Colon Cancer: Gene >> HAUS3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000243706
Start	2236455:2236455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351C>A
AA Mutation	p.Leu451Ile(p.L451I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243706
Start	2238771:2238771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182A>C
AA Mutation	p.Glu394Asp(p.E394D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243706
Start	2238778:2238778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1175A>G
AA Mutation	p.Glu392Gly(p.E392G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243706
Start	2238912:2238912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1041G>T
AA Mutation	p.Leu347Phe(p.L347F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000243706
Start	2240171:2240171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145093973
CDS Mutation	c.776G>A
AA Mutation	p.Arg259Gln(p.R259Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000243706
Start	2236244:2236244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562T>G
AA Mutation	p.Leu521Arg(p.L521R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243706
Start	2240359:2240359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149074489
CDS Mutation	c.588G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000243706
Start	2238878:2238878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075C>T
AA Mutation	p.Gln359Ter(p.Q359*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000243706
Start	2232028:2232028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200438056
CDS Mutation	c.1711G>T
AA Mutation	p.Glu571Ter(p.E571*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243706
Start	2232013:2232014(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1725_1726insA
AA Mutation	p.Phe576IlefsTer5(p.F576Ifs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243706
Start	2240351:2240352(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.595dupT
AA Mutation	p.Ser199PhefsTer30(p.S199Ffs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000243706
Start	2240517:2240519(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755784281
CDS Mutation	c.428_430delAAG
AA Mutation	p.Glu143del(p.E143del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HAUS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243706
Start	2240360:2240360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770168907
CDS Mutation	c.587C>T
AA Mutation	p.Ser196Leu(p.S196L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243706
Start	2238734:2238734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1219A>C
AA Mutation	p.Asn407His(p.N407H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243706
Start	2240757:2240757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.190C>A
AA Mutation	p.Leu64Ile(p.L64I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript