Transcript #00001235 (NM_024344.1, CAPN3 gene)

Transcript name transcript variant 2
Gene name CAPN3 (calpain 3, (p94))
Chromosome 15
Transcript - NCBI ID NM_024344.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_077320.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 11:01:21 +01:00 (CET)
Date last edited N/A


Variants

79 entries on 1 page. Showing entries 1 - 79.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.62G>A 62 r.(?) p.(Gly21Glu) - missense -
./. - c.78G>A 78 r.(?) p.(=) - coding-synonymous -
./. - c.96T>C 96 r.(?) p.(=) - coding-synonymous -
./. - c.96T>C 96 r.(?) p.(=) - coding-synonymous -
./. - c.96T>C 96 r.(?) p.(=) - coding-synonymous -
./. - c.97G>A 97 r.(?) p.(Glu33Lys) - missense -
./. - c.97G>A 97 r.(?) p.(Glu33Lys) - missense -
./. - c.97G>A 97 r.(?) p.(Glu33Lys) - missense -
./. - c.97G>A 97 r.(?) p.(Glu33Lys) - missense -
./. - c.310-44A>G 310 r.(=) p.(=) - intron 44
./. - c.380-27C>T 380 r.(=) p.(=) - intron 27
./. - c.498+32A>C 498 r.(=) p.(=) - intron 32
./. - c.498+35G>T 498 r.(=) p.(=) - intron 35
./. - c.498+35G>T 498 r.(=) p.(=) - intron 35
./. - c.498+35G>T 498 r.(=) p.(=) - intron 35
./. - c.498+35G>T 498 r.(=) p.(=) - intron 35
./. - c.499-18C>T 499 r.(=) p.(=) - intron 18
./. - c.606T>C 606 r.(?) p.(=) - coding-synonymous -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.706G>A 706 r.(?) p.(Ala236Thr) - missense -
./. - c.984C>T 984 r.(?) p.(=) - coding-synonymous -
./. - c.1194-45C>T 1194 r.(=) p.(=) - intron 45
./. - c.1194-45C>T 1194 r.(=) p.(=) - intron 45
./. - c.1194-45C>T 1194 r.(=) p.(=) - intron 45
./. - c.1194-26C>G 1194 r.(=) p.(=) - intron 26
./. - c.1194-26C>G 1194 r.(=) p.(=) - intron 26
./. - c.1194-26C>G 1194 r.(=) p.(=) - intron 26
./. - c.1525-35delC 1525 r.(=) p.(=) - intron 35
./. - c.1525-35delC 1525 r.(=) p.(=) - intron 35
./. - c.1525-35delC 1525 r.(=) p.(=) - intron 35
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-48T>C 1537 r.(=) p.(=) - intron 48
./. - c.1537-33G>A 1537 r.(=) p.(=) - intron 33
./. - c.1896+30G>A 1896 r.(=) p.(=) - intron 30
./. - c.1896+30G>A 1896 r.(=) p.(=) - intron 30
./. - c.1896+30G>A 1896 r.(=) p.(=) - intron 30
./. - c.1974+42C>G 1974 r.(=) p.(=) - intron 42
./. - c.2033-29C>T 2033 r.(=) p.(=) - intron 29
./. - c.2033-3C>A 2033 r.spl? p.? - splice 3
./. - c.2033-3C>A 2033 r.spl? p.? - splice 3
./. - c.2199C>T 2199 r.(?) p.(=) - coding-synonymous -
./. - c.2251C>T 2251 r.(?) p.(His751Tyr) - missense -
./. - c.2422-48G>C 2422 r.(=) p.(=) - intron 48
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