Colon Cancer: Gene >> HYAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266031
Start	50302823:50302823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134A>G
AA Mutation	p.Glu45Gly(p.E45G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266031
Start	50302778:50302778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179C>T
AA Mutation	p.Ala60Val(p.A60V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266031
Start	50302302:50302302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781935297
CDS Mutation	c.655G>A
AA Mutation	p.Gly219Ser(p.G219S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266031
Start	50300615:50300615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587680396
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266031
Start	50301034:50301035(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.943dupG
AA Mutation	p.Ala315GlyfsTer69(p.A315Gfs*69)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HYAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266031
Start	50300500:50300500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782616691
CDS Mutation	c.1291C>T
AA Mutation	p.Arg431Trp(p.R431W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript