Transcript #00000040 (NM_024422.3, DSC2 gene)

Transcript name desmocollin 2
Gene name DSC2 (desmocollin 2)
Chromosome 18
Transcript - NCBI ID NM_024422.3
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

77 entries on 1 page. Showing entries 1 - 77.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 06 c.631 - -
./. 01 c.4G>A - p.Glu2Lys
./. 01 c.32A>G - p.Asn11Ser
./. 02 c.82G>T - p.Ala28Ser
./. 02 c.111A>G - p.Leu37Leu
./. 03 c.155-22_155-3del - -
./. 03 c.172T>G - p.Phe58Val
./. 03 c.266C>T - p.Ser89Leu
./. 03 c.304G>A - p.Glu102Lys
./. 03 c.304G>A - p.Glu102Lys
./. 03 c.304G>A - p.Glu102Lys
./. 03 c.321G>T - p.Lys107Asn
./. 03 c.341del - p.Glu114GlyfsX7
./. 03 c.351A>G - p.Thr117Thr
./. 04 c.394C>T - p.Arg132Cys
./. 04 c.449G>C - p.Gly150Ala
./. 05 c.536A>G - p.Asp179Gly
./. 05 c.562G>T - p.Val188Leu
./. 06 c.631-2A>G - -
./. 06 c.663T>A - p.Tyr221Ter
./. 06 c.745A>C - p.Thr249Pro
./. 06 c.748T>C - p.Phe250Leu
./. 07 c.865C>T - p.Pro289Ser
./. 07 c.874C>T - p.Pro292Ser
./. 07 c.880C>A - p.Leu294Ile
./. 07 c.907G>A - p.Val303Met
./. 07 c.924A>T - p.Ser308Ser
./. 08 c.977A>C - p.Gln326Pro
./. 08 c.1024A>G - p.Ile342Val
./. 08 c.1034T>C - p.Ile345Thr
./. 08 c.1034T>C - p.Ile345Thr
./. 08 c.1048G>T - p.Asp350Tyr
./. 08 c.1073C>T - p.Thr358Ile
./. 08 c.1073C>T - p.Thr358Ile
./. 09 c.1108G>A - p.Asp370Asn
./. 10 c.1315A>G - p.Asn439Asp
./. 10 c.1402G>A - p.Gly468Ser
./. 10 c.1430delC - p.Thr477MetfsX4
./. 10 c.1435C>T - p.Arg479Cys
./. 11 c.1660C>T - p.Gln554X
./. 12 c.1706A>T - p.Asp569Val
./. 12 c.1721G>A - p.Ser574Asn
./. 12 c.1775C>T - p.Ala592Val
./. 12 c.1787C>T - p.Ala596Val
./. 12 c.1789G>T - p.Val597Phe
./. 12 c.1808T>C - p.Ile603Thr
./. 12 c.1841delG - p.Ser614IlefsX12
./. 13 c.1914G>C - p.Gln638His
./. 13 c.2036A>G - p.His679Arg
./. 14 c.2126G>A - p.Cys709Tyr
./. 14 c.2194T>G - p.Leu732Val
./. 14 c.2194T>G - p.Leu732Val
./. 15 c.2298G>C - p.Gln766His
./. 15 c.2314G>A - p.Val772Met
./. 15 c.2326A>G - p.Ile776Val
./. 15 c.2326A>G - p.Ile776Val
./. 15 c.2326A>G - p.Ile776Val
./. 15 c.2328C>G - p.Ile776Met
./. 25 c.2335G>A - p.Gly779Arg
./. 15 c.2359G>A - p.Val787Met
./. 15 c.2368_2370del - p.Gly790del
./. 25 c.2371C>A - p.His791Asn
./. 15 c.2375A>G - p.Gln792Arg
./. 25 c.2381C>T - p.Ser794Leu
./. 15 c.2393G>A - p.Arg798Gln
./. 15 c.2393G>A - p.Arg798Gln
./. 15 c.2393G>A - p.Arg798Gln
./. 25 c.2393G>A - p.Arg798Gln
./. 25 c.2408A>G - p.His803Arg
./. 15 c.2471C>T - p.Ser824Leu
./. 25 c.2471C>T - p.Ser824Leu
./. 25 c.2497C>T - p.Arg833Cys
./. 15 c.2508+5G>A - -
./. 26 c.2509-132G>T - -
./. 16 c.2603C>T - p.Ser868Phe
./. 16 c.2686_2687dup - p.Ala897LysfsX4
./. 16 c.2686_2687insGA - p.Glu896GlyfsX5
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