Colon Cancer: Gene >> TANK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259075
Start	161179726:161179726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.64G>A
AA Mutation	p.Asp22Asn(p.D22N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259075
Start	161235379:161235379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759803420
CDS Mutation	c.1139C>T
AA Mutation	p.Ser380Leu(p.S380L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259075
Start	161224698:161224698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472G>A
AA Mutation	p.Ala158Thr(p.A158T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259075
Start	161224738:161224738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512C>T
AA Mutation	p.Thr171Ile(p.T171I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259075
Start	161179680:161179680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376080393
CDS Mutation	c.18C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259075
Start	161231230:161231230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142460004
CDS Mutation	c.780G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259075
Start	161204780:161204780(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.318delA
AA Mutation	p.Lys106AsnfsTer5(p.K106Nfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TANK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259075
Start	161231025:161231025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762974211
CDS Mutation	c.575C>T
AA Mutation	p.Ala192Val(p.A192V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259075
Start	161231361:161231361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.911A>C
AA Mutation	p.Lys304Thr(p.K304T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript