Colon Cancer: Gene >> GDF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378673
Start	132862340:132862340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614T>A
AA Mutation	p.Phe205Tyr(p.F205Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378673
Start	132862001:132862001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.953G>T
AA Mutation	p.Arg318Leu(p.R318L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378673
Start	132862022:132862022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932G>A
AA Mutation	p.Arg311Lys(p.R311K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378673
Start	132864343:132864343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751002918
CDS Mutation	c.191C>T
AA Mutation	p.Ala64Val(p.A64V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378673
Start	132862008:132862008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751894227
CDS Mutation	c.946C>T
AA Mutation	p.Arg316Cys(p.R316C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378673
Start	132861915:132861915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039C>A
AA Mutation	p.Leu347Ile(p.L347I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378673
Start	132861778:132861778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378673
Start	132864396:132864396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776452563
CDS Mutation	c.138T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378673
Start	132861742:132861742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378673
Start	132861628:132861628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000378673
Start	132864317:132864317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770828556
CDS Mutation	c.217C>T
AA Mutation	p.Arg73Ter(p.R73*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GDF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378673
Start	132861915:132861915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039C>A
AA Mutation	p.Leu347Ile(p.L347I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript