Transcript #00005625 (NM_000439.4, PCSK1 gene)

Transcript name transcript variant 1
Gene name PCSK1 (proprotein convertase subtilisin/kexin type 1)
Chromosome 5
Transcript - NCBI ID NM_000439.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000430.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-30 09:51:58 +01:00 (CET)
Date last edited N/A


Variants

70 entries on 1 page. Showing entries 1 - 70.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.111G>A 111 r.(?) p.(=) - coding-synonymous -
./. - c.180+37C>T 180 r.(=) p.(=) - intron 37
./. - c.180+37C>T 180 r.(=) p.(=) - intron 37
./. - c.180+37C>T 180 r.(=) p.(=) - intron 37
./. - c.180+37C>T 180 r.(=) p.(=) - intron 37
./. - c.181-34C>T 181 r.(=) p.(=) - intron 34
./. - c.181-34C>T 181 r.(=) p.(=) - intron 34
./. - c.181-34C>T 181 r.(=) p.(=) - intron 34
./. - c.181-34C>T 181 r.(=) p.(=) - intron 34
./. - c.181-33G>T 181 r.(=) p.(=) - intron 33
./. - c.285+38G>A 285 r.(=) p.(=) - intron 38
./. - c.285+38G>A 285 r.(=) p.(=) - intron 38
./. - c.396+22A>G 396 r.(=) p.(=) - intron 22
./. - c.396+22A>G 396 r.(=) p.(=) - intron 22
./. - c.543+31T>A 543 r.(=) p.(=) - intron 31
./. - c.612C>T 612 r.(?) p.(=) - coding-synonymous -
./. - c.612C>T 612 r.(?) p.(=) - coding-synonymous -
./. - c.612C>T 612 r.(?) p.(=) - coding-synonymous -
./. - c.612C>T 612 r.(?) p.(=) - coding-synonymous -
./. - c.612C>T 612 r.(?) p.(=) - coding-synonymous -
./. - c.612C>T 612 r.(?) p.(=) - coding-synonymous -
./. - c.661A>G 661 r.(?) p.(Asn221Asp) - missense -
./. - c.709+32A>G 709 r.(=) p.(=) - intron 32
./. - c.882+41C>A 882 r.(=) p.(=) - intron 41
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1650T>C 1650 r.(?) p.(=) - coding-synonymous -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.1993C>G 1993 r.(?) p.(Gln665Glu) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
./. - c.2069G>C 2069 r.(?) p.(Ser690Thr) - missense -
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