Transcript #00012394 (NM_000899.4, KITLG gene)

Transcript name transcript variant b
Gene name KITLG (KIT ligand)
Chromosome 12
Transcript - NCBI ID NM_000899.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000890.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

18 entries on 1 page. Showing entries 1 - 18.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.129+21C>T 129 r.(=) p.(=) - intron 21
./. - c.129+38A>G 129 r.(=) p.(=) - intron 38
./. - c.130-11dupT 130 r.(=) p.(=) - intron 11
./. - c.130-11dupT 130 r.(=) p.(=) - intron 11
./. - c.130-11dupT 130 r.(=) p.(=) - intron 11
./. - c.130-11dupT 130 r.(=) p.(=) - intron 11
./. - c.130-11dupT 130 r.(=) p.(=) - intron 11
./. - c.130-11dupT 130 r.(=) p.(=) - intron 11
./. - c.130-11dupT 130 r.(=) p.(=) - intron 11
./. - c.130-11dupT 130 r.(=) p.(=) - intron 11
./. - c.160A>G 160 r.(?) p.(Thr54Ala) - missense -
./. - c.160A>G 160 r.(?) p.(Thr54Ala) - missense -
./. - c.177C>T 177 r.(?) p.(=) - coding-synonymous -
./. - c.363+16T>A 363 r.(=) p.(=) - intron 16
./. - c.363+16T>A 363 r.(=) p.(=) - intron 16
./. - c.364-40G>A 364 r.(=) p.(=) - intron 40
./. - c.364-40G>A 364 r.(=) p.(=) - intron 40
./. - c.628G>T 628 r.(?) p.(Asp210Tyr) - missense -
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