Colon Cancer: Gene >> GFM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000486715
Start	158652203:158652203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797A>G
AA Mutation	p.Glu266Gly(p.E266G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000486715
Start	158646827:158646827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452T>C
AA Mutation	p.Val151Ala(p.V151A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000486715
Start	158662659:158662659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1355C>T
AA Mutation	p.Ser452Leu(p.S452L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000486715
Start	158646265:158646265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335A>C
AA Mutation	p.Lys112Thr(p.K112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000486715
Start	158682119:158682119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1726T>C
AA Mutation	p.Ser576Pro(p.S576P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000486715
Start	158645662:158645662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.115G>T
AA Mutation	p.Gly39Trp(p.G39W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000486715
Start	158684648:158684648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1889G>A
AA Mutation	p.Gly630Glu(p.G630E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000486715
Start	158690195:158690195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758611209
CDS Mutation	c.1942C>T
AA Mutation	p.Pro648Ser(p.P648S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000486715
Start	158646838:158646838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463A>G
AA Mutation	p.Thr155Ala(p.T155A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000486715
Start	158646867:158646867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000486715
Start	158691401:158691401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149049400
CDS Mutation	c.2190C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000486715
Start	158645715:158645715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768555221
CDS Mutation	c.168T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000486715
Start	158666358:158666358(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1575delT
AA Mutation	p.Arg526GlufsTer27(p.R526Efs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000486715
Start	158658928:158658928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775919783
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Ter(p.R364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000486715
Start	158691450:158691451(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2239_2240insAGAGGGTTTTTT
AA Mutation	p.Gly747delinsGluArgValPheTer(p.G747delinsERVF*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000486715
Start	158652217:158652218(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.817dupA
AA Mutation	p.Ile273AsnfsTer6(p.I273Nfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000486715
Start	158649104:158649105(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.636_637insAAATCAGT
AA Mutation	p.Gly213LysfsTer6(p.G213Kfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000486715
Start	158646299:158646299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.367+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GFM1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000486715
Start	158660963:158660963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199976566
CDS Mutation	c.1311C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000486715
Start	158653319:158653319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771890880
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Ter(p.R284*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript