Colon Cancer: Gene >> TRIM37

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59032085:59032085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1759A>T
AA Mutation	p.Ser587Cys(p.S587C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262294
Start	59079754:59079754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616G>T
AA Mutation	p.Gly206Cys(p.G206C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59079855:59079855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515G>T
AA Mutation	p.Arg172Ile(p.R172I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262294
Start	59104393:59104393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374747161
CDS Mutation	c.23G>C
AA Mutation	p.Ser8Thr(p.S8T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59088372:59088372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201317687
CDS Mutation	c.200G>A
AA Mutation	p.Arg67His(p.R67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59051318:59051318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210C>T
AA Mutation	p.Arg404Cys(p.R404C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59012334:59012334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2689G>A
AA Mutation	p.Glu897Lys(p.E897K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59047756:59047756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1594G>A
AA Mutation	p.Asp532Asn(p.D532N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59062640:59062640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778383295
CDS Mutation	c.869G>A
AA Mutation	p.Arg290His(p.R290H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59079838:59079838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532C>T
AA Mutation	p.Arg178Cys(p.R178C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59001702:59001702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2708A>G
AA Mutation	p.Asp903Gly(p.D903G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59064363:59064363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.852G>T
AA Mutation	p.Glu284Asp(p.E284D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59070833:59070833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799G>A
AA Mutation	p.Asp267Asn(p.D267N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59084071:59084071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.300A>C
AA Mutation	p.Glu100Asp(p.E100D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59028604:59028604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2068A>G
AA Mutation	p.Thr690Ala(p.T690A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59079802:59079802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568A>C
AA Mutation	p.Ile190Leu(p.I190L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262294
Start	58999422:58999422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771052261
CDS Mutation	c.2850C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262294
Start	59041883:59041883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1683T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262294
Start	59088398:59088398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262294
Start	59070936:59070936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.696T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262294
Start	59001606:59001606(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2804delC
AA Mutation	p.Pro935ArgfsTer15(p.P935Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262294
Start	59081105:59081106(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.483_484delTC
AA Mutation	p.Gln162ArgfsTer15(p.Q162Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000262294
Start	59075691:59075691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640G>T
AA Mutation	p.Glu214Ter(p.E214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM37

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59047795:59047795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555G>A
AA Mutation	p.Asp519Asn(p.D519N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59028420:59028420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2252G>A
AA Mutation	p.Arg751Gln(p.R751Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262294
Start	59104349:59104349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753562399
CDS Mutation	c.67C>T
AA Mutation	p.Arg23Trp(p.R23W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262294
Start	59064363:59064363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.852G>A
Mutation Classification	Silent
Feature Type	Transcript