Colon Cancer: Gene >> LGMN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334869
Start	92712824:92712824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.591C>A
AA Mutation	p.His197Gln(p.H197Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334869
Start	92714378:92714378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478G>A
AA Mutation	p.Asp160Asn(p.D160N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334869
Start	92712814:92712814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.601A>G
AA Mutation	p.Asn201Asp(p.N201D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334869
Start	92713830:92713830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.536A>G
AA Mutation	p.Tyr179Cys(p.Y179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334869
Start	92706600:92706600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146747445
CDS Mutation	c.1074G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334869
Start	92706618:92706618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141204016
CDS Mutation	c.1056C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334869
Start	92711921:92711921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753838339
CDS Mutation	c.645G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334869
Start	92713829:92713829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334869
Start	92709819:92709819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.873T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334869
Start	92709677:92709677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334869
Start	92704340:92704340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773071207
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LGMN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334869
Start	92704357:92704357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264A>C
AA Mutation	p.Lys422Gln(p.K422Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript