Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51302 |
| ensemblid | ENSG00000146233.8 |
| hgncid | 17449 |
| symbol | CYP39A1 |
| name | cytochrome P450 family 39 subfamily A member 1 |
| refseq_nuc | NM_016593.5 |
| refseq_prot | NP_057677.2 |
| ensembl_nuc | ENST00000275016.3 |
| ensembl_prot | ENSP00000275016.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 46549580 |
| end | 46652818 |
| strand | - |
| ver | v1.2 |
| region | chr6:46549580-46652818 |
| region5000 | chr6:46544580-46657818 |
| regionname0 | CYP39A1_chr6_46549580_46652818 |
| regionname5000 | CYP39A1_chr6_46544580_46657818 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 469 | 114 | 47 | 9 | 43 | 3 | 12 | 37 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(464): Show |
chr6 | 46544580 | 46657818 |
| a0002 | 1/0 | 469 | 100 | 26 | 22 | 37 | 4 | 10 | 24 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(464): Show |
chr6 | 46544580 | 46657818 |
| a0003 | 0/1 | 469 | 26 | 4 | 6 | 12 | 1 | 2 | 11 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(464): Show |
chr6 | 46544580 | 46657818 |
| a0004 | 0/0 | 469 | 23 | 0 | 1 | 20 | 0 | 2 | 16 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(464): Show |
chr6 | 46544580 | 46657818 |
| a0005 | 0/0 | 469 | 23 | 12 | 3 | 5 | 0 | 3 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(464): Show |
chr6 | 46544580 | 46657818 |
| a0006 | 0/0 | 469 | 10 | 0 | 2 | 1 | 2 | 5 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(464): Show |
chr6 | 46544580 | 46657818 |
| a0007 | 0/0 | 469 | 9 | 0 | 3 | 2 | 0 | 4 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(464): Show |
chr6 | 46544580 | 46657818 |
| a0008 | 0/0 | 469 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(464): Show |
chr6 | 46544580 | 46657818 |
| a0009 | 0/0 | 469 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(464): Show |
chr6 | 46544580 | 46657818 |
| a0010 | 0/0 | 433 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | MELIS others(428): Show |
chr6 | 46544580 | 46657818 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1407 | 114 | 47 | 9 | 43 | 3 | 12 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1402): Show |
chr6 | 46544580 | 46657818 | ||
| a0002c0002 | 1/0 | 1407 | 100 | 26 | 22 | 37 | 4 | 10 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1402): Show |
chr6 | 46544580 | 46657818 | ||
| a0003c0003 | 0/1 | 1407 | 26 | 4 | 6 | 12 | 1 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1402): Show |
chr6 | 46544580 | 46657818 | ||
| a0004c0004 | 0/0 | 1407 | 23 | 0 | 1 | 20 | 0 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1402): Show |
chr6 | 46544580 | 46657818 | ||
| a0005c0005 | 0/0 | 1407 | 23 | 12 | 3 | 5 | 0 | 3 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1402): Show |
chr6 | 46544580 | 46657818 | ||
| a0006c0006 | 0/0 | 1407 | 10 | 0 | 2 | 1 | 2 | 5 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1402): Show |
chr6 | 46544580 | 46657818 | ||
| a0007c0007 | 0/0 | 1407 | 9 | 0 | 3 | 2 | 0 | 4 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1402): Show |
chr6 | 46544580 | 46657818 | ||
| a0008c0008 | 0/0 | 1407 | 3 | 0 | 3 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1402): Show |
chr6 | 46544580 | 46657818 | ||
| a0009c0009 | 0/0 | 1407 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1402): Show |
chr6 | 46544580 | 46657818 | ||
| a0010c0010 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | ATGGA others(1294): Show |
chr6 | 46544580 | 46657818 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2432 | 104 | 38 | 9 | 43 | 3 | 11 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0001c0001t0002 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0001c0001t0003 | 0/0 | 2432 | 7 | 7 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0001c0001t0005 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0001c0001t0007 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0002c0002t0001 | 1/0 | 2432 | 56 | 5 | 16 | 21 | 3 | 10 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0002c0002t0002 | 0/0 | 2432 | 38 | 16 | 6 | 15 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0002c0002t0004 | 0/0 | 2432 | 5 | 5 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0002c0002t0006 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0003c0003t0001 | 0/0 | 2432 | 22 | 2 | 5 | 12 | 1 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0003c0003t0002 | 0/1 | 2432 | 4 | 2 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0004c0004t0001 | 0/0 | 2432 | 23 | 0 | 1 | 20 | 0 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0005c0005t0001 | 0/0 | 2432 | 21 | 11 | 3 | 5 | 0 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0005c0005t0008 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0005c0005t0009 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0006c0006t0001 | 0/0 | 2432 | 10 | 0 | 2 | 1 | 2 | 5 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0007c0007t0001 | 0/0 | 2432 | 6 | 0 | 1 | 2 | 0 | 3 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0007c0007t0002 | 0/0 | 2432 | 3 | 0 | 2 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0008c0008t0001 | 0/0 | 2432 | 2 | 0 | 2 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0008c0008t0002 | 0/0 | 2432 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0009c0009t0001 | 0/0 | 2432 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2427): Show |
chr6 | 46544580 | 46657818 |
| a0010c0010t0001 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | GCATT others(2319): Show |
chr6 | 46544580 | 46657818 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0002c0002t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0002g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0003c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0004c0004t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0008g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0005c0005t0009g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0006c0006t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0006c0006t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0006c0006t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0006c0006t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0006c0006t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0006c0006t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0006c0006t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0006c0006t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0006c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0007c0007t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0007c0007t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0007c0007t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0007c0007t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0007c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0007c0007t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0007c0007t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0007c0007t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0007c0007t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0008c0008t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0008c0008t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0008c0008t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0009c0009t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| a0010c0010t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0180 | EUR | GBR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | GBR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0279 | EUR | FIN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00408 | hp2 | a0004 | c0004 | t0001 | g0034 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00609 | hp2 | a0007 | c0007 | t0001 | g0039 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00738 | hp1 | a0007 | c0007 | t0002 | g0036 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01069 | hp2 | a0005 | c0005 | t0001 | g0283 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0218 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0205 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0200 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0201 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01175 | hp1 | a0006 | c0006 | t0001 | g0010 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01192 | hp1 | a0003 | c0003 | t0002 | g0213 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01243 | hp1 | a0005 | c0005 | t0001 | g0285 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01243 | hp2 | a0008 | c0008 | t0001 | g0029 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01255 | hp2 | a0005 | c0005 | t0001 | g0280 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01256 | hp2 | a0008 | c0008 | t0001 | g0017 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0163 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01261 | hp1 | a0006 | c0006 | t0001 | g0006 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0118 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01346 | hp2 | a0004 | c0004 | t0001 | g0044 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01433 | hp1 | a0009 | c0009 | t0001 | g0197 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01433 | hp2 | a0007 | c0007 | t0002 | g0035 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0051 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01516 | hp1 | a0006 | c0006 | t0001 | g0043 | EUR | IBS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0212 | EUR | IBS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0211 | EUR | IBS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0261 | EUR | IBS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01891 | hp2 | a0003 | c0003 | t0002 | g0255 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0048 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01975 | hp1 | a0007 | c0007 | t0001 | g0007 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0144 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02015 | hp2 | a0004 | c0004 | t0001 | g0033 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02027 | hp1 | a0004 | c0004 | t0001 | g0019 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02027 | hp2 | a0006 | c0006 | t0001 | g0005 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0257 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0226 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0305 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02056 | hp1 | a0005 | c0005 | t0001 | g0267 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02083 | hp2 | a0007 | c0007 | t0001 | g0004 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02132 | hp1 | a0004 | c0004 | t0001 | g0026 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0100 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02165 | hp1 | a0005 | c0005 | t0001 | g0192 | EAS | CDX | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | CDX | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0272 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02300 | hp2 | a0008 | c0008 | t0002 | g0016 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02451 | hp1 | a0003 | c0003 | t0002 | g0270 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02451 | hp2 | a0005 | c0005 | t0001 | g0269 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02523 | hp1 | a0005 | c0005 | t0001 | g0276 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02602 | hp1 | a0006 | c0006 | t0001 | g0025 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0199 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0207 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02622 | hp2 | a0005 | c0005 | t0001 | g0284 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02630 | hp1 | a0005 | c0005 | t0001 | g0237 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02647 | hp1 | a0005 | c0005 | t0001 | g0287 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02647 | hp2 | a0002 | c0002 | t0004 | g0304 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0166 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02683 | hp2 | a0006 | c0006 | t0001 | g0009 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02698 | hp1 | a0005 | c0005 | t0001 | g0281 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02698 | hp2 | a0006 | c0006 | t0001 | g0001 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0168 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02723 | hp2 | a0010 | c0010 | t0001 | g0178 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02738 | hp2 | a0006 | c0006 | t0001 | g0008 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02886 | hp2 | a0005 | c0005 | t0001 | g0273 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0254 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0300 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0236 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02965 | hp2 | a0005 | c0005 | t0001 | g0274 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02970 | hp2 | a0005 | c0005 | t0009 | g0302 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03017 | hp2 | a0007 | c0007 | t0001 | g0028 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03041 | hp2 | a0002 | c0002 | t0004 | g0306 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03098 | hp1 | a0005 | c0005 | t0001 | g0277 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0203 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0298 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03195 | hp1 | a0005 | c0005 | t0001 | g0286 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03239 | hp1 | a0004 | c0004 | t0001 | g0015 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0299 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03579 | hp2 | a0002 | c0002 | t0004 | g0303 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0147 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0021 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03688 | hp2 | a0007 | c0007 | t0001 | g0013 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03704 | hp1 | a0003 | c0003 | t0001 | g0217 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03834 | hp2 | a0007 | c0007 | t0002 | g0037 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03927 | hp1 | a0005 | c0005 | t0001 | g0233 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0105 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0049 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG04115 | hp1 | a0005 | c0005 | t0008 | g0301 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG04199 | hp2 | a0007 | c0007 | t0001 | g0018 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0094 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG04204 | hp2 | a0006 | c0006 | t0001 | g0011 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0102 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | CHB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18940 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18942 | hp2 | a0004 | c0004 | t0001 | g0020 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18949 | hp1 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18951 | hp2 | a0004 | c0004 | t0001 | g0024 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0222 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18968 | hp1 | a0004 | c0004 | t0001 | g0038 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18975 | hp1 | a0003 | c0003 | t0001 | g0214 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18977 | hp2 | a0004 | c0004 | t0001 | g0031 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0196 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18982 | hp1 | a0004 | c0004 | t0001 | g0041 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0219 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0216 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18994 | hp2 | a0004 | c0004 | t0001 | g0012 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18997 | hp1 | a0003 | c0003 | t0001 | g0202 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19000 | hp1 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19000 | hp2 | a0002 | c0002 | t0006 | g0109 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19002 | hp2 | a0004 | c0004 | t0001 | g0030 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19005 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19030 | hp2 | a0005 | c0005 | t0001 | g0278 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19058 | hp2 | a0004 | c0004 | t0001 | g0042 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19065 | hp1 | a0004 | c0004 | t0001 | g0032 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19068 | hp1 | a0005 | c0005 | t0001 | g0268 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0204 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0206 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19070 | hp2 | a0004 | c0004 | t0001 | g0023 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19078 | hp1 | a0004 | c0004 | t0001 | g0027 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19083 | hp2 | a0005 | c0005 | t0001 | g0266 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19086 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19090 | hp2 | a0004 | c0004 | t0001 | g0040 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0143 | AFR | ASW | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA20129 | hp2 | a0005 | c0005 | t0001 | g0282 | AFR | ASW | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0119 | EUR | TSI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA20752 | hp2 | a0006 | c0006 | t0001 | g0001 | EUR | TSI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | GIH | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0165 | SAS | GIH | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0294 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0133 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA20300 | hp2 | a0002 | c0002 | t0004 | g0307 | AFR | USA | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| NA21309 | hp2 | a0005 | c0005 | t0001 | g0256 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0002 | g0221 | REF | REF | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0209 | REF | REF | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46596080 | A | T | 5 | a0001 a0004 a0005 others(2): Show |
171 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(168): Show |
missense_variant | MODERATE | c.972T>A | p.Asn324Lys | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/12 | 1208/2432 | 972/1410 | 324/469 | chr6 | 46596080 | |||
| chr6:46625487 | A | G | 1 | a0009 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.862T>C | p.Tyr288His | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/12 | 1098/2432 | 862/1410 | 288/469 | chr6 | 46625487 | |||
| chr6:46629865 | ACTGTTGG others(1424): Show |
A | 1 | a0010 | 1 | HG02723.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.733-226_840+1097de others(1): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/12 | chr6 | 46629865 | |||||||
| chr6:46642168 | C | T | 4 | a0003 a0004 a0005 others(1): Show |
80 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(77): Show |
missense_variant | MODERATE | c.308G>A | p.Arg103His | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/12 | 544/2432 | 308/1410 | 103/469 | chr6 | 46642168 | |||
| chr6:46652515 | C | G | 4 | a0004 a0006 a0007 others(1): Show |
45 | HG00408.hp2 HG00609.hp2 HG00738.hp1 others(42): Show |
missense_variant | MODERATE | c.68G>C | p.Arg23Pro | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/12 | 304/2432 | 68/1410 | 23/469 | chr6 | 46652515 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46631035 | C | T | 1 | a0004c0004 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.768G>A | p.Thr256Thr | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/12 | 1004/2432 | 768/1410 | 256/469 | chr6 | 46631035 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46549729 | A | G | 1 | a0001c0001t0005 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 637 | chr6 | 46549729 | ||||||
| chr6:46550005 | C | T | 6 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0004 others(3): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*361G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 361 | chr6 | 46550005 | ||||||
| chr6:46550010 | A | G | 1 | a0001c0001t0003 | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*356T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 356 | chr6 | 46550010 | ||||||
| chr6:46550228 | C | A | 1 | a0002c0002t0006 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 138 | chr6 | 46550228 | ||||||
| chr6:46550341 | T | C | 1 | a0001c0001t0007 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 25 | chr6 | 46550341 | ||||||
| chr6:46652588 | T | C | 1 | a0005c0005t0008 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/12 | 6 | chr6 | 46652588 | ||||||
| chr6:46652664 | C | A | 1 | a0005c0005t0009 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/12 | 82 | chr6 | 46652664 | ||||||
| chr6:46652700 | G | C | 1 | a0002c0002t0004 | 5 | HG02055.hp2 HG02647.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-118C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/12 | 118 | chr6 | 46652700 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46550450 | A | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1339-13T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550450 | |||||||
| chr6:46550670 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1339-233G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550670 | |||||||
| chr6:46550725 | C | G | 1 | a0002c0002t0001g0198 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1339-288G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550725 | |||||||
| chr6:46550896 | T | A | 3 | a0002c0002t0001g0265 a0003c0003t0001g0200 a0008c0008t0001g0029 |
3 | HG01109.hp1 HG01243.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1339-459A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550896 | |||||||
| chr6:46550925 | C | G | 1 | a0002c0002t0001g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1339-488G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550925 | |||||||
| chr6:46550956 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1339-519T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550956 | |||||||
| chr6:46550970 | C | T | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1339-533G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550970 | |||||||
| chr6:46551001 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1339-564C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551001 | |||||||
| chr6:46551283 | GTA | G | 45 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0092 others(42): Show |
45 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.1339-848_1339-847d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551283 | |||||||
| chr6:46551284 | T | A | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1339-847A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551284 | |||||||
| chr6:46551369 | G | GAA | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1339-934_1339-933d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551369 | |||||||
| chr6:46551369 | GA | G | 7 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(4): Show |
7 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1339-933delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551369 | |||||||
| chr6:46551459 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1339-1022A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551459 | |||||||
| chr6:46551473 | C | T | 31 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(28): Show |
31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1339-1036G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551473 | |||||||
| chr6:46551489 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1339-1052A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551489 | |||||||
| chr6:46551748 | C | T | 31 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(28): Show |
31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1339-1311G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551748 | |||||||
| chr6:46551812 | T | A | 1 | a0005c0005t0001g0256 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1339-1375A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551812 | |||||||
| chr6:46552004 | T | C | 1 | a0005c0005t0001g0276 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1339-1567A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552004 | |||||||
| chr6:46552128 | A | G | 2 | a0003c0003t0001g0199 a0007c0007t0001g0013 |
2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1338+1639T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552128 | |||||||
| chr6:46552434 | A | G | 1 | a0004c0004t0001g0027 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1338+1333T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552434 | |||||||
| chr6:46552519 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1338+1248A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552519 | |||||||
| chr6:46552980 | G | A | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1338+787C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552980 | |||||||
| chr6:46553066 | C | T | 1 | a0001c0001t0003g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1338+701G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553066 | |||||||
| chr6:46553073 | C | CA | 8 | a0002c0002t0002g0107 a0002c0002t0002g0152 a0002c0002t0002g0161 others(5): Show |
8 | HG01071.hp1 HG02015.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1338+693dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553073 | |||||||
| chr6:46553073 | CA | C | 83 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0068 others(80): Show |
83 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1338+693delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553073 | |||||||
| chr6:46553093 | A | C | 3 | a0001c0001t0001g0230 a0002c0002t0001g0194 a0002c0002t0001g0198 |
3 | NA18972.hp1 NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1338+674T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553093 | |||||||
| chr6:46553096 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1338+671C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553096 | |||||||
| chr6:46553123 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1338+644G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553123 | |||||||
| chr6:46553185 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1338+582G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553185 | |||||||
| chr6:46553218 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1338+549T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553218 | |||||||
| chr6:46553309 | T | A | 1 | a0002c0002t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1338+458A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553309 | |||||||
| chr6:46553446 | T | C | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1338+321A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553446 | |||||||
| chr6:46553512 | A | T | 5 | a0002c0002t0002g0129 a0003c0003t0002g0213 a0007c0007t0002g0035 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+255T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553512 | |||||||
| chr6:46553602 | G | A | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1338+165C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553602 | |||||||
| chr6:46553639 | C | A | 1 | a0002c0002t0002g0162 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1338+128G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553639 | |||||||
| chr6:46553699 | G | A | 1 | a0002c0002t0002g0162 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1338+68C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553699 | |||||||
| chr6:46553733 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1338+34A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553733 | |||||||
| chr6:46553865 | C | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1251-11G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46553865 | |||||||
| chr6:46553983 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-129A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46553983 | |||||||
| chr6:46554240 | T | C | 1 | a0002c0002t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1251-386A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554240 | |||||||
| chr6:46554317 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-463A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554317 | |||||||
| chr6:46554369 | C | A | 3 | a0001c0001t0001g0235 a0004c0004t0001g0019 a0005c0005t0001g0192 |
3 | HG02027.hp1 HG02165.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1251-515G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554369 | |||||||
| chr6:46554442 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-588A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554442 | |||||||
| chr6:46554493 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0001g0258 a0001c0001t0001g0260 others(1): Show |
4 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-639G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554493 | |||||||
| chr6:46554519 | G | C | 1 | a0002c0002t0002g0160 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1251-665C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554519 | |||||||
| chr6:46554520 | C | A | 1 | a0002c0002t0002g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1251-666G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554520 | |||||||
| chr6:46554595 | CACAT | C | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1251-745_1251-742d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554595 | |||||||
| chr6:46554654 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1251-800G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554654 | |||||||
| chr6:46554655 | C | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-801G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554655 | |||||||
| chr6:46554801 | A | T | 1 | a0002c0002t0002g0107 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1251-947T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554801 | |||||||
| chr6:46554814 | T | C | 2 | a0004c0004t0001g0023 a0004c0004t0001g0024 |
2 | NA18951.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1251-960A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554814 | |||||||
| chr6:46554817 | A | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1251-963T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554817 | |||||||
| chr6:46554840 | A | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-986T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554840 | |||||||
| chr6:46555050 | G | GAC | 6 | a0001c0001t0001g0096 a0002c0002t0001g0173 a0002c0002t0002g0111 others(3): Show |
6 | HG02027.hp2 HG02109.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-1198_1251-119 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555050 | |||||||
| chr6:46555050 | G | GACAC | 23 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(20): Show |
23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-1200_1251-119 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555050 | |||||||
| chr6:46555050 | GAC | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(83): Show |
88 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1251-1198_1251-119 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555050 | |||||||
| chr6:46555141 | C | T | 6 | a0002c0002t0001g0051 a0002c0002t0001g0108 a0002c0002t0001g0112 others(3): Show |
6 | HG00558.hp2 HG00597.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-1287G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555141 | |||||||
| chr6:46555177 | T | C | 1 | a0002c0002t0002g0149 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1251-1323A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555177 | |||||||
| chr6:46555191 | C | T | 1 | a0002c0002t0001g0155 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1251-1337G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555191 | |||||||
| chr6:46555220 | T | C | 23 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(20): Show |
23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-1366A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555220 | |||||||
| chr6:46555260 | A | G | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-1406T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555260 | |||||||
| chr6:46555423 | C | A | 2 | a0001c0001t0003g0188 a0001c0001t0003g0190 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1251-1569G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555423 | |||||||
| chr6:46555559 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-1705A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555559 | |||||||
| chr6:46555573 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1251-1719T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555573 | |||||||
| chr6:46555845 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1251-1991G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555845 | |||||||
| chr6:46556142 | T | G | 1 | a0001c0001t0001g0259 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1251-2288A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556142 | |||||||
| chr6:46556237 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-2383C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556237 | |||||||
| chr6:46556372 | T | C | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-2518A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556372 | |||||||
| chr6:46556408 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-2554T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556408 | |||||||
| chr6:46556610 | C | A | 2 | a0002c0002t0001g0147 a0004c0004t0001g0015 |
2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1251-2756G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556610 | |||||||
| chr6:46556665 | G | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-2811C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556665 | |||||||
| chr6:46556793 | A | G | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-2939T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556793 | |||||||
| chr6:46556803 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1251-2949G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556803 | |||||||
| chr6:46556862 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0223 |
2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1251-3008G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556862 | |||||||
| chr6:46557071 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1251-3217T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557071 | |||||||
| chr6:46557245 | C | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-3391G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557245 | |||||||
| chr6:46557470 | G | A | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-3616C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557470 | |||||||
| chr6:46557603 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-3749T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557603 | |||||||
| chr6:46557643 | T | TA | 51 | a0001c0001t0001g0078 a0001c0001t0002g0238 a0002c0002t0002g0046 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1251-3790dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557643 | |||||||
| chr6:46557643 | T | TAA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-3791_1251-379 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557643 | |||||||
| chr6:46557705 | G | A | 2 | a0002c0002t0001g0080 a0002c0002t0001g0085 |
2 | HG00423.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1251-3851C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557705 | |||||||
| chr6:46557783 | AAAAATTA others(8): Show |
A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-3944_1251-393 others(19): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557783 | |||||||
| chr6:46557830 | C | T | 4 | a0001c0001t0003g0075 a0001c0001t0003g0188 a0001c0001t0003g0189 others(1): Show |
4 | HG02572.hp2 HG03540.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-3976G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557830 | |||||||
| chr6:46557933 | C | CA | 81 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(78): Show |
83 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1251-4080dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557933 | |||||||
| chr6:46557933 | C | CAA | 9 | a0001c0001t0001g0293 a0001c0001t0003g0075 a0001c0001t0003g0186 others(6): Show |
9 | HG00741.hp1 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1251-4081_1251-408 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557933 | |||||||
| chr6:46557933 | CA | C | 12 | a0001c0001t0001g0121 a0001c0001t0001g0290 a0002c0002t0001g0074 others(9): Show |
12 | HG01884.hp1 HG01975.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-4080delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557933 | |||||||
| chr6:46557959 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-4105T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557959 | |||||||
| chr6:46558076 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1251-4222G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558076 | |||||||
| chr6:46558241 | G | A | 1 | a0005c0005t0001g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1251-4387C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558241 | |||||||
| chr6:46558398 | C | T | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-4544G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558398 | |||||||
| chr6:46558402 | C | G | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1251-4548G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558402 | |||||||
| chr6:46558433 | A | T | 1 | a0010c0010t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1251-4579T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558433 | |||||||
| chr6:46558518 | C | T | 1 | a0004c0004t0001g0026 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1251-4664G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558518 | |||||||
| chr6:46558544 | A | C | 1 | a0003c0003t0001g0206 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1251-4690T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558544 | |||||||
| chr6:46558545 | T | A | 1 | a0003c0003t0001g0206 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1251-4691A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558545 | |||||||
| chr6:46558551 | A | G | 1 | a0002c0002t0002g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1251-4697T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558551 | |||||||
| chr6:46558691 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-4837A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558691 | |||||||
| chr6:46558694 | A | C | 1 | a0005c0005t0001g0269 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1251-4840T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558694 | |||||||
| chr6:46558700 | A | G | 1 | a0005c0005t0001g0269 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1251-4846T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558700 | |||||||
| chr6:46558701 | A | G | 44 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(41): Show |
46 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1251-4847T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558701 | |||||||
| chr6:46558725 | C | T | 1 | a0005c0005t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1251-4871G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558725 | |||||||
| chr6:46558804 | T | C | 1 | a0005c0005t0001g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1251-4950A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558804 | |||||||
| chr6:46558866 | C | T | 1 | a0005c0005t0001g0282 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1251-5012G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558866 | |||||||
| chr6:46558945 | G | A | 7 | a0002c0002t0002g0133 a0002c0002t0002g0191 a0002c0002t0002g0236 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-5091C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558945 | |||||||
| chr6:46558994 | C | CA | 22 | a0001c0001t0001g0058 a0001c0001t0001g0125 a0001c0001t0001g0179 others(19): Show |
22 | HG00735.hp1 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1251-5141dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558994 | |||||||
| chr6:46558994 | CA | C | 7 | a0001c0001t0001g0167 a0001c0001t0001g0288 a0001c0001t0001g0289 others(4): Show |
7 | HG00408.hp2 HG00741.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-5141delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558994 | |||||||
| chr6:46559033 | T | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1251-5179A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559033 | |||||||
| chr6:46559063 | G | A | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-5209C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559063 | |||||||
| chr6:46559103 | GAATT | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-5253_1251-525 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559103 | |||||||
| chr6:46559116 | G | A | 1 | a0003c0003t0001g0048 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1251-5262C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559116 | |||||||
| chr6:46559279 | A | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1251-5425T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559279 | |||||||
| chr6:46559354 | A | C | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1251-5500T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559354 | |||||||
| chr6:46559604 | C | T | 2 | a0002c0002t0001g0051 a0002c0002t0001g0112 |
2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1251-5750G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559604 | |||||||
| chr6:46559623 | G | A | 1 | a0010c0010t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1251-5769C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559623 | |||||||
| chr6:46559673 | C | T | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-5819G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559673 | |||||||
| chr6:46559890 | T | C | 1 | a0010c0010t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1251-6036A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559890 | |||||||
| chr6:46559967 | A | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1251-6113T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559967 | |||||||
| chr6:46560374 | A | AC | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-6521_1251-652 others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560374 | |||||||
| chr6:46560560 | T | A | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1251-6706A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560560 | |||||||
| chr6:46560614 | A | G | 1 | a0002c0002t0001g0163 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1251-6760T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560614 | |||||||
| chr6:46560778 | T | TA | 178 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(175): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1251-6925dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560778 | |||||||
| chr6:46560791 | C | T | 6 | a0004c0004t0001g0002 a0004c0004t0001g0014 a0004c0004t0001g0031 others(3): Show |
7 | NA18940.hp1 NA18968.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-6937G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560791 | |||||||
| chr6:46560807 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-6953C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560807 | |||||||
| chr6:46560847 | G | A | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-6993C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560847 | |||||||
| chr6:46561076 | A | C | 1 | a0003c0003t0002g0270 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1251-7222T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561076 | |||||||
| chr6:46561139 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-7285A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561139 | |||||||
| chr6:46561272 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-7418A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561272 | |||||||
| chr6:46561393 | G | A | 2 | a0002c0002t0001g0210 a0008c0008t0001g0017 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1251-7539C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561393 | |||||||
| chr6:46561436 | G | A | 5 | a0005c0005t0001g0282 a0005c0005t0001g0285 a0005c0005t0001g0286 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-7582C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561436 | |||||||
| chr6:46561459 | C | T | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1251-7605G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561459 | |||||||
| chr6:46561635 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1251-7781G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561635 | |||||||
| chr6:46561684 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-7830C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561684 | |||||||
| chr6:46561702 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0010c0010t0001g0178 |
3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1251-7848C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561702 | |||||||
| chr6:46561867 | G | C | 6 | a0002c0002t0001g0153 a0002c0002t0001g0158 a0002c0002t0001g0181 others(3): Show |
6 | HG00639.hp2 HG01109.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-8013C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561867 | |||||||
| chr6:46562126 | G | GA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-8273dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562126 | |||||||
| chr6:46562183 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-8329A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562183 | |||||||
| chr6:46562283 | A | G | 44 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1251-8429T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562283 | |||||||
| chr6:46562353 | C | CA | 9 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(6): Show |
9 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-8500dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562353 | |||||||
| chr6:46562377 | T | G | 1 | a0003c0003t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1251-8523A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562377 | |||||||
| chr6:46562625 | C | T | 3 | a0003c0003t0001g0201 a0003c0003t0001g0205 a0003c0003t0001g0218 |
3 | HG01071.hp1 HG01074.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1251-8771G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562625 | |||||||
| chr6:46562695 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1251-8841C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562695 | |||||||
| chr6:46562754 | C | T | 5 | a0002c0002t0002g0114 a0002c0002t0004g0304 a0002c0002t0004g0305 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-8900G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562754 | |||||||
| chr6:46562867 | T | C | 1 | a0005c0005t0001g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1251-9013A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562867 | |||||||
| chr6:46562963 | T | G | 1 | a0005c0005t0001g0276 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1251-9109A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562963 | |||||||
| chr6:46563113 | G | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-9259C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563113 | |||||||
| chr6:46563115 | C | CA | 23 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0288 others(20): Show |
23 | HG00741.hp1 HG01069.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-9262dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563115 | |||||||
| chr6:46563115 | C | CAA | 39 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(36): Show |
41 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1251-9263_1251-926 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563115 | |||||||
| chr6:46563115 | CA | C | 6 | a0001c0001t0001g0121 a0001c0001t0001g0225 a0001c0001t0002g0238 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-9262delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563115 | |||||||
| chr6:46563201 | T | C | 1 | a0003c0003t0001g0257 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1251-9347A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563201 | |||||||
| chr6:46563243 | G | C | 1 | a0007c0007t0001g0039 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1251-9389C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563243 | |||||||
| chr6:46563257 | C | T | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-9403G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563257 | |||||||
| chr6:46563439 | A | G | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-9585T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563439 | |||||||
| chr6:46563598 | T | G | 1 | a0003c0003t0001g0196 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1251-9744A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563598 | |||||||
| chr6:46563748 | G | C | 23 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(20): Show |
23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-9894C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563748 | |||||||
| chr6:46563750 | G | T | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-9896C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563750 | |||||||
| chr6:46563911 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(175): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1251-10057A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563911 | |||||||
| chr6:46564087 | GTTTTTTA others(11): Show |
G | 12 | a0001c0001t0001g0045 a0001c0001t0001g0062 a0001c0001t0001g0064 others(9): Show |
12 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-10251_1251-10 others(24): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564087 | |||||||
| chr6:46564087 | GTTTTTTA others(26): Show |
G | 9 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0116 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10266_1251-10 others(39): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564087 | |||||||
| chr6:46564088 | TTTTTTAT others(6): Show |
T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0053 others(26): Show |
31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10247_1251-10 others(19): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564088 | |||||||
| chr6:46564089 | T | A | 32 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0056 others(29): Show |
32 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1251-10235A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564089 | |||||||
| chr6:46564090 | TTTTATTT others(21): Show |
T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0288 others(1): Show |
4 | HG02723.hp2 HG02818.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-10264_1251-10 others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564090 | |||||||
| chr6:46564090 | TTTTATTT others(31): Show |
T | 26 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(23): Show |
26 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1251-10274_1251-10 others(44): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564090 | |||||||
| chr6:46564090 | TTTTATTT others(41): Show |
T | 2 | a0001c0001t0003g0187 a0001c0001t0005g0271 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-10284_1251-10 others(54): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564090 | |||||||
| chr6:46564096 | T | TTTATTTT others(248): Show |
1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-10243_1251-10 others(261): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564096 | |||||||
| chr6:46564099 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-10245C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564099 | |||||||
| chr6:46564102 | T | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0053 others(26): Show |
31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10248A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564102 | |||||||
| chr6:46564105 | T | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0053 others(26): Show |
31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10251A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564105 | |||||||
| chr6:46564107 | T | A | 12 | a0001c0001t0001g0045 a0001c0001t0001g0062 a0001c0001t0001g0064 others(9): Show |
12 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-10253A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564107 | |||||||
| chr6:46564108 | TTATTTTA others(3): Show |
T | 1 | a0002c0002t0002g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1251-10264_1251-10 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564108 | |||||||
| chr6:46564117 | TCTA | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0053 others(26): Show |
31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10266_1251-10 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564117 | |||||||
| chr6:46564118 | C | T | 13 | a0001c0001t0001g0045 a0001c0001t0001g0062 a0001c0001t0001g0064 others(10): Show |
13 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.1251-10264G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564118 | |||||||
| chr6:46564120 | ATT | A | 12 | a0001c0001t0001g0045 a0001c0001t0001g0062 a0001c0001t0001g0064 others(9): Show |
12 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-10268_1251-10 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564120 | |||||||
| chr6:46564121 | T | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0053 others(26): Show |
31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10267A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564121 | |||||||
| chr6:46564122 | T | A | 9 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0116 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10268A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564122 | |||||||
| chr6:46564127 | TC | T | 12 | a0001c0001t0001g0045 a0001c0001t0001g0062 a0001c0001t0001g0064 others(9): Show |
12 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-10274delG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564127 | |||||||
| chr6:46564128 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0052 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-10274G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564128 | |||||||
| chr6:46564130 | ATT | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0288 others(1): Show |
4 | HG02723.hp2 HG02818.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-10278_1251-10 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564130 | |||||||
| chr6:46564136 | TTC | T | 9 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0116 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10284_1251-10 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564136 | |||||||
| chr6:46564137 | TC | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0288 others(1): Show |
4 | HG02723.hp2 HG02818.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-10284delG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564137 | |||||||
| chr6:46564138 | C | CTATTCTA others(3): Show |
1 | a0001c0001t0001g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1251-10294_1251-10 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564138 | |||||||
| chr6:46564138 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(65): Show |
70 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1251-10284G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564138 | |||||||
| chr6:46564138 | CTATTCTA others(3): Show |
C | 14 | a0001c0001t0002g0238 a0002c0002t0001g0067 a0002c0002t0001g0110 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1251-10294_1251-10 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564138 | |||||||
| chr6:46564142 | TC | T | 9 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0116 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10289delG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564142 | |||||||
| chr6:46564142 | TCTA | T | 26 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(23): Show |
26 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1251-10291_1251-10 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564142 | |||||||
| chr6:46564143 | C | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(45): Show |
50 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1251-10289G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564143 | |||||||
| chr6:46564146 | T | A | 26 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(23): Show |
26 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1251-10292A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564146 | |||||||
| chr6:46564153 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-10299G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564153 | |||||||
| chr6:46564163 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-10309G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564163 | |||||||
| chr6:46564173 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-10319G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564173 | |||||||
| chr6:46564180 | ATTCTAT | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(26): Show |
30 | HG00735.hp2 HG00741.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1251-10332_1251-10 others(12): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564180 | |||||||
| chr6:46564183 | C | T | 54 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0055 others(51): Show |
55 | HG00597.hp2 HG00639.hp1 HG01884.hp2 others(52): Show |
intron_variant | MODIFIER | c.1251-10329G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564183 | |||||||
| chr6:46564185 | AT | A | 52 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0055 others(49): Show |
53 | HG00597.hp2 HG00639.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.1251-10332delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564185 | |||||||
| chr6:46564210 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-10356T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564210 | |||||||
| chr6:46564223 | C | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-10369G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564223 | |||||||
| chr6:46564260 | C | T | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-10406G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564260 | |||||||
| chr6:46564367 | T | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-10513A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564367 | |||||||
| chr6:46564377 | G | A | 44 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1251-10523C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564377 | |||||||
| chr6:46564398 | A | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-10544T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564398 | |||||||
| chr6:46564577 | C | A | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1251-10723G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564577 | |||||||
| chr6:46564727 | C | T | 9 | a0001c0001t0002g0238 a0002c0002t0002g0100 a0002c0002t0002g0102 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10873G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564727 | |||||||
| chr6:46565078 | C | T | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-11224G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565078 | |||||||
| chr6:46565087 | C | CA | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-11234dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565087 | |||||||
| chr6:46565205 | G | A | 1 | a0003c0003t0001g0196 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1251-11351C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565205 | |||||||
| chr6:46565259 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-11405G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565259 | |||||||
| chr6:46565343 | C | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-11489G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565343 | |||||||
| chr6:46565356 | A | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-11502T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565356 | |||||||
| chr6:46565417 | A | G | 1 | a0002c0002t0001g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1251-11563T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565417 | |||||||
| chr6:46565507 | GAAATAAA others(2): Show |
G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(78): Show |
83 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.1251-11662_1251-11 others(15): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565507 | |||||||
| chr6:46565511 | TAAATAAA others(3): Show |
T | 1 | a0004c0004t0001g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1251-11667_1251-11 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565511 | |||||||
| chr6:46565693 | C | G | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-11839G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565693 | |||||||
| chr6:46565709 | G | A | 1 | a0005c0005t0001g0268 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1251-11855C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565709 | |||||||
| chr6:46565805 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1251-11951C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565805 | |||||||
| chr6:46565971 | G | T | 1 | a0005c0005t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1251-12117C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565971 | |||||||
| chr6:46565988 | C | T | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1251-12134G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565988 | |||||||
| chr6:46566003 | T | G | 1 | a0002c0002t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1251-12149A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566003 | |||||||
| chr6:46566035 | C | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-12181G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566035 | |||||||
| chr6:46566166 | C | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-12312G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566166 | |||||||
| chr6:46566182 | G | C | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1251-12328C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566182 | |||||||
| chr6:46566248 | T | C | 1 | a0010c0010t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1251-12394A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566248 | |||||||
| chr6:46566530 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1251-12676C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566530 | |||||||
| chr6:46566561 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-12707G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566561 | |||||||
| chr6:46566739 | T | C | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-12885A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566739 | |||||||
| chr6:46566742 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-12888G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566742 | |||||||
| chr6:46566767 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-12913T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566767 | |||||||
| chr6:46566834 | TTA | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-12982_1251-12 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566834 | |||||||
| chr6:46566836 | A | T | 1 | a0002c0002t0001g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1251-12982T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566836 | |||||||
| chr6:46566843 | T | A | 1 | a0005c0005t0001g0276 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1251-12989A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566843 | |||||||
| chr6:46566874 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-13020T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566874 | |||||||
| chr6:46566889 | C | T | 1 | a0002c0002t0001g0174 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1251-13035G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566889 | |||||||
| chr6:46567035 | A | G | 1 | a0002c0002t0001g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1251-13181T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567035 | |||||||
| chr6:46567134 | A | G | 1 | a0002c0002t0001g0135 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1251-13280T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567134 | |||||||
| chr6:46567262 | T | C | 1 | a0002c0002t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1251-13408A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567262 | |||||||
| chr6:46567340 | A | ATG | 83 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-13487_1251-13 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567340 | |||||||
| chr6:46567606 | T | C | 1 | a0002c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1251-13752A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567606 | |||||||
| chr6:46567740 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-13886G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567740 | |||||||
| chr6:46567994 | TTTA | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(35): Show |
40 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1251-14143_1251-14 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567994 | |||||||
| chr6:46567995 | TTAA | T | 89 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(86): Show |
89 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1251-14144_1251-14 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567995 | |||||||
| chr6:46567996 | T | A | 3 | a0005c0005t0001g0273 a0005c0005t0001g0278 a0007c0007t0001g0013 |
3 | HG02886.hp2 HG03688.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1251-14142A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567996 | |||||||
| chr6:46567996 | TA | T | 44 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1251-14143delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567996 | |||||||
| chr6:46567996 | TAAA | T | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG01255.hp2 HG02572.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-14145_1251-14 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567996 | |||||||
| chr6:46567997 | A | T | 3 | a0002c0002t0001g0165 a0002c0002t0001g0166 a0004c0004t0001g0031 |
3 | HG02683.hp1 NA18977.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1251-14143T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567997 | |||||||
| chr6:46567998 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0225 |
3 | HG02976.hp1 HG03139.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1251-14144T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567998 | |||||||
| chr6:46568126 | G | C | 2 | a0002c0002t0002g0129 a0003c0003t0002g0213 |
2 | HG00735.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1251-14272C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568126 | |||||||
| chr6:46568157 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1251-14303A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568157 | |||||||
| chr6:46568215 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1251-14361A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568215 | |||||||
| chr6:46568250 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1251-14396C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568250 | |||||||
| chr6:46568500 | CT | C | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1251-14647delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568500 | |||||||
| chr6:46568678 | G | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1251-14824C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568678 | |||||||
| chr6:46568918 | G | T | 7 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0002c0002t0001g0113 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-15064C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568918 | |||||||
| chr6:46568920 | C | CA | 91 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(88): Show |
93 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1251-15067dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568920 | |||||||
| chr6:46568920 | C | CAA | 37 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(34): Show |
37 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.1251-15068_1251-15 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568920 | |||||||
| chr6:46569229 | T | C | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-15375A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569229 | |||||||
| chr6:46569266 | A | G | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-15412T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569266 | |||||||
| chr6:46569382 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-15528C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569382 | |||||||
| chr6:46569477 | A | T | 6 | a0004c0004t0001g0002 a0004c0004t0001g0014 a0004c0004t0001g0031 others(3): Show |
7 | NA18940.hp1 NA18968.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-15623T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569477 | |||||||
| chr6:46569698 | C | G | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1251-15844G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569698 | |||||||
| chr6:46569803 | T | C | 5 | a0002c0002t0001g0113 a0002c0002t0001g0169 a0002c0002t0001g0170 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-15949A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569803 | |||||||
| chr6:46569819 | G | A | 23 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(20): Show |
23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-15965C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569819 | |||||||
| chr6:46569891 | T | C | 1 | a0002c0002t0006g0109 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1251-16037A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569891 | |||||||
| chr6:46569925 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-16071C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569925 | |||||||
| chr6:46570110 | C | G | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1251-16256G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570110 | |||||||
| chr6:46570174 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-16320A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570174 | |||||||
| chr6:46570175 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-16321C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570175 | |||||||
| chr6:46570264 | T | A | 5 | a0002c0002t0002g0129 a0003c0003t0002g0213 a0007c0007t0002g0035 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-16410A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570264 | |||||||
| chr6:46570395 | C | T | 2 | a0003c0003t0001g0216 a0003c0003t0001g0222 |
2 | NA18960.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1251-16541G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570395 | |||||||
| chr6:46570424 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-16570A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570424 | |||||||
| chr6:46570666 | G | A | 1 | a0001c0001t0003g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1250+16411C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570666 | |||||||
| chr6:46570737 | T | G | 1 | a0002c0002t0001g0131 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1250+16340A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570737 | |||||||
| chr6:46570824 | C | T | 2 | a0002c0002t0002g0129 a0003c0003t0002g0213 |
2 | HG00735.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1250+16253G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570824 | |||||||
| chr6:46570907 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1250+16170G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570907 | |||||||
| chr6:46570914 | A | G | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+16163T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570914 | |||||||
| chr6:46571034 | C | T | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+16043G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571034 | |||||||
| chr6:46571045 | C | T | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+16032G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571045 | |||||||
| chr6:46571099 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1250+15978G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571099 | |||||||
| chr6:46571176 | T | C | 2 | a0002c0002t0002g0298 a0002c0002t0002g0299 |
2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1250+15901A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571176 | |||||||
| chr6:46571271 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+15806A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571271 | |||||||
| chr6:46571515 | C | A | 4 | a0001c0001t0001g0242 a0001c0001t0001g0258 a0001c0001t0001g0260 others(1): Show |
4 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250+15562G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571515 | |||||||
| chr6:46571539 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+15538A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571539 | |||||||
| chr6:46571558 | CATTT | C | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+15515_1250+15 others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571558 | |||||||
| chr6:46571662 | C | CT | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+15414dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571662 | |||||||
| chr6:46571675 | C | T | 7 | a0002c0002t0001g0074 a0002c0002t0001g0080 a0002c0002t0001g0085 others(4): Show |
7 | HG00423.hp2 HG01258.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+15402G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571675 | |||||||
| chr6:46571723 | C | T | 1 | a0003c0003t0001g0257 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1250+15354G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571723 | |||||||
| chr6:46571998 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1250+15079A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571998 | |||||||
| chr6:46572070 | T | A | 5 | a0005c0005t0001g0282 a0005c0005t0001g0285 a0005c0005t0001g0286 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1250+15007A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572070 | |||||||
| chr6:46572094 | A | G | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+14983T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572094 | |||||||
| chr6:46572115 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+14962A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572115 | |||||||
| chr6:46572187 | TA | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+14889delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572187 | |||||||
| chr6:46572241 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1250+14836T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572241 | |||||||
| chr6:46572274 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+14803A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572274 | |||||||
| chr6:46572297 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1250+14780A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572297 | |||||||
| chr6:46572717 | G | A | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+14360C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572717 | |||||||
| chr6:46572944 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+14133A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572944 | |||||||
| chr6:46573081 | G | A | 1 | a0002c0002t0002g0144 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1250+13996C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573081 | |||||||
| chr6:46573149 | A | T | 1 | a0004c0004t0001g0020 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1250+13928T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573149 | |||||||
| chr6:46573171 | G | A | 31 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(28): Show |
31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1250+13906C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573171 | |||||||
| chr6:46573339 | G | C | 1 | a0004c0004t0001g0022 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1250+13738C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573339 | |||||||
| chr6:46573364 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1250+13713A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573364 | |||||||
| chr6:46573494 | G | A | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+13583C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573494 | |||||||
| chr6:46573524 | G | T | 298 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(295): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1250+13553C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573524 | |||||||
| chr6:46573725 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+13352A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573725 | |||||||
| chr6:46574353 | C | T | 1 | a0002c0002t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1250+12724G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574353 | |||||||
| chr6:46574489 | G | A | 31 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(28): Show |
31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1250+12588C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574489 | |||||||
| chr6:46574581 | T | C | 16 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(13): Show |
16 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1250+12496A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574581 | |||||||
| chr6:46574830 | A | G | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+12247T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574830 | |||||||
| chr6:46574878 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1250+12199G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574878 | |||||||
| chr6:46574987 | C | T | 2 | a0001c0001t0001g0096 a0010c0010t0001g0178 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1250+12090G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574987 | |||||||
| chr6:46575010 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0243 |
2 | NA18985.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1250+12067A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575010 | |||||||
| chr6:46575020 | T | C | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1250+12057A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575020 | |||||||
| chr6:46575067 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1250+12010A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575067 | |||||||
| chr6:46575096 | T | G | 24 | a0001c0001t0001g0091 a0001c0001t0001g0130 a0001c0001t0001g0132 others(21): Show |
25 | HG02015.hp2 HG02027.hp2 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.1250+11981A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575096 | |||||||
| chr6:46575151 | C | T | 31 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(28): Show |
31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1250+11926G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575151 | |||||||
| chr6:46575460 | A | T | 1 | a0002c0002t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1250+11617T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575460 | |||||||
| chr6:46575596 | CT | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+11480delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575596 | |||||||
| chr6:46575725 | C | T | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+11352G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575725 | |||||||
| chr6:46575746 | C | T | 1 | a0004c0004t0001g0022 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1250+11331G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575746 | |||||||
| chr6:46575946 | T | A | 1 | a0005c0005t0001g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1250+11131A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575946 | |||||||
| chr6:46576098 | G | A | 7 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0002c0002t0001g0113 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1250+10979C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46576098 | |||||||
| chr6:46576261 | C | T | 3 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0010c0010t0001g0178 |
3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1250+10816G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46576261 | |||||||
| chr6:46576397 | G | A | 1 | a0004c0004t0001g0027 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1250+10680C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46576397 | |||||||
| chr6:46576522 | T | C | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+10555A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46576522 | |||||||
| chr6:46577312 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1250+9765G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577312 | |||||||
| chr6:46577335 | C | T | 2 | a0002c0002t0001g0210 a0008c0008t0001g0017 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1250+9742G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577335 | |||||||
| chr6:46577575 | T | C | 1 | a0002c0002t0001g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1250+9502A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577575 | |||||||
| chr6:46577620 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1250+9457C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577620 | |||||||
| chr6:46577631 | T | G | 1 | a0004c0004t0001g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1250+9446A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577631 | |||||||
| chr6:46577674 | G | A | 23 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(20): Show |
23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1250+9403C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577674 | |||||||
| chr6:46577775 | TA | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+9301delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577775 | |||||||
| chr6:46577828 | G | A | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+9249C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577828 | |||||||
| chr6:46577855 | G | A | 1 | a0002c0002t0001g0296 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1250+9222C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577855 | |||||||
| chr6:46578008 | G | A | 1 | a0003c0003t0001g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1250+9069C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578008 | |||||||
| chr6:46578157 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+8920A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578157 | |||||||
| chr6:46578173 | T | C | 1 | a0002c0002t0001g0165 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1250+8904A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578173 | |||||||
| chr6:46578298 | C | A | 23 | a0001c0001t0001g0091 a0001c0001t0001g0130 a0001c0001t0001g0132 others(20): Show |
24 | HG02015.hp2 HG02027.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.1250+8779G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578298 | |||||||
| chr6:46578384 | C | T | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+8693G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578384 | |||||||
| chr6:46578653 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1250+8424T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578653 | |||||||
| chr6:46578756 | C | A | 1 | a0002c0002t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1250+8321G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578756 | |||||||
| chr6:46579109 | C | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(72): Show |
77 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.1250+7968G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579109 | |||||||
| chr6:46579293 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+7784G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579293 | |||||||
| chr6:46579444 | G | A | 1 | a0002c0002t0002g0152 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1250+7633C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579444 | |||||||
| chr6:46579584 | C | T | 2 | a0002c0002t0001g0119 a0002c0002t0001g0128 |
2 | HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1250+7493G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579584 | |||||||
| chr6:46579765 | C | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+7312G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579765 | |||||||
| chr6:46580312 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+6765G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580312 | |||||||
| chr6:46580337 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(130): Show |
135 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1250+6740A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580337 | |||||||
| chr6:46580495 | A | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(72): Show |
77 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.1250+6582T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580495 | |||||||
| chr6:46580554 | C | T | 1 | a0005c0005t0001g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1250+6523G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580554 | |||||||
| chr6:46580614 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0010c0010t0001g0178 |
3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1250+6463C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580614 | |||||||
| chr6:46580931 | A | G | 1 | a0005c0005t0008g0301 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1250+6146T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580931 | |||||||
| chr6:46581083 | C | A | 2 | a0002c0002t0001g0163 a0002c0002t0001g0176 |
2 | HG01258.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1250+5994G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581083 | |||||||
| chr6:46581095 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+5982G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581095 | |||||||
| chr6:46581192 | G | C | 2 | a0003c0003t0001g0199 a0007c0007t0001g0013 |
2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1250+5885C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581192 | |||||||
| chr6:46581199 | G | A | 26 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0123 others(23): Show |
26 | HG00408.hp2 HG00609.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1250+5878C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581199 | |||||||
| chr6:46581233 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1250+5844G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581233 | |||||||
| chr6:46581269 | G | A | 1 | a0002c0002t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1250+5808C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581269 | |||||||
| chr6:46581366 | C | T | 5 | a0002c0002t0002g0129 a0003c0003t0002g0213 a0007c0007t0002g0035 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+5711G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581366 | |||||||
| chr6:46581405 | GA | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(130): Show |
135 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1250+5671delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581405 | |||||||
| chr6:46581419 | A | G | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1250+5658T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581419 | |||||||
| chr6:46581767 | C | T | 23 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(20): Show |
23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1250+5310G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581767 | |||||||
| chr6:46581768 | C | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0010c0010t0001g0178 |
3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1250+5309G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581768 | |||||||
| chr6:46581805 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+5272G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581805 | |||||||
| chr6:46581822 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+5255A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581822 | |||||||
| chr6:46581858 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+5219C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581858 | |||||||
| chr6:46581986 | A | G | 4 | a0005c0005t0001g0282 a0005c0005t0001g0286 a0005c0005t0001g0287 others(1): Show |
4 | HG02647.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+5091T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581986 | |||||||
| chr6:46582027 | G | A | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+5050C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582027 | |||||||
| chr6:46582233 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(131): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+4844G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582233 | |||||||
| chr6:46582239 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(175): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1250+4838A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582239 | |||||||
| chr6:46582262 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+4815G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582262 | |||||||
| chr6:46582313 | A | G | 1 | a0002c0002t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1250+4764T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582313 | |||||||
| chr6:46582545 | C | T | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+4532G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582545 | |||||||
| chr6:46583121 | T | C | 3 | a0002c0002t0001g0182 a0002c0002t0001g0296 a0002c0002t0001g0297 |
3 | NA18971.hp1 NA19058.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1250+3956A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583121 | |||||||
| chr6:46583447 | A | T | 5 | a0002c0002t0002g0129 a0003c0003t0002g0213 a0007c0007t0002g0035 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+3630T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583447 | |||||||
| chr6:46583453 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1250+3624G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583453 | |||||||
| chr6:46583600 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+3477C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583600 | |||||||
| chr6:46583648 | T | C | 1 | a0002c0002t0001g0110 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1250+3429A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583648 | |||||||
| chr6:46583779 | C | T | 2 | a0007c0007t0001g0018 a0007c0007t0001g0028 |
2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1250+3298G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583779 | |||||||
| chr6:46583892 | G | C | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+3185C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583892 | |||||||
| chr6:46584006 | C | T | 44 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1250+3071G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584006 | |||||||
| chr6:46584121 | T | G | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+2956A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584121 | |||||||
| chr6:46584124 | G | C | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+2953C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584124 | |||||||
| chr6:46584205 | G | A | 1 | a0002c0002t0001g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1250+2872C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584205 | |||||||
| chr6:46584370 | C | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(41): Show |
46 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1250+2707G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584370 | |||||||
| chr6:46584463 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+2614G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584463 | |||||||
| chr6:46584508 | C | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(175): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1250+2569G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584508 | |||||||
| chr6:46584582 | C | T | 6 | a0002c0002t0001g0051 a0002c0002t0001g0108 a0002c0002t0001g0112 others(3): Show |
6 | HG00558.hp2 HG00597.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1250+2495G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584582 | |||||||
| chr6:46584807 | C | T | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1250+2270G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584807 | |||||||
| chr6:46584905 | A | G | 44 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1250+2172T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584905 | |||||||
| chr6:46584935 | A | G | 1 | a0006c0006t0001g0001 | 2 | HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1250+2142T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584935 | |||||||
| chr6:46584966 | G | A | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+2111C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584966 | |||||||
| chr6:46585322 | T | TATAG | 93 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0053 others(90): Show |
94 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1250+1751_1250+175 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | |||||||
| chr6:46585322 | T | TATAGATA others(1): Show |
4 | a0001c0001t0001g0066 a0002c0002t0001g0106 a0002c0002t0002g0298 others(1): Show |
4 | HG02647.hp1 HG03139.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+1747_1250+175 others(12): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | |||||||
| chr6:46585322 | TATAG | T | 47 | a0001c0001t0001g0050 a0001c0001t0001g0088 a0001c0001t0001g0089 others(44): Show |
48 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1250+1751_1250+175 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | |||||||
| chr6:46585322 | TATAGATA others(1): Show |
T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0137 others(7): Show |
10 | HG01175.hp1 HG02145.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1250+1747_1250+175 others(12): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | |||||||
| chr6:46585322 | TATAGATA others(5): Show |
T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+1743_1250+175 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | |||||||
| chr6:46585360 | T | C | 3 | a0002c0002t0001g0080 a0002c0002t0001g0085 a0002c0002t0001g0150 |
3 | HG00423.hp2 NA18951.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1250+1717A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585360 | |||||||
| chr6:46585561 | G | A | 1 | a0002c0002t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1250+1516C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585561 | |||||||
| chr6:46585586 | T | C | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+1491A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585586 | |||||||
| chr6:46585711 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+1366G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585711 | |||||||
| chr6:46585716 | A | G | 16 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(13): Show |
16 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1250+1361T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585716 | |||||||
| chr6:46585917 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(130): Show |
135 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1250+1160T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585917 | |||||||
| chr6:46585933 | G | A | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1250+1144C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585933 | |||||||
| chr6:46586079 | G | C | 1 | a0005c0005t0001g0276 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1250+998C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586079 | |||||||
| chr6:46586088 | T | C | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+989A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586088 | |||||||
| chr6:46586126 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+951G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586126 | |||||||
| chr6:46586192 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+885G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586192 | |||||||
| chr6:46586331 | A | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(35): Show |
40 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+746T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586331 | |||||||
| chr6:46586388 | T | C | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+689A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586388 | |||||||
| chr6:46586829 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0096 |
3 | HG02109.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1250+248G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586829 | |||||||
| chr6:46587414 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1162-249G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587414 | |||||||
| chr6:46587437 | G | A | 7 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0002c0002t0001g0113 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1162-272C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587437 | |||||||
| chr6:46587664 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(130): Show |
135 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1161+370C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587664 | |||||||
| chr6:46587711 | A | G | 1 | a0002c0002t0001g0296 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1161+323T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587711 | |||||||
| chr6:46587736 | C | T | 7 | a0001c0001t0003g0075 a0001c0001t0003g0186 a0001c0001t0003g0187 others(4): Show |
7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+298G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587736 | |||||||
| chr6:46588004 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1161+30C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46588004 | |||||||
| chr6:46588138 | G | C | 1 | a0002c0002t0002g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1066-9C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588138 | |||||||
| chr6:46588373 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(35): Show |
40 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1066-244C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588373 | |||||||
| chr6:46588588 | T | C | 51 | a0001c0001t0002g0238 a0002c0002t0002g0046 a0002c0002t0002g0076 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1066-459A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588588 | |||||||
| chr6:46588663 | G | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-534C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588663 | |||||||
| chr6:46588696 | G | A | 2 | a0002c0002t0002g0129 a0003c0003t0002g0213 |
2 | HG00735.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1066-567C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588696 | |||||||
| chr6:46588697 | G | C | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066-568C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588697 | |||||||
| chr6:46588725 | G | A | 1 | a0010c0010t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1066-596C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588725 | |||||||
| chr6:46588727 | C | G | 1 | a0005c0005t0001g0276 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1066-598G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588727 | |||||||
| chr6:46589073 | G | A | 1 | a0001c0001t0005g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1066-944C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589073 | |||||||
| chr6:46589282 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0225 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1066-1153C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589282 | |||||||
| chr6:46589346 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1066-1217C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589346 | |||||||
| chr6:46589453 | G | A | 1 | a0002c0002t0002g0143 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1066-1324C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589453 | |||||||
| chr6:46589772 | T | A | 2 | a0001c0001t0001g0290 a0005c0005t0001g0284 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1066-1643A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589772 | |||||||
| chr6:46589912 | T | C | 1 | a0002c0002t0001g0155 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1066-1783A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589912 | |||||||
| chr6:46590013 | T | C | 6 | a0002c0002t0002g0148 a0002c0002t0002g0149 a0002c0002t0002g0152 others(3): Show |
6 | HG02015.hp1 HG02165.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1066-1884A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590013 | |||||||
| chr6:46590171 | G | A | 38 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(35): Show |
38 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(35): Show |
intron_variant | MODIFIER | c.1066-2042C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590171 | |||||||
| chr6:46590538 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1066-2409C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590538 | |||||||
| chr6:46590568 | T | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(79): Show |
84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1066-2439A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590568 | |||||||
| chr6:46590719 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1066-2590A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590719 | |||||||
| chr6:46590974 | T | C | 7 | a0002c0002t0002g0133 a0002c0002t0002g0191 a0002c0002t0002g0236 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1066-2845A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590974 | |||||||
| chr6:46591041 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1066-2912A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591041 | |||||||
| chr6:46591069 | C | A | 1 | a0002c0002t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1066-2940G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591069 | |||||||
| chr6:46591311 | C | A | 1 | a0007c0007t0001g0013 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1066-3182G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591311 | |||||||
| chr6:46591348 | T | C | 5 | a0005c0005t0001g0282 a0005c0005t0001g0285 a0005c0005t0001g0286 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066-3219A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591348 | |||||||
| chr6:46591395 | A | T | 1 | a0001c0001t0001g0247 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1066-3266T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591395 | |||||||
| chr6:46591532 | T | C | 1 | a0002c0002t0002g0161 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1066-3403A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591532 | |||||||
| chr6:46591734 | A | T | 2 | a0001c0001t0001g0179 a0004c0004t0001g0034 |
2 | HG00408.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1066-3605T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591734 | |||||||
| chr6:46591936 | A | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02280.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1066-3807T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591936 | |||||||
| chr6:46592081 | T | G | 1 | a0004c0004t0001g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1065+3906A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592081 | |||||||
| chr6:46592266 | A | C | 46 | a0001c0001t0001g0091 a0001c0001t0001g0130 a0001c0001t0001g0132 others(43): Show |
47 | HG01243.hp1 HG01346.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.1065+3721T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592266 | |||||||
| chr6:46592323 | T | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0177 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1065+3664A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592323 | |||||||
| chr6:46592323 | T | C | 1 | a0002c0002t0001g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1065+3664A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592323 | |||||||
| chr6:46592661 | C | T | 1 | a0003c0003t0001g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1065+3326G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592661 | |||||||
| chr6:46592679 | A | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(165): Show |
171 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1065+3308T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592679 | |||||||
| chr6:46592930 | TGGG | T | 3 | a0001c0001t0001g0134 a0004c0004t0001g0030 a0006c0006t0001g0005 |
3 | HG02027.hp2 NA18970.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1065+3054_1065+305 others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592930 | |||||||
| chr6:46593013 | A | G | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1065+2974T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46593013 | |||||||
| chr6:46593231 | C | T | 16 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(13): Show |
16 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1065+2756G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46593231 | |||||||
| chr6:46593822 | C | T | 1 | a0006c0006t0001g0011 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1065+2165G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46593822 | |||||||
| chr6:46594150 | G | A | 1 | a0003c0003t0001g0218 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1065+1837C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594150 | |||||||
| chr6:46594403 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1065+1584G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594403 | |||||||
| chr6:46594463 | C | T | 1 | a0004c0004t0001g0031 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1065+1524G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594463 | |||||||
| chr6:46594483 | T | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065+1504A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594483 | |||||||
| chr6:46594554 | T | C | 7 | a0006c0006t0001g0006 a0006c0006t0001g0008 a0006c0006t0001g0009 others(4): Show |
7 | HG01175.hp1 HG01261.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1065+1433A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594554 | |||||||
| chr6:46594651 | A | G | 8 | a0001c0001t0001g0064 a0001c0001t0003g0186 a0001c0001t0003g0187 others(5): Show |
8 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065+1336T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594651 | |||||||
| chr6:46595032 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0010c0010t0001g0178 |
3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1065+955C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595032 | |||||||
| chr6:46595205 | C | T | 8 | a0001c0001t0001g0290 a0001c0001t0003g0186 a0001c0001t0003g0187 others(5): Show |
8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065+782G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595205 | |||||||
| chr6:46595226 | T | C | 1 | a0004c0004t0001g0022 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1065+761A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595226 | |||||||
| chr6:46595440 | T | C | 2 | a0002c0002t0002g0298 a0002c0002t0002g0299 |
2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1065+547A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595440 | |||||||
| chr6:46595461 | T | G | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1065+526A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595461 | |||||||
| chr6:46595674 | A | G | 8 | a0001c0001t0001g0290 a0001c0001t0003g0186 a0001c0001t0003g0187 others(5): Show |
8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065+313T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595674 | |||||||
| chr6:46595981 | G | C | 1 | a0002c0002t0001g0163 | 1 | HG01258.hp2 | splice_region_variant&intron_variant | LOW | c.1065+6C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595981 | |||||||
| chr6:46596390 | T | C | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-270A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46596390 | |||||||
| chr6:46596564 | C | CT | 13 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(10): Show |
13 | HG00741.hp1 HG01884.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.932-445dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46596564 | |||||||
| chr6:46596755 | C | T | 1 | a0002c0002t0001g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.932-635G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46596755 | |||||||
| chr6:46597063 | G | T | 1 | a0002c0002t0001g0176 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.932-943C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597063 | |||||||
| chr6:46597230 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0290 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.932-1110G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597230 | |||||||
| chr6:46597231 | G | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(41): Show |
46 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.932-1111C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597231 | |||||||
| chr6:46597327 | C | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(37): Show |
42 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.932-1207G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597327 | |||||||
| chr6:46597350 | A | T | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.932-1230T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597350 | |||||||
| chr6:46597398 | A | G | 7 | a0002c0002t0002g0133 a0002c0002t0002g0191 a0002c0002t0002g0236 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-1278T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597398 | |||||||
| chr6:46597439 | C | T | 6 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(3): Show |
6 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-1319G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597439 | |||||||
| chr6:46597582 | A | T | 1 | a0006c0006t0001g0001 | 2 | HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.932-1462T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597582 | |||||||
| chr6:46597742 | C | T | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-1622G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597742 | |||||||
| chr6:46597770 | G | A | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-1650C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597770 | |||||||
| chr6:46597831 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.932-1711A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597831 | |||||||
| chr6:46597927 | T | C | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-1807A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597927 | |||||||
| chr6:46598048 | C | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-1928G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598048 | |||||||
| chr6:46598227 | T | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(166): Show |
172 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.932-2107A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598227 | |||||||
| chr6:46598330 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.932-2210T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598330 | |||||||
| chr6:46598387 | A | T | 1 | a0001c0001t0001g0245 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.932-2267T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598387 | |||||||
| chr6:46598419 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.932-2299G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598419 | |||||||
| chr6:46598548 | C | G | 1 | a0005c0005t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.932-2428G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598548 | |||||||
| chr6:46598931 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.932-2811C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598931 | |||||||
| chr6:46599058 | G | A | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-2938C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599058 | |||||||
| chr6:46599087 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.932-2967C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599087 | |||||||
| chr6:46599112 | C | T | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-2992G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599112 | |||||||
| chr6:46599255 | C | T | 1 | a0007c0007t0001g0013 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.932-3135G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599255 | |||||||
| chr6:46599270 | G | C | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-3150C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599270 | |||||||
| chr6:46599313 | C | CG | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-3194dupC | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599313 | |||||||
| chr6:46599313 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.932-3193G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599313 | |||||||
| chr6:46599498 | C | T | 1 | a0002c0002t0001g0051 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.932-3378G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599498 | |||||||
| chr6:46599556 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0223 |
2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.932-3436G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599556 | |||||||
| chr6:46599558 | C | T | 1 | a0004c0004t0001g0015 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.932-3438G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599558 | |||||||
| chr6:46599620 | C | T | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-3500G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599620 | |||||||
| chr6:46599757 | C | T | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-3637G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599757 | |||||||
| chr6:46599848 | T | C | 1 | a0003c0003t0002g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.932-3728A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599848 | |||||||
| chr6:46600107 | CTTTCT | C | 42 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0002c0002t0001g0131 others(39): Show |
43 | HG00609.hp2 HG01243.hp1 HG01346.hp2 others(40): Show |
intron_variant | MODIFIER | c.932-3992_932-3988d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600107 | |||||||
| chr6:46600116 | C | A | 1 | a0002c0002t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.932-3996G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600116 | |||||||
| chr6:46600151 | T | A | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-4031A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600151 | |||||||
| chr6:46600152 | G | T | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-4032C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600152 | |||||||
| chr6:46600160 | G | C | 1 | a0006c0006t0001g0043 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.932-4040C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600160 | |||||||
| chr6:46600325 | T | C | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-4205A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600325 | |||||||
| chr6:46600367 | C | G | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-4247G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600367 | |||||||
| chr6:46600488 | T | G | 2 | a0002c0002t0001g0151 a0002c0002t0001g0156 |
2 | NA18968.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.932-4368A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600488 | |||||||
| chr6:46600666 | G | A | 3 | a0002c0002t0002g0272 a0002c0002t0002g0294 a0002c0002t0004g0303 |
3 | HG02257.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.932-4546C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600666 | |||||||
| chr6:46600850 | G | A | 1 | a0002c0002t0001g0297 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.932-4730C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600850 | |||||||
| chr6:46600921 | G | C | 1 | a0002c0002t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.932-4801C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600921 | |||||||
| chr6:46601207 | GT | G | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-5088delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601207 | |||||||
| chr6:46601281 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0083 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-5161C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601281 | |||||||
| chr6:46601308 | G | T | 2 | a0002c0002t0001g0151 a0002c0002t0001g0156 |
2 | NA18968.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.932-5188C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601308 | |||||||
| chr6:46601353 | C | A | 5 | a0002c0002t0002g0129 a0003c0003t0002g0213 a0007c0007t0002g0035 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-5233G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601353 | |||||||
| chr6:46601628 | A | C | 2 | a0003c0003t0001g0193 a0003c0003t0001g0195 |
2 | NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.932-5508T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601628 | |||||||
| chr6:46601665 | C | CTAT | 60 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(57): Show |
62 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.932-5548_932-5546d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | |||||||
| chr6:46601665 | C | CTATTAT | 10 | a0001c0001t0001g0059 a0001c0001t0001g0073 a0001c0001t0001g0099 others(7): Show |
11 | HG02258.hp1 HG02602.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.932-5551_932-5546d others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | |||||||
| chr6:46601665 | C | CTATTATT others(5): Show |
1 | a0004c0004t0001g0026 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.932-5557_932-5546d others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | |||||||
| chr6:46601665 | CTAT | C | 7 | a0001c0001t0001g0116 a0001c0001t0001g0177 a0001c0001t0001g0259 others(4): Show |
7 | HG00738.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-5548_932-5546d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | |||||||
| chr6:46601665 | CTATTAT | C | 34 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(31): Show |
34 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.932-5551_932-5546d others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | |||||||
| chr6:46601688 | A | G | 2 | a0002c0002t0002g0076 a0002c0002t0002g0077 |
2 | HG00408.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.932-5568T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601688 | |||||||
| chr6:46601817 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(42): Show |
47 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.932-5697C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601817 | |||||||
| chr6:46602023 | C | T | 2 | a0002c0002t0001g0211 a0002c0002t0001g0212 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.932-5903G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602023 | |||||||
| chr6:46602072 | C | G | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-5952G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602072 | |||||||
| chr6:46602147 | AATGGATG others(9): Show |
A | 5 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0117 others(2): Show |
5 | HG02083.hp1 NA18945.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-6043_932-6028d others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602147 | |||||||
| chr6:46602238 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.932-6118T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602238 | |||||||
| chr6:46602250 | T | C | 2 | a0005c0005t0001g0277 a0005c0005t0001g0280 |
2 | HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.932-6130A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602250 | |||||||
| chr6:46602289 | G | T | 3 | a0002c0002t0002g0298 a0002c0002t0002g0299 a0002c0002t0002g0300 |
3 | HG02896.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.932-6169C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602289 | |||||||
| chr6:46602336 | T | C | 25 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(22): Show |
25 | HG00741.hp1 HG01884.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-6216A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602336 | |||||||
| chr6:46602379 | T | G | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-6259A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602379 | |||||||
| chr6:46602578 | C | T | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.932-6458G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602578 | |||||||
| chr6:46602641 | C | T | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-6521G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602641 | |||||||
| chr6:46602684 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(218): Show |
224 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.932-6564G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602684 | |||||||
| chr6:46602689 | C | CA | 19 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0122 others(16): Show |
19 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.932-6570dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602689 | |||||||
| chr6:46602689 | CA | C | 63 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(60): Show |
63 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.932-6570delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602689 | |||||||
| chr6:46602689 | CAA | C | 9 | a0001c0001t0001g0124 a0001c0001t0001g0245 a0001c0001t0001g0248 others(6): Show |
9 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.932-6571_932-6570d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602689 | |||||||
| chr6:46602689 | CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0002g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.932-6581_932-6570d others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602689 | |||||||
| chr6:46602723 | T | G | 1 | a0005c0005t0001g0276 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.932-6603A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602723 | |||||||
| chr6:46602806 | T | C | 1 | a0003c0003t0001g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.932-6686A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602806 | |||||||
| chr6:46602901 | C | T | 2 | a0007c0007t0002g0035 a0007c0007t0002g0037 |
2 | HG01433.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.932-6781G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602901 | |||||||
| chr6:46602923 | T | TG | 177 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0054 others(174): Show |
180 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.932-6804dupC | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602923 | |||||||
| chr6:46602923 | T | TGG | 63 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0053 others(60): Show |
63 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.932-6805_932-6804d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602923 | |||||||
| chr6:46602925 | G | GC | 4 | a0001c0001t0001g0066 a0002c0002t0001g0120 a0002c0002t0001g0172 others(1): Show |
4 | HG01175.hp2 HG02965.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-6806_932-6805i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602925 | |||||||
| chr6:46602933 | G | GA | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-6814dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602933 | |||||||
| chr6:46603019 | A | G | 2 | a0005c0005t0001g0266 a0005c0005t0001g0268 |
2 | NA19068.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.932-6899T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603019 | |||||||
| chr6:46603046 | C | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(218): Show |
224 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.932-6926G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603046 | |||||||
| chr6:46603119 | T | C | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-6999A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603119 | |||||||
| chr6:46603167 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.932-7047G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603167 | |||||||
| chr6:46603236 | A | C | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-7116T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603236 | |||||||
| chr6:46603451 | C | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0116 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-7331G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603451 | |||||||
| chr6:46603467 | T | A | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-7347A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603467 | |||||||
| chr6:46603469 | C | T | 1 | a0002c0002t0002g0250 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.932-7349G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603469 | |||||||
| chr6:46603538 | C | T | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-7418G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603538 | |||||||
| chr6:46603539 | T | C | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-7419A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603539 | |||||||
| chr6:46603541 | C | T | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-7421G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603541 | |||||||
| chr6:46603691 | T | C | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-7571A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603691 | |||||||
| chr6:46603724 | G | C | 1 | a0010c0010t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-7604C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603724 | |||||||
| chr6:46603802 | T | C | 25 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(22): Show |
25 | HG00741.hp1 HG01884.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-7682A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603802 | |||||||
| chr6:46604176 | AGAGCAAA others(7): Show |
A | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-8070_932-8057d others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604176 | |||||||
| chr6:46604334 | C | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.932-8214G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604334 | |||||||
| chr6:46604354 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.932-8234G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604354 | |||||||
| chr6:46604560 | C | A | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-8440G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604560 | |||||||
| chr6:46604560 | C | T | 2 | a0002c0002t0001g0251 a0002c0002t0001g0264 |
2 | HG00558.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.932-8440G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604560 | |||||||
| chr6:46604723 | C | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0223 |
2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.932-8603G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604723 | |||||||
| chr6:46604749 | A | T | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-8629T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604749 | |||||||
| chr6:46604791 | A | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-8671T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604791 | |||||||
| chr6:46604807 | C | T | 1 | a0007c0007t0002g0037 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.932-8687G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604807 | |||||||
| chr6:46604939 | T | C | 1 | a0005c0005t0001g0274 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.932-8819A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604939 | |||||||
| chr6:46604982 | C | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-8862G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604982 | |||||||
| chr6:46605052 | C | T | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-8932G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605052 | |||||||
| chr6:46605084 | C | T | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-8964G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605084 | |||||||
| chr6:46605391 | G | A | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-9271C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605391 | |||||||
| chr6:46605399 | C | A | 1 | a0003c0003t0001g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.932-9279G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605399 | |||||||
| chr6:46605509 | A | C | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-9389T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605509 | |||||||
| chr6:46605536 | G | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(4): Show |
8 | HG00735.hp2 HG01993.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.932-9416C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605536 | |||||||
| chr6:46605573 | G | A | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-9453C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605573 | |||||||
| chr6:46605705 | A | G | 8 | a0001c0001t0001g0290 a0001c0001t0003g0186 a0001c0001t0003g0187 others(5): Show |
8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.932-9585T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605705 | |||||||
| chr6:46605748 | T | A | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-9628A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605748 | |||||||
| chr6:46605943 | G | A | 1 | a0005c0005t0001g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.932-9823C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605943 | |||||||
| chr6:46605966 | A | T | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.932-9846T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605966 | |||||||
| chr6:46606167 | C | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.932-10047G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606167 | |||||||
| chr6:46606238 | T | C | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-10118A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606238 | |||||||
| chr6:46606378 | C | T | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-10258G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606378 | |||||||
| chr6:46606540 | A | G | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.932-10420T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606540 | |||||||
| chr6:46606568 | A | AC | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-10449dupG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606568 | |||||||
| chr6:46606701 | G | T | 1 | a0005c0005t0001g0283 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.932-10581C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606701 | |||||||
| chr6:46606710 | G | A | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-10590C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606710 | |||||||
| chr6:46606730 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.932-10610C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606730 | |||||||
| chr6:46607004 | C | A | 5 | a0002c0002t0002g0129 a0003c0003t0002g0213 a0007c0007t0002g0035 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-10884G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607004 | |||||||
| chr6:46607067 | G | C | 25 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(22): Show |
25 | HG00741.hp1 HG01884.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-10947C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607067 | |||||||
| chr6:46607125 | T | C | 1 | a0005c0005t0001g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.932-11005A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607125 | |||||||
| chr6:46607153 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.932-11033C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607153 | |||||||
| chr6:46607203 | A | C | 1 | a0002c0002t0002g0152 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.932-11083T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607203 | |||||||
| chr6:46607241 | A | C | 1 | a0003c0003t0001g0201 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.932-11121T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607241 | |||||||
| chr6:46607430 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.932-11310G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607430 | |||||||
| chr6:46607464 | T | TAC | 56 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(53): Show |
56 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.932-11346_932-1134 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607464 | |||||||
| chr6:46607464 | T | TACAC | 21 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(18): Show |
21 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.932-11348_932-1134 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607464 | |||||||
| chr6:46607464 | T | TACACAC | 14 | a0001c0001t0001g0224 a0001c0001t0001g0288 a0001c0001t0001g0289 others(11): Show |
14 | HG00741.hp1 HG02572.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.932-11350_932-1134 others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607464 | |||||||
| chr6:46607514 | G | GT | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-11395dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607514 | |||||||
| chr6:46607531 | C | T | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-11411G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607531 | |||||||
| chr6:46607563 | T | G | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-11443A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607563 | |||||||
| chr6:46607565 | C | T | 4 | a0002c0002t0001g0151 a0002c0002t0001g0156 a0003c0003t0001g0048 others(1): Show |
4 | HG01952.hp2 HG01975.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-11445G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607565 | |||||||
| chr6:46607659 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.932-11539A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607659 | |||||||
| chr6:46608233 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(165): Show |
171 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.932-12113A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608233 | |||||||
| chr6:46608475 | A | T | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-12355T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608475 | |||||||
| chr6:46608559 | C | T | 33 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-12439G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608559 | |||||||
| chr6:46608624 | T | A | 1 | a0002c0002t0002g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.932-12504A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608624 | |||||||
| chr6:46608746 | C | A | 1 | a0002c0002t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.932-12626G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608746 | |||||||
| chr6:46608834 | G | A | 6 | a0002c0002t0002g0191 a0002c0002t0002g0236 a0002c0002t0002g0254 others(3): Show |
6 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-12714C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608834 | |||||||
| chr6:46608927 | A | G | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.932-12807T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608927 | |||||||
| chr6:46608948 | C | T | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-12828G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608948 | |||||||
| chr6:46609058 | A | G | 2 | a0002c0002t0001g0120 a0002c0002t0006g0109 |
2 | HG01175.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.932-12938T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609058 | |||||||
| chr6:46609113 | T | C | 2 | a0002c0002t0001g0210 a0002c0002t0001g0220 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.932-12993A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609113 | |||||||
| chr6:46609162 | G | A | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-13042C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609162 | |||||||
| chr6:46609215 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.932-13095G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609215 | |||||||
| chr6:46609316 | T | C | 3 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0190 |
3 | HG03540.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.932-13196A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609316 | |||||||
| chr6:46609349 | G | GCTGAGTC others(7): Show |
1 | a0002c0002t0002g0300 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.932-13243_932-1323 others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609349 | |||||||
| chr6:46609349 | GCTGAGTC others(7): Show |
G | 1 | a0005c0005t0001g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.932-13243_932-1323 others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609349 | |||||||
| chr6:46609359 | C | T | 1 | a0005c0005t0001g0192 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.932-13239G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609359 | |||||||
| chr6:46609414 | C | CA | 12 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0061 others(9): Show |
12 | HG01175.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-13295dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609414 | |||||||
| chr6:46609475 | A | C | 1 | a0002c0002t0001g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.932-13355T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609475 | |||||||
| chr6:46609763 | A | G | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-13643T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609763 | |||||||
| chr6:46610042 | G | A | 1 | a0002c0002t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.932-13922C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610042 | |||||||
| chr6:46610092 | A | G | 1 | a0004c0004t0001g0044 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.932-13972T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610092 | |||||||
| chr6:46610167 | T | G | 1 | a0005c0005t0001g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.932-14047A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610167 | |||||||
| chr6:46610307 | G | A | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-14187C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610307 | |||||||
| chr6:46610350 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.932-14230G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610350 | |||||||
| chr6:46610410 | T | C | 6 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(3): Show |
6 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-14290A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610410 | |||||||
| chr6:46610731 | G | T | 3 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0010c0010t0001g0178 |
3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.932-14611C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610731 | |||||||
| chr6:46610983 | G | A | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+14435C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610983 | |||||||
| chr6:46611002 | A | G | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+14416T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611002 | |||||||
| chr6:46611116 | G | C | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+14302C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611116 | |||||||
| chr6:46611313 | C | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0177 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.931+14105G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611313 | |||||||
| chr6:46611399 | A | G | 3 | a0001c0001t0001g0234 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | NA18942.hp1 NA18977.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.931+14019T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611399 | |||||||
| chr6:46611470 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.931+13948G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611470 | |||||||
| chr6:46611479 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.931+13939T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611479 | |||||||
| chr6:46611705 | C | A | 4 | a0002c0002t0001g0194 a0002c0002t0001g0198 a0002c0002t0002g0101 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+13713G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611705 | |||||||
| chr6:46612119 | C | T | 4 | a0001c0001t0001g0134 a0002c0002t0001g0251 a0002c0002t0001g0264 others(1): Show |
4 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+13299G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612119 | |||||||
| chr6:46612265 | T | C | 1 | a0002c0002t0001g0110 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.931+13153A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612265 | |||||||
| chr6:46612287 | G | T | 8 | a0001c0001t0001g0290 a0001c0001t0003g0186 a0001c0001t0003g0187 others(5): Show |
8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.931+13131C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612287 | |||||||
| chr6:46612297 | T | C | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+13121A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612297 | |||||||
| chr6:46612322 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0177 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.931+13096C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612322 | |||||||
| chr6:46612607 | ATGTGAGA others(3): Show |
A | 1 | a0001c0001t0001g0241 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.931+12801_931+1281 others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612607 | |||||||
| chr6:46612645 | G | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(166): Show |
172 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.931+12773C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612645 | |||||||
| chr6:46612716 | T | G | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+12702A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612716 | |||||||
| chr6:46613165 | G | C | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+12253C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613165 | |||||||
| chr6:46613170 | T | A | 1 | a0008c0008t0002g0016 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.931+12248A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613170 | |||||||
| chr6:46613364 | C | T | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+12054G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613364 | |||||||
| chr6:46613395 | C | A | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+12023G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613395 | |||||||
| chr6:46613450 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.931+11968A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613450 | |||||||
| chr6:46613473 | T | C | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+11945A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613473 | |||||||
| chr6:46613704 | G | GTT | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+11712_931+1171 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613704 | |||||||
| chr6:46613871 | G | C | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.931+11547C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613871 | |||||||
| chr6:46613939 | C | CA | 19 | a0002c0002t0001g0113 a0002c0002t0001g0156 a0002c0002t0001g0157 others(16): Show |
19 | HG00280.hp2 HG00597.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.931+11478dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613939 | |||||||
| chr6:46613939 | CA | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(161): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.931+11478delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613939 | |||||||
| chr6:46613945 | A | G | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+11473T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613945 | |||||||
| chr6:46614012 | A | G | 1 | a0002c0002t0002g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.931+11406T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614012 | |||||||
| chr6:46614142 | T | C | 2 | a0002c0002t0001g0080 a0002c0002t0001g0085 |
2 | HG00423.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.931+11276A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614142 | |||||||
| chr6:46614180 | T | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+11238A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614180 | |||||||
| chr6:46614243 | C | G | 69 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+11175G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614243 | |||||||
| chr6:46614250 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.931+11168A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614250 | |||||||
| chr6:46614342 | T | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(42): Show |
47 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.931+11076A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614342 | |||||||
| chr6:46614396 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+11022G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614396 | |||||||
| chr6:46614419 | G | T | 127 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(124): Show |
129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.931+10999C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614419 | |||||||
| chr6:46614530 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.931+10888C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614530 | |||||||
| chr6:46614580 | T | A | 1 | a0002c0002t0001g0181 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.931+10838A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614580 | |||||||
| chr6:46614674 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.931+10744G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614674 | |||||||
| chr6:46614717 | GA | G | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+10700delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614717 | |||||||
| chr6:46614900 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+10518A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614900 | |||||||
| chr6:46615174 | C | T | 8 | a0001c0001t0001g0290 a0001c0001t0003g0186 a0001c0001t0003g0187 others(5): Show |
8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.931+10244G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615174 | |||||||
| chr6:46615237 | ATATAT | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(42): Show |
47 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.931+10176_931+1018 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615237 | |||||||
| chr6:46615253 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.931+10165A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615253 | |||||||
| chr6:46615384 | G | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+10034C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615384 | |||||||
| chr6:46615399 | G | A | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.931+10019C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615399 | |||||||
| chr6:46615446 | C | A | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9972G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615446 | |||||||
| chr6:46615463 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.931+9955G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615463 | |||||||
| chr6:46615576 | C | T | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+9842G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615576 | |||||||
| chr6:46615584 | C | T | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+9834G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615584 | |||||||
| chr6:46615596 | T | A | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9822A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615596 | |||||||
| chr6:46615734 | TA | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(41): Show |
46 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.931+9683delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615734 | |||||||
| chr6:46615951 | A | G | 1 | a0001c0001t0003g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+9467T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615951 | |||||||
| chr6:46615973 | A | G | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+9445T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615973 | |||||||
| chr6:46616005 | T | TC | 10 | a0001c0001t0001g0177 a0002c0002t0001g0110 a0002c0002t0001g0164 others(7): Show |
10 | HG01261.hp2 HG02027.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.931+9412dupG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616005 | |||||||
| chr6:46616006 | C | T | 1 | a0003c0003t0001g0196 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.931+9412G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616006 | |||||||
| chr6:46616006 | CCCCCCTC others(3): Show |
C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(115): Show |
120 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.931+9402_931+9411d others(12): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616006 | |||||||
| chr6:46616016 | T | TC | 148 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0132 others(145): Show |
148 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.931+9401dupG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616016 | |||||||
| chr6:46616016 | T | TCC | 35 | a0001c0001t0001g0130 a0001c0001t0001g0223 a0002c0002t0001g0105 others(32): Show |
35 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.931+9400_931+9401d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616016 | |||||||
| chr6:46616042 | CTTTCT | C | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+9371_931+9375d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616042 | |||||||
| chr6:46616113 | C | CTCTT | 3 | a0001c0001t0001g0288 a0001c0001t0001g0293 a0001c0001t0003g0186 |
3 | HG00741.hp1 HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.931+9301_931+9304d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616113 | |||||||
| chr6:46616119 | CT | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0224 a0001c0001t0001g0227 others(1): Show |
4 | NA18522.hp1 NA18978.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9298delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616119 | |||||||
| chr6:46616123 | T | C | 68 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.931+9295A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616123 | |||||||
| chr6:46616124 | C | T | 68 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.931+9294G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616124 | |||||||
| chr6:46616125 | TTTC | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG01952.hp2 NA18522.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9290_931+9292d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616125 | |||||||
| chr6:46616140 | CTTTCTTT others(16): Show |
C | 5 | a0002c0002t0001g0181 a0002c0002t0002g0161 a0002c0002t0002g0298 others(2): Show |
5 | HG01192.hp2 HG02015.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9255_931+9277d others(25): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616140 | |||||||
| chr6:46616144 | CTTTCTTT others(12): Show |
C | 10 | a0002c0002t0002g0046 a0002c0002t0002g0111 a0002c0002t0002g0152 others(7): Show |
10 | HG02165.hp2 HG02615.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.931+9255_931+9273d others(21): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616144 | |||||||
| chr6:46616148 | CTTTCTTT others(8): Show |
C | 29 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0179 others(26): Show |
30 | HG00597.hp1 HG00609.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.931+9255_931+9269d others(17): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616148 | |||||||
| chr6:46616152 | CTTTCTTT others(4): Show |
C | 34 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0097 others(31): Show |
34 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.931+9255_931+9265d others(13): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616152 | |||||||
| chr6:46616156 | CTTTCTTT | C | 40 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(37): Show |
40 | HG00558.hp1 HG00558.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.931+9255_931+9261d others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616156 | |||||||
| chr6:46616160 | CTTT | C | 54 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0063 others(51): Show |
54 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.931+9255_931+9257d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616160 | |||||||
| chr6:46616162 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931+9256A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616162 | |||||||
| chr6:46616163 | T | C | 40 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(37): Show |
40 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.931+9255A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | |||||||
| chr6:46616163 | T | TC | 42 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(39): Show |
42 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.931+9254_931+9255i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | |||||||
| chr6:46616163 | T | TCTTTC | 13 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0235 others(10): Show |
13 | HG00738.hp1 HG01071.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.931+9254_931+9255i others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | |||||||
| chr6:46616163 | T | TCTTTCTT others(2): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG00735.hp2 HG01109.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.931+9254_931+9255i others(11): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | |||||||
| chr6:46616163 | T | TCTTTCTT others(6): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0065 others(3): Show |
6 | HG01258.hp1 HG01258.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.931+9254_931+9255i others(15): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | |||||||
| chr6:46616163 | T | TCTTTCTT others(10): Show |
2 | a0002c0002t0001g0220 a0008c0008t0001g0017 |
2 | HG01256.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.931+9254_931+9255i others(19): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | |||||||
| chr6:46616163 | T | TCTTTCTT others(14): Show |
1 | a0001c0001t0001g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.931+9254_931+9255i others(23): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | |||||||
| chr6:46616164 | T | A | 1 | a0001c0001t0001g0230 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.931+9254A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616164 | |||||||
| chr6:46616164 | T | C | 23 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0084 others(20): Show |
23 | HG00140.hp2 HG01175.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.931+9254A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616164 | |||||||
| chr6:46616165 | TTCTTTCT others(11): Show |
T | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931+9235_931+9252d others(20): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616165 | |||||||
| chr6:46616166 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.931+9252A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616166 | |||||||
| chr6:46616167 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9251G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616167 | |||||||
| chr6:46616168 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0230 |
2 | NA18972.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.931+9250A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616168 | |||||||
| chr6:46616168 | T | TC | 14 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0082 others(11): Show |
14 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.931+9249_931+9250i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616168 | |||||||
| chr6:46616169 | T | C | 23 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0072 others(20): Show |
23 | HG00280.hp1 HG00408.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.931+9249A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616169 | |||||||
| chr6:46616170 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0230 |
2 | NA18949.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.931+9248A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616170 | |||||||
| chr6:46616171 | C | T | 37 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(34): Show |
37 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.931+9247G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616171 | |||||||
| chr6:46616172 | T | A | 14 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0082 others(11): Show |
14 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.931+9246A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616172 | |||||||
| chr6:46616172 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0230 |
2 | NA18949.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.931+9246A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616172 | |||||||
| chr6:46616172 | T | TC | 5 | a0001c0001t0001g0139 a0001c0001t0001g0261 a0006c0006t0001g0010 others(2): Show |
5 | HG01175.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9245_931+9246i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616172 | |||||||
| chr6:46616173 | T | A | 23 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0072 others(20): Show |
23 | HG00280.hp1 HG00408.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.931+9245A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616173 | |||||||
| chr6:46616173 | T | C | 17 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0084 others(14): Show |
17 | HG00140.hp2 HG01261.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.931+9245A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616173 | |||||||
| chr6:46616174 | T | C | 16 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0082 others(13): Show |
16 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.931+9244A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616174 | |||||||
| chr6:46616175 | C | T | 22 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0084 others(19): Show |
22 | HG00140.hp2 HG01175.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.931+9243G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616175 | |||||||
| chr6:46616175 | CTTT | C | 22 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0072 others(19): Show |
22 | HG00408.hp2 HG01884.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.931+9240_931+9242d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616175 | |||||||
| chr6:46616176 | T | A | 5 | a0001c0001t0001g0139 a0001c0001t0001g0261 a0006c0006t0001g0010 others(2): Show |
5 | HG01175.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9242A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616176 | |||||||
| chr6:46616176 | T | C | 16 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0082 others(13): Show |
16 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.931+9242A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616176 | |||||||
| chr6:46616177 | T | A | 17 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0084 others(14): Show |
17 | HG00140.hp2 HG01261.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.931+9241A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616177 | |||||||
| chr6:46616177 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9241A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616177 | |||||||
| chr6:46616178 | T | C | 22 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0082 others(19): Show |
22 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.931+9240A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616178 | |||||||
| chr6:46616179 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9239G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616179 | |||||||
| chr6:46616179 | CTTT | C | 17 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0084 others(14): Show |
17 | HG00140.hp2 HG01261.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.931+9236_931+9238d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616179 | |||||||
| chr6:46616180 | T | C | 44 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(41): Show |
44 | HG00408.hp2 HG00609.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+9238A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616180 | |||||||
| chr6:46616181 | T | A | 1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9237A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616181 | |||||||
| chr6:46616181 | T | C | 1 | a0002c0002t0004g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.931+9237A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616181 | |||||||
| chr6:46616182 | T | C | 45 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(42): Show |
45 | HG00408.hp2 HG00609.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.931+9236A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616182 | |||||||
| chr6:46616183 | C | T | 1 | a0008c0008t0002g0016 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.931+9235G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616183 | |||||||
| chr6:46616183 | CT | C | 3 | a0001c0001t0001g0122 a0002c0002t0002g0127 a0002c0002t0004g0305 |
3 | HG00733.hp2 HG02055.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.931+9234delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616183 | |||||||
| chr6:46616184 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931+9234A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616184 | |||||||
| chr6:46616184 | T | C | 62 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(59): Show |
62 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.931+9234A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616184 | |||||||
| chr6:46616186 | T | C | 64 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.931+9232A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616186 | |||||||
| chr6:46616187 | C | CT | 6 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(3): Show |
6 | HG02055.hp1 HG02886.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9230dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616187 | |||||||
| chr6:46616187 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+9231G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616187 | |||||||
| chr6:46616188 | T | A | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+9230A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616188 | |||||||
| chr6:46616188 | T | C | 66 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(63): Show |
66 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.931+9230A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616188 | |||||||
| chr6:46616190 | C | T | 2 | a0001c0001t0003g0190 a0002c0002t0002g0127 |
2 | HG00733.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9228G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616190 | |||||||
| chr6:46616191 | T | C | 71 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.931+9227A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616191 | |||||||
| chr6:46616191 | T | TTTCTCTT others(5): Show |
4 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9226_931+9227i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616191 | |||||||
| chr6:46616192 | T | C | 69 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+9226A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616192 | T | TTCCC | 26 | a0002c0002t0001g0094 a0002c0002t0001g0163 a0002c0002t0001g0176 others(23): Show |
26 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.931+9222_931+9225d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616192 | TTCCC | T | 42 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0134 others(39): Show |
42 | HG00558.hp2 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.931+9222_931+9225d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616192 | TTCCCTCC others(1): Show |
T | 52 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0052 others(49): Show |
54 | HG00597.hp2 HG00639.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.931+9218_931+9225d others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616192 | TTCCCTCC others(5): Show |
T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0065 others(13): Show |
17 | HG00735.hp2 HG01069.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.931+9214_931+9225d others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616192 | TTCCCTCC others(9): Show |
T | 8 | a0001c0001t0001g0053 a0002c0002t0002g0102 a0002c0002t0002g0146 others(5): Show |
8 | HG01891.hp2 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.931+9210_931+9225d others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616192 | TTCCCTCC others(11): Show |
T | 1 | a0004c0004t0001g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.931+9208_931+9225d others(20): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616192 | TTCCCTCC others(13): Show |
T | 6 | a0001c0001t0003g0275 a0005c0005t0001g0233 a0005c0005t0001g0282 others(3): Show |
6 | HG02647.hp1 HG02970.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9206_931+9225d others(22): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616192 | TTCCCTCC others(17): Show |
T | 1 | a0001c0001t0003g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+9202_931+9225d others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616192 | TTCCCTCC others(21): Show |
T | 1 | a0004c0004t0001g0022 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.931+9198_931+9225d others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | |||||||
| chr6:46616193 | TCCCTCCC others(6): Show |
T | 2 | a0001c0001t0003g0187 a0001c0001t0003g0189 |
2 | HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.931+9212_931+9224d others(15): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616193 | |||||||
| chr6:46616193 | TCCCTCCC others(10): Show |
T | 1 | a0001c0001t0003g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.931+9208_931+9224d others(19): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616193 | |||||||
| chr6:46616194 | C | T | 1 | a0001c0001t0003g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.931+9224G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616194 | |||||||
| chr6:46616195 | C | T | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.931+9223G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616195 | |||||||
| chr6:46616196 | C | T | 2 | a0001c0001t0003g0190 a0002c0002t0001g0194 |
2 | NA18972.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9222G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616196 | |||||||
| chr6:46616198 | C | T | 1 | a0001c0001t0003g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.931+9220G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616198 | |||||||
| chr6:46616200 | C | T | 1 | a0001c0001t0003g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.931+9218G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616200 | |||||||
| chr6:46616202 | C | T | 1 | a0001c0001t0003g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.931+9216G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616202 | |||||||
| chr6:46616204 | C | T | 2 | a0001c0001t0003g0190 a0005c0005t0001g0273 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9214G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616204 | |||||||
| chr6:46616206 | C | T | 2 | a0001c0001t0003g0190 a0005c0005t0001g0273 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9212G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616206 | |||||||
| chr6:46616208 | C | T | 4 | a0001c0001t0003g0187 a0001c0001t0003g0189 a0001c0001t0003g0190 others(1): Show |
4 | HG02886.hp2 HG03540.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9210G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616208 | |||||||
| chr6:46616210 | C | CCCTTCCT others(5): Show |
2 | a0001c0001t0001g0260 a0006c0006t0001g0009 |
2 | HG00738.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.931+9207_931+9208i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616210 | |||||||
| chr6:46616210 | C | T | 3 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0005c0005t0001g0273 |
3 | HG02886.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9208G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616210 | |||||||
| chr6:46616211 | C | T | 1 | a0001c0001t0003g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.931+9207G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616211 | |||||||
| chr6:46616212 | C | T | 6 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(3): Show |
6 | HG02027.hp1 HG02886.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9206G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616212 | |||||||
| chr6:46616214 | C | CCCTTCCT others(1): Show |
4 | a0001c0001t0001g0093 a0001c0001t0001g0230 a0001c0001t0001g0253 others(1): Show |
4 | HG01175.hp1 NA18942.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9203_931+9204i others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | |||||||
| chr6:46616214 | C | CCCTTCCT others(5): Show |
2 | a0001c0001t0001g0229 a0006c0006t0001g0043 |
2 | HG00609.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.931+9203_931+9204i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | |||||||
| chr6:46616214 | C | CCCTTCCT others(9): Show |
2 | a0001c0001t0001g0245 a0001c0001t0001g0252 |
2 | NA18962.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.931+9203_931+9204i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | |||||||
| chr6:46616214 | C | CCCTTCCT others(17): Show |
1 | a0001c0001t0001g0124 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.931+9203_931+9204i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | |||||||
| chr6:46616214 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0249 a0001c0001t0001g0260 others(1): Show |
4 | HG00738.hp2 HG02074.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9204G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | |||||||
| chr6:46616215 | C | T | 6 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(3): Show |
6 | HG02886.hp2 HG03540.hp1 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9203G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616215 | |||||||
| chr6:46616216 | C | T | 4 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0190 others(1): Show |
4 | HG02886.hp2 HG03540.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9202G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616216 | |||||||
| chr6:46616218 | C | CCCTTCCT others(5): Show |
1 | a0001c0001t0001g0261 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.931+9199_931+9200i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | |||||||
| chr6:46616218 | C | CCCTTCCT others(9): Show |
1 | a0001c0001t0001g0126 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.931+9199_931+9200i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | |||||||
| chr6:46616218 | C | CCCTTCCT others(17): Show |
2 | a0001c0001t0001g0258 a0006c0006t0001g0025 |
2 | HG00140.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.931+9199_931+9200i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | |||||||
| chr6:46616218 | C | CCCTTCCT others(21): Show |
1 | a0001c0001t0001g0123 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.931+9199_931+9200i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | |||||||
| chr6:46616218 | C | T | 16 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0124 others(13): Show |
16 | HG00280.hp1 HG00609.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.931+9200G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | |||||||
| chr6:46616219 | C | T | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+9199G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616219 | |||||||
| chr6:46616220 | C | A | 2 | a0001c0001t0003g0187 a0001c0001t0003g0275 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.931+9198G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616220 | |||||||
| chr6:46616222 | C | CCCTTCCT others(5): Show |
1 | a0001c0001t0001g0263 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.931+9195_931+9196i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | |||||||
| chr6:46616222 | C | CCCTTCCT others(9): Show |
1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.931+9195_931+9196i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | |||||||
| chr6:46616222 | C | CCCTTCCT others(17): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0228 a0006c0006t0001g0006 |
3 | HG01261.hp1 NA18963.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.931+9195_931+9196i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | |||||||
| chr6:46616222 | C | CCCTTCCT others(21): Show |
2 | a0001c0001t0001g0247 a0006c0006t0001g0008 |
2 | HG02738.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.931+9195_931+9196i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | |||||||
| chr6:46616222 | C | CCCTTCCT others(25): Show |
2 | a0001c0001t0001g0227 a0001c0001t0001g0234 |
2 | NA18977.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.931+9195_931+9196i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | |||||||
| chr6:46616222 | C | CCCTTCCT others(29): Show |
2 | a0001c0001t0001g0244 a0001c0001t0001g0246 |
2 | NA18954.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.931+9195_931+9196i others(38): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | |||||||
| chr6:46616222 | C | T | 26 | a0001c0001t0001g0081 a0001c0001t0001g0091 a0001c0001t0001g0093 others(23): Show |
26 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.931+9196G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | |||||||
| chr6:46616223 | C | T | 5 | a0001c0001t0003g0186 a0001c0001t0003g0188 a0001c0001t0003g0189 others(2): Show |
5 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9195G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616223 | |||||||
| chr6:46616224 | C | A | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+9194G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616224 | |||||||
| chr6:46616226 | C | CCCTTCCT others(9): Show |
1 | a0001c0001t0001g0262 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.931+9191_931+9192i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | |||||||
| chr6:46616226 | C | CCCTTCCT others(17): Show |
2 | a0001c0001t0001g0231 a0001c0001t0001g0239 |
2 | NA18995.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.931+9191_931+9192i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | |||||||
| chr6:46616226 | C | CCCTTCCT others(21): Show |
2 | a0001c0001t0001g0121 a0001c0001t0001g0125 |
2 | HG02976.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.931+9191_931+9192i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | |||||||
| chr6:46616226 | C | CCCTTCCT others(25): Show |
2 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
2 | NA18959.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.931+9191_931+9192i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | |||||||
| chr6:46616226 | C | T | 32 | a0001c0001t0001g0061 a0001c0001t0001g0081 a0001c0001t0001g0091 others(29): Show |
32 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.931+9192G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | |||||||
| chr6:46616228 | C | A | 5 | a0001c0001t0003g0186 a0001c0001t0003g0188 a0001c0001t0003g0189 others(2): Show |
5 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9190G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616228 | |||||||
| chr6:46616230 | C | CCCTTCCT others(25): Show |
1 | a0001c0001t0001g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.931+9187_931+9188i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616230 | |||||||
| chr6:46616230 | C | CCCTTCCT others(29): Show |
1 | a0001c0001t0001g0259 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.931+9187_931+9188i others(38): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616230 | |||||||
| chr6:46616230 | C | CCCTTCCT others(33): Show |
1 | a0004c0004t0001g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.931+9187_931+9188i others(42): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616230 | |||||||
| chr6:46616230 | C | T | 41 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0081 others(38): Show |
41 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.931+9188G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616230 | |||||||
| chr6:46616234 | C | T | 46 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0071 others(43): Show |
46 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.931+9184G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616234 | |||||||
| chr6:46616238 | C | T | 51 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0069 others(48): Show |
51 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.931+9180G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616238 | |||||||
| chr6:46616242 | C | CCCTCCCT others(37): Show |
1 | a0001c0001t0001g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.931+9175_931+9176i others(46): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | |||||||
| chr6:46616242 | C | CCCTCCCT others(29): Show |
1 | a0001c0001t0001g0293 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.931+9175_931+9176i others(38): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | |||||||
| chr6:46616242 | C | CCCTCCCT others(21): Show |
2 | a0001c0001t0001g0288 a0001c0001t0001g0290 |
2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.931+9175_931+9176i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | |||||||
| chr6:46616242 | C | CCCTCCCT others(25): Show |
2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.931+9175_931+9176i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | |||||||
| chr6:46616242 | C | CCCTTCCT others(29): Show |
1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9175_931+9176i others(38): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | |||||||
| chr6:46616242 | C | CCCTTCCT others(33): Show |
1 | a0001c0001t0001g0232 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.931+9175_931+9176i others(42): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | |||||||
| chr6:46616242 | C | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(110): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.931+9176G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | |||||||
| chr6:46616255 | C | T | 1 | a0005c0005t0001g0192 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.931+9163G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616255 | |||||||
| chr6:46616259 | T | C | 78 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(75): Show |
78 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.931+9159A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616259 | |||||||
| chr6:46616282 | T | TCCTTCCT others(9): Show |
2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.931+9135_931+9136i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | |||||||
| chr6:46616282 | T | TCCTTCCT others(17): Show |
4 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0083 others(1): Show |
4 | HG03130.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9135_931+9136i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | |||||||
| chr6:46616282 | T | TCCTTCCT others(21): Show |
4 | a0001c0001t0001g0104 a0001c0001t0001g0138 a0001c0001t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02895.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9135_931+9136i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | |||||||
| chr6:46616282 | T | TCCTTCCT others(25): Show |
5 | a0001c0001t0001g0050 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9135_931+9136i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | |||||||
| chr6:46616282 | T | TCCTTCCT others(33): Show |
5 | a0001c0001t0001g0068 a0001c0001t0001g0084 a0001c0001t0001g0089 others(2): Show |
5 | HG02280.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9135_931+9136i others(42): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | |||||||
| chr6:46616311 | G | A | 6 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(3): Show |
6 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9107C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616311 | |||||||
| chr6:46616362 | A | G | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+9056T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616362 | |||||||
| chr6:46616531 | C | A | 1 | a0004c0004t0001g0033 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.931+8887G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616531 | |||||||
| chr6:46616574 | T | G | 1 | a0002c0002t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.931+8844A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616574 | |||||||
| chr6:46616587 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.931+8831A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616587 | |||||||
| chr6:46616706 | A | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(39): Show |
44 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+8712T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616706 | |||||||
| chr6:46616738 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.931+8680A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616738 | |||||||
| chr6:46616855 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.931+8563A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616855 | |||||||
| chr6:46616949 | T | C | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.931+8469A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616949 | |||||||
| chr6:46616953 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+8465G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616953 | |||||||
| chr6:46617140 | T | G | 1 | a0003c0003t0001g0206 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.931+8278A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617140 | |||||||
| chr6:46617286 | C | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+8132G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617286 | |||||||
| chr6:46617356 | T | G | 69 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+8062A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617356 | |||||||
| chr6:46617409 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.931+8009T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617409 | |||||||
| chr6:46617416 | C | A | 1 | a0001c0001t0001g0243 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.931+8002G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617416 | |||||||
| chr6:46617454 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(39): Show |
44 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+7964C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617454 | |||||||
| chr6:46617661 | G | A | 1 | a0004c0004t0001g0033 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.931+7757C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617661 | |||||||
| chr6:46617737 | G | A | 1 | a0002c0002t0002g0146 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.931+7681C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617737 | |||||||
| chr6:46617855 | T | C | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.931+7563A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617855 | |||||||
| chr6:46618165 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.931+7253G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618165 | |||||||
| chr6:46618175 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+7243G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618175 | |||||||
| chr6:46618421 | A | C | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+6997T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618421 | |||||||
| chr6:46618534 | A | G | 8 | a0001c0001t0001g0290 a0001c0001t0003g0186 a0001c0001t0003g0187 others(5): Show |
8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.931+6884T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618534 | |||||||
| chr6:46618576 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.931+6842G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618576 | |||||||
| chr6:46618812 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+6606A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618812 | |||||||
| chr6:46618915 | T | C | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+6503A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618915 | |||||||
| chr6:46618973 | C | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.931+6445G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618973 | |||||||
| chr6:46619008 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.931+6410A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619008 | |||||||
| chr6:46619203 | C | T | 1 | a0003c0003t0001g0215 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.931+6215G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619203 | |||||||
| chr6:46619462 | T | C | 1 | a0002c0002t0002g0250 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.931+5956A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619462 | |||||||
| chr6:46619783 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5635G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619783 | |||||||
| chr6:46619913 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5505G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619913 | |||||||
| chr6:46619927 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5491G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619927 | |||||||
| chr6:46620096 | C | A | 13 | a0002c0002t0001g0113 a0002c0002t0001g0169 a0002c0002t0001g0170 others(10): Show |
13 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.931+5322G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620096 | |||||||
| chr6:46620149 | T | C | 1 | a0007c0007t0002g0036 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.931+5269A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620149 | |||||||
| chr6:46620179 | T | C | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+5239A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620179 | |||||||
| chr6:46620235 | C | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5183G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620235 | |||||||
| chr6:46620260 | C | G | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5158G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620260 | |||||||
| chr6:46620290 | G | T | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+5128C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620290 | |||||||
| chr6:46620312 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5106G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620312 | |||||||
| chr6:46620625 | T | C | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4793A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620625 | |||||||
| chr6:46620668 | TG | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4749delC | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620668 | |||||||
| chr6:46620684 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4734G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620684 | |||||||
| chr6:46620733 | G | A | 1 | a0005c0005t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.931+4685C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620733 | |||||||
| chr6:46620897 | A | G | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4521T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620897 | |||||||
| chr6:46620899 | A | C | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4519T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620899 | |||||||
| chr6:46620905 | ACAAT | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4509_931+4512d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620905 | |||||||
| chr6:46620915 | A | G | 1 | a0005c0005t0001g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.931+4503T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620915 | |||||||
| chr6:46620966 | G | A | 1 | a0004c0004t0001g0038 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.931+4452C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620966 | |||||||
| chr6:46621089 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.931+4329C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621089 | |||||||
| chr6:46621202 | G | C | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4216C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621202 | |||||||
| chr6:46621216 | T | TCA | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4201_931+4202i others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621216 | |||||||
| chr6:46621231 | T | C | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+4187A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621231 | |||||||
| chr6:46621318 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+4100T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621318 | |||||||
| chr6:46621323 | AAAATT | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4090_931+4094d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621323 | |||||||
| chr6:46621422 | G | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3996C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621422 | |||||||
| chr6:46621434 | A | G | 1 | a0002c0002t0001g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.931+3984T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621434 | |||||||
| chr6:46621490 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3928G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621490 | |||||||
| chr6:46621513 | G | T | 1 | a0005c0005t0001g0192 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.931+3905C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621513 | |||||||
| chr6:46621546 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3872G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621546 | |||||||
| chr6:46621558 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0177 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.931+3860A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621558 | |||||||
| chr6:46621606 | C | G | 5 | a0005c0005t0001g0282 a0005c0005t0001g0285 a0005c0005t0001g0286 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+3812G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621606 | |||||||
| chr6:46621742 | A | C | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+3676T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621742 | |||||||
| chr6:46621764 | C | G | 127 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(124): Show |
129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.931+3654G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621764 | |||||||
| chr6:46621765 | C | A | 5 | a0005c0005t0001g0282 a0005c0005t0001g0285 a0005c0005t0001g0286 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+3653G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621765 | |||||||
| chr6:46621816 | T | C | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3602A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621816 | |||||||
| chr6:46621958 | T | C | 1 | a0010c0010t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.931+3460A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621958 | |||||||
| chr6:46622008 | G | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3410C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622008 | |||||||
| chr6:46622066 | A | C | 1 | a0002c0002t0001g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.931+3352T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622066 | |||||||
| chr6:46622071 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3347G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622071 | |||||||
| chr6:46622155 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.931+3263G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622155 | |||||||
| chr6:46622259 | T | G | 1 | a0002c0002t0004g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.931+3159A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622259 | |||||||
| chr6:46622334 | C | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3084G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622334 | |||||||
| chr6:46622440 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2978G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622440 | |||||||
| chr6:46622471 | A | G | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2947T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622471 | |||||||
| chr6:46622523 | G | A | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+2895C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622523 | |||||||
| chr6:46622560 | C | CTATGATC others(55): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02280.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.931+2857_931+2858i others(64): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622560 | |||||||
| chr6:46622577 | T | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(166): Show |
172 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.931+2841A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622577 | |||||||
| chr6:46622693 | A | G | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2725T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622693 | |||||||
| chr6:46622943 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.931+2475G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622943 | |||||||
| chr6:46622944 | T | C | 1 | a0001c0001t0001g0243 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.931+2474A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622944 | |||||||
| chr6:46622966 | T | A | 2 | a0002c0002t0002g0129 a0003c0003t0002g0213 |
2 | HG00735.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.931+2452A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622966 | |||||||
| chr6:46623019 | A | G | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2399T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623019 | |||||||
| chr6:46623148 | T | C | 40 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(37): Show |
42 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.931+2270A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623148 | |||||||
| chr6:46623187 | C | CA | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2230_931+2231i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623187 | |||||||
| chr6:46623265 | A | C | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+2153T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623265 | |||||||
| chr6:46623302 | T | C | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2116A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623302 | |||||||
| chr6:46623354 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.931+2064A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623354 | |||||||
| chr6:46623480 | C | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+1938G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623480 | |||||||
| chr6:46623836 | T | C | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | NA18949.hp2 NA18963.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.931+1582A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623836 | |||||||
| chr6:46623940 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+1478G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623940 | |||||||
| chr6:46623983 | C | T | 1 | a0004c0004t0001g0030 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.931+1435G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623983 | |||||||
| chr6:46623984 | A | AT | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+1433dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623984 | |||||||
| chr6:46624290 | G | T | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+1128C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624290 | |||||||
| chr6:46624361 | C | T | 1 | a0002c0002t0002g0146 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.931+1057G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624361 | |||||||
| chr6:46624372 | C | A | 69 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+1046G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624372 | |||||||
| chr6:46624428 | A | G | 1 | a0001c0001t0003g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.931+990T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624428 | |||||||
| chr6:46624452 | T | C | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+966A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624452 | |||||||
| chr6:46624501 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+917G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624501 | |||||||
| chr6:46624564 | A | G | 1 | a0002c0002t0001g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.931+854T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624564 | |||||||
| chr6:46624571 | A | G | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+847T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624571 | |||||||
| chr6:46624653 | T | C | 7 | a0002c0002t0002g0102 a0002c0002t0002g0168 a0002c0002t0002g0272 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+765A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624653 | |||||||
| chr6:46624681 | T | C | 44 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+737A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624681 | |||||||
| chr6:46624776 | A | T | 69 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+642T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624776 | |||||||
| chr6:46624886 | C | T | 69 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+532G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624886 | |||||||
| chr6:46624889 | C | T | 127 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(124): Show |
129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.931+529G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624889 | |||||||
| chr6:46624946 | C | T | 20 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+472G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624946 | |||||||
| chr6:46625142 | G | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+276C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625142 | |||||||
| chr6:46625152 | T | C | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+266A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625152 | |||||||
| chr6:46625290 | T | C | 1 | a0004c0004t0001g0038 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.931+128A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625290 | |||||||
| chr6:46625339 | A | G | 1 | a0007c0007t0001g0039 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.931+79T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625339 | |||||||
| chr6:46625342 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.931+76C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625342 | |||||||
| chr6:46625349 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+69T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625349 | |||||||
| chr6:46625535 | A | C | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.841-27T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625535 | |||||||
| chr6:46625584 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.841-76G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625584 | |||||||
| chr6:46625759 | A | G | 1 | a0002c0002t0001g0181 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.841-251T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625759 | |||||||
| chr6:46625815 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.841-307T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625815 | |||||||
| chr6:46625870 | A | G | 1 | a0002c0002t0001g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.841-362T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625870 | |||||||
| chr6:46626061 | C | CT | 68 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.841-554dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626061 | |||||||
| chr6:46626099 | A | T | 77 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.841-591T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626099 | |||||||
| chr6:46626329 | T | C | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.841-821A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626329 | |||||||
| chr6:46626384 | G | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0068 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.841-876C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626384 | |||||||
| chr6:46626803 | A | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-1295T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626803 | |||||||
| chr6:46626908 | T | C | 23 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0099 others(20): Show |
23 | HG01069.hp2 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.841-1400A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626908 | |||||||
| chr6:46626909 | G | A | 23 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0099 others(20): Show |
23 | HG01069.hp2 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.841-1401C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626909 | |||||||
| chr6:46626912 | T | C | 16 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0099 others(13): Show |
16 | HG01069.hp2 HG01255.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-1404A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626912 | |||||||
| chr6:46627080 | A | G | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.841-1572T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627080 | |||||||
| chr6:46627208 | C | T | 2 | a0001c0001t0001g0045 a0006c0006t0001g0001 |
3 | HG02056.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.841-1700G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627208 | |||||||
| chr6:46627243 | C | G | 56 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(53): Show |
56 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.841-1735G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627243 | |||||||
| chr6:46627344 | A | G | 1 | a0005c0005t0001g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.841-1836T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627344 | |||||||
| chr6:46627380 | C | G | 20 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0140 others(17): Show |
20 | HG01069.hp2 HG01255.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.841-1872G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627380 | |||||||
| chr6:46627410 | TTTTA | T | 30 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(27): Show |
30 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.841-1906_841-1903d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627410 | |||||||
| chr6:46627418 | ATTTAT | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(63): Show |
68 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.841-1915_841-1911d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627418 | |||||||
| chr6:46627419 | TTTA | T | 16 | a0001c0001t0001g0061 a0001c0001t0001g0224 a0001c0001t0001g0225 others(13): Show |
16 | HG00741.hp1 HG01175.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-1914_841-1912d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627419 | |||||||
| chr6:46627422 | AT | A | 112 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0134 others(109): Show |
112 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.841-1915delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627422 | |||||||
| chr6:46627422 | ATTTTT | A | 23 | a0003c0003t0001g0257 a0004c0004t0001g0002 a0004c0004t0001g0012 others(20): Show |
24 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.841-1919_841-1915d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627422 | |||||||
| chr6:46627422 | ATTTTTT | A | 20 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0140 others(17): Show |
20 | HG01069.hp2 HG01255.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.841-1920_841-1915d others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627422 | |||||||
| chr6:46627426 | T | A | 6 | a0001c0001t0001g0096 a0001c0001t0001g0290 a0003c0003t0001g0205 others(3): Show |
6 | HG01071.hp1 HG01074.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-1918A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627426 | |||||||
| chr6:46627427 | T | A | 2 | a0002c0002t0001g0164 a0002c0002t0002g0207 |
2 | HG01261.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.841-1919A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627427 | |||||||
| chr6:46627480 | G | A | 1 | a0006c0006t0001g0006 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.841-1972C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627480 | |||||||
| chr6:46627504 | C | T | 20 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0140 others(17): Show |
20 | HG01069.hp2 HG01255.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.841-1996G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627504 | |||||||
| chr6:46627505 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | NA18955.hp1 NA19002.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-1997C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627505 | |||||||
| chr6:46627698 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.841-2190C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627698 | |||||||
| chr6:46627750 | A | T | 19 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0103 others(16): Show |
19 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.841-2242T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627750 | |||||||
| chr6:46627753 | A | T | 57 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(54): Show |
57 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.841-2245T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627753 | |||||||
| chr6:46627768 | A | T | 1 | a0001c0001t0001g0243 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.841-2260T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627768 | |||||||
| chr6:46627777 | A | G | 27 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0103 others(24): Show |
27 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.841-2269T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627777 | |||||||
| chr6:46628068 | C | A | 1 | a0002c0002t0001g0074 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.841-2560G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628068 | |||||||
| chr6:46628120 | G | C | 8 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(5): Show |
8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-2612C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628120 | |||||||
| chr6:46628184 | G | C | 1 | a0007c0007t0002g0037 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.841-2676C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628184 | |||||||
| chr6:46628366 | G | A | 2 | a0002c0002t0002g0168 a0003c0003t0002g0255 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.840+2597C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628366 | |||||||
| chr6:46628549 | A | C | 66 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0134 others(63): Show |
66 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.840+2414T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628549 | |||||||
| chr6:46628642 | A | T | 19 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0103 others(16): Show |
19 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.840+2321T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628642 | |||||||
| chr6:46628780 | C | T | 2 | a0002c0002t0002g0101 a0002c0002t0002g0136 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.840+2183G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628780 | |||||||
| chr6:46629111 | G | A | 1 | a0005c0005t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.840+1852C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629111 | |||||||
| chr6:46629227 | G | A | 1 | a0005c0005t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.840+1736C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629227 | |||||||
| chr6:46629277 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.840+1686C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629277 | |||||||
| chr6:46629525 | A | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0010c0010t0001g0178 |
3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.840+1438T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629525 | |||||||
| chr6:46629771 | T | C | 4 | a0002c0002t0001g0194 a0002c0002t0001g0198 a0002c0002t0002g0101 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+1192A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629771 | |||||||
| chr6:46629871 | G | T | 27 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(24): Show |
27 | HG01069.hp2 HG01255.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.840+1092C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629871 | |||||||
| chr6:46629903 | T | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+1060A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629903 | |||||||
| chr6:46629918 | G | A | 1 | a0002c0002t0001g0153 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.840+1045C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629918 | |||||||
| chr6:46630025 | A | G | 26 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0103 others(23): Show |
26 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.840+938T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630025 | |||||||
| chr6:46630130 | C | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0262 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+833G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630130 | |||||||
| chr6:46630130 | C | CAAAAA | 13 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0137 others(10): Show |
13 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.840+828_840+832dup others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630130 | |||||||
| chr6:46630130 | C | CAACAA | 10 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0003g0186 others(7): Show |
10 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.840+832_840+833ins others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630130 | |||||||
| chr6:46630137 | A | C | 8 | a0005c0005t0001g0281 a0005c0005t0001g0282 a0005c0005t0001g0284 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+826T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630137 | |||||||
| chr6:46630142 | C | CA | 8 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(5): Show |
8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+820dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630142 | |||||||
| chr6:46630526 | A | G | 12 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0002g0238 others(9): Show |
12 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.840+437T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630526 | |||||||
| chr6:46630672 | A | C | 1 | a0002c0002t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.840+291T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630672 | |||||||
| chr6:46631105 | CTA | C | 4 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0002g0238 others(1): Show |
4 | HG02258.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-37_733-36delTA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631105 | |||||||
| chr6:46631120 | C | T | 13 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.733-50G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631120 | |||||||
| chr6:46631450 | A | G | 52 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(49): Show |
52 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.733-380T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631450 | |||||||
| chr6:46631537 | C | T | 8 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(5): Show |
8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-467G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631537 | |||||||
| chr6:46631803 | T | C | 1 | a0002c0002t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.733-733A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631803 | |||||||
| chr6:46632105 | T | C | 5 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0002g0238 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-1035A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632105 | |||||||
| chr6:46632326 | A | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(44): Show |
49 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.733-1256T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632326 | |||||||
| chr6:46632350 | A | G | 1 | a0002c0002t0001g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.733-1280T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632350 | |||||||
| chr6:46632412 | C | T | 1 | a0003c0003t0001g0279 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.733-1342G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632412 | |||||||
| chr6:46632604 | TC | T | 19 | a0004c0004t0001g0002 a0004c0004t0001g0012 a0004c0004t0001g0014 others(16): Show |
20 | HG00609.hp2 HG02015.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.733-1535delG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632604 | |||||||
| chr6:46632610 | C | T | 8 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(5): Show |
8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-1540G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632610 | |||||||
| chr6:46632705 | AT | A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0002g0238 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-1636delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632705 | |||||||
| chr6:46632954 | A | G | 3 | a0003c0003t0001g0202 a0003c0003t0001g0214 a0007c0007t0001g0004 |
3 | HG02083.hp2 NA18975.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.733-1884T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632954 | |||||||
| chr6:46632969 | T | TAGAGACT others(315): Show |
1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733-1900_733-1899i others(324): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632969 | |||||||
| chr6:46633132 | G | C | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.733-2062C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633132 | |||||||
| chr6:46633395 | C | T | 1 | a0002c0002t0002g0250 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.733-2325G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633395 | |||||||
| chr6:46633578 | G | T | 3 | a0002c0002t0002g0127 a0002c0002t0002g0143 a0002c0002t0002g0144 |
3 | HG00733.hp2 HG01975.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.733-2508C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633578 | |||||||
| chr6:46633597 | G | A | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.733-2527C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633597 | |||||||
| chr6:46633614 | T | G | 5 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0002g0238 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-2544A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633614 | |||||||
| chr6:46633617 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02280.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.733-2547C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633617 | |||||||
| chr6:46633625 | G | A | 3 | a0002c0002t0001g0051 a0002c0002t0001g0112 a0003c0003t0002g0270 |
3 | HG01496.hp2 HG01952.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.733-2555C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633625 | |||||||
| chr6:46633631 | G | A | 3 | a0002c0002t0001g0265 a0008c0008t0001g0029 a0008c0008t0002g0016 |
3 | HG01243.hp2 HG01496.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.733-2561C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633631 | |||||||
| chr6:46633640 | C | T | 8 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(5): Show |
8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-2570G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633640 | |||||||
| chr6:46633819 | T | C | 54 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(51): Show |
54 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.732+2570A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633819 | |||||||
| chr6:46633844 | A | C | 4 | a0001c0001t0001g0242 a0001c0001t0001g0258 a0001c0001t0001g0260 others(1): Show |
4 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+2545T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633844 | |||||||
| chr6:46633848 | C | G | 2 | a0003c0003t0001g0200 a0003c0003t0001g0201 |
2 | HG01109.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.732+2541G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633848 | |||||||
| chr6:46633863 | G | GA | 11 | a0001c0001t0001g0167 a0001c0001t0002g0238 a0001c0001t0003g0186 others(8): Show |
11 | HG02615.hp1 HG02886.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.732+2525dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633863 | |||||||
| chr6:46634175 | G | A | 113 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(110): Show |
114 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.732+2214C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634175 | |||||||
| chr6:46634267 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+2122C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634267 | |||||||
| chr6:46634507 | C | CT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(46): Show |
51 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.732+1881dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634507 | |||||||
| chr6:46634523 | G | GT | 26 | a0001c0001t0001g0061 a0001c0001t0001g0121 a0001c0001t0001g0185 others(23): Show |
26 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.732+1865_732+1866i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634523 | |||||||
| chr6:46634523 | G | GTT | 72 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(69): Show |
74 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.732+1865_732+1866i others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634523 | |||||||
| chr6:46634523 | G | GTTT | 4 | a0001c0001t0001g0062 a0001c0001t0001g0123 a0001c0001t0001g0227 others(1): Show |
4 | HG03688.hp1 NA18955.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+1865_732+1866i others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634523 | |||||||
| chr6:46634524 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(109): Show |
114 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.732+1865G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634524 | |||||||
| chr6:46634524 | CT | C | 72 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0134 others(69): Show |
72 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.732+1864delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634524 | |||||||
| chr6:46634603 | C | A | 1 | a0001c0001t0003g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.732+1786G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634603 | |||||||
| chr6:46634668 | C | T | 2 | a0002c0002t0002g0101 a0002c0002t0002g0136 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.732+1721G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634668 | |||||||
| chr6:46634826 | C | T | 146 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(143): Show |
147 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.732+1563G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634826 | |||||||
| chr6:46635123 | T | C | 1 | a0004c0004t0001g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.732+1266A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635123 | |||||||
| chr6:46635145 | T | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0177 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+1244A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635145 | |||||||
| chr6:46635230 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+1159A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635230 | |||||||
| chr6:46635301 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.732+1088G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635301 | |||||||
| chr6:46635344 | G | A | 24 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(21): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.732+1045C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635344 | |||||||
| chr6:46635441 | C | A | 2 | a0002c0002t0001g0251 a0002c0002t0001g0264 |
2 | HG00558.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.732+948G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635441 | |||||||
| chr6:46635479 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.732+910G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635479 | |||||||
| chr6:46635531 | C | T | 24 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(21): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.732+858G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635531 | |||||||
| chr6:46635542 | G | GTGTT | 3 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0002c0002t0001g0135 |
3 | HG02109.hp1 HG03453.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.732+843_732+846dup others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635542 | |||||||
| chr6:46635583 | G | A | 1 | a0005c0005t0001g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.732+806C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635583 | |||||||
| chr6:46635728 | A | T | 23 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0099 others(20): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+661T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635728 | |||||||
| chr6:46635783 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.732+606C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635783 | |||||||
| chr6:46635950 | G | A | 146 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(143): Show |
147 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.732+439C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635950 | |||||||
| chr6:46636141 | T | G | 1 | a0004c0004t0001g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.732+248A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46636141 | |||||||
| chr6:46636220 | G | A | 3 | a0002c0002t0002g0168 a0003c0003t0002g0255 a0003c0003t0002g0270 |
3 | HG01891.hp2 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.732+169C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46636220 | |||||||
| chr6:46636263 | G | C | 70 | a0002c0002t0001g0176 a0003c0003t0001g0048 a0003c0003t0001g0193 others(67): Show |
71 | HG00408.hp2 HG00609.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.732+126C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46636263 | |||||||
| chr6:46636533 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.639-51A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636533 | |||||||
| chr6:46636749 | A | T | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.639-267T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636749 | |||||||
| chr6:46636775 | GGCTGCTG others(3): Show |
G | 1 | a0002c0002t0001g0210 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.639-303_639-294del others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636775 | |||||||
| chr6:46636821 | A | G | 5 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0002c0002t0002g0236 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-339T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636821 | |||||||
| chr6:46636911 | G | A | 3 | a0005c0005t0001g0237 a0005c0005t0001g0256 a0005c0005t0001g0269 |
3 | HG02451.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.639-429C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636911 | |||||||
| chr6:46637037 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.639-555T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637037 | |||||||
| chr6:46637175 | T | C | 21 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0116 others(18): Show |
21 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.638+654A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637175 | |||||||
| chr6:46637360 | A | T | 1 | a0007c0007t0001g0018 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.638+469T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637360 | |||||||
| chr6:46637437 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.638+392C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637437 | |||||||
| chr6:46637463 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.638+366G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637463 | |||||||
| chr6:46637605 | G | A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0002c0002t0002g0236 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+224C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637605 | |||||||
| chr6:46637732 | A | G | 9 | a0001c0001t0001g0290 a0001c0001t0003g0186 a0001c0001t0003g0187 others(6): Show |
9 | HG01884.hp1 HG02615.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.638+97T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637732 | |||||||
| chr6:46638013 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0240 a0001c0001t0001g0241 |
4 | NA18960.hp1 NA18971.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-35C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638013 | |||||||
| chr6:46638042 | A | C | 27 | a0002c0002t0001g0176 a0003c0003t0001g0048 a0003c0003t0001g0257 others(24): Show |
28 | HG00408.hp2 HG00609.hp2 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.489-64T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638042 | |||||||
| chr6:46638105 | G | A | 2 | a0003c0003t0001g0193 a0003c0003t0001g0195 |
2 | NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.489-127C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638105 | |||||||
| chr6:46638137 | G | C | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.489-159C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638137 | |||||||
| chr6:46638394 | C | T | 19 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0116 others(16): Show |
19 | HG00741.hp1 HG01891.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.489-416G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638394 | |||||||
| chr6:46638534 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.489-556T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638534 | |||||||
| chr6:46638591 | T | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(222): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.489-613A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638591 | |||||||
| chr6:46638698 | G | A | 8 | a0002c0002t0001g0113 a0002c0002t0001g0169 a0002c0002t0001g0170 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.489-720C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638698 | |||||||
| chr6:46638708 | C | T | 1 | a0010c0010t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.489-730G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638708 | |||||||
| chr6:46638813 | G | A | 1 | a0005c0005t0001g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.488+681C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638813 | |||||||
| chr6:46638842 | C | T | 3 | a0005c0005t0001g0237 a0005c0005t0001g0256 a0005c0005t0001g0269 |
3 | HG02451.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.488+652G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638842 | |||||||
| chr6:46638877 | G | A | 8 | a0002c0002t0001g0113 a0002c0002t0001g0169 a0002c0002t0001g0170 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+617C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638877 | |||||||
| chr6:46638979 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.488+515G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638979 | |||||||
| chr6:46639330 | T | C | 20 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(17): Show |
20 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.488+164A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639330 | |||||||
| chr6:46639335 | C | CA | 16 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.488+158dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639335 | |||||||
| chr6:46639344 | AT | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(141): Show |
146 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.488+149delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639344 | |||||||
| chr6:46639345 | T | A | 9 | a0002c0002t0001g0113 a0002c0002t0001g0169 a0002c0002t0001g0170 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.488+149A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639345 | |||||||
| chr6:46639488 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.488+6T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639488 | |||||||
| chr6:46639724 | T | A | 1 | a0002c0002t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.314-56A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639724 | |||||||
| chr6:46639740 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.314-72T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639740 | |||||||
| chr6:46639800 | A | T | 1 | a0001c0001t0003g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.314-132T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639800 | |||||||
| chr6:46639826 | T | C | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-158A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639826 | |||||||
| chr6:46639833 | G | A | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.314-165C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639833 | |||||||
| chr6:46639834 | A | G | 20 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(17): Show |
20 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-166T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639834 | |||||||
| chr6:46639841 | G | C | 48 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(45): Show |
48 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.314-173C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639841 | |||||||
| chr6:46639858 | T | C | 20 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(17): Show |
20 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-190A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639858 | |||||||
| chr6:46639943 | T | C | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-275A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639943 | |||||||
| chr6:46639971 | C | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(223): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.314-303G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639971 | |||||||
| chr6:46639980 | C | T | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-312G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639980 | |||||||
| chr6:46640055 | G | A | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(2): Show |
5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-387C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640055 | |||||||
| chr6:46640069 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.314-401G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640069 | |||||||
| chr6:46640152 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(223): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.314-484C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640152 | |||||||
| chr6:46640192 | G | T | 1 | a0001c0001t0003g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-524C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640192 | |||||||
| chr6:46640735 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.314-1067G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640735 | |||||||
| chr6:46640770 | G | A | 1 | a0004c0004t0001g0022 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.314-1102C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640770 | |||||||
| chr6:46640806 | T | A | 1 | a0002c0002t0001g0174 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.314-1138A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640806 | |||||||
| chr6:46640862 | C | T | 1 | a0003c0003t0001g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.314-1194G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640862 | |||||||
| chr6:46640937 | C | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0177 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.313+1226G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640937 | |||||||
| chr6:46641002 | T | C | 1 | a0002c0002t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.313+1161A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641002 | |||||||
| chr6:46641029 | G | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(223): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.313+1134C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641029 | |||||||
| chr6:46641221 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+942G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641221 | |||||||
| chr6:46641346 | A | T | 4 | a0002c0002t0002g0133 a0002c0002t0002g0298 a0002c0002t0002g0299 others(1): Show |
4 | HG02896.hp2 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+817T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641346 | |||||||
| chr6:46641347 | A | T | 4 | a0002c0002t0002g0133 a0002c0002t0002g0298 a0002c0002t0002g0299 others(1): Show |
4 | HG02896.hp2 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+816T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641347 | |||||||
| chr6:46641594 | T | C | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.313+569A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641594 | |||||||
| chr6:46641833 | G | A | 5 | a0003c0003t0002g0255 a0003c0003t0002g0270 a0005c0005t0001g0237 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+330C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641833 | |||||||
| chr6:46641939 | T | C | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.313+224A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641939 | |||||||
| chr6:46642047 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.313+116A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46642047 | |||||||
| chr6:46642361 | T | A | 5 | a0005c0005t0001g0282 a0005c0005t0001g0285 a0005c0005t0001g0286 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-63A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642361 | |||||||
| chr6:46642450 | G | C | 1 | a0002c0002t0002g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.178-152C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642450 | |||||||
| chr6:46642608 | T | C | 1 | a0005c0005t0001g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-310A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642608 | |||||||
| chr6:46642757 | G | C | 1 | a0006c0006t0001g0011 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-459C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642757 | |||||||
| chr6:46642779 | A | G | 2 | a0001c0001t0001g0290 a0001c0001t0003g0075 |
2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.178-481T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642779 | |||||||
| chr6:46642952 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.178-654G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642952 | |||||||
| chr6:46643274 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0177 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.178-976G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46643274 | |||||||
| chr6:46643807 | TTTG | T | 13 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(10): Show |
13 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.178-1512_178-1510d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46643807 | |||||||
| chr6:46643850 | G | A | 6 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(3): Show |
6 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-1552C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46643850 | |||||||
| chr6:46644028 | T | C | 48 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0092 others(45): Show |
48 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.178-1730A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644028 | |||||||
| chr6:46644112 | T | C | 5 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0002c0002t0002g0236 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-1814A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644112 | |||||||
| chr6:46644166 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.178-1868G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644166 | |||||||
| chr6:46644233 | T | C | 1 | a0002c0002t0001g0176 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.178-1935A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644233 | |||||||
| chr6:46644398 | A | C | 5 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0002c0002t0002g0236 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-2100T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644398 | |||||||
| chr6:46644432 | C | G | 1 | a0002c0002t0002g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.178-2134G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644432 | |||||||
| chr6:46644629 | T | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(6): Show |
9 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.178-2331A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644629 | |||||||
| chr6:46644910 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.178-2612C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644910 | |||||||
| chr6:46644916 | C | T | 300 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(297): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.178-2618G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644916 | |||||||
| chr6:46645261 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.178-2963A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645261 | |||||||
| chr6:46645317 | A | G | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-3019T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645317 | |||||||
| chr6:46645346 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(197): Show |
203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.178-3048A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645346 | |||||||
| chr6:46645617 | A | G | 1 | a0002c0002t0002g0127 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.178-3319T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645617 | |||||||
| chr6:46645795 | C | A | 1 | a0003c0003t0001g0219 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.178-3497G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645795 | |||||||
| chr6:46645977 | A | T | 2 | a0001c0001t0002g0238 a0001c0001t0005g0271 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.178-3679T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645977 | |||||||
| chr6:46646089 | C | T | 1 | a0004c0004t0001g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.178-3791G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646089 | |||||||
| chr6:46646255 | T | G | 1 | a0008c0008t0001g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.178-3957A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646255 | |||||||
| chr6:46646322 | A | T | 13 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(10): Show |
13 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.178-4024T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646322 | |||||||
| chr6:46646702 | T | G | 44 | a0003c0003t0001g0048 a0003c0003t0001g0226 a0003c0003t0001g0257 others(41): Show |
45 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.178-4404A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646702 | |||||||
| chr6:46646793 | G | A | 1 | a0003c0003t0002g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.178-4495C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646793 | |||||||
| chr6:46647093 | C | G | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-4795G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46647093 | |||||||
| chr6:46647651 | T | G | 1 | a0002c0002t0001g0119 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.177+4755A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46647651 | |||||||
| chr6:46647675 | C | T | 1 | a0004c0004t0001g0038 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.177+4731G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46647675 | |||||||
| chr6:46647947 | C | G | 3 | a0002c0002t0002g0298 a0002c0002t0002g0299 a0002c0002t0002g0300 |
3 | HG02896.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.177+4459G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46647947 | |||||||
| chr6:46648055 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.177+4351G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648055 | |||||||
| chr6:46648506 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0002c0002t0001g0131 |
3 | NA18995.hp1 NA19054.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.177+3900G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648506 | |||||||
| chr6:46648524 | A | AG | 28 | a0001c0001t0001g0050 a0001c0001t0001g0121 a0001c0001t0001g0239 others(25): Show |
28 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.177+3881dupC | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648524 | |||||||
| chr6:46648531 | A | G | 1 | a0004c0004t0001g0012 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.177+3875T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648531 | |||||||
| chr6:46648555 | A | G | 1 | a0002c0002t0002g0250 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.177+3851T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648555 | |||||||
| chr6:46648743 | G | A | 1 | a0002c0002t0001g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.177+3663C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648743 | |||||||
| chr6:46648929 | A | G | 1 | a0002c0002t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.177+3477T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648929 | |||||||
| chr6:46649094 | T | C | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(4): Show |
7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+3312A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649094 | |||||||
| chr6:46649131 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0177 |
3 | HG01891.hp1 HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.177+3275C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649131 | |||||||
| chr6:46649206 | T | A | 1 | a0002c0002t0001g0074 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.177+3200A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649206 | |||||||
| chr6:46649317 | T | C | 1 | a0002c0002t0002g0118 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.177+3089A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649317 | |||||||
| chr6:46649490 | T | C | 2 | a0001c0001t0001g0290 a0001c0001t0003g0075 |
2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.177+2916A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649490 | |||||||
| chr6:46649581 | C | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.177+2825G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649581 | |||||||
| chr6:46649891 | G | A | 3 | a0002c0002t0001g0251 a0002c0002t0001g0264 a0002c0002t0002g0250 |
3 | HG00558.hp1 HG02074.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.177+2515C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649891 | |||||||
| chr6:46650067 | C | T | 1 | a0002c0002t0001g0119 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.177+2339G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650067 | |||||||
| chr6:46650111 | T | TAC | 92 | a0001c0001t0001g0003 a0001c0001t0001g0095 a0001c0001t0001g0096 others(89): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.177+2293_177+2294d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | |||||||
| chr6:46650111 | T | TACAC | 14 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(11): Show |
14 | HG00741.hp1 HG02257.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.177+2291_177+2294d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | |||||||
| chr6:46650111 | T | TACACAC | 4 | a0001c0001t0002g0238 a0001c0001t0005g0271 a0004c0004t0001g0023 others(1): Show |
4 | HG03516.hp1 NA18951.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+2289_177+2294d others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | |||||||
| chr6:46650111 | T | TACACACA others(7): Show |
1 | a0003c0003t0002g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.177+2281_177+2294d others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | |||||||
| chr6:46650111 | T | TACACACA others(9): Show |
21 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(18): Show |
21 | HG00735.hp2 HG01071.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.177+2279_177+2294d others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | |||||||
| chr6:46650111 | T | TACACACA others(11): Show |
1 | a0003c0003t0001g0206 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.177+2277_177+2294d others(20): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | |||||||
| chr6:46650111 | TAC | T | 4 | a0001c0001t0001g0179 a0001c0001t0007g0049 a0002c0002t0002g0118 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+2293_177+2294d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | |||||||
| chr6:46650295 | G | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02738.hp1 HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.177+2111C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650295 | |||||||
| chr6:46650375 | C | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0092 others(37): Show |
41 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.177+2031G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650375 | |||||||
| chr6:46650383 | C | CT | 264 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(261): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.177+2022dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650383 | |||||||
| chr6:46650484 | C | CT | 34 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0258 others(31): Show |
35 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.177+1921dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | |||||||
| chr6:46650484 | C | CTT | 39 | a0001c0001t0001g0003 a0001c0001t0001g0086 a0001c0001t0001g0091 others(36): Show |
41 | HG00280.hp1 HG00408.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.177+1920_177+1921d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | |||||||
| chr6:46650484 | C | CTTT | 31 | a0001c0001t0001g0096 a0001c0001t0001g0227 a0001c0001t0001g0228 others(28): Show |
31 | HG00609.hp1 HG01175.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.177+1919_177+1921d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | |||||||
| chr6:46650484 | C | CTTTT | 8 | a0001c0001t0001g0095 a0001c0001t0001g0223 a0001c0001t0001g0224 others(5): Show |
8 | HG01261.hp1 HG01975.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+1918_177+1921d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | |||||||
| chr6:46650484 | CT | C | 12 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(9): Show |
12 | HG01069.hp2 HG01243.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.177+1921delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | |||||||
| chr6:46650484 | CTT | C | 8 | a0001c0001t0001g0047 a0001c0001t0001g0097 a0001c0001t0001g0288 others(5): Show |
8 | HG00423.hp1 HG01109.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+1920_177+1921d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | |||||||
| chr6:46650484 | CTTT | C | 42 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0052 others(39): Show |
42 | HG00558.hp2 HG00639.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.177+1919_177+1921d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | |||||||
| chr6:46650484 | CTTTT | C | 91 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.177+1918_177+1921d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | |||||||
| chr6:46650484 | CTTTTT | C | 11 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(8): Show |
11 | HG00140.hp1 HG01192.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+1917_177+1921d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | |||||||
| chr6:46650552 | C | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0047 others(270): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.177+1854G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650552 | |||||||
| chr6:46650586 | C | A | 1 | a0002c0002t0002g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.177+1820G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650586 | |||||||
| chr6:46650678 | AT | A | 105 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(102): Show |
105 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.177+1727delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650678 | |||||||
| chr6:46650716 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.177+1690T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650716 | |||||||
| chr6:46650719 | T | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0092 others(116): Show |
122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.177+1687A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650719 | |||||||
| chr6:46650732 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.177+1674A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650732 | |||||||
| chr6:46651063 | A | G | 1 | a0002c0002t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.177+1343T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46651063 | |||||||
| chr6:46651739 | A | T | 103 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(100): Show |
103 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.177+667T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46651739 | |||||||
| chr6:46652194 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | NA18949.hp2 NA18963.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.177+212G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652194 | |||||||
| chr6:46652302 | G | A | 3 | a0002c0002t0001g0296 a0002c0002t0001g0297 a0002c0002t0002g0295 |
3 | NA18945.hp1 NA18971.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.177+104C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652302 | |||||||
| chr6:46652360 | G | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.177+46C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652360 | |||||||
| chr6:46652367 | T | C | 3 | a0002c0002t0002g0298 a0002c0002t0002g0299 a0002c0002t0002g0300 |
3 | HG02896.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.177+39A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652367 | |||||||
| chr6:46652398 | C | T | 46 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0050 others(43): Show |
46 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(43): Show |
splice_region_variant&intron_variant | LOW | c.177+8G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652398 |