Colon Cancer: Gene >> LZTS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20253000:20253000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931C>T
AA Mutation	p.Pro311Ser(p.P311S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20250218:20250218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1295G>T
AA Mutation	p.Arg432Met(p.R432M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20253317:20253317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200343127
CDS Mutation	c.614G>A
AA Mutation	p.Arg205His(p.R205H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20253374:20253374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557G>A
AA Mutation	p.Ser186Asn(p.S186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20253153:20253153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767923160
CDS Mutation	c.778G>A
AA Mutation	p.Glu260Lys(p.E260K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20253005:20253005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199863998
CDS Mutation	c.926C>T
AA Mutation	p.Pro309Leu(p.P309L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20250248:20250248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370068074
CDS Mutation	c.1265C>T
AA Mutation	p.Thr422Met(p.T422M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20252811:20252811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577366847
CDS Mutation	c.1120G>A
AA Mutation	p.Gly374Ser(p.G374S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20255064:20255064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118G>A
AA Mutation	p.Gly40Arg(p.G40R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20254898:20254898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284G>T
AA Mutation	p.Gly95Val(p.G95V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20250056:20250056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759562008
CDS Mutation	c.1457G>A
AA Mutation	p.Arg486His(p.R486H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20253516:20253516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415C>A
AA Mutation	p.His139Asn(p.H139N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20249863:20249863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778252648
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20253307:20253307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20250313:20250313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20253046:20253046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768481706
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20253346:20253346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758900574
CDS Mutation	c.585G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20254948:20254948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20254921:20254921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20253469:20253469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20254882:20254882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368947201
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LZTS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20253173:20253173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758G>A
AA Mutation	p.Arg253His(p.R253H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265801
Start	20249937:20249937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1576C>A
AA Mutation	p.Gln526Lys(p.Q526K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20252968:20252968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20252812:20252812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139017329
CDS Mutation	c.1119C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265801
Start	20254996:20254996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748915529
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript