Transcript #00000069 (NM_000222.2, KIT gene)

Transcript name v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
Gene name KIT (v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog)
Chromosome 4
Transcript - NCBI ID NM_000222.2
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

152 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 01 c.2T>C - p.Met1Thr
./. 01 c.67+4G>A - -
./. 02 c.101C>T - p.Pro34Leu
./. 02 c.142delG - p.Val48SerfsX56
./. 02 c.199A>T - p.Thr67Ser
./. 02 c.200C>G - p.Thr67Ser
./. 02 c.221C>T - p.Thr74Met
./. 02 c.253delG - p.Glu85LysfsX16
./. 02 c.253G>C - p.Glu85Gln
./. 02 c.280A>G - p.Lys94Glu
./. 03 c.358delG - p.Val120LeufsX24
./. 03 c.369dup - p.Tyr125ValfsX41
./. 03 c.406T>C - p.Cys136Arg
./. 03 c.406T>C - p.Cys136Arg
./. 03 c.454C>G - p.Gln152Glu
./. 03 c.503C>T - p.Ala168Val
./. 03 c.532G>A - p.Ala178Thr
./. 04 c.655G>C - p.Ala219Pro
./. 05 c.821C>T - p.Thr274Met
./. 05 c.836_837insT - p.Ala280SerfsX4
./. 05 c.842G>A - p.Arg281Lys
./. 05 c.878A>G - p.Asn293Ser
./. 06 c.952A>G - p.Met318Val
./. 06 c.952A>G - p.Met318Val
./. 06 c.964A>G - p.Thr322Ala
./. 06 c.972del - p.Phe324LeufsX2
./. 06 c.1036C>T - p.Gln346X
./. 06 c.1039C>T - p.Gln347X
./. 07 c.1120G>A - p.Val374Ile
./. 07 c.1195G>A - p.Val399Ile
./. 07 c.1199A>G - p.Asn400Ser
./. 07 c.1228A>C - p.Asn410His
./. 08 c.1255_1257delGAC - p.Asp419del
./. 09 c.1351T>C - p.Ser451Pro
./. 09 c.1413_1414insA - p.Leu472ThrfsX10
./. 09 c.1463C>T - p.Thr488Met
./. 09 c.1486G>A - p.Asp496Asn
./. 09 c.1493dup - p.Lys499GlnfsX7
./. 09 c.1526A>T - p.Lys509Ile
./. 09 c.1530_1531insGCCTAT - p.Gly510_Asn511insAlaTyr
./. 10 c.1564T>G - p.Phe522Val
./. 10 c.1588G>A - p.Val530Ile
./. 10 c.1594G>A - p.Val532Ile
./. 10 c.1598C>A - p.Ala533Asp
./. 10 c.1621A>C - p.Met541Leu
./. 10 c.1621A>C - p.Met541Leu
./. 10 c.1621A>C - p.Met541Leu
./. 11 c.1649A>T - p.Lys550Ile
./. 11 c.1653_1670del - p.Met552_Trp557del
./. 11 c.1654_1668del - p.Met552_Gln556del
./. 11 c.1655T>A - p.Met552Lys
./. 11 c.1655_1672del - p.Met552_Trp557del
./. 11 c.1657_1658delinsGT - p.Tyr553Val
./. 11 c.1661_1675del - p.Glu554_Lys558del
./. 11 c.1669T>C - p.Trp557Arg
./. 11 c.1669T>C - p.Trp557Arg
./. 11 c.1669_1674del - p.Trp557_Lys558del
./. 11 c.1669_1674del - p.Trp557_Lys558del
./. 11 c.1669_1683del - p.Trp557_Glu561del
./. 11 c.1669_1683del - p.Trp557_Glu561del
./. 11 c.1669_1683del - p.Trp557_Glu561del
./. 11 c.1670G>A - p.Trp557X
./. 11 c.1670G>C - p.Trp557Ser
./. 11 c.1674_1680del - p.Val559ArgfsX3
./. 11 c.1675_1680del - p.Val559_Val560del
./. 11 c.1675_1680delGTTGTT - p.Val559_Val560del
./. 11 c.1676T>A - p.Val559Asp
./. 11 c.1676T>C - p.Val559Ala
./. 11 c.1679delT - Glu561ArgfsX3
./. 11 c.1679T>A - p.Val560Asp
./. 11 c.1679T>G - p.Val560Gly
./. 11 c.1679T>G - p.Val560Gly
./. 11 c.1679T>G - p.Val560Gly
./. 11 c.1679T>G - p.Val560Gly
./. 11 c.1679_1680delinsAG - p.Val560Glu
./. 11 c.1679_1681del - p.Val560del
./. 11 c.1681dupG - p.Glu561GlyfsX19
./. 11 c.1702_1722del - p.Tyr568_Thr574del
./. 11 c.1726_1731dupCAACTT - p.Leu576_Pro577dup
./. 11 c.1727T>C - p.Leu576Pro
./. 11 c.1747G>A - p.Glu583Lys
./. 11 c.1751T>G - p.Phe584Cys
./. 10 c.1752delT - p.Arg586GlufsX4
./. 11 c.1752T>A - p.Phe584Leu
./. 11 c.1768_1769delAG - p.Ser590PhefsX15
./. 12 c.1784T>C - p.Leu595Pro
./. 12 c.1801G>A - p.Gly601Arg
./. 12 c.1810G>A - p.Val604Ile
./. 12 c.1853T>C - p.Met618Thr
./. 12 c.1859T>C - p.Val620Ala
./. 12 c.1861G>A - p.Ala621Thr
./. 12 c.1862C>A - p.Ala621Asp
./. 12 c.1879+1G>A - -
./. 13 c.1889dup - p.His630GlnfsX11
./. 13 c.1900C>T - p.Arg634Trp
./. 13 c.1924A>G - p.Lys642Glu
./. 13 c.1924A>G - p.Lys642Glu
./. 13 c.1924A>G - p.Lys642Glu
./. 13 c.1925_1926delAA - p.Lys642SerfsX7
./. 13 c.1949A>T - p.His650Leu
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