Colon Cancer: Gene >> CREB3L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46300006:46300006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174C>A
AA Mutation	p.Phe58Leu(p.F58L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46312455:46312455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749140671
CDS Mutation	c.884G>A
AA Mutation	p.Arg295Gln(p.R295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46299992:46299992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160C>A
AA Mutation	p.Leu54Met(p.L54M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46307896:46307896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375217169
CDS Mutation	c.412G>A
AA Mutation	p.Val138Met(p.V138M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46311104:46311104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771754544
CDS Mutation	c.668G>A
AA Mutation	p.Arg223His(p.R223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46312373:46312373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Trp(p.R268W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46317454:46317454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1225C>A
AA Mutation	p.Leu409Met(p.L409M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46320320:46320320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774678396
CDS Mutation	c.1315C>T
AA Mutation	p.Arg439Cys(p.R439C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46320276:46320276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1271G>A
AA Mutation	p.Ser424Asn(p.S424N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621158
Start	46311141:46311141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545047399
CDS Mutation	c.705G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621158
Start	46317477:46317477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1248G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621158
Start	46320481:46320481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756003422
CDS Mutation	c.1476C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000621158
Start	46311190:46311190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.753+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000621158
Start	46312324:46312324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000621158
Start	46278213:46278224(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.102+3_102+14delAAGATGAAGGGT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CREB3L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000621158
Start	46312872:46312872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984G>T
AA Mutation	p.Glu328Asp(p.E328D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript