Colon Cancer: Gene >> SH3PXD2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172339145:172339145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1960C>T
AA Mutation	p.Pro654Ser(p.P654S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172339324:172339324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1781T>G
AA Mutation	p.Met594Arg(p.M594R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172350371:172350371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004C>G
AA Mutation	p.Ala335Gly(p.A335G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172339484:172339484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621C>T
AA Mutation	p.Arg541Trp(p.R541W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172422445:172422445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267607046
CDS Mutation	c.127C>T
AA Mutation	p.Arg43Trp(p.R43W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172350450:172350450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200725740
CDS Mutation	c.925G>A
AA Mutation	p.Ala309Thr(p.A309T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172350524:172350524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851C>T
AA Mutation	p.Pro284Leu(p.P284L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172346195:172346195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779664507
CDS Mutation	c.1129G>A
AA Mutation	p.Ala377Thr(p.A377T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172339169:172339169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1936C>A
AA Mutation	p.Pro646Thr(p.P646T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172339790:172339790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1315C>A
AA Mutation	p.Pro439Thr(p.P439T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172346167:172346167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Gly386Asp(p.G386D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172353981:172353981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.692C>T
AA Mutation	p.Pro231Leu(p.P231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311601
Start	172339740:172339740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374958326
CDS Mutation	c.1365G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311601
Start	172338981:172338981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370525113
CDS Mutation	c.2124C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311601
Start	172339901:172339901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311601
Start	172338664:172338664(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2441delG
AA Mutation	p.Gly814AlafsTer37(p.G814Afs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SH3PXD2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172362791:172362791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777163334
CDS Mutation	c.506C>T
AA Mutation	p.Ser169Leu(p.S169L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172338779:172338779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2326C>A
AA Mutation	p.Pro776Thr(p.P776T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172347303:172347303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1042C>A
AA Mutation	p.Pro348Thr(p.P348T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172339666:172339666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781378826
CDS Mutation	c.1439C>T
AA Mutation	p.Ser480Leu(p.S480L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311601
Start	172339232:172339232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1873G>A
AA Mutation	p.Glu625Lys(p.E625K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311601
Start	172338531:172338531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2574G>A
Mutation Classification	Silent
Feature Type	Transcript