Colon Cancer: Gene >> GYPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360771
Start	144140621:144140621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15A>G
AA Mutation	p.Ile5Met(p.I5M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360771
Start	144119697:144119697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221A>T
AA Mutation	p.Glu74Val(p.E74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360771
Start	144120549:144120549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77C>T
AA Mutation	p.Ala26Val(p.A26V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360771
Start	144118724:144118724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261C>A
AA Mutation	p.Phe87Leu(p.F87L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360771
Start	144119757:144119757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161C>A
AA Mutation	p.Ala54Glu(p.A54E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360771
Start	144119768:144119768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000360771
Start	144119737:144119737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>T
AA Mutation	p.Glu61Ter(p.E61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GYPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360771
Start	144116864:144116864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772099477
CDS Mutation	c.347G>A
AA Mutation	p.Arg116Gln(p.R116Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript