Mutation

Primary Site >> Stomach Cancer

Gene >> MERTK

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111975463:111975463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1135A>C
AA Mutation	p.Thr379Pro(p.T379P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	112021451:112021451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2219C>T
AA Mutation	p.Ala740Val(p.A740V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111965205:111965205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.772G>A
AA Mutation	p.Ala258Thr(p.A258T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111975395:111975395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067G>A
AA Mutation	p.Ser356Asn(p.S356N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111968152:111968152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860C>A
AA Mutation	p.Pro287Gln(p.P287Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295408
Start	111929334:111929334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571353346
CDS Mutation	c.276G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295408
Start	111975465:111975465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295408
Start	112010015:112010015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56225811
CDS Mutation	c.2028C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295408
Start	111947405:111947405(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.597delT
AA Mutation	p.Phe199LeufsTer8(p.F199Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000295408
Start	112028677:112028677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2813G>A
AA Mutation	p.Trp938Ter(p.W938*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript