Transcript #00004023 (NM_004518.4, KCNQ2 gene)

Transcript name transcript variant 3
Gene name KCNQ2 (potassium voltage-gated channel, KQT-like subfamily, member 2)
Chromosome 20
Transcript - NCBI ID NM_004518.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_004509.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 16:26:17 +01:00 (CET)
Date last edited N/A


Variants

67 entries on 1 page. Showing entries 1 - 67.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.388-26G>T 388 r.(=) p.(=) - intron 26
./. - c.515-38C>T 515 r.(=) p.(=) - intron 38
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.912C>T 912 r.(?) p.(=) - coding-synonymous -
./. - c.1419C>G 1419 r.(?) p.(=) - coding-synonymous -
./. - c.1419C>G 1419 r.(?) p.(=) - coding-synonymous -
./. - c.1419C>G 1419 r.(?) p.(=) - coding-synonymous -
./. - c.1419C>G 1419 r.(?) p.(=) - coding-synonymous -
./. - c.1419C>G 1419 r.(?) p.(=) - coding-synonymous -
./. - c.1419C>G 1419 r.(?) p.(=) - coding-synonymous -
./. - c.1419C>G 1419 r.(?) p.(=) - coding-synonymous -
./. - c.1635C>T 1635 r.(?) p.(=) - coding-synonymous -
./. - c.1635C>T 1635 r.(?) p.(=) - coding-synonymous -
./. - c.1804-29G>A 1804 r.(=) p.(=) - intron 29
./. - c.1804-29G>A 1804 r.(=) p.(=) - intron 29
./. - c.1804-29G>A 1804 r.(=) p.(=) - intron 29
./. - c.2151G>A 2151 r.(?) p.(=) - coding-synonymous -
./. - c.2154T>A 2154 r.(?) p.(=) - coding-synonymous -
./. - c.2154T>A 2154 r.(?) p.(=) - coding-synonymous -
./. - c.2154T>A 2154 r.(?) p.(=) - coding-synonymous -
./. - c.2154T>A 2154 r.(?) p.(=) - coding-synonymous -
./. - c.2154T>A 2154 r.(?) p.(=) - coding-synonymous -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
./. - c.2255A>C 2255 r.(?) p.(Asn752Thr) - missense -
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