Colon Cancer: Gene >> LAMC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183243234:183243234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144652590
CDS Mutation	c.3416G>A
AA Mutation	p.Arg1139Gln(p.R1139Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183227587:183227587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147781376
CDS Mutation	c.1358C>T
AA Mutation	p.Pro453Leu(p.P453L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183218478:183218478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142335339
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Cys(p.R165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183222152:183222152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374756027
CDS Mutation	c.704G>A
AA Mutation	p.Arg235His(p.R235H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183243270:183243270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3452A>G
AA Mutation	p.Gln1151Arg(p.Q1151R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183223192:183223192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821G>A
AA Mutation	p.Arg274His(p.R274H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183223173:183223173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802A>C
AA Mutation	p.Ser268Arg(p.S268R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183225640:183225640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986C>A
AA Mutation	p.Pro329His(p.P329H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183239533:183239533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3039G>T
AA Mutation	p.Glu1013Asp(p.E1013D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183232786:183232786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762028260
CDS Mutation	c.2149C>T
AA Mutation	p.Arg717Trp(p.R717W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183220910:183220910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184817147
CDS Mutation	c.589C>T
AA Mutation	p.Arg197Cys(p.R197C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183243204:183243204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3386G>A
AA Mutation	p.Arg1129Gln(p.R1129Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183220911:183220911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376553923
CDS Mutation	c.590G>A
AA Mutation	p.Arg197His(p.R197H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183222136:183222136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688C>T
AA Mutation	p.Leu230Phe(p.L230F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264144
Start	183227627:183227627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189665394
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264144
Start	183227688:183227688(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1462delG
AA Mutation	p.Val488SerfsTer24(p.V488Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LAMC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183237441:183237441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2691G>T
AA Mutation	p.Lys897Asn(p.K897N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183218424:183218424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754947872
CDS Mutation	c.439G>A
AA Mutation	p.Ala147Thr(p.A147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183226736:183226736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552102778
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Cys(p.R369C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183240332:183240332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3269A>G
AA Mutation	p.Asn1090Ser(p.N1090S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183237483:183237483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752530548
CDS Mutation	c.2733G>T
AA Mutation	p.Gln911His(p.Q911H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript