Colon Cancer: Gene >> FAN1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000362065
Start	30913860:30913860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580C>T
AA Mutation	p.Ala527Val(p.A527V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30922239:30922239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2057C>T
AA Mutation	p.Ala686Val(p.A686V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30904749:30904749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.86C>A
AA Mutation	p.Ser29Tyr(p.S29Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30905036:30905036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373A>G
AA Mutation	p.Ile125Val(p.I125V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30905627:30905627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964A>C
AA Mutation	p.Lys322Gln(p.K322Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30925182:30925182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2228G>A
AA Mutation	p.Arg743His(p.R743H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30905884:30905884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221T>G
AA Mutation	p.Phe407Leu(p.F407L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30925802:30925802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2351G>A
AA Mutation	p.Gly784Asp(p.G784D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30905217:30905217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554A>G
AA Mutation	p.Lys185Arg(p.K185R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30908177:30908177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1294A>G
AA Mutation	p.Thr432Ala(p.T432A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30925224:30925224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56258078
CDS Mutation	c.2270C>T
AA Mutation	p.Pro757Leu(p.P757L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30904937:30904937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>A
AA Mutation	p.Val92Ile(p.V92I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30922272:30922272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2090G>T
AA Mutation	p.Arg697Ile(p.R697I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30905724:30905724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758141872
CDS Mutation	c.1061G>A
AA Mutation	p.Ser354Asn(p.S354N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30918193:30918193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1841A>G
AA Mutation	p.Asp614Gly(p.D614G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30929324:30929324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200517390
CDS Mutation	c.2714C>T
AA Mutation	p.Thr905Met(p.T905M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30905172:30905172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.509T>C
AA Mutation	p.Ile170Thr(p.I170T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362065
Start	30930587:30930587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2832C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362065
Start	30925156:30925156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777269185
CDS Mutation	c.2202G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000362065
Start	30925188:30925188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2234C>G
AA Mutation	p.Ser745Ter(p.S745*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FAN1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000362065
Start	30928553:30928553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2489G>T
AA Mutation	p.Gly830Val(p.G830V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30922272:30922272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2090G>T
AA Mutation	p.Arg697Ile(p.R697I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30904735:30904735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72A>C
AA Mutation	p.Lys24Asn(p.K24N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30920609:30920609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2008T>G
AA Mutation	p.Leu670Val(p.L670V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000362065
Start	30928558:30928558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776828162
CDS Mutation	c.2494C>A
AA Mutation	p.His832Asn(p.H832N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362065
Start	30937130:30937130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2928T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362065
Start	30904951:30904951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288T>C
Mutation Classification	Silent
Feature Type	Transcript