Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84640 |
| ensemblid | ENSG00000170185.11 |
| hgncid | 20067 |
| symbol | USP38 |
| name | ubiquitin specific peptidase 38 |
| refseq_nuc | NM_032557.6 |
| refseq_prot | NP_115946.2 |
| ensembl_nuc | ENST00000307017.9 |
| ensembl_prot | ENSP00000303434.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 143184917 |
| end | 143223874 |
| strand | + |
| ver | v1.2 |
| region | chr4:143184917-143223874 |
| region5000 | chr4:143179917-143228874 |
| regionname0 | USP38_chr4_143184917_143223874 |
| regionname5000 | USP38_chr4_143179917_143228874 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1042 | 247 | 89 | 49 | 66 | 8 | 33 | 50 | USP38_chr4_143179917_143228874 | USP38 | MDKIL others(1037): Show |
chr4 | 143179917 | 143228874 |
| a0002 | 0/0 | 1042 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | MDKIL others(1037): Show |
chr4 | 143179917 | 143228874 |
| a0003 | 0/0 | 1042 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | USP38_chr4_143179917_143228874 | USP38 | MDKIL others(1037): Show |
chr4 | 143179917 | 143228874 |
| a0004 | 0/0 | 1042 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | MDKIL others(1037): Show |
chr4 | 143179917 | 143228874 |
| a0005 | 0/0 | 1042 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | MDKIL others(1037): Show |
chr4 | 143179917 | 143228874 |
| a0006 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | MDKIL others(1037): Show |
chr4 | 143179917 | 143228874 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3126 | 140 | 57 | 30 | 33 | 3 | 16 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0001c0002 | 1/0 | 3126 | 76 | 14 | 15 | 30 | 2 | 14 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0001c0003 | 0/0 | 3126 | 26 | 18 | 3 | 1 | 3 | 1 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0001c0006 | 0/0 | 3126 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0001c0008 | 0/0 | 3126 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0001c0009 | 0/0 | 3126 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0001c0011 | 0/0 | 3126 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0002c0004 | 0/0 | 3126 | 5 | 4 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0003c0005 | 0/0 | 3126 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0004c0010 | 0/0 | 3126 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0005c0007 | 0/0 | 3126 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 | ||
| a0006c0012 | 0/0 | 3126 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ATGGA others(3121): Show |
chr4 | 143179917 | 143228874 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7080 | 88 | 17 | 23 | 33 | 3 | 11 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0003 | 0/0 | 7080 | 14 | 12 | 2 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0005 | 0/0 | 7080 | 12 | 9 | 1 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0007 | 0/0 | 7080 | 8 | 7 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0008 | 0/0 | 7082 | 5 | 5 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7077): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0010 | 0/0 | 7080 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0014 | 0/0 | 7081 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0016 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0017 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0018 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0019 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0020 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0021 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0022 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0023 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0001t0024 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0002t0002 | 1/0 | 7081 | 69 | 14 | 12 | 30 | 0 | 12 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0001c0002t0009 | 0/0 | 7081 | 4 | 0 | 2 | 0 | 2 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0001c0002t0015 | 0/0 | 7081 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0001c0002t0025 | 0/0 | 7081 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0001c0002t0026 | 0/0 | 7081 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0001c0003t0004 | 0/0 | 7080 | 13 | 13 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0003t0006 | 0/0 | 7080 | 9 | 1 | 3 | 1 | 3 | 1 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0003t0011 | 0/0 | 7080 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0003t0012 | 0/0 | 7080 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0006t0006 | 0/0 | 7080 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0001c0008t0002 | 0/0 | 7081 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0001c0009t0002 | 0/0 | 7081 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0001c0011t0002 | 0/0 | 7081 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0002c0004t0003 | 0/0 | 7080 | 5 | 4 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0003c0005t0001 | 0/0 | 7080 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0004c0010t0013 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| a0005c0007t0002 | 0/0 | 7081 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7076): Show |
chr4 | 143179917 | 143228874 |
| a0006c0012t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | ACTTC others(7075): Show |
chr4 | 143179917 | 143228874 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 34 | 1 | 12 | 15 | 2 | 4 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0003g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0005g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0005g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0005g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0007g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0007g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0007g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0008g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0010g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0014g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0016g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0018g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0019g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0020g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0022g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0023g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0001t0024g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0002 | 0/0 | 15 | 3 | 4 | 4 | 0 | 4 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0003 | 0/0 | 14 | 0 | 1 | 11 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0020 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0009g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0009g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0009g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0015g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0025g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0002t0026g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0006g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0006g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0011g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0003t0012g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0006t0006g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0006t0006g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0008t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0009t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0001c0011t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0002c0004t0003g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0002c0004t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0002c0004t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0003c0005t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0004c0010t0013g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0005c0007t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| a0006c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00140 | hp2 | a0001 | c0003 | t0006 | g0011 | EUR | GBR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00280 | hp1 | a0001 | c0003 | t0006 | g0011 | EUR | FIN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00280 | hp2 | a0001 | c0002 | t0009 | g0003 | EUR | FIN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | CHS | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00639 | hp1 | a0001 | c0002 | t0009 | g0003 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00642 | hp2 | a0001 | c0001 | t0017 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00741 | hp1 | a0001 | c0002 | t0015 | g0002 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01081 | hp1 | a0001 | c0002 | t0009 | g0053 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01099 | hp2 | a0001 | c0011 | t0002 | g0050 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01109 | hp1 | a0001 | c0003 | t0006 | g0041 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0126 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01243 | hp2 | a0002 | c0004 | t0003 | g0015 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01516 | hp1 | a0001 | c0002 | t0009 | g0059 | EUR | IBS | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01884 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01891 | hp2 | a0001 | c0003 | t0004 | g0037 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01978 | hp1 | a0001 | c0003 | t0006 | g0038 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01993 | hp2 | a0001 | c0001 | t0020 | g0106 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02055 | hp1 | a0001 | c0003 | t0004 | g0016 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02055 | hp2 | a0001 | c0001 | t0023 | g0074 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02145 | hp2 | a0001 | c0003 | t0011 | g0006 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02258 | hp1 | a0001 | c0001 | t0018 | g0070 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02258 | hp2 | a0001 | c0003 | t0011 | g0006 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02300 | hp1 | a0001 | c0001 | t0014 | g0111 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02451 | hp2 | a0002 | c0004 | t0003 | g0121 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02615 | hp2 | a0001 | c0003 | t0004 | g0065 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02622 | hp2 | a0002 | c0004 | t0003 | g0015 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02647 | hp2 | a0001 | c0003 | t0012 | g0033 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02717 | hp2 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0128 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02895 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02896 | hp1 | a0001 | c0003 | t0004 | g0068 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0046 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02976 | hp1 | a0004 | c0010 | t0013 | g0118 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0127 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0124 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0047 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0032 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0066 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03490 | hp1 | a0001 | c0001 | t0022 | g0102 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0018 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0054 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03540 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03540 | hp2 | a0001 | c0003 | t0006 | g0067 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03579 | hp1 | a0001 | c0001 | t0024 | g0072 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03654 | hp1 | a0001 | c0003 | t0006 | g0042 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0055 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03688 | hp2 | a0001 | c0002 | t0026 | g0021 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03834 | hp1 | a0001 | c0001 | t0021 | g0001 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03834 | hp2 | a0001 | c0006 | t0006 | g0039 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03942 | hp1 | a0001 | c0006 | t0006 | g0017 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0044 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG04184 | hp2 | a0001 | c0002 | t0025 | g0021 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0057 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG04228 | hp1 | a0005 | c0007 | t0002 | g0002 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG04228 | hp2 | a0001 | c0001 | t0016 | g0108 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18522 | hp1 | a0002 | c0004 | t0003 | g0015 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18952 | hp1 | a0003 | c0005 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18952 | hp2 | a0001 | c0003 | t0006 | g0040 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18961 | hp2 | a0003 | c0005 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18991 | hp2 | a0001 | c0009 | t0002 | g0064 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18999 | hp1 | a0003 | c0005 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19011 | hp1 | a0001 | c0008 | t0002 | g0071 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0078 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19043 | hp1 | a0001 | c0003 | t0004 | g0016 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19063 | hp2 | a0006 | c0012 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ASW | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA20129 | hp2 | a0002 | c0004 | t0003 | g0120 | AFR | ASW | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA20805 | hp1 | a0001 | c0003 | t0006 | g0017 | EUR | TSI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01123 | hp1 | a0001 | c0003 | t0006 | g0011 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG03471 | hp2 | a0001 | c0003 | t0012 | g0033 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | USA | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | USA | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA21309 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0117 | REF | REF | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0020 | REF | REF | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:143185533 | C | T | 1 | a0006 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.83C>T | p.Ser28Leu | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 617/7081 | 83/3129 | 28/1042 | chr4 | 143185533 | |||
| chr4:143186034 | T | C | 1 | a0005 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.584T>C | p.Val195Ala | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 1118/7081 | 584/3129 | 195/1042 | chr4 | 143186034 | |||
| chr4:143213771 | C | T | 1 | a0002 | 5 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
missense_variant | MODERATE | c.1795C>T | p.Arg599Cys | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 2329/7081 | 1795/3129 | 599/1042 | chr4 | 143213771 | |||
| chr4:143214059 | A | G | 1 | a0004 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.2083A>G | p.Asn695Asp | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 2617/7081 | 2083/3129 | 695/1042 | chr4 | 143214059 | |||
| chr4:143214828 | G | A | 1 | a0003 | 3 | NA18952.hp1 NA18961.hp2 NA18999.hp1 |
missense_variant | MODERATE | c.2852G>A | p.Ser951Asn | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 3386/7081 | 2852/3129 | 951/1042 | chr4 | 143214828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:143185618 | C | T | 1 | a0001c0006 | 2 | HG03834.hp2 HG03942.hp1 |
synonymous_variant | LOW | c.168C>T | p.Phe56Phe | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 702/7081 | 168/3129 | 56/1042 | chr4 | 143185618 | |||
| chr4:143186098 | C | T | 1 | a0001c0011 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.648C>T | p.Ser216Ser | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 1182/7081 | 648/3129 | 216/1042 | chr4 | 143186098 | |||
| chr4:143209597 | T | C | 2 | a0001c0003 a0001c0006 |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
synonymous_variant | LOW | c.1437T>C | p.Asn479Asn | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/10 | 1971/7081 | 1437/3129 | 479/1042 | chr4 | 143209597 | |||
| chr4:143213827 | G | C | 1 | a0001c0008 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.1851G>C | p.Ser617Ser | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 2385/7081 | 1851/3129 | 617/1042 | chr4 | 143213827 | |||
| chr4:143214565 | G | A | 7 | a0001c0001 a0001c0003 a0001c0006 others(4): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
synonymous_variant | LOW | c.2589G>A | p.Arg863Arg | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 3123/7081 | 2589/3129 | 863/1042 | chr4 | 143214565 | |||
| chr4:143214880 | A | G | 1 | a0001c0009 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.2904A>G | p.Gly968Gly | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 3438/7081 | 2904/3129 | 968/1042 | chr4 | 143214880 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:143184961 | C | T | 2 | a0001c0002t0025 a0001c0002t0026 |
2 | HG03688.hp2 HG04184.hp2 |
5_prime_UTR_variant | MODIFIER | c.-490C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 490 | chr4 | 143184961 | ||||||
| chr4:143185278 | G | A | 1 | a0004c0010t0013 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-173G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 173 | chr4 | 143185278 | ||||||
| chr4:143185308 | G | A | 1 | a0001c0001t0010 | 3 | HG03130.hp2 HG03209.hp2 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-143G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 143 | chr4 | 143185308 | ||||||
| chr4:143220522 | C | G | 1 | a0001c0001t0024 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 66 | chr4 | 143220522 | ||||||
| chr4:143220632 | GA | G | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(21): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*185delA | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 185 | INFO_REALIGN_3_PRIME | chr4 | 143220632 | |||||
| chr4:143220684 | T | C | 1 | a0001c0001t0016 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*228T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 228 | chr4 | 143220684 | ||||||
| chr4:143220715 | C | A | 1 | a0001c0002t0025 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*259C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 259 | chr4 | 143220715 | ||||||
| chr4:143220798 | T | A | 1 | a0001c0001t0005 | 12 | HG01496.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*342T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 342 | chr4 | 143220798 | ||||||
| chr4:143220843 | A | T | 1 | a0001c0001t0023 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 387 | chr4 | 143220843 | ||||||
| chr4:143220880 | A | T | 1 | a0001c0003t0012 | 2 | HG02647.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*424A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 424 | chr4 | 143220880 | ||||||
| chr4:143220888 | C | T | 1 | a0001c0002t0015 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 432 | chr4 | 143220888 | ||||||
| chr4:143221398 | G | C | 1 | a0001c0001t0017 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942G>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 942 | chr4 | 143221398 | ||||||
| chr4:143221448 | T | C | 1 | a0001c0002t0009 | 4 | HG00280.hp2 HG00639.hp1 HG01081.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*992T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 992 | chr4 | 143221448 | ||||||
| chr4:143221728 | A | C | 1 | a0001c0001t0022 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1272A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1272 | chr4 | 143221728 | ||||||
| chr4:143221806 | C | G | 1 | a0001c0001t0021 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1350C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1350 | chr4 | 143221806 | ||||||
| chr4:143221829 | G | A | 2 | a0001c0001t0008 a0001c0001t0018 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1373G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1373 | chr4 | 143221829 | ||||||
| chr4:143221867 | C | T | 5 | a0001c0003t0004 a0001c0003t0006 a0001c0003t0011 others(2): Show |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1411C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1411 | chr4 | 143221867 | ||||||
| chr4:143221967 | T | TTA | 1 | a0001c0001t0008 | 5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1514_*1515dupTA | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1516 | INFO_REALIGN_3_PRIME | chr4 | 143221967 | |||||
| chr4:143222187 | T | G | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(22): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1731T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1731 | chr4 | 143222187 | ||||||
| chr4:143222243 | A | T | 1 | a0001c0001t0008 | 5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1787A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1787 | chr4 | 143222243 | ||||||
| chr4:143222256 | A | C | 1 | a0001c0001t0024 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1800A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1800 | chr4 | 143222256 | ||||||
| chr4:143222425 | C | T | 11 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(8): Show |
110 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1969C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1969 | chr4 | 143222425 | ||||||
| chr4:143222521 | T | C | 1 | a0001c0001t0019 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2065T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 2065 | chr4 | 143222521 | ||||||
| chr4:143223093 | A | G | 1 | a0001c0001t0020 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2637A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 2637 | chr4 | 143223093 | ||||||
| chr4:143223121 | T | C | 1 | a0001c0003t0011 | 2 | HG02145.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2665T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 2665 | chr4 | 143223121 | ||||||
| chr4:143223209 | T | G | 2 | a0001c0001t0007 a0001c0001t0019 |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2753T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 2753 | chr4 | 143223209 | ||||||
| chr4:143223514 | C | A | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(22): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*3058C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 3058 | chr4 | 143223514 | ||||||
| chr4:143223570 | T | C | 2 | a0001c0001t0007 a0001c0001t0019 |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3114T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 3114 | chr4 | 143223570 | ||||||
| chr4:143223808 | T | G | 2 | a0001c0003t0006 a0001c0006t0006 |
11 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3352T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 3352 | chr4 | 143223808 | ||||||
| chr4:143223839 | C | T | 1 | a0001c0001t0024 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3383C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 3383 | chr4 | 143223839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:143186184 | T | C | 4 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0037 others(1): Show |
8 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.682+52T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186184 | |||||||
| chr4:143186191 | C | T | 6 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.682+59C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186191 | |||||||
| chr4:143186453 | T | C | 8 | a0001c0003t0006g0011 a0001c0003t0006g0017 a0001c0003t0006g0038 others(5): Show |
10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+321T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186453 | |||||||
| chr4:143186652 | C | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.682+520C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186652 | |||||||
| chr4:143186669 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(74): Show |
143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.682+537A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186669 | |||||||
| chr4:143186871 | C | T | 18 | a0001c0001t0003g0004 a0001c0001t0003g0031 a0001c0001t0003g0119 others(15): Show |
32 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.682+739C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186871 | |||||||
| chr4:143187008 | A | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(55): Show |
110 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.683-818A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187008 | |||||||
| chr4:143187011 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.683-815C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187011 | |||||||
| chr4:143187036 | A | G | 2 | a0001c0002t0002g0024 a0001c0008t0002g0071 |
3 | NA18906.hp1 NA19011.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.683-790A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187036 | |||||||
| chr4:143187089 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.683-737T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187089 | |||||||
| chr4:143187091 | T | G | 1 | a0001c0003t0004g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.683-735T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187091 | |||||||
| chr4:143187132 | A | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-694A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187132 | |||||||
| chr4:143187360 | A | G | 1 | a0001c0001t0018g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.683-466A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187360 | |||||||
| chr4:143187372 | T | C | 1 | a0001c0002t0002g0043 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.683-454T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187372 | |||||||
| chr4:143187417 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.683-409A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187417 | |||||||
| chr4:143187456 | G | C | 2 | a0001c0002t0002g0018 a0001c0002t0002g0044 |
3 | HG03490.hp2 HG03492.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.683-370G>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187456 | |||||||
| chr4:143187488 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(55): Show |
110 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.683-338A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187488 | |||||||
| chr4:143187622 | A | G | 1 | a0001c0002t0002g0069 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.683-204A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187622 | |||||||
| chr4:143188382 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(55): Show |
110 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.818+421T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143188382 | |||||||
| chr4:143188482 | C | T | 2 | a0001c0001t0008g0013 a0001c0001t0008g0023 |
5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.818+521C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143188482 | |||||||
| chr4:143188527 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.818+566G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143188527 | |||||||
| chr4:143188789 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.818+828A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143188789 | |||||||
| chr4:143189099 | AT | A | 2 | a0001c0003t0006g0011 a0001c0003t0006g0038 |
4 | HG00140.hp2 HG00280.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.818+1142delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143189099 | ||||||
| chr4:143189179 | G | C | 1 | a0001c0002t0002g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.818+1218G>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189179 | |||||||
| chr4:143189344 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.818+1383C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189344 | |||||||
| chr4:143189737 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.818+1776A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189737 | |||||||
| chr4:143189823 | T | C | 1 | a0001c0003t0004g0016 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.818+1862T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189823 | |||||||
| chr4:143189874 | T | C | 1 | a0004c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.818+1913T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189874 | |||||||
| chr4:143190054 | C | T | 1 | a0001c0003t0004g0068 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.818+2093C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190054 | |||||||
| chr4:143190114 | G | A | 2 | a0001c0003t0004g0046 a0001c0003t0004g0047 |
2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.818+2153G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190114 | |||||||
| chr4:143190262 | ATAG | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(72): Show |
141 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.818+2305_818+2307d others(5): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143190262 | ||||||
| chr4:143190290 | A | C | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.818+2329A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190290 | |||||||
| chr4:143190493 | C | CT | 10 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(7): Show |
10 | HG01099.hp1 HG01361.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.818+2534dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143190493 | ||||||
| chr4:143190579 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.818+2618A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190579 | |||||||
| chr4:143190679 | T | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.818+2718T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190679 | |||||||
| chr4:143190744 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.818+2783G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190744 | |||||||
| chr4:143190802 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(96): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.818+2841C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190802 | |||||||
| chr4:143190896 | A | G | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.818+2935A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190896 | |||||||
| chr4:143191048 | G | GTGATCCT others(6): Show |
1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.818+3099_818+3100i others(15): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143191048 | ||||||
| chr4:143191276 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.818+3315A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143191276 | |||||||
| chr4:143191844 | G | A | 1 | a0001c0002t0002g0043 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.819-3872G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143191844 | |||||||
| chr4:143192145 | T | A | 5 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0002c0004t0003g0015 others(2): Show |
7 | HG01243.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.819-3571T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192145 | |||||||
| chr4:143192345 | G | T | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.819-3371G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192345 | |||||||
| chr4:143192459 | C | T | 8 | a0001c0003t0006g0011 a0001c0003t0006g0017 a0001c0003t0006g0038 others(5): Show |
10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.819-3257C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192459 | |||||||
| chr4:143192479 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.819-3237A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192479 | |||||||
| chr4:143192550 | C | CT | 12 | a0001c0001t0001g0026 a0001c0001t0001g0073 a0001c0001t0001g0075 others(9): Show |
13 | HG01099.hp1 HG02027.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.819-3145dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | ||||||
| chr4:143192550 | C | CTT | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(48): Show |
107 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.819-3146_819-3145d others(4): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | ||||||
| chr4:143192550 | C | CTTT | 15 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0099 others(12): Show |
23 | HG01243.hp2 HG01993.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.819-3147_819-3145d others(5): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | ||||||
| chr4:143192550 | CT | C | 10 | a0001c0001t0018g0070 a0001c0002t0002g0048 a0001c0002t0002g0049 others(7): Show |
15 | HG01099.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.819-3145delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | ||||||
| chr4:143192550 | CTT | C | 2 | a0001c0001t0008g0013 a0001c0001t0008g0023 |
5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-3146_819-3145d others(4): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | ||||||
| chr4:143192574 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.819-3142T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192574 | |||||||
| chr4:143192647 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(74): Show |
143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.819-3069T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192647 | |||||||
| chr4:143192769 | G | A | 18 | a0001c0001t0003g0004 a0001c0001t0003g0031 a0001c0001t0003g0119 others(15): Show |
32 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.819-2947G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192769 | |||||||
| chr4:143192827 | T | A | 1 | a0001c0002t0002g0019 | 2 | NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.819-2889T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192827 | |||||||
| chr4:143192828 | A | G | 1 | a0001c0002t0002g0019 | 2 | NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.819-2888A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192828 | |||||||
| chr4:143192888 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.819-2828G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192888 | |||||||
| chr4:143193042 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(45): Show |
95 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.819-2674C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193042 | |||||||
| chr4:143193126 | T | C | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.819-2590T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193126 | |||||||
| chr4:143193260 | A | G | 18 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(15): Show |
25 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.819-2456A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193260 | |||||||
| chr4:143193274 | A | G | 3 | a0002c0004t0003g0015 a0002c0004t0003g0120 a0002c0004t0003g0121 |
5 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-2442A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193274 | |||||||
| chr4:143193521 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.819-2195G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193521 | |||||||
| chr4:143193778 | C | A | 4 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0037 others(1): Show |
8 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.819-1938C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193778 | |||||||
| chr4:143193878 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.819-1838G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193878 | |||||||
| chr4:143194149 | T | C | 1 | a0001c0002t0002g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.819-1567T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194149 | |||||||
| chr4:143194513 | C | CT | 12 | a0001c0001t0001g0095 a0001c0001t0003g0004 a0001c0001t0003g0031 others(9): Show |
23 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.819-1192dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143194513 | ||||||
| chr4:143194536 | C | G | 1 | a0001c0001t0007g0036 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.819-1180C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194536 | |||||||
| chr4:143194577 | G | A | 2 | a0001c0001t0010g0032 a0001c0001t0010g0124 |
3 | HG03130.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.819-1139G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194577 | |||||||
| chr4:143194610 | C | T | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.819-1106C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194610 | |||||||
| chr4:143194630 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.819-1086C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194630 | |||||||
| chr4:143194870 | G | T | 1 | a0001c0001t0023g0074 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.819-846G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194870 | |||||||
| chr4:143194892 | T | A | 1 | a0001c0001t0003g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819-824T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194892 | |||||||
| chr4:143194893 | A | C | 1 | a0001c0001t0003g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819-823A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194893 | |||||||
| chr4:143194894 | C | CT | 32 | a0001c0001t0003g0031 a0001c0001t0003g0119 a0001c0001t0007g0034 others(29): Show |
57 | HG00280.hp2 HG00408.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.819-807dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143194894 | ||||||
| chr4:143194894 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819-822C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194894 | |||||||
| chr4:143194894 | CT | C | 17 | a0001c0001t0001g0081 a0001c0001t0003g0125 a0001c0001t0005g0027 others(14): Show |
24 | HG00140.hp2 HG00280.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.819-807delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143194894 | ||||||
| chr4:143195024 | TTTG | T | 3 | a0002c0004t0003g0015 a0002c0004t0003g0120 a0002c0004t0003g0121 |
5 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-689_819-687del others(3): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143195024 | ||||||
| chr4:143195457 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0099 |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.819-259C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143195457 | |||||||
| chr4:143195458 | G | A | 1 | a0001c0003t0004g0068 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.819-258G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143195458 | |||||||
| chr4:143195486 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.819-230C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143195486 | |||||||
| chr4:143195539 | A | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.819-177A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143195539 | |||||||
| chr4:143195944 | GTTA | G | 6 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.948+102_948+104del others(3): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 143195944 | ||||||
| chr4:143195950 | GTTGTT | G | 20 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(17): Show |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.948+114_948+118del others(5): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 143195950 | ||||||
| chr4:143196135 | G | A | 1 | a0001c0002t0002g0044 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.948+290G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196135 | |||||||
| chr4:143196237 | C | T | 1 | a0001c0002t0002g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.948+392C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196237 | |||||||
| chr4:143196278 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(54): Show |
109 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.948+433C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196278 | |||||||
| chr4:143196332 | A | T | 1 | a0001c0003t0006g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.948+487A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196332 | |||||||
| chr4:143196499 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(97): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.948+654G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196499 | |||||||
| chr4:143196515 | A | G | 7 | a0001c0001t0005g0014 a0001c0001t0005g0025 a0001c0001t0005g0027 others(4): Show |
12 | HG01496.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.948+670A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196515 | |||||||
| chr4:143196740 | T | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.948+895T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196740 | |||||||
| chr4:143196905 | T | A | 1 | a0001c0002t0002g0018 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.949-918T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196905 | |||||||
| chr4:143197019 | C | T | 6 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.949-804C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143197019 | |||||||
| chr4:143197097 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.949-726T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143197097 | |||||||
| chr4:143198020 | A | G | 1 | a0001c0001t0007g0035 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1050+96A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198020 | |||||||
| chr4:143198169 | G | A | 1 | a0001c0001t0003g0031 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1050+245G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198169 | |||||||
| chr4:143198171 | A | C | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1050+247A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198171 | |||||||
| chr4:143198290 | A | G | 1 | a0001c0002t0002g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1050+366A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198290 | |||||||
| chr4:143198529 | T | A | 20 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(17): Show |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1050+605T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198529 | |||||||
| chr4:143198780 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.1050+856G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198780 | |||||||
| chr4:143198961 | T | G | 20 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(17): Show |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1050+1037T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198961 | |||||||
| chr4:143199051 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(97): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1050+1127A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199051 | |||||||
| chr4:143199053 | G | A | 1 | a0004c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1050+1129G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199053 | |||||||
| chr4:143199146 | G | T | 12 | a0001c0001t0003g0004 a0001c0001t0003g0031 a0001c0001t0003g0119 others(9): Show |
23 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1050+1222G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199146 | |||||||
| chr4:143199212 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1050+1288C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199212 | |||||||
| chr4:143199213 | G | A | 6 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1050+1289G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199213 | |||||||
| chr4:143199377 | A | G | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1050+1453A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199377 | |||||||
| chr4:143199527 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.1050+1603C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199527 | |||||||
| chr4:143199776 | GTCT | G | 6 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1050+1857_1050+185 others(7): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 143199776 | ||||||
| chr4:143200011 | A | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(96): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1050+2087A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200011 | |||||||
| chr4:143200158 | G | A | 1 | a0001c0003t0006g0011 | 3 | HG00140.hp2 HG00280.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1050+2234G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200158 | |||||||
| chr4:143200231 | G | A | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1050+2307G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200231 | |||||||
| chr4:143200659 | G | T | 9 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(6): Show |
14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1050+2735G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200659 | |||||||
| chr4:143200714 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051-2694G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200714 | |||||||
| chr4:143200890 | T | C | 1 | a0001c0001t0005g0078 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1051-2518T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200890 | |||||||
| chr4:143201024 | C | T | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1051-2384C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201024 | |||||||
| chr4:143201074 | A | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(35): Show |
85 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1051-2334A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201074 | |||||||
| chr4:143201220 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0020g0106 |
2 | HG01993.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1051-2188C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201220 | |||||||
| chr4:143201277 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051-2131G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201277 | |||||||
| chr4:143201294 | C | T | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1051-2114C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201294 | |||||||
| chr4:143201359 | C | T | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1051-2049C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201359 | |||||||
| chr4:143201401 | A | G | 1 | a0001c0001t0005g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1051-2007A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201401 | |||||||
| chr4:143201523 | T | C | 20 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(17): Show |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1051-1885T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201523 | |||||||
| chr4:143201646 | G | T | 2 | a0001c0001t0008g0013 a0001c0001t0008g0023 |
5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-1762G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201646 | |||||||
| chr4:143201989 | C | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0100 |
2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1051-1419C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201989 | |||||||
| chr4:143202029 | ATTAC | A | 1 | a0001c0003t0004g0016 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1051-1376_1051-137 others(8): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 143202029 | ||||||
| chr4:143202101 | CTT | C | 9 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(6): Show |
14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1051-1304_1051-130 others(6): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 143202101 | ||||||
| chr4:143202219 | A | G | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1051-1189A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202219 | |||||||
| chr4:143202257 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1051-1151A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202257 | |||||||
| chr4:143202337 | A | G | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1051-1071A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202337 | |||||||
| chr4:143202339 | G | A | 1 | a0001c0001t0003g0031 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1051-1069G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202339 | |||||||
| chr4:143202414 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(97): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1051-994C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202414 | |||||||
| chr4:143202473 | T | G | 1 | a0004c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1051-935T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202473 | |||||||
| chr4:143202492 | T | G | 6 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1051-916T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202492 | |||||||
| chr4:143203065 | G | A | 2 | a0001c0002t0002g0048 a0001c0002t0002g0052 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1051-343G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143203065 | |||||||
| chr4:143203119 | G | T | 8 | a0001c0003t0006g0011 a0001c0003t0006g0017 a0001c0003t0006g0038 others(5): Show |
10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1051-289G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143203119 | |||||||
| chr4:143203125 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(97): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1051-283T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143203125 | |||||||
| chr4:143203339 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.1051-69G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143203339 | |||||||
| chr4:143203694 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1209+128A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143203694 | |||||||
| chr4:143203894 | G | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0123 a0001c0001t0003g0125 |
10 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1209+328G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143203894 | |||||||
| chr4:143203932 | A | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(55): Show |
110 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.1209+366A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143203932 | |||||||
| chr4:143204008 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1209+442G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204008 | |||||||
| chr4:143204095 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1209+529C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204095 | |||||||
| chr4:143204142 | C | T | 1 | a0001c0009t0002g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1209+576C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204142 | |||||||
| chr4:143204303 | G | A | 1 | a0001c0002t0002g0012 | 3 | NA18945.hp1 NA18957.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1209+737G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204303 | |||||||
| chr4:143204351 | G | T | 6 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1209+785G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204351 | |||||||
| chr4:143204453 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0100 |
2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1209+887G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204453 | |||||||
| chr4:143204458 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1209+892C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204458 | |||||||
| chr4:143204516 | A | G | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1209+950A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204516 | |||||||
| chr4:143204577 | CG | C | 3 | a0001c0003t0004g0006 a0001c0003t0004g0037 a0001c0003t0011g0006 |
6 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1209+1015delG | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 143204577 | ||||||
| chr4:143204814 | T | C | 3 | a0001c0001t0005g0027 a0001c0001t0005g0078 a0001c0001t0005g0097 |
4 | HG02630.hp2 HG02886.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-1219T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204814 | |||||||
| chr4:143204824 | A | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1210-1209A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204824 | |||||||
| chr4:143204948 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1210-1085T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204948 | |||||||
| chr4:143205139 | T | G | 1 | a0001c0003t0006g0040 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1210-894T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205139 | |||||||
| chr4:143205190 | C | T | 5 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0002c0004t0003g0015 others(2): Show |
7 | HG01243.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-843C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205190 | |||||||
| chr4:143205219 | C | T | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1210-814C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205219 | |||||||
| chr4:143205324 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210-709G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205324 | |||||||
| chr4:143205349 | T | C | 8 | a0001c0003t0006g0011 a0001c0003t0006g0017 a0001c0003t0006g0038 others(5): Show |
10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1210-684T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205349 | |||||||
| chr4:143205697 | A | G | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1210-336A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205697 | |||||||
| chr4:143205833 | A | G | 20 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(17): Show |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1210-200A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205833 | |||||||
| chr4:143205943 | T | TAAGAATC others(348): Show |
1 | a0001c0001t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1210-71_1210-70ins others(355): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 143205943 | ||||||
| chr4:143206029 | A | G | 1 | a0001c0006t0006g0039 | 1 | HG03834.hp2 | splice_region_variant&intron_variant | LOW | c.1210-4A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143206029 | |||||||
| chr4:143206246 | T | G | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403+20T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206246 | |||||||
| chr4:143206330 | A | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1403+104A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206330 | |||||||
| chr4:143206333 | A | G | 1 | a0004c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1403+107A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206333 | |||||||
| chr4:143206372 | T | C | 20 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(17): Show |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1403+146T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206372 | |||||||
| chr4:143206428 | G | A | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1403+202G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206428 | |||||||
| chr4:143206582 | C | T | 5 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0002c0004t0003g0015 others(2): Show |
7 | HG01243.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403+356C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206582 | |||||||
| chr4:143206600 | G | T | 1 | a0001c0003t0004g0016 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1403+374G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206600 | |||||||
| chr4:143206625 | G | A | 16 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0045 others(13): Show |
33 | HG00280.hp2 HG00408.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403+399G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206625 | |||||||
| chr4:143207252 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1403+1026G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207252 | |||||||
| chr4:143207288 | C | G | 1 | a0001c0001t0018g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1403+1062C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207288 | |||||||
| chr4:143207325 | G | A | 2 | a0001c0001t0010g0032 a0001c0001t0010g0124 |
3 | HG03130.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1403+1099G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207325 | |||||||
| chr4:143207326 | T | G | 1 | a0001c0001t0007g0036 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1403+1100T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207326 | |||||||
| chr4:143207327 | C | T | 18 | a0001c0001t0003g0004 a0001c0001t0003g0031 a0001c0001t0003g0119 others(15): Show |
32 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1403+1101C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207327 | |||||||
| chr4:143207337 | A | G | 1 | a0004c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1403+1111A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207337 | |||||||
| chr4:143207380 | A | T | 8 | a0001c0003t0006g0011 a0001c0003t0006g0017 a0001c0003t0006g0038 others(5): Show |
10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1403+1154A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207380 | |||||||
| chr4:143207408 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(96): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1403+1182T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207408 | |||||||
| chr4:143207427 | A | G | 1 | a0004c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1403+1201A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207427 | |||||||
| chr4:143207648 | GGTTT | G | 3 | a0001c0001t0001g0109 a0001c0001t0016g0108 a0001c0001t0022g0102 |
3 | HG03490.hp1 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1403+1429_1403+143 others(8): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 143207648 | ||||||
| chr4:143207666 | AT | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(96): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1403+1454delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 143207666 | ||||||
| chr4:143207821 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0076 others(2): Show |
14 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1403+1595G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207821 | |||||||
| chr4:143207884 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403+1658G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207884 | |||||||
| chr4:143207923 | C | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.1404-1641C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207923 | |||||||
| chr4:143208409 | A | C | 1 | a0001c0002t0002g0061 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1404-1155A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208409 | |||||||
| chr4:143208526 | A | G | 1 | a0001c0002t0002g0024 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1404-1038A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208526 | |||||||
| chr4:143208698 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(133): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1404-866A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208698 | |||||||
| chr4:143208716 | G | A | 6 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1404-848G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208716 | |||||||
| chr4:143208808 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(97): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1404-756A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208808 | |||||||
| chr4:143208851 | T | A | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1404-713T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208851 | |||||||
| chr4:143208950 | C | T | 1 | a0001c0002t0002g0009 | 4 | HG01346.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1404-614C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208950 | |||||||
| chr4:143208965 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(74): Show |
143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1404-599C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208965 | |||||||
| chr4:143209013 | C | T | 2 | a0001c0001t0010g0032 a0001c0001t0010g0124 |
3 | HG03130.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1404-551C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209013 | |||||||
| chr4:143209035 | T | C | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1404-529T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209035 | |||||||
| chr4:143209065 | A | AT | 8 | a0001c0003t0006g0011 a0001c0003t0006g0017 a0001c0003t0006g0038 others(5): Show |
10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1404-492dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 143209065 | ||||||
| chr4:143209104 | ACTTAT | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.1404-454_1404-450d others(7): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 143209104 | ||||||
| chr4:143209129 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1404-435A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209129 | |||||||
| chr4:143209371 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1404-193G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209371 | |||||||
| chr4:143209444 | T | C | 20 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(17): Show |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1404-120T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209444 | |||||||
| chr4:143209509 | A | G | 18 | a0001c0001t0003g0004 a0001c0001t0003g0031 a0001c0001t0003g0119 others(15): Show |
32 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1404-55A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209509 | |||||||
| chr4:143209812 | C | T | 6 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+155C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143209812 | |||||||
| chr4:143209826 | A | AT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.1497+177dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 143209826 | ||||||
| chr4:143210153 | T | A | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1497+496T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210153 | |||||||
| chr4:143210188 | G | A | 1 | a0001c0001t0008g0023 | 2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1497+531G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210188 | |||||||
| chr4:143210204 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(97): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1497+547G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210204 | |||||||
| chr4:143210216 | A | G | 1 | a0001c0002t0002g0008 | 4 | HG01069.hp2 HG01934.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+559A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210216 | |||||||
| chr4:143210217 | A | G | 1 | a0001c0002t0002g0056 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1497+560A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210217 | |||||||
| chr4:143210586 | C | CA | 5 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 others(2): Show |
8 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1497+941dupA | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 143210586 | ||||||
| chr4:143210609 | G | T | 1 | a0001c0003t0006g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1497+952G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210609 | |||||||
| chr4:143210910 | TATACTCA others(1): Show |
T | 5 | a0001c0002t0002g0045 a0001c0002t0002g0051 a0001c0002t0002g0060 others(2): Show |
5 | HG00408.hp1 HG02040.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1497+1257_1497+126 others(12): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 143210910 | ||||||
| chr4:143210946 | A | G | 1 | a0001c0001t0019g0127 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1497+1289A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210946 | |||||||
| chr4:143211191 | T | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(97): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1498-1127T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211191 | |||||||
| chr4:143211339 | T | A | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1498-979T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211339 | |||||||
| chr4:143211384 | A | G | 1 | a0001c0001t0005g0029 | 2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1498-934A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211384 | |||||||
| chr4:143211395 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1498-923C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211395 | |||||||
| chr4:143211469 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(96): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1498-849A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211469 | |||||||
| chr4:143211519 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(74): Show |
143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1498-799T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211519 | |||||||
| chr4:143211767 | A | C | 1 | a0001c0001t0003g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1498-551A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211767 | |||||||
| chr4:143211813 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1498-505A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211813 | |||||||
| chr4:143211939 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1498-379T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211939 | |||||||
| chr4:143212021 | T | G | 2 | a0001c0002t0025g0021 a0001c0002t0026g0021 |
2 | HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1498-297T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212021 | |||||||
| chr4:143212045 | C | T | 8 | a0001c0003t0006g0011 a0001c0003t0006g0017 a0001c0003t0006g0038 others(5): Show |
10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1498-273C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212045 | |||||||
| chr4:143212099 | T | A | 1 | a0001c0001t0003g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1498-219T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212099 | |||||||
| chr4:143212104 | A | G | 1 | a0001c0003t0004g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1498-214A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212104 | |||||||
| chr4:143212264 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1498-54T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212264 | |||||||
| chr4:143212305 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1498-13T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212305 | |||||||
| chr4:143212592 | C | CT | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(74): Show |
143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1604+173dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 143212592 | ||||||
| chr4:143212704 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(74): Show |
143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1604+280G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143212704 | |||||||
| chr4:143212890 | A | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.1604+466A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143212890 | |||||||
| chr4:143213115 | G | A | 3 | a0002c0004t0003g0015 a0002c0004t0003g0120 a0002c0004t0003g0121 |
5 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1605-466G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213115 | |||||||
| chr4:143213124 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(55): Show |
110 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.1605-457C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213124 | |||||||
| chr4:143213179 | G | A | 1 | a0001c0001t0008g0023 | 2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1605-402G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213179 | |||||||
| chr4:143213420 | T | G | 1 | a0001c0001t0016g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1605-161T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213420 | |||||||
| chr4:143213567 | A | G | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1605-14A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213567 | |||||||
| chr4:143215040 | T | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(97): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.2967+97T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215040 | |||||||
| chr4:143215053 | A | G | 20 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(17): Show |
28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.2967+110A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215053 | |||||||
| chr4:143215068 | C | T | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2967+125C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215068 | |||||||
| chr4:143215252 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(74): Show |
143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.2967+309T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215252 | |||||||
| chr4:143215689 | A | T | 2 | a0001c0001t0005g0027 a0001c0001t0005g0078 |
3 | HG02886.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2967+746A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215689 | |||||||
| chr4:143215833 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(97): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.2967+890C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215833 | |||||||
| chr4:143216069 | C | T | 4 | a0001c0002t0002g0007 a0001c0002t0002g0024 a0001c0002t0002g0048 others(1): Show |
8 | HG02486.hp1 HG02622.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2967+1126C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216069 | |||||||
| chr4:143216182 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2967+1239T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216182 | |||||||
| chr4:143216206 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(74): Show |
143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.2967+1263A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216206 | |||||||
| chr4:143216478 | AT | A | 23 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0024g0072 others(20): Show |
34 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.2967+1549delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 143216478 | ||||||
| chr4:143216655 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2967+1712T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216655 | |||||||
| chr4:143216673 | G | A | 11 | a0001c0001t0003g0004 a0001c0001t0003g0031 a0001c0001t0003g0119 others(8): Show |
22 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2967+1730G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216673 | |||||||
| chr4:143216728 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2967+1785G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216728 | |||||||
| chr4:143216809 | C | CATTT | 2 | a0001c0001t0008g0013 a0001c0001t0008g0023 |
5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2967+1882_2967+188 others(8): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 143216809 | ||||||
| chr4:143217083 | A | G | 1 | a0001c0003t0006g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2967+2140A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143217083 | |||||||
| chr4:143217377 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2967+2434C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143217377 | |||||||
| chr4:143217906 | A | C | 1 | a0001c0003t0006g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2968-2389A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143217906 | |||||||
| chr4:143218244 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2968-2051G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218244 | |||||||
| chr4:143218320 | C | A | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2968-1975C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218320 | |||||||
| chr4:143218471 | A | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2968-1824A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218471 | |||||||
| chr4:143218559 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(74): Show |
143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.2968-1736T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218559 | |||||||
| chr4:143218815 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0008g0023 a0001c0001t0018g0070 |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2968-1480T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218815 | |||||||
| chr4:143218920 | T | A | 1 | a0001c0002t0002g0055 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2968-1375T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218920 | |||||||
| chr4:143218925 | C | T | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2968-1370C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218925 | |||||||
| chr4:143219223 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.2968-1072G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219223 | |||||||
| chr4:143219255 | A | G | 9 | a0001c0003t0006g0011 a0001c0003t0006g0017 a0001c0003t0006g0038 others(6): Show |
11 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2968-1040A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219255 | |||||||
| chr4:143219439 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.2968-856G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219439 | |||||||
| chr4:143219482 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2968-813T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219482 | |||||||
| chr4:143219512 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.2968-783C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219512 | |||||||
| chr4:143219560 | C | G | 9 | a0001c0003t0004g0006 a0001c0003t0004g0016 a0001c0003t0004g0022 others(6): Show |
14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2968-735C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219560 | |||||||
| chr4:143220179 | T | C | 1 | a0001c0001t0007g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2968-116T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143220179 |