Transcript #00000082 (NM_000249.3, MLH1 gene)

Transcript name mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli)
Gene name MLH1 (mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli))
Chromosome 3
Transcript - NCBI ID NM_000249.3
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 00 c.-93G>A - -
./. 00 c.-93G>A - -
./. 00 c.-28A>G - -
./. 01 c.-28A>G - -
./. 01 c.-28A>G - -
./. 02 c.(115-?)_(545+?)del - -
./. 07 c.(546_?)_(588+?)del - -
./. 09 c.(676_?)_(1667+?)del - -
./. 11 c.(883_?)_(1038+?)del - -
./. 00 c.(?_-60)_(588+?)del - -
./. 00 c.(?_-60)_116+?del - -
./. 00 c.(?_-60)_116+?dup - -
./. 00 c.(?_-60)_884+?del - -
./. 12 c.1226_1227AG>GT - p.Gln409Arg
./. 19 c.2104-?_(*193_?)dup - -
./. 01 c.107T>A - p.Ile36Asn
./. 02 c.137G>T - p.Ser46Ile
./. 02 c.137G>T - p.Ser46Ile
./. 02 c.137G>T - p.Ser46Ile
./. 02 c.194G>A - p.Gly65Asp
./. 02 c.194G>A - p.Gly65Asp
./. 02 c.199G>A - p.Gly67Arg
./. 02 c.199G>A - p.Gly67Arg
./. 02 c.199G>A - p.Gly67Arg
./. 03 c.208-1G>A - -
./. 03 c.208-?_306+?dup - -
./. 03 c.265G>T - p.Glu89X
./. 03 c.265G>T - p.Glu89X
./. 03 c.265G>T - p.Glu89X
./. 03 c.265G>T - p.Glu89X
./. 04 c.350C>T - p.Thr117Met
./. 05 c.453+1G>T - -
./. 06 c.488delG - p.Arg163LysfsX4
./. 06 c.497T>A - p.Leu166X
./. 06 c.498A>C - p.Leu166Phe
./. 06 c.503_504insA - p.Asn168LysfsX4
./. 06 c.545+3A>G - -
./. 06 c.545+3A>G - -
./. 07 c.546-?_884+?del - -
./. 07 c.572G>T - p.Ser191Ile
./. 08 c.637G>T - p.Val213Leu
./. 08 c.637G>T - p.Val213Leu
./. 08 c.649C>T - p.Arg217Cys
./. 08 c.649C>T - p.Arg217Cys
./. 08 c.649C>T - p.Arg217Cys
./. 08 c.649C>T - p.Arg217Cys
./. 08 c.649C>T - p.Arg217Cys
./. 08 c.649C>T - p.Arg217Cys
./. 08 c.655A>G - p.Ile219Val
./. 08 c.655A>G - p.Ile219Val
./. 08 c.655A>G - p.Ile219Val
./. 08 c.655A>G - p.Ile219Val
./. 08 c.655A>G - p.Ile219Val
./. 08 c.655A>G - p.Ile219Val
./. 08 c.676C>T - p.Arg226X
./. 08 c.676C>T - p. Arg226X
./. 08 c.677G>A - p.Arg226Gln
./. 08 c.677G>A - p.Arg226Gln
./. 08 c.677G>A - p.Arg226Gln
./. 08 c.677G>T - p.Arg226Leu
./. 09 c.753C>T - p.Ser252Phe
./. 10 c.790C>T - p.His264Tyr
./. 09 c.790+1G>A - -
./. 09 c.790+1G>A - -
./. 09 c.790+2T>A - -
./. 10 c.808_811delACTT - p.Thr270ProfsX2
./. 11 c.885-597_1038+1120del - -
./. 11 c.887T>G - p.Leu296X
./. 11 c.887T>G - p.Leu296X
./. 11 c.888delA - p.Leu296LeufsX71
./. 11 c.901C>T - p.Gln301X
./. 11 c.914_937del24 - -
./. 11 c.914_937del24 - p.Val305_His312del
./. 11 c.920T>A - p.Val307Glu
./. 11 c.927C>T - p.Pro309Pro
./. 11 c.927C>T - p.Pro309Pro
./. 11 c.932_933insA - p.Lys311LysfsX3
./. 11 c.949C>A - p.Leu317Met
./. 11 c.985C>A - p.His329Asn
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1151T>A - p.Val384Asp
./. 12 c.1198C>G - p.Leu400Val
./. 12 c.1246A>G - p.Lys416Glu
./. 12 c.1362dupG - p.Thr455Aspfx24
./. 12 c.1402A>G - p.Asn468Asp
./. 13 c.1459C>T - p.Arg487X
./. 13 c.1459C>T - p.Arg487X
./. 13 c.1558+14G>A - -
./. 13 c.1558+14G>A - -
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