| geneid | 1056 |
|---|---|
| ensemblid | ENSG00000170835.17 |
| hgncid | 1848 |
| symbol | CEL |
| name | carboxyl ester lipase |
| refseq_nuc | NM_001807.6 |
| refseq_prot | NP_001798.3 |
| ensembl_nuc | ENST00000372080.8 |
| ensembl_prot | ENSP00000361151.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 133061981 |
| end | 133071861 |
| strand | + |
| ver | v1.2 |
| region | chr9:133061981-133071861 |
| region5000 | chr9:133056981-133076861 |
| regionname0 | CEL_chr9_133061981_133071861 |
| regionname5000 | CEL_chr9_133056981_133076861 |
| chr:pos | ref | alt | af | annotation | impact | samples | AHAPIDS | ACHAPIDS | ACTHAPIDS | ACTGHAPIDS | ac | an | len | genename | geneid | featuretype | featureid | transcript_biotype | rank | hgvs_c | hgvs_p | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr9:133071337
|
CCCCCCCC others(25): Show |
C | 0.0481 | frameshift_variant | HIGH | HG01099.hp1 HG01106.hp1 HG01433.hp1 others(17): Show |
a0001a0008 | a0001c0063a0001c0065a0001c0067others(12): Show | a0001c0063t0001a0001c0065t0001a0001c0067t0001others(12): Show | a0001c0063t0001g0003a0001c0065t0001g0001a0001c0067t0001g0003others(14): Show | 20 | 416 | -32 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.1843_1874delGTGCCGCCCACGGGTGACTCCGGGGCCCCCCC | p.Val615fs | 1865/2381 | 1843/2262 | 615/753 | INFO_REALIGN_3_PRIME | |
|
chr9:133071337
|
CCCCCCCC others(58): Show |
C | 0.0120 | frameshift_variant | HIGH | HG01099.hp2 HG02055.hp2 HG02698.hp2 others(2): Show |
a0001a0008a0067 | a0001c0064a0001c0066a0008c0103others(2): Show | a0001c0064t0001a0001c0066t0003a0008c0103t0001others(2): Show | a0001c0064t0001g0003a0001c0066t0003g0001a0008c0103t0001g0006others(2): Show | 5 | 416 | -65 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.1843_1907delGTGCCGCCCACGGGTGACTCCGGGGCCCCCCCCGTGCCGCCCACGGGTGACTCCGGGGCCCCCCC | p.Val615fs | 1865/2381 | 1843/2262 | 615/753 | INFO_REALIGN_3_PRIME | |
|
chr9:133071337
|
CCCCCCCC others(91): Show |
C | 0.0024 | frameshift_variant | HIGH | NA19072.hp1 | a0008 | a0008c0098 | a0008c0098t0001 | a0008c0098t0001g0004 | 1 | 416 | -98 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.1843_1940delGTGCCGCCCACGGGTGACTCCGGGGCCCCCCCCGTGCCGCCCACGGGTGACTCCGGGGCCCCCCCCGTGCCGCCCACGGGTGACTCCGGGGCCCCCCC | p.Val615fs | 1865/2381 | 1843/2262 | 615/753 | INFO_REALIGN_3_PRIME | |
|
chr9:133071402
|
G | GC | 0.0673 | frameshift_variant | HIGH | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(25): Show |
a0001a0005a0006others(2): Show | a0001c0019a0001c0054a0001c0056others(24): Show | a0001c0019t0001a0001c0054t0001a0001c0056t0001others(24): Show | a0001c0019t0001g0001a0001c0019t0001g0003a0001c0054t0001g0056others(25): Show | 28 | 416 | 1 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.1908dupC | p.Val637fs | 1931/2381 | 1909/2262 | 637/753 | INFO_REALIGN_3_PRIME | |
|
chr9:133071435
|
G | GC | 0.0553 | frameshift_variant | HIGH | HG00544.hp1 HG00597.hp2 HG01099.hp2 others(20): Show |
a0001a0005a0006others(5): Show | a0001c0019a0001c0055a0001c0063others(19): Show | a0001c0019t0001a0001c0055t0001a0001c0063t0001others(19): Show | a0001c0019t0001g0001a0001c0019t0001g0003a0001c0055t0001g0001others(20): Show | 23 | 416 | 1 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.1941dupC | p.Val648fs | 1964/2381 | 1942/2262 | 648/753 | INFO_REALIGN_3_PRIME | |
|
chr9:133071468
|
G | GC | 0.0553 | frameshift_variant | HIGH | HG01109.hp2 HG01169.hp2 HG01175.hp1 others(20): Show |
a0001a0004a0005others(6): Show | a0001c0055a0001c0062a0001c0063others(19): Show | a0001c0055t0001a0001c0062t0001a0001c0063t0001others(19): Show | a0001c0055t0001g0001a0001c0062t0001g0007a0001c0063t0001g0003others(19): Show | 23 | 416 | 1 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.1974dupC | p.Val659fs | 1997/2381 | 1975/2262 | 659/753 | INFO_REALIGN_3_PRIME | |
|
chr9:133071501
|
G | C | 0.0096 | missense_variant | MODERATE | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
a0007a0008a0044others(1): Show | a0007c0119a0008c0109a0044c0164others(1): Show | a0007c0119t0001a0008c0109t0001a0044c0164t0001others(1): Show | a0007c0119t0001g0032a0008c0109t0001g0008a0044c0164t0001g0020others(1): Show | 4 | 416 | 0 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.1999G>C | p.Ala667Pro | 2021/2381 | 1999/2262 | 667/753 | ||
|
chr9:133071501
|
G | GC | 0.1250 | frameshift_variant | HIGH | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(49): Show |
a0001a0004a0005others(10): Show | a0001c0054a0001c0060a0001c0061others(48): Show | a0001c0054t0001a0001c0060t0001a0001c0061t0001others(48): Show | a0001c0054t0001g0056a0001c0060t0001g0001a0001c0061t0001g0006others(48): Show | 52 | 416 | 1 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.2007dupC | p.Val670fs | 2030/2381 | 2008/2262 | 670/753 | INFO_REALIGN_3_PRIME | |
|
chr9:133071533
|
G | GC | 0.4375 | frameshift_variant | HIGH | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(179): Show |
a0001a0002a0004others(26): Show | a0001c0019a0001c0020a0001c0054others(112): Show | a0001c0019t0001a0001c0020t0001a0001c0054t0001others(112): Show | a0001c0019t0001g0001a0001c0019t0001g0003a0001c0020t0001g0001others(140): Show | 182 | 416 | 1 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.2040dupC | p.Val681fs | 2063/2381 | 2041/2262 | 681/753 | INFO_REALIGN_3_PRIME | |
|
chr9:133071567
|
G | C | 0.0120 | missense_variant | MODERATE | HG00642.hp1 HG01069.hp2 HG01433.hp2 others(2): Show |
a0001a0004a0008others(2): Show | a0001c0191a0004c0233a0008c0101others(2): Show | a0001c0191t0001a0004c0233t0001a0008c0101t0001others(2): Show | a0001c0191t0001g0026a0004c0233t0001g0002a0008c0101t0001g0001others(2): Show | 5 | 416 | 0 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.2065G>C | p.Ala689Pro | 2087/2381 | 2065/2262 | 689/753 | ||
|
chr9:133071567
|
G | GC | 0.2043 | frameshift_variant | HIGH | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
a0001a0002a0004others(19): Show | a0001c0054a0001c0055a0001c0056others(60): Show | a0001c0054t0001a0001c0055t0001a0001c0056t0001others(60): Show | a0001c0054t0001g0056a0001c0055t0001g0001a0001c0056t0001g0008others(73): Show | 85 | 416 | 1 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.2073dupC | p.Val692fs | 2096/2381 | 2074/2262 | 692/753 | INFO_REALIGN_3_PRIME | |
|
chr9:133071600
|
G | GC | 0.1130 | frameshift_variant | HIGH | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
a0001a0002a0004others(11): Show | a0001c0019a0001c0055a0001c0058others(42): Show | a0001c0019t0001a0001c0055t0001a0001c0058t0001others(42): Show | a0001c0019t0001g0001a0001c0019t0001g0003a0001c0055t0001g0001others(44): Show | 47 | 416 | 1 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | c.2106dupC | p.Val703fs | 2129/2381 | 2107/2262 | 703/753 | INFO_REALIGN_3_PRIME |
| chr:pos | ref | alt | af | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | len | genename | geneid | featuretype | featureid | transcript_biotype | rank | hgvs_c | hgvs_p | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status |
|---|
| chr:pos | ref | alt | af | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | len | genename | geneid | featuretype | featureid | transcript_biotype | rank | hgvs_c | hgvs_p | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status |
|---|
| chr:pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | genename | geneid | featuretype | featureid | transcript_biotype | rank | hgvs_c | hgvs_p | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr9:133063218
|
C | T | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(71): Show |
a0001a0002a0003others(18): Show | a0001c0019a0001c0059a0001c0063others(45): Show | a0001c0019t0001a0001c0059t0001a0001c0063t0001others(45): Show | a0001c0019t0001g0003a0001c0059t0001g0003a0001c0063t0001g0003others(52): Show | 74 | 416 | 0.1779 | 0 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | c.66+1150C>T | ||||||
|
chr9:133065846
|
C | CA | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
a0001a0002a0004others(22): Show | a0001c0020a0001c0056a0001c0057others(73): Show | a0001c0020t0001a0001c0056t0001a0001c0057t0001others(73): Show | a0001c0020t0001g0043a0001c0056t0001g0008a0001c0057t0001g0008others(77): Show | 104 | 416 | 0.2500 | 1 | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | c.538+632dupA | INFO_REALIGN_3_PRIME |
| genename | 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
|
ahapid | alen | total | AFR | AMR | EAS | EUR | SAS | aseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| CEL | 0/0 | a0008 | 619 | 20 | 4 | 2 | 12 | 0 | 2 | subcellular location copy fasta | chr9 | 133056981 | 133076861 |
| genename | 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
|
chapid | clen | total | AFR | AMR | EAS | EUR | SAS | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| CEL | 0/0 | c0011 | 2231 | 5 | 2 | 0 | 3 | 0 | 0 | copy fasta | chr9 | 133056981 | 133076861 |
| genename | grch38/chm13v2 | thapid | tlen | total | AFR | AMR | EAS | EUR | SAS | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| CEL | 1/1 | t0001 | 120 | 410 | 89 | 84 | 179 | 16 | 40 | copy fasta | chr9 | 133056981 | 133076861 |
| genename | grch38/chm13v2 | ghapid | total | AFR | AMR | EAS | EUR | SAS | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|
| CEL | 0/0 | g0009 | 7 | 0 | 1 | 5 | 0 | 1 | chr9 | 133056981 | 133076861 |
| genename | 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 |
achapid | total | AFR | AMR | EAS | EUR | SAS | clen | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| CEL | 0/0 | a0008c0011 | 5 | 2 | 0 | 3 | 0 | 0 | 2231 | copy fasta | chr9 | 133056981 | 133076861 |
| genename | 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 |
acthapid | total | AFR | AMR | EAS | EUR | SAS | tlen | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| CEL | 0/0 | a0008c0011t0001 | 5 | 2 | 0 | 3 | 0 | 0 | 2350 | copy fasta | chr9 | 133056981 | 133076861 |
| genename | 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 |
actghapid | total | AFR | AMR | EAS | EUR | SAS | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|
| CEL | 0/0 | a0008c0011t0001g0009 | 1 | 0 | 0 | 1 | 0 | 0 | chr9 | 133056981 | 133076861 |
Click to load Haplotype QTL data...
| pos | S. Strand |
E# Exon Number |
max | median | min | diff | type | haplotypeid | max_hap_list | min_hap_list | symbol | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 133062068 | + | 1 | -0.1452 | -0.1452 | -0.1452 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133064404 | + | 2 | 0.9986 | 0.9986 | 0.9986 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133064554 | + | 2 | -0.9931 | -0.9931 | -0.9931 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133064640 | + | 3 | 0.9989 | 0.9989 | 0.9989 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133064762 | + | 3 | -0.9954 | -0.9954 | -0.9954 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133065040 | + | 4 | 0.9784 | 0.9784 | 0.9784 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133065237 | + | 4 | -0.9957 | -0.9957 | -0.9957 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133066530 | + | 5 | 0.9967 | 0.9967 | 0.9967 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133066660 | + | 5 | -0.8706 | -0.8706 | -0.8706 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133066838 | + | 6 | 0.9954 | 0.9953 | 0.9954 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133066945 | + | 6 | -0.9957 | -0.9957 | -0.9957 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133067088 | + | 7 | 0.9801 | 0.9800 | 0.9801 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133067205 | + | 7 | -0.9863 | -0.9862 | -0.9863 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133068672 | + | 8 | 0.9995 | 0.9995 | 0.9995 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133068858 | + | 8 | -0.9954 | -0.9954 | -0.9954 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133069056 | + | 9 | 0.9932 | 0.9932 | 0.9932 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133069259 | + | 9 | -0.9932 | -0.9932 | -0.9932 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133070461 | + | 10 | 0.9829 | 0.9829 | 0.9829 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133070658 | + | 10 | -0.9905 | -0.9905 | -0.9905 | 0.0000 | acceptor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| 133070987 | + | 11 | 0.9885 | 0.9885 | 0.9885 | 0.0000 | donor | a0008c0011t0001g0009 | HG02129.hp2 | HG02129.hp2 | CEL | chr9 | 133056981 | 133076861 |
| pos | annotationhgvs_chgvs_p | clinvarid | clnsig | geneinfo | mc | clndisdb | strand strand
|
ahapid ahapid_count
|
chapid chapid count
|
thapid thapid_count
|
ghapid ghapid_count
|
AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
impact | chr | ref | alt | external |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 133071533:splice 133071533:variant goto | c.2040dupCp.Val681fs | 3779506 | Uncertain_significance | CEL:1056 | SO:0001589 frameshift_variant |
MONDO:MONDO:0012348 MedGen:C1853297 OMIM:609812 Orphanet:552 |
+ | 29 | 115 | 115 | 143 | a0001a0002a0004a0005a0006others(24): Show | a0001c0019a0001c0020a0001c0054a0001c0055a0001c0056others(110): Show | a0001c0019t0001a0001c0020t0001a0001c0054t0001a0001c0055t0001a0001c0056t0001others(110): Show | a0001c0019t0001g0001a0001c0019t0001g0003a0001c0020t0001g0001a0001c0020t0001g0043a0001c0054t0001g0056others(138): Show | HG00280.hp2 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(177): Show |
HIGH | chr9 | G | GC | TogoVar |
| CHR:POS | annotationhgvs_chgvs_p | disease trait-log10podds or beta | AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
study | initial sample size/replication sample size | report genes | mapped gene | strongest snp risk allele | strand strand
|
impact | chr | ref | alt |
|---|
| pos | genenamehgvs_chgvs_pannotation | tissueexpression gene-log10(pval)slope Tissue name in GTEx database(the target eQTL tissue name of the GTEx database)The -log10(nominal pvalue) in GTEx databaseSlope in GTEx database (positive value:alt allele has higher gene expression) |
ahapidchapidthapidghapid ahapid_countchapid_countthapid_countghapid_count
|
AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
af allele frequency in GTEx database |
ms The number of samples with minor allele in GTEx database |
ma The number of minor allele count in GTEx database |
ver GTEx version |
vid Variant ID in GTEx database |
strand strand
|
impact | chr | ref | alt | external |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 133057735:splice 133057735:variant goto | CELupstream_gene_variantc.-4268C>T | ADAMTSL2 Thyroid 4.664 0.230 | 23515158 | a0001a0002a0003a0004a0005others(18): Show | a0001c0019a0001c0059a0001c0063a0001c0064a0001c0067others(46): Show | a0001c0019t0001a0001c0059t0001a0001c0063t0001a0001c0064t0001a0001c0067t0001others(46): Show | a0001c0019t0001g0003a0001c0059t0001g0003a0001c0063t0001g0003a0001c0064t0001g0003a0001c0067t0001g0003others(53): Show | HG00423.hp2 HG00438.hp2 HG00544.hp2 HG00741.hp1 HG01074.hp2 others(71): Show |
0.097 | 127 | 132 | 10 | chr9_133057735_C_T_b38 | + | MODIFIER | chr9 | C | T | TogoVar |
| 133063218:splice 133063218:variant goto | CELintron_variantc.66+1150C>T | ADAMTSL2 Thyroid 4.664 0.230 | 21484855 | a0001a0002a0003a0004a0005others(16): Show | a0001c0019a0001c0059a0001c0063a0001c0064a0001c0067others(43): Show | a0001c0019t0001a0001c0059t0001a0001c0063t0001a0001c0064t0001a0001c0067t0001others(43): Show | a0001c0019t0001g0003a0001c0059t0001g0003a0001c0063t0001g0003a0001c0064t0001g0003a0001c0067t0001g0003others(50): Show | HG00423.hp2 HG00438.hp2 HG00544.hp2 HG00741.hp1 HG01074.hp2 others(69): Show |
0.097 | 127 | 132 | 10 | chr9_133063218_C_T_b38 | + | MODIFIER | chr9 | C | T | TogoVar |