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geneid	338321
ensemblid	ENSG00000185792.10
hgncid	22941
symbol	NLRP9
name	NLR family pyrin domain containing 9
refseq_nuc	NM_176820.4
refseq_prot	NP_789790.2
ensembl_nuc	ENST00000332836.7
ensembl_prot	ENSP00000331857.2
mane_status	MANE Select
chr	chr19
start	55708438
end	55738402
strand	-
ver	v1.2
region	chr19:55708438-55738402
region5000	chr19:55703438-55743402
regionname0	NLRP9_chr19_55708438_55738402
regionname5000	NLRP9_chr19_55703438_55743402

ahapid	grch38/ chm13v2 1/0: The haplotype type is the same as GRCh38 0/1: The haplotype type is the same as CHM13v2 0/0: The haplotype type matches neither GRCh38 nor CHM13v2 1/1: The haplotype type is the same on both GRCh38 and CHM13v2	alen	total	AFR	AMR	EAS	EUR	SAS	JPT	regionname	genename	aa	chr	start	end
a0001	1/1	991	2	0	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	copy fasta	chr19	55703438	55743402

chapid	grch38/ chm13v2 1/0: The haplotype type is the same as GRCh38 0/1: The haplotype type is the same as CHM13v2 0/0: The haplotype type matches neither GRCh38 nor CHM13v2 1/1: The haplotype type is the same on both GRCh38 and CHM13v2	clen	total	AFR	AMR	EAS	EUR	SAS	regionname	genename	cseq	chr	start	end
c0001	0/1	2976	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	copy fasta	chr19	55703438	55743402
c0002	1/0	2976	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	copy fasta	chr19	55703438	55743402

thapid	grch38 chm13v2 1/0: The haplotype type is the same as GRCh38 0/1: The haplotype type is the same as CHM13v2 0/0: The haplotype type matches neither GRCh38 nor CHM13v2 1/1: The haplotype type is the same on both GRCh38 and CHM13v2	tlen	total	AFR	AMR	EAS	EUR	SAS	regionname	genename	tseq	chr	start	end
t0001	1/1	503	2	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	copy fasta	chr19	55703438	55743402

ghapid	grch38/ chm13v2 1/0: The haplotype type is the same as GRCh38 0/1: The haplotype type is the same as CHM13v2 0/0: The haplotype type matches neither GRCh38 nor CHM13v2 1/1: The haplotype type is the same on both GRCh38 and CHM13v2	total	AFR	AMR	EAS	EUR	SAS	regionname	genename	chr	start	end
g0001	0/1	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	chr19	55703438	55743402
g0002	1/0	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	chr19	55703438	55743402

achapid	grch38/ chm13v2 1/0: The haplotype type is the same as GRCh38 0/1: The haplotype type is the same as CHM13v2 0/0: The haplotype type matches neither GRCh38 nor CHM13v2 1/1: The haplotype type is the same on both GRCh38 and CHM13v2	clen	total	AFR	AMR	EAS	EUR	SAS	regionname	genename	cseq	chr	start	end
a0001c0001	0/1	2976	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	copy fasta	chr19	55703438	55743402
a0001c0002	1/0	2976	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	copy fasta	chr19	55703438	55743402

acthapid	grch38 chm13v2	tlen	total	AFR	AMR	EAS	EUR	SAS	regionname	genename	tseq	chr	start	end
a0001c0001t0001	0/1	3478	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	copy fasta	chr19	55703438	55743402
a0001c0002t0001	1/0	3478	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	copy fasta	chr19	55703438	55743402

actghapid	grch38/ chm13v2 1/0: The haplotype type is the same as GRCh38 0/1: The haplotype type is the same as CHM13v2 0/0: The haplotype type matches neither GRCh38 nor CHM13v2 1/1: The haplotype type is the same on both GRCh38 and CHM13v2	total	AFR	AMR	EAS	EUR	SAS	regionname	genename	chr	start	end
a0001c0001t0001g0001	0/1	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	chr19	55703438	55743402
a0001c0002t0001g0002	1/0	1	0	0	0	0	0	NLRP9_chr19_55703438_55743402	NLRP9	chr19	55703438	55743402

sampleid	ID haplotypeid	ahapid	chapid	thapid	ghapid	gpopname	popname	regionname	genename	chr	start	end
homoSapiens_chm13v2	hp1	a0001	c0001	t0001	g0001	REF	REF	NLRP9_chr19_55703438_55743402	NLRP9	chr19	55703438	55743402
homoSapiens_grch38	hp1	a0001	c0002	t0001	g0002	REF	REF	NLRP9_chr19_55703438_55743402	NLRP9	chr19	55703438	55743402

chr:pos	ref	alt	# # of ahapid:amino-acid(protein) level	ahapids	# # of haplotypeids	haplotypeids	annotation	impact	hgvs_c	hgvs_p	genename	geneid	featuretype	featureid	transcript_biotype	rank	cdna cdna pos length	cds cds pos length	aa aa pos length	distance	status	chr	pos

chr:pos	ref	alt	# # of chapid	chapids	# # of haplotypeids	haplotypeids	annotation	impact	hgvs_c	hgvs_p	genename	geneid	featuretype	featureid	transcript_biotype	rank	cdna cdna pos length	cds cds pos length	aa aa pos length	distance	status	chr	pos
chr19:55738306	A A	G G	1	a0001c0001 a0001c0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	synonymous_variant	LOW	c.69T>C c.69T>C	p.Phe23Phe p.Phe23Phe	NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	1/9	97/3478	69/2976	23/991			chr19	55738306

chr:pos	ref	alt	# # of thapid:transcript level	thapids	# # of haplotypeids	haplotypeids	annotation	impact	hgvs_c	hgvs_p	genename	geneid	featuretype	featureid	transcript_biotype	rank	cdna cdna pos length	cds cds pos length	aa aa pos length	distance	status	chr	pos

chr:pos	ref	alt	# # of ghapid:genebody level	ghapids	# # of haplotypeids	haplotypeids	annotation	impact	hgvs_c	hgvs_p	genename	geneid	featuretype	featureid	genebody_biotype	rank	cdna cdna pos length	cds cds pos length	aa aa pos length	distance	status	chr	pos
chr19:55712950	G G	GGAAGGGG others(1837): Show GGAAGGGGAGGGGAGGAGAGGAGGGGAAGGGGAGGGGAGGAGGGAGGGGG AGGGGAGGAGAGGAGCGGAGGGGGAGGAGAGGAGGGAGGGGGGAGGAGAG GAGCGGGAGGGGAGGGGGAGGGAGGAGGGGAGGGGGAGGAGAGGAGGGGA GGGGAGAGGAGGGGGGAGGAGAGGAGGAGGAGGGGGAGGAGGGGATGGGA GGGGGAGGAGAGGAGGGGGAGGAGAGGGGGAGAGGAGGGGGAGAGGAGGG AGGAGGGGGGGAGAGGGGGAGAGGAGGGGAGAGGAGGGGAGAGGAGGGGG GGAGAGGAGGGGGAGGAGAGGAGGGGGAGGAGAGGGGGAGAGGAGAGGGG GAGAGGAGGGGAGGAGAGGAGGGGAGAGGAGGGGGGAGGAGAGGAGGGGA GGAGAGGGGAGAGGAGAGGGGGAGAGGAGGGGGAGGGAGAGGAGGGGAGG GGAGAGAGGAGAGGAGGGGGAGGAAGAGGGGAGGAGGAGGAGGGGGAGGG GAGGAAGAGGGGGGAGGAAGAGGGGAGGAGGAGGAGGGGAGGGGAGGAGA GGAGGGGGAGGGGAGGAGGAGGGAGGAGAGGGGGAGGGGAGGGGAGGAGG AGGGAAAGAGAGGAGGGAGGGGAGGAGAGGAGGGGGAGGAGGAGGGGGAG GAGGAGGGGGAGGAGGAGGGGGAGGAGGAGGGGGAGGAGGAGGGAGGGGT AGAAGGGGGAGAAAGGGCAGAAAGGGCAGAAAGGGAAGGGGGAGAAGTGG CAGAAAGGGAAGGGGGAGAAGGGGAGGGGGAGAAGGGGAAGGAAGGGGAG GGTGAGAAGGAGTCGGAAGGGGAGGGGGAGAAGGGGAGGAAGGGGAGGGG TGGGAGGAGGAGGAGGGAGAAGGAGGAGGGGGAGGAAGGGGAGGTGGAGG GGAGGAAGGGGAGGGAGGGGAGGAAGGGGAGGTGAGGGGAGGAAGGGGAG GGGGAGGTAGGGGAGGGGGAGAAGGGGAGGGGAGGGAGAGGAGGGAAAGG GGAGGGGAGGATGGGAGGGAGGGCAAAGGGGGCAAAGGAAGGGGAAGGGG AAGGGGAAGGGGAAGGGGGAAGGGGAAGGGGAAGGGGAAGGGGAAGGGGG GAAGGGGGAAGGGGGAAGGGGGAGGGGAAGGGGAAGGGGAGGGGAAGGGG GAGGGTGCGGGGAAGGGGGAGGGGAAAGGGAATGGGGAGGGGAAAGGGGA ATGGGAGGGAAGGGGGAGGGAAGGAGGGGGGAAGGGGAGGGAGGAGGGAA TGGGAGGGAAAAGGGGGAGGAGGGAGAGAGAAGGAGGAATAGGGAGGAGG GGAAAGGGGAGGAGGGAAGGGAGGGGAAAGGGGAGGAGGGAAGGGAGGGA AAGGGGAGGAGGGAGGGAAAGGGGGAGGAGGGAAGGGAGGGGAAAGGGGA GGAGGGAAGGGAGGGGAAAGGGGGAGGAGGGAAGGGAGGGGAAAGGGGGA GGAGGGAAGGGAGGGAAAGGGGGAGGGAGGAGGAAGGGGGAGGGAGGAGG AAGGGGGAGGGAGGCGGGGGAGGAGGAGGAGGGGAGGGAGGGGGGAGGGA GGGGGGAGGGGAGGAGGGGGAGGGGGGAGGGGAGGAGGGGGAGGGAGGAG GAAGGAGGGGGAGGGAGGAGGAAGGGAGGGGGAGGGAGGAGGAACGGAGG GGGAGGGAGGAGGAACGGAGGGGGAGGGAGGAGGAACGGAGGGGGAGGGA GGAGGAACGGAGGGGGGAGGGAGGAGGAACGGAGGGGGAGGGAGGAGGGA GGGGAGGGAGGAGGGAGGGGGAGGGAGGAGGGAGGGGAGGGAGGAGGGAG GAGGGAGGGGAGGGGGAGGAGGGGGAGGGAGGAGGGAGGGGAGGA	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.2502-361_2502-360i others(1846): Show c.2502-361_2502-360insTCCTCCCCTCCCTCCTCCCTCCCCCTCC TCCCCCTCCCCTCCCTCCTCCCTCCTCCCTCCCCTCCCTCCTCCCTCCCC CTCCCTCCTCCCTCCCCTCCCTCCTCCCTCCCCCTCCGTTCCTCCTCCCT CCCCCCTCCGTTCCTCCTCCCTCCCCCTCCGTTCCTCCTCCCTCCCCCTC CGTTCCTCCTCCCTCCCCCTCCGTTCCTCCTCCCTCCCCCTCCCTTCCTC CTCCCTCCCCCTCCTTCCTCCTCCCTCCCCCTCCTCCCCTCCCCCCTCCC CCTCCTCCCCTCCCCCCTCCCTCCCCCCTCCCTCCCCTCCTCCTCCTCCC CCGCCTCCCTCCCCCTTCCTCCTCCCTCCCCCTTCCTCCTCCCTCCCCCT TTCCCTCCCTTCCCTCCTCCCCCTTTCCCCTCCCTTCCCTCCTCCCCCTT TCCCCTCCCTTCCCTCCTCCCCTTTCCCCTCCCTTCCCTCCTCCCCCTTT CCCTCCCTCCTCCCCTTTCCCTCCCTTCCCTCCTCCCCTTTCCCCTCCCT TCCCTCCTCCCCTTTCCCCTCCTCCCTATTCCTCCTTCTCTCTCCCTCCT CCCCCTTTTCCCTCCCATTCCCTCCTCCCTCCCCTTCCCCCCTCCTTCCC TCCCCCTTCCCTCCCATTCCCCTTTCCCCTCCCCATTCCCTTTCCCCTCC CCCTTCCCCGCACCCTCCCCCTTCCCCTCCCCTTCCCCTTCCCCTCCCCC TTCCCCCTTCCCCCTTCCCCCCTTCCCCTTCCCCTTCCCCTTCCCCTTCC CCCTTCCCCTTCCCCTTCCCCTTCCCCTTCCTTTGCCCCCTTTGCCCTCC CTCCCATCCTCCCCTCCCCTTTCCCTCCTCTCCCTCCCCTCCCCTTCTCC CCCTCCCCTACCTCCCCCTCCCCTTCCTCCCCTCACCTCCCCTTCCTCCC CTCCCTCCCCTTCCTCCCCTCCACCTCCCCTTCCTCCCCCTCCTCCTTCT CCCTCCTCCTCCTCCCACCCCTCCCCTTCCTCCCCTTCTCCCCCTCCCCT TCCGACTCCTTCTCACCCTCCCCTTCCTTCCCCTTCTCCCCCTCCCCTTC TCCCCCTTCCCTTTCTGCCACTTCTCCCCCTTCCCTTTCTGCCCTTTCTG CCCTTTCTCCCCCTTCTACCCCTCCCTCCTCCTCCCCCTCCTCCTCCCCC TCCTCCTCCCCCTCCTCCTCCCCCTCCTCCTCCCCCTCCTCTCCTCCCCT CCCTCCTCTCTTTCCCTCCTCCTCCCCTCCCCTCCCCCTCTCCTCCCTCC TCCTCCCCTCCCCCTCCTCTCCTCCCCTCCCCTCCTCCTCCTCCCCTCTT CCTCCCCCCTCTTCCTCCCCTCCCCCTCCTCCTCCTCCCCTCTTCCTCCC CCTCCTCTCCTCTCTCCCCTCCCCTCCTCTCCCTCCCCCTCCTCTCCCCC TCTCCTCTCCCCTCTCCTCCCCTCCTCTCCTCCCCCCTCCTCTCCCCTCC TCTCCTCCCCTCCTCTCCCCCTCTCCTCTCCCCCTCTCCTCCCCCTCCTC TCCTCCCCCTCCTCTCCCCCCCTCCTCTCCCCTCCTCTCCCCTCCTCTCC CCCTCTCCCCCCCTCCTCCCTCCTCTCCCCCTCCTCTCCCCCTCTCCTCC CCCTCCTCTCCTCCCCCTCCCATCCCCTCCTCCCCCTCCTCCTCCTCTCC TCCCCCCTCCTCTCCCCTCCCCTCCTCTCCTCCCCCTCCCCTCCTCCCTC CCCCTCCCCTCCCGCTCCTCTCCTCCCCCCTCCCTCCTCTCCTCCCCCTC CGCTCCTCTCCTCCCCTCCCCCTCCCTCCTCCCCTCCCCTTCCCCTCCTC TCCTCCCCTCCCCTTC		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	6/8						chr19	55712950
chr19:55712954	A A	G G	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.2502-364T>C c.2502-364T>C		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	6/8						chr19	55712954
chr19:55713548	C C	T T	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.2502-958G>A c.2502-958G>A		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	6/8						chr19	55713548
chr19:55713636	T T	TCTCCCCT others(167): Show TCTCCCCTCCCTCCCCACCTCTCCCTCTCCCCTCCCCACCTCTCCCCTCT CCCTCCCCACCTCTCCCCTCCCTCCCCACCTCTCCCCTCTCCCTCCCCAC CTCTCCCCTCCCTCCCCACCTCTCCCTCTCCCTCCCCACCTCCCCTCTCC CTCCCCACCTCCCCTCTCCTCCCCA	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.2502-1047_2502-104 others(178): Show c.2502-1047_2502-1046insTGGGGAGGAGAGGGGAGGTGGGGAGG GAGAGGGGAGGTGGGGAGGGAGAGGGAGAGGTGGGGAGGGAGGGGAGAGG TGGGGAGGGAGAGGGGAGAGGTGGGGAGGGAGGGGAGAGGTGGGGAGGGA GAGGGGAGAGGTGGGGAGGGGAGAGGGAGAGGTGGGGAGGGAGGGGAG		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	6/8						chr19	55713636
chr19:55713697	C C	CCACCTCT others(202): Show CCACCTCTCCCTCTCCCTCCCCACCTCTTCCCCCCCGCCTCCCCCACCTC TTCCCCCCGCCTCCCACCCTCTTCCCCCCCCTGCCTCCCCACCTCTTCCC CCCTCCTCCCACCTCTCCCCCTCTCCCCTCCCCACCTCTTCCCCCTCCTC CCCACCTCTCCCCTCTCCCTCCCCACCTCTTCCCCCCGCCTCCCCACCTC TTCCCCCCCG	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.2502-1108_2502-110 others(213): Show c.2502-1108_2502-1107insCGGGGGGGAAGAGGTGGGGAGGCGGG GGGAAGAGGTGGGGAGGGAGAGGGGAGAGGTGGGGAGGAGGGGGAAGAGG TGGGGAGGGGAGAGGGGGAGAGGTGGGAGGAGGGGGGAAGAGGTGGGGAG GCAGGGGGGGGAAGAGGGTGGGAGGCGGGGGGAAGAGGTGGGGGAGGCGG GGGGGAAGAGGTGGGGAGGGAGAGGGAGAGGTG		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	6/8						chr19	55713697
chr19:55713753	T T	TCCCCCTC others(143): Show TCCCCCTCCTCCCCACCTCTTCCCCCCTCCTCCCCACCTCTTCCCCCCCG CCTCCCCACCTCTTCCCCCCCCCTCCTCCCCACCTCTTCCCCCTCCTCCC CACCTCTTCCCCCTCCTCCCCACCTCTTCCCCCTCCTCCCCCACCTCTTC C	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.2502-1164_2502-116 others(154): Show c.2502-1164_2502-1163insGGAAGAGGTGGGGGAGGAGGGGGAAG AGGTGGGGAGGAGGGGGAAGAGGTGGGGAGGAGGGGGAAGAGGTGGGGAG GAGGGGGGGGGAAGAGGTGGGGAGGCGGGGGGGAAGAGGTGGGGAGGAGG GGGGAAGAGGTGGGGAGGAGGGGG		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	6/8						chr19	55713753
chr19:55713774	T T	TCCCCCCT others(15): Show TCCCCCCTCCTCCCCACCTCTTC	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.2502-1185_2502-118 others(26): Show c.2502-1185_2502-1184insGAAGAGGTGGGGAGGAGGGGGG		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	6/8						chr19	55713774
chr19:55720467	C C	T T	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.2159+3513G>A c.2159+3513G>A		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	4/8						chr19	55720467
chr19:55727757	T T	G G	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.1994+2074A>C c.1994+2074A>C		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	3/8						chr19	55727757
chr19:55735423	A A	G G	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.281-1873T>C c.281-1873T>C		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	1/8						chr19	55735423
chr19:55735738	A A	C C	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.281-2188T>G c.281-2188T>G		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	1/8						chr19	55735738
chr19:55736260	A A	G G	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.280+1835T>C c.280+1835T>C		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	1/8						chr19	55736260
chr19:55736261	G G	A A	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.280+1834C>T c.280+1834C>T		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	1/8						chr19	55736261
chr19:55736861	A A	C C	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.280+1234T>G c.280+1234T>G		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	1/8						chr19	55736861
chr19:55738079	A A	G G	1	a0001c0001t0001g0001 a0001c0001t0001g0001	1	homoSapiens_chm13v2.hp1 homoSapiens_chm13v2.hp1	intron_variant	MODIFIER	c.280+16T>C c.280+16T>C		NLRP9	ENSG00000185792.10	transcript	ENST00000332836.7	protein_coding	1/8						chr19	55738079