Colon Cancer: Gene >> DPY19L3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000342179
Start	32482081:32482081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1992G>A
AA Mutation	p.Met664Ile(p.M664I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342179
Start	32480465:32480465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1897G>T
AA Mutation	p.Asp633Tyr(p.D633Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342179
Start	32437223:32437223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480T>G
AA Mutation	p.Ile160Met(p.I160M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342179
Start	32436473:32436473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356A>C
AA Mutation	p.Lys119Thr(p.K119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342179
Start	32439146:32439146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342179
Start	32458486:32458486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1299C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342179
Start	32480551:32480551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775192273
CDS Mutation	c.1983C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342179
Start	32482168:32482168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2079C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000342179
Start	32454938:32454939(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.992dupA
AA Mutation	p.Asn331LysfsTer9(p.N331Kfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DPY19L3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342179
Start	32439821:32439821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766C>A
AA Mutation	p.Leu256Met(p.L256M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342179
Start	32458106:32458106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096C>A
AA Mutation	p.Leu366Ile(p.L366I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342179
Start	32436486:32436486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748028225
CDS Mutation	c.369G>T
AA Mutation	p.Met123Ile(p.M123I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342179
Start	32464754:32464754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150059190
CDS Mutation	c.1584G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342179
Start	32411366:32411366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000342179
Start	32468770:32468770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654G>T
AA Mutation	p.Glu552Ter(p.E552*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript