Colon Cancer: Gene >> GATA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252997
Start	62464906:62464906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124C>T
AA Mutation	p.Ala375Val(p.A375V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252997
Start	62466542:62466542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367777789
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Cys(p.R237C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252997
Start	62464949:62464949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081G>A
AA Mutation	p.Glu361Lys(p.E361K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252997
Start	62473446:62473446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375617512
CDS Mutation	c.656T>C
AA Mutation	p.Met219Thr(p.M219T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252997
Start	62473573:62473573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529G>A
AA Mutation	p.Asp177Asn(p.D177N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252997
Start	62473508:62473508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781910978
CDS Mutation	c.594G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252997
Start	62475135:62475135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252997
Start	62475144:62475144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782141667
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GATA5

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000252997
Start	62473498:62473498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604C>T
AA Mutation	p.Arg202Ter(p.R202*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript