| geneid | 29974 |
|---|---|
| ensemblid | ENSG00000148584.16 |
| hgncid | 24086 |
| symbol | A1CF |
| name | APOBEC1 complementation factor |
| refseq_nuc | NM_014576.4 |
| refseq_prot | NP_055391.2 |
| ensembl_nuc | ENST00000373997.8 |
| ensembl_prot | ENSP00000363109.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 50799409 |
| end | 50885627 |
| strand | - |
| ver | v1.2 |
| region | chr10:50799409-50885627 |
| region5000 | chr10:50794409-50890627 |
| regionname0 | A1CF_chr10_50799409_50885627 |
| regionname5000 | A1CF_chr10_50794409_50890627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr10:50813938
|
G | A | 0.1124 | synonymous_variant | LOW | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
a0001 | a0001c0002a0001c0009a0001c0012 | a0001c0002t0004a0001c0002t0013a0001c0009t0004others(1): Show | a0001c0002t0004g0002a0001c0002t0004g0019a0001c0002t0004g0036others(30): Show | 38 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/13 | c.1242C>T | p.Leu414Leu | 1382/9221 | 1242/1761 | 414/586 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr10:50799874
|
A | G | 0.1598 | 3_prime_UTR_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(51): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0008others(4): Show | a0001c0001t0016a0001c0001t0017a0001c0002t0004others(9): Show | a0001c0001t0016g0040a0001c0001t0016g0041a0001c0001t0017g0266others(45): Show | 54 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | c.*6855T>C | 6855 | |||||
|
chr10:50800083
|
T | G | 0.8491 | 3_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(241): Show | 287 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | c.*6646A>C | 6646 | |||||
|
chr10:50800699
|
G | A | 0.9970 | 3_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(283): Show | 337 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | c.*6030C>T | 6030 | |||||
|
chr10:50800797
|
G | A | 0.8491 | 3_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(241): Show | 287 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | c.*5932C>T | 5932 | |||||
|
chr10:50802043
|
A | G | 0.1183 | 3_prime_UTR_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(37): Show |
a0001 | a0001c0001a0001c0002a0001c0009others(1): Show | a0001c0001t0016a0001c0002t0004a0001c0002t0013others(2): Show | a0001c0001t0016g0040a0001c0001t0016g0041a0001c0002t0004g0002others(32): Show | 40 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | c.*4686T>C | 4686 | |||||
|
chr10:50802069
|
C | A | 0.8491 | 3_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(241): Show | 287 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | c.*4660G>T | 4660 | |||||
|
chr10:50804661
|
G | A | 0.8284 | 3_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 280 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | c.*2068C>T | 2068 | |||||
|
chr10:50805008
|
G | A | 0.1095 | 3_prime_UTR_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
a0001 | a0001c0002a0001c0009 | a0001c0002t0004a0001c0002t0013a0001c0009t0004 | a0001c0002t0004g0002a0001c0002t0004g0019a0001c0002t0004g0036others(29): Show | 37 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | c.*1721C>T | 1721 | |||||
|
chr10:50806180
|
A | C | 0.8343 | 3_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(237): Show | 282 | 338 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | c.*549T>G | 549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr10:50807215
|
G | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(255): Show | 303 | 338 | 0.8965 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | c.1610-335C>A | ||||||
|
chr10:50808105
|
A | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(243): Show | 289 | 338 | 0.8550 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | c.1610-1225T>C | ||||||
|
chr10:50808856
|
T | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(241): Show | 287 | 338 | 0.8491 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | c.1609+1038A>G | ||||||
|
chr10:50810457
|
A | G | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
a0001 | a0001c0002a0001c0009 | a0001c0002t0004a0001c0002t0013a0001c0009t0004 | a0001c0002t0004g0002a0001c0002t0004g0019a0001c0002t0004g0036others(29): Show | 37 | 338 | 0.1095 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | c.1461-415T>C | ||||||
|
chr10:50811287
|
C | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(283): Show | 337 | 338 | 0.9970 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | c.1324-111G>A | ||||||
|
chr10:50811742
|
C | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(255): Show | 303 | 338 | 0.8965 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | c.1324-566G>C | ||||||
|
chr10:50812749
|
C | T | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
a0001 | a0001c0002a0001c0009 | a0001c0002t0004a0001c0002t0013a0001c0009t0004 | a0001c0002t0004g0002a0001c0002t0004g0019a0001c0002t0004g0036others(29): Show | 37 | 338 | 0.1095 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | c.1323+1108G>A | ||||||
|
chr10:50816308
|
G | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(244): Show | 292 | 338 | 0.8639 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | c.868-29C>T | ||||||
|
chr10:50816670
|
A | G | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
a0001 | a0001c0001a0001c0002a0001c0009others(1): Show | a0001c0001t0005a0001c0001t0016a0001c0002t0004others(3): Show | a0001c0001t0005g0010a0001c0001t0016g0040a0001c0001t0016g0041others(33): Show | 43 | 338 | 0.1272 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | c.868-391T>C | ||||||
|
chr10:50818518
|
C | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(274): Show | 327 | 338 | 0.9675 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | c.867+2034G>A | ||||||
|
chr10:50821541
|
A | AT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(127): Show | 149 | 338 | 0.4408 | 1 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | c.770-893dupA | ||||||
|
chr10:50826860
|
T | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 330 | 338 | 0.9763 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | c.769+1271A>G | ||||||
|
chr10:50832494
|
C | T | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG01109.hp2 others(33): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(4): Show | a0001c0001t0001g0074a0001c0001t0005g0251a0001c0001t0005g0253others(29): Show | 36 | 338 | 0.1065 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | c.604+3580G>A | ||||||
|
chr10:50840035
|
T | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(277): Show | 331 | 338 | 0.9793 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | c.365+1827A>G | ||||||
|
chr10:50840276
|
A | AT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(111): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(97): Show | 114 | 338 | 0.3373 | 1 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | c.365+1585dupA | ||||||
|
chr10:50843482
|
T | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(124): Show | 145 | 338 | 0.4290 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | c.234+506A>G | ||||||
|
chr10:50844563
|
A | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(281): Show | 335 | 338 | 0.9911 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.100-441T>G | ||||||
|
chr10:50845953
|
C | CA | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(84): Show | 97 | 338 | 0.2870 | 1 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.100-1832dupT | ||||||
|
chr10:50846728
|
A | G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(82): Show | 98 | 338 | 0.2899 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.100-2606T>C | ||||||
|
chr10:50848897
|
A | G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(123): Show | 144 | 338 | 0.4260 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.100-4775T>C | ||||||
|
chr10:50849786
|
C | CT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(166): Show | 204 | 338 | 0.6036 | 1 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.100-5665dupA | ||||||
|
chr10:50853275
|
C | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(281): Show | 335 | 338 | 0.9911 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.99+6567G>A | ||||||
|
chr10:50853750
|
AT | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(159): Show | 188 | 338 | 0.5562 | -1 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.99+6091delA | ||||||
|
chr10:50853804
|
A | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(252): Show | 302 | 338 | 0.8935 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.99+6038T>A | ||||||
|
chr10:50856463
|
C | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(114): Show | 134 | 338 | 0.3965 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.99+3379G>A | ||||||
|
chr10:50856509
|
G | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(111): Show | 131 | 338 | 0.3876 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.99+3333C>A | ||||||
|
chr10:50857237
|
G | A | intron_variant | MODIFIER | HG03225.hp2 NA20905.hp2 |
a0001 | a0001c0002a0001c0012 | a0001c0002t0004a0001c0012t0034 | a0001c0002t0004g0087a0001c0012t0034g0154 | 2 | 338 | 0.0059 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | c.99+2605C>T | ||||||
|
chr10:50860705
|
G | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(265): Show | 318 | 338 | 0.9408 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | c.-45-720C>T | ||||||
|
chr10:50861856
|
A | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(274): Show | 328 | 338 | 0.9704 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | c.-45-1871T>C | ||||||
|
chr10:50866087
|
C | T | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG01109.hp2 others(32): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(4): Show | a0001c0001t0001g0074a0001c0001t0005g0251a0001c0001t0005g0253others(28): Show | 35 | 338 | 0.1036 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-93-2007G>A | ||||||
|
chr10:50870968
|
T | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(277): Show | 331 | 338 | 0.9793 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-93-6888A>T | ||||||
|
chr10:50871981
|
A | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(281): Show | 335 | 338 | 0.9911 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-93-7901T>A | ||||||
|
chr10:50873248
|
G | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(37): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(241): Show | 291 | 338 | 0.8610 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-93-9168C>A | ||||||
|
chr10:50878165
|
A | G | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(43): Show | 58 | 338 | 0.1716 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+7416T>C | ||||||
|
chr10:50879173
|
T | G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(278): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(236): Show | 281 | 338 | 0.8314 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+6408A>C | ||||||
|
chr10:50879236
|
T | C | intron_variant | MODIFIER | HG02738.hp2 NA20905.hp2 |
a0001 | a0001c0002 | a0001c0002t0004a0001c0002t0013 | a0001c0002t0004g0087a0001c0002t0013g0088 | 2 | 338 | 0.0059 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+6345A>G | ||||||
|
chr10:50879897
|
G | C | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(45): Show | 60 | 338 | 0.1775 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+5684C>G | ||||||
|
chr10:50880116
|
C | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(283): Show | 337 | 338 | 0.9970 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+5465G>A | ||||||
|
chr10:50881804
|
T | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(267): Show | 321 | 338 | 0.9497 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+3777A>G | ||||||
|
chr10:50882028
|
T | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(267): Show | 321 | 338 | 0.9497 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+3553A>C | ||||||
|
chr10:50882624
|
A | G | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(43): Show | 58 | 338 | 0.1716 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+2957T>C | ||||||
|
chr10:50883419
|
C | T | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(45): Show | 60 | 338 | 0.1775 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+2162G>A | ||||||
|
chr10:50884062
|
A | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 326 | 338 | 0.9645 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+1519T>C | ||||||
|
chr10:50884324
|
G | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 326 | 338 | 0.9645 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+1257C>T | ||||||
|
chr10:50884559
|
A | T | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(45): Show | 60 | 338 | 0.1775 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+1022T>A | ||||||
|
chr10:50884716
|
T | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 326 | 338 | 0.9645 | 0 | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | c.-94+865A>G |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| A1CF | 1/1 | a0001 | 586 | 325 | 77 | 49 | 145 | 12 | 40 | subcellular location copy fasta | chr10 | 50794409 | 50890627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| A1CF | 0/0 | c0002 | 1761 | 35 | 10 | 1 | 19 | 0 | 5 | copy fasta | chr10 | 50794409 | 50890627 |
| genename | grch38/chm13v2 | thapid | tlen | total | AFR | AMR | EAS | EUR | SAS | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| A1CF | 0/0 | t0004 | 7461 | 35 | 12 | 1 | 19 | 0 | 3 | copy fasta | chr10 | 50794409 | 50890627 |
| genename | grch38/chm13v2 | ghapid | total | AFR | AMR | EAS | EUR | SAS | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|
| A1CF | 0/0 | g0087 | 1 | 0 | 0 | 0 | 0 | 1 | chr10 | 50794409 | 50890627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| A1CF | 0/0 | a0001c0002 | 35 | 10 | 1 | 19 | 0 | 5 | 1761 | copy fasta | chr10 | 50794409 | 50890627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| A1CF | 0/0 | a0001c0002t0004 | 33 | 10 | 1 | 19 | 0 | 3 | 9221 | copy fasta | chr10 | 50794409 | 50890627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| A1CF | 0/0 | a0001c0002t0004g0087 | 1 | 0 | 0 | 0 | 0 | 1 | chr10 | 50794409 | 50890627 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 50864033 | - | 2 | -0.2386 | -0.2386 | -0.2386 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50864080 | - | 2 | 0.3885 | 0.3885 | 0.3885 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50859842 | - | 3 | -0.7501 | -0.7501 | -0.7501 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50859985 | - | 3 | 0.8116 | 0.8116 | 0.8116 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50843988 | - | 4 | -0.9973 | -0.9973 | -0.9973 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50844122 | - | 4 | 0.9885 | 0.9885 | 0.9885 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50841862 | - | 5 | -0.9955 | -0.9955 | -0.9955 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50841992 | - | 5 | 0.9926 | 0.9926 | 0.9926 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50836074 | - | 6 | -0.9694 | -0.9694 | -0.9694 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50836312 | - | 6 | 0.9282 | 0.9282 | 0.9282 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50828131 | - | 7 | -0.9959 | -0.9959 | -0.9959 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50828295 | - | 7 | 0.9735 | 0.9735 | 0.9735 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50820552 | - | 8 | -0.9951 | -0.9950 | -0.9951 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50820649 | - | 8 | 0.9932 | 0.9932 | 0.9932 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50816006 | - | 9 | -0.6994 | -0.6994 | -0.6994 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50816279 | - | 9 | 0.7920 | 0.7920 | 0.7920 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50813857 | - | 10 | -0.7176 | -0.7176 | -0.7176 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50814038 | - | 10 | 0.5549 | 0.5549 | 0.5549 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50811040 | - | 11 | -0.8908 | -0.8908 | -0.8908 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50811176 | - | 11 | 0.7929 | 0.7929 | 0.7929 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50809894 | - | 12 | -0.9811 | -0.9811 | -0.9811 | 0.0000 | acceptor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50810042 | - | 12 | 0.9799 | 0.9798 | 0.9799 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 50806880 | - | 13 | 0.9093 | 0.9093 | 0.9093 | 0.0000 | donor | a0001c0002t0004g0087 | NA20905.hp2 | NA20905.hp2 | A1CF | chr10 | 50794409 | 50890627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr10:50808856
|
c.1609+1038A>G | Urate levels in lean individuals0.08 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0003a0001c0005a0001c0007others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0007a0001c0001t0009others(40): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0021others(239): Show | HG00140.hp1 HG00140.hp2 HG00280.hp1 HG00280.hp2 HG00423.hp1 others(282): Show |
Modulation of genetic associations with serum urat others(38): Show |
up to 5,529 European ancestry male individuals, up others(47): Show |
ASAH2B, A1CF | ASAH2B, A1CF | rs4256922-C | - | MODIFIER | chr10 | T | C |
|
chr10:50879173
|
c.-94+6408A>C | Cognitive function0.58 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0003a0001c0005a0001c0009others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0007others(34): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(234): Show | HG00140.hp2 HG00280.hp1 HG00280.hp2 HG00423.hp2 HG00438.hp1 others(276): Show |
Genome-wide association study of population-standa others(75): Show |
2,211 Sub-Saharan African ancestry individuals/ | A1CF | rs6479768-G | - | MODIFIER | chr10 | T | G | |
|
chr10:50889433
|
c.-3946A>G | Colorectal cancer0.173862 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0003a0001c0005a0001c0011others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0007others(25): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0021others(184): Show | HG00140.hp1 HG00140.hp2 HG00280.hp1 HG00423.hp1 HG00423.hp2 others(221): Show |
New role of fat-free mass in cancer risk linked wi others(26): Show |
4,988 European ancestry cases, 310,272 European an others(16): Show |
A1CF - MIX23P2 | rs10761587-C | - | MODIFIER | chr10 | T | C | |
|
chr10:50878165
|
c.-94+7416T>C | Random glucose levels0.002197784 | a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0007a0001c0001t0012others(9): Show | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0074others(41): Show | HG00140.hp1 HG00423.hp1 HG00423.hp2 HG00597.hp2 HG00735.hp1 others(53): Show |
GWAS of random glucose in 476,326 individuals prov others(87): Show |
7,644 African ancestry individuals, 1,503 Chinese others(106): Show |
A1CF | rs61856594-A | - | MODIFIER | chr10 | A | G | |
|
chr10:50878165
|
c.-94+7416T>C | Random glucose levels0.0022 | a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0007a0001c0001t0012others(9): Show | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0074others(41): Show | HG00140.hp1 HG00423.hp1 HG00423.hp2 HG00597.hp2 HG00735.hp1 others(53): Show |
GWAS of random glucose in 476,326 individuals prov others(87): Show |
458,862 European ancestry individuals/ | A1CF | rs61856594-A | - | MODIFIER | chr10 | A | G | |
|
chr10:50883419
|
c.-94+2162G>A | Height0.0078 | a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0007a0001c0001t0012others(10): Show | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0074others(43): Show | HG00140.hp1 HG00423.hp1 HG00423.hp2 HG00597.hp2 HG00735.hp1 others(55): Show |
A saturated map of common genetic variants associa others(22): Show |
5,314,291 European ancestry, Hispanic or Latin Ame others(79): Show |
A1CF | rs12244405-T | - | MODIFIER | chr10 | C | T | |
|
chr10:50882624
|
c.-94+2957T>C | Colorectal cancer0.0596 | a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0007a0001c0001t0012others(9): Show | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0074others(41): Show | HG00140.hp1 HG00423.hp1 HG00423.hp2 HG00597.hp2 HG00735.hp1 others(53): Show |
Developing an optimal stratification model for col others(98): Show |
15,714 European ancestry cases, 621,182 European a others(88): Show |
A1CF | rs17500846-A | - | MODIFIER | chr10 | A | G |