Colon Cancer: Gene >> CATSPER3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282611
Start	134970001:134970001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161T>G
AA Mutation	p.Ile54Arg(p.I54R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282611
Start	134996281:134996281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261G>T
AA Mutation	p.Glu87Asp(p.E87D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000282611
Start	135007958:135007958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778365595
CDS Mutation	c.494C>T
AA Mutation	p.Thr165Met(p.T165M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282611
Start	135008009:135008009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.545T>C
AA Mutation	p.Leu182Pro(p.L182P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282611
Start	134996508:134996508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488T>A
AA Mutation	p.Ile163Asn(p.I163N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282611
Start	134996342:134996342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322A>G
AA Mutation	p.Asn108Asp(p.N108D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282611
Start	135009421:135009421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.867G>A
AA Mutation	p.Met289Ile(p.M289I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282611
Start	135009414:135009414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860A>G
AA Mutation	p.Gln287Arg(p.Q287R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282611
Start	134996491:134996491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146770599
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282611
Start	134996356:134996356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749172456
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282611
Start	134996332:134996332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.312G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282611
Start	134996392:134996393(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.373_374delAT
AA Mutation	p.Met125ValfsTer21(p.M125Vfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CATSPER3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282611
Start	134996333:134996333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313G>T
AA Mutation	p.Asp105Tyr(p.D105Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript