Colon Cancer: Gene >> LRRC8A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128907317:128907317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153G>T
AA Mutation	p.Lys51Asn(p.K51N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128908422:128908422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258C>T
AA Mutation	p.Leu420Phe(p.L420F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128907450:128907450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286G>T
AA Mutation	p.Gly96Cys(p.G96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128907762:128907762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598A>G
AA Mutation	p.Thr200Ala(p.T200A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128908095:128908095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931G>A
AA Mutation	p.Ala311Thr(p.A311T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128907229:128907229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757315550
CDS Mutation	c.65C>T
AA Mutation	p.Pro22Leu(p.P22L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128909200:128909200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748626839
CDS Mutation	c.2036C>T
AA Mutation	p.Thr679Ile(p.T679I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128908234:128908234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357His(p.R357H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259324
Start	128907395:128907395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259324
Start	128908433:128908433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750593208
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259324
Start	128907410:128907410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259324
Start	128908538:128908538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259324
Start	128908622:128908622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11999276
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259324
Start	128907563:128907563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778279829
CDS Mutation	c.399G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259324
Start	128908775:128908775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201808589
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000259324
Start	128907757:128907757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593C>A
AA Mutation	p.Ser198Ter(p.S198*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LRRC8A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128908536:128908536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372G>T
AA Mutation	p.Asp458Tyr(p.D458Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259324
Start	128916103:128916103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2165C>T
AA Mutation	p.Thr722Met(p.T722M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript