Colon Cancer: Gene >> GDF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47325491:47325491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35129734
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Trp(p.R333W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47325195:47325195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701G>T
AA Mutation	p.Arg234Met(p.R234M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47325503:47325503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009G>A
AA Mutation	p.Glu337Lys(p.E337K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47322840:47322840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172T>C
AA Mutation	p.Phe58Leu(p.F58L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47322958:47322958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290C>T
AA Mutation	p.Thr97Met(p.T97M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47324916:47324916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422G>T
AA Mutation	p.Arg141Met(p.R141M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47325776:47325776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1282T>C
AA Mutation	p.Cys428Arg(p.C428R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47325761:47325761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1267G>A
AA Mutation	p.Val423Met(p.V423M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47325341:47325341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847G>A
AA Mutation	p.Val283Met(p.V283M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47325119:47325119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.625A>G
AA Mutation	p.Ser209Gly(p.S209G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47322870:47322870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Cys(p.R68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47325603:47325603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1109C>T
AA Mutation	p.Pro370Leu(p.P370L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000581492
Start	47322879:47322879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211A>G
AA Mutation	p.Asn71Asp(p.N71D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581492
Start	47325325:47325325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581492
Start	47325502:47325502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581492
Start	47325661:47325661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1167C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581492
Start	47325748:47325748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GDF2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581492
Start	47322878:47322878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581492
Start	47325502:47325502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript