Colon Cancer: Gene >> ESR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341099
Start	64268858:64268858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589C>T
AA Mutation	p.Arg197Trp(p.R197W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341099
Start	64268895:64268895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552T>G
AA Mutation	p.Ile184Met(p.I184M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341099
Start	64280122:64280122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Cys(p.R132C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341099
Start	64233235:64233235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141940742
CDS Mutation	c.1495G>A
AA Mutation	p.Val499Met(p.V499M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341099
Start	64282880:64282880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106T>C
AA Mutation	p.Tyr36His(p.Y36H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341099
Start	64249671:64249671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100G>A
AA Mutation	p.Gly367Glu(p.G367E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341099
Start	64260617:64260617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>A
AA Mutation	p.Ala262Thr(p.A262T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341099
Start	64260742:64260742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341099
Start	64282905:64282905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145033525
CDS Mutation	c.81C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341099
Start	64282944:64282944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341099
Start	64233155:64233155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758569519
CDS Mutation	c.1575G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341099
Start	64280102:64280102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341099
Start	64260629:64260629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143949374
CDS Mutation	c.772C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341099
Start	64260743:64260743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.658C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000341099
Start	64282862:64282862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124G>T
AA Mutation	p.Glu42Ter(p.E42*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ESR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341099
Start	64233226:64233226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766524153
CDS Mutation	c.1504G>A
AA Mutation	p.Gly502Arg(p.G502R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341099
Start	64260540:64260540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000341099
Start	64249585:64249585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186G>T
AA Mutation	p.Glu396Ter(p.E396*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript