Colon Cancer: Gene >> FERMT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52858439:52858439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1981A>C
AA Mutation	p.Lys661Gln(p.K661Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52860350:52860350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1718T>C
AA Mutation	p.Phe573Ser(p.F573S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52950463:52950463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106A>G
AA Mutation	p.Thr36Ala(p.T36A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52864526:52864526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752746667
CDS Mutation	c.1477C>A
AA Mutation	p.Leu493Ile(p.L493I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52858444:52858444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1976G>A
AA Mutation	p.Arg659His(p.R659H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52864811:52864811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1316T>G
AA Mutation	p.Phe439Cys(p.F439C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52881276:52881276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.720A>T
AA Mutation	p.Gln240His(p.Q240H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52859659:52859659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751620780
CDS Mutation	c.1783C>T
AA Mutation	p.Arg595Trp(p.R595W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52919169:52919169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.345C>A
AA Mutation	p.Phe115Leu(p.F115L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341590
Start	52859579:52859579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1863C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341590
Start	52872821:52872821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341590
Start	52859645:52859645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1797C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FERMT2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000341590
Start	52881469:52881469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527G>A
AA Mutation	p.Gly176Glu(p.G176E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52919169:52919169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.345C>A
AA Mutation	p.Phe115Leu(p.F115L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341590
Start	52919170:52919170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344T>G
AA Mutation	p.Phe115Cys(p.F115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341590
Start	52860451:52860451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1617C>T
Mutation Classification	Silent
Feature Type	Transcript