Colon Cancer: Gene >> SIGLEC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317643
Start	51146082:51146082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988C>A
AA Mutation	p.His330Asn(p.H330N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317643
Start	51144535:51144535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563C>A
AA Mutation	p.Ser188Tyr(p.S188Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317643
Start	51142675:51142675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306G>T
AA Mutation	p.Gln102His(p.Q102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317643
Start	51145991:51145991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897G>T
AA Mutation	p.Gln299His(p.Q299H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317643
Start	51145863:51145863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.769G>T
AA Mutation	p.Ala257Ser(p.A257S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317643
Start	51142455:51142455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140841032
CDS Mutation	c.86C>T
AA Mutation	p.Thr29Met(p.T29M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317643
Start	51146791:51146791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143153982
CDS Mutation	c.1065G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317643
Start	51142456:51142456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317643
Start	51144674:51144674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702C>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SIGLEC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317643
Start	51153143:51153143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1302G>T
AA Mutation	p.Glu434Asp(p.E434D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317643
Start	51142740:51142740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368230574
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317643
Start	51142703:51142703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334G>A
AA Mutation	p.Asp112Asn(p.D112N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317643
Start	51146783:51146783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317643
Start	51153134:51153134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1293G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000317643
Start	51153141:51153141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1300G>T
AA Mutation	p.Glu434Ter(p.E434*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript