Colon Cancer: Gene >> SASH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148548362:148548362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3548C>T
AA Mutation	p.Ser1183Leu(p.S1183L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148532901:148532901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769499189
CDS Mutation	c.1669G>A
AA Mutation	p.Gly557Arg(p.G557R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148527493:148527493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1325C>T
AA Mutation	p.Ser442Leu(p.S442L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148532880:148532880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648C>T
AA Mutation	p.Pro550Ser(p.P550S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148544754:148544754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547938889
CDS Mutation	c.3284C>T
AA Mutation	p.Thr1095Met(p.T1095M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148532905:148532905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369655037
CDS Mutation	c.1673G>A
AA Mutation	p.Arg558His(p.R558H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148519717:148519717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033G>T
AA Mutation	p.Gly345Trp(p.G345W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148546118:148546118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3452A>G
AA Mutation	p.Lys1151Arg(p.K1151R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148544796:148544796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767736360
CDS Mutation	c.3326C>T
AA Mutation	p.Thr1109Met(p.T1109M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148544351:148544351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2881C>T
AA Mutation	p.His961Tyr(p.H961Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148543993:148543993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2523T>G
AA Mutation	p.Asp841Glu(p.D841E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148543688:148543688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218C>T
AA Mutation	p.Arg740Trp(p.R740W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148532878:148532878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139081709
CDS Mutation	c.1646C>T
AA Mutation	p.Pro549Leu(p.P549L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148474148:148474148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553A>C
AA Mutation	p.Ser185Arg(p.S185R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148548425:148548425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3611G>C
AA Mutation	p.Ser1204Thr(p.S1204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148548334:148548334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577978226
CDS Mutation	c.3520G>A
AA Mutation	p.Val1174Ile(p.V1174I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148546103:148546103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3437A>G
AA Mutation	p.Asp1146Gly(p.D1146G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367467
Start	148533929:148533929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1893A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367467
Start	148544134:148544134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763114501
CDS Mutation	c.2664C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367467
Start	148544665:148544665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758923254
CDS Mutation	c.3195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367467
Start	148544641:148544641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3171G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367467
Start	148487646:148487646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756344953
CDS Mutation	c.660G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367467
Start	148543927:148543927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2457C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367467
Start	148474144:148474144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367467
Start	148474150:148474150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764763178
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367467
Start	148543895:148543895(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2429delA
AA Mutation	p.Asn810ThrfsTer48(p.N810Tfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SASH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148544780:148544780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3310G>A
AA Mutation	p.Glu1104Lys(p.E1104K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148544206:148544206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746649534
CDS Mutation	c.2736G>T
AA Mutation	p.Glu912Asp(p.E912D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148544123:148544123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2653G>T
AA Mutation	p.Asp885Tyr(p.D885Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367467
Start	148534863:148534863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2057T>G
AA Mutation	p.Val686Gly(p.V686G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367467
Start	148527587:148527587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1419C>A
Mutation Classification	Silent
Feature Type	Transcript