Transcript #00017654 (NM_172108.3, KCNQ2 gene)

Transcript name Manually created transcript. (removed from reference sequence)
Gene name KCNQ2 (potassium voltage-gated channel, KQT-like subfamily, member 2)
Chromosome 20
Transcript - NCBI ID NM_172108.3
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

69 entries on 1 page. Showing entries 1 - 69.
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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.1148+38_1148+39del 1148 r.(=) p.(=) - intron 38
./. - c.1148+38_1148+39del 1148 r.(=) p.(=) - intron 38
./. - c.1413C>G 1413 r.(?) p.(=) - coding-synonymous -
./. - c.1413C>G 1413 r.(?) p.(=) - coding-synonymous -
./. - c.1413C>G 1413 r.(?) p.(=) - coding-synonymous -
./. - c.1413C>G 1413 r.(?) p.(=) - coding-synonymous -
./. - c.1413C>G 1413 r.(?) p.(=) - coding-synonymous -
./. - c.1413C>G 1413 r.(?) p.(=) - coding-synonymous -
./. - c.1413C>G 1413 r.(?) p.(=) - coding-synonymous -
./. - c.1626C>T 1626 r.(?) p.(=) - coding-synonymous -
./. - c.1626C>T 1626 r.(?) p.(=) - coding-synonymous -
./. - c.1795-29G>A 1795 r.(=) p.(=) - intron 29
./. - c.1795-29G>A 1795 r.(=) p.(=) - intron 29
./. - c.1795-29G>A 1795 r.(=) p.(=) - intron 29
./. - c.2142G>A 2142 r.(?) p.(=) - coding-synonymous -
./. - c.2145T>A 2145 r.(?) p.(=) - coding-synonymous -
./. - c.2145T>A 2145 r.(?) p.(=) - coding-synonymous -
./. - c.2145T>A 2145 r.(?) p.(=) - coding-synonymous -
./. - c.2145T>A 2145 r.(?) p.(=) - coding-synonymous -
./. - c.2145T>A 2145 r.(?) p.(=) - coding-synonymous -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
./. - c.2246A>C 2246 r.(?) p.(Asn749Thr) - missense -
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