Colon Cancer: Gene >> DICER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95090601:95090601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5666A>C
AA Mutation	p.Lys1889Thr(p.K1889T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95107680:95107680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2732G>T
AA Mutation	p.Ser911Ile(p.S911I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95096145:95096145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4775C>T
AA Mutation	p.Pro1592Leu(p.P1592L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95091302:95091302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775912475
CDS Mutation	c.5428G>A
AA Mutation	p.Asp1810Asn(p.D1810N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95103495:95103495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3901T>A
AA Mutation	p.Leu1301Met(p.L1301M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95106197:95106197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2831G>A
AA Mutation	p.Arg944Gln(p.R944Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95108337:95108337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2423A>C
AA Mutation	p.Lys808Thr(p.K808T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95105180:95105180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3160C>T
AA Mutation	p.Leu1054Phe(p.L1054F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95103365:95103365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4031C>T
AA Mutation	p.Ser1344Leu(p.S1344L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95106177:95106177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2851T>C
AA Mutation	p.Tyr951His(p.Y951H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000343455
Start	95111454:95111454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2119G>A
AA Mutation	p.Glu707Lys(p.E707K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95124273:95124273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299T>A
AA Mutation	p.Asn433Lys(p.N433K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95090613:95090613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5654T>C
AA Mutation	p.Val1885Ala(p.V1885A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95108391:95108391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762784970
CDS Mutation	c.2369G>A
AA Mutation	p.Arg790Gln(p.R790Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95096241:95096241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4679C>T
AA Mutation	p.Ala1560Val(p.A1560V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95094139:95094139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5113G>C
AA Mutation	p.Glu1705Gln(p.E1705Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95103438:95103438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3958G>A
AA Mutation	p.Asp1320Asn(p.D1320N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95090590:95090590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5677G>T
AA Mutation	p.Val1893Phe(p.V1893F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95095919:95095919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5001A>C
AA Mutation	p.Glu1667Asp(p.E1667D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95133325:95133325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Arg45Lys(p.R45K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95103626:95103626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3770T>C
AA Mutation	p.Val1257Ala(p.V1257A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95106095:95106095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2933T>G
AA Mutation	p.Leu978Arg(p.L978R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95112234:95112234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2054G>A
AA Mutation	p.Ser685Asn(p.S685N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95096071:95096071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4849C>A
AA Mutation	p.Leu1617Ile(p.L1617I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343455
Start	95111344:95111344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753276132
CDS Mutation	c.2229G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343455
Start	95105780:95105780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2991T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343455
Start	95091288:95091288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759875628
CDS Mutation	c.5442G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343455
Start	95106205:95106205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2823G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343455
Start	95095928:95095928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781268313
CDS Mutation	c.4992G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343455
Start	95113158:95113158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1974G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343455
Start	95096462:95096462(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4458delA
AA Mutation	p.Lys1486AsnfsTer4(p.K1486Nfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000343455
Start	95116635:95116635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1570G>T
AA Mutation	p.Glu524Ter(p.E524*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000343455
Start	95129554:95129554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652G>T
AA Mutation	p.Glu218Ter(p.E218*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000343455
Start	95124356:95124356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1216C>T
AA Mutation	p.Gln406Ter(p.Q406*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000343455
Start	95124590:95124590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.982G>T
AA Mutation	p.Glu328Ter(p.E328*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343455
Start	95096502:95096503(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.4417dupT
AA Mutation	p.Ser1473PhefsTer4(p.S1473Ffs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DICER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95105763:95105763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3008G>A
AA Mutation	p.Arg1003Gln(p.R1003Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95115688:95115688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750410087
CDS Mutation	c.1886C>T
AA Mutation	p.Thr629Met(p.T629M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95106152:95106152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2876A>C
AA Mutation	p.Lys959Thr(p.K959T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95106197:95106197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2831G>A
AA Mutation	p.Arg944Gln(p.R944Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95113105:95113105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2027G>A
AA Mutation	p.Arg676Gln(p.R676Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95124428:95124428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144G>A
AA Mutation	p.Glu382Lys(p.E382K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343455
Start	95094122:95094122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769974404
CDS Mutation	c.5130G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343455
Start	95111344:95111344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753276132
CDS Mutation	c.2229G>A
Mutation Classification	Silent
Feature Type	Transcript