Colon Cancer: Gene >> DHX9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182866478:182866478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1367G>A
AA Mutation	p.Arg456Gln(p.R456Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182881334:182881334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2695C>T
AA Mutation	p.Arg899Trp(p.R899W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182887424:182887424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3803G>A
AA Mutation	p.Gly1268Asp(p.G1268D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182876081:182876081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1847A>G
AA Mutation	p.Tyr616Cys(p.Y616C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182872380:182872380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1601A>G
AA Mutation	p.Tyr534Cys(p.Y534C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182884758:182884758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3406C>T
AA Mutation	p.Arg1136Cys(p.R1136C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182878122:182878122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2300G>A
AA Mutation	p.Arg767Gln(p.R767Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182887360:182887360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3739T>G
AA Mutation	p.Phe1247Val(p.F1247V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182881579:182881579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2846C>T
AA Mutation	p.Thr949Ile(p.T949I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182867005:182867005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519C>T
AA Mutation	p.His507Tyr(p.H507Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182842585:182842585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19T>G
AA Mutation	p.Phe7Val(p.F7V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182878065:182878065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2243A>G
AA Mutation	p.Tyr748Cys(p.Y748C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182853405:182853405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464A>T
AA Mutation	p.Gln155Leu(p.Q155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182878128:182878128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2306G>A
AA Mutation	p.Arg769Gln(p.R769Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182887219:182887219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3598G>A
AA Mutation	p.Gly1200Ser(p.G1200S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367549
Start	182858786:182858786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.954C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367549
Start	182876145:182876145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771546846
CDS Mutation	c.1911C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367549
Start	182876118:182876118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191883464
CDS Mutation	c.1884C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367549
Start	182887209:182887209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781296469
CDS Mutation	c.3588C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367549
Start	182887179:182887179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367549
Start	182883563:182883563(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3193delC
AA Mutation	p.Leu1065CysfsTer20(p.L1065Cfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000367549
Start	182866531:182866531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1420C>T
AA Mutation	p.Arg474Ter(p.R474*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000367549
Start	182858799:182858799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.967C>T
AA Mutation	p.Arg323Ter(p.R323*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367549
Start	182876197:182876198(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1970dupT
AA Mutation	p.Leu657PhefsTer44(p.L657Ffs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367549
Start	182853404:182853405(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.463_464insTG
AA Mutation	p.Gln155LeufsTer8(p.Q155Lfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000367549
Start	182858642:182858642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DHX9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182860155:182860155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303G>T
AA Mutation	p.Ala435Ser(p.A435S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182872444:182872444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1665C>A
AA Mutation	p.Phe555Leu(p.F555L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182842585:182842585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19T>G
AA Mutation	p.Phe7Val(p.F7V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367549
Start	182876200:182876200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1966T>G
AA Mutation	p.Phe656Val(p.F656V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367549
Start	182859051:182859051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367549
Start	182883293:182883293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3069C>T
Mutation Classification	Silent
Feature Type	Transcript