Colon Cancer: Gene >> TNS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47303451:47303451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2956T>G
AA Mutation	p.Ser986Ala(p.S986A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47304904:47304904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760674078
CDS Mutation	c.2750C>T
AA Mutation	p.Thr917Met(p.T917M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47368689:47368689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542060079
CDS Mutation	c.1957C>T
AA Mutation	p.Pro653Ser(p.P653S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47368482:47368482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367961192
CDS Mutation	c.2164G>A
AA Mutation	p.Ala722Thr(p.A722T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47303340:47303340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3067G>A
AA Mutation	p.Gly1023Ser(p.G1023S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47396899:47396899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925G>A
AA Mutation	p.Glu309Lys(p.E309K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47439494:47439494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143A>G
AA Mutation	p.Asn48Ser(p.N48S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47280178:47280178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4179T>A
AA Mutation	p.Asp1393Glu(p.D1393E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47400794:47400794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844G>A
AA Mutation	p.Ala282Thr(p.A282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47302206:47302206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375909974
CDS Mutation	c.3524C>T
AA Mutation	p.Ala1175Val(p.A1175V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47435374:47435374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232G>A
AA Mutation	p.Ala78Thr(p.A78T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47435352:47435352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.254G>A
AA Mutation	p.Cys85Tyr(p.C85Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47303334:47303334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3073G>A
AA Mutation	p.Ala1025Thr(p.A1025T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47368969:47368969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1677G>T
AA Mutation	p.Glu559Asp(p.E559D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47369481:47369481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165G>A
AA Mutation	p.Val389Ile(p.V389I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47369199:47369199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1447C>A
AA Mutation	p.Pro483Thr(p.P483T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47344823:47344823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2582G>A
AA Mutation	p.Arg861His(p.R861H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311160
Start	47369191:47369191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745634291
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311160
Start	47439523:47439523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774321914
CDS Mutation	c.114G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311160
Start	47297209:47297209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116297963
CDS Mutation	c.3549C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311160
Start	47344828:47344828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369474794
CDS Mutation	c.2577G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311160
Start	47415107:47415107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368113552
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311160
Start	47369532:47369532(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1114delC
AA Mutation	p.Gln372ArgfsTer46(p.Q372Rfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311160
Start	47278165:47278165(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4249delC
AA Mutation	p.Leu1417CysfsTer22(p.L1417Cfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000311160
Start	47304836:47304836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2818G>T
AA Mutation	p.Glu940Ter(p.E940*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000311160
Start	47369090:47369090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1556C>A
AA Mutation	p.Ser519Ter(p.S519*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311160
Start	47283791:47283792(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4002_4003insGGCATCACCCTGGTCCAGGATGAAGGCCCTG
AA Mutation	p.Ser1335GlyfsTer89(p.S1335Gfs*89)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000311160
Start	47368364:47368364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2281+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000311160
Start	47396885:47396887(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.937_939delAAC
AA Mutation	p.Asn313del(p.N313del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TNS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47368560:47368560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748272175
CDS Mutation	c.2086G>A
AA Mutation	p.Asp696Asn(p.D696N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47439620:47439620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.17G>A
AA Mutation	p.Gly6Glu(p.G6E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47428363:47428363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338G>A
AA Mutation	p.Arg113His(p.R113H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47303267:47303267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764207972
CDS Mutation	c.3140C>T
AA Mutation	p.Ala1047Val(p.A1047V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47302989:47302989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3418G>A
AA Mutation	p.Asp1140Asn(p.D1140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311160
Start	47302239:47302239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3491T>G
AA Mutation	p.Phe1164Cys(p.F1164C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311160
Start	47369062:47369062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770876695
CDS Mutation	c.1584C>T
Mutation Classification	Silent
Feature Type	Transcript