Colon Cancer: Gene >> SH3PXD2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103601950:103601950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3268G>A
AA Mutation	p.Ala1090Thr(p.A1090T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103602471:103602471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2747G>A
AA Mutation	p.Gly916Asp(p.G916D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103602625:103602625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144776136
CDS Mutation	c.2593G>A
AA Mutation	p.Val865Met(p.V865M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103602311:103602311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2907G>T
AA Mutation	p.Arg969Ser(p.R969S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103602631:103602631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766798828
CDS Mutation	c.2587G>A
AA Mutation	p.Ala863Thr(p.A863T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103602830:103602830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751249053
CDS Mutation	c.2388G>C
AA Mutation	p.Lys796Asn(p.K796N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103661072:103661072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515T>C
AA Mutation	p.Val172Ala(p.V172A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103611598:103611598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370598379
CDS Mutation	c.1291C>T
AA Mutation	p.Arg431Cys(p.R431C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103605817:103605817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374221356
CDS Mutation	c.1409G>A
AA Mutation	p.Arg470Gln(p.R470Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000369774
Start	103724361:103724361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372408078
CDS Mutation	c.307G>A
AA Mutation	p.Ala103Thr(p.A103T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103603615:103603615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603G>A
AA Mutation	p.Glu535Lys(p.E535K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103603681:103603681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751092364
CDS Mutation	c.1537C>T
AA Mutation	p.Arg513Cys(p.R513C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103603713:103603713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1505T>C
AA Mutation	p.Ile502Thr(p.I502T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103603113:103603113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755571944
CDS Mutation	c.2105C>G
AA Mutation	p.Ser702Cys(p.S702C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369774
Start	103601828:103601828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369774
Start	103602200:103602200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758214698
CDS Mutation	c.3018T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369774
Start	103661101:103661101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369774
Start	103603634:103603634(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1584delC
AA Mutation	p.Ser529AlafsTer43(p.S529Afs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369774
Start	103602018:103602019(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3199_3200delCA
AA Mutation	p.Gln1067ValfsTer5(p.Q1067Vfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369774
Start	103601932:103601932(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3286delG
AA Mutation	p.Val1096CysfsTer22(p.V1096Cfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SH3PXD2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369774
Start	103602993:103602993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765874609
CDS Mutation	c.2225C>T
AA Mutation	p.Ala742Val(p.A742V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript