Colon Cancer: Gene >> LRRC32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260061
Start	76659752:76659752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138705487
CDS Mutation	c.1841G>A
AA Mutation	p.Arg614His(p.R614H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260061
Start	76660931:76660931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552037826
CDS Mutation	c.662G>A
AA Mutation	p.Arg221Gln(p.R221Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260061
Start	76660242:76660242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351G>T
AA Mutation	p.Val451Leu(p.V451L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260061
Start	76659753:76659753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1840C>T
AA Mutation	p.Arg614Cys(p.R614C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260061
Start	76661022:76661022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Gly191Ser(p.G191S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260061
Start	76660520:76660520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566149427
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358His(p.R358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260061
Start	76659705:76659705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1888A>G
AA Mutation	p.Ile630Val(p.I630V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260061
Start	76660110:76660110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483G>A
AA Mutation	p.Val495Ile(p.V495I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000260061
Start	76661123:76661123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767579768
CDS Mutation	c.470C>T
AA Mutation	p.Ala157Val(p.A157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260061
Start	76660816:76660816(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.777delC
AA Mutation	p.Asp260ThrfsTer11(p.D260Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LRRC32

No Mutation Annotation!