Colon Cancer: Gene >> INF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104711124:104711124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2356C>A
AA Mutation	p.Leu786Met(p.L786M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104709372:104709372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771072587
CDS Mutation	c.2041G>A
AA Mutation	p.Glu681Lys(p.E681K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104711116:104711116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2348G>A
AA Mutation	p.Ser783Asn(p.S783N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104701602:104701602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237G>T
AA Mutation	p.Glu79Asp(p.E79D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104703203:104703203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755015990
CDS Mutation	c.490G>A
AA Mutation	p.Ala164Thr(p.A164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104707643:104707643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766510967
CDS Mutation	c.1376C>T
AA Mutation	p.Pro459Leu(p.P459L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104701549:104701549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>A
AA Mutation	p.Gly62Ser(p.G62S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000392634
Start	104713309:104713309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2878G>T
AA Mutation	p.Val960Phe(p.V960F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104701613:104701613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248G>A
AA Mutation	p.Arg83Gln(p.R83Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104714592:104714592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769598010
CDS Mutation	c.3430G>A
AA Mutation	p.Glu1144Lys(p.E1144K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104713232:104713232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2801C>T
AA Mutation	p.Ala934Val(p.A934V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104708719:104708719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1936A>G
AA Mutation	p.Lys646Glu(p.K646E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104701525:104701525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Cys(p.R54C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104701684:104701684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319G>A
AA Mutation	p.Ala107Thr(p.A107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104707918:104707918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1651G>A
AA Mutation	p.Val551Ile(p.V551I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104714597:104714597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780026536
CDS Mutation	c.3435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104703408:104703408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104711096:104711096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771802606
CDS Mutation	c.2328C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104703351:104703351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746732992
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104701401:104701401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104713269:104713269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2838G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104707845:104707845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1578C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104701668:104701668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779780698
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104703154:104703154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104714288:104714288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392634
Start	104707848:104707848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1587delC
AA Mutation	p.Val530TrpfsTer28(p.V530Wfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392634
Start	104714323:104714323(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3165delC
AA Mutation	p.Gly1056AlafsTer31(p.G1056Afs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392634
Start	104707576:104707576(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1313delC
AA Mutation	p.Pro438LeufsTer120(p.P438Lfs*120)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392634
Start	104707676:104707676(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1415delC
AA Mutation	p.Pro472GlnfsTer86(p.P472Qfs*86)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392634
Start	104714794:104714810(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3635_3651delGCCGGGCCTCAAAGGGG
AA Mutation	p.Gly1212AspfsTer19(p.G1212Dfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> INF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104712889:104712889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777498088
CDS Mutation	c.2672G>A
AA Mutation	p.Arg891Gln(p.R891Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript