Colon Cancer: Gene >> GAS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327773
Start	113863654:113863654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176G>A
AA Mutation	p.Gly59Asp(p.G59D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327773
Start	113822048:113822048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1792G>A
AA Mutation	p.Glu598Lys(p.E598K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327773
Start	113827052:113827052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767144171
CDS Mutation	c.1421C>T
AA Mutation	p.Thr474Met(p.T474M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327773
Start	113820928:113820928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1973C>T
AA Mutation	p.Ala658Val(p.A658V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327773
Start	113820954:113820954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1947C>G
AA Mutation	p.Asn649Lys(p.N649K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327773
Start	113822044:113822044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1796T>A
AA Mutation	p.Val599Glu(p.V599E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327773
Start	113820870:113820870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2031A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327773
Start	113828691:113828691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375788560
CDS Mutation	c.1164G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327773
Start	113846564:113846564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373068496
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327773
Start	113834626:113834626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376542109
CDS Mutation	c.759C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327773
Start	113820921:113820921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1980C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327773
Start	113820885:113820885(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs766199351
CDS Mutation	c.2016delC
AA Mutation	p.Val673TrpfsTer85(p.V673Wfs*85)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327773
Start	113839745:113839745(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.449delG
AA Mutation	p.Gly150AlafsTer49(p.G150Afs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327773
Start	113846552:113846553(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.317dupA
AA Mutation	p.Asn106LysfsTer13(p.N106Kfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327773
Start	113839744:113839745(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs773341392
CDS Mutation	c.449dupG
AA Mutation	p.Arg151ProfsTer27(p.R151Pfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GAS6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327773
Start	113828610:113828610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1245A>G
Mutation Classification	Silent
Feature Type	Transcript