Colon Cancer: Gene >> SIGLEC10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51413777:51413777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756C>T
AA Mutation	p.Pro586Ser(p.P586S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51415253:51415253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769528072
CDS Mutation	c.1258G>A
AA Mutation	p.Glu420Lys(p.E420K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51415058:51415058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381C>T
AA Mutation	p.His461Tyr(p.H461Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51411361:51411361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772709558
CDS Mutation	c.1832G>A
AA Mutation	p.Arg611Gln(p.R611Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51416822:51416822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550G>A
AA Mutation	p.Ala184Thr(p.A184T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51417141:51417141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362A>G
AA Mutation	p.Glu121Gly(p.E121G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51414476:51414476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201868126
CDS Mutation	c.1655C>T
AA Mutation	p.Ala552Val(p.A552V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51417556:51417556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201054656
CDS Mutation	c.26C>T
AA Mutation	p.Ser9Leu(p.S9L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51416854:51416854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.518G>A
AA Mutation	p.Cys173Tyr(p.C173Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51414487:51414487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1644C>A
AA Mutation	p.Phe548Leu(p.F548L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51416842:51416842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530C>A
AA Mutation	p.Ser177Tyr(p.S177Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51413724:51413724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144827503
CDS Mutation	c.1809G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51413817:51413817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1716G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51415413:51415413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780126295
CDS Mutation	c.1098G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51416889:51416889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200977765
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51415233:51415233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536361935
CDS Mutation	c.1278C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51415950:51415950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.972A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51416694:51416694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.678A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000339313
Start	51416681:51416681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779337135
CDS Mutation	c.691C>T
AA Mutation	p.Arg231Ter(p.R231*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000339313
Start	51417433:51417433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770204126
CDS Mutation	c.70C>T
AA Mutation	p.Arg24Ter(p.R24*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339313
Start	51415360:51415361(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1149_1150dupCA
AA Mutation	p.Ser384ThrfsTer8(p.S384Tfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SIGLEC10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51417148:51417148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374849658
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Trp(p.R119W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51416842:51416842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530C>A
AA Mutation	p.Ser177Tyr(p.S177Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339313
Start	51417462:51417462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41C>T
AA Mutation	p.Ser14Phe(p.S14F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51415419:51415419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555512085
CDS Mutation	c.1092C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51417407:51417407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571577019
CDS Mutation	c.96G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339313
Start	51417131:51417131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript