| geneid | 100507747 |
|---|---|
| ensemblid | ENSG00000283199.3 |
| hgncid | 53786 |
| symbol | C13orf46 |
| name | chromosome 13 open reading frame 46 |
| refseq_nuc | NM_001365455.2 |
| refseq_prot | NP_001352384.1 |
| ensembl_nuc | ENST00000636427.3 |
| ensembl_prot | ENSP00000490032.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 113953705 |
| end | 113974076 |
| strand | - |
| ver | v1.2 |
| region | chr13:113953705-113974076 |
| region5000 | chr13:113948705-113979076 |
| regionname0 | C13orf46_chr13_113953705_113974076 |
| regionname5000 | C13orf46_chr13_113948705_113979076 |
| 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 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr13:113954158
|
A | G | 0.9565 | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(393): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0008a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(108): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(232): Show | 396 | 414 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | c.*2615T>C | 2615 | |||||
|
chr13:113955662
|
A | G | 0.8792 | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0008a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(95): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(212): Show | 364 | 414 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | c.*1111T>C | 1111 | |||||
|
chr13:113955994
|
A | G | 0.6570 | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(82): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(161): Show | 272 | 414 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | c.*779T>C | 779 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr13:113961341
|
C | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0008a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(113): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(241): Show | 409 | 414 | 0.9879 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | c.572+3586G>A | ||||||
|
chr13:113965237
|
A | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(89): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(171): Show | 285 | 414 | 0.6884 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.505-243T>C | ||||||
|
chr13:113965746
|
G | GTGA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | a0001c0001t0001g0063a0001c0001t0002g0004a0001c0001t0002g0010others(162): Show | 275 | 414 | 0.6643 | 3 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.505-755_505-753dupTCA | ||||||
|
chr13:113965758
|
A | ATGG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(85): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(160): Show | 271 | 414 | 0.6546 | 3 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.505-767_505-765dupCCA | ||||||
|
chr13:113965842
|
ATGATGGT others(8): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0002a0001c0001t0010a0001c0001t0018others(13): Show | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0039others(23): Show | 44 | 414 | 0.1063 | -15 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.505-863_505-849delCCACCATCACCATCA | ||||||
|
chr13:113965875
|
A | G | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0002a0001c0001t0010a0001c0001t0018others(13): Show | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0039others(23): Show | 44 | 414 | 0.1063 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.505-881T>C | ||||||
|
chr13:113965880
|
GGTGGTA | G | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0002a0001c0001t0010a0001c0001t0018others(13): Show | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0039others(23): Show | 44 | 414 | 0.1063 | -6 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.505-892_505-887delTACCAC | ||||||
|
chr13:113965922
|
A | AATG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(86): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(161): Show | 269 | 414 | 0.6498 | 3 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.505-931_505-929dupCAT | ||||||
|
chr13:113966105
|
ATGATGAT others(2): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(53): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 195 | 414 | 0.4710 | -9 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.505-1120_505-1112delCCATCATCA | ||||||
|
chr13:113966184
|
T | TGGC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(88): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(168): Show | 281 | 414 | 0.6787 | 3 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.504+1156_504+1157insGCC | ||||||
|
chr13:113967217
|
T | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(89): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(171): Show | 285 | 414 | 0.6884 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | c.504+124A>G | ||||||
|
chr13:113968015
|
G | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(89): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(171): Show | 285 | 414 | 0.6884 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | c.456+452C>G | ||||||
|
chr13:113968465
|
A | G | splice_donor_variant others(1): Show |
HIGH | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0008a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(115): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(241): Show | 406 | 414 | 0.9807 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | c.456+2T>C | ||||||
|
chr13:113968830
|
T | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(89): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(171): Show | 285 | 414 | 0.6884 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | c.243-70A>G | ||||||
|
chr13:113969452
|
C | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(89): Show | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0014others(171): Show | 285 | 414 | 0.6884 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | c.243-692G>C | ||||||
|
chr13:113971664
|
C | T | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(40): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0002a0001c0001t0010a0001c0001t0018others(12): Show | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0039others(22): Show | 43 | 414 | 0.1039 | 0 | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | c.191-1442G>A |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| C13orf46 | 1/1 | a0001 | 212 | 390 | 88 | 82 | 159 | 16 | 43 | subcellular location copy fasta | chr13 | 113948705 | 113979076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| C13orf46 | 1/1 | c0001 | 639 | 389 | 88 | 82 | 158 | 16 | 43 | copy fasta | chr13 | 113948705 | 113979076 |
| genename | grch38/chm13v2 | thapid | tlen | total | AFR | AMR | EAS | EUR | SAS | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| C13orf46 | 0/0 | t0002 | 3148 | 59 | 13 | 12 | 17 | 3 | 14 | copy fasta | chr13 | 113948705 | 113979076 |
| genename | grch38/chm13v2 | ghapid | total | AFR | AMR | EAS | EUR | SAS | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|
| C13orf46 | 0/0 | g0010 | 5 | 1 | 2 | 1 | 0 | 1 | chr13 | 113948705 | 113979076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| C13orf46 | 1/1 | a0001c0001 | 389 | 88 | 82 | 158 | 16 | 43 | 639 | copy fasta | chr13 | 113948705 | 113979076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| C13orf46 | 0/0 | a0001c0001t0002 | 58 | 12 | 12 | 17 | 3 | 14 | 3786 | copy fasta | chr13 | 113948705 | 113979076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| C13orf46 | 0/0 | a0001c0001t0002g0010 | 5 | 1 | 2 | 1 | 0 | 1 | chr13 | 113948705 | 113979076 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113973808 | - | 1 | -0.0830 | -0.0830 | -0.0829 | 0.0001 | acceptor | a0001c0001t0002g0010 | HG02080.hp2 HG02647.hp1 |
HG00639.hp1 | C13orf46 | chr13 | 113948705 | 113979076 |
| 113970171 | - | 2 | -0.9884 | -0.9884 | -0.9884 | 0.0000 | acceptor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113970222 | - | 2 | 0.9909 | 0.9909 | 0.9909 | 0.0000 | donor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113968595 | - | 3 | -0.5494 | -0.5494 | -0.5494 | 0.0000 | acceptor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113968760 | - | 3 | 0.6891 | 0.6891 | 0.6891 | 0.0000 | donor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113968467 | - | 4 | -0.1840 | -0.1840 | -0.1840 | 0.0000 | acceptor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113968514 | - | 4 | 0.5309 | 0.5309 | 0.5309 | 0.0000 | donor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113967341 | - | 5 | -0.3217 | -0.3217 | -0.3217 | 0.0000 | acceptor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113967388 | - | 5 | 0.3023 | 0.3023 | 0.3023 | 0.0000 | donor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113964927 | - | 6 | -0.9968 | -0.9968 | -0.9968 | 0.0000 | acceptor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113964994 | - | 6 | 0.9935 | 0.9935 | 0.9935 | 0.0000 | donor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02647.hp1 HG02738.hp2 |
C13orf46 | chr13 | 113948705 | 113979076 |
| 113956839 | - | 7 | 0.8508 | 0.8508 | 0.8504 | 0.0004 | donor | a0001c0001t0002g0010 | HG00639.hp1 HG01361.hp1 HG02080.hp2 HG02738.hp2 |
HG02647.hp1 | C13orf46 | chr13 | 113948705 | 113979076 |
| 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 |
|---|
| 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 |
|---|
