Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SSH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29636758:29636758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1391A>G
AA Mutation	p.Asp464Gly(p.D464G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29636640:29636640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1509A>G
AA Mutation	p.Ile503Met(p.I503M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29630902:29630902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4211G>T
AA Mutation	p.Arg1404Met(p.R1404M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29631510:29631510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3603G>T
AA Mutation	p.Glu1201Asp(p.E1201D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29631970:29631970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3143A>C
AA Mutation	p.Lys1048Thr(p.K1048T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29631938:29631938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3175A>C
AA Mutation	p.Asn1059His(p.N1059H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29648234:29648234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1256A>G
AA Mutation	p.Tyr419Cys(p.Y419C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29632048:29632048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369139548
CDS Mutation	c.3065A>G
AA Mutation	p.Asn1022Ser(p.N1022S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29636722:29636722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1427G>T
AA Mutation	p.Gly476Val(p.G476V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29631145:29631145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3968T>C
AA Mutation	p.Phe1323Ser(p.F1323S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29793920:29793920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81G>T
AA Mutation	p.Glu27Asp(p.E27D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29631436:29631436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3677A>G
AA Mutation	p.His1226Arg(p.H1226R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29650727:29650727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072C>T
AA Mutation	p.Arg358Trp(p.R358W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29632927:29632927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2186T>G
AA Mutation	p.Ile729Ser(p.I729S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29632022:29632022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3091G>A
AA Mutation	p.Ala1031Thr(p.A1031T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29636392:29636392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757C>A
AA Mutation	p.Ala586Asp(p.A586D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29632191:29632191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2922A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29632494:29632494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56047313
CDS Mutation	c.2619C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29636742:29636742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367567775
CDS Mutation	c.1407C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29648176:29648176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1314A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269033
Start	29636277:29636277(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1872delC
AA Mutation	p.Met625CysfsTer32(p.M625Cfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269033
Start	29636190:29636190(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1959delT
AA Mutation	p.Phe653LeufsTer4(p.F653Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269033
Start	29631607:29631608(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3505_3506delTC
AA Mutation	p.Ser1169GlnfsTer4(p.S1169Qfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269033
Start	29632716:29632716(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2397delA
AA Mutation	p.Lys799AsnfsTer18(p.K799Nfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000269033
Start	29636128:29636128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2021C>A
AA Mutation	p.Ser674Ter(p.S674*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SSH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29793907:29793907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94T>C
AA Mutation	p.Ser32Pro(p.S32P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29630924:29630924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4189C>T
AA Mutation	p.His1397Tyr(p.H1397Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29630926:29630926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4187A>C
AA Mutation	p.Gln1396Pro(p.Q1396P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29630917:29630917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4196G>T
AA Mutation	p.Arg1399Ile(p.R1399I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000269033
Start	29631482:29631482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3631C>T
AA Mutation	p.Arg1211Ter(p.R1211*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269033
Start	29632736:29632737(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2376_2377insT
AA Mutation	p.Ala793CysfsTer15(p.A793Cfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript