Colon Cancer: Gene >> SASS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287482
Start	100102989:100102989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749784408
CDS Mutation	c.1640C>T
AA Mutation	p.Ala547Val(p.A547V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287482
Start	100123277:100123277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541086017
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Cys(p.R47C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287482
Start	100085341:100085341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1961T>C
AA Mutation	p.Leu654Ser(p.L654S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287482
Start	100107488:100107488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212G>T
AA Mutation	p.Lys404Asn(p.K404N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287482
Start	100120398:100120398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374162430
CDS Mutation	c.545G>A
AA Mutation	p.Arg182Gln(p.R182Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287482
Start	100107967:100107967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774060441
CDS Mutation	c.899G>A
AA Mutation	p.Arg300Gln(p.R300Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287482
Start	100105824:100105824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779107653
CDS Mutation	c.1488G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287482
Start	100119024:100119024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000287482
Start	100106969:100106969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351G>T
AA Mutation	p.Glu451Ter(p.E451*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287482
Start	100121519:100121520(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.341_342insCATTGATACT
AA Mutation	p.Leu116AspfsTer6(p.L116Dfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287482
Start	100119119:100119120(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs778258887
CDS Mutation	c.567dupA
AA Mutation	p.Gln190ThrfsTer5(p.Q190Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SASS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287482
Start	100107453:100107453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247C>G
AA Mutation	p.Ala416Gly(p.A416G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287482
Start	100121404:100121404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457C>A
AA Mutation	p.Leu153Ile(p.L153I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript