Colon Cancer: Gene >> ANXA6

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000354546
Start	151123011:151123011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1139G>A
AA Mutation	p.Gly380Glu(p.G380E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151122954:151122954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196A>G
AA Mutation	p.Gln399Arg(p.Q399R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151132538:151132538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674C>A
AA Mutation	p.Pro225Gln(p.P225Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151131248:151131248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778C>A
AA Mutation	p.Leu260Ile(p.L260I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151105276:151105276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1808T>A
AA Mutation	p.Phe603Tyr(p.F603Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151139409:151139409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758088547
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Trp(p.R50W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151133118:151133118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616C>T
AA Mutation	p.Arg206Cys(p.R206C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151105264:151105264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1820A>C
AA Mutation	p.Lys607Thr(p.K607T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151123003:151123003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748009214
CDS Mutation	c.1147G>A
AA Mutation	p.Glu383Lys(p.E383K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151139426:151139426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131T>A
AA Mutation	p.Leu44Gln(p.L44Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151117818:151117818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1458G>T
AA Mutation	p.Glu486Asp(p.E486D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354546
Start	151129488:151129488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354546
Start	151136304:151136304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181203511
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354546
Start	151132485:151132485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000354546
Start	151122943:151122943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1207C>T
AA Mutation	p.Gln403Ter(p.Q403*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000354546
Start	151110645:151110645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1573-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	start_lost
Transcription ID	ENST00000354546
Start	151147900:151147900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ANXA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151105268:151105268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771610573
CDS Mutation	c.1816G>A
AA Mutation	p.Asp606Asn(p.D606N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151105290:151105290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1794G>T
AA Mutation	p.Lys598Asn(p.K598N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354546
Start	151110633:151110633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1584G>T
AA Mutation	p.Glu528Asp(p.E528D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript