Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 340533 |
| ensemblid | ENSG00000050030.16 |
| hgncid | 29433 |
| symbol | NEXMIF |
| name | neurite extension and migration factor |
| refseq_nuc | NM_001008537.3 |
| refseq_prot | NP_001008537.1 |
| ensembl_nuc | ENST00000055682.12 |
| ensembl_prot | ENSP00000055682.5 |
| mane_status | MANE Select |
| chr | chrX |
| start | 74732856 |
| end | 74925452 |
| strand | - |
| ver | v1.2 |
| region | chrX:74732856-74925452 |
| region5000 | chrX:74727856-74930452 |
| regionname0 | NEXMIF_chrX_74732856_74925452 |
| regionname5000 | NEXMIF_chrX_74727856_74930452 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1516 | 216 | 60 | 43 | 77 | 7 | 27 | 52 | NEXMIF_chrX_74727856_74930452 | NEXMIF | MDNQQ others(1511): Show |
chrX | 74727856 | 74930452 |
| a0002 | 0/0 | 1516 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | MDNQQ others(1511): Show |
chrX | 74727856 | 74930452 |
| a0003 | 0/0 | 1516 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | MDNQQ others(1511): Show |
chrX | 74727856 | 74930452 |
| a0004 | 0/0 | 1516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | MDNQQ others(1511): Show |
chrX | 74727856 | 74930452 |
| a0005 | 0/0 | 1516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | MDNQQ others(1511): Show |
chrX | 74727856 | 74930452 |
| a0006 | 0/0 | 1516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | MDNQQ others(1511): Show |
chrX | 74727856 | 74930452 |
| a0007 | 0/0 | 1516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | MDNQQ others(1511): Show |
chrX | 74727856 | 74930452 |
| a0008 | 0/0 | 1516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | MDNQQ others(1511): Show |
chrX | 74727856 | 74930452 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4548 | 201 | 59 | 39 | 70 | 6 | 25 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0001c0002 | 0/0 | 4548 | 6 | 0 | 3 | 0 | 1 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0001c0003 | 0/0 | 4548 | 3 | 0 | 0 | 3 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0001c0005 | 0/0 | 4548 | 2 | 0 | 1 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0001c0007 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0001c0010 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0001c0012 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0001c0015 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0002c0004 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0003c0011 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0004c0006 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0005c0009 | 0/0 | 4548 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0006c0014 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0007c0008 | 0/0 | 4548 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 | ||
| a0008c0013 | 0/0 | 4548 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | ATGGA others(4543): Show |
chrX | 74727856 | 74930452 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 11717 | 108 | 33 | 13 | 51 | 1 | 9 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0002 | 0/1 | 11717 | 48 | 8 | 23 | 1 | 4 | 11 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0003 | 0/0 | 11717 | 11 | 0 | 0 | 11 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0004 | 0/0 | 11715 | 6 | 3 | 1 | 0 | 0 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11710): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0005 | 0/0 | 11717 | 5 | 5 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0006 | 0/0 | 11717 | 3 | 3 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0007 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0008 | 0/0 | 11717 | 2 | 0 | 0 | 2 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0009 | 0/0 | 11714 | 2 | 0 | 0 | 0 | 0 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11709): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0010 | 0/0 | 11719 | 2 | 1 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11714): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0012 | 0/0 | 11717 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0013 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0014 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0015 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0017 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0018 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0019 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0020 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0021 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0022 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0023 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0024 | 0/0 | 11717 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0001t0025 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0002t0001 | 0/0 | 11717 | 6 | 0 | 3 | 0 | 1 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0003t0001 | 0/0 | 11717 | 3 | 0 | 0 | 3 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0005t0001 | 0/0 | 11717 | 2 | 0 | 1 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0007t0001 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0010t0001 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0012t0001 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0001c0015t0001 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0002c0004t0001 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0002c0004t0011 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0003c0011t0002 | 0/0 | 11717 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0004c0006t0016 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0005c0009t0001 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0006c0014t0007 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0007c0008t0002 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| a0008c0013t0001 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | AAAAC others(11712): Show |
chrX | 74727856 | 74930452 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0009g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0012g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0013g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0014g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0015g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0017g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0018g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0019g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0020g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0021g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0022g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0023g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0024g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0025g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0005t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0005t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0007t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0010t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0012t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0015t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0002c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0002c0004t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0003c0011t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0004c0006t0016g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0005c0009t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0006c0014t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0007c0008t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0008c0013t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0170 | EUR | GBR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0030 | EUR | FIN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00323 | hp2 | a0001 | c0001 | t0025 | g0130 | EUR | FIN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00408 | hp1 | a0001 | c0001 | t0018 | g0178 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01168 | hp1 | a0001 | c0001 | t0024 | g0167 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0003 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | IBS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01975 | hp1 | a0001 | c0005 | t0001 | g0011 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0049 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02135 | hp1 | a0001 | c0001 | t0019 | g0017 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02273 | hp1 | a0003 | c0011 | t0002 | g0141 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02886 | hp2 | a0004 | c0006 | t0016 | g0118 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02896 | hp1 | a0002 | c0004 | t0011 | g0002 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0113 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0219 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03130 | hp1 | a0001 | c0001 | t0013 | g0004 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03239 | hp1 | a0005 | c0009 | t0001 | g0182 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03490 | hp1 | a0001 | c0001 | t0023 | g0171 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03491 | hp1 | a0001 | c0001 | t0009 | g0135 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0136 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03516 | hp2 | a0006 | c0014 | t0007 | g0112 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0201 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03540 | hp2 | a0001 | c0001 | t0017 | g0216 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03831 | hp2 | a0007 | c0008 | t0002 | g0132 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0133 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18522 | hp1 | a0001 | c0001 | t0021 | g0207 | AFR | YRI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | CHB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0091 | EAS | CHB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18944 | hp1 | a0001 | c0007 | t0001 | g0029 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18962 | hp1 | a0001 | c0001 | t0022 | g0037 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18965 | hp1 | a0001 | c0001 | t0020 | g0027 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18971 | hp1 | a0001 | c0015 | t0001 | g0008 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0095 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19011 | hp2 | a0001 | c0012 | t0001 | g0142 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19030 | hp1 | a0001 | c0001 | t0015 | g0210 | AFR | LWK | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | LWK | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0189 | AFR | LWK | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19056 | hp1 | a0001 | c0005 | t0001 | g0012 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ASW | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0169 | EUR | TSI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0151 | EUR | TSI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20905 | hp1 | a0008 | c0013 | t0001 | g0076 | SAS | GIH | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0114 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03471 | hp1 | a0001 | c0010 | t0001 | g0212 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | USA | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0153 | REF | REF | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0131 | REF | REF | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:74740311 | G | A | 1 | a0007 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.4246C>T | p.Pro1416Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 4863/11717 | 4246/4551 | 1416/1516 | chrX | 74740311 | |||
| chrX:74740734 | T | C | 1 | a0005 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.3823A>G | p.Ser1275Gly | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 4440/11717 | 3823/4551 | 1275/1516 | chrX | 74740734 | |||
| chrX:74740848 | T | A | 1 | a0004 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.3709A>T | p.Met1237Leu | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 4326/11717 | 3709/4551 | 1237/1516 | chrX | 74740848 | |||
| chrX:74741756 | T | C | 1 | a0003 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.2801A>G | p.Asn934Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3418/11717 | 2801/4551 | 934/1516 | chrX | 74741756 | |||
| chrX:74742020 | G | A | 1 | a0008 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.2537C>T | p.Thr846Ile | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3154/11717 | 2537/4551 | 846/1516 | chrX | 74742020 | |||
| chrX:74742711 | T | C | 1 | a0006 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1846A>G | p.Ser616Gly | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 2463/11717 | 1846/4551 | 616/1516 | chrX | 74742711 | |||
| chrX:74744406 | G | T | 1 | a0002 | 2 | HG02896.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.151C>A | p.Pro51Thr | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 768/11717 | 151/4551 | 51/1516 | chrX | 74744406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:74739492 | G | T | 1 | a0001c0007 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.4464C>A | p.Ser1488Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5081/11717 | 4464/4551 | 1488/1516 | chrX | 74739492 | |||
| chrX:74741002 | C | A | 1 | a0001c0003 | 3 | HG02040.hp1 HG02071.hp1 HG02523.hp2 |
synonymous_variant | LOW | c.3555G>T | p.Gly1185Gly | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 4172/11717 | 3555/4551 | 1185/1516 | chrX | 74741002 | |||
| chrX:74741383 | G | A | 1 | a0001c0010 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.3174C>T | p.Phe1058Phe | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3791/11717 | 3174/4551 | 1058/1516 | chrX | 74741383 | |||
| chrX:74741821 | T | C | 1 | a0001c0012 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.2736A>G | p.Gln912Gln | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3353/11717 | 2736/4551 | 912/1516 | chrX | 74741821 | |||
| chrX:74741959 | G | T | 1 | a0001c0002 | 6 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
synonymous_variant | LOW | c.2598C>A | p.Ser866Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3215/11717 | 2598/4551 | 866/1516 | chrX | 74741959 | |||
| chrX:74742184 | T | G | 1 | a0004c0006 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.2373A>C | p.Thr791Thr | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 2990/11717 | 2373/4551 | 791/1516 | chrX | 74742184 | |||
| chrX:74742403 | A | G | 1 | a0004c0006 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.2154T>C | p.Asn718Asn | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 2771/11717 | 2154/4551 | 718/1516 | chrX | 74742403 | |||
| chrX:74743483 | G | A | 1 | a0001c0015 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.1074C>T | p.Ser358Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 1691/11717 | 1074/4551 | 358/1516 | chrX | 74743483 | |||
| chrX:74743702 | T | C | 1 | a0001c0005 | 2 | HG01975.hp1 NA19056.hp1 |
synonymous_variant | LOW | c.855A>G | p.Leu285Leu | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 1472/11717 | 855/4551 | 285/1516 | chrX | 74743702 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:74733025 | T | C | 1 | a0001c0001t0005 | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6380A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 6380 | chrX | 74733025 | ||||||
| chrX:74733441 | T | G | 1 | a0001c0001t0021 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5964A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5964 | chrX | 74733441 | ||||||
| chrX:74734190 | C | T | 1 | a0001c0001t0005 | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5215G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5215 | chrX | 74734190 | ||||||
| chrX:74734588 | T | C | 1 | a0001c0001t0022 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4817A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4817 | chrX | 74734588 | ||||||
| chrX:74735289 | A | C | 1 | a0001c0001t0020 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4116T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4116 | chrX | 74735289 | ||||||
| chrX:74735330 | T | A | 1 | a0001c0001t0023 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4075A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4075 | chrX | 74735330 | ||||||
| chrX:74735710 | G | A | 1 | a0001c0001t0008 | 2 | NA18747.hp1 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3695C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 3695 | chrX | 74735710 | ||||||
| chrX:74736139 | C | T | 1 | a0001c0001t0019 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 3266 | chrX | 74736139 | ||||||
| chrX:74736562 | C | G | 1 | a0001c0001t0018 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2843G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2843 | chrX | 74736562 | ||||||
| chrX:74736630 | C | T | 1 | a0001c0001t0017 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2775G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2775 | chrX | 74736630 | ||||||
| chrX:74736853 | G | A | 1 | a0001c0001t0024 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2552C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2552 | chrX | 74736853 | ||||||
| chrX:74737338 | TAGA | T | 1 | a0001c0001t0009 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2064_*2066delTCT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2064 | chrX | 74737338 | ||||||
| chrX:74737341 | A | G | 1 | a0001c0001t0006 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2064T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2064 | chrX | 74737341 | ||||||
| chrX:74737705 | G | T | 1 | a0004c0006t0016 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1700C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1700 | chrX | 74737705 | ||||||
| chrX:74737833 | A | G | 2 | a0001c0001t0003 a0001c0001t0008 |
13 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1572T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1572 | chrX | 74737833 | ||||||
| chrX:74737895 | C | T | 1 | a0001c0001t0015 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1510G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1510 | chrX | 74737895 | ||||||
| chrX:74737903 | A | T | 2 | a0001c0001t0007 a0006c0014t0007 |
2 | HG02922.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1502T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1502 | chrX | 74737903 | ||||||
| chrX:74738764 | G | T | 1 | a0001c0001t0014 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*641C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 641 | chrX | 74738764 | ||||||
| chrX:74738794 | G | A | 6 | a0001c0001t0002 a0001c0001t0023 a0001c0001t0024 others(3): Show |
52 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*611C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 611 | chrX | 74738794 | ||||||
| chrX:74738857 | T | C | 2 | a0001c0001t0006 a0001c0001t0025 |
4 | HG00323.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*548A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 548 | chrX | 74738857 | ||||||
| chrX:74738857 | T | TAC | 1 | a0001c0001t0010 | 2 | NA19043.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546_*547dupGT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 547 | chrX | 74738857 | ||||||
| chrX:74738857 | TAC | T | 1 | a0001c0001t0004 | 6 | HG01243.hp1 HG02055.hp1 HG02735.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*546_*547delGT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 546 | chrX | 74738857 | ||||||
| chrX:74738859 | C | T | 2 | a0001c0001t0001 a0001c0001t0012 |
2 | HG00738.hp1 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 546 | chrX | 74738859 | ||||||
| chrX:74739271 | G | C | 1 | a0001c0001t0006 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*134C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 134 | chrX | 74739271 | ||||||
| chrX:74924904 | C | T | 1 | a0001c0001t0013 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/4 | 179254 | chrX | 74924904 | ||||||
| chrX:74925213 | C | T | 1 | a0001c0001t0012 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-378G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/4 | 179563 | chrX | 74925213 | ||||||
| chrX:74925232 | C | T | 1 | a0002c0004t0011 | 1 | HG02896.hp1 | 5_prime_UTR_variant | MODIFIER | c.-397G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/4 | 179582 | chrX | 74925232 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:74739692 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4458-194A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/3 | chrX | 74739692 | |||||||
| chrX:74744736 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.80-259T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744736 | |||||||
| chrX:74744911 | C | CTCT | 7 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-437_80-435dupAG others(1): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744911 | |||||||
| chrX:74744915 | C | CT | 6 | a0001c0001t0001g0202 a0001c0001t0005g0119 a0001c0001t0005g0120 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-439dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744915 | |||||||
| chrX:74744920 | T | C | 1 | a0001c0001t0010g0025 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.80-443A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744920 | |||||||
| chrX:74744920 | T | TC | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-444_80-443insG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744920 | |||||||
| chrX:74744921 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0032 others(5): Show |
8 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-444A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744921 | |||||||
| chrX:74744923 | T | TC | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(1): Show |
4 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-447dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744923 | |||||||
| chrX:74744929 | TC | T | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(1): Show |
4 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-453delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744929 | |||||||
| chrX:74744930 | C | CCT | 5 | a0001c0001t0001g0071 a0001c0001t0001g0193 a0001c0001t0001g0198 others(2): Show |
5 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-455_80-454dupAG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | |||||||
| chrX:74744930 | C | CCTCT | 3 | a0001c0001t0001g0138 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG02717.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.80-457_80-454dupAG others(2): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | |||||||
| chrX:74744930 | C | CCTCTCT | 17 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0103 others(14): Show |
17 | HG00323.hp1 HG02015.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-459_80-454dupAG others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | |||||||
| chrX:74744930 | C | CCTCTCTC others(1): Show |
64 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0115 others(61): Show |
65 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.80-461_80-454dupAG others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | |||||||
| chrX:74744930 | C | CCTCTCTC others(3): Show |
87 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(84): Show |
87 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.80-463_80-454dupAG others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | |||||||
| chrX:74744930 | C | CCTCTCTC others(5): Show |
13 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0064 others(10): Show |
13 | HG00673.hp1 HG02523.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-465_80-454dupAG others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | |||||||
| chrX:74744930 | C | CCTCTCTC others(7): Show |
4 | a0001c0001t0001g0019 a0001c0001t0019g0017 a0001c0003t0001g0041 others(1): Show |
4 | HG02040.hp1 HG02071.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-467_80-454dupAG others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | |||||||
| chrX:74744930 | C | CT | 10 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0032 others(7): Show |
10 | HG02970.hp1 NA18945.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-454_80-453insA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | |||||||
| chrX:74744930 | C | CTCTCTCT others(4): Show |
1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.80-454_80-453insAG others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | |||||||
| chrX:74744962 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.80-485G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744962 | |||||||
| chrX:74745111 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.79+461T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74745111 | |||||||
| chrX:74745278 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.79+294G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74745278 | |||||||
| chrX:74745394 | C | T | 2 | a0002c0004t0001g0201 a0002c0004t0011g0002 |
2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+178G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74745394 | |||||||
| chrX:74746462 | TAGG | T | 2 | a0001c0001t0002g0160 a0003c0011t0002g0141 |
2 | HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-47-768_-47-766del others(3): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74746462 | |||||||
| chrX:74747161 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-47-1464G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747161 | |||||||
| chrX:74747642 | C | CT | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
150 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-47-1946dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747642 | |||||||
| chrX:74747835 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47-2138A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747835 | |||||||
| chrX:74747869 | G | A | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-2172C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747869 | |||||||
| chrX:74748406 | G | A | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-2709C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74748406 | |||||||
| chrX:74748759 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-3062T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74748759 | |||||||
| chrX:74748838 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-3141A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74748838 | |||||||
| chrX:74749194 | G | A | 2 | a0001c0001t0007g0113 a0006c0014t0007g0112 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-3497C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749194 | |||||||
| chrX:74749215 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0180 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-47-3518G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749215 | |||||||
| chrX:74749494 | G | A | 2 | a0001c0001t0009g0135 a0001c0001t0009g0136 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-3797C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749494 | |||||||
| chrX:74749525 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-47-3828A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749525 | |||||||
| chrX:74749739 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-47-4042C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749739 | |||||||
| chrX:74749891 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-4194T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749891 | |||||||
| chrX:74750094 | G | C | 1 | a0001c0001t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-47-4397C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750094 | |||||||
| chrX:74750096 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(18): Show |
21 | HG00408.hp1 HG01243.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.-47-4399C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750096 | |||||||
| chrX:74750326 | T | C | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-4629A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750326 | |||||||
| chrX:74750606 | G | C | 1 | a0001c0001t0002g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-47-4909C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750606 | |||||||
| chrX:74750865 | G | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-5168C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750865 | |||||||
| chrX:74751031 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-47-5334G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751031 | |||||||
| chrX:74751057 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-5360C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751057 | |||||||
| chrX:74751185 | G | A | 151 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
151 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-47-5488C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751185 | |||||||
| chrX:74751309 | C | T | 1 | a0001c0001t0003g0092 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-47-5612G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751309 | |||||||
| chrX:74751494 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-5797A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751494 | |||||||
| chrX:74751505 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47-5808A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751505 | |||||||
| chrX:74751592 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0004g0186 |
2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-47-5895G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751592 | |||||||
| chrX:74751623 | C | CCCTT | 25 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0115 others(22): Show |
25 | HG00408.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-47-5930_-47-5927d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | |||||||
| chrX:74751623 | C | CCCTTCCT others(1): Show |
12 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0193 others(9): Show |
12 | HG02015.hp1 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-47-5934_-47-5927d others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | |||||||
| chrX:74751623 | C | CCCTTCCT others(5): Show |
3 | a0001c0001t0001g0223 a0001c0001t0006g0098 a0001c0001t0006g0218 |
3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-47-5938_-47-5927d others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | |||||||
| chrX:74751623 | C | CCCTTCCT others(9): Show |
1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-5942_-47-5927d others(18): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | |||||||
| chrX:74751623 | CCCTT | C | 4 | a0001c0001t0002g0168 a0001c0001t0002g0170 a0001c0001t0002g0183 others(1): Show |
4 | HG00140.hp1 HG03654.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-5930_-47-5927d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | |||||||
| chrX:74751658 | T | TTCC | 17 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0055 others(14): Show |
17 | HG01978.hp1 HG01993.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47-5962_-47-5961i others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751658 | |||||||
| chrX:74751658 | T | TTCCTTCC | 68 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(65): Show |
68 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-47-5962_-47-5961i others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751658 | |||||||
| chrX:74751658 | T | TTCCTTCC others(4): Show |
27 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(24): Show |
27 | HG00609.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-47-5962_-47-5961i others(13): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751658 | |||||||
| chrX:74751658 | T | TTCCTTCC others(8): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0084 a0001c0001t0001g0099 |
3 | HG00323.hp1 NA18984.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-47-5962_-47-5961i others(17): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751658 | |||||||
| chrX:74751660 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-5963A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751660 | |||||||
| chrX:74751662 | C | CT | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(110): Show |
113 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-47-5966dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751662 | |||||||
| chrX:74751662 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-5965G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751662 | |||||||
| chrX:74751675 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-5978G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751675 | |||||||
| chrX:74751679 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-5982G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751679 | |||||||
| chrX:74751688 | T | TC | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-5992dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751688 | |||||||
| chrX:74752048 | C | G | 1 | a0001c0001t0025g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-6351G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74752048 | |||||||
| chrX:74752064 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-47-6367G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74752064 | |||||||
| chrX:74752491 | T | C | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-6794A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74752491 | |||||||
| chrX:74752535 | CAAG | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-6841_-47-6839d others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74752535 | |||||||
| chrX:74753534 | G | C | 2 | a0001c0001t0002g0159 a0001c0001t0025g0130 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-47-7837C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753534 | |||||||
| chrX:74753598 | G | A | 1 | a0003c0011t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-47-7901C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753598 | |||||||
| chrX:74753715 | G | GCA | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-47-8020_-47-8019d others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753715 | |||||||
| chrX:74753715 | GCA | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0005g0119 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-8020_-47-8019d others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753715 | |||||||
| chrX:74753950 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-47-8253C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753950 | |||||||
| chrX:74754312 | AT | A | 4 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-8616delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754312 | |||||||
| chrX:74754317 | T | A | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-8620A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754317 | |||||||
| chrX:74754318 | T | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-8621A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754318 | |||||||
| chrX:74754410 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-8713C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754410 | |||||||
| chrX:74754512 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-47-8815A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754512 | |||||||
| chrX:74754596 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-8899G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754596 | |||||||
| chrX:74754812 | C | G | 1 | a0001c0001t0002g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-47-9115G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754812 | |||||||
| chrX:74755187 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-47-9490T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755187 | |||||||
| chrX:74755218 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-47-9521C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755218 | |||||||
| chrX:74755240 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47-9543C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755240 | |||||||
| chrX:74755560 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-9863G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755560 | |||||||
| chrX:74755892 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-47-10195T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755892 | |||||||
| chrX:74756025 | GCCACCAT others(81): Show |
G | 2 | a0001c0001t0002g0166 a0001c0001t0002g0184 |
2 | HG01106.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.-47-10416_-47-1032 others(92): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74756025 | |||||||
| chrX:74756048 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-47-10351C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74756048 | |||||||
| chrX:74756803 | C | T | 5 | a0001c0001t0009g0135 a0001c0001t0009g0136 a0001c0003t0001g0041 others(2): Show |
5 | HG02040.hp1 HG02071.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-11106G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74756803 | |||||||
| chrX:74756860 | C | CA | 3 | a0001c0001t0001g0208 a0001c0001t0013g0004 a0001c0010t0001g0212 |
3 | HG00738.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-47-11164dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74756860 | |||||||
| chrX:74757031 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-11334G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74757031 | |||||||
| chrX:74757282 | C | T | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-47-11585G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74757282 | |||||||
| chrX:74757798 | T | C | 1 | a0005c0009t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47-12101A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74757798 | |||||||
| chrX:74757820 | G | A | 11 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0193 others(8): Show |
11 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-12123C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74757820 | |||||||
| chrX:74758149 | C | T | 2 | a0002c0004t0001g0201 a0002c0004t0011g0002 |
2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-12452G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758149 | |||||||
| chrX:74758156 | T | C | 3 | a0001c0003t0001g0041 a0001c0003t0001g0049 a0001c0003t0001g0050 |
3 | HG02040.hp1 HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-47-12459A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758156 | |||||||
| chrX:74758193 | A | G | 219 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(216): Show |
220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-47-12496T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758193 | |||||||
| chrX:74758199 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0075 |
2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-47-12502A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758199 | |||||||
| chrX:74758235 | A | T | 1 | a0001c0001t0017g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-12538T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758235 | |||||||
| chrX:74758367 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47-12670G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758367 | |||||||
| chrX:74758430 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0126 a0001c0001t0002g0127 others(48): Show |
52 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.-47-12733T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758430 | |||||||
| chrX:74758475 | G | C | 2 | a0001c0001t0003g0085 a0001c0001t0003g0086 |
2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-47-12778C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758475 | |||||||
| chrX:74758694 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-12997T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758694 | |||||||
| chrX:74759053 | C | T | 1 | a0005c0009t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47-13356G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759053 | |||||||
| chrX:74759157 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0023 |
2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-47-13460G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759157 | |||||||
| chrX:74759297 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-13600C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759297 | |||||||
| chrX:74759653 | C | T | 1 | a0001c0001t0004g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47-13956G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759653 | |||||||
| chrX:74759842 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-47-14145G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759842 | |||||||
| chrX:74760461 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-14764C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760461 | |||||||
| chrX:74760551 | A | T | 7 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0005g0119 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-14854T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760551 | |||||||
| chrX:74760671 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-47-14974A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760671 | |||||||
| chrX:74760713 | T | C | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-15016A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760713 | |||||||
| chrX:74760841 | G | GATTT | 4 | a0001c0001t0001g0102 a0001c0001t0001g0213 a0001c0001t0003g0097 others(1): Show |
4 | HG02080.hp2 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-15148_-47-1514 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | |||||||
| chrX:74760841 | G | GATTTATT others(1): Show |
2 | a0001c0001t0001g0208 a0001c0001t0001g0214 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-47-15152_-47-1514 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | |||||||
| chrX:74760841 | GATTT | G | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-47-15148_-47-1514 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | |||||||
| chrX:74760841 | GATTTATT others(1): Show |
G | 45 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 others(42): Show |
45 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.-47-15152_-47-1514 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | |||||||
| chrX:74760841 | GATTTATT others(5): Show |
G | 2 | a0001c0001t0006g0098 a0001c0001t0006g0218 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-47-15156_-47-1514 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | |||||||
| chrX:74760841 | GATTTATT others(9): Show |
G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-15160_-47-1514 others(20): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | |||||||
| chrX:74760845 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-47-15148A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760845 | |||||||
| chrX:74760906 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-47-15209A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760906 | |||||||
| chrX:74760925 | C | T | 1 | a0001c0001t0018g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-15228G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760925 | |||||||
| chrX:74761022 | C | A | 1 | a0001c0001t0003g0089 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-47-15325G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761022 | |||||||
| chrX:74761092 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-15395C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761092 | |||||||
| chrX:74761112 | C | A | 2 | a0001c0001t0002g0168 a0001c0001t0002g0183 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-47-15415G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761112 | |||||||
| chrX:74761157 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-15460G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761157 | |||||||
| chrX:74761343 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-15646C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761343 | |||||||
| chrX:74761431 | C | T | 1 | a0001c0001t0025g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-15734G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761431 | |||||||
| chrX:74761449 | G | T | 1 | a0001c0001t0025g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-15752C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761449 | |||||||
| chrX:74761737 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-47-16040T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761737 | |||||||
| chrX:74761881 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-16184G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761881 | |||||||
| chrX:74761997 | G | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-16300C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761997 | |||||||
| chrX:74762014 | G | A | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-16317C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762014 | |||||||
| chrX:74762180 | T | C | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-16483A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762180 | |||||||
| chrX:74762235 | T | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
155 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-47-16538A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762235 | |||||||
| chrX:74762490 | C | G | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-16793G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762490 | |||||||
| chrX:74762581 | C | T | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-16884G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762581 | |||||||
| chrX:74762622 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-47-16925G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762622 | |||||||
| chrX:74762707 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-17010G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762707 | |||||||
| chrX:74762810 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-47-17113A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762810 | |||||||
| chrX:74762891 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47-17194T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762891 | |||||||
| chrX:74763250 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-47-17553G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763250 | |||||||
| chrX:74763301 | C | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-17604G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763301 | |||||||
| chrX:74763320 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-17623C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763320 | |||||||
| chrX:74763320 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-47-17623C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763320 | |||||||
| chrX:74763342 | C | A | 1 | a0001c0005t0001g0011 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-47-17645G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763342 | |||||||
| chrX:74763447 | C | T | 2 | a0001c0001t0007g0113 a0006c0014t0007g0112 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-17750G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763447 | |||||||
| chrX:74763526 | T | G | 1 | a0001c0001t0002g0165 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-47-17829A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763526 | |||||||
| chrX:74763550 | C | T | 130 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-17853G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763550 | |||||||
| chrX:74763557 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-17860G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763557 | |||||||
| chrX:74763557 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47-17860G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763557 | |||||||
| chrX:74763596 | T | A | 1 | a0001c0001t0001g0079 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-47-17899A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763596 | |||||||
| chrX:74763650 | T | C | 1 | a0001c0001t0018g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-17953A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763650 | |||||||
| chrX:74763726 | GC | G | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-47-18030delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763726 | |||||||
| chrX:74763944 | T | C | 8 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0005g0119 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-18247A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763944 | |||||||
| chrX:74764068 | C | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): Show |
117 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-47-18371G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764068 | |||||||
| chrX:74764154 | T | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-18457A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764154 | |||||||
| chrX:74764299 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-18602A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764299 | |||||||
| chrX:74764515 | G | A | 1 | a0001c0001t0004g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47-18818C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764515 | |||||||
| chrX:74764558 | T | A | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-18861A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764558 | |||||||
| chrX:74764596 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-47-18899G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764596 | |||||||
| chrX:74764670 | A | T | 2 | a0001c0002t0001g0072 a0001c0002t0001g0073 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-47-18973T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764670 | |||||||
| chrX:74765812 | G | A | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-20115C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74765812 | |||||||
| chrX:74765871 | C | CA | 25 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0058 others(22): Show |
25 | HG00408.hp1 HG00408.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-47-20175dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74765871 | |||||||
| chrX:74765871 | CA | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0105 a0001c0001t0001g0217 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-20175delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74765871 | |||||||
| chrX:74766012 | G | A | 2 | a0001c0001t0007g0113 a0006c0014t0007g0112 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-20315C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766012 | |||||||
| chrX:74766041 | C | CA | 14 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0101 others(11): Show |
14 | HG02135.hp1 HG02165.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-47-20345dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766041 | |||||||
| chrX:74766041 | CAA | C | 49 | a0001c0001t0002g0001 a0001c0001t0002g0126 a0001c0001t0002g0128 others(46): Show |
50 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-47-20346_-47-2034 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766041 | |||||||
| chrX:74766177 | C | T | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-20480G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766177 | |||||||
| chrX:74766872 | C | G | 2 | a0001c0001t0007g0113 a0006c0014t0007g0112 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-21175G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766872 | |||||||
| chrX:74766968 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47-21271C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766968 | |||||||
| chrX:74766999 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-47-21302C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766999 | |||||||
| chrX:74767108 | C | G | 41 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 others(38): Show |
41 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.-47-21411G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767108 | |||||||
| chrX:74767321 | A | G | 1 | a0001c0007t0001g0029 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-47-21624T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767321 | |||||||
| chrX:74767373 | G | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): Show |
117 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-47-21676C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767373 | |||||||
| chrX:74767429 | C | A | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47-21732G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767429 | |||||||
| chrX:74767697 | C | A | 11 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0162 others(8): Show |
11 | HG00408.hp1 HG02015.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-22000G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767697 | |||||||
| chrX:74768054 | C | T | 1 | a0001c0001t0021g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-47-22357G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768054 | |||||||
| chrX:74768250 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-22553T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768250 | |||||||
| chrX:74768487 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-22790G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768487 | |||||||
| chrX:74768503 | C | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
98 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-47-22806G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768503 | |||||||
| chrX:74768833 | C | A | 1 | a0001c0001t0002g0185 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-23136G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768833 | |||||||
| chrX:74768878 | C | T | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-23181G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768878 | |||||||
| chrX:74769210 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-47-23513G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74769210 | |||||||
| chrX:74769605 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-23908T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74769605 | |||||||
| chrX:74770121 | T | C | 1 | a0001c0001t0004g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47-24424A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74770121 | |||||||
| chrX:74770331 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-24634A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74770331 | |||||||
| chrX:74770448 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-47-24751C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74770448 | |||||||
| chrX:74770679 | G | A | 12 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47-24982C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74770679 | |||||||
| chrX:74771119 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-47-25422A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771119 | |||||||
| chrX:74771304 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-47-25607T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771304 | |||||||
| chrX:74771550 | T | C | 130 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-25853A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771550 | |||||||
| chrX:74771821 | C | CTG | 3 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0138 |
3 | HG02630.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-47-26126_-47-2612 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771821 | |||||||
| chrX:74771829 | G | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-26132C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771829 | |||||||
| chrX:74771865 | G | A | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-26168C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771865 | |||||||
| chrX:74772039 | C | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-26342G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74772039 | |||||||
| chrX:74772091 | T | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-26394A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74772091 | |||||||
| chrX:74772685 | A | T | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-26988T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74772685 | |||||||
| chrX:74773097 | A | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(18): Show |
21 | HG00408.hp1 HG01243.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.-47-27400T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773097 | |||||||
| chrX:74773220 | G | A | 2 | a0001c0001t0002g0164 a0001c0001t0023g0171 |
2 | HG01515.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-47-27523C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773220 | |||||||
| chrX:74773476 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-47-27779G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773476 | |||||||
| chrX:74773547 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-47-27850G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773547 | |||||||
| chrX:74773775 | G | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): Show |
117 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-47-28078C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773775 | |||||||
| chrX:74773801 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-47-28104G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773801 | |||||||
| chrX:74773887 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-47-28190G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773887 | |||||||
| chrX:74773888 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-28191C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773888 | |||||||
| chrX:74773908 | CA | C | 47 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0138 others(44): Show |
48 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-47-28212delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | |||||||
| chrX:74773908 | CAA | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0134 others(33): Show |
36 | HG00408.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-47-28213_-47-2821 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | |||||||
| chrX:74773908 | CAAA | C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0023 others(25): Show |
28 | HG01109.hp1 HG01243.hp1 HG02040.hp1 others(25): Show |
intron_variant | MODIFIER | c.-47-28214_-47-2821 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | |||||||
| chrX:74773908 | CAAAA | C | 95 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(92): Show |
95 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.-47-28215_-47-2821 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | |||||||
| chrX:74773908 | CAAAAA | C | 8 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0217 others(5): Show |
8 | HG01070.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-28216_-47-2821 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | |||||||
| chrX:74773925 | A | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-28228T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773925 | |||||||
| chrX:74774330 | T | A | 36 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0021 others(33): Show |
36 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-28633A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74774330 | |||||||
| chrX:74774813 | A | C | 1 | a0001c0001t0002g0222 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-47-29116T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74774813 | |||||||
| chrX:74775390 | T | A | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47-29693A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74775390 | |||||||
| chrX:74775794 | T | C | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-30097A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74775794 | |||||||
| chrX:74776056 | G | T | 1 | a0001c0005t0001g0011 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-47-30359C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776056 | |||||||
| chrX:74776596 | G | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): Show |
117 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-47-30899C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776596 | |||||||
| chrX:74776724 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-47-31027A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776724 | |||||||
| chrX:74776727 | C | CA | 46 | a0001c0001t0001g0205 a0001c0001t0002g0126 a0001c0001t0002g0127 others(43): Show |
46 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-47-31031dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | |||||||
| chrX:74776727 | C | CAAA | 4 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-31033_-47-3103 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | |||||||
| chrX:74776727 | CA | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0102 a0001c0001t0014g0114 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-31031delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | |||||||
| chrX:74776727 | CAA | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-47-31032_-47-3103 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | |||||||
| chrX:74777275 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-31578C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74777275 | |||||||
| chrX:74777481 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0116 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-47-31784T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74777481 | |||||||
| chrX:74777681 | T | C | 2 | a0001c0001t0002g0159 a0001c0001t0025g0130 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-47-31984A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74777681 | |||||||
| chrX:74777756 | A | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG02818.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-47-32059T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74777756 | |||||||
| chrX:74778117 | T | A | 1 | a0001c0001t0002g0191 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-47-32420A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74778117 | |||||||
| chrX:74778425 | C | T | 12 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47-32728G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74778425 | |||||||
| chrX:74778804 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-47-33107G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74778804 | |||||||
| chrX:74779729 | G | A | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-34032C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74779729 | |||||||
| chrX:74779869 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-34172A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74779869 | |||||||
| chrX:74779986 | A | G | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-47-34289T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74779986 | |||||||
| chrX:74780375 | G | GT | 8 | a0001c0001t0001g0023 a0001c0001t0001g0088 a0001c0001t0001g0101 others(5): Show |
8 | HG01074.hp1 HG02080.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-34679dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780375 | |||||||
| chrX:74780375 | GT | G | 7 | a0001c0001t0002g0156 a0001c0001t0005g0119 a0001c0001t0005g0120 others(4): Show |
7 | HG01884.hp1 HG01943.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-34679delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780375 | |||||||
| chrX:74780383 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-34686A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780383 | |||||||
| chrX:74780535 | AT | A | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-34839delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780535 | |||||||
| chrX:74780558 | C | G | 7 | a0001c0001t0002g0143 a0001c0001t0002g0156 a0001c0001t0002g0157 others(4): Show |
7 | HG01256.hp1 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-34861G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780558 | |||||||
| chrX:74780575 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0074 |
2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-47-34878G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780575 | |||||||
| chrX:74780582 | G | T | 1 | a0001c0001t0004g0196 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-47-34885C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780582 | |||||||
| chrX:74780588 | A | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-47-34891T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780588 | |||||||
| chrX:74780618 | C | T | 3 | a0001c0001t0001g0211 a0001c0001t0002g0164 a0001c0001t0023g0171 |
3 | HG01515.hp1 HG02257.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-47-34921G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780618 | |||||||
| chrX:74781150 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-47-35453G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74781150 | |||||||
| chrX:74781312 | T | A | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-35615A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74781312 | |||||||
| chrX:74781708 | T | TGTGTATG others(12): Show |
51 | a0001c0001t0002g0001 a0001c0001t0002g0126 a0001c0001t0002g0127 others(48): Show |
52 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.-47-36030_-47-3601 others(23): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74781708 | |||||||
| chrX:74781901 | T | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-36204A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74781901 | |||||||
| chrX:74782005 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-36308G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782005 | |||||||
| chrX:74782072 | C | T | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-47-36375G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782072 | |||||||
| chrX:74782495 | C | A | 2 | a0001c0001t0007g0113 a0006c0014t0007g0112 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-36798G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782495 | |||||||
| chrX:74782509 | T | C | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-47-36812A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782509 | |||||||
| chrX:74782512 | A | T | 1 | a0001c0001t0003g0060 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-47-36815T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782512 | |||||||
| chrX:74782674 | C | T | 5 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0148 others(2): Show |
5 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-36977G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782674 | |||||||
| chrX:74782862 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-47-37165A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782862 | |||||||
| chrX:74783374 | C | A | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-37677G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74783374 | |||||||
| chrX:74783462 | T | G | 2 | a0001c0001t0002g0155 a0001c0001t0002g0181 |
2 | HG02602.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-47-37765A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74783462 | |||||||
| chrX:74783893 | C | T | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-38196G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74783893 | |||||||
| chrX:74783936 | T | C | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-47-38239A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74783936 | |||||||
| chrX:74784178 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-47-38481G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74784178 | |||||||
| chrX:74784587 | A | G | 4 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-38890T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74784587 | |||||||
| chrX:74784612 | T | TTA | 3 | a0001c0001t0002g0175 a0001c0001t0005g0123 a0004c0006t0016g0118 |
3 | HG01070.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-47-38917_-47-3891 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74784612 | |||||||
| chrX:74784802 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-47-39105T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74784802 | |||||||
| chrX:74785522 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-39825A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74785522 | |||||||
| chrX:74785809 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-47-40112G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74785809 | |||||||
| chrX:74785947 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-40250A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74785947 | |||||||
| chrX:74786032 | C | A | 130 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-40335G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786032 | |||||||
| chrX:74786139 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-47-40442C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786139 | |||||||
| chrX:74786342 | G | A | 1 | a0001c0001t0017g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-40645C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786342 | |||||||
| chrX:74786557 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-47-40860C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786557 | |||||||
| chrX:74786621 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-40924T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786621 | |||||||
| chrX:74786816 | T | TAC | 9 | a0001c0001t0001g0053 a0001c0001t0001g0066 a0001c0001t0001g0079 others(6): Show |
9 | HG01261.hp1 HG02602.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47-41121_-47-4112 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786816 | |||||||
| chrX:74786823 | ACACACAC others(35): Show |
A | 2 | a0001c0001t0001g0034 a0001c0001t0019g0017 |
2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-47-41168_-47-4112 others(46): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786823 | |||||||
| chrX:74786827 | ACACACAC others(31): Show |
A | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-47-41168_-47-4113 others(42): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786827 | |||||||
| chrX:74786848 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-41151A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786848 | |||||||
| chrX:74786864 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-41167A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786864 | |||||||
| chrX:74786865 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-41168C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786865 | |||||||
| chrX:74787093 | T | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-41396A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787093 | |||||||
| chrX:74787104 | C | CA | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-41408dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787104 | |||||||
| chrX:74787104 | C | CAA | 6 | a0001c0001t0001g0068 a0001c0001t0001g0081 a0001c0001t0001g0088 others(3): Show |
6 | HG02559.hp1 NA18906.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-41409_-47-4140 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787104 | |||||||
| chrX:74787104 | CA | C | 5 | a0001c0001t0001g0005 a0001c0001t0002g0181 a0001c0001t0004g0186 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-41408delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787104 | |||||||
| chrX:74787269 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-41572G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787269 | |||||||
| chrX:74787294 | G | GA | 56 | a0001c0001t0001g0101 a0001c0001t0001g0162 a0001c0001t0001g0172 others(53): Show |
57 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-47-41598dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787294 | |||||||
| chrX:74787294 | GA | G | 6 | a0001c0001t0001g0052 a0001c0001t0005g0119 a0001c0001t0005g0120 others(3): Show |
6 | HG01884.hp1 HG01981.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-41598delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787294 | |||||||
| chrX:74787386 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-41689C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787386 | |||||||
| chrX:74787470 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-41773A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787470 | |||||||
| chrX:74787769 | G | T | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-42072C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787769 | |||||||
| chrX:74787999 | C | T | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-42302G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787999 | |||||||
| chrX:74788169 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-47-42472T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788169 | |||||||
| chrX:74788371 | T | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-42674A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788371 | |||||||
| chrX:74788390 | T | G | 1 | a0001c0001t0002g0174 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-47-42693A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788390 | |||||||
| chrX:74788420 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-42723T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788420 | |||||||
| chrX:74788484 | A | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-42787T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788484 | |||||||
| chrX:74788520 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-47-42823A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788520 | |||||||
| chrX:74788714 | T | G | 3 | a0001c0001t0001g0215 a0002c0004t0001g0201 a0002c0004t0011g0002 |
3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-43017A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788714 | |||||||
| chrX:74789105 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47-43408G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789105 | |||||||
| chrX:74789127 | T | TC | 34 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0066 others(31): Show |
34 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.-47-43431dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789127 | |||||||
| chrX:74789169 | C | T | 56 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0002g0001 others(53): Show |
57 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-47-43472G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789169 | |||||||
| chrX:74789216 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-43519A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789216 | |||||||
| chrX:74789404 | T | C | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-43707A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789404 | |||||||
| chrX:74789479 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-47-43782C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789479 | |||||||
| chrX:74789505 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47-43808C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789505 | |||||||
| chrX:74789544 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-43847A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789544 | |||||||
| chrX:74789572 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-47-43875G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789572 | |||||||
| chrX:74789660 | T | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-43963A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789660 | |||||||
| chrX:74789671 | C | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-43974G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789671 | |||||||
| chrX:74789697 | G | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-44000C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789697 | |||||||
| chrX:74789801 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47-44104G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789801 | |||||||
| chrX:74789921 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-44224C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789921 | |||||||
| chrX:74790057 | G | A | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-47-44360C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790057 | |||||||
| chrX:74790099 | A | T | 1 | a0001c0001t0002g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-47-44402T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790099 | |||||||
| chrX:74790279 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-47-44582A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790279 | |||||||
| chrX:74790311 | C | G | 3 | a0001c0001t0001g0215 a0002c0004t0001g0201 a0002c0004t0011g0002 |
3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-44614G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790311 | |||||||
| chrX:74790350 | A | C | 2 | a0001c0001t0009g0135 a0001c0001t0009g0136 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-44653T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790350 | |||||||
| chrX:74790361 | A | C | 3 | a0001c0001t0002g0129 a0001c0001t0009g0135 a0001c0001t0009g0136 |
3 | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-44664T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790361 | |||||||
| chrX:74790374 | T | C | 2 | a0001c0001t0009g0135 a0001c0001t0009g0136 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-44677A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790374 | |||||||
| chrX:74790456 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-47-44759G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790456 | |||||||
| chrX:74790495 | T | G | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-44798A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790495 | |||||||
| chrX:74790586 | T | G | 7 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0005g0119 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-44889A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790586 | |||||||
| chrX:74790588 | C | T | 7 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0005g0119 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-44891G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790588 | |||||||
| chrX:74790638 | C | G | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-44941G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790638 | |||||||
| chrX:74790742 | C | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-47-45045G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790742 | |||||||
| chrX:74790903 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-45206T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790903 | |||||||
| chrX:74790937 | G | C | 1 | a0001c0001t0001g0007 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47-45240C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790937 | |||||||
| chrX:74791145 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-45448G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791145 | |||||||
| chrX:74791205 | A | C | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47-45508T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791205 | |||||||
| chrX:74791237 | T | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-45540A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791237 | |||||||
| chrX:74791340 | C | G | 2 | a0001c0001t0009g0135 a0001c0001t0009g0136 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-45643G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791340 | |||||||
| chrX:74791417 | A | G | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-45720T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791417 | |||||||
| chrX:74791447 | T | C | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-45750A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791447 | |||||||
| chrX:74791574 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-45877G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791574 | |||||||
| chrX:74791711 | T | A | 1 | a0001c0001t0002g0192 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-47-46014A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791711 | |||||||
| chrX:74791763 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-46066T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791763 | |||||||
| chrX:74791775 | T | G | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-47-46078A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791775 | |||||||
| chrX:74791846 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-46149G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791846 | |||||||
| chrX:74791907 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-46210T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791907 | |||||||
| chrX:74792073 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-46376A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792073 | |||||||
| chrX:74792104 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-46407C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792104 | |||||||
| chrX:74792281 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-47-46584C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792281 | |||||||
| chrX:74792342 | G | T | 2 | a0001c0001t0009g0135 a0001c0001t0009g0136 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-46645C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792342 | |||||||
| chrX:74792430 | G | A | 1 | a0001c0012t0001g0142 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-47-46733C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792430 | |||||||
| chrX:74792785 | C | A | 1 | a0001c0001t0004g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47-47088G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792785 | |||||||
| chrX:74792901 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-47204A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792901 | |||||||
| chrX:74792984 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-47-47287A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792984 | |||||||
| chrX:74792989 | T | G | 2 | a0001c0001t0001g0005 a0001c0001t0004g0186 |
2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-47-47292A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792989 | |||||||
| chrX:74793210 | T | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-47513A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793210 | |||||||
| chrX:74793215 | A | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-47518T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793215 | |||||||
| chrX:74793345 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0179 |
2 | HG01433.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-47-47648C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793345 | |||||||
| chrX:74793379 | C | T | 3 | a0001c0001t0001g0215 a0002c0004t0001g0201 a0002c0004t0011g0002 |
3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-47682G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793379 | |||||||
| chrX:74793586 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-47889G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793586 | |||||||
| chrX:74793691 | C | G | 1 | a0001c0002t0001g0031 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-47-47994G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793691 | |||||||
| chrX:74793709 | G | A | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-48012C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793709 | |||||||
| chrX:74793722 | C | A | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(7): Show |
10 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-48025G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793722 | |||||||
| chrX:74793737 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-48040A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793737 | |||||||
| chrX:74793952 | G | A | 1 | a0001c0001t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-47-48255C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793952 | |||||||
| chrX:74794006 | T | C | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-47-48309A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794006 | |||||||
| chrX:74794015 | G | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-48318C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794015 | |||||||
| chrX:74794235 | G | A | 1 | a0007c0008t0002g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47-48538C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794235 | |||||||
| chrX:74794299 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-47-48602C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794299 | |||||||
| chrX:74794322 | A | G | 1 | a0001c0001t0003g0124 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-47-48625T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794322 | |||||||
| chrX:74794519 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-48822G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794519 | |||||||
| chrX:74794602 | G | A | 5 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02559.hp2 HG02698.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-48905C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794602 | |||||||
| chrX:74794625 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-48928C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794625 | |||||||
| chrX:74794674 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-47-48977G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794674 | |||||||
| chrX:74794698 | G | A | 130 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-49001C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794698 | |||||||
| chrX:74794700 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-47-49003G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794700 | |||||||
| chrX:74794708 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-47-49011G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794708 | |||||||
| chrX:74794712 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49015T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794712 | |||||||
| chrX:74794834 | C | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG02818.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-47-49137G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794834 | |||||||
| chrX:74794865 | C | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49168G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794865 | |||||||
| chrX:74794900 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49203A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794900 | |||||||
| chrX:74794948 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49251G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794948 | |||||||
| chrX:74794962 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0004g0186 |
2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-47-49265C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794962 | |||||||
| chrX:74795026 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47-49329G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795026 | |||||||
| chrX:74795198 | T | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0116 a0001c0001t0001g0217 others(1): Show |
4 | HG02257.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-49501A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795198 | |||||||
| chrX:74795423 | A | G | 1 | a0001c0001t0017g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-49726T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795423 | |||||||
| chrX:74795523 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49826T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795523 | |||||||
| chrX:74795800 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-47-50103C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795800 | |||||||
| chrX:74795954 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-47-50257A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795954 | |||||||
| chrX:74796104 | T | TTATATAT others(23): Show |
4 | a0001c0001t0001g0215 a0001c0001t0010g0189 a0002c0004t0001g0201 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-50437_-47-5040 others(34): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796104 | |||||||
| chrX:74796126 | T | A | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-50429A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796126 | |||||||
| chrX:74796126 | T | TATATATA others(21): Show |
1 | a0001c0001t0003g0086 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-47-50457_-47-5043 others(32): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796126 | |||||||
| chrX:74796134 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-47-50465_-47-5043 others(32): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796134 | |||||||
| chrX:74796135 | T | TATATATA others(12): Show |
1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-47-50457_-47-5043 others(23): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796135 | |||||||
| chrX:74796144 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-47-50447A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796144 | |||||||
| chrX:74796151 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-47-50454T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796151 | |||||||
| chrX:74796153 | A | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50456T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796153 | |||||||
| chrX:74796154 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50457G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796154 | |||||||
| chrX:74796159 | ATAT | A | 2 | a0001c0001t0002g0174 a0001c0001t0002g0180 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-47-50465_-47-5046 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796159 | |||||||
| chrX:74796162 | T | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-50465A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796162 | |||||||
| chrX:74796181 | A | ATTTATAT others(90): Show |
3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50485_-47-5048 others(101): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796181 | |||||||
| chrX:74796181 | AC | A | 3 | a0001c0001t0001g0215 a0002c0004t0001g0201 a0002c0004t0011g0002 |
3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-50485delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796181 | |||||||
| chrX:74796182 | C | T | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50485G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796182 | |||||||
| chrX:74796200 | A | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50503T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796200 | |||||||
| chrX:74796201 | C | CT | 2 | a0001c0001t0002g0168 a0001c0001t0002g0183 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-47-50505_-47-5050 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796201 | |||||||
| chrX:74796201 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50504G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796201 | |||||||
| chrX:74796203 | T | TATATATT others(10): Show |
1 | a0007c0008t0002g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47-50507_-47-5050 others(21): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796203 | |||||||
| chrX:74796209 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-47-50512A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | |||||||
| chrX:74796209 | T | TTATATAT others(14): Show |
1 | a0001c0001t0002g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47-50533_-47-5051 others(25): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | |||||||
| chrX:74796209 | T | TTATATAT others(16): Show |
42 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 others(39): Show |
42 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.-47-50535_-47-5051 others(27): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | |||||||
| chrX:74796209 | T | TTATATAT others(18): Show |
1 | a0001c0001t0001g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-50537_-47-5051 others(29): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | |||||||
| chrX:74796209 | TTA | T | 11 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01884.hp1 NA18945.hp1 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-50514_-47-5051 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | |||||||
| chrX:74796210 | T | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50513A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796210 | |||||||
| chrX:74796220 | T | C | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50523A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796220 | |||||||
| chrX:74796220 | T | TACATATA others(16): Show |
1 | a0001c0001t0002g0164 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-47-50524_-47-5052 others(27): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796220 | |||||||
| chrX:74796222 | C | T | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50525G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796222 | |||||||
| chrX:74796229 | A | T | 6 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0001c0001t0006g0098 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-50532T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796229 | |||||||
| chrX:74796229 | AAT | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0047 others(11): Show |
14 | HG00323.hp1 HG00558.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-50534_-47-5053 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796229 | |||||||
| chrX:74796231 | T | TATATATA others(10): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 |
4 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-50535_-47-5053 others(21): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796231 | |||||||
| chrX:74796231 | T | TATATATA others(14): Show |
3 | a0001c0001t0002g0152 a0001c0001t0002g0184 a0001c0001t0018g0178 |
3 | HG00408.hp1 HG01106.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-47-50535_-47-5053 others(25): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796231 | |||||||
| chrX:74796235 | T | TATACATA others(4): Show |
3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50539_-47-5053 others(15): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796235 | |||||||
| chrX:74796236 | A | ATATATAC others(19): Show |
2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-47-50540_-47-5053 others(30): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796236 | |||||||
| chrX:74796243 | T | TACATATA others(16): Show |
3 | a0001c0001t0002g0161 a0001c0001t0002g0174 a0001c0001t0002g0180 |
3 | HG01433.hp1 HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-47-50547_-47-5054 others(27): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796243 | |||||||
| chrX:74796245 | C | CACATATA others(21): Show |
1 | a0001c0001t0021g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-47-50576_-47-5054 others(32): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796245 | |||||||
| chrX:74796245 | C | T | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0006g0098 others(2): Show |
5 | HG02615.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-50548G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796245 | |||||||
| chrX:74796266 | A | C | 1 | a0001c0001t0017g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-50569T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796266 | |||||||
| chrX:74796266 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0004g0186 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-47-50595_-47-5057 others(30): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796266 | |||||||
| chrX:74796268 | ATATATAC others(17): Show |
A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50595_-47-5057 others(28): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796268 | |||||||
| chrX:74796292 | T | TTATATAT others(32): Show |
2 | a0001c0001t0001g0080 a0001c0001t0010g0189 |
2 | HG03239.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-47-50596_-47-5059 others(43): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796292 | |||||||
| chrX:74796301 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50604A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796301 | |||||||
| chrX:74796303 | T | C | 5 | a0001c0001t0001g0080 a0001c0001t0004g0133 a0001c0001t0004g0186 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-50606A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796303 | |||||||
| chrX:74796303 | T | TAC | 200 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-47-50608_-47-5060 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796303 | |||||||
| chrX:74796456 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50759A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796456 | |||||||
| chrX:74796626 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-47-50929G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796626 | |||||||
| chrX:74796798 | T | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-51101A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796798 | |||||||
| chrX:74797050 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47-51353A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74797050 | |||||||
| chrX:74797173 | G | T | 1 | a0001c0001t0002g0183 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-47-51476C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74797173 | |||||||
| chrX:74797613 | TCTAA | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-51920_-47-5191 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74797613 | |||||||
| chrX:74797744 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-52047T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74797744 | |||||||
| chrX:74798102 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-47-52405G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798102 | |||||||
| chrX:74798247 | CAAACCAA others(6): Show |
C | 1 | a0001c0001t0001g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-47-52563_-47-5255 others(17): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798247 | |||||||
| chrX:74798400 | G | A | 2 | a0001c0001t0001g0215 a0002c0004t0001g0201 |
2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-52703C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798400 | |||||||
| chrX:74798439 | G | C | 2 | a0001c0001t0001g0009 a0001c0015t0001g0008 |
2 | NA18971.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-47-52742C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798439 | |||||||
| chrX:74798466 | T | G | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-47-52769A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798466 | |||||||
| chrX:74798798 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-53101A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798798 | |||||||
| chrX:74798799 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-53102G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798799 | |||||||
| chrX:74798964 | T | TA | 5 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02559.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-53268dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798964 | |||||||
| chrX:74799502 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-47-53805G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74799502 | |||||||
| chrX:74799588 | T | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0179 |
2 | HG01433.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-47-53891A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74799588 | |||||||
| chrX:74799699 | C | T | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-47-54002G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74799699 | |||||||
| chrX:74799967 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-47-54270G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74799967 | |||||||
| chrX:74800162 | A | G | 1 | a0001c0007t0001g0029 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-47-54465T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800162 | |||||||
| chrX:74800166 | T | C | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-47-54469A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800166 | |||||||
| chrX:74800435 | T | G | 1 | a0001c0001t0002g0222 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-47-54738A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800435 | |||||||
| chrX:74800437 | C | T | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-54740G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800437 | |||||||
| chrX:74800595 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-54898C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800595 | |||||||
| chrX:74800596 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-54899A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800596 | |||||||
| chrX:74800712 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-55015A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800712 | |||||||
| chrX:74800776 | C | T | 209 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
210 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-47-55079G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800776 | |||||||
| chrX:74800779 | T | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-55082A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800779 | |||||||
| chrX:74800915 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0075 |
2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-47-55218G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800915 | |||||||
| chrX:74801250 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0079 |
2 | NA18960.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-47-55553A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801250 | |||||||
| chrX:74801407 | T | C | 1 | a0001c0001t0006g0219 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47-55710A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801407 | |||||||
| chrX:74801659 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-55962G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801659 | |||||||
| chrX:74801670 | G | T | 7 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0005g0119 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-55973C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801670 | |||||||
| chrX:74801936 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-47-56239C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801936 | |||||||
| chrX:74801938 | C | T | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-56241G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801938 | |||||||
| chrX:74802136 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-56439G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802136 | |||||||
| chrX:74802460 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47-56763G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802460 | |||||||
| chrX:74802467 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0019g0017 |
2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-47-56770C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802467 | |||||||
| chrX:74802607 | C | A | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-56910G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802607 | |||||||
| chrX:74802756 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-47-57059G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802756 | |||||||
| chrX:74802834 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-47-57137A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802834 | |||||||
| chrX:74803194 | C | T | 1 | a0001c0001t0025g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-57497G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803194 | |||||||
| chrX:74803228 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-57531C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803228 | |||||||
| chrX:74803246 | C | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-57549G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803246 | |||||||
| chrX:74803346 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-57649G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803346 | |||||||
| chrX:74803422 | G | T | 3 | a0001c0001t0001g0215 a0002c0004t0001g0201 a0002c0004t0011g0002 |
3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-57725C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803422 | |||||||
| chrX:74803554 | C | T | 1 | a0001c0001t0004g0188 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-47-57857G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803554 | |||||||
| chrX:74803563 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-47-57866C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803563 | |||||||
| chrX:74803574 | AT | A | 2 | a0001c0001t0001g0199 a0001c0001t0005g0120 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-47-57878delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803574 | |||||||
| chrX:74803575 | T | A | 10 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0193 others(7): Show |
10 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-57878A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803575 | |||||||
| chrX:74803579 | T | A | 11 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0193 others(8): Show |
11 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-57882A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803579 | |||||||
| chrX:74803763 | GA | G | 52 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0002g0126 others(49): Show |
52 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.-47-58067delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803763 | |||||||
| chrX:74803772 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-58075T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803772 | |||||||
| chrX:74803779 | A | C | 1 | a0001c0001t0002g0166 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-47-58082T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803779 | |||||||
| chrX:74803827 | C | T | 2 | a0001c0003t0001g0041 a0001c0003t0001g0049 |
2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-47-58130G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803827 | |||||||
| chrX:74803877 | CA | C | 9 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0047 others(6): Show |
9 | HG02027.hp1 HG02074.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47-58181delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803877 | |||||||
| chrX:74803992 | A | G | 1 | a0001c0001t0001g0007 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47-58295T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803992 | |||||||
| chrX:74804344 | C | T | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-58647G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804344 | |||||||
| chrX:74804350 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-47-58653C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804350 | |||||||
| chrX:74804383 | T | C | 3 | a0001c0001t0001g0215 a0002c0004t0001g0201 a0002c0004t0011g0002 |
3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-58686A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804383 | |||||||
| chrX:74804791 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-59094G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804791 | |||||||
| chrX:74804950 | G | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-59253C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804950 | |||||||
| chrX:74805219 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47-59522C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74805219 | |||||||
| chrX:74805343 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-59646G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74805343 | |||||||
| chrX:74805464 | T | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0023 |
2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-47-59767A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74805464 | |||||||
| chrX:74806181 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-60484C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806181 | |||||||
| chrX:74806273 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-60576G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806273 | |||||||
| chrX:74806651 | T | A | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-60954A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806651 | |||||||
| chrX:74806887 | CTATT | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0078 others(1): Show |
4 | HG00408.hp2 NA18967.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-61194_-47-6119 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806887 | |||||||
| chrX:74806899 | A | C | 2 | a0001c0001t0005g0120 a0001c0001t0005g0121 |
2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-47-61202T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806899 | |||||||
| chrX:74806921 | A | G | 1 | a0001c0001t0017g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-61224T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806921 | |||||||
| chrX:74806931 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-61234C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806931 | |||||||
| chrX:74807213 | T | C | 1 | a0001c0001t0005g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47-61516A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74807213 | |||||||
| chrX:74807468 | C | A | 1 | a0001c0001t0002g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-47-61771G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74807468 | |||||||
| chrX:74807698 | A | G | 56 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0002g0001 others(53): Show |
57 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-47-62001T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74807698 | |||||||
| chrX:74807814 | A | G | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-47-62117T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74807814 | |||||||
| chrX:74808036 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-62339T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74808036 | |||||||
| chrX:74808143 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-62446G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74808143 | |||||||
| chrX:74808843 | T | C | 1 | a0001c0001t0002g0154 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-47-63146A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74808843 | |||||||
| chrX:74809520 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47-63823G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74809520 | |||||||
| chrX:74809585 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-63888A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74809585 | |||||||
| chrX:74809611 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-63914C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74809611 | |||||||
| chrX:74810249 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-47-64552G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810249 | |||||||
| chrX:74810562 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-64865C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810562 | |||||||
| chrX:74810635 | C | CA | 57 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0001g0220 others(54): Show |
58 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.-47-64939dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810635 | |||||||
| chrX:74810723 | G | C | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-65026C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810723 | |||||||
| chrX:74810795 | A | T | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-65098T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810795 | |||||||
| chrX:74811285 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-65588C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811285 | |||||||
| chrX:74811348 | TC | T | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-65652delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811348 | |||||||
| chrX:74811350 | C | T | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-65653G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811350 | |||||||
| chrX:74811351 | A | T | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-65654T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811351 | |||||||
| chrX:74811352 | T | C | 130 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-65655A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811352 | |||||||
| chrX:74811435 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47-65738T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811435 | |||||||
| chrX:74811813 | T | C | 3 | a0001c0001t0001g0215 a0002c0004t0001g0201 a0002c0004t0011g0002 |
3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-66116A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811813 | |||||||
| chrX:74811972 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-66275T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811972 | |||||||
| chrX:74812259 | A | G | 1 | a0001c0001t0025g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-66562T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812259 | |||||||
| chrX:74812373 | T | A | 1 | a0001c0001t0021g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-47-66676A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812373 | |||||||
| chrX:74812434 | T | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0004g0186 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-66737A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812434 | |||||||
| chrX:74812454 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-66757C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812454 | |||||||
| chrX:74812505 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-66808A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812505 | |||||||
| chrX:74812762 | C | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-67065G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812762 | |||||||
| chrX:74812819 | G | T | 6 | a0001c0001t0001g0088 a0001c0001t0003g0089 a0001c0001t0003g0124 others(3): Show |
6 | NA18612.hp1 NA18747.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-67122C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812819 | |||||||
| chrX:74813472 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-47-67775G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74813472 | |||||||
| chrX:74813515 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-47-67818C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74813515 | |||||||
| chrX:74813532 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-67835G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74813532 | |||||||
| chrX:74814125 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-47-68428G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814125 | |||||||
| chrX:74814159 | C | T | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-68462G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814159 | |||||||
| chrX:74814390 | T | G | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-68693A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814390 | |||||||
| chrX:74814723 | G | T | 1 | a0001c0001t0002g0158 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-47-69026C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814723 | |||||||
| chrX:74814759 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-47-69062G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814759 | |||||||
| chrX:74814951 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-47-69254C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814951 | |||||||
| chrX:74815703 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-47-70006G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74815703 | |||||||
| chrX:74815789 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-70092G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74815789 | |||||||
| chrX:74815927 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-47-70230G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74815927 | |||||||
| chrX:74816181 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-47-70484G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74816181 | |||||||
| chrX:74816891 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0116 a0001c0001t0001g0217 others(1): Show |
4 | HG02257.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-71194C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74816891 | |||||||
| chrX:74816965 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-47-71268A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74816965 | |||||||
| chrX:74817043 | T | C | 1 | a0003c0011t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-47-71346A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74817043 | |||||||
| chrX:74817463 | G | T | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-71766C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74817463 | |||||||
| chrX:74817781 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-72084G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74817781 | |||||||
| chrX:74817878 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-47-72181T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74817878 | |||||||
| chrX:74818095 | AAAAAAAA others(5): Show |
A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-72410_-47-7239 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818095 | |||||||
| chrX:74818253 | T | A | 2 | a0001c0001t0001g0005 a0001c0001t0004g0186 |
2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-47-72556A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818253 | |||||||
| chrX:74818258 | C | T | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-72561G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818258 | |||||||
| chrX:74818299 | A | G | 1 | a0003c0011t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-47-72602T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818299 | |||||||
| chrX:74818340 | T | C | 1 | a0008c0013t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-47-72643A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818340 | |||||||
| chrX:74818667 | A | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-72970T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818667 | |||||||
| chrX:74819004 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-73307C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819004 | |||||||
| chrX:74819061 | C | T | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-73364G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819061 | |||||||
| chrX:74819459 | A | T | 1 | a0001c0001t0001g0051 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-73762T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819459 | |||||||
| chrX:74819599 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-47-73902G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819599 | |||||||
| chrX:74819679 | A | G | 3 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 |
4 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-73982T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819679 | |||||||
| chrX:74819738 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-74041C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819738 | |||||||
| chrX:74819995 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-74298A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819995 | |||||||
| chrX:74820108 | T | G | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-47-74411A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820108 | |||||||
| chrX:74820122 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-47-74425C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820122 | |||||||
| chrX:74820175 | T | C | 207 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
208 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.-47-74478A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820175 | |||||||
| chrX:74820198 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-74501A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820198 | |||||||
| chrX:74820304 | G | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-74607C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820304 | |||||||
| chrX:74820330 | T | TATA | 2 | a0001c0001t0001g0079 a0002c0004t0011g0002 |
2 | HG02896.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-47-74636_-47-7463 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820330 | |||||||
| chrX:74820330 | T | TATAATAA others(8): Show |
1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-74648_-47-7463 others(19): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820330 | |||||||
| chrX:74820506 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-74809T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820506 | |||||||
| chrX:74820649 | T | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0074 |
2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-47-74952A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820649 | |||||||
| chrX:74820677 | G | T | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-74980C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820677 | |||||||
| chrX:74820704 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-75007C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820704 | |||||||
| chrX:74820819 | C | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-75122G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820819 | |||||||
| chrX:74820948 | G | T | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-47-75251C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820948 | |||||||
| chrX:74821112 | AT | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-47-75416delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821112 | |||||||
| chrX:74821113 | T | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
98 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-47-75416A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821113 | |||||||
| chrX:74821168 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-75471G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821168 | |||||||
| chrX:74821430 | G | A | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-75733C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821430 | |||||||
| chrX:74821598 | CTTAAT | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0221 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-47-75906_-47-7590 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821598 | |||||||
| chrX:74822002 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-76305G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822002 | |||||||
| chrX:74822300 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-47-76603G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822300 | |||||||
| chrX:74822330 | T | C | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-76633A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822330 | |||||||
| chrX:74822466 | T | C | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-76769A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822466 | |||||||
| chrX:74822751 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47-77054C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822751 | |||||||
| chrX:74823031 | G | A | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-77334C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823031 | |||||||
| chrX:74823563 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-77866G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823563 | |||||||
| chrX:74823697 | C | CAGAT | 21 | a0001c0001t0001g0005 a0001c0001t0001g0138 a0001c0001t0001g0204 others(18): Show |
21 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-47-78004_-47-7800 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | |||||||
| chrX:74823697 | C | CAGATAGA others(1): Show |
5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0203 others(2): Show |
5 | HG02809.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-78008_-47-7800 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | |||||||
| chrX:74823697 | CAGAT | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(116): Show |
120 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-47-78004_-47-7800 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | |||||||
| chrX:74823697 | CAGATAGA others(1): Show |
C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0063 others(3): Show |
6 | HG01952.hp1 HG02074.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-78008_-47-7800 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | |||||||
| chrX:74823697 | CAGATAGA others(5): Show |
C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG01109.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-78012_-47-7800 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | |||||||
| chrX:74823824 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-47-78127A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823824 | |||||||
| chrX:74824139 | A | G | 3 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-78442T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824139 | |||||||
| chrX:74824254 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-78557C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824254 | |||||||
| chrX:74824284 | C | A | 1 | a0001c0001t0024g0167 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-47-78587G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824284 | |||||||
| chrX:74824397 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-47-78700G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824397 | |||||||
| chrX:74824652 | G | GT | 18 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0205 others(15): Show |
18 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-47-78956dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824652 | |||||||
| chrX:74824797 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-47-79100G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824797 | |||||||
| chrX:74824884 | G | A | 2 | a0001c0001t0001g0215 a0002c0004t0001g0201 |
2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-79187C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824884 | |||||||
| chrX:74824891 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0075 |
2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-47-79194C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824891 | |||||||
| chrX:74824912 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-79215A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824912 | |||||||
| chrX:74825594 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-47-79897C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74825594 | |||||||
| chrX:74825679 | C | T | 8 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-79982G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74825679 | |||||||
| chrX:74826206 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47-80509G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826206 | |||||||
| chrX:74826228 | G | A | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-80531C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826228 | |||||||
| chrX:74826764 | A | G | 1 | a0001c0001t0021g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-47-81067T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826764 | |||||||
| chrX:74826865 | A | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-81168T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826865 | |||||||
| chrX:74826932 | C | T | 2 | a0001c0001t0002g0160 a0003c0011t0002g0141 |
2 | HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-47-81235G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826932 | |||||||
| chrX:74827130 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-81433G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74827130 | |||||||
| chrX:74827343 | C | T | 1 | a0001c0001t0005g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47-81646G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74827343 | |||||||
| chrX:74827849 | C | T | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-82152G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74827849 | |||||||
| chrX:74827886 | T | G | 1 | a0001c0001t0018g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-82189A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74827886 | |||||||
| chrX:74828454 | A | G | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-82757T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828454 | |||||||
| chrX:74828720 | G | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-83023C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828720 | |||||||
| chrX:74828785 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-47-83088G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828785 | |||||||
| chrX:74828789 | G | T | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-83092C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828789 | |||||||
| chrX:74828989 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-47-83292A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828989 | |||||||
| chrX:74829006 | C | A | 2 | a0001c0001t0002g0129 a0001c0001t0002g0163 |
2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-47-83309G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74829006 | |||||||
| chrX:74829712 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47-84015A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74829712 | |||||||
| chrX:74829756 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-84059C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74829756 | |||||||
| chrX:74829834 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-84137G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74829834 | |||||||
| chrX:74830158 | T | A | 1 | a0001c0001t0002g0174 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-47-84461A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830158 | |||||||
| chrX:74830474 | A | T | 1 | a0001c0001t0002g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-47-84777T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830474 | |||||||
| chrX:74830519 | T | G | 1 | a0001c0001t0001g0023 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-47-84822A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830519 | |||||||
| chrX:74830543 | T | C | 1 | a0008c0013t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-47-84846A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830543 | |||||||
| chrX:74830662 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-84965A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830662 | |||||||
| chrX:74830832 | T | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0102 |
2 | HG00323.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-47-85135A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830832 | |||||||
| chrX:74830958 | CGTT | C | 2 | a0001c0001t0002g0159 a0001c0001t0025g0130 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-47-85264_-47-8526 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830958 | |||||||
| chrX:74831027 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47-85330A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831027 | |||||||
| chrX:74831196 | T | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-85499A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831196 | |||||||
| chrX:74831315 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0075 |
2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-47-85618C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831315 | |||||||
| chrX:74831350 | A | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-85653T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831350 | |||||||
| chrX:74831592 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-47-85895C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831592 | |||||||
| chrX:74831621 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-85924G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831621 | |||||||
| chrX:74831642 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-85945G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831642 | |||||||
| chrX:74831903 | A | G | 1 | a0001c0001t0020g0027 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-47-86206T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831903 | |||||||
| chrX:74832390 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-86693A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74832390 | |||||||
| chrX:74833662 | C | T | 2 | a0001c0001t0002g0160 a0003c0011t0002g0141 |
2 | HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-47-87965G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74833662 | |||||||
| chrX:74833858 | A | T | 2 | a0001c0001t0005g0122 a0001c0001t0005g0123 |
2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-47-88161T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74833858 | |||||||
| chrX:74834134 | C | CA | 15 | a0001c0001t0001g0100 a0001c0001t0001g0138 a0001c0001t0001g0140 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-88438dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834134 | |||||||
| chrX:74834134 | CA | C | 20 | a0001c0001t0001g0039 a0001c0001t0001g0051 a0001c0001t0001g0202 others(17): Show |
20 | HG00735.hp2 HG00738.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.-47-88438delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834134 | |||||||
| chrX:74834334 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-88637A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834334 | |||||||
| chrX:74834659 | G | C | 1 | a0001c0001t0003g0086 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-47-88962C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834659 | |||||||
| chrX:74834837 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-89140A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834837 | |||||||
| chrX:74834858 | A | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-89161T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834858 | |||||||
| chrX:74834914 | C | T | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-89217G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834914 | |||||||
| chrX:74835208 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-89511G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835208 | |||||||
| chrX:74835585 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-48+89298A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835585 | |||||||
| chrX:74835832 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+89051A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835832 | |||||||
| chrX:74835907 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-48+88976T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835907 | |||||||
| chrX:74835953 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+88930G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835953 | |||||||
| chrX:74835977 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+88906C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835977 | |||||||
| chrX:74836946 | C | T | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+87937G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74836946 | |||||||
| chrX:74837135 | CACAG | C | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
98 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-48+87744_-48+8774 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837135 | |||||||
| chrX:74837203 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+87680A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837203 | |||||||
| chrX:74837360 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-48+87523T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837360 | |||||||
| chrX:74837609 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-48+87274G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837609 | |||||||
| chrX:74837856 | G | GA | 6 | a0001c0001t0001g0038 a0001c0001t0001g0193 a0001c0001t0001g0198 others(3): Show |
6 | HG02559.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+87026dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837856 | |||||||
| chrX:74839684 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-48+85199G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74839684 | |||||||
| chrX:74840148 | C | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-48+84735G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840148 | |||||||
| chrX:74840180 | T | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+84703A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840180 | |||||||
| chrX:74840372 | CAG | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+84509_-48+8451 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840372 | |||||||
| chrX:74840841 | G | T | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+84042C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840841 | |||||||
| chrX:74841758 | T | C | 1 | a0001c0001t0004g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-48+83125A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74841758 | |||||||
| chrX:74842065 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0023 |
2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-48+82818A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842065 | |||||||
| chrX:74842092 | T | C | 3 | a0001c0001t0001g0215 a0002c0004t0001g0201 a0002c0004t0011g0002 |
3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-48+82791A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842092 | |||||||
| chrX:74842536 | T | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+82347A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842536 | |||||||
| chrX:74842596 | A | C | 4 | a0001c0001t0001g0223 a0001c0001t0004g0187 a0001c0001t0004g0188 others(1): Show |
4 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+82287T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842596 | |||||||
| chrX:74842779 | T | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+82104A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842779 | |||||||
| chrX:74842907 | T | A | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+81976A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842907 | |||||||
| chrX:74843138 | T | G | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-48+81745A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843138 | |||||||
| chrX:74843421 | T | G | 1 | a0003c0011t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-48+81462A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843421 | |||||||
| chrX:74843555 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-48+81328G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843555 | |||||||
| chrX:74843571 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48+81312G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843571 | |||||||
| chrX:74843572 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0096 |
2 | NA18961.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-48+81311C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843572 | |||||||
| chrX:74843741 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48+81142G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843741 | |||||||
| chrX:74843845 | T | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0004c0006t0016g0118 |
3 | HG02717.hp1 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-48+81038A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843845 | |||||||
| chrX:74844202 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-48+80681G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74844202 | |||||||
| chrX:74845060 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-48+79823A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74845060 | |||||||
| chrX:74845126 | A | T | 1 | a0001c0001t0002g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-48+79757T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74845126 | |||||||
| chrX:74845180 | G | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+79703C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74845180 | |||||||
| chrX:74845508 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-48+79375G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74845508 | |||||||
| chrX:74846020 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-48+78863T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846020 | |||||||
| chrX:74846094 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-48+78789C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846094 | |||||||
| chrX:74846118 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+78765G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846118 | |||||||
| chrX:74846769 | A | G | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-48+78114T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846769 | |||||||
| chrX:74846835 | T | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+78048A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846835 | |||||||
| chrX:74846900 | C | T | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+77983G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846900 | |||||||
| chrX:74847310 | G | T | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+77573C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847310 | |||||||
| chrX:74847472 | C | T | 1 | a0007c0008t0002g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-48+77411G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847472 | |||||||
| chrX:74847529 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+77354T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847529 | |||||||
| chrX:74847584 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-48+77299G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847584 | |||||||
| chrX:74847758 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-48+77125A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847758 | |||||||
| chrX:74848285 | G | A | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+76598C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74848285 | |||||||
| chrX:74848413 | T | G | 1 | a0001c0001t0002g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-48+76470A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74848413 | |||||||
| chrX:74848962 | G | T | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+75921C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74848962 | |||||||
| chrX:74849502 | C | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+75381G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849502 | |||||||
| chrX:74849548 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-48+75335C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849548 | |||||||
| chrX:74849707 | G | A | 2 | a0001c0001t0002g0168 a0001c0001t0002g0183 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-48+75176C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849707 | |||||||
| chrX:74849839 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48+75044G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849839 | |||||||
| chrX:74849974 | T | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+74909A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849974 | |||||||
| chrX:74850136 | C | A | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+74747G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850136 | |||||||
| chrX:74850456 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-48+74427G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850456 | |||||||
| chrX:74850557 | C | T | 3 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0018g0178 |
3 | HG00408.hp1 HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-48+74326G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850557 | |||||||
| chrX:74850659 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-48+74224G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850659 | |||||||
| chrX:74850686 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0163 |
2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-48+74197G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850686 | |||||||
| chrX:74850780 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+74103T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850780 | |||||||
| chrX:74850781 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+74102C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850781 | |||||||
| chrX:74850782 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+74101T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850782 | |||||||
| chrX:74850784 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+74099T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850784 | |||||||
| chrX:74851086 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+73797A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851086 | |||||||
| chrX:74851161 | C | A | 14 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0104 others(11): Show |
14 | HG00323.hp1 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48+73722G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851161 | |||||||
| chrX:74851267 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-48+73616T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851267 | |||||||
| chrX:74851379 | T | G | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-48+73504A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851379 | |||||||
| chrX:74851523 | G | A | 4 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+73360C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851523 | |||||||
| chrX:74851581 | T | C | 220 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(217): Show |
221 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-48+73302A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851581 | |||||||
| chrX:74851582 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0013g0004 a0001c0010t0001g0212 |
3 | HG00738.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-48+73301C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851582 | |||||||
| chrX:74851590 | G | GA | 9 | a0001c0001t0001g0026 a0001c0001t0001g0217 a0001c0001t0005g0119 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+73292dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851590 | |||||||
| chrX:74851590 | GA | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(16): Show |
19 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-48+73292delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851590 | |||||||
| chrX:74851595 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+73288T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851595 | |||||||
| chrX:74851807 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-48+73076T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851807 | |||||||
| chrX:74851896 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+72987T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851896 | |||||||
| chrX:74852982 | T | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+71901A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74852982 | |||||||
| chrX:74853002 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+71881A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853002 | |||||||
| chrX:74853008 | GT | G | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+71874delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853008 | |||||||
| chrX:74853027 | T | A | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+71856A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853027 | |||||||
| chrX:74853086 | TTGTCACA others(438): Show |
T | 1 | a0001c0001t0019g0017 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-48+71352_-48+7179 others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853086 | |||||||
| chrX:74853296 | G | C | 1 | a0001c0001t0002g0179 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-48+71587C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853296 | |||||||
| chrX:74853402 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+71481A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853402 | |||||||
| chrX:74853445 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0067 |
2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-48+71438G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853445 | |||||||
| chrX:74853785 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-48+71098A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853785 | |||||||
| chrX:74854055 | G | A | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+70828C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854055 | |||||||
| chrX:74854265 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+70618C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854265 | |||||||
| chrX:74854296 | C | T | 3 | a0001c0001t0001g0208 a0001c0001t0013g0004 a0001c0010t0001g0212 |
3 | HG00738.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-48+70587G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854296 | |||||||
| chrX:74854315 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+70568G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854315 | |||||||
| chrX:74854435 | A | G | 4 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+70448T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854435 | |||||||
| chrX:74854442 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+70441C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854442 | |||||||
| chrX:74854734 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+70149G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854734 | |||||||
| chrX:74854784 | C | A | 1 | a0001c0001t0003g0016 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-48+70099G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854784 | |||||||
| chrX:74854816 | A | G | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+70067T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854816 | |||||||
| chrX:74854861 | G | A | 4 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+70022C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854861 | |||||||
| chrX:74855057 | G | GA | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0007g0113 others(1): Show |
4 | HG02027.hp1 HG02922.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+69825dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855057 | |||||||
| chrX:74855065 | A | T | 1 | a0001c0002t0001g0048 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-48+69818T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855065 | |||||||
| chrX:74855289 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+69594T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855289 | |||||||
| chrX:74855389 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+69494G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855389 | |||||||
| chrX:74855599 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-48+69284G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855599 | |||||||
| chrX:74855774 | T | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+69109A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855774 | |||||||
| chrX:74856181 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+68702A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856181 | |||||||
| chrX:74856218 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-48+68665A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856218 | |||||||
| chrX:74856245 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+68638G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856245 | |||||||
| chrX:74856307 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+68576A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856307 | |||||||
| chrX:74856519 | C | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0083 others(19): Show |
22 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.-48+68364G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856519 | |||||||
| chrX:74856663 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-48+68220G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856663 | |||||||
| chrX:74856862 | G | A | 3 | a0001c0001t0002g0164 a0001c0001t0002g0173 a0001c0001t0023g0171 |
3 | HG01255.hp1 HG01515.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-48+68021C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856862 | |||||||
| chrX:74856882 | AC | A | 14 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0104 others(11): Show |
14 | HG00323.hp1 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48+68000delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856882 | |||||||
| chrX:74857149 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+67734C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857149 | |||||||
| chrX:74857158 | G | A | 1 | a0002c0004t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+67725C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857158 | |||||||
| chrX:74857212 | C | T | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+67671G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857212 | |||||||
| chrX:74857243 | A | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+67640T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857243 | |||||||
| chrX:74857970 | G | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66913C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857970 | |||||||
| chrX:74858045 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66838G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858045 | |||||||
| chrX:74858145 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66738A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858145 | |||||||
| chrX:74858155 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-48+66728G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858155 | |||||||
| chrX:74858213 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG02818.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-48+66670G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858213 | |||||||
| chrX:74858216 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-48+66667T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858216 | |||||||
| chrX:74858312 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0006g0098 |
2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-48+66571C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858312 | |||||||
| chrX:74858359 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48+66524T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858359 | |||||||
| chrX:74858509 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66374A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858509 | |||||||
| chrX:74858517 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-48+66366G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858517 | |||||||
| chrX:74858594 | T | A | 1 | a0001c0001t0012g0003 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-48+66289A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858594 | |||||||
| chrX:74858615 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-48+66268G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858615 | |||||||
| chrX:74858616 | G | A | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+66267C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858616 | |||||||
| chrX:74858689 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-48+66194C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858689 | |||||||
| chrX:74858790 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66093G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858790 | |||||||
| chrX:74858885 | TCA | T | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-48+65996_-48+6599 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858885 | |||||||
| chrX:74858971 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+65912T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858971 | |||||||
| chrX:74859002 | C | T | 130 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-48+65881G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859002 | |||||||
| chrX:74859261 | C | A | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+65622G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859261 | |||||||
| chrX:74859369 | G | T | 1 | a0001c0001t0004g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-48+65514C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859369 | |||||||
| chrX:74859738 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-48+65145G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859738 | |||||||
| chrX:74859755 | G | A | 6 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0197 others(3): Show |
6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+65128C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859755 | |||||||
| chrX:74859919 | A | C | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-48+64964T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859919 | |||||||
| chrX:74860201 | G | A | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-48+64682C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860201 | |||||||
| chrX:74860336 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-48+64547A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860336 | |||||||
| chrX:74860391 | C | G | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+64492G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860391 | |||||||
| chrX:74860642 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+64241G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860642 | |||||||
| chrX:74860890 | G | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+63993C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860890 | |||||||
| chrX:74860989 | G | C | 1 | a0008c0013t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-48+63894C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860989 | |||||||
| chrX:74861077 | C | A | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-48+63806G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861077 | |||||||
| chrX:74861293 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+63590T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861293 | |||||||
| chrX:74861890 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-48+62993G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861890 | |||||||
| chrX:74861923 | A | T | 3 | a0001c0001t0001g0088 a0001c0001t0003g0124 a0001c0001t0003g0125 |
3 | NA18983.hp1 NA18985.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-48+62960T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861923 | |||||||
| chrX:74861966 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-48+62917A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861966 | |||||||
| chrX:74862103 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0093 |
2 | NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-48+62780C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74862103 | |||||||
| chrX:74862115 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-48+62768T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74862115 | |||||||
| chrX:74862122 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48+62761G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74862122 | |||||||
| chrX:74862894 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-48+61989C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74862894 | |||||||
| chrX:74863007 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-48+61876G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863007 | |||||||
| chrX:74863171 | CA | C | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
167 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.-48+61711delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863171 | |||||||
| chrX:74863195 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+61688G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863195 | |||||||
| chrX:74863421 | C | T | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.-48+61462G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863421 | |||||||
| chrX:74863781 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+61102A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863781 | |||||||
| chrX:74863856 | T | A | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+61027A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863856 | |||||||
| chrX:74864113 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-48+60770G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864113 | |||||||
| chrX:74864453 | A | T | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+60430T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864453 | |||||||
| chrX:74864473 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-48+60410A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864473 | |||||||
| chrX:74864624 | A | G | 1 | a0003c0011t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-48+60259T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864624 | |||||||
| chrX:74864674 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0004g0187 a0001c0001t0004g0188 others(1): Show |
4 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+60209G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864674 | |||||||
| chrX:74865361 | C | G | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-48+59522G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865361 | |||||||
| chrX:74865541 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+59342T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865541 | |||||||
| chrX:74865604 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-48+59279C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865604 | |||||||
| chrX:74865772 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-48+59111C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865772 | |||||||
| chrX:74865892 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0093 |
2 | NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-48+58991C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865892 | |||||||
| chrX:74866430 | ACTTGT | A | 2 | a0001c0001t0001g0221 a0001c0001t0006g0098 |
2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-48+58448_-48+5845 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866430 | |||||||
| chrX:74866452 | CTT | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+58429_-48+5843 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866452 | |||||||
| chrX:74866463 | G | T | 1 | a0001c0001t0002g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-48+58420C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866463 | |||||||
| chrX:74866818 | C | T | 1 | a0001c0001t0004g0196 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48+58065G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866818 | |||||||
| chrX:74866991 | A | G | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+57892T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866991 | |||||||
| chrX:74867248 | T | C | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+57635A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74867248 | |||||||
| chrX:74867614 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0078 others(1): Show |
4 | HG00408.hp2 NA18967.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+57269G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74867614 | |||||||
| chrX:74868056 | A | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+56827T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868056 | |||||||
| chrX:74868110 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+56773T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868110 | |||||||
| chrX:74868614 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-48+56269A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868614 | |||||||
| chrX:74868616 | G | A | 12 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+56267C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868616 | |||||||
| chrX:74868686 | T | A | 1 | a0001c0001t0021g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-48+56197A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868686 | |||||||
| chrX:74868766 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-48+56117A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868766 | |||||||
| chrX:74868923 | T | C | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 |
3 | HG00639.hp1 HG00642.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-48+55960A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868923 | |||||||
| chrX:74868965 | T | C | 2 | a0001c0001t0003g0085 a0001c0001t0003g0086 |
2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-48+55918A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868965 | |||||||
| chrX:74868980 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-48+55903T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868980 | |||||||
| chrX:74869227 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-48+55656C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869227 | |||||||
| chrX:74869383 | A | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0020g0027 |
3 | NA18965.hp1 NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-48+55500T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869383 | |||||||
| chrX:74869585 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0078 |
3 | HG00408.hp2 NA18982.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-48+55298G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869585 | |||||||
| chrX:74869629 | A | G | 148 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
148 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-48+55254T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869629 | |||||||
| chrX:74869684 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+55199C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869684 | |||||||
| chrX:74870249 | G | T | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-48+54634C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74870249 | |||||||
| chrX:74870358 | C | T | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+54525G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74870358 | |||||||
| chrX:74870997 | A | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+53886T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74870997 | |||||||
| chrX:74871169 | G | A | 1 | a0001c0001t0006g0219 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-48+53714C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74871169 | |||||||
| chrX:74871749 | C | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+53134G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74871749 | |||||||
| chrX:74871807 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-48+53076G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74871807 | |||||||
| chrX:74871914 | G | A | 7 | a0001c0001t0002g0143 a0001c0001t0002g0156 a0001c0001t0002g0157 others(4): Show |
7 | HG01256.hp1 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+52969C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74871914 | |||||||
| chrX:74872552 | T | G | 12 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(9): Show |
12 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+52331A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872552 | |||||||
| chrX:74872604 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-48+52279C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872604 | |||||||
| chrX:74872947 | G | T | 2 | a0001c0001t0005g0122 a0001c0001t0005g0123 |
2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-48+51936C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872947 | |||||||
| chrX:74872962 | A | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(19): Show |
22 | HG01243.hp1 HG01884.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.-48+51921T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872962 | |||||||
| chrX:74872980 | T | G | 4 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+51903A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872980 | |||||||
| chrX:74872993 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-48+51890T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872993 | |||||||
| chrX:74873005 | T | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-48+51878A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873005 | |||||||
| chrX:74873180 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-48+51703G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873180 | |||||||
| chrX:74873398 | T | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0160 a0003c0011t0002g0141 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+51485A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873398 | |||||||
| chrX:74873406 | T | C | 1 | a0001c0001t0002g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+51477A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873406 | |||||||
| chrX:74873440 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+51443T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873440 | |||||||
| chrX:74873452 | C | A | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+51431G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873452 | |||||||
| chrX:74873452 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+51431G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873452 | |||||||
| chrX:74873453 | G | A | 2 | a0001c0001t0025g0130 a0004c0006t0016g0118 |
2 | HG00323.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+51430C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873453 | |||||||
| chrX:74873631 | T | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+51252A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873631 | |||||||
| chrX:74873772 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-48+51111A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873772 | |||||||
| chrX:74873800 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+51083T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873800 | |||||||
| chrX:74873947 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-48+50936C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873947 | |||||||
| chrX:74874049 | A | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50834T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874049 | |||||||
| chrX:74874108 | G | T | 1 | a0001c0001t0002g0179 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-48+50775C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874108 | |||||||
| chrX:74874139 | G | C | 1 | a0001c0001t0002g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+50744C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874139 | |||||||
| chrX:74874173 | G | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50710C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874173 | |||||||
| chrX:74874209 | C | A | 7 | a0001c0001t0002g0143 a0001c0001t0002g0156 a0001c0001t0002g0157 others(4): Show |
7 | HG01256.hp1 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+50674G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874209 | |||||||
| chrX:74874213 | C | G | 1 | a0001c0001t0002g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-48+50670G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874213 | |||||||
| chrX:74874258 | C | T | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+50625G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874258 | |||||||
| chrX:74874310 | T | C | 128 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-48+50573A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874310 | |||||||
| chrX:74874311 | G | A | 128 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-48+50572C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874311 | |||||||
| chrX:74874414 | A | G | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+50469T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874414 | |||||||
| chrX:74874450 | A | G | 2 | a0001c0001t0001g0059 a0004c0006t0016g0118 |
2 | HG02886.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-48+50433T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874450 | |||||||
| chrX:74874473 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+50410A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874473 | |||||||
| chrX:74874492 | A | C | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+50391T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874492 | |||||||
| chrX:74874510 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+50373G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874510 | |||||||
| chrX:74874601 | G | C | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+50282C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874601 | |||||||
| chrX:74874652 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50231C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874652 | |||||||
| chrX:74874688 | C | A | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-48+50195G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874688 | |||||||
| chrX:74874688 | C | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50195G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874688 | |||||||
| chrX:74874743 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+50140G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874743 | |||||||
| chrX:74874776 | A | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50107T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874776 | |||||||
| chrX:74874784 | GCTCT | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0205 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-48+50095_-48+5009 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874784 | |||||||
| chrX:74874900 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-48+49983G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874900 | |||||||
| chrX:74874924 | C | T | 149 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
149 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-48+49959G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874924 | |||||||
| chrX:74874978 | A | C | 2 | a0001c0001t0001g0107 a0004c0006t0016g0118 |
2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+49905T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874978 | |||||||
| chrX:74874979 | T | C | 2 | a0001c0001t0001g0107 a0004c0006t0016g0118 |
2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+49904A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874979 | |||||||
| chrX:74875127 | A | G | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-48+49756T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875127 | |||||||
| chrX:74875160 | C | T | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.-48+49723G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875160 | |||||||
| chrX:74875258 | GTTT | G | 11 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0193 others(8): Show |
11 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+49622_-48+4962 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875258 | |||||||
| chrX:74875294 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-48+49589T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875294 | |||||||
| chrX:74875497 | C | T | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-48+49386G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875497 | |||||||
| chrX:74875563 | G | T | 2 | a0001c0001t0001g0221 a0001c0001t0006g0098 |
2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-48+49320C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875563 | |||||||
| chrX:74875585 | G | C | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+49298C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875585 | |||||||
| chrX:74875602 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+49281G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875602 | |||||||
| chrX:74875767 | C | G | 1 | a0001c0001t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-48+49116G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875767 | |||||||
| chrX:74875779 | T | C | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+49104A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875779 | |||||||
| chrX:74875780 | G | A | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+49103C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875780 | |||||||
| chrX:74875843 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+49040G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875843 | |||||||
| chrX:74875863 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+49020A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875863 | |||||||
| chrX:74875892 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+48991G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875892 | |||||||
| chrX:74876007 | T | C | 1 | a0001c0001t0002g0154 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48+48876A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876007 | |||||||
| chrX:74876070 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48813G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876070 | |||||||
| chrX:74876072 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48811A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876072 | |||||||
| chrX:74876144 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+48739G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876144 | |||||||
| chrX:74876199 | C | T | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-48+48684G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876199 | |||||||
| chrX:74876228 | C | A | 2 | a0001c0001t0001g0206 a0001c0001t0015g0210 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48655G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876228 | |||||||
| chrX:74876231 | C | A | 2 | a0001c0001t0001g0206 a0001c0001t0015g0210 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48652G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876231 | |||||||
| chrX:74876236 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0015g0210 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48647C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876236 | |||||||
| chrX:74876241 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0015g0210 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48642T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876241 | |||||||
| chrX:74876246 | G | T | 2 | a0001c0001t0001g0206 a0001c0001t0015g0210 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48637C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876246 | |||||||
| chrX:74876260 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+48623A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876260 | |||||||
| chrX:74876275 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0015g0210 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48608G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876275 | |||||||
| chrX:74876284 | A | C | 2 | a0001c0001t0001g0206 a0001c0001t0015g0210 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48599T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876284 | |||||||
| chrX:74876287 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0015g0210 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48596C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876287 | |||||||
| chrX:74876288 | T | C | 1 | a0005c0009t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48+48595A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876288 | |||||||
| chrX:74876356 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-48+48527G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876356 | |||||||
| chrX:74876405 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+48478A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876405 | |||||||
| chrX:74876449 | G | GA | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0101 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+48433dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876449 | |||||||
| chrX:74876507 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-48+48376A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876507 | |||||||
| chrX:74876508 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0193 |
2 | HG02165.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-48+48375G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876508 | |||||||
| chrX:74876519 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-48+48364C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876519 | |||||||
| chrX:74876562 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+48321G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876562 | |||||||
| chrX:74876567 | A | G | 1 | a0001c0001t0003g0094 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-48+48316T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876567 | |||||||
| chrX:74876568 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+48315A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876568 | |||||||
| chrX:74876597 | A | C | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-48+48286T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876597 | |||||||
| chrX:74876609 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-48+48274A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876609 | |||||||
| chrX:74876612 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48271T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876612 | |||||||
| chrX:74876643 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+48240T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876643 | |||||||
| chrX:74876662 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+48221T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876662 | |||||||
| chrX:74876816 | C | T | 1 | a0001c0001t0004g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-48+48067G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876816 | |||||||
| chrX:74877153 | C | T | 2 | a0001c0001t0008g0091 a0001c0001t0008g0095 |
2 | NA18747.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-48+47730G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877153 | |||||||
| chrX:74877318 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+47565G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877318 | |||||||
| chrX:74877325 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47558A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877325 | |||||||
| chrX:74877335 | C | T | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+47548G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877335 | |||||||
| chrX:74877338 | G | C | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+47545C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877338 | |||||||
| chrX:74877361 | G | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0001g0068 others(2): Show |
5 | HG02074.hp1 HG02135.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+47522C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877361 | |||||||
| chrX:74877434 | A | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(15): Show |
18 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-48+47449T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877434 | |||||||
| chrX:74877483 | C | T | 1 | a0001c0001t0004g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-48+47400G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877483 | |||||||
| chrX:74877485 | C | A | 1 | a0001c0001t0002g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-48+47398G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877485 | |||||||
| chrX:74877504 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+47379C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877504 | |||||||
| chrX:74877611 | G | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47272C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877611 | |||||||
| chrX:74877613 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47270G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877613 | |||||||
| chrX:74877614 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47269T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877614 | |||||||
| chrX:74877779 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48+47104C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877779 | |||||||
| chrX:74877784 | G | A | 1 | a0001c0001t0007g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-48+47099C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877784 | |||||||
| chrX:74877801 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+47082G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877801 | |||||||
| chrX:74877810 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+47073G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877810 | |||||||
| chrX:74877811 | G | A | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+47072C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877811 | |||||||
| chrX:74877908 | G | T | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+46975C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877908 | |||||||
| chrX:74877953 | G | A | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+46930C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877953 | |||||||
| chrX:74878105 | C | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+46778G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878105 | |||||||
| chrX:74878141 | T | A | 1 | a0001c0001t0017g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-48+46742A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878141 | |||||||
| chrX:74878243 | C | T | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+46640G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878243 | |||||||
| chrX:74878391 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+46492T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878391 | |||||||
| chrX:74878397 | TCAGA | T | 8 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+46482_-48+4648 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878397 | |||||||
| chrX:74878418 | G | T | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+46465C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878418 | |||||||
| chrX:74878638 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+46245C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878638 | |||||||
| chrX:74878705 | A | G | 4 | a0001c0001t0001g0223 a0001c0001t0004g0187 a0001c0001t0004g0188 others(1): Show |
4 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+46178T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878705 | |||||||
| chrX:74878863 | G | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-48+46020C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878863 | |||||||
| chrX:74878871 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+46012A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878871 | |||||||
| chrX:74878879 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-48+46004C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878879 | |||||||
| chrX:74878913 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-48+45970C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878913 | |||||||
| chrX:74878944 | G | A | 12 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+45939C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878944 | |||||||
| chrX:74878995 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45888C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878995 | |||||||
| chrX:74879007 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+45876A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879007 | |||||||
| chrX:74879023 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45860A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879023 | |||||||
| chrX:74879024 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45859A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879024 | |||||||
| chrX:74879025 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45858A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879025 | |||||||
| chrX:74879026 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45857A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879026 | |||||||
| chrX:74879029 | T | G | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45854A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879029 | |||||||
| chrX:74879030 | C | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45853G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879030 | |||||||
| chrX:74879053 | C | G | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+45830G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879053 | |||||||
| chrX:74879222 | G | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+45661C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879222 | |||||||
| chrX:74879283 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-48+45600A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879283 | |||||||
| chrX:74879490 | A | G | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+45393T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879490 | |||||||
| chrX:74879493 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0018g0178 others(1): Show |
4 | HG00408.hp1 HG02165.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+45390C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879493 | |||||||
| chrX:74879494 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0018g0178 others(1): Show |
4 | HG00408.hp1 HG02165.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+45389C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879494 | |||||||
| chrX:74879628 | C | G | 1 | a0001c0001t0018g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-48+45255G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879628 | |||||||
| chrX:74879816 | T | C | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+45067A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879816 | |||||||
| chrX:74879912 | T | C | 2 | a0001c0001t0001g0215 a0002c0004t0001g0201 |
2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-48+44971A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879912 | |||||||
| chrX:74879932 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-48+44951C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879932 | |||||||
| chrX:74880001 | C | T | 1 | a0001c0012t0001g0142 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-48+44882G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880001 | |||||||
| chrX:74880005 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+44878A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880005 | |||||||
| chrX:74880017 | A | G | 1 | a0005c0009t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48+44866T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880017 | |||||||
| chrX:74880397 | G | A | 1 | a0001c0001t0006g0219 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-48+44486C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880397 | |||||||
| chrX:74880629 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+44254A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880629 | |||||||
| chrX:74880754 | A | G | 148 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
148 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-48+44129T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880754 | |||||||
| chrX:74880942 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+43941T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880942 | |||||||
| chrX:74881050 | G | A | 1 | a0001c0010t0001g0212 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48+43833C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881050 | |||||||
| chrX:74881058 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+43825G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881058 | |||||||
| chrX:74881232 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-48+43651G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881232 | |||||||
| chrX:74881392 | G | GCA | 42 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0001g0199 others(39): Show |
42 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.-48+43489_-48+4349 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | |||||||
| chrX:74881392 | G | GCACA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0198 a0001c0001t0001g0206 others(6): Show |
9 | HG00639.hp1 HG01884.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+43487_-48+4349 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | |||||||
| chrX:74881392 | G | GCACACA | 6 | a0001c0001t0001g0193 a0001c0001t0001g0202 a0001c0001t0001g0217 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+43485_-48+4349 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | |||||||
| chrX:74881392 | G | GCACACAC others(1): Show |
5 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0006g0219 others(2): Show |
5 | HG02717.hp1 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+43483_-48+4349 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | |||||||
| chrX:74881392 | G | GCACACAC others(3): Show |
9 | a0001c0001t0001g0138 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
9 | HG02109.hp1 HG02273.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+43481_-48+4349 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | |||||||
| chrX:74881392 | G | GCACACAC others(5): Show |
28 | a0001c0001t0001g0103 a0001c0001t0001g0134 a0001c0001t0001g0137 others(25): Show |
28 | HG00738.hp1 HG01081.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-48+43479_-48+4349 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | |||||||
| chrX:74881392 | G | GCACACAC others(7): Show |
3 | a0001c0001t0001g0115 a0001c0001t0001g0209 a0002c0004t0001g0201 |
3 | HG00735.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-48+43477_-48+4349 others(18): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | |||||||
| chrX:74881419 | CACACAG | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0093 |
3 | HG01109.hp1 NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-48+43458_-48+4346 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881419 | |||||||
| chrX:74881421 | CACAG | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(102): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-48+43458_-48+4346 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881421 | |||||||
| chrX:74881423 | CAG | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
8 | HG01952.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+43458_-48+4345 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881423 | |||||||
| chrX:74881425 | G | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+43458C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881425 | |||||||
| chrX:74881611 | T | TCCTCTAC others(67): Show |
120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
120 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-48+43271_-48+4327 others(78): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881611 | |||||||
| chrX:74881611 | T | TCCTCTAC others(67): Show |
1 | a0001c0005t0001g0011 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-48+43271_-48+4327 others(78): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881611 | |||||||
| chrX:74881676 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+43207A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881676 | |||||||
| chrX:74881872 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-48+43011G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881872 | |||||||
| chrX:74882134 | A | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+42749T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882134 | |||||||
| chrX:74882221 | G | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+42662C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882221 | |||||||
| chrX:74882244 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42639C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882244 | |||||||
| chrX:74882247 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42636A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882247 | |||||||
| chrX:74882249 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42634A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882249 | |||||||
| chrX:74882250 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42633G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882250 | |||||||
| chrX:74882251 | C | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42632G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882251 | |||||||
| chrX:74882252 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42631T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882252 | |||||||
| chrX:74882253 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42630T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882253 | |||||||
| chrX:74882254 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42629G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882254 | |||||||
| chrX:74882255 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42628A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882255 | |||||||
| chrX:74882257 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42626T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882257 | |||||||
| chrX:74882259 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42624C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882259 | |||||||
| chrX:74882331 | G | A | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+42552C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882331 | |||||||
| chrX:74882342 | T | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+42541A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882342 | |||||||
| chrX:74882360 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-48+42523G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882360 | |||||||
| chrX:74882415 | G | A | 5 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0048 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+42468C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882415 | |||||||
| chrX:74882549 | C | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+42334G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882549 | |||||||
| chrX:74882595 | G | C | 5 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0048 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+42288C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882595 | |||||||
| chrX:74882636 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+42247G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882636 | |||||||
| chrX:74882996 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+41887C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882996 | |||||||
| chrX:74883215 | C | G | 5 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0048 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+41668G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883215 | |||||||
| chrX:74883216 | C | T | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+41667G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883216 | |||||||
| chrX:74883278 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-48+41605G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883278 | |||||||
| chrX:74883309 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-48+41574C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883309 | |||||||
| chrX:74883347 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-48+41536G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883347 | |||||||
| chrX:74883358 | A | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+41525T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883358 | |||||||
| chrX:74883363 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+41520C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883363 | |||||||
| chrX:74883444 | A | G | 7 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0193 others(4): Show |
7 | HG02559.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+41439T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883444 | |||||||
| chrX:74883573 | A | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+41310T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883573 | |||||||
| chrX:74883663 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-48+41220G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883663 | |||||||
| chrX:74884030 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+40853G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884030 | |||||||
| chrX:74884109 | A | C | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+40774T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884109 | |||||||
| chrX:74884188 | C | A | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+40695G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884188 | |||||||
| chrX:74884347 | T | C | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0002g0185 |
3 | HG02145.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+40536A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884347 | |||||||
| chrX:74884409 | T | G | 1 | a0001c0001t0001g0009 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-48+40474A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884409 | |||||||
| chrX:74884658 | G | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+40225C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884658 | |||||||
| chrX:74884928 | G | C | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+39955C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884928 | |||||||
| chrX:74884976 | C | G | 6 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0197 others(3): Show |
6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+39907G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884976 | |||||||
| chrX:74885375 | A | T | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+39508T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885375 | |||||||
| chrX:74885394 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+39489G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885394 | |||||||
| chrX:74885395 | G | A | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(111): Show |
114 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-48+39488C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885395 | |||||||
| chrX:74885477 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+39406G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885477 | |||||||
| chrX:74885495 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-48+39388T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885495 | |||||||
| chrX:74885524 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48+39359G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885524 | |||||||
| chrX:74885588 | C | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0179 |
2 | HG01433.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-48+39295G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885588 | |||||||
| chrX:74885603 | G | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+39280C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885603 | |||||||
| chrX:74885729 | G | A | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+39154C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885729 | |||||||
| chrX:74885785 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+39098G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885785 | |||||||
| chrX:74885808 | A | G | 149 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(146): Show |
149 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-48+39075T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885808 | |||||||
| chrX:74886020 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-48+38863C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886020 | |||||||
| chrX:74886054 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-48+38829C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886054 | |||||||
| chrX:74886100 | C | A | 1 | a0002c0004t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+38783G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886100 | |||||||
| chrX:74886101 | T | C | 1 | a0002c0004t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+38782A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886101 | |||||||
| chrX:74886114 | A | T | 1 | a0002c0004t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+38769T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886114 | |||||||
| chrX:74886142 | C | T | 2 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-48+38741G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886142 | |||||||
| chrX:74886203 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-48+38680T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886203 | |||||||
| chrX:74886208 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-48+38675T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886208 | |||||||
| chrX:74886348 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+38535C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886348 | |||||||
| chrX:74886382 | T | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+38501A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886382 | |||||||
| chrX:74886503 | A | C | 2 | a0001c0001t0001g0220 a0001c0007t0001g0029 |
2 | HG01258.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-48+38380T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886503 | |||||||
| chrX:74886537 | A | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+38346T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886537 | |||||||
| chrX:74886813 | T | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(112): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-48+38070A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886813 | |||||||
| chrX:74886832 | A | G | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(139): Show |
142 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-48+38051T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886832 | |||||||
| chrX:74886837 | A | G | 26 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(23): Show |
26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-48+38046T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886837 | |||||||
| chrX:74886881 | G | A | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+38002C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886881 | |||||||
| chrX:74886997 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-48+37886C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886997 | |||||||
| chrX:74887001 | G | C | 1 | a0001c0001t0002g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-48+37882C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887001 | |||||||
| chrX:74887026 | G | C | 4 | a0001c0001t0001g0223 a0001c0001t0004g0187 a0001c0001t0004g0188 others(1): Show |
4 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+37857C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887026 | |||||||
| chrX:74887080 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-48+37803T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887080 | |||||||
| chrX:74887096 | G | T | 1 | a0001c0001t0002g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-48+37787C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887096 | |||||||
| chrX:74887133 | T | A | 1 | a0001c0001t0002g0192 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-48+37750A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887133 | |||||||
| chrX:74887147 | A | T | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+37736T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887147 | |||||||
| chrX:74887187 | C | G | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+37696G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887187 | |||||||
| chrX:74887205 | A | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+37678T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887205 | |||||||
| chrX:74887278 | G | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+37605C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887278 | |||||||
| chrX:74887285 | C | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+37598G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887285 | |||||||
| chrX:74887311 | A | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-48+37572T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887311 | |||||||
| chrX:74887371 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-48+37512C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887371 | |||||||
| chrX:74887400 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-48+37483T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887400 | |||||||
| chrX:74887482 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-48+37401G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887482 | |||||||
| chrX:74887489 | T | C | 2 | a0001c0001t0003g0085 a0001c0001t0003g0086 |
2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-48+37394A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887489 | |||||||
| chrX:74887492 | T | G | 3 | a0001c0001t0001g0071 a0001c0001t0003g0085 a0001c0001t0003g0086 |
3 | HG00673.hp1 NA18943.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-48+37391A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887492 | |||||||
| chrX:74887562 | G | C | 1 | a0001c0001t0002g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+37321C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887562 | |||||||
| chrX:74887582 | C | G | 12 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+37301G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887582 | |||||||
| chrX:74887691 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48+37192A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887691 | |||||||
| chrX:74887929 | A | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+36954T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887929 | |||||||
| chrX:74888039 | A | T | 1 | a0001c0001t0001g0005 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-48+36844T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888039 | |||||||
| chrX:74888254 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0205 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-48+36629G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888254 | |||||||
| chrX:74888314 | A | C | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(122): Show |
125 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-48+36569T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888314 | |||||||
| chrX:74888561 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-48+36322T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888561 | |||||||
| chrX:74888647 | A | C | 2 | a0001c0005t0001g0011 a0001c0005t0001g0012 |
2 | HG01975.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-48+36236T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888647 | |||||||
| chrX:74888705 | AAAAC | A | 121 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-48+36174_-48+3617 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888705 | |||||||
| chrX:74889292 | A | G | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+35591T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889292 | |||||||
| chrX:74889590 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+35293C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889590 | |||||||
| chrX:74889694 | A | AAG | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(139): Show |
142 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-48+35187_-48+3518 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889694 | |||||||
| chrX:74889895 | TTTC | T | 4 | a0001c0001t0001g0217 a0001c0001t0002g0175 a0001c0001t0006g0218 others(1): Show |
4 | HG01070.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+34985_-48+3498 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889895 | |||||||
| chrX:74889952 | GTC | G | 10 | a0001c0001t0001g0053 a0001c0001t0001g0066 a0001c0001t0001g0079 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+34929_-48+3493 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889952 | |||||||
| chrX:74889952 | GTCTC | G | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(111): Show |
114 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-48+34927_-48+3493 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889952 | |||||||
| chrX:74889952 | GTCTCTCT others(1): Show |
G | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+34923_-48+3493 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889952 | |||||||
| chrX:74890009 | CCT | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+34872_-48+3487 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890009 | |||||||
| chrX:74890256 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+34627T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890256 | |||||||
| chrX:74890264 | GT | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+34618delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890264 | |||||||
| chrX:74890495 | T | A | 1 | a0001c0001t0004g0196 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48+34388A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890495 | |||||||
| chrX:74890596 | T | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+34287A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890596 | |||||||
| chrX:74890801 | T | G | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+34082A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890801 | |||||||
| chrX:74891170 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+33713G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891170 | |||||||
| chrX:74891193 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-48+33690C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891193 | |||||||
| chrX:74891316 | GT | G | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(122): Show |
125 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-48+33566delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891316 | |||||||
| chrX:74891525 | G | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+33358C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891525 | |||||||
| chrX:74891778 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-48+33105T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891778 | |||||||
| chrX:74892346 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-48+32537G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892346 | |||||||
| chrX:74892612 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-48+32271A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892612 | |||||||
| chrX:74892816 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0015g0210 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+32067T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892816 | |||||||
| chrX:74892940 | G | GGA | 148 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
148 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-48+31941_-48+3194 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892940 | |||||||
| chrX:74892994 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0074 |
2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-48+31889A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892994 | |||||||
| chrX:74893519 | G | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+31364C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74893519 | |||||||
| chrX:74893947 | T | G | 1 | a0001c0001t0002g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-48+30936A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74893947 | |||||||
| chrX:74894084 | G | C | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+30799C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894084 | |||||||
| chrX:74894137 | CA | C | 121 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-48+30745delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894137 | |||||||
| chrX:74894147 | A | T | 5 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG00735.hp2 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+30736T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894147 | |||||||
| chrX:74894384 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-48+30499T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894384 | |||||||
| chrX:74894558 | C | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+30325G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894558 | |||||||
| chrX:74894797 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+30086T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894797 | |||||||
| chrX:74895834 | TA | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0102 others(14): Show |
17 | HG00323.hp1 HG01109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-48+29048delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74895834 | |||||||
| chrX:74895850 | C | A | 1 | a0001c0001t0022g0037 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-48+29033G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74895850 | |||||||
| chrX:74895946 | T | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+28937A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74895946 | |||||||
| chrX:74896422 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-48+28461T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74896422 | |||||||
| chrX:74896832 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+28051A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74896832 | |||||||
| chrX:74897324 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-48+27559C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74897324 | |||||||
| chrX:74897473 | T | C | 6 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0197 others(3): Show |
6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+27410A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74897473 | |||||||
| chrX:74897888 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-48+26995T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74897888 | |||||||
| chrX:74897890 | A | G | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+26993T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74897890 | |||||||
| chrX:74898111 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-48+26772C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74898111 | |||||||
| chrX:74898195 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0006g0218 |
2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-48+26688A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74898195 | |||||||
| chrX:74898221 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0067 others(1): Show |
4 | HG02027.hp1 HG02132.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+26662T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74898221 | |||||||
| chrX:74898896 | A | C | 1 | a0001c0001t0004g0196 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48+25987T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74898896 | |||||||
| chrX:74899007 | G | A | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+25876C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74899007 | |||||||
| chrX:74899087 | A | G | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+25796T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74899087 | |||||||
| chrX:74899342 | A | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+25541T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74899342 | |||||||
| chrX:74900006 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-48+24877G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900006 | |||||||
| chrX:74900188 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+24695C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900188 | |||||||
| chrX:74900457 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0185 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+24426G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900457 | |||||||
| chrX:74900462 | C | CA | 9 | a0001c0001t0001g0223 a0001c0001t0002g0145 a0001c0001t0002g0146 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+24420dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900462 | |||||||
| chrX:74900474 | A | AAAAAAAG | 6 | a0001c0001t0001g0081 a0001c0001t0001g0108 a0001c0001t0001g0110 others(3): Show |
6 | HG02080.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+24408_-48+2440 others(11): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900474 | |||||||
| chrX:74900474 | A | AAAAAAG | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(100): Show |
103 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.-48+24403_-48+2440 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900474 | |||||||
| chrX:74900632 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-48+24251G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900632 | |||||||
| chrX:74900660 | G | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+24223C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900660 | |||||||
| chrX:74900700 | G | T | 1 | a0001c0001t0012g0003 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-48+24183C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900700 | |||||||
| chrX:74900804 | T | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+24079A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900804 | |||||||
| chrX:74900977 | T | C | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+23906A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900977 | |||||||
| chrX:74901010 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+23873A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901010 | |||||||
| chrX:74901026 | A | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+23857T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901026 | |||||||
| chrX:74901031 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+23852C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901031 | |||||||
| chrX:74901094 | T | C | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+23789A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901094 | |||||||
| chrX:74901120 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-48+23763G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901120 | |||||||
| chrX:74901587 | T | TCACA | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+23295_-48+2329 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901587 | |||||||
| chrX:74901777 | T | C | 1 | a0001c0001t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-48+23106A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901777 | |||||||
| chrX:74901939 | T | A | 1 | a0001c0001t0002g0158 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-48+22944A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901939 | |||||||
| chrX:74902183 | C | T | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+22700G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902183 | |||||||
| chrX:74902427 | A | G | 1 | a0001c0001t0002g0185 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-48+22456T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902427 | |||||||
| chrX:74902582 | T | C | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(112): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-48+22301A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902582 | |||||||
| chrX:74902698 | A | T | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+22185T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902698 | |||||||
| chrX:74902989 | G | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+21894C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902989 | |||||||
| chrX:74903325 | T | TAC | 24 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0026 others(21): Show |
25 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-48+21556_-48+2155 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACAC | 28 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0033 others(25): Show |
28 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.-48+21554_-48+2155 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACACAC | 20 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(17): Show |
20 | HG01168.hp2 HG01169.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.-48+21552_-48+2155 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACACACA others(1): Show |
17 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0051 others(14): Show |
17 | HG00558.hp1 HG01981.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-48+21550_-48+2155 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACACACA others(3): Show |
17 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0055 others(14): Show |
17 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+21548_-48+2155 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACACACA others(5): Show |
12 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0063 others(9): Show |
12 | HG00621.hp1 HG01258.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+21546_-48+2155 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACACACA others(7): Show |
11 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0018 others(8): Show |
11 | HG00609.hp1 HG01358.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+21544_-48+2155 others(18): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACACACA others(9): Show |
7 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0096 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+21542_-48+2155 others(20): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACACACA others(11): Show |
5 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0102 others(2): Show |
5 | HG01261.hp1 HG02083.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+21540_-48+2155 others(22): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACACACA others(17): Show |
1 | a0001c0001t0001g0078 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-48+21534_-48+2155 others(28): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | T | TACACACA others(19): Show |
1 | a0001c0001t0001g0079 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-48+21532_-48+2155 others(30): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | TAC | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0081 others(11): Show |
14 | HG00408.hp1 HG00735.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48+21556_-48+2155 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | TACAC | T | 20 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0099 others(17): Show |
20 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-48+21554_-48+2155 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | TACACAC | T | 5 | a0001c0001t0002g0154 a0001c0001t0002g0166 a0001c0001t0002g0175 others(2): Show |
5 | HG01070.hp1 HG01099.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+21552_-48+2155 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | TACACACA others(1): Show |
T | 7 | a0001c0001t0001g0107 a0001c0001t0001g0193 a0001c0001t0001g0195 others(4): Show |
7 | HG00673.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+21550_-48+2155 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | TACACACA others(3): Show |
T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0221 a0001c0001t0006g0098 others(1): Show |
4 | HG02486.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+21548_-48+2155 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0194 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-48+21546_-48+2155 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | TACACACA others(9): Show |
T | 2 | a0001c0001t0001g0115 a0001c0001t0004g0188 |
2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-48+21542_-48+2155 others(20): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903325 | TACACACA others(21): Show |
T | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48+21530_-48+2155 others(32): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | |||||||
| chrX:74903703 | T | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0165 a0001c0001t0002g0185 |
3 | HG02145.hp1 HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+21180A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903703 | |||||||
| chrX:74903782 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+21101C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903782 | |||||||
| chrX:74903880 | C | CGT | 5 | a0001c0001t0001g0103 a0001c0001t0001g0138 a0001c0001t0001g0200 others(2): Show |
5 | HG01515.hp1 HG02818.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+21001_-48+2100 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | |||||||
| chrX:74903880 | CGT | C | 38 | a0001c0001t0001g0115 a0001c0001t0001g0137 a0001c0001t0001g0162 others(35): Show |
38 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.-48+21001_-48+2100 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | |||||||
| chrX:74903880 | CGTGT | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0202 a0001c0001t0001g0203 others(15): Show |
18 | HG00735.hp2 HG01192.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-48+20999_-48+2100 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | |||||||
| chrX:74903880 | CGTGTGT | C | 2 | a0001c0001t0006g0218 a0004c0006t0016g0118 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+20997_-48+2100 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | |||||||
| chrX:74903880 | CGTGTGTG others(1): Show |
C | 3 | a0001c0001t0001g0217 a0001c0001t0002g0001 a0001c0001t0006g0219 |
4 | HG01069.hp1 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+20995_-48+2100 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | |||||||
| chrX:74903880 | CGTGTGTG others(3): Show |
C | 6 | a0001c0001t0001g0105 a0001c0001t0005g0119 a0001c0001t0005g0120 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+20993_-48+2100 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | |||||||
| chrX:74903880 | CGTGTGTG others(5): Show |
C | 113 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(110): Show |
113 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-48+20991_-48+2100 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | |||||||
| chrX:74903880 | CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+20989_-48+2100 others(18): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | |||||||
| chrX:74903880 | CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0001g0006 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-48+20987_-48+2100 others(20): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | |||||||
| chrX:74904222 | T | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+20661A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74904222 | |||||||
| chrX:74905048 | G | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+19835C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905048 | |||||||
| chrX:74905093 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+19790A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905093 | |||||||
| chrX:74905456 | A | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+19427T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905456 | |||||||
| chrX:74905468 | A | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+19415T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905468 | |||||||
| chrX:74905639 | G | A | 1 | a0001c0001t0004g0196 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48+19244C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905639 | |||||||
| chrX:74905678 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+19205G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905678 | |||||||
| chrX:74905744 | A | T | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48+19139T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905744 | |||||||
| chrX:74905828 | AC | A | 2 | a0001c0001t0007g0113 a0006c0014t0007g0112 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-48+19054delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905828 | |||||||
| chrX:74905829 | C | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(117): Show |
120 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-48+19054G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905829 | |||||||
| chrX:74905897 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+18986G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905897 | |||||||
| chrX:74905988 | G | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+18895C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905988 | |||||||
| chrX:74906098 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+18785A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906098 | |||||||
| chrX:74906120 | T | A | 8 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+18763A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906120 | |||||||
| chrX:74906145 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+18738G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906145 | |||||||
| chrX:74906154 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+18729A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906154 | |||||||
| chrX:74906156 | C | T | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+18727G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906156 | |||||||
| chrX:74906429 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+18454C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906429 | |||||||
| chrX:74906754 | A | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+18129T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906754 | |||||||
| chrX:74906789 | A | C | 13 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(10): Show |
13 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-48+18094T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906789 | |||||||
| chrX:74906796 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+18087A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906796 | |||||||
| chrX:74906900 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+17983A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906900 | |||||||
| chrX:74906996 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+17887C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906996 | |||||||
| chrX:74907007 | G | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+17876C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907007 | |||||||
| chrX:74907048 | T | C | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+17835A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907048 | |||||||
| chrX:74907334 | A | AC | 34 | a0001c0001t0001g0138 a0001c0001t0001g0162 a0001c0001t0001g0193 others(31): Show |
34 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-48+17548dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907334 | |||||||
| chrX:74907334 | ACC | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+17547_-48+1754 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907334 | |||||||
| chrX:74907339 | C | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+17544G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907339 | |||||||
| chrX:74907701 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+17182A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907701 | |||||||
| chrX:74907974 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+16909G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907974 | |||||||
| chrX:74908187 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-48+16696G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908187 | |||||||
| chrX:74908225 | A | C | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+16658T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908225 | |||||||
| chrX:74908383 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+16500G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908383 | |||||||
| chrX:74908432 | T | C | 1 | a0001c0001t0004g0188 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-48+16451A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908432 | |||||||
| chrX:74908527 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-48+16356G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908527 | |||||||
| chrX:74909384 | C | T | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-48+15499G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909384 | |||||||
| chrX:74909386 | C | T | 1 | a0001c0012t0001g0142 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-48+15497G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909386 | |||||||
| chrX:74909459 | C | T | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+15424G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909459 | |||||||
| chrX:74909523 | A | G | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+15360T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909523 | |||||||
| chrX:74909709 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-48+15174G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909709 | |||||||
| chrX:74909750 | A | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+15133T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909750 | |||||||
| chrX:74909912 | G | A | 1 | a0001c0001t0010g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+14971C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909912 | |||||||
| chrX:74909965 | G | C | 1 | a0001c0001t0005g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-48+14918C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909965 | |||||||
| chrX:74910032 | CTGCTAGG others(3): Show |
C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14841_-48+1485 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910032 | |||||||
| chrX:74910043 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14840C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910043 | |||||||
| chrX:74910047 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14836T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910047 | |||||||
| chrX:74910049 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14834T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910049 | |||||||
| chrX:74910053 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14830T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910053 | |||||||
| chrX:74910064 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14819A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910064 | |||||||
| chrX:74910080 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14803C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910080 | |||||||
| chrX:74910081 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14802T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910081 | |||||||
| chrX:74910082 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14801C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910082 | |||||||
| chrX:74910090 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14793A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910090 | |||||||
| chrX:74910092 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14791C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910092 | |||||||
| chrX:74910093 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14790C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910093 | |||||||
| chrX:74910094 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14789C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910094 | |||||||
| chrX:74910095 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14788G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910095 | |||||||
| chrX:74910096 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14787T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910096 | |||||||
| chrX:74910104 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14779C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910104 | |||||||
| chrX:74910107 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-48+14776C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910107 | |||||||
| chrX:74910112 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14771C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910112 | |||||||
| chrX:74910151 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14732C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910151 | |||||||
| chrX:74910152 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14731T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910152 | |||||||
| chrX:74910153 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14730A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910153 | |||||||
| chrX:74910154 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14729G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910154 | |||||||
| chrX:74910158 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14725A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910158 | |||||||
| chrX:74910159 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14724C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910159 | |||||||
| chrX:74910160 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14723T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910160 | |||||||
| chrX:74910162 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14721T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910162 | |||||||
| chrX:74910164 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14719G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910164 | |||||||
| chrX:74910165 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14718A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910165 | |||||||
| chrX:74910167 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14716C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910167 | |||||||
| chrX:74910172 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14711T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910172 | |||||||
| chrX:74910294 | G | A | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+14589C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910294 | |||||||
| chrX:74910475 | C | T | 6 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+14408G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910475 | |||||||
| chrX:74910502 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+14381T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910502 | |||||||
| chrX:74910758 | G | A | 2 | a0001c0001t0002g0139 a0001c0001t0002g0185 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+14125C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910758 | |||||||
| chrX:74910816 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0003g0097 |
2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-48+14067C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910816 | |||||||
| chrX:74911223 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+13660G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74911223 | |||||||
| chrX:74911288 | C | T | 123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(120): Show |
123 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-48+13595G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74911288 | |||||||
| chrX:74911629 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-48+13254A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74911629 | |||||||
| chrX:74911738 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-48+13145G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74911738 | |||||||
| chrX:74912705 | G | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+12178C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74912705 | |||||||
| chrX:74913240 | C | T | 1 | a0001c0012t0001g0142 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-48+11643G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913240 | |||||||
| chrX:74913377 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+11506G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913377 | |||||||
| chrX:74913413 | T | C | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+11470A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913413 | |||||||
| chrX:74913531 | T | C | 1 | a0001c0001t0013g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-48+11352A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913531 | |||||||
| chrX:74913628 | GA | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0194 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+11254delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913628 | |||||||
| chrX:74914389 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-48+10494G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74914389 | |||||||
| chrX:74914554 | G | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+10329C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74914554 | |||||||
| chrX:74914713 | C | A | 1 | a0004c0006t0016g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+10170G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74914713 | |||||||
| chrX:74914739 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0004g0186 |
2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-48+10144A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74914739 | |||||||
| chrX:74915001 | G | T | 1 | a0003c0011t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-48+9882C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915001 | |||||||
| chrX:74915034 | C | A | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+9849G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915034 | |||||||
| chrX:74915307 | A | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+9576T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915307 | |||||||
| chrX:74915337 | G | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+9546C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915337 | |||||||
| chrX:74915431 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+9452G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915431 | |||||||
| chrX:74915465 | C | G | 1 | a0002c0004t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+9418G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915465 | |||||||
| chrX:74915508 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-48+9375T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915508 | |||||||
| chrX:74915602 | G | A | 7 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0193 others(4): Show |
7 | HG02559.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+9281C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915602 | |||||||
| chrX:74915713 | T | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+9170A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915713 | |||||||
| chrX:74915899 | T | C | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-48+8984A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915899 | |||||||
| chrX:74915917 | A | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+8966T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915917 | |||||||
| chrX:74916649 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-48+8234G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74916649 | |||||||
| chrX:74917010 | C | G | 2 | a0001c0001t0001g0005 a0001c0001t0004g0186 |
2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-48+7873G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917010 | |||||||
| chrX:74917057 | AC | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+7825delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917057 | |||||||
| chrX:74917286 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+7597G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917286 | |||||||
| chrX:74917421 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0137 others(13): Show |
16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+7462A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917421 | |||||||
| chrX:74917840 | G | A | 2 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-48+7043C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917840 | |||||||
| chrX:74917841 | T | C | 1 | a0001c0001t0002g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-48+7042A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917841 | |||||||
| chrX:74918029 | G | A | 1 | a0002c0004t0011g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+6854C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918029 | |||||||
| chrX:74918062 | G | A | 1 | a0001c0001t0014g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+6821C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918062 | |||||||
| chrX:74918396 | A | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+6487T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918396 | |||||||
| chrX:74918854 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(1): Show |
4 | NA18971.hp1 NA19005.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+6029A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918854 | |||||||
| chrX:74918892 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+5991C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918892 | |||||||
| chrX:74919426 | G | A | 18 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 others(15): Show |
18 | HG00558.hp2 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.-48+5457C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919426 | |||||||
| chrX:74919429 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-48+5454A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919429 | |||||||
| chrX:74919629 | T | A | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+5254A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919629 | |||||||
| chrX:74919633 | T | C | 5 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+5250A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919633 | |||||||
| chrX:74919691 | C | T | 1 | a0001c0001t0019g0017 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-48+5192G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919691 | |||||||
| chrX:74919773 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-48+5110G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919773 | |||||||
| chrX:74919815 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+5068G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919815 | |||||||
| chrX:74919867 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+5016G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919867 | |||||||
| chrX:74919869 | C | T | 119 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(116): Show |
119 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-48+5014G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919869 | |||||||
| chrX:74919871 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-48+5012G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919871 | |||||||
| chrX:74920196 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+4687C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920196 | |||||||
| chrX:74920208 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+4675A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920208 | |||||||
| chrX:74920239 | G | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+4644C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920239 | |||||||
| chrX:74920248 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-48+4635A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920248 | |||||||
| chrX:74920541 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-48+4342T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920541 | |||||||
| chrX:74920549 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+4334C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920549 | |||||||
| chrX:74920775 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-48+4108G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920775 | |||||||
| chrX:74921356 | C | T | 17 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+3527G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74921356 | |||||||
| chrX:74921663 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0006g0098 |
2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-48+3220G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74921663 | |||||||
| chrX:74921722 | GA | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+3160delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74921722 | |||||||
| chrX:74921985 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-48+2898T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74921985 | |||||||
| chrX:74922113 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-48+2770A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922113 | |||||||
| chrX:74922337 | GGT | G | 157 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(154): Show |
158 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-48+2544_-48+2545d others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922337 | |||||||
| chrX:74922337 | GGTGT | G | 11 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(8): Show |
11 | HG00323.hp1 HG02615.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.-48+2542_-48+2545d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922337 | |||||||
| chrX:74922337 | GGTGTGT | G | 32 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(29): Show |
32 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-48+2540_-48+2545d others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922337 | |||||||
| chrX:74922337 | GGTGTGTG others(1): Show |
G | 6 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+2538_-48+2545d others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922337 | |||||||
| chrX:74922584 | T | C | 2 | a0001c0001t0003g0124 a0001c0001t0003g0125 |
2 | NA18983.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-48+2299A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922584 | |||||||
| chrX:74922642 | A | G | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 |
3 | HG00639.hp1 HG00642.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-48+2241T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922642 | |||||||
| chrX:74922734 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+2149A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922734 | |||||||
| chrX:74922888 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+1995G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922888 | |||||||
| chrX:74922899 | A | T | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+1984T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922899 | |||||||
| chrX:74923102 | A | AG | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(1): Show |
4 | NA18971.hp1 NA19005.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+1780dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74923102 | |||||||
| chrX:74923447 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-48+1436C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74923447 | |||||||
| chrX:74923924 | A | G | 1 | a0001c0001t0001g0006 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-48+959T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74923924 | |||||||
| chrX:74924073 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-48+810G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74924073 | |||||||
| chrX:74924159 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-48+724G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74924159 | |||||||
| chrX:74924162 | G | C | 1 | a0001c0001t0002g0222 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-48+721C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74924162 | |||||||
| chrX:74924838 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-48+45C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74924838 |