Colon Cancer: Gene >> DNAJB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262177
Start	157409954:157409954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851A>T
AA Mutation	p.Asp284Val(p.D284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262177
Start	157384957:157384957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771003490
CDS Mutation	c.569C>T
AA Mutation	p.Ser190Leu(p.S190L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262177
Start	157363165:157363165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70C>T
AA Mutation	p.Arg24Trp(p.R24W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262177
Start	157366554:157366554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779138971
CDS Mutation	c.228A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262177
Start	157409916:157409916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000262177
Start	157416065:157416067(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778749161
CDS Mutation	c.958_960delAAG
AA Mutation	p.Lys320del(p.K320del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DNAJB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262177
Start	157384955:157384955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567A>C
AA Mutation	p.Lys189Asn(p.K189N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262177
Start	157366518:157366518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192C>A
Mutation Classification	Silent
Feature Type	Transcript