Colon Cancer: Gene >> FAM83H

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143726795:143726795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2666G>A
AA Mutation	p.Arg889Gln(p.R889Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143726609:143726609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201459659
CDS Mutation	c.2852C>T
AA Mutation	p.Ala951Val(p.A951V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143730441:143730441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142G>T
AA Mutation	p.Ala48Ser(p.A48S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143727687:143727687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1774G>A
AA Mutation	p.Gly592Ser(p.G592S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143726712:143726712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2749C>T
AA Mutation	p.Pro917Ser(p.P917S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143729028:143729028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>T
AA Mutation	p.Gly226Cys(p.G226C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143728055:143728055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406C>T
AA Mutation	p.Pro469Leu(p.P469L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143728290:143728290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1171G>A
AA Mutation	p.Ala391Thr(p.A391T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143730548:143730548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782638461
CDS Mutation	c.35A>G
AA Mutation	p.Asp12Gly(p.D12G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143728349:143728349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112C>T
AA Mutation	p.Ala371Val(p.A371V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143730335:143730335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248T>G
AA Mutation	p.Leu83Arg(p.L83R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143730482:143730482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101C>A
AA Mutation	p.Ala34Glu(p.A34E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143726100:143726100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782236631
CDS Mutation	c.3361C>T
AA Mutation	p.Arg1121Cys(p.R1121C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143726492:143726492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201196465
CDS Mutation	c.2969C>T
AA Mutation	p.Pro990Leu(p.P990L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143726813:143726813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782246101
CDS Mutation	c.2648C>T
AA Mutation	p.Thr883Met(p.T883M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143728454:143728454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007A>G
AA Mutation	p.Glu336Gly(p.E336G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000388913
Start	143730144:143730144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439G>A
AA Mutation	p.Ala147Thr(p.A147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388913
Start	143728192:143728192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388913
Start	143728114:143728114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1347C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388913
Start	143726431:143726431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3030G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388913
Start	143726134:143726134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3327G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388913
Start	143726068:143726068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782491323
CDS Mutation	c.3393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388913
Start	143728183:143728183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1278G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388913
Start	143728066:143728066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1395G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000388913
Start	143728367:143728367(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1094delG
AA Mutation	p.Gly365AlafsTer180(p.G365Afs*180)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000388913
Start	143730138:143730138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445C>T
AA Mutation	p.Gln149Ter(p.Q149*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FAM83H

No Mutation Annotation!