Colon Cancer: Gene >> PALM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338448
Start	746785:746785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1135C>T
AA Mutation	p.His379Tyr(p.H379Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338448
Start	727624:727624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Asp67Asn(p.D67N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000338448
Start	726187:726187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763907757
CDS Mutation	c.55G>A
AA Mutation	p.Ala19Thr(p.A19T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338448
Start	727015:727015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65G>A
AA Mutation	p.Arg22Gln(p.R22Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338448
Start	746400:746400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145938736
CDS Mutation	c.750G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338448
Start	736061:736061(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.489delC
AA Mutation	p.Met164Ter(p.M164*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000338448
Start	726191:726191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PALM

No Mutation Annotation!