Colon Cancer: Gene >> MORC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30958684:30958684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79G>A
AA Mutation	p.Glu27Lys(p.E27K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30956775:30956775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.145G>T
AA Mutation	p.Asp49Tyr(p.D49Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30934875:30934875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772866972
CDS Mutation	c.2099T>C
AA Mutation	p.Leu700Pro(p.L700P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000397641
Start	30937583:30937583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201852637
CDS Mutation	c.1498G>A
AA Mutation	p.Asp500Asn(p.D500N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30941541:30941541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716C>T
AA Mutation	p.Ser239Leu(p.S239L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30949803:30949803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266A>G
AA Mutation	p.Lys89Arg(p.K89R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30932970:30932970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2441C>T
AA Mutation	p.Ala814Val(p.A814V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30932642:30932642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372297066
CDS Mutation	c.2650G>A
AA Mutation	p.Ala884Thr(p.A884T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30942213:30942213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485T>C
AA Mutation	p.Val162Ala(p.V162A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30937630:30937630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143046507
CDS Mutation	c.1451G>A
AA Mutation	p.Arg484His(p.R484H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000397641
Start	30939697:30939697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746698035
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Ter(p.R333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MORC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30956780:30956780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140G>T
AA Mutation	p.Arg47Ile(p.R47I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30958684:30958684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79G>A
AA Mutation	p.Glu27Lys(p.E27K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30933006:30933006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2405G>A
AA Mutation	p.Arg802His(p.R802H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30936555:30936555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1693A>G
AA Mutation	p.Thr565Ala(p.T565A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397641
Start	30950421:30950421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.182G>T
AA Mutation	p.Gly61Val(p.G61V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript