Colon Cancer: Gene >> LMOD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201946274:201946274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67A>T
AA Mutation	p.Thr23Ser(p.T23S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201899677:201899677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1336A>G
AA Mutation	p.Thr446Ala(p.T446A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201899965:201899965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763440069
CDS Mutation	c.1048C>T
AA Mutation	p.Arg350Trp(p.R350W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201900333:201900333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199655500
CDS Mutation	c.680G>A
AA Mutation	p.Arg227His(p.R227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201899518:201899518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1495C>T
AA Mutation	p.Pro499Ser(p.P499S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201899787:201899787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572664263
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409Gln(p.R409Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201946318:201946318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23G>A
AA Mutation	p.Arg8His(p.R8H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201946256:201946256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85A>C
AA Mutation	p.Met29Leu(p.M29L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201900206:201900206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807A>C
AA Mutation	p.Glu269Asp(p.E269D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201900004:201900004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>A
AA Mutation	p.Val337Ile(p.V337I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201899920:201899920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372721398
CDS Mutation	c.1093G>A
AA Mutation	p.Ala365Thr(p.A365T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367288
Start	201899681:201899681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1332T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LMOD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201900291:201900291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722G>T
AA Mutation	p.Arg241Ile(p.R241I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201899360:201899360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1653G>T
AA Mutation	p.Lys551Asn(p.K551N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367288
Start	201899447:201899447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1566G>T
AA Mutation	p.Lys522Asn(p.K522N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript