Colon Cancer: Gene >> SARDH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133730130:133730130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Trp(p.R250W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133730156:133730156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755017202
CDS Mutation	c.722G>A
AA Mutation	p.Arg241His(p.R241H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133666764:133666764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2602G>A
AA Mutation	p.Gly868Ser(p.G868S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133717386:133717386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775453942
CDS Mutation	c.1090G>A
AA Mutation	p.Ala364Thr(p.A364T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133717419:133717419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057G>T
AA Mutation	p.Asp353Tyr(p.D353Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133664010:133664010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563709194
CDS Mutation	c.2636C>T
AA Mutation	p.Ser879Leu(p.S879L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133708315:133708315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35699831
CDS Mutation	c.1442G>A
AA Mutation	p.Arg481His(p.R481H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133717404:133717404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767136747
CDS Mutation	c.1072A>G
AA Mutation	p.Thr358Ala(p.T358A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133670735:133670735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563087933
CDS Mutation	c.2344G>A
AA Mutation	p.Ala782Thr(p.A782T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133730126:133730126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760282297
CDS Mutation	c.752G>A
AA Mutation	p.Arg251Gln(p.R251Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371872
Start	133732601:133732601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332G>A
AA Mutation	p.Gly111Asp(p.G111D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133666844:133666844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2522C>A
AA Mutation	p.Ala841Asp(p.A841D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133719027:133719027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Cys(p.R311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133730080:133730080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133731419:133731419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133732444:133732444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133671575:133671575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373435029
CDS Mutation	c.2286C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133702976:133702976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1608C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133690520:133690520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1929T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133671629:133671629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2232C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133708365:133708365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781432712
CDS Mutation	c.1392C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000371872
Start	133708388:133708388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199802293
CDS Mutation	c.1369C>T
AA Mutation	p.Arg457Ter(p.R457*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000371872
Start	133713074:133713074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61737867
CDS Mutation	c.1201C>T
AA Mutation	p.Arg401Ter(p.R401*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SARDH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133712653:133712653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79196288
CDS Mutation	c.1294C>T
AA Mutation	p.Arg432Cys(p.R432C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371872
Start	133717424:133717424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052A>G
AA Mutation	p.Asp351Gly(p.D351G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133664009:133664009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775373624
CDS Mutation	c.2637G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371872
Start	133729810:133729810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript