Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 283820 |
|---|---|
| ensemblid | ENSG00000185164.15 |
| hgncid | 22652 |
| symbol | NOMO2 |
| name | NODAL modulator 2 |
| refseq_nuc | NM_173614.4 |
| refseq_prot | NP_775885.1 |
| ensembl_nuc | ENST00000622306.5 |
| ensembl_prot | ENSP00000478653.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 18499927 |
| end | 18562097 |
| strand | - |
| ver | v1.2 |
| region | chr16:18499927-18562097 |
| region5000 | chr16:18494927-18567097 |
| regionname0 | NOMO2_chr16_18499927_18562097 |
| regionname5000 | NOMO2_chr16_18494927_18567097 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: 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 | 0/0 | 1222 | 11 | 1 | 1 | 1 | 0 | 8 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0002 | 0/0 | 1222 | 4 | 0 | 1 | 1 | 0 | 2 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0003 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: 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 | 0/0 | 3669 | 9 | 1 | 1 | 1 | 0 | 6 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| c0002 | 0/0 | 3669 | 4 | 0 | 1 | 1 | 0 | 2 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| c0003 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| c0004 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| c0005 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: 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 | 0/0 | 567 | 14 | 1 | 2 | 1 | 0 | 10 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| t0002 | 0/0 | 567 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| t0003 | 0/0 | 567 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: 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 | 0/0 | 3669 | 9 | 1 | 1 | 1 | 0 | 6 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0001c0003 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0001c0005 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0002c0002 | 0/0 | 3669 | 4 | 0 | 1 | 1 | 0 | 2 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0003c0004 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4235 | 8 | 0 | 1 | 1 | 0 | 6 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0001c0001t0002 | 0/0 | 4235 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0001c0003t0001 | 0/0 | 4235 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0001c0005t0001 | 0/0 | 4235 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0002c0002t0001 | 0/0 | 4235 | 3 | 0 | 1 | 0 | 0 | 2 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0002c0002t0003 | 0/0 | 4235 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| a0003c0004t0001 | 0/0 | 4235 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | copy fasta | chr16 | 18494927 | 18567097 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0001c0005t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0002c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0002c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| a0003c0004t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG02451 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | ACB | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG02683 | hp1 | a0001 | c0005 | t0001 | g0009 | SAS | PJL | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0011 | SAS | PJL | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| NA19001 | hp1 | a0002 | c0002 | t0003 | g0013 | EAS | JPT | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NOMO2_chr16_18494927_18567097 | NOMO2 | chr16 | 18494927 | 18567097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:18517230
|
G | A | 1 | a0002 | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
missense_variant | MODERATE | c.2716C>T | p.Leu906Phe | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 23/31 | 2773/4235 | 2716/3669 | 906/1222 | chr16 | 18517230 | ||
| chr16:18531526
|
C | T | 2 | a0002a0003 | 5 | HG01167.hp2 HG02451.hp2 HG03492.hp1 others(2): Show |
missense_variant | MODERATE | c.1477G>A | p.Val493Met | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 13/31 | 1534/4235 | 1477/3669 | 493/1222 | chr16 | 18531526 | ||
| chr16:18531535
|
C | T | 2 | a0002a0003 | 5 | HG01167.hp2 HG02451.hp2 HG03492.hp1 others(2): Show |
missense_variant | MODERATE | c.1468G>A | p.Asp490Asn | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 13/31 | 1525/4235 | 1468/3669 | 490/1222 | chr16 | 18531535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:18501009
|
G | A | 1 | a0001c0005 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.3519C>T | p.Ala1173Ala | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 30/31 | 3576/4235 | 3519/3669 | 1173/1222 | chr16 | 18501009 | ||
| chr16:18519629
|
G | A | 1 | a0003c0004 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.2388C>T | p.His796His | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 21/31 | 2445/4235 | 2388/3669 | 796/1222 | chr16 | 18519629 | ||
| chr16:18538561
|
C | T | 1 | a0001c0003 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.1185G>A | p.Pro395Pro | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/31 | 1242/4235 | 1185/3669 | 395/1222 | chr16 | 18538561 | ||
| chr16:18543656
|
C | G | 1 | a0001c0003 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.696G>C | p.Gly232Gly | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 7/31 | 753/4235 | 696/3669 | 232/1222 | chr16 | 18543656 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:18500061
|
C | G | 1 | a0001c0001t0002 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*375G>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 31/31 | 375 | chr16 | 18500061 | |||||
| chr16:18500079
|
A | G | 1 | a0002c0002t0003 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 31/31 | 357 | chr16 | 18500079 | |||||
| chr16:18500405
|
C | T | 1 | a0001c0001t0002 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 31/31 | 31 | chr16 | 18500405 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:18501640
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3445-557C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 29/30 | chr16 | 18501640 | ||||||
| chr16:18502797
|
G | C | 1 | a0002c0002t0003g0013 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3445-1714C>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 29/30 | chr16 | 18502797 | ||||||
| chr16:18503964
|
T | G | 1 | a0001c0005t0001g0009 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3445-2881A>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 29/30 | chr16 | 18503964 | ||||||
| chr16:18504172
|
G | A | 4 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.3444+2701C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 29/30 | chr16 | 18504172 | ||||||
| chr16:18505004
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3444+1869T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 29/30 | chr16 | 18505004 | ||||||
| chr16:18505080
|
G | C | 3 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0003g0013 | 3 | HG01167.hp2 HG03688.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.3444+1793C>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 29/30 | chr16 | 18505080 | ||||||
| chr16:18509323
|
C | T | 4 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.3223-56G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 27/30 | chr16 | 18509323 | ||||||
| chr16:18511724
|
G | A | 1 | a0001c0005t0001g0009 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3112-68C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 26/30 | chr16 | 18511724 | ||||||
| chr16:18512658
|
G | A | 4 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.3111+692C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 26/30 | chr16 | 18512658 | ||||||
| chr16:18513115
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0010 | 2 | HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3111+235A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 26/30 | chr16 | 18513115 | ||||||
| chr16:18514093
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3027+249G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 25/30 | chr16 | 18514093 | ||||||
| chr16:18518174
|
A | G | 1 | a0002c0002t0001g0002 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2644-872T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 22/30 | chr16 | 18518174 | ||||||
| chr16:18518204
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG01167.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2644-902A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 22/30 | chr16 | 18518204 | ||||||
| chr16:18518724
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2643+505C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 22/30 | chr16 | 18518724 | ||||||
| chr16:18520695
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2274-16A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 19/30 | chr16 | 18520695 | ||||||
| chr16:18521252
|
T | C | 4 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2055-269A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 18/30 | chr16 | 18521252 | ||||||
| chr16:18521835
|
C | T | 5 | a0001c0001t0001g0001a0002c0002t0001g0002a0002c0002t0001g0014others(2): Show | 5 | HG01167.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2055-852G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 18/30 | chr16 | 18521835 | ||||||
| chr16:18521913
|
G | C | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2055-930C>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 18/30 | chr16 | 18521913 | ||||||
| chr16:18522503
|
C | T | 3 | a0002c0002t0001g0002a0002c0002t0001g0016a0002c0002t0003g0013 | 3 | HG03492.hp1 HG03688.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.2054+1341G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 18/30 | chr16 | 18522503 | ||||||
| chr16:18522609
|
A | G | 4 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2054+1235T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 18/30 | chr16 | 18522609 | ||||||
| chr16:18523254
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2054+590T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 18/30 | chr16 | 18523254 | ||||||
| chr16:18527105
|
T | A | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1894+432A>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 16/30 | chr16 | 18527105 | ||||||
| chr16:18528843
|
C | T | 1 | a0003c0004t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1806+658G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18528843 | ||||||
| chr16:18528861
|
G | A | 1 | a0002c0002t0001g0014 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1806+640C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18528861 | ||||||
| chr16:18528925
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0015others(2): Show | 5 | HG02451.hp2 HG02683.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1806+576C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18528925 | ||||||
| chr16:18528987
|
AAATACAT others(6): Show |
A | 2 | a0001c0001t0001g0006a0001c0001t0001g0012 | 2 | HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1806+501_1806+513d others(15): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18528987 | ||||||
| chr16:18528987
|
AAATACAT others(8): Show |
A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(1): Show | 4 | HG01167.hp1 HG02683.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806+499_1806+513d others(17): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18528987 | ||||||
| chr16:18528987
|
AAATACAT others(30): Show |
A | 4 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0003t0001g0011others(1): Show | 4 | HG02451.hp2 HG02683.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806+477_1806+513d others(39): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18528987 | ||||||
| chr16:18528992
|
CATATATA others(5): Show |
C | 3 | a0001c0001t0002g0007a0002c0002t0001g0002a0002c0002t0003g0013 | 3 | HG02451.hp1 HG03688.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1806+497_1806+508d others(14): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18528992 | ||||||
| chr16:18528992
|
CATATATA others(7): Show |
C | 3 | a0001c0001t0001g0001a0002c0002t0001g0014a0002c0002t0001g0016 | 3 | HG01167.hp2 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1806+495_1806+508d others(16): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18528992 | ||||||
| chr16:18529004
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0012 | 2 | HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1806+497A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18529004 | ||||||
| chr16:18529006
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(1): Show | 4 | HG01167.hp1 HG02683.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806+495A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18529006 | ||||||
| chr16:18529028
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0003t0001g0011others(1): Show | 4 | HG02451.hp2 HG02683.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806+473A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18529028 | ||||||
| chr16:18529071
|
G | A | 1 | a0001c0005t0001g0009 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1806+430C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18529071 | ||||||
| chr16:18529189
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1806+312A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 15/30 | chr16 | 18529189 | ||||||
| chr16:18529968
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1670-331C>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 14/30 | chr16 | 18529968 | ||||||
| chr16:18531416
|
T | C | 1 | a0003c0004t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1537+50A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 13/30 | chr16 | 18531416 | ||||||
| chr16:18532175
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1396-568G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 12/30 | chr16 | 18532175 | ||||||
| chr16:18532431
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1395+574G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 12/30 | chr16 | 18532431 | ||||||
| chr16:18532891
|
A | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1395+114T>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 12/30 | chr16 | 18532891 | ||||||
| chr16:18533449
|
G | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0002g0007others(4): Show | 7 | HG01167.hp2 HG02451.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1221-270C>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18533449 | ||||||
| chr16:18533839
|
G | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG01167.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1221-660C>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18533839 | ||||||
| chr16:18534352
|
AT | A | 4 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1221-1174delA | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18534352 | ||||||
| chr16:18535279
|
T | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2100A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535279 | ||||||
| chr16:18535313
|
T | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2134A>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535313 | ||||||
| chr16:18535319
|
A | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2140T>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535319 | ||||||
| chr16:18535383
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2204C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535383 | ||||||
| chr16:18535391
|
A | AT | 2 | a0001c0001t0001g0003a0001c0003t0001g0011 | 2 | HG01167.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1221-2213dupA | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535391 | ||||||
| chr16:18535404
|
A | AT | 5 | a0001c0003t0001g0011a0002c0002t0001g0002a0002c0002t0001g0014others(2): Show | 5 | HG01167.hp2 HG03239.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-2226dupA | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535404 | ||||||
| chr16:18535496
|
T | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2317A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535496 | ||||||
| chr16:18535506
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2327C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535506 | ||||||
| chr16:18535509
|
T | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2330A>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535509 | ||||||
| chr16:18535610
|
C | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2431G>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535610 | ||||||
| chr16:18535639
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2460C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535639 | ||||||
| chr16:18535669
|
C | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2490G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535669 | ||||||
| chr16:18535670
|
C | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2491G>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535670 | ||||||
| chr16:18535813
|
C | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2634G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535813 | ||||||
| chr16:18535837
|
G | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1221-2658C>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535837 | ||||||
| chr16:18535892
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+2634T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535892 | ||||||
| chr16:18535937
|
C | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+2589G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535937 | ||||||
| chr16:18535941
|
A | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+2585T>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535941 | ||||||
| chr16:18535942
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+2584T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18535942 | ||||||
| chr16:18536086
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+2440T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536086 | ||||||
| chr16:18536445
|
T | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+2081A>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536445 | ||||||
| chr16:18536541
|
T | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+1985A>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536541 | ||||||
| chr16:18536548
|
C | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+1978G>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536548 | ||||||
| chr16:18536594
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+1932T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536594 | ||||||
| chr16:18536598
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+1928C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536598 | ||||||
| chr16:18536688
|
A | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+1838T>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536688 | ||||||
| chr16:18536829
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1220+1697C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536829 | ||||||
| chr16:18536875
|
C | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+1651G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536875 | ||||||
| chr16:18536966
|
C | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+1560G>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18536966 | ||||||
| chr16:18537022
|
C | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+1504G>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18537022 | ||||||
| chr16:18537344
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0015a0003c0004t0001g0005 | 3 | HG02451.hp2 HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1220+1182G>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18537344 | ||||||
| chr16:18537394
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0003t0001g0011others(1): Show | 4 | HG02451.hp2 HG02683.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220+1132G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18537394 | ||||||
| chr16:18537637
|
G | T | 1 | a0002c0002t0001g0016 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1220+889C>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18537637 | ||||||
| chr16:18538265
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+261T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18538265 | ||||||
| chr16:18538389
|
C | CAA | 4 | a0001c0001t0001g0001a0002c0002t0001g0002a0002c0002t0001g0016others(1): Show | 4 | HG03492.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1220+135_1220+136d others(4): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 11/30 | chr16 | 18538389 | ||||||
| chr16:18538717
|
T | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1070-41A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 10/30 | chr16 | 18538717 | ||||||
| chr16:18539357
|
C | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-393G>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539357 | ||||||
| chr16:18539567
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-603T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539567 | ||||||
| chr16:18539626
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-662T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539626 | ||||||
| chr16:18539672
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-708C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539672 | ||||||
| chr16:18539681
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.964-717G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539681 | ||||||
| chr16:18539689
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-725C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539689 | ||||||
| chr16:18539710
|
C | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-746G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539710 | ||||||
| chr16:18539728
|
C | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-764G>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539728 | ||||||
| chr16:18539815
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-851T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539815 | ||||||
| chr16:18539858
|
T | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-894A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539858 | ||||||
| chr16:18539875
|
C | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-911G>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539875 | ||||||
| chr16:18539945
|
C | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-981G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539945 | ||||||
| chr16:18539952
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-988C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18539952 | ||||||
| chr16:18540263
|
C | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-1299G>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18540263 | ||||||
| chr16:18540264
|
C | T | 6 | a0001c0001t0001g0001a0001c0003t0001g0011a0002c0002t0001g0002others(3): Show | 6 | HG01167.hp2 HG03239.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-1300G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18540264 | ||||||
| chr16:18540328
|
T | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-1364A>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18540328 | ||||||
| chr16:18540408
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-1444C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18540408 | ||||||
| chr16:18540604
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.963+1568T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18540604 | ||||||
| chr16:18540690
|
G | A | 1 | a0002c0002t0001g0016 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.963+1482C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18540690 | ||||||
| chr16:18540759
|
T | C | 4 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+1413A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18540759 | ||||||
| chr16:18541135
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.963+1037C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18541135 | ||||||
| chr16:18541291
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.963+881C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18541291 | ||||||
| chr16:18541364
|
A | C | 2 | a0001c0001t0001g0001a0001c0003t0001g0011 | 2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.963+808T>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18541364 | ||||||
| chr16:18541447
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0003t0001g0011 | 3 | HG01167.hp1 HG03239.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.963+725C>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18541447 | ||||||
| chr16:18541531
|
A | G | 5 | a0001c0001t0001g0001a0002c0002t0001g0002a0002c0002t0001g0014others(2): Show | 5 | HG01167.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+641T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18541531 | ||||||
| chr16:18541763
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.963+409C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18541763 | ||||||
| chr16:18541837
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.963+335T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 9/30 | chr16 | 18541837 | ||||||
| chr16:18542399
|
C | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.874-138G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 8/30 | chr16 | 18542399 | ||||||
| chr16:18542480
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.873+114C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 8/30 | chr16 | 18542480 | ||||||
| chr16:18542860
|
C | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.736-129G>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 7/30 | chr16 | 18542860 | ||||||
| chr16:18543059
|
C | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.736-328G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 7/30 | chr16 | 18543059 | ||||||
| chr16:18543549
|
T | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.735+68A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 7/30 | chr16 | 18543549 | ||||||
| chr16:18543872
|
T | G | 2 | a0001c0001t0001g0001a0001c0003t0001g0011 | 2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.583-103A>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18543872 | ||||||
| chr16:18544140
|
T | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-371A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18544140 | ||||||
| chr16:18544395
|
C | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-626G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18544395 | ||||||
| chr16:18544666
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-897T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18544666 | ||||||
| chr16:18544691
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-922C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18544691 | ||||||
| chr16:18544836
|
G | A | 4 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-1067C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18544836 | ||||||
| chr16:18544868
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-1099C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18544868 | ||||||
| chr16:18544882
|
G | T | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-1113C>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18544882 | ||||||
| chr16:18544940
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-1171C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18544940 | ||||||
| chr16:18545026
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0015 | 2 | HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.583-1257G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18545026 | ||||||
| chr16:18545049
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG01167.hp1 HG01167.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.583-1280G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18545049 | ||||||
| chr16:18545097
|
A | AT | 5 | a0001c0001t0001g0001a0002c0002t0001g0002a0002c0002t0001g0014others(2): Show | 5 | HG01167.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.583-1329dupA | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18545097 | ||||||
| chr16:18545182
|
C | A | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-1413G>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18545182 | ||||||
| chr16:18545389
|
A | G | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-1620T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18545389 | ||||||
| chr16:18545398
|
T | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-1629A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18545398 | ||||||
| chr16:18545457
|
T | C | 1 | a0001c0003t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-1688A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18545457 | ||||||
| chr16:18545882
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0002g0007a0001c0003t0001g0011others(4): Show | 7 | HG01167.hp2 HG02451.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.582+1346T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18545882 | ||||||
| chr16:18546347
|
CTTT | C | 6 | a0001c0001t0001g0001a0001c0003t0001g0011a0002c0002t0001g0002others(3): Show | 6 | HG01167.hp2 HG03239.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+878_582+880del others(3): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18546347 | ||||||
| chr16:18546595
|
TA | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(12): Show | 15 | HG01167.hp1 HG01167.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.582+632delT | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 6/30 | chr16 | 18546595 | ||||||
| chr16:18548082
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.510-782T>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 5/30 | chr16 | 18548082 | ||||||
| chr16:18548404
|
T | A | 5 | a0001c0001t0001g0001a0002c0002t0001g0002a0002c0002t0001g0014others(2): Show | 5 | HG01167.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-1104A>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 5/30 | chr16 | 18548404 | ||||||
| chr16:18549104
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.509+417C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 5/30 | chr16 | 18549104 | ||||||
| chr16:18550116
|
C | T | 1 | a0003c0004t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-489G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 4/30 | chr16 | 18550116 | ||||||
| chr16:18550159
|
TA | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(7): Show | 10 | HG01167.hp1 HG02451.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-533delT | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 4/30 | chr16 | 18550159 | ||||||
| chr16:18552035
|
G | A | 2 | a0001c0001t0001g0010a0001c0003t0001g0011 | 2 | HG03239.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.302-496C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 3/30 | chr16 | 18552035 | ||||||
| chr16:18552469
|
G | GCA | 5 | a0001c0001t0001g0001a0002c0002t0001g0002a0002c0002t0001g0014others(2): Show | 5 | HG01167.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-932_302-931dup others(2): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 3/30 | chr16 | 18552469 | ||||||
| chr16:18552469
|
GCACA | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG01167.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.302-934_302-931del others(4): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 3/30 | chr16 | 18552469 | ||||||
| chr16:18552702
|
T | C | 5 | a0001c0001t0001g0001a0002c0002t0001g0002a0002c0002t0001g0014others(2): Show | 5 | HG01167.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-1163A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 3/30 | chr16 | 18552702 | ||||||
| chr16:18553000
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.302-1461C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 3/30 | chr16 | 18553000 | ||||||
| chr16:18553595
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.301+1212C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 3/30 | chr16 | 18553595 | ||||||
| chr16:18553695
|
C | G | 5 | a0001c0001t0001g0001a0002c0002t0001g0002a0002c0002t0001g0014others(2): Show | 5 | HG01167.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+1112G>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 3/30 | chr16 | 18553695 | ||||||
| chr16:18554630
|
G | A | 1 | a0002c0002t0001g0014 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.301+177C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 3/30 | chr16 | 18554630 | ||||||
| chr16:18556816
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.255+886A>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 2/30 | chr16 | 18556816 | ||||||
| chr16:18558037
|
C | T | 4 | a0002c0002t0001g0002a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-246G>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 1/30 | chr16 | 18558037 | ||||||
| chr16:18558071
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.166-280C>T | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 1/30 | chr16 | 18558071 | ||||||
| chr16:18558510
|
G | T | 5 | a0001c0001t0001g0001a0002c0002t0001g0002a0002c0002t0001g0014others(2): Show | 5 | HG01167.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-719C>A | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 1/30 | chr16 | 18558510 | ||||||
| chr16:18558679
|
T | G | 1 | a0002c0002t0001g0016 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.166-888A>C | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 1/30 | chr16 | 18558679 | ||||||
| chr16:18561173
|
T | TA | 4 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0003t0001g0011others(1): Show | 4 | HG02683.hp1 HG03239.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+702dupT | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 1/30 | chr16 | 18561173 | ||||||
| chr16:18561173
|
T | TAA | 4 | a0001c0001t0001g0015a0002c0002t0001g0014a0002c0002t0001g0016others(1): Show | 4 | HG01167.hp2 HG02683.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+701_165+702dup others(2): Show |
NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 1/30 | chr16 | 18561173 | ||||||
| chr16:18561195
|
A | C | 1 | a0001c0001t0001g0001 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.165+681T>G | NOMO2 | ENSG00000185164.15 | transcript | ENST00000622306.5 | protein_coding | 1/30 | chr16 | 18561195 |