Colon Cancer: Gene >> AFAP1L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304129
Start	114304876:114304876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1127G>C
AA Mutation	p.Arg376Thr(p.R376T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304129
Start	114314011:114314011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561584886
CDS Mutation	c.652G>A
AA Mutation	p.Val218Met(p.V218M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304129
Start	114313890:114313890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773A>G
AA Mutation	p.Gln258Arg(p.Q258R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304129
Start	114299323:114299323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2050G>T
AA Mutation	p.Gly684Trp(p.G684W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304129
Start	114299292:114299292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201695310
CDS Mutation	c.2081G>A
AA Mutation	p.Arg694Gln(p.R694Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304129
Start	114300314:114300314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760017215
CDS Mutation	c.1837G>A
AA Mutation	p.Val613Ile(p.V613I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000304129
Start	114299305:114299305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767778015
CDS Mutation	c.2068C>T
AA Mutation	p.Arg690Trp(p.R690W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000304129
Start	114333282:114333282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159G>C
AA Mutation	p.Glu53Asp(p.E53D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000304129
Start	114297248:114297248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750411935
CDS Mutation	c.2279C>G
AA Mutation	p.Thr760Ser(p.T760S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000304129
Start	114300690:114300690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1543G>A
AA Mutation	p.Val515Met(p.V515M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304129
Start	114297337:114297337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115650575
CDS Mutation	c.2190C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304129
Start	114308497:114308497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304129
Start	114315737:114315737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751640593
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304129
Start	114300553:114300553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367606214
CDS Mutation	c.1680G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304129
Start	114301426:114301426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1470C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304129
Start	114315647:114315647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373379522
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AFAP1L2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304129
Start	114315668:114315668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185015833
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304129
Start	114308470:114308470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761578304
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304129
Start	114314009:114314010(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.653_654insAA
AA Mutation	p.Asn219ArgfsTer22(p.N219Rfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript