Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79041 |
| ensemblid | ENSG00000072954.7 |
| hgncid | 28462 |
| symbol | TMEM38A |
| name | transmembrane protein 38A |
| refseq_nuc | NM_024074.4 |
| refseq_prot | NP_076979.1 |
| ensembl_nuc | ENST00000187762.7 |
| ensembl_prot | ENSP00000187762.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 16661139 |
| end | 16690023 |
| strand | + |
| ver | v1.2 |
| region | chr19:16661139-16690023 |
| region5000 | chr19:16656139-16695023 |
| regionname0 | TMEM38A_chr19_16661139_16690023 |
| regionname5000 | TMEM38A_chr19_16656139_16695023 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 299 | 327 | 92 | 60 | 126 | 10 | 37 | 96 | TMEM38A_chr19_16656139_16695023 | TMEM38A | MELLS others(294): Show |
chr19 | 16656139 | 16695023 |
| a0002 | 0/0 | 299 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | MELLS others(294): Show |
chr19 | 16656139 | 16695023 |
| a0003 | 0/0 | 299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | MELLS others(294): Show |
chr19 | 16656139 | 16695023 |
| a0004 | 0/0 | 299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | MELLL others(294): Show |
chr19 | 16656139 | 16695023 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 897 | 248 | 77 | 51 | 79 | 7 | 33 | TMEM38A_chr19_16656139_16695023 | TMEM38A | ATGGA others(892): Show |
chr19 | 16656139 | 16695023 | ||
| a0001c0002 | 0/0 | 897 | 69 | 7 | 9 | 47 | 2 | 4 | TMEM38A_chr19_16656139_16695023 | TMEM38A | ATGGA others(892): Show |
chr19 | 16656139 | 16695023 | ||
| a0001c0003 | 0/0 | 897 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | ATGGA others(892): Show |
chr19 | 16656139 | 16695023 | ||
| a0001c0005 | 0/1 | 897 | 2 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | ATGGA others(892): Show |
chr19 | 16656139 | 16695023 | ||
| a0001c0007 | 0/0 | 897 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | ATGGA others(892): Show |
chr19 | 16656139 | 16695023 | ||
| a0002c0004 | 0/0 | 897 | 3 | 1 | 2 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | ATGGA others(892): Show |
chr19 | 16656139 | 16695023 | ||
| a0003c0006 | 0/0 | 897 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | ATGGA others(892): Show |
chr19 | 16656139 | 16695023 | ||
| a0004c0008 | 0/0 | 897 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | ATGGA others(892): Show |
chr19 | 16656139 | 16695023 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2632 | 97 | 0 | 25 | 54 | 5 | 13 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0002 | 0/0 | 2631 | 14 | 10 | 1 | 3 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2626): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0003 | 0/0 | 2630 | 24 | 18 | 1 | 1 | 0 | 4 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2625): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0004 | 0/0 | 2627 | 14 | 14 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2622): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0005 | 1/0 | 2631 | 26 | 5 | 10 | 8 | 0 | 2 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2626): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0006 | 0/0 | 2636 | 18 | 17 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2631): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0007 | 0/0 | 2627 | 15 | 4 | 4 | 0 | 1 | 6 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2622): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0008 | 0/0 | 2632 | 6 | 0 | 2 | 0 | 0 | 4 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0009 | 0/0 | 2632 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0010 | 0/0 | 2631 | 5 | 0 | 2 | 1 | 0 | 2 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2626): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0011 | 0/0 | 2635 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2630): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0012 | 0/0 | 2633 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2628): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0014 | 0/0 | 2635 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2630): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0015 | 0/0 | 2635 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2630): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0017 | 0/0 | 2633 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2628): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0018 | 0/0 | 2632 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0020 | 0/0 | 2631 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2626): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0021 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2636): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0022 | 0/0 | 2638 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2633): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0024 | 0/0 | 2633 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2628): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0025 | 0/0 | 2633 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2628): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0026 | 0/0 | 2632 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0027 | 0/0 | 2632 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0028 | 0/0 | 2630 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2625): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0030 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2666): Show |
chr19 | 16656139 | 16695023 |
| a0001c0001t0031 | 0/0 | 2632 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0002t0002 | 0/0 | 2631 | 50 | 2 | 7 | 35 | 2 | 4 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2626): Show |
chr19 | 16656139 | 16695023 |
| a0001c0002t0003 | 0/0 | 2630 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2625): Show |
chr19 | 16656139 | 16695023 |
| a0001c0002t0004 | 0/0 | 2627 | 7 | 5 | 2 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2622): Show |
chr19 | 16656139 | 16695023 |
| a0001c0002t0013 | 0/0 | 2630 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2625): Show |
chr19 | 16656139 | 16695023 |
| a0001c0002t0016 | 0/0 | 2630 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2625): Show |
chr19 | 16656139 | 16695023 |
| a0001c0002t0019 | 0/0 | 2632 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0003t0004 | 0/0 | 2627 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2622): Show |
chr19 | 16656139 | 16695023 |
| a0001c0003t0029 | 0/0 | 2627 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2622): Show |
chr19 | 16656139 | 16695023 |
| a0001c0005t0018 | 0/0 | 2632 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0005t0023 | 0/1 | 2632 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| a0001c0007t0004 | 0/0 | 2627 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2622): Show |
chr19 | 16656139 | 16695023 |
| a0002c0004t0002 | 0/0 | 2631 | 3 | 1 | 2 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2626): Show |
chr19 | 16656139 | 16695023 |
| a0003c0006t0003 | 0/0 | 2630 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2625): Show |
chr19 | 16656139 | 16695023 |
| a0004c0008t0008 | 0/0 | 2632 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | GCAGT others(2627): Show |
chr19 | 16656139 | 16695023 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0007g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0010g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0011g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0011g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0012g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0012g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0012g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0014g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0014g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0015g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0015g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0017g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0017g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0018g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0020g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0020g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0021g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0022g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0024g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0025g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0026g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0027g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0028g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0030g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0001t0031g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0013g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0013g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0013g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0016g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0016g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0019g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0002t0019g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0003t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0003t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0003t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0003t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0003t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0003t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0003t0029g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0005t0018g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0005t0023g0012 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0001c0007t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0002c0004t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0002c0004t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0002c0004t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0003c0006t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| a0004c0008t0008g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0018 | g0106 | EUR | GBR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0286 | EUR | FIN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0164 | EUR | FIN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00558 | hp1 | a0001 | c0001 | t0024 | g0007 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00609 | hp1 | a0001 | c0001 | t0009 | g0007 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0292 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00738 | hp2 | a0001 | c0001 | t0017 | g0119 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0270 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0269 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0205 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01099 | hp1 | a0002 | c0004 | t0002 | g0088 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0112 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0258 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01168 | hp1 | a0001 | c0001 | t0010 | g0004 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0280 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0281 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0046 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01175 | hp2 | a0001 | c0001 | t0031 | g0115 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01243 | hp1 | a0002 | c0004 | t0002 | g0127 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0120 | AMR | PUR | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0147 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0210 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01358 | hp1 | a0001 | c0001 | t0007 | g0064 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01361 | hp1 | a0001 | c0001 | t0025 | g0224 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01496 | hp2 | a0001 | c0001 | t0018 | g0113 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0202 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0209 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0231 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0146 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0252 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02083 | hp1 | a0001 | c0001 | t0012 | g0034 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | CDX | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | CDX | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0277 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0208 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0138 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02280 | hp2 | a0001 | c0001 | t0021 | g0227 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0296 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0225 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0256 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0221 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02615 | hp1 | a0001 | c0001 | t0028 | g0305 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0257 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0181 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0273 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02647 | hp1 | a0001 | c0001 | t0015 | g0251 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0260 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0174 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02698 | hp2 | a0001 | c0001 | t0010 | g0013 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0297 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0264 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0184 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02895 | hp2 | a0001 | c0003 | t0004 | g0182 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02897 | hp1 | a0001 | c0003 | t0004 | g0226 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0212 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0291 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0259 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02976 | hp1 | a0001 | c0003 | t0029 | g0229 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0234 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03041 | hp1 | a0002 | c0004 | t0002 | g0092 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0265 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0236 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0274 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0302 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03139 | hp1 | a0001 | c0003 | t0004 | g0180 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03195 | hp1 | a0001 | c0007 | t0004 | g0271 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0237 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03209 | hp1 | a0001 | c0003 | t0004 | g0179 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0267 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03486 | hp2 | a0001 | c0001 | t0015 | g0235 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0278 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0122 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03491 | hp1 | a0001 | c0001 | t0010 | g0068 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0121 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0272 | AFR | ESN | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03579 | hp2 | a0003 | c0006 | t0003 | g0026 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03654 | hp2 | a0004 | c0008 | t0008 | g0124 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0246 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0287 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03710 | hp1 | a0001 | c0001 | t0026 | g0086 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03834 | hp1 | a0001 | c0001 | t0007 | g0282 | SAS | BEB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0294 | SAS | BEB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0006 | SAS | BEB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0268 | SAS | STU | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0161 | SAS | BEB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0093 | SAS | STU | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0171 | SAS | STU | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0283 | SAS | STU | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | STU | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG04228 | hp2 | a0001 | c0001 | t0012 | g0111 | SAS | STU | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | YRI | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0279 | AFR | YRI | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | CHB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18942 | hp1 | a0001 | c0002 | t0013 | g0150 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18942 | hp2 | a0001 | c0001 | t0009 | g0051 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18943 | hp1 | a0001 | c0002 | t0016 | g0016 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18943 | hp2 | a0001 | c0001 | t0027 | g0036 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18945 | hp2 | a0001 | c0002 | t0016 | g0159 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18948 | hp1 | a0001 | c0001 | t0010 | g0031 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18954 | hp2 | a0001 | c0001 | t0009 | g0070 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18956 | hp2 | a0001 | c0001 | t0030 | g0006 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0207 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18973 | hp2 | a0001 | c0001 | t0009 | g0081 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18983 | hp1 | a0001 | c0002 | t0013 | g0016 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18992 | hp1 | a0001 | c0001 | t0012 | g0037 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18999 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19011 | hp1 | a0001 | c0001 | t0020 | g0104 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | LWK | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | LWK | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0250 | AFR | LWK | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | LWK | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19057 | hp2 | a0001 | c0002 | t0019 | g0183 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0152 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19064 | hp2 | a0001 | c0002 | t0019 | g0021 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19070 | hp1 | a0001 | c0002 | t0013 | g0155 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0158 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19085 | hp1 | a0001 | c0001 | t0020 | g0103 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19089 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0262 | AFR | YRI | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0304 | AFR | YRI | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | ASW | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ASW | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA20752 | hp2 | a0001 | c0001 | t0017 | g0123 | EUR | TSI | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0139 | EUR | TSI | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01123 | hp1 | a0001 | c0001 | t0022 | g0276 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0289 | AFR | ACB | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0275 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0254 | AFR | MSL | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | USA | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | USA | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0253 | AFR | LWK | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0238 | AFR | LWK | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| homoSapiens | chm13v2 | a0001 | c0005 | t0023 | g0012 | REF | REF | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0080 | REF | REF | TMEM38A_chr19_16656139_16695023 | TMEM38A | chr19 | 16656139 | 16695023 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16661231 | C | T | 1 | a0004 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.14C>T | p.Ser5Leu | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/6 | 93/2631 | 14/900 | 5/299 | chr19 | 16661231 | |||
| chr19:16688210 | G | A | 1 | a0002 | 3 | HG01099.hp1 HG01243.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.739G>A | p.Val247Met | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 818/2631 | 739/900 | 247/299 | chr19 | 16688210 | |||
| chr19:16688309 | G | A | 1 | a0003 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.838G>A | p.Ala280Thr | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 917/2631 | 838/900 | 280/299 | chr19 | 16688309 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16680048 | C | T | 2 | a0001c0002 a0001c0007 |
70 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
synonymous_variant | LOW | c.189C>T | p.Phe63Phe | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 2/6 | 268/2631 | 189/900 | 63/299 | chr19 | 16680048 | |||
| chr19:16680132 | A | G | 1 | a0001c0003 | 7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
synonymous_variant | LOW | c.273A>G | p.Ser91Ser | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 2/6 | 352/2631 | 273/900 | 91/299 | chr19 | 16680132 | |||
| chr19:16680547 | G | C | 1 | a0001c0007 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.432G>C | p.Gly144Gly | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/6 | 511/2631 | 432/900 | 144/299 | chr19 | 16680547 | |||
| chr19:16688332 | C | T | 1 | a0001c0005 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.861C>T | p.Ser287Ser | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 940/2631 | 861/900 | 287/299 | chr19 | 16688332 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16661158 | C | T | 1 | a0001c0001t0031 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/6 | 60 | chr19 | 16661158 | ||||||
| chr19:16661195 | C | CGGCAGGC others(1): Show |
6 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0014 others(3): Show |
27 | HG01109.hp2 HG01123.hp1 HG02055.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-11_-4dupAGGCGGGC | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/6 | 3 | INFO_REALIGN_3_PRIME | chr19 | 16661195 | |||||
| chr19:16688447 | T | TCTATCCT others(31): Show |
1 | a0001c0001t0030 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77_*114dupCTATCCT others(31): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 115 | INFO_REALIGN_3_PRIME | chr19 | 16688447 | |||||
| chr19:16688515 | T | C | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(20): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*144T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 144 | chr19 | 16688515 | ||||||
| chr19:16688523 | T | C | 1 | a0001c0001t0028 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*152T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 152 | chr19 | 16688523 | ||||||
| chr19:16688764 | G | A | 1 | a0001c0002t0016 | 2 | NA18943.hp1 NA18945.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 393 | chr19 | 16688764 | ||||||
| chr19:16688809 | A | T | 1 | a0001c0001t0006 | 18 | HG01109.hp2 HG02109.hp1 HG02572.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*438A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 438 | chr19 | 16688809 | ||||||
| chr19:16688853 | C | T | 1 | a0001c0001t0027 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 482 | chr19 | 16688853 | ||||||
| chr19:16689003 | C | CA | 10 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(7): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*649dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 650 | INFO_REALIGN_3_PRIME | chr19 | 16689003 | |||||
| chr19:16689003 | C | CAA | 6 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0021 others(3): Show |
9 | HG00558.hp1 HG00738.hp2 HG01361.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*648_*649dupAA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 650 | INFO_REALIGN_3_PRIME | chr19 | 16689003 | |||||
| chr19:16689003 | CA | C | 7 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0028 others(4): Show |
37 | HG00597.hp1 HG01123.hp1 HG01123.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*649delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 649 | INFO_REALIGN_3_PRIME | chr19 | 16689003 | |||||
| chr19:16689003 | CAAA | C | 1 | a0001c0001t0006 | 18 | HG01109.hp2 HG02109.hp1 HG02572.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*647_*649delAAA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 647 | INFO_REALIGN_3_PRIME | chr19 | 16689003 | |||||
| chr19:16689003 | CAAAA | C | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(6): Show |
51 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*646_*649delAAAA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 646 | INFO_REALIGN_3_PRIME | chr19 | 16689003 | |||||
| chr19:16689133 | C | T | 4 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0021 others(1): Show |
22 | HG01109.hp2 HG01361.hp1 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*762C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 762 | chr19 | 16689133 | ||||||
| chr19:16689258 | C | T | 1 | a0001c0001t0007 | 15 | HG00280.hp2 HG00735.hp2 HG01168.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*887C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 887 | chr19 | 16689258 | ||||||
| chr19:16689322 | C | T | 3 | a0001c0001t0008 a0001c0001t0017 a0004c0008t0008 |
9 | HG00738.hp2 HG01109.hp1 HG01243.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*951C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 951 | chr19 | 16689322 | ||||||
| chr19:16689641 | T | G | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(23): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1270T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 1270 | chr19 | 16689641 | ||||||
| chr19:16689741 | G | A | 3 | a0001c0001t0009 a0001c0001t0020 a0001c0001t0024 |
8 | HG00558.hp1 HG00609.hp1 NA18942.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1370G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 1370 | chr19 | 16689741 | ||||||
| chr19:16689752 | T | C | 3 | a0001c0001t0018 a0001c0001t0031 a0001c0005t0018 |
3 | HG00099.hp1 HG01175.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1381T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 1381 | chr19 | 16689752 | ||||||
| chr19:16689797 | G | T | 1 | a0001c0003t0029 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1426G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 1426 | chr19 | 16689797 | ||||||
| chr19:16689839 | G | A | 2 | a0001c0001t0014 a0001c0001t0026 |
3 | HG03098.hp1 HG03471.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1468G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 6/6 | 1468 | chr19 | 16689839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16661429 | C | A | 1 | a0003c0006t0003g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+88C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16661429 | |||||||
| chr19:16661763 | A | T | 10 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0299 others(7): Show |
10 | HG02258.hp1 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+422A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16661763 | |||||||
| chr19:16661768 | C | CTA | 184 | a0001c0001t0001g0140 a0001c0001t0001g0206 a0001c0001t0001g0285 others(181): Show |
196 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.124+430_124+431dup others(2): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16661768 | ||||||
| chr19:16661825 | C | T | 1 | a0001c0001t0004g0296 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124+484C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16661825 | |||||||
| chr19:16662070 | C | T | 30 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(27): Show |
30 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.124+729C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16662070 | |||||||
| chr19:16662436 | C | CT | 55 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(52): Show |
57 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.124+1117dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16662436 | ||||||
| chr19:16662436 | C | CTTTTT | 12 | a0001c0001t0001g0285 a0001c0001t0002g0284 a0001c0001t0007g0277 others(9): Show |
12 | HG00280.hp2 HG01123.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.124+1113_124+1117d others(7): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16662436 | ||||||
| chr19:16662436 | C | CTTTTTT | 8 | a0001c0001t0002g0290 a0001c0001t0002g0293 a0001c0001t0002g0295 others(5): Show |
8 | HG00735.hp2 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+1112_124+1117d others(8): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16662436 | ||||||
| chr19:16662436 | CT | C | 61 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0140 others(58): Show |
67 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.124+1117delT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16662436 | ||||||
| chr19:16662462 | G | GT | 11 | a0001c0001t0001g0028 a0001c0001t0001g0117 a0001c0001t0001g0118 others(8): Show |
11 | HG02615.hp1 HG03130.hp1 HG03225.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1131dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16662462 | ||||||
| chr19:16662490 | G | A | 23 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(20): Show |
23 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+1149G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16662490 | |||||||
| chr19:16662518 | A | T | 23 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0237 others(20): Show |
25 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.124+1177A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16662518 | |||||||
| chr19:16662631 | T | G | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.124+1290T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16662631 | |||||||
| chr19:16662720 | G | A | 1 | a0001c0001t0011g0250 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124+1379G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16662720 | |||||||
| chr19:16662781 | A | G | 15 | a0001c0001t0001g0013 a0001c0001t0001g0105 a0001c0001t0001g0107 others(12): Show |
15 | HG00099.hp1 HG00558.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+1440A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16662781 | |||||||
| chr19:16662869 | T | G | 22 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(19): Show |
22 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.124+1528T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16662869 | |||||||
| chr19:16662944 | T | C | 1 | a0001c0002t0002g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124+1603T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16662944 | |||||||
| chr19:16663021 | C | T | 1 | a0001c0001t0007g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.124+1680C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663021 | |||||||
| chr19:16663188 | G | A | 1 | a0001c0001t0005g0199 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.124+1847G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663188 | |||||||
| chr19:16663281 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.124+1940G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663281 | |||||||
| chr19:16663378 | C | T | 2 | a0001c0001t0020g0103 a0001c0001t0020g0104 |
2 | NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.124+2037C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663378 | |||||||
| chr19:16663489 | C | G | 1 | a0001c0001t0005g0234 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.124+2148C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663489 | |||||||
| chr19:16663567 | C | T | 2 | a0001c0002t0002g0021 a0001c0002t0019g0021 |
2 | NA19064.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.124+2226C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663567 | |||||||
| chr19:16663584 | G | A | 54 | a0001c0001t0001g0285 a0001c0001t0002g0185 a0001c0001t0002g0240 others(51): Show |
54 | HG00280.hp2 HG00597.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.124+2243G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663584 | |||||||
| chr19:16663593 | G | A | 6 | a0001c0001t0008g0120 a0001c0001t0008g0121 a0001c0001t0008g0122 others(3): Show |
6 | HG00738.hp2 HG01243.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+2252G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663593 | |||||||
| chr19:16663601 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.124+2260T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663601 | |||||||
| chr19:16663664 | G | C | 2 | a0001c0002t0002g0021 a0001c0002t0019g0021 |
2 | NA19064.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.124+2323G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663664 | |||||||
| chr19:16663695 | A | AT | 19 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0116 others(16): Show |
19 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.124+2368dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16663695 | ||||||
| chr19:16663768 | C | A | 4 | a0001c0002t0002g0014 a0001c0002t0002g0138 a0001c0002t0002g0139 others(1): Show |
5 | HG01074.hp2 HG01975.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+2427C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663768 | |||||||
| chr19:16663814 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.124+2473G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663814 | |||||||
| chr19:16663827 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.124+2486C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663827 | |||||||
| chr19:16663832 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0038 others(10): Show |
14 | HG00423.hp2 HG01934.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.124+2491G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663832 | |||||||
| chr19:16663853 | C | T | 1 | a0001c0003t0029g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.124+2512C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16663853 | |||||||
| chr19:16664182 | G | A | 23 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(20): Show |
23 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+2841G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16664182 | |||||||
| chr19:16664218 | C | G | 1 | a0001c0002t0002g0228 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.124+2877C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16664218 | |||||||
| chr19:16664244 | C | T | 1 | a0001c0002t0019g0183 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.124+2903C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16664244 | |||||||
| chr19:16664251 | A | G | 31 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(28): Show |
31 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.124+2910A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16664251 | |||||||
| chr19:16664261 | CA | C | 153 | a0001c0001t0001g0140 a0001c0001t0001g0285 a0001c0001t0002g0185 others(150): Show |
161 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.124+2927delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16664261 | ||||||
| chr19:16664286 | G | A | 31 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(28): Show |
31 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.124+2945G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16664286 | |||||||
| chr19:16664289 | C | T | 24 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0237 others(21): Show |
26 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.124+2948C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16664289 | |||||||
| chr19:16664403 | C | A | 1 | a0001c0001t0015g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124+3062C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16664403 | |||||||
| chr19:16664864 | T | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00642.hp2 HG01074.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+3523T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16664864 | |||||||
| chr19:16664876 | T | TA | 58 | a0001c0001t0001g0140 a0001c0002t0002g0014 a0001c0002t0002g0015 others(55): Show |
62 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.124+3542dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16664876 | ||||||
| chr19:16664879 | A | T | 17 | a0001c0001t0001g0134 a0001c0001t0006g0024 a0001c0001t0006g0025 others(14): Show |
19 | HG01070.hp1 HG01109.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.124+3538A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16664879 | |||||||
| chr19:16665150 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.124+3809C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665150 | |||||||
| chr19:16665151 | G | A | 23 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(20): Show |
23 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+3810G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665151 | |||||||
| chr19:16665290 | G | A | 1 | a0001c0001t0006g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.124+3949G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665290 | |||||||
| chr19:16665317 | A | T | 10 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0299 others(7): Show |
10 | HG02258.hp1 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+3976A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665317 | |||||||
| chr19:16665411 | C | A | 1 | a0001c0001t0017g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.124+4070C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665411 | |||||||
| chr19:16665489 | C | CA | 31 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(28): Show |
35 | HG01109.hp2 HG01361.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.124+4158dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16665489 | ||||||
| chr19:16665665 | A | C | 23 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(20): Show |
23 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+4324A>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665665 | |||||||
| chr19:16665712 | G | T | 1 | a0004c0008t0008g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.124+4371G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665712 | |||||||
| chr19:16665728 | T | C | 2 | a0001c0001t0015g0235 a0001c0001t0015g0251 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.124+4387T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665728 | |||||||
| chr19:16665812 | C | CT | 23 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(20): Show |
23 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+4485dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16665812 | ||||||
| chr19:16665871 | C | T | 57 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0017 others(54): Show |
61 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.124+4530C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665871 | |||||||
| chr19:16665969 | C | T | 2 | a0001c0001t0005g0215 a0001c0001t0005g0248 |
2 | NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.124+4628C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16665969 | |||||||
| chr19:16666042 | T | A | 8 | a0001c0002t0004g0267 a0001c0002t0004g0269 a0001c0002t0004g0270 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+4701T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666042 | |||||||
| chr19:16666042 | T | G | 166 | a0001c0001t0001g0028 a0001c0001t0001g0206 a0001c0001t0001g0285 others(163): Show |
177 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.124+4701T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666042 | |||||||
| chr19:16666084 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.124+4743G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666084 | |||||||
| chr19:16666221 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124+4880C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666221 | |||||||
| chr19:16666274 | T | C | 53 | a0001c0001t0001g0285 a0001c0001t0002g0185 a0001c0001t0002g0240 others(50): Show |
53 | HG00280.hp2 HG00597.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.124+4933T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666274 | |||||||
| chr19:16666427 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.124+5086T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666427 | |||||||
| chr19:16666434 | A | T | 3 | a0001c0001t0007g0287 a0001c0001t0010g0031 a0001c0001t0014g0254 |
3 | HG03471.hp2 HG03704.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.124+5093A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666434 | |||||||
| chr19:16666435 | T | A | 9 | a0001c0001t0015g0235 a0001c0001t0015g0251 a0001c0003t0004g0179 others(6): Show |
9 | HG02572.hp1 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+5094T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666435 | |||||||
| chr19:16666562 | C | A | 31 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(28): Show |
31 | HG00597.hp1 HG01070.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.124+5221C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666562 | |||||||
| chr19:16666612 | C | T | 2 | a0001c0001t0006g0239 a0001c0001t0006g0265 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.124+5271C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666612 | |||||||
| chr19:16666641 | T | G | 2 | a0001c0001t0015g0235 a0001c0001t0015g0251 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.124+5300T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666641 | |||||||
| chr19:16666854 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0010g0004 |
2 | HG00099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.124+5513G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666854 | |||||||
| chr19:16666952 | C | CA | 128 | a0001c0001t0001g0117 a0001c0001t0002g0185 a0001c0001t0002g0240 others(125): Show |
136 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.124+5625dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16666952 | ||||||
| chr19:16666952 | C | CAA | 24 | a0001c0001t0001g0028 a0001c0001t0001g0206 a0001c0001t0003g0204 others(21): Show |
27 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.124+5624_124+5625d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16666952 | ||||||
| chr19:16666962 | A | G | 1 | a0001c0001t0007g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.124+5621A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666962 | |||||||
| chr19:16666977 | G | A | 32 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(29): Show |
36 | HG01109.hp2 HG01123.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.124+5636G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16666977 | |||||||
| chr19:16667216 | C | T | 23 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(20): Show |
23 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+5875C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16667216 | |||||||
| chr19:16667255 | G | A | 2 | a0001c0001t0015g0235 a0001c0001t0015g0251 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.124+5914G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16667255 | |||||||
| chr19:16667279 | G | GA | 145 | a0001c0001t0001g0028 a0001c0001t0001g0206 a0001c0001t0002g0185 others(142): Show |
154 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.124+5949dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16667279 | ||||||
| chr19:16667279 | G | GAAA | 6 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(3): Show |
8 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+5947_124+5949d others(5): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16667279 | ||||||
| chr19:16667282 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.124+5941A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16667282 | |||||||
| chr19:16667556 | G | T | 1 | a0001c0001t0007g0286 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.124+6215G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16667556 | |||||||
| chr19:16667684 | G | A | 10 | a0001c0002t0002g0015 a0001c0002t0002g0141 a0001c0002t0002g0142 others(7): Show |
11 | HG01257.hp2 HG02004.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.124+6343G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16667684 | |||||||
| chr19:16667717 | C | A | 1 | a0001c0001t0004g0023 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.124+6376C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16667717 | |||||||
| chr19:16667861 | G | GA | 24 | a0001c0001t0001g0049 a0001c0001t0001g0117 a0001c0001t0002g0185 others(21): Show |
24 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.124+6537dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16667861 | ||||||
| chr19:16667861 | GA | G | 42 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0023 others(39): Show |
47 | HG01109.hp2 HG01123.hp1 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.124+6537delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16667861 | ||||||
| chr19:16667861 | GAA | G | 59 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0017 others(56): Show |
63 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.124+6536_124+6537d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16667861 | ||||||
| chr19:16667899 | C | T | 1 | a0001c0001t0005g0246 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.124+6558C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16667899 | |||||||
| chr19:16668001 | A | G | 131 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(128): Show |
139 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.124+6660A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16668001 | |||||||
| chr19:16668302 | TG | T | 4 | a0001c0001t0004g0230 a0001c0001t0004g0233 a0001c0001t0004g0249 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+6964delG | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16668302 | ||||||
| chr19:16668502 | C | CA | 53 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0050 others(50): Show |
55 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.124+7181dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16668502 | ||||||
| chr19:16668502 | CA | C | 10 | a0001c0001t0001g0028 a0001c0001t0001g0099 a0001c0001t0005g0212 others(7): Show |
10 | HG02155.hp1 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+7181delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16668502 | ||||||
| chr19:16668589 | C | G | 1 | a0001c0001t0015g0251 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.124+7248C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16668589 | |||||||
| chr19:16668603 | G | A | 1 | a0001c0001t0006g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.124+7262G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16668603 | |||||||
| chr19:16668635 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.124+7294C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16668635 | |||||||
| chr19:16668832 | CT | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0140 others(3): Show |
6 | HG00099.hp1 HG00323.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+7505delT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16668832 | ||||||
| chr19:16668855 | C | CT | 130 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(127): Show |
141 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.124+7517dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16668855 | ||||||
| chr19:16668999 | T | A | 4 | a0001c0001t0004g0230 a0001c0001t0004g0233 a0001c0001t0004g0249 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+7658T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16668999 | |||||||
| chr19:16669077 | G | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
6 | HG00735.hp1 HG01070.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+7736G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669077 | |||||||
| chr19:16669085 | C | T | 18 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0237 others(15): Show |
20 | HG01109.hp2 HG02109.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.124+7744C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669085 | |||||||
| chr19:16669233 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.124+7892G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669233 | |||||||
| chr19:16669297 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.124+7956C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669297 | |||||||
| chr19:16669330 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124+7989C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669330 | |||||||
| chr19:16669427 | G | A | 114 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(111): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.124+8086G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669427 | |||||||
| chr19:16669720 | C | T | 2 | a0001c0001t0014g0236 a0001c0001t0014g0254 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.124+8379C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669720 | |||||||
| chr19:16669741 | G | A | 1 | a0001c0001t0025g0224 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.124+8400G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669741 | |||||||
| chr19:16669813 | T | C | 123 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(120): Show |
134 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.124+8472T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669813 | |||||||
| chr19:16669938 | C | G | 6 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(3): Show |
8 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+8597C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669938 | |||||||
| chr19:16669978 | TA | T | 7 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+8638delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16669978 | |||||||
| chr19:16670129 | C | T | 32 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(29): Show |
32 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.124+8788C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670129 | |||||||
| chr19:16670229 | A | G | 57 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0017 others(54): Show |
61 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.124+8888A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670229 | |||||||
| chr19:16670269 | G | GT | 9 | a0001c0002t0002g0184 a0001c0002t0004g0267 a0001c0002t0004g0269 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+8934dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16670269 | ||||||
| chr19:16670276 | G | GT | 9 | a0001c0001t0002g0042 a0001c0001t0003g0194 a0001c0001t0003g0195 others(6): Show |
9 | HG01169.hp2 HG01261.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+8950dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16670276 | ||||||
| chr19:16670276 | G | T | 10 | a0001c0002t0002g0184 a0001c0002t0002g0231 a0001c0002t0004g0267 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.124+8935G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670276 | |||||||
| chr19:16670314 | T | G | 130 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(127): Show |
141 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.124+8973T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670314 | |||||||
| chr19:16670343 | C | T | 1 | a0001c0001t0011g0252 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.124+9002C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670343 | |||||||
| chr19:16670530 | C | T | 1 | a0001c0001t0007g0287 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.124+9189C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670530 | |||||||
| chr19:16670584 | A | G | 1 | a0001c0001t0017g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+9243A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670584 | |||||||
| chr19:16670709 | A | C | 184 | a0001c0001t0001g0206 a0001c0001t0001g0285 a0001c0001t0002g0185 others(181): Show |
196 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.125-9275A>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670709 | |||||||
| chr19:16670917 | C | T | 113 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(110): Show |
124 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.125-9067C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670917 | |||||||
| chr19:16670932 | C | G | 5 | a0001c0001t0011g0250 a0001c0001t0011g0252 a0001c0001t0011g0253 others(2): Show |
5 | HG02055.hp1 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-9052C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16670932 | |||||||
| chr19:16671012 | C | G | 1 | a0001c0001t0003g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125-8972C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671012 | |||||||
| chr19:16671150 | C | G | 1 | a0001c0001t0005g0246 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.125-8834C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671150 | |||||||
| chr19:16671201 | C | CT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0065 a0001c0001t0001g0095 others(8): Show |
11 | HG01433.hp1 HG03710.hp1 HG03710.hp2 others(8): Show |
intron_variant | MODIFIER | c.125-8761dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTT | 7 | a0001c0002t0002g0015 a0001c0002t0002g0141 a0001c0002t0002g0142 others(4): Show |
7 | HG01257.hp2 HG02004.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-8766_125-8761d others(8): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(6): Show |
11 | HG02055.hp1 HG02280.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.125-8769_125-8761d others(11): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTTT others(3): Show |
9 | a0001c0001t0004g0178 a0001c0001t0004g0223 a0001c0001t0004g0232 others(6): Show |
9 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-8770_125-8761d others(12): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0025g0224 a0001c0003t0004g0179 a0001c0003t0004g0181 others(3): Show |
6 | HG01361.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-8771_125-8761d others(13): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0004g0230 a0001c0001t0004g0249 a0001c0001t0004g0296 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-8772_125-8761d others(14): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTTT others(6): Show |
14 | a0001c0001t0004g0233 a0001c0001t0015g0251 a0001c0002t0002g0017 others(11): Show |
14 | HG00609.hp2 HG01975.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-8773_125-8761d others(15): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTTT others(7): Show |
30 | a0001c0001t0006g0257 a0001c0002t0002g0014 a0001c0002t0002g0017 others(27): Show |
32 | HG00323.hp1 HG00408.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.125-8774_125-8761d others(16): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTTT others(8): Show |
17 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0237 others(14): Show |
17 | HG00423.hp1 HG00741.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.125-8775_125-8761d others(17): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTTT others(9): Show |
7 | a0001c0001t0006g0025 a0001c0001t0006g0239 a0001c0001t0006g0256 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-8776_125-8761d others(18): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0006g0024 a0001c0001t0006g0259 a0001c0001t0006g0262 |
3 | HG02717.hp1 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.125-8777_125-8761d others(19): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | CT | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0033 others(53): Show |
58 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.125-8761delT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671201 | CTT | C | 34 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0003g0300 others(31): Show |
36 | HG00280.hp2 HG01081.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.125-8762_125-8761d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16671201 | ||||||
| chr19:16671202 | T | G | 1 | a0001c0001t0012g0034 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.125-8782T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671202 | |||||||
| chr19:16671392 | G | A | 101 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(98): Show |
109 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.125-8592G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671392 | |||||||
| chr19:16671420 | C | T | 9 | a0001c0002t0002g0184 a0001c0002t0004g0267 a0001c0002t0004g0269 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-8564C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671420 | |||||||
| chr19:16671721 | C | T | 21 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0005g0002 others(18): Show |
24 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.125-8263C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671721 | |||||||
| chr19:16671801 | T | C | 22 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(19): Show |
22 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.125-8183T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671801 | |||||||
| chr19:16671808 | G | C | 129 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(126): Show |
140 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.125-8176G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671808 | |||||||
| chr19:16671811 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.125-8173A>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671811 | |||||||
| chr19:16671838 | G | A | 1 | a0001c0003t0004g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.125-8146G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16671838 | |||||||
| chr19:16672003 | C | A | 1 | a0001c0001t0012g0034 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.125-7981C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16672003 | |||||||
| chr19:16672014 | T | C | 1 | a0001c0001t0005g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.125-7970T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16672014 | |||||||
| chr19:16672056 | C | CCCTA | 22 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(19): Show |
22 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.125-7927_125-7924d others(6): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672056 | ||||||
| chr19:16672385 | A | C | 8 | a0001c0002t0004g0267 a0001c0002t0004g0269 a0001c0002t0004g0270 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-7599A>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16672385 | |||||||
| chr19:16672385 | A | G | 2 | a0001c0001t0021g0227 a0001c0001t0025g0224 |
2 | HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.125-7599A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16672385 | |||||||
| chr19:16672442 | C | A | 5 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(2): Show |
5 | HG02109.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-7542C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16672442 | |||||||
| chr19:16672446 | A | AT | 15 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0058 others(12): Show |
15 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-7518dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTT | 9 | a0001c0001t0003g0204 a0001c0001t0004g0230 a0001c0001t0005g0203 others(6): Show |
9 | HG01361.hp1 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-7520_125-7518d others(5): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTTT | 76 | a0001c0001t0001g0206 a0001c0001t0004g0177 a0001c0001t0005g0022 others(73): Show |
83 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.125-7521_125-7518d others(6): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTTTT | 28 | a0001c0001t0004g0019 a0001c0001t0004g0178 a0001c0001t0004g0223 others(25): Show |
31 | HG00423.hp1 HG01943.hp2 HG01978.hp2 others(28): Show |
intron_variant | MODIFIER | c.125-7522_125-7518d others(7): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTTTTT | 25 | a0001c0001t0002g0284 a0001c0001t0002g0290 a0001c0001t0002g0295 others(22): Show |
26 | HG00280.hp2 HG01168.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.125-7523_125-7518d others(8): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTTTTTT | 10 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0293 others(7): Show |
10 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-7524_125-7518d others(9): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTTTTTT others(2): Show |
12 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0243 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.125-7526_125-7518d others(11): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTTTTTT others(3): Show |
10 | a0001c0001t0002g0241 a0001c0001t0003g0029 a0001c0001t0003g0187 others(7): Show |
10 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-7527_125-7518d others(12): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0003g0191 a0001c0001t0003g0244 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.125-7528_125-7518d others(13): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0002g0242 a0001c0001t0003g0192 |
2 | HG02622.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.125-7529_125-7518d others(14): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0003g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.125-7531_125-7518d others(16): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672446 | AT | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0060 others(5): Show |
9 | HG00673.hp1 HG01934.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-7518delT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16672446 | ||||||
| chr19:16672505 | G | A | 1 | a0001c0001t0005g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.125-7479G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16672505 | |||||||
| chr19:16672584 | G | T | 1 | a0004c0008t0008g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.125-7400G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16672584 | |||||||
| chr19:16672593 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.125-7391C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16672593 | |||||||
| chr19:16672670 | G | A | 1 | a0001c0001t0009g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.125-7314G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16672670 | |||||||
| chr19:16673049 | CT | C | 4 | a0001c0001t0004g0230 a0001c0001t0004g0233 a0001c0001t0004g0249 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-6934delT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16673049 | |||||||
| chr19:16673057 | CTTTTCT | C | 9 | a0001c0002t0002g0184 a0001c0002t0004g0267 a0001c0002t0004g0269 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-6916_125-6911d others(8): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16673057 | ||||||
| chr19:16673205 | C | G | 1 | a0001c0001t0018g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.125-6779C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16673205 | |||||||
| chr19:16673310 | G | A | 7 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(4): Show |
7 | HG00558.hp2 HG00673.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-6674G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16673310 | |||||||
| chr19:16673370 | C | A | 1 | a0001c0001t0008g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.125-6614C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16673370 | |||||||
| chr19:16673455 | T | G | 2 | a0001c0001t0014g0236 a0001c0001t0014g0254 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.125-6529T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16673455 | |||||||
| chr19:16673468 | A | C | 1 | a0001c0001t0003g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.125-6516A>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16673468 | |||||||
| chr19:16673591 | G | C | 1 | a0001c0002t0013g0155 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.125-6393G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16673591 | |||||||
| chr19:16673790 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.125-6194T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16673790 | |||||||
| chr19:16673859 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.125-6125A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16673859 | |||||||
| chr19:16673932 | GA | G | 27 | a0001c0001t0001g0028 a0001c0001t0005g0203 a0001c0001t0006g0024 others(24): Show |
29 | HG01109.hp2 HG01257.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.125-6040delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16673932 | ||||||
| chr19:16674041 | G | A | 1 | a0001c0001t0004g0023 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.125-5943G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674041 | |||||||
| chr19:16674141 | T | C | 1 | a0001c0001t0005g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.125-5843T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674141 | |||||||
| chr19:16674201 | T | A | 122 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(119): Show |
133 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.125-5783T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674201 | |||||||
| chr19:16674330 | G | A | 2 | a0001c0001t0003g0029 a0001c0001t0003g0187 |
2 | HG00597.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.125-5654G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674330 | |||||||
| chr19:16674389 | C | CA | 37 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0105 others(34): Show |
37 | HG00597.hp1 HG01123.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.125-5576dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16674389 | ||||||
| chr19:16674389 | CA | C | 110 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(107): Show |
121 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.125-5576delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16674389 | ||||||
| chr19:16674389 | CAA | C | 10 | a0001c0002t0002g0176 a0001c0002t0002g0184 a0001c0002t0004g0267 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-5577_125-5576d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16674389 | ||||||
| chr19:16674599 | A | G | 113 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(110): Show |
124 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.125-5385A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674599 | |||||||
| chr19:16674656 | G | T | 2 | a0001c0001t0001g0050 a0001c0002t0002g0184 |
2 | HG02886.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.125-5328G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674656 | |||||||
| chr19:16674666 | G | A | 1 | a0001c0001t0003g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125-5318G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674666 | |||||||
| chr19:16674718 | A | T | 1 | a0001c0001t0005g0208 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.125-5266A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674718 | |||||||
| chr19:16674816 | C | CA | 22 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(19): Show |
22 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.125-5159dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16674816 | ||||||
| chr19:16674819 | A | C | 129 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(126): Show |
140 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.125-5165A>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674819 | |||||||
| chr19:16674903 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0105 a0001c0001t0008g0112 others(1): Show |
4 | HG01109.hp1 HG01175.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-5081A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674903 | |||||||
| chr19:16674910 | A | G | 130 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(127): Show |
142 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.125-5074A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674910 | |||||||
| chr19:16674933 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125-5051G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674933 | |||||||
| chr19:16674964 | C | T | 9 | a0001c0002t0002g0184 a0001c0002t0004g0267 a0001c0002t0004g0269 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-5020C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674964 | |||||||
| chr19:16674974 | C | T | 22 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(19): Show |
22 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.125-5010C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16674974 | |||||||
| chr19:16675094 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.125-4890T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675094 | |||||||
| chr19:16675096 | C | A | 6 | a0001c0001t0007g0277 a0001c0001t0007g0279 a0001c0001t0007g0280 others(3): Show |
6 | HG00280.hp2 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-4888C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675096 | |||||||
| chr19:16675130 | A | G | 1 | a0001c0002t0002g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.125-4854A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675130 | |||||||
| chr19:16675335 | G | T | 1 | a0001c0001t0007g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.125-4649G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675335 | |||||||
| chr19:16675344 | C | G | 57 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0017 others(54): Show |
61 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-4640C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675344 | |||||||
| chr19:16675359 | C | A | 21 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0005g0002 others(18): Show |
24 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.125-4625C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675359 | |||||||
| chr19:16675401 | T | C | 113 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(110): Show |
124 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.125-4583T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675401 | |||||||
| chr19:16675544 | A | AT | 37 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0062 others(34): Show |
39 | HG00673.hp1 HG00741.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.125-4419dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16675544 | ||||||
| chr19:16675544 | AT | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0060 a0001c0001t0005g0214 others(3): Show |
6 | HG01496.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-4419delT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16675544 | ||||||
| chr19:16675544 | ATT | A | 8 | a0001c0002t0002g0184 a0001c0002t0004g0267 a0001c0002t0004g0269 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-4420_125-4419d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16675544 | ||||||
| chr19:16675588 | G | T | 113 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(110): Show |
124 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.125-4396G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675588 | |||||||
| chr19:16675651 | C | T | 57 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0017 others(54): Show |
61 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-4333C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675651 | |||||||
| chr19:16675701 | G | A | 7 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-4283G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675701 | |||||||
| chr19:16675738 | A | G | 7 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-4246A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675738 | |||||||
| chr19:16675751 | A | C | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4233A>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675751 | |||||||
| chr19:16675760 | G | C | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4224G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675760 | |||||||
| chr19:16675771 | A | T | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4213A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675771 | |||||||
| chr19:16675776 | T | A | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4208T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675776 | |||||||
| chr19:16675782 | T | G | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4202T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675782 | |||||||
| chr19:16675791 | C | A | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4193C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675791 | |||||||
| chr19:16675793 | C | T | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4191C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675793 | |||||||
| chr19:16675798 | C | G | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4186C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675798 | |||||||
| chr19:16675803 | T | G | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4181T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675803 | |||||||
| chr19:16675805 | C | T | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4179C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675805 | |||||||
| chr19:16675818 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.125-4166A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675818 | |||||||
| chr19:16675858 | G | A | 4 | a0001c0001t0001g0285 a0001c0001t0007g0064 a0001c0001t0007g0278 others(1): Show |
4 | HG01358.hp1 HG03490.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-4126G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675858 | |||||||
| chr19:16675861 | C | A | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4123C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675861 | |||||||
| chr19:16675864 | G | T | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4120G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675864 | |||||||
| chr19:16675866 | G | A | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4118G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675866 | |||||||
| chr19:16675869 | G | C | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4115G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675869 | |||||||
| chr19:16675884 | A | C | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4100A>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675884 | |||||||
| chr19:16675904 | C | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0039 others(5): Show |
9 | HG01934.hp1 HG02132.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-4080C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675904 | |||||||
| chr19:16675910 | C | T | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4074C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675910 | |||||||
| chr19:16675918 | T | C | 1 | a0001c0001t0005g0246 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.125-4066T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675918 | |||||||
| chr19:16675918 | T | G | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4066T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675918 | |||||||
| chr19:16675927 | C | T | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4057C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675927 | |||||||
| chr19:16675928 | G | T | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4056G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675928 | |||||||
| chr19:16675929 | G | T | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4055G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675929 | |||||||
| chr19:16675950 | TACGAATT others(5): Show |
T | 1 | a0001c0001t0005g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.125-4033_125-4022d others(14): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675950 | |||||||
| chr19:16675966 | A | G | 1 | a0001c0002t0002g0173 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.125-4018A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675966 | |||||||
| chr19:16675967 | C | G | 1 | a0001c0002t0002g0173 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.125-4017C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16675967 | |||||||
| chr19:16676089 | G | A | 57 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0017 others(54): Show |
61 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-3895G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16676089 | |||||||
| chr19:16676089 | GGTGGCTC others(201): Show |
G | 31 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(28): Show |
35 | HG01109.hp2 HG01361.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.125-3891_125-3684d others(2): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16676089 | ||||||
| chr19:16676128 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.125-3856A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16676128 | |||||||
| chr19:16676142 | C | T | 4 | a0001c0001t0004g0230 a0001c0001t0004g0233 a0001c0001t0004g0249 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3842C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16676142 | |||||||
| chr19:16676217 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0010g0004 |
2 | HG00099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.125-3767G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16676217 | |||||||
| chr19:16676592 | C | G | 57 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0017 others(54): Show |
61 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-3392C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16676592 | |||||||
| chr19:16676755 | C | CT | 21 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0058 others(18): Show |
23 | HG00423.hp2 HG01074.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-3208dupT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16676755 | ||||||
| chr19:16676755 | C | CTT | 30 | a0001c0001t0001g0095 a0001c0001t0001g0285 a0001c0001t0002g0266 others(27): Show |
30 | HG00280.hp2 HG00735.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.125-3209_125-3208d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16676755 | ||||||
| chr19:16676755 | CT | C | 34 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0065 others(31): Show |
34 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.125-3208delT | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16676755 | ||||||
| chr19:16676783 | T | G | 130 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(127): Show |
141 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.125-3201T>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16676783 | |||||||
| chr19:16676885 | C | G | 21 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0005g0002 others(18): Show |
24 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.125-3099C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16676885 | |||||||
| chr19:16676945 | G | A | 1 | a0001c0005t0018g0106 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.125-3039G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16676945 | |||||||
| chr19:16677065 | T | C | 7 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-2919T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16677065 | |||||||
| chr19:16677074 | G | GA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0095 others(7): Show |
10 | HG01433.hp1 HG01891.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-2895dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16677074 | ||||||
| chr19:16677074 | G | GAA | 22 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0005g0002 others(19): Show |
25 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.125-2896_125-2895d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16677074 | ||||||
| chr19:16677074 | G | GAAA | 23 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0237 others(20): Show |
25 | HG01123.hp1 HG01361.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.125-2897_125-2895d others(5): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16677074 | ||||||
| chr19:16677074 | G | GAAAA | 58 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(55): Show |
64 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.125-2898_125-2895d others(6): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16677074 | ||||||
| chr19:16677074 | G | GAAAAA | 7 | a0001c0002t0002g0143 a0001c0002t0002g0144 a0001c0002t0002g0154 others(4): Show |
7 | HG00423.hp1 HG02071.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-2899_125-2895d others(7): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16677074 | ||||||
| chr19:16677074 | GA | G | 18 | a0001c0001t0001g0013 a0001c0001t0001g0105 a0001c0001t0001g0109 others(15): Show |
18 | HG00099.hp1 HG00558.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.125-2895delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16677074 | ||||||
| chr19:16677080 | A | G | 1 | a0001c0001t0003g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.125-2904A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16677080 | |||||||
| chr19:16677441 | C | G | 1 | a0001c0001t0007g0291 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.125-2543C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16677441 | |||||||
| chr19:16677516 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0058 |
2 | HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.125-2468T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16677516 | |||||||
| chr19:16677533 | C | CACTGTGT others(59): Show |
8 | a0001c0002t0004g0267 a0001c0002t0004g0269 a0001c0002t0004g0270 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-2450_125-2385d others(68): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16677533 | ||||||
| chr19:16677582 | CCCTCT | C | 6 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(3): Show |
8 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-2400_125-2396d others(7): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16677582 | ||||||
| chr19:16677683 | A | G | 1 | a0001c0002t0002g0169 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.125-2301A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16677683 | |||||||
| chr19:16677778 | G | C | 4 | a0001c0001t0004g0230 a0001c0001t0004g0233 a0001c0001t0004g0249 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-2206G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16677778 | |||||||
| chr19:16677796 | G | C | 7 | a0001c0001t0001g0285 a0001c0001t0007g0268 a0001c0001t0007g0278 others(4): Show |
7 | HG03490.hp1 HG03704.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-2188G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16677796 | |||||||
| chr19:16677832 | A | G | 9 | a0001c0002t0002g0184 a0001c0002t0004g0267 a0001c0002t0004g0269 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-2152A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16677832 | |||||||
| chr19:16678359 | G | A | 5 | a0001c0001t0003g0188 a0001c0001t0003g0191 a0001c0001t0003g0192 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-1625G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16678359 | |||||||
| chr19:16678390 | CCGCG | C | 66 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0017 others(63): Show |
70 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.125-1592_125-1589d others(6): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16678390 | ||||||
| chr19:16678394 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.125-1590G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16678394 | |||||||
| chr19:16678427 | C | CA | 34 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0067 others(31): Show |
34 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.125-1536dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16678427 | ||||||
| chr19:16678427 | CA | C | 79 | a0001c0001t0001g0053 a0001c0001t0001g0095 a0001c0001t0001g0101 others(76): Show |
86 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.125-1536delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16678427 | ||||||
| chr19:16678427 | CAA | C | 14 | a0001c0001t0003g0204 a0001c0001t0005g0201 a0001c0001t0005g0203 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-1537_125-1536d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16678427 | ||||||
| chr19:16678766 | C | CA | 22 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0056 others(19): Show |
22 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.125-1195dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16678766 | ||||||
| chr19:16678766 | CA | C | 14 | a0001c0001t0001g0066 a0001c0001t0001g0089 a0001c0001t0001g0285 others(11): Show |
14 | HG01109.hp2 HG02055.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-1195delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16678766 | ||||||
| chr19:16678766 | CAA | C | 50 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(47): Show |
57 | HG01123.hp1 HG01261.hp1 HG01346.hp1 others(54): Show |
intron_variant | MODIFIER | c.125-1196_125-1195d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16678766 | ||||||
| chr19:16678819 | CA | C | 21 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(18): Show |
21 | HG00280.hp2 HG00735.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.125-1156delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16678819 | ||||||
| chr19:16678981 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.125-1003T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16678981 | |||||||
| chr19:16679166 | TA | T | 15 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0083 others(12): Show |
15 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-800delA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679166 | ||||||
| chr19:16679182 | A | AAAAG | 72 | a0001c0001t0003g0191 a0001c0001t0003g0301 a0001c0001t0003g0302 others(69): Show |
76 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.125-800_125-799ins others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679182 | ||||||
| chr19:16679182 | A | AAAG | 98 | a0001c0001t0001g0206 a0001c0001t0001g0285 a0001c0001t0002g0185 others(95): Show |
106 | HG00280.hp2 HG00597.hp1 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.125-799_125-797dup others(3): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679182 | ||||||
| chr19:16679182 | A | AAG | 13 | a0001c0001t0002g0245 a0001c0001t0003g0196 a0001c0001t0003g0300 others(10): Show |
13 | HG01070.hp2 HG01169.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.125-801_125-800ins others(2): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679182 | ||||||
| chr19:16679182 | A | G | 1 | a0001c0001t0005g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.125-802A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679182 | |||||||
| chr19:16679252 | C | CGT | 20 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0038 others(17): Show |
20 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.125-687_125-686dup others(2): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | C | CGTGT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0044 others(6): Show |
10 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-689_125-686dup others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0001t0001g0117 |
3 | NA18960.hp1 NA18965.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.125-693_125-686dup others(8): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | CGT | C | 21 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0053 others(18): Show |
22 | HG00323.hp2 HG00735.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.125-687_125-686del others(2): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | CGTGT | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0108 others(17): Show |
22 | HG00099.hp1 HG01071.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.125-689_125-686del others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | CGTGTGT | C | 32 | a0001c0001t0001g0054 a0001c0001t0001g0071 a0001c0001t0002g0185 others(29): Show |
32 | HG00323.hp1 HG00597.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.125-691_125-686del others(6): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | CGTGTGTG others(1): Show |
C | 46 | a0001c0001t0001g0107 a0001c0001t0001g0116 a0001c0001t0001g0133 others(43): Show |
50 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.125-693_125-686del others(8): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | CGTGTGTG others(3): Show |
C | 17 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0140 others(14): Show |
17 | HG00558.hp2 HG02071.hp2 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.125-695_125-686del others(10): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0109 |
2 | HG00673.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.125-697_125-686del others(12): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | CGTGTGTG others(9): Show |
C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0137 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.125-701_125-686del others(16): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | CGTGTGTG others(11): Show |
C | 6 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(3): Show |
6 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-703_125-686del others(18): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679252 | CGTGTGTG others(13): Show |
C | 1 | a0001c0003t0029g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.125-705_125-686del others(20): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679252 | ||||||
| chr19:16679275 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0025g0224 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.125-699_125-676del others(24): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679275 | ||||||
| chr19:16679277 | GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0021g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-697_125-676del others(22): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679277 | ||||||
| chr19:16679281 | GTGTGTGT others(11): Show |
G | 17 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(14): Show |
20 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.125-693_125-676del others(18): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679281 | ||||||
| chr19:16679283 | GTGTGTGT others(9): Show |
G | 18 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0005g0002 others(15): Show |
21 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.125-691_125-676del others(16): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679283 | ||||||
| chr19:16679285 | GTGTGTGT others(7): Show |
G | 13 | a0001c0001t0005g0208 a0001c0001t0006g0025 a0001c0001t0006g0237 others(10): Show |
14 | HG02055.hp1 HG02273.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.125-689_125-676del others(14): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679285 | ||||||
| chr19:16679287 | GTGTGTGT others(5): Show |
G | 2 | a0001c0001t0005g0213 a0001c0001t0022g0276 |
2 | HG01123.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.125-687_125-676del others(12): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679287 | ||||||
| chr19:16679289 | GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0004g0230 a0001c0001t0004g0233 a0001c0001t0004g0249 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-685_125-676del others(10): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679289 | ||||||
| chr19:16679297 | G | A | 1 | a0001c0001t0004g0023 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.125-687G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679297 | |||||||
| chr19:16679301 | G | A | 57 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0004g0019 others(54): Show |
64 | HG01081.hp2 HG01109.hp2 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.125-683G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679301 | |||||||
| chr19:16679383 | C | G | 1 | a0001c0001t0002g0242 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.125-601C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679383 | |||||||
| chr19:16679479 | G | A | 7 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-505G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679479 | |||||||
| chr19:16679494 | T | C | 6 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(3): Show |
8 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-490T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679494 | |||||||
| chr19:16679539 | C | CA | 32 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(29): Show |
32 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.125-444dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 16679539 | ||||||
| chr19:16679800 | A | G | 5 | a0001c0002t0004g0267 a0001c0002t0004g0272 a0001c0002t0004g0273 others(2): Show |
5 | HG02630.hp2 HG03098.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-184A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679800 | |||||||
| chr19:16679809 | G | A | 7 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-175G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679809 | |||||||
| chr19:16679847 | G | A | 4 | a0001c0001t0004g0230 a0001c0001t0004g0233 a0001c0001t0004g0249 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-137G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679847 | |||||||
| chr19:16679937 | G | A | 1 | a0001c0001t0003g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.125-47G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 1/5 | chr19 | 16679937 | |||||||
| chr19:16680369 | C | G | 7 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-28C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 2/5 | chr19 | 16680369 | |||||||
| chr19:16680632 | T | C | 184 | a0001c0001t0001g0206 a0001c0001t0001g0285 a0001c0001t0002g0185 others(181): Show |
196 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.466+51T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16680632 | |||||||
| chr19:16680733 | G | A | 2 | a0001c0001t0021g0227 a0001c0001t0025g0224 |
2 | HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.466+152G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16680733 | |||||||
| chr19:16680901 | C | G | 2 | a0001c0001t0015g0235 a0001c0001t0015g0251 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.466+320C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16680901 | |||||||
| chr19:16680940 | C | T | 66 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0017 others(63): Show |
70 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.466+359C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16680940 | |||||||
| chr19:16681093 | G | A | 1 | a0001c0002t0002g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.466+512G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681093 | |||||||
| chr19:16681125 | C | T | 20 | a0001c0001t0001g0206 a0001c0001t0003g0204 a0001c0001t0005g0002 others(17): Show |
23 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.466+544C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681125 | |||||||
| chr19:16681133 | G | A | 30 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(27): Show |
34 | HG01109.hp2 HG01123.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.466+552G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681133 | |||||||
| chr19:16681149 | A | G | 1 | a0001c0001t0005g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.466+568A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681149 | |||||||
| chr19:16681395 | A | G | 6 | a0001c0001t0011g0250 a0001c0001t0011g0252 a0001c0001t0011g0253 others(3): Show |
6 | HG01123.hp1 HG02055.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+814A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681395 | |||||||
| chr19:16681419 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.466+838G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681419 | |||||||
| chr19:16681545 | A | G | 1 | a0001c0001t0003g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.467-876A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681545 | |||||||
| chr19:16681577 | G | A | 1 | a0001c0001t0005g0199 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.467-844G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681577 | |||||||
| chr19:16681711 | C | T | 16 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0237 others(13): Show |
18 | HG01109.hp2 HG02109.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.467-710C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681711 | |||||||
| chr19:16681718 | C | A | 16 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0237 others(13): Show |
18 | HG01109.hp2 HG02109.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.467-703C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681718 | |||||||
| chr19:16681818 | C | T | 1 | a0001c0001t0008g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.467-603C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681818 | |||||||
| chr19:16681960 | C | T | 6 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(3): Show |
8 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-461C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16681960 | |||||||
| chr19:16682008 | G | A | 35 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(32): Show |
39 | HG01109.hp2 HG01361.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.467-413G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16682008 | |||||||
| chr19:16682030 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-391T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16682030 | |||||||
| chr19:16682083 | C | T | 7 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-338C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16682083 | |||||||
| chr19:16682092 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.467-329G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16682092 | |||||||
| chr19:16682282 | C | G | 4 | a0001c0001t0003g0188 a0001c0001t0003g0191 a0001c0001t0003g0192 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-139C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 3/5 | chr19 | 16682282 | |||||||
| chr19:16682739 | A | G | 1 | a0001c0001t0005g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.554+231A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16682739 | |||||||
| chr19:16682744 | G | T | 29 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(26): Show |
33 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.554+236G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16682744 | |||||||
| chr19:16682891 | A | G | 184 | a0001c0001t0001g0206 a0001c0001t0001g0285 a0001c0001t0002g0185 others(181): Show |
196 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.554+383A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16682891 | |||||||
| chr19:16682953 | A | G | 1 | a0004c0008t0008g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.554+445A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16682953 | |||||||
| chr19:16683136 | G | C | 1 | a0001c0001t0007g0291 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.554+628G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683136 | |||||||
| chr19:16683248 | A | G | 3 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 |
3 | HG02109.hp2 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.554+740A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683248 | |||||||
| chr19:16683427 | A | T | 3 | a0002c0004t0002g0088 a0002c0004t0002g0092 a0002c0004t0002g0127 |
3 | HG01099.hp1 HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.554+919A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683427 | |||||||
| chr19:16683441 | A | G | 1 | a0001c0001t0006g0264 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.554+933A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683441 | |||||||
| chr19:16683584 | C | T | 1 | a0001c0002t0002g0146 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.554+1076C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683584 | |||||||
| chr19:16683592 | C | CA | 49 | a0001c0001t0001g0003 a0001c0001t0001g0097 a0001c0001t0001g0102 others(46): Show |
53 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.554+1103dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16683592 | ||||||
| chr19:16683592 | C | CAA | 28 | a0001c0001t0002g0185 a0001c0001t0002g0241 a0001c0001t0002g0242 others(25): Show |
28 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.554+1102_554+1103d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16683592 | ||||||
| chr19:16683592 | C | CAAA | 14 | a0001c0001t0002g0240 a0001c0001t0003g0191 a0001c0001t0003g0204 others(11): Show |
14 | HG02055.hp2 HG02109.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.554+1101_554+1103d others(5): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16683592 | ||||||
| chr19:16683592 | C | CAAAA | 21 | a0001c0001t0001g0206 a0001c0001t0005g0002 a0001c0001t0005g0022 others(18): Show |
24 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.554+1100_554+1103d others(6): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16683592 | ||||||
| chr19:16683592 | C | CAAAAA | 53 | a0001c0001t0005g0202 a0001c0002t0002g0014 a0001c0002t0002g0015 others(50): Show |
57 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.554+1099_554+1103d others(7): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16683592 | ||||||
| chr19:16683780 | G | A | 1 | a0001c0001t0005g0208 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.554+1272G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683780 | |||||||
| chr19:16683845 | C | T | 1 | a0001c0001t0011g0250 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.554+1337C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683845 | |||||||
| chr19:16683899 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.554+1391G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683899 | |||||||
| chr19:16683969 | T | TA | 57 | a0001c0001t0001g0285 a0001c0001t0002g0185 a0001c0001t0002g0240 others(54): Show |
57 | HG00280.hp2 HG00597.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.554+1461_554+1462i others(3): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683969 | |||||||
| chr19:16683969 | T | TAA | 117 | a0001c0001t0004g0230 a0001c0001t0004g0233 a0001c0001t0004g0249 others(114): Show |
126 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.554+1461_554+1462i others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683969 | |||||||
| chr19:16683969 | T | TAAA | 8 | a0001c0001t0001g0206 a0001c0001t0004g0019 a0001c0001t0004g0020 others(5): Show |
10 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.554+1461_554+1462i others(5): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683969 | |||||||
| chr19:16683970 | C | A | 183 | a0001c0001t0001g0206 a0001c0001t0001g0285 a0001c0001t0002g0185 others(180): Show |
194 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.554+1462C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16683970 | |||||||
| chr19:16684047 | T | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0095 others(4): Show |
7 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.554+1539T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16684047 | |||||||
| chr19:16684112 | AG | A | 32 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(29): Show |
32 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.554+1605delG | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16684112 | |||||||
| chr19:16684141 | C | CAG | 17 | a0001c0001t0005g0201 a0001c0001t0006g0024 a0001c0001t0006g0025 others(14): Show |
19 | HG01109.hp2 HG02109.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.554+1652_554+1653d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16684141 | ||||||
| chr19:16684141 | C | CAGAGAGA others(3): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0137 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.554+1644_554+1653d others(12): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16684141 | ||||||
| chr19:16684141 | CAG | C | 21 | a0001c0001t0001g0285 a0001c0001t0002g0266 a0001c0001t0002g0284 others(18): Show |
21 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.554+1652_554+1653d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16684141 | ||||||
| chr19:16684395 | G | T | 3 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 |
3 | HG02109.hp2 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.554+1887G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16684395 | |||||||
| chr19:16684445 | A | G | 1 | a0001c0002t0002g0139 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.555-1843A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16684445 | |||||||
| chr19:16684733 | T | C | 1 | a0001c0001t0006g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.555-1555T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16684733 | |||||||
| chr19:16684805 | G | A | 5 | a0001c0001t0011g0250 a0001c0001t0011g0252 a0001c0001t0011g0253 others(2): Show |
5 | HG02055.hp1 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-1483G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16684805 | |||||||
| chr19:16684875 | C | CA | 52 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0096 others(49): Show |
57 | HG00609.hp2 HG00741.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.555-1397dupA | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16684875 | ||||||
| chr19:16684875 | C | CAA | 6 | a0001c0001t0004g0230 a0001c0001t0004g0233 a0001c0001t0004g0249 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-1398_555-1397d others(4): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16684875 | ||||||
| chr19:16684926 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.555-1362C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16684926 | |||||||
| chr19:16685049 | T | A | 1 | a0001c0001t0015g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.555-1239T>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685049 | |||||||
| chr19:16685049 | T | TATAA | 18 | a0001c0001t0001g0050 a0001c0001t0001g0078 a0001c0001t0001g0079 others(15): Show |
19 | HG01099.hp1 HG01099.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.555-1239_555-1238i others(6): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685049 | |||||||
| chr19:16685049 | T | TATAAATA others(1): Show |
25 | a0001c0001t0001g0074 a0001c0001t0004g0019 a0001c0001t0004g0020 others(22): Show |
28 | HG01109.hp2 HG02071.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.555-1239_555-1238i others(10): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685049 | |||||||
| chr19:16685049 | T | TATAAATA others(5): Show |
69 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(66): Show |
73 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.555-1239_555-1238i others(14): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685049 | |||||||
| chr19:16685049 | T | TATAAATA others(9): Show |
28 | a0001c0001t0002g0266 a0001c0001t0002g0295 a0001c0001t0003g0187 others(25): Show |
29 | HG00597.hp1 HG00741.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.555-1239_555-1238i others(18): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685049 | |||||||
| chr19:16685049 | T | TATAAATA others(13): Show |
21 | a0001c0001t0002g0245 a0001c0001t0002g0284 a0001c0001t0002g0290 others(18): Show |
21 | HG01070.hp2 HG01071.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.555-1239_555-1238i others(22): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685049 | |||||||
| chr19:16685049 | T | TATAAATA others(17): Show |
2 | a0001c0001t0022g0276 a0001c0002t0002g0160 |
2 | HG01123.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.555-1239_555-1238i others(26): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685049 | |||||||
| chr19:16685049 | TGTAA | T | 5 | a0001c0002t0004g0267 a0001c0002t0004g0272 a0001c0002t0004g0273 others(2): Show |
5 | HG02630.hp2 HG03098.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-1238_555-1235d others(6): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685049 | |||||||
| chr19:16685050 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.555-1238G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685050 | |||||||
| chr19:16685050 | G | GTAAATAA others(5): Show |
1 | a0001c0001t0005g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.555-1213_555-1202d others(14): Show |
TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 16685050 | ||||||
| chr19:16685122 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.555-1166C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685122 | |||||||
| chr19:16685173 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.555-1115G>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685173 | |||||||
| chr19:16685254 | C | T | 7 | a0001c0003t0004g0179 a0001c0003t0004g0180 a0001c0003t0004g0181 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.555-1034C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685254 | |||||||
| chr19:16685371 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.555-917A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685371 | |||||||
| chr19:16685440 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0010g0068 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.555-848A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685440 | |||||||
| chr19:16685484 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.555-804T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685484 | |||||||
| chr19:16685690 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.555-598G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685690 | |||||||
| chr19:16685693 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.555-595G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685693 | |||||||
| chr19:16685850 | A | G | 1 | a0001c0001t0009g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.555-438A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685850 | |||||||
| chr19:16685893 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.555-395C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685893 | |||||||
| chr19:16685901 | C | G | 3 | a0001c0001t0003g0188 a0001c0001t0003g0191 a0001c0001t0003g0194 |
3 | HG01884.hp2 HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.555-387C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685901 | |||||||
| chr19:16685934 | G | A | 2 | a0001c0001t0004g0019 a0001c0001t0004g0223 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.555-354G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16685934 | |||||||
| chr19:16686040 | G | A | 1 | a0001c0001t0031g0115 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.555-248G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 4/5 | chr19 | 16686040 | |||||||
| chr19:16686429 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.672+24A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16686429 | |||||||
| chr19:16686459 | C | T | 36 | a0001c0001t0002g0185 a0001c0001t0002g0240 a0001c0001t0002g0241 others(33): Show |
36 | HG00597.hp1 HG01123.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.672+54C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16686459 | |||||||
| chr19:16686569 | A | T | 53 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(50): Show |
57 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.672+164A>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16686569 | |||||||
| chr19:16686604 | A | G | 65 | a0001c0001t0002g0035 a0001c0001t0002g0040 a0001c0001t0002g0042 others(62): Show |
69 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.672+199A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16686604 | |||||||
| chr19:16686653 | C | T | 67 | a0001c0001t0002g0035 a0001c0001t0002g0040 a0001c0001t0002g0042 others(64): Show |
71 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.672+248C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16686653 | |||||||
| chr19:16686712 | C | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.672+307C>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16686712 | |||||||
| chr19:16686856 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.672+451T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16686856 | |||||||
| chr19:16686907 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.672+502C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16686907 | |||||||
| chr19:16687000 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.672+595G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687000 | |||||||
| chr19:16687085 | A | C | 1 | a0001c0002t0002g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.672+680A>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687085 | |||||||
| chr19:16687153 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0097 |
3 | HG00597.hp2 NA18945.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.672+748G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687153 | |||||||
| chr19:16687225 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0137 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.672+820G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687225 | |||||||
| chr19:16687256 | C | T | 3 | a0001c0002t0002g0162 a0001c0002t0002g0219 a0001c0002t0002g0222 |
3 | NA19055.hp1 NA19060.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.672+851C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687256 | |||||||
| chr19:16687368 | A | G | 64 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0177 others(61): Show |
68 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.673-776A>G | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687368 | |||||||
| chr19:16687562 | G | C | 19 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0191 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.673-582G>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687562 | |||||||
| chr19:16687658 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.673-486C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687658 | |||||||
| chr19:16687660 | C | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.673-484C>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687660 | |||||||
| chr19:16687667 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.673-477G>A | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687667 | |||||||
| chr19:16687798 | C | T | 2 | a0001c0001t0021g0227 a0001c0001t0025g0224 |
2 | HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.673-346C>T | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16687798 | |||||||
| chr19:16688116 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.673-28T>C | TMEM38A | ENSG00000072954.7 | transcript | ENST00000187762.7 | protein_coding | 5/5 | chr19 | 16688116 |