD2 (SET domain containing 2)
Chromosome 3
Transcript - NCBI ID NM_014159.6
Transcript - Ensembl ID -
Protein - NCBI ID NP_054878.5
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.19C>T r.(?) p.(Gln7*)
-?/. - c.71+9696G>A r.(=) p.(=)
-?/. - c.72-8298A>G r.(=) p.(=)
-?/. - c.72-8205G>A r.(=) p.(=)
?/. - c.149C>T r.(?) p.(Ala50Val)
-?/. - c.361G>A r.(?) p.(Gly121Ser)
-?/. - c.376A>G r.(?) p.(Thr126Ala)
-?/. - c.388T>C r.(?) p.(Ser130Pro)
-?/. - c.393C>T r.(?) p.(Ser131=)
?/. - c.424A>G r.(?) p.(Ile142Val)
?/. - c.557C>T r.(?) p.(Pro186Leu)
-?/. - c.579_587del r.(?) p.(Pro194_Pro196del)
-?/. - c.595G>A r.(?) p.(Ala199Thr)
?/. - c.757G>T r.(?) p.(Asp253Tyr)
+?/. - c.788del r.(?) p.(Leu263*)
+?/. 3 c.820C>T r.(?) p.(Gln274*)
-?/. - c.1066G>A r.(?) p.(Ala356Thr)
?/. - c.1117A>G r.(?) p.(Arg373Gly)
?/. - c.1180T>C r.(?) p.(Cys394Arg)
?/. - c.1204C>T r.(?) p.(Arg402Trp)
?/. - c.1204C>T r.(?) p.(Arg402Trp)
-?/. - c.1205G>A r.(?) p.(Arg402Gln)
?/. - c.1294C>G r.(?) p.(Arg432Gly)
-?/. - c.1343G>A r.(?) p.(Arg448Gln)
-?/. - c.1412G>A r.(?) p.(Arg471Lys)
?/. - c.1415G>A r.(?) p.(Arg472His)
-?/. - c.1415G>A r.(?) p.(Arg472His)
-?/. - c.1562C>T r.(?) p.(Thr521Ile)
?/. - c.1619G>A r.(?) p.(Arg540Gln)
-?/. - c.1626G>C r.(?) p.(Gly542=)
?/. - c.1647_1652del r.(?) p.(Ser550_Ser551del)
?/. - c.1655_1667del r.(?) p.(Ala552AspfsTer23)
?/. - c.1706T>G r.(?) p.(Phe569Cys)
-?/. - c.1734A>T r.(?) p.(Leu578Phe)
?/. - c.1775C>A r.(?) p.(Thr592Lys)
-?/. - c.1833G>T r.(?) p.(Lys611Asn)
?/. - c.1859G>T r.(?) p.(Arg620Leu)
-?/. - c.1885A>G r.(?) p.(Lys629Glu)
+?/. - c.1984del r.(?) p.(Gln662AsnfsTer2)
?/. 3 c.2000G>A r.(?) p.(Cys667Tyr)
?/. - c.2057T>C r.(?) p.(Phe686Ser)
-?/. - c.2096A>G r.(?) p.(Asp699Gly)
-?/. - c.2101A>C r.(?) p.(Ser701Arg)
-?/. - c.2114C>T r.(?) p.(Ser705Leu)
?/. - c.2155A>G r.(?) p.(Asn719Asp)
-?/. - c.2155A>G r.(?) p.(Asn719Asp)
-?/. - c.2155A>G r.(?) p.(Asn719Asp)
-?/. - c.2251C>A r.(?) p.(Pro751Thr)
-?/. - c.2251C>A r.(?) p.(Pro751Thr)
-?/. - c.2275A>G r.(?) p.(Lys759Glu)
?/. - c.2281A>T r.(?) p.(Met761Leu)
-?/. - c.2302G>C r.(?) p.(Val768Leu)
?/. - c.2309A>G r.(?) p.(Tyr770Cys)
-?/. - c.2315A>G r.(?) p.(Lys772Arg)
-?/. - c.2450T>C r.(?) p.(Met817Thr)
?/. - c.2474T>A r.(?) p.(Met825Lys)
-?/. - c.2543C>T r.(?) p.(Ala848Val)
?/. - c.2549A>C r.(?) p.(Glu850Ala)
?/. - c.2569G>A r.(?) p.(Gly857Ser)
-?/. - c.2603A>G r.(?) p.(Asp868Gly)
-/. - c.2603A>G r.(?) p.(Asp868Gly)
-?/. - c.2704G>C r.(?) p.(Glu902Gln)
?/. - c.2723T>G r.(?) p.(Leu908Arg)
?/. - c.2723T>G r.(?) p.(Leu908Arg)
+?/. - c.2749dup r.(?) p.(Ser917LysfsTer18)
-/. - c.2783C>G r.(?) p.(Thr928Arg)
?/. - c.2785A>T r.(?) p.(Ile929Leu)
-?/. - c.2785A>T r.(?) p.(Ile929Leu)
-?/. - c.2791G>A r.(?) p.(Glu931Lys)
?/. - c.2791G>A r.(?) p.(Glu931Lys)
-?/. - c.2798G>T r.(?) p.(Gly933Val)
-?/. - c.2813A>G r.(?) p.(Asp938Gly)
+?/. 3 c.2942dup r.(?) p.(Leu981Phefs*3)
-?/. - c.2982T>A r.(?) p.(Asp994Glu)
-?/. - c.2988A>G r.(?) p.(Ser996=)
-?/. - c.3095C>T r.(?) p.(Ser1032Phe)
?/. - c.3113A>T r.(?) p.(Tyr1038Phe)
?/. - c.3130A>T r.(?) p.(Ser1044Cys)
-?/. - c.3229A>G r.(?) p.(Thr1077Ala)
-?/. - c.3229A>G r.(?) p.(Thr1077Ala)
?/. - c.3240G>A r.(?) p.(Met1080Ile)
?/. - c.3240G>A r.(?) p.(Met1080Ile)
-?/. - c.3422C>T r.(?) p.(Pro1141Leu)
-?/. - c.3422C>T r.(?) p.(Pro1141Leu)
-?/. - c.3422C>T r.(?) p.(Pro1141Leu)
?/. - c.3554A>G r.(?) p.(Asn1185Ser)
-?/. - c.3567C>T r.(?) p.(Thr1189=)
-/. - c.3567C>T r.(?) p.(Thr1189=)
?/. - c.3595C>A r.(?) p.(Gln1199Lys)
-?/. - c.3610A>G r.(?) p.(Ile1204Val)
-?/. - c.3610A>G r.(?) p.(Ile1204Val)
?/. - c.3697A>C r.(?) p.(Thr1233Pro)
?/. 3 c.3776G>A r.(?) p.(Gly1259Asp)
?/. - c.3861G>C r.(?) p.(Gln1287His)
?/. - c.3908A>G r.(?) p.(Asn1303Ser)
-?/. - c.3908A>G r.(?) p.(Asn1303Ser)
-?/. - c.3937C>T r.(?) p.(Pro1313Ser)
-?/. - c.3943G>C r.(?) p.(Gly1315Arg)
?/. - c.3974G>A r.(?) p.(Gly1325Glu)
?/. - c.3979G>T r.(?) p.Val1327Leu
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