Colon Cancer: Gene >> FZD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266238:91266238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358C>T
AA Mutation	p.Ala453Val(p.A453V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91265577:91265577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697T>C
AA Mutation	p.Ser233Pro(p.S233P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91265808:91265808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.928T>G
AA Mutation	p.Tyr310Asp(p.Y310D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91265392:91265392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512C>T
AA Mutation	p.Ser171Phe(p.S171F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91265985:91265985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105T>C
AA Mutation	p.Tyr369His(p.Y369H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266708:91266708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1828A>T
AA Mutation	p.Thr610Ser(p.T610S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266819:91266819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1939G>T
AA Mutation	p.Val647Phe(p.V647F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266195:91266195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315G>A
AA Mutation	p.Ala439Thr(p.A439T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91266350:91266350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1470C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91265819:91265819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91266188:91266188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91266383:91266383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1503C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91265771:91265771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91265579:91265579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91266035:91266035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91265414:91265414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287934
Start	91265669:91265669(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.794delG
AA Mutation	p.Gly265AlafsTer143(p.G265Afs*143)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FZD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266231:91266231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1351G>A
AA Mutation	p.Ala451Thr(p.A451T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266384:91266384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1504G>A
AA Mutation	p.Gly502Ser(p.G502S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91266035:91266035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript