Transcript #00019110 (NM_080921.3, PTPRC gene)

Transcript name Manually created transcript.
Gene name PTPRC (protein tyrosine phosphatase, receptor type, C)
Chromosome 1
Transcript - NCBI ID NM_080921.3
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

43 entries on 1 page. Showing entries 1 - 43.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.550+30T>A 550 r.(=) p.(=) - intron 30
./. - c.550+30T>A 550 r.(=) p.(=) - intron 30
./. - c.550+30T>A 550 r.(=) p.(=) - intron 30
./. - c.550+30T>A 550 r.(=) p.(=) - intron 30
./. - c.550+30T>A 550 r.(=) p.(=) - intron 30
./. - c.551-21C>T 551 r.(=) p.(=) - intron 21
./. - c.551-21C>T 551 r.(=) p.(=) - intron 21
./. - c.551-21C>T 551 r.(=) p.(=) - intron 21
./. - c.785C>T 785 r.(?) p.(Thr262Ile) - missense -
./. - c.785C>T 785 r.(?) p.(Thr262Ile) - missense -
./. - c.1085A>T 1085 r.(?) p.(Glu362Val) - missense -
./. - c.1227T>A 1227 r.(?) p.(His409Gln) - missense -
./. - c.1346+14T>A 1346 r.(=) p.(=) - intron 14
./. - c.1346+14T>A 1346 r.(=) p.(=) - intron 14
./. - c.1660-36C>T 1660 r.(=) p.(=) - intron 36
./. - c.1660-36C>T 1660 r.(=) p.(=) - intron 36
./. - c.1660-19C>T 1660 r.(=) p.(=) - intron 19
./. - c.1660-19C>T 1660 r.(=) p.(=) - intron 19
./. - c.1660-19C>T 1660 r.(=) p.(=) - intron 19
./. - c.1660-19C>T 1660 r.(=) p.(=) - intron 19
./. - c.1660-19C>T 1660 r.(=) p.(=) - intron 19
./. - c.1660-19C>T 1660 r.(=) p.(=) - intron 19
./. - c.1660-19C>T 1660 r.(=) p.(=) - intron 19
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.1833C>T 1833 r.(?) p.(=) - coding-synonymous -
./. - c.2078+27_2078+28del 2078 r.(=) p.(=) - intron 27
./. - c.2078+27_2078+28del 2078 r.(=) p.(=) - intron 27
./. - c.2078+27_2078+28del 2078 r.(=) p.(=) - intron 27
./. - c.2589+14T>C 2589 r.(=) p.(=) - intron 14
./. - c.2589+14T>C 2589 r.(=) p.(=) - intron 14
./. - c.2589+14T>C 2589 r.(=) p.(=) - intron 14
./. - c.3095A>C 3095 r.(?) p.(Glu1032Ala) - missense -
./. - c.3349G>T 3349 r.(?) p.(Ala1117Ser) - missense -
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