Colon Cancer: Gene >> SIGLEC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000425629
Start	51531442:51531442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759524109
CDS Mutation	c.145G>A
AA Mutation	p.Val49Ile(p.V49I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000425629
Start	51531319:51531319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Trp(p.R90W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000425629
Start	51529862:51529862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874G>A
AA Mutation	p.Ala292Thr(p.A292T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000425629
Start	51527798:51527798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137G>T
AA Mutation	p.Gln379His(p.Q379H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000425629
Start	51527778:51527778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157A>G
AA Mutation	p.Asp386Gly(p.D386G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425629
Start	51530742:51530742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425629
Start	51529935:51529935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425629
Start	51520160:51520160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1284C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425629
Start	51531607:51531607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425629
Start	51531515:51531515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SIGLEC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000425629
Start	51531340:51531340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247G>A
AA Mutation	p.Glu83Lys(p.E83K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000425629
Start	51531223:51531223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772851483
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Trp(p.R122W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000425629
Start	51531615:51531615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34A>G
AA Mutation	p.Met12Val(p.M12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425629
Start	51529875:51529875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript