Colon Cancer: Gene >> GDF10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000580279
Start	47312604:47312604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1249G>A
AA Mutation	p.Val417Ile(p.V417I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000580279
Start	47300667:47300667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16G>A
AA Mutation	p.Ala6Thr(p.A6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000580279
Start	47310486:47310486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337His(p.R337H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000580279
Start	47309933:47309933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Trp(p.R153W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000580279
Start	47310649:47310649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1173T>A
AA Mutation	p.Asn391Lys(p.N391K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000580279
Start	47310341:47310341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865C>T
AA Mutation	p.Arg289Cys(p.R289C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000580279
Start	47300680:47300680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29C>T
AA Mutation	p.Pro10Leu(p.P10L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000580279
Start	47310327:47310327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851C>A
AA Mutation	p.Ala284Glu(p.A284E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000580279
Start	47309915:47309915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782809728
CDS Mutation	c.439G>C
AA Mutation	p.Glu147Gln(p.E147Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580279
Start	47310532:47310532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580279
Start	47300837:47300837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580279
Start	47310103:47310103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580279
Start	47312768:47312768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1413C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580279
Start	47309960:47309960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580279
Start	47309944:47309944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580279
Start	47300921:47300921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580279
Start	47310631:47310631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GDF10

Mutation ID	1
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000580279
Start	47312654:47312655(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1300_1308dupATCATCCCT
AA Mutation	p.Ile434_Pro436dup(p.I434_P436dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript