Colon Cancer: Gene >> TIMD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274532
Start	156963187:156963187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12A>C
AA Mutation	p.Glu4Asp(p.E4D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274532
Start	156954615:156954615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200184575
CDS Mutation	c.200C>T
AA Mutation	p.Ala67Val(p.A67V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274532
Start	156949678:156949678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733G>A
AA Mutation	p.Ala245Thr(p.A245T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274532
Start	156954729:156954729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375659101
CDS Mutation	c.86C>T
AA Mutation	p.Thr29Met(p.T29M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274532
Start	156954432:156954432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774551130
CDS Mutation	c.383G>A
AA Mutation	p.Arg128His(p.R128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000274532
Start	156922113:156922113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773468118
CDS Mutation	c.998C>T
AA Mutation	p.Ala333Val(p.A333V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000274532
Start	156920497:156920497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019T>A
AA Mutation	p.Leu340His(p.L340H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274532
Start	156951678:156951678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747523800
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274532
Start	156919496:156919496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274532
Start	156922127:156922127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200813433
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274532
Start	156949718:156949718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274532
Start	156954437:156954437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761841993
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274532
Start	156954452:156954452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766204987
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000274532
Start	156949651:156949652(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.759dupA
AA Mutation	p.Glu254ArgfsTer20(p.E254Rfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TIMD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274532
Start	156954540:156954540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275G>T
AA Mutation	p.Arg92Ile(p.R92I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274532
Start	156922127:156922127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200813433
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript