Colon Cancer: Gene >> HNRNPC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420743
Start	21234162:21234162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32C>T
AA Mutation	p.Pro11Leu(p.P11L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000420743
Start	21211450:21211450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793G>A
AA Mutation	p.Asp265Asn(p.D265N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000420743
Start	21231005:21231005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.309G>T
AA Mutation	p.Glu103Asp(p.E103D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000420743
Start	21231015:21231015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299C>A
AA Mutation	p.Ser100Tyr(p.S100Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420743
Start	21231068:21231068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420743
Start	21212985:21212985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.537G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000420743
Start	21211414:21211414(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.829delG
AA Mutation	p.Asp277MetfsTer6(p.D277Mfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000420743
Start	21213081:21213082(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.440dupC
AA Mutation	p.Pro148SerfsTer29(p.P148Sfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPC

Mutation ID	1
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000420743
Start	21211404:21211404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript