Colon Cancer: Gene >> HNRNPH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179617574:179617574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997G>A
AA Mutation	p.Val333Ile(p.V333I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179618244:179618244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616C>T
AA Mutation	p.Arg206Trp(p.R206W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179618273:179618273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587A>C
AA Mutation	p.Asp196Ala(p.D196A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179617065:179617065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1103G>T
AA Mutation	p.Ser368Ile(p.S368I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179619281:179619281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524G>T
AA Mutation	p.Arg175Ile(p.R175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179616888:179616888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188G>T
AA Mutation	p.Met396Ile(p.M396I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179621284:179621284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211C>A
AA Mutation	p.Leu71Met(p.L71M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356731
Start	179617625:179617625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179618264:179618264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596G>A
AA Mutation	p.Arg199Gln(p.R199Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179618225:179618225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635G>A
AA Mutation	p.Arg212Lys(p.R212K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356731
Start	179617101:179617101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067A>C
AA Mutation	p.Tyr356Ser(p.Y356S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000356731
Start	179617933:179617933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript