Colon Cancer: Gene >> HNRNPM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325495
Start	8488777:8488777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2116G>A
AA Mutation	p.Glu706Lys(p.E706K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325495
Start	8485659:8485659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1231C>T
AA Mutation	p.Leu411Phe(p.L411F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325495
Start	8467547:8467547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797G>A
AA Mutation	p.Gly266Asp(p.G266D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325495
Start	8463619:8463619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.371G>T
AA Mutation	p.Ser124Ile(p.S124I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000325495
Start	8468834:8468834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895C>T
AA Mutation	p.His299Tyr(p.H299Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325495
Start	8488708:8488708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2047G>A
AA Mutation	p.Asp683Asn(p.D683N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000325495
Start	8483159:8483159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1122A>C
AA Mutation	p.Glu374Asp(p.E374D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325495
Start	8486077:8486077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775519970
CDS Mutation	c.1649G>A
AA Mutation	p.Arg550His(p.R550H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325495
Start	8488704:8488704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754289633
CDS Mutation	c.2043C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325495
Start	8463656:8463656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778365609
CDS Mutation	c.408T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325495
Start	8473699:8473699(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1036delA
AA Mutation	p.Met346TrpfsTer22(p.M346Wfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000325495
Start	8463687:8463688(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.438+1_438+2insA
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325495
Start	8485720:8485720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1292G>A
AA Mutation	p.Gly431Asp(p.G431D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325495
Start	8488758:8488758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201359498
CDS Mutation	c.2097C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000325495
Start	8463684:8463684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436G>T
AA Mutation	p.Glu146Ter(p.E146*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript