Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 952 |
| ensemblid | ENSG00000004468.13 |
| hgncid | 1667 |
| symbol | CD38 |
| name | CD38 molecule |
| refseq_nuc | NM_001775.4 |
| refseq_prot | NP_001766.2 |
| ensembl_nuc | ENST00000226279.8 |
| ensembl_prot | ENSP00000226279.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 15778328 |
| end | 15853232 |
| strand | + |
| ver | v1.2 |
| region | chr4:15778328-15853232 |
| region5000 | chr4:15773328-15858232 |
| regionname0 | CD38_chr4_15778328_15853232 |
| regionname5000 | CD38_chr4_15773328_15858232 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 300 | 341 | 76 | 66 | 149 | 12 | 36 | 121 | CD38_chr4_15773328_15858232 | CD38 | MANCE others(295): Show |
chr4 | 15773328 | 15858232 |
| a0002 | 0/0 | 300 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CD38_chr4_15773328_15858232 | CD38 | MANCE others(295): Show |
chr4 | 15773328 | 15858232 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 900 | 298 | 70 | 61 | 121 | 12 | 32 | CD38_chr4_15773328_15858232 | CD38 | ATGGC others(895): Show |
chr4 | 15773328 | 15858232 | ||
| a0001c0002 | 0/0 | 900 | 39 | 6 | 4 | 25 | 0 | 4 | CD38_chr4_15773328_15858232 | CD38 | ATGGC others(895): Show |
chr4 | 15773328 | 15858232 | ||
| a0001c0004 | 0/0 | 900 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | ATGGC others(895): Show |
chr4 | 15773328 | 15858232 | ||
| a0001c0005 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | ATGGC others(895): Show |
chr4 | 15773328 | 15858232 | ||
| a0001c0006 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | ATGGC others(895): Show |
chr4 | 15773328 | 15858232 | ||
| a0002c0003 | 0/0 | 900 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | ATGGC others(895): Show |
chr4 | 15773328 | 15858232 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5620 | 60 | 1 | 20 | 28 | 4 | 6 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0002 | 0/0 | 5619 | 59 | 5 | 16 | 21 | 5 | 12 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0003 | 0/0 | 5622 | 23 | 0 | 13 | 6 | 2 | 2 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0004 | 0/0 | 5619 | 20 | 4 | 1 | 9 | 1 | 5 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0005 | 0/0 | 5622 | 6 | 0 | 0 | 6 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0006 | 0/0 | 5620 | 15 | 0 | 0 | 15 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0007 | 0/0 | 5622 | 6 | 2 | 2 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0008 | 0/0 | 5619 | 9 | 0 | 0 | 9 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0009 | 0/0 | 5622 | 6 | 2 | 0 | 3 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0010 | 0/0 | 5623 | 5 | 0 | 1 | 3 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5618): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0011 | 0/0 | 5619 | 6 | 6 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0013 | 0/0 | 5621 | 4 | 0 | 0 | 3 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0014 | 0/0 | 5623 | 4 | 1 | 0 | 1 | 0 | 2 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5618): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0015 | 0/0 | 5621 | 3 | 2 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0016 | 0/0 | 5623 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5618): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0017 | 0/0 | 5619 | 3 | 3 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0018 | 0/0 | 5619 | 3 | 0 | 3 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0019 | 0/0 | 5619 | 3 | 3 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0020 | 0/0 | 5619 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0021 | 0/0 | 5622 | 2 | 0 | 0 | 1 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0022 | 0/0 | 5620 | 2 | 1 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0023 | 0/0 | 5619 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0024 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0025 | 0/0 | 5619 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0026 | 0/0 | 5619 | 2 | 1 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0028 | 0/0 | 5620 | 2 | 1 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0030 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0031 | 0/0 | 5619 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0032 | 0/0 | 5621 | 2 | 1 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0033 | 0/0 | 5619 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0034 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GAAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0035 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0036 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0038 | 0/0 | 5619 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0039 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5618): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0040 | 0/0 | 5620 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0041 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0042 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0043 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0044 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0045 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0046 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0047 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0048 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0049 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0050 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0051 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0052 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0053 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0054 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0055 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0056 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0057 | 0/1 | 5619 | 1 | 0 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0058 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5618): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0059 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0060 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0061 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0062 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5606): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0063 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0064 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0065 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0066 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0067 | 0/0 | 5621 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0068 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5618): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0069 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0070 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0071 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0072 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5606): Show |
chr4 | 15773328 | 15858232 |
| a0001c0001t0073 | 0/0 | 5619 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0001 | 0/0 | 5620 | 5 | 0 | 0 | 5 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0002 | 0/0 | 5619 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0003 | 0/0 | 5622 | 6 | 1 | 0 | 5 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0004 | 0/0 | 5619 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0005 | 0/0 | 5622 | 10 | 0 | 2 | 7 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0006 | 0/0 | 5620 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0007 | 0/0 | 5622 | 3 | 0 | 0 | 2 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0009 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0010 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5618): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0012 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0016 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5618): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0024 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5616): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0027 | 0/0 | 5619 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0029 | 0/0 | 5619 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0030 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0002t0037 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5614): Show |
chr4 | 15773328 | 15858232 |
| a0001c0004t0001 | 0/0 | 5620 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0001c0005t0007 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| a0001c0006t0001 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5615): Show |
chr4 | 15773328 | 15858232 |
| a0002c0003t0012 | 0/0 | 5622 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | GCAGT others(5617): Show |
chr4 | 15773328 | 15858232 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0008g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0008g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0009g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0010g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0010g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0010g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0010g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0010g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0011g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0013g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0013g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0013g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0013g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0014g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0014g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0014g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0014g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0015g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0015g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0016g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0016g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0017g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0017g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0018g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0018g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0019g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0019g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0019g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0020g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0021g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0021g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0022g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0022g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0023g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0023g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0024g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0025g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0025g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0026g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0026g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0028g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0028g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0030g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0031g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0031g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0032g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0032g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0033g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0033g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0034g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0035g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0036g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0038g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0039g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0040g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0041g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0042g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0043g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0044g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0045g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0046g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0047g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0048g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0049g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0050g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0051g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0052g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0053g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0054g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0055g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0056g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0057g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0058g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0059g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0060g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0061g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0062g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0063g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0064g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0065g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0066g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0067g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0068g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0069g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0070g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0071g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0072g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0001t0073g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0007g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0009g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0010g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0012g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0016g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0024g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0027g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0027g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0029g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0029g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0030g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0002t0037g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0005t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0001c0006t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0002c0003t0012g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0002c0003t0012g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| a0002c0003t0012g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0299 | EUR | GBR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | GBR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0291 | EUR | GBR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0261 | EUR | GBR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | FIN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0269 | EUR | FIN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00408 | hp2 | a0001 | c0002 | t0004 | g0007 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00423 | hp1 | a0001 | c0004 | t0001 | g0249 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00423 | hp2 | a0001 | c0002 | t0005 | g0093 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00438 | hp1 | a0001 | c0001 | t0032 | g0175 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0250 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00621 | hp2 | a0001 | c0002 | t0007 | g0086 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00642 | hp1 | a0001 | c0001 | t0041 | g0292 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00733 | hp2 | a0001 | c0001 | t0018 | g0011 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00735 | hp1 | a0001 | c0001 | t0018 | g0190 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01069 | hp2 | a0001 | c0001 | t0018 | g0011 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01106 | hp2 | a0001 | c0002 | t0009 | g0085 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0031 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0045 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0294 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01192 | hp2 | a0001 | c0002 | t0016 | g0108 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01243 | hp2 | a0001 | c0001 | t0067 | g0075 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01256 | hp1 | a0001 | c0005 | t0007 | g0029 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0287 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0289 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0295 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01358 | hp2 | a0001 | c0001 | t0038 | g0014 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0298 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01433 | hp2 | a0001 | c0001 | t0026 | g0072 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0214 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01884 | hp2 | a0001 | c0001 | t0024 | g0185 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0002 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0064 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0081 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0307 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0061 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02055 | hp2 | a0001 | c0001 | t0032 | g0313 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02074 | hp1 | a0001 | c0001 | t0008 | g0128 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0157 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0087 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02083 | hp2 | a0001 | c0001 | t0010 | g0300 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0124 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02145 | hp1 | a0001 | c0001 | t0014 | g0210 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02145 | hp2 | a0001 | c0001 | t0056 | g0303 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02148 | hp1 | a0001 | c0002 | t0005 | g0097 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | CDX | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02165 | hp2 | a0001 | c0001 | t0014 | g0166 | EAS | CDX | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02257 | hp1 | a0001 | c0001 | t0047 | g0200 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02257 | hp2 | a0001 | c0001 | t0030 | g0040 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02280 | hp1 | a0001 | c0001 | t0045 | g0202 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02293 | hp1 | a0001 | c0001 | t0028 | g0209 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02451 | hp2 | a0001 | c0001 | t0023 | g0052 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02523 | hp1 | a0001 | c0001 | t0007 | g0171 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02572 | hp1 | a0001 | c0001 | t0015 | g0068 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02572 | hp2 | a0001 | c0001 | t0042 | g0082 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02622 | hp1 | a0001 | c0001 | t0019 | g0199 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02622 | hp2 | a0001 | c0001 | t0069 | g0043 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0197 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02630 | hp2 | a0001 | c0001 | t0064 | g0038 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0050 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02647 | hp2 | a0001 | c0001 | t0019 | g0159 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0304 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0139 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02738 | hp1 | a0001 | c0001 | t0014 | g0176 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02738 | hp2 | a0001 | c0001 | t0010 | g0288 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02809 | hp2 | a0001 | c0002 | t0024 | g0084 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02818 | hp1 | a0001 | c0002 | t0037 | g0090 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02818 | hp2 | a0001 | c0001 | t0055 | g0060 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0051 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02896 | hp1 | a0001 | c0001 | t0028 | g0076 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02922 | hp1 | a0001 | c0001 | t0071 | g0180 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02922 | hp2 | a0001 | c0001 | t0062 | g0110 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02965 | hp1 | a0001 | c0001 | t0034 | g0112 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02965 | hp2 | a0001 | c0001 | t0039 | g0156 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02970 | hp1 | a0001 | c0001 | t0063 | g0059 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0067 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02976 | hp1 | a0001 | c0001 | t0061 | g0054 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02976 | hp2 | a0001 | c0001 | t0070 | g0039 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03017 | hp1 | a0001 | c0001 | t0040 | g0014 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0201 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03098 | hp1 | a0001 | c0002 | t0030 | g0073 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03098 | hp2 | a0001 | c0001 | t0022 | g0047 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03130 | hp1 | a0001 | c0001 | t0058 | g0302 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03130 | hp2 | a0001 | c0001 | t0049 | g0069 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03139 | hp1 | a0001 | c0001 | t0035 | g0155 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0083 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03209 | hp1 | a0001 | c0001 | t0060 | g0055 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0048 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03453 | hp1 | a0001 | c0001 | t0015 | g0181 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03453 | hp2 | a0001 | c0001 | t0017 | g0066 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0002 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03486 | hp2 | a0001 | c0001 | t0036 | g0160 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03491 | hp2 | a0001 | c0002 | t0007 | g0101 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0306 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0309 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03831 | hp2 | a0001 | c0002 | t0010 | g0088 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03834 | hp1 | a0001 | c0001 | t0014 | g0149 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03834 | hp2 | a0001 | c0002 | t0005 | g0103 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03942 | hp1 | a0001 | c0001 | t0013 | g0286 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03942 | hp2 | a0001 | c0002 | t0006 | g0102 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0267 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0174 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG04228 | hp1 | a0001 | c0001 | t0021 | g0219 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0145 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18906 | hp1 | a0001 | c0002 | t0029 | g0164 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18906 | hp2 | a0001 | c0001 | t0020 | g0179 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18942 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18943 | hp1 | a0001 | c0002 | t0005 | g0094 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18944 | hp1 | a0001 | c0002 | t0007 | g0008 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18944 | hp2 | a0001 | c0001 | t0013 | g0239 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0245 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18950 | hp1 | a0002 | c0003 | t0012 | g0105 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18950 | hp2 | a0001 | c0001 | t0044 | g0241 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18951 | hp1 | a0002 | c0003 | t0012 | g0107 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18953 | hp2 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18960 | hp2 | a0001 | c0001 | t0052 | g0218 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18965 | hp2 | a0001 | c0001 | t0059 | g0153 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18968 | hp2 | a0001 | c0001 | t0054 | g0146 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18969 | hp1 | a0001 | c0001 | t0010 | g0305 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18972 | hp2 | a0001 | c0001 | t0051 | g0127 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18974 | hp1 | a0001 | c0001 | t0025 | g0240 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0130 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18978 | hp1 | a0002 | c0003 | t0012 | g0106 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18981 | hp1 | a0001 | c0002 | t0005 | g0092 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18981 | hp2 | a0001 | c0001 | t0031 | g0148 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18982 | hp1 | a0001 | c0001 | t0009 | g0232 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18984 | hp1 | a0001 | c0002 | t0012 | g0007 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18984 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18986 | hp1 | a0001 | c0001 | t0053 | g0285 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18993 | hp2 | a0001 | c0002 | t0005 | g0008 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0114 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA18999 | hp2 | a0001 | c0001 | t0025 | g0057 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19000 | hp1 | a0001 | c0002 | t0005 | g0095 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19000 | hp2 | a0001 | c0001 | t0013 | g0310 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0134 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0243 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19006 | hp1 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19006 | hp2 | a0001 | c0001 | t0009 | g0314 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19009 | hp2 | a0001 | c0002 | t0005 | g0089 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19011 | hp2 | a0001 | c0001 | t0010 | g0275 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19012 | hp2 | a0001 | c0001 | t0008 | g0133 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19030 | hp1 | a0001 | c0001 | t0020 | g0154 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0077 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0178 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19043 | hp2 | a0001 | c0001 | t0026 | g0071 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0273 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19062 | hp1 | a0001 | c0001 | t0073 | g0183 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19062 | hp2 | a0001 | c0001 | t0022 | g0260 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19064 | hp1 | a0001 | c0002 | t0005 | g0098 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19067 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19074 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19075 | hp2 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19077 | hp2 | a0001 | c0002 | t0027 | g0100 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19080 | hp1 | a0001 | c0001 | t0013 | g0281 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19080 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19081 | hp1 | a0001 | c0006 | t0001 | g0022 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19081 | hp2 | a0001 | c0001 | t0031 | g0147 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19084 | hp2 | a0001 | c0001 | t0008 | g0168 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19087 | hp2 | a0001 | c0001 | t0021 | g0056 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19088 | hp1 | a0001 | c0002 | t0027 | g0080 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19240 | hp1 | a0001 | c0001 | t0046 | g0053 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA19240 | hp2 | a0001 | c0001 | t0066 | g0115 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA20129 | hp1 | a0001 | c0001 | t0033 | g0182 | AFR | ASW | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA20129 | hp2 | a0001 | c0001 | t0033 | g0037 | AFR | ASW | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0207 | EUR | TSI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02109 | hp2 | a0001 | c0001 | t0050 | g0278 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02486 | hp2 | a0001 | c0001 | t0048 | g0002 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0049 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG02559 | hp2 | a0001 | c0001 | t0065 | g0104 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03471 | hp1 | a0001 | c0002 | t0029 | g0163 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG03471 | hp2 | a0001 | c0001 | t0017 | g0058 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG06807 | hp1 | a0001 | c0001 | t0072 | g0198 | AFR | USA | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | USA | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA21309 | hp1 | a0001 | c0001 | t0068 | g0184 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| NA21309 | hp2 | a0001 | c0001 | t0043 | g0109 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0057 | g0208 | REF | REF | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0021 | REF | REF | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15824935 | C | T | 1 | a0002 | 3 | NA18950.hp1 NA18951.hp1 NA18978.hp1 |
missense_variant | MODERATE | c.418C>T | p.Arg140Trp | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/8 | 505/5620 | 418/903 | 140/300 | chr4 | 15824935 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15778483 | A | G | 1 | a0001c0006 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.69A>G | p.Gln23Gln | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/8 | 156/5620 | 69/903 | 23/300 | chr4 | 15778483 | |||
| chr4:15816625 | C | T | 1 | a0001c0004 | 2 | HG00423.hp1 HG00609.hp1 |
synonymous_variant | LOW | c.348C>T | p.Thr116Thr | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/8 | 435/5620 | 348/903 | 116/300 | chr4 | 15816625 | |||
| chr4:15834221 | A | C | 2 | a0001c0002 a0002c0003 |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
synonymous_variant | LOW | c.504A>C | p.Ile168Ile | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/8 | 591/5620 | 504/903 | 168/300 | chr4 | 15834221 | |||
| chr4:15840107 | A | G | 1 | a0001c0005 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.741A>G | p.Arg247Arg | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/8 | 828/5620 | 741/903 | 247/300 | chr4 | 15840107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15778329 | C | A | 1 | a0001c0001t0034 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-86C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/8 | 86 | chr4 | 15778329 | ||||||
| chr4:15848707 | T | G | 7 | a0001c0001t0020 a0001c0001t0035 a0001c0001t0036 others(4): Show |
8 | HG01358.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*105T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 105 | chr4 | 15848707 | ||||||
| chr4:15848740 | T | C | 1 | a0001c0001t0041 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*138T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 138 | chr4 | 15848740 | ||||||
| chr4:15848759 | A | G | 1 | a0001c0001t0073 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*157A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 157 | chr4 | 15848759 | ||||||
| chr4:15848790 | T | C | 1 | a0001c0001t0042 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*188T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 188 | chr4 | 15848790 | ||||||
| chr4:15848936 | C | G | 5 | a0001c0001t0033 a0001c0001t0069 a0001c0001t0070 others(2): Show |
6 | HG02622.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*334C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 334 | chr4 | 15848936 | ||||||
| chr4:15849029 | G | A | 1 | a0001c0001t0043 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*427G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 427 | chr4 | 15849029 | ||||||
| chr4:15849048 | A | G | 1 | a0001c0001t0068 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*446A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 446 | chr4 | 15849048 | ||||||
| chr4:15849062 | C | T | 47 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(44): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*460C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 460 | chr4 | 15849062 | ||||||
| chr4:15849196 | A | T | 1 | a0001c0001t0067 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*594A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 594 | chr4 | 15849196 | ||||||
| chr4:15849526 | C | T | 1 | a0001c0001t0053 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*924C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 924 | chr4 | 15849526 | ||||||
| chr4:15850345 | G | A | 75 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(72): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1743G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 1743 | chr4 | 15850345 | ||||||
| chr4:15850406 | A | T | 2 | a0001c0001t0065 a0001c0001t0066 |
2 | HG02559.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1804A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 1804 | chr4 | 15850406 | ||||||
| chr4:15850481 | T | C | 18 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(15): Show |
64 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1879T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 1879 | chr4 | 15850481 | ||||||
| chr4:15850506 | A | C | 2 | a0001c0001t0017 a0001c0001t0049 |
4 | HG03041.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1904A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 1904 | chr4 | 15850506 | ||||||
| chr4:15850692 | C | T | 1 | a0001c0001t0052 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2090C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2090 | chr4 | 15850692 | ||||||
| chr4:15850704 | C | G | 2 | a0001c0001t0073 a0001c0002t0027 |
3 | NA19062.hp1 NA19077.hp2 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2102C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2102 | chr4 | 15850704 | ||||||
| chr4:15850841 | G | A | 1 | a0001c0001t0056 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2239G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2239 | chr4 | 15850841 | ||||||
| chr4:15851012 | T | C | 1 | a0001c0001t0020 | 2 | NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2410T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2410 | chr4 | 15851012 | ||||||
| chr4:15851174 | G | C | 1 | a0001c0001t0034 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2572G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2572 | chr4 | 15851174 | ||||||
| chr4:15851235 | C | T | 6 | a0001c0001t0026 a0001c0001t0062 a0001c0001t0063 others(3): Show |
7 | HG01243.hp2 HG01433.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2633C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2633 | chr4 | 15851235 | ||||||
| chr4:15851261 | C | T | 2 | a0001c0001t0060 a0001c0001t0061 |
2 | HG02976.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2659C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2659 | chr4 | 15851261 | ||||||
| chr4:15851390 | C | A | 15 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(12): Show |
60 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2788C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2788 | chr4 | 15851390 | ||||||
| chr4:15851617 | A | T | 1 | a0001c0001t0031 | 2 | NA18981.hp2 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3015A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3015 | chr4 | 15851617 | ||||||
| chr4:15851726 | A | G | 3 | a0001c0001t0008 a0001c0001t0025 a0001c0001t0059 |
12 | HG02074.hp1 HG02135.hp1 NA18942.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3124A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3124 | chr4 | 15851726 | ||||||
| chr4:15851759 | G | A | 1 | a0001c0001t0050 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3157G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3157 | chr4 | 15851759 | ||||||
| chr4:15851854 | A | T | 1 | a0001c0001t0049 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3252A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3252 | chr4 | 15851854 | ||||||
| chr4:15851948 | GTATCTAA others(3): Show |
G | 2 | a0001c0001t0062 a0001c0001t0072 |
2 | HG02922.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3359_*3368delTCTA others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3359 | INFO_REALIGN_3_PRIME | chr4 | 15851948 | |||||
| chr4:15852061 | T | C | 22 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(19): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*3459T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3459 | chr4 | 15852061 | ||||||
| chr4:15852343 | G | C | 1 | a0001c0001t0020 | 2 | NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3741G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3741 | chr4 | 15852343 | ||||||
| chr4:15852484 | T | C | 1 | a0001c0001t0070 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3882T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3882 | chr4 | 15852484 | ||||||
| chr4:15852594 | C | A | 1 | a0001c0001t0065 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3992C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3992 | chr4 | 15852594 | ||||||
| chr4:15852607 | C | T | 2 | a0001c0001t0024 a0001c0002t0024 |
2 | HG01884.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4005C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4005 | chr4 | 15852607 | ||||||
| chr4:15852797 | G | A | 37 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(34): Show |
144 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*4195G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4195 | chr4 | 15852797 | ||||||
| chr4:15852809 | C | CT | 14 | a0001c0001t0013 a0001c0001t0015 a0001c0001t0024 others(11): Show |
20 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4225dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4226 | INFO_REALIGN_3_PRIME | chr4 | 15852809 | |||||
| chr4:15852809 | C | CTT | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(14): Show |
73 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4224_*4225dupTT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4226 | INFO_REALIGN_3_PRIME | chr4 | 15852809 | |||||
| chr4:15852809 | C | CTTT | 8 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0016 others(5): Show |
16 | HG01192.hp2 HG01361.hp2 HG01891.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4223_*4225dupTTT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4226 | INFO_REALIGN_3_PRIME | chr4 | 15852809 | |||||
| chr4:15852809 | CT | C | 29 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(26): Show |
134 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*4225delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4225 | INFO_REALIGN_3_PRIME | chr4 | 15852809 | |||||
| chr4:15852843 | G | A | 1 | a0001c0001t0044 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4241G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4241 | chr4 | 15852843 | ||||||
| chr4:15852901 | C | G | 1 | a0001c0002t0037 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4299C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4299 | chr4 | 15852901 | ||||||
| chr4:15852905 | G | T | 2 | a0001c0001t0046 a0001c0002t0029 |
3 | HG03471.hp1 NA18906.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4303G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4303 | chr4 | 15852905 | ||||||
| chr4:15852955 | C | T | 1 | a0001c0001t0064 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4353C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4353 | chr4 | 15852955 | ||||||
| chr4:15853011 | C | T | 4 | a0001c0001t0044 a0001c0001t0054 a0001c0002t0012 others(1): Show |
6 | NA18950.hp1 NA18950.hp2 NA18951.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4409C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4409 | chr4 | 15853011 | ||||||
| chr4:15853102 | G | A | 36 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(33): Show |
138 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*4500G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4500 | chr4 | 15853102 | ||||||
| chr4:15853202 | A | G | 1 | a0001c0001t0026 | 2 | HG01433.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4600A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4600 | chr4 | 15853202 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15778735 | G | A | 25 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.233+88G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778735 | |||||||
| chr4:15778820 | T | G | 207 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(204): Show |
220 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.233+173T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778820 | |||||||
| chr4:15778830 | C | G | 35 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(32): Show |
37 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.233+183C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778830 | |||||||
| chr4:15778862 | C | CG | 86 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0113 others(83): Show |
93 | HG00408.hp1 HG00733.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.233+224dupG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15778862 | ||||||
| chr4:15778862 | C | CGG | 21 | a0001c0001t0001g0167 a0001c0001t0002g0044 a0001c0001t0002g0165 others(18): Show |
21 | HG00438.hp1 HG01169.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.233+223_233+224dup others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15778862 | ||||||
| chr4:15778916 | C | T | 63 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(60): Show |
67 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.233+269C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778916 | |||||||
| chr4:15778962 | G | A | 2 | a0001c0001t0003g0212 a0001c0001t0003g0213 |
2 | NA19079.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.233+315G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778962 | |||||||
| chr4:15779012 | C | T | 2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | NA18956.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.233+365C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779012 | |||||||
| chr4:15779106 | G | A | 9 | a0001c0001t0011g0002 a0001c0001t0011g0048 a0001c0001t0011g0049 others(6): Show |
10 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+459G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779106 | |||||||
| chr4:15779107 | G | C | 9 | a0001c0001t0011g0002 a0001c0001t0011g0048 a0001c0001t0011g0049 others(6): Show |
10 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+460G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779107 | |||||||
| chr4:15779110 | AC | A | 9 | a0001c0001t0011g0002 a0001c0001t0011g0048 a0001c0001t0011g0049 others(6): Show |
10 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+464delC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779110 | |||||||
| chr4:15779463 | G | A | 2 | a0001c0001t0002g0111 a0001c0001t0002g0165 |
2 | HG02055.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.233+816G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779463 | |||||||
| chr4:15779555 | C | T | 1 | a0001c0001t0028g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.233+908C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779555 | |||||||
| chr4:15779701 | T | C | 2 | a0001c0001t0060g0055 a0001c0001t0061g0054 |
2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+1054T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779701 | |||||||
| chr4:15779791 | C | T | 1 | a0001c0001t0043g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.233+1144C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779791 | |||||||
| chr4:15779963 | A | G | 1 | a0001c0002t0016g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.233+1316A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779963 | |||||||
| chr4:15780042 | G | A | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233+1395G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780042 | |||||||
| chr4:15780264 | A | G | 2 | a0001c0001t0003g0023 a0001c0001t0003g0307 |
3 | HG00738.hp2 HG01099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.233+1617A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780264 | |||||||
| chr4:15780298 | A | G | 45 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0020g0154 others(42): Show |
48 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.233+1651A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780298 | |||||||
| chr4:15780302 | C | G | 16 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+1655C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780302 | |||||||
| chr4:15780413 | A | G | 1 | a0001c0001t0004g0306 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.233+1766A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780413 | |||||||
| chr4:15780518 | T | TCA | 7 | a0001c0001t0001g0019 a0001c0001t0001g0277 a0001c0001t0001g0279 others(4): Show |
8 | HG00280.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+1920_233+1921d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780518 | T | TCACACAC others(11): Show |
4 | a0001c0001t0015g0068 a0001c0001t0017g0066 a0001c0001t0023g0067 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(20): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780518 | T | TCACACAC others(15): Show |
4 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0016g0064 others(1): Show |
4 | HG01891.hp2 HG02896.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(24): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780518 | T | TCACACAC others(17): Show |
4 | a0001c0001t0016g0077 a0001c0001t0026g0071 a0001c0001t0026g0072 others(1): Show |
4 | HG01433.hp2 HG03098.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(26): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780518 | T | TCACACAC others(21): Show |
3 | a0001c0001t0002g0074 a0001c0001t0028g0076 a0001c0001t0067g0075 |
3 | HG01243.hp2 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.233+1882_233+1883i others(30): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780518 | TCA | T | 104 | a0001c0001t0001g0018 a0001c0001t0001g0137 a0001c0001t0001g0217 others(101): Show |
111 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.233+1920_233+1921d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780518 | TCACA | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(86): Show |
93 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.233+1918_233+1921d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780518 | TCACACA | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0024 others(33): Show |
36 | HG00741.hp1 HG01192.hp1 HG02622.hp2 others(33): Show |
intron_variant | MODIFIER | c.233+1916_233+1921d others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780518 | TCACACAC others(1): Show |
T | 9 | a0001c0001t0001g0215 a0001c0001t0001g0244 a0001c0001t0001g0247 others(6): Show |
9 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+1914_233+1921d others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780518 | TCACACAC others(13): Show |
T | 1 | a0001c0001t0001g0223 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.233+1902_233+1921d others(22): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | ||||||
| chr4:15780524 | A | ACACACG | 3 | a0001c0002t0004g0079 a0001c0002t0005g0081 a0001c0002t0027g0080 |
3 | HG01928.hp2 NA19074.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.233+1882_233+1883i others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780524 | ||||||
| chr4:15780524 | A | T | 2 | a0001c0001t0005g0235 a0001c0001t0021g0056 |
2 | NA18952.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.233+1877A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780524 | |||||||
| chr4:15780526 | A | ACACG | 25 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0158 others(22): Show |
28 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780526 | ||||||
| chr4:15780526 | A | T | 3 | a0001c0001t0001g0022 a0001c0001t0010g0305 a0001c0006t0001g0022 |
3 | NA18969.hp1 NA18970.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.233+1879A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780526 | |||||||
| chr4:15780528 | A | ACG | 11 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780528 | ||||||
| chr4:15780528 | A | ACGCACAC others(25): Show |
1 | a0001c0001t0004g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+1882_233+1883i others(34): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780528 | ||||||
| chr4:15780528 | A | ACGCG | 3 | a0002c0003t0012g0105 a0002c0003t0012g0106 a0002c0003t0012g0107 |
3 | NA18950.hp1 NA18951.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.233+1882_233+1883i others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780528 | ||||||
| chr4:15780530 | A | G | 13 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0207 others(10): Show |
13 | HG02145.hp2 HG02559.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+1883A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780530 | |||||||
| chr4:15780532 | A | G | 98 | a0001c0001t0001g0137 a0001c0001t0001g0297 a0001c0001t0002g0010 others(95): Show |
104 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.233+1885A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780532 | |||||||
| chr4:15780534 | A | G | 114 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0137 others(111): Show |
123 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.233+1887A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780534 | |||||||
| chr4:15780536 | A | G | 29 | a0001c0001t0001g0024 a0001c0001t0001g0113 a0001c0001t0001g0167 others(26): Show |
29 | HG01361.hp1 HG01891.hp2 HG02165.hp2 others(26): Show |
intron_variant | MODIFIER | c.233+1889A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780536 | |||||||
| chr4:15780538 | A | G | 6 | a0001c0001t0001g0113 a0001c0001t0017g0058 a0001c0001t0034g0112 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+1891A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780538 | |||||||
| chr4:15780540 | A | G | 1 | a0001c0001t0063g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.233+1893A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780540 | |||||||
| chr4:15780563 | C | T | 10 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+1916C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780563 | |||||||
| chr4:15780918 | G | A | 2 | a0001c0001t0007g0116 a0001c0001t0066g0115 |
2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.233+2271G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780918 | |||||||
| chr4:15781070 | G | T | 4 | a0001c0001t0030g0040 a0001c0001t0064g0038 a0001c0001t0069g0043 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+2423G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781070 | |||||||
| chr4:15781270 | T | C | 1 | a0001c0001t0019g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.233+2623T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781270 | |||||||
| chr4:15781339 | T | C | 1 | a0001c0001t0015g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233+2692T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781339 | |||||||
| chr4:15781358 | G | C | 16 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+2711G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781358 | |||||||
| chr4:15781595 | T | C | 1 | a0001c0001t0016g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.233+2948T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781595 | |||||||
| chr4:15782043 | G | A | 1 | a0001c0001t0055g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233+3396G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782043 | |||||||
| chr4:15782364 | T | A | 1 | a0001c0001t0009g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.233+3717T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782364 | |||||||
| chr4:15782595 | G | A | 1 | a0001c0002t0003g0083 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.233+3948G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782595 | |||||||
| chr4:15782600 | G | A | 5 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(2): Show |
5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+3953G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782600 | |||||||
| chr4:15782639 | C | T | 1 | a0001c0001t0013g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.233+3992C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782639 | |||||||
| chr4:15782764 | T | C | 2 | a0001c0001t0056g0303 a0001c0001t0058g0302 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.233+4117T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782764 | |||||||
| chr4:15782975 | T | C | 53 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+4328T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782975 | |||||||
| chr4:15783256 | G | A | 1 | a0001c0002t0007g0101 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.233+4609G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783256 | |||||||
| chr4:15783278 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.233+4631G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783278 | |||||||
| chr4:15783393 | G | C | 53 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+4746G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783393 | |||||||
| chr4:15783404 | T | C | 1 | a0001c0002t0024g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.233+4757T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783404 | |||||||
| chr4:15783528 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.233+4881T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783528 | |||||||
| chr4:15783578 | C | T | 140 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(137): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.233+4931C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783578 | |||||||
| chr4:15783698 | G | A | 21 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(18): Show |
23 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.233+5051G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783698 | |||||||
| chr4:15783715 | T | C | 2 | a0001c0001t0026g0071 a0001c0001t0026g0072 |
2 | HG01433.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.233+5068T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783715 | |||||||
| chr4:15784036 | C | T | 20 | a0001c0001t0001g0297 a0001c0001t0003g0023 a0001c0001t0003g0287 others(17): Show |
21 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.233+5389C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784036 | |||||||
| chr4:15784063 | C | T | 2 | a0001c0001t0009g0178 a0001c0001t0010g0300 |
2 | HG02083.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+5416C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784063 | |||||||
| chr4:15784288 | G | A | 16 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+5641G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784288 | |||||||
| chr4:15784379 | C | A | 67 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(64): Show |
72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.233+5732C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784379 | |||||||
| chr4:15784452 | C | T | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+5805C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784452 | |||||||
| chr4:15784525 | G | C | 206 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(203): Show |
219 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.233+5878G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784525 | |||||||
| chr4:15784532 | C | T | 1 | a0001c0001t0059g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.233+5885C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784532 | |||||||
| chr4:15784605 | A | G | 1 | a0001c0001t0053g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.233+5958A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784605 | |||||||
| chr4:15784661 | A | G | 1 | a0001c0001t0006g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.233+6014A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784661 | |||||||
| chr4:15784701 | T | C | 139 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(136): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+6054T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784701 | |||||||
| chr4:15784785 | C | T | 35 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(32): Show |
37 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.233+6138C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784785 | |||||||
| chr4:15784884 | C | T | 53 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+6237C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784884 | |||||||
| chr4:15784885 | G | A | 28 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(25): Show |
30 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.233+6238G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784885 | |||||||
| chr4:15784900 | A | T | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(31): Show |
36 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.233+6253A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784900 | |||||||
| chr4:15784970 | C | T | 53 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+6323C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784970 | |||||||
| chr4:15784998 | A | G | 139 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(136): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+6351A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784998 | |||||||
| chr4:15785055 | T | TA | 189 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(186): Show |
202 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.233+6420dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785055 | ||||||
| chr4:15785055 | T | TAA | 6 | a0001c0001t0004g0065 a0001c0001t0007g0197 a0001c0001t0017g0058 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+6419_233+6420d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785055 | ||||||
| chr4:15785093 | A | G | 10 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+6446A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785093 | |||||||
| chr4:15785148 | T | C | 3 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0036g0160 |
3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.233+6501T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785148 | |||||||
| chr4:15785157 | A | T | 139 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(136): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+6510A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785157 | |||||||
| chr4:15785191 | T | C | 1 | a0001c0001t0004g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.233+6544T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785191 | |||||||
| chr4:15785208 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.233+6561T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785208 | |||||||
| chr4:15785257 | G | C | 2 | a0001c0001t0026g0071 a0001c0001t0026g0072 |
2 | HG01433.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.233+6610G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785257 | |||||||
| chr4:15785403 | C | T | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+6756C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785403 | |||||||
| chr4:15785459 | A | G | 139 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(136): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+6812A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785459 | |||||||
| chr4:15785463 | C | A | 10 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+6816C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785463 | |||||||
| chr4:15785539 | C | CTTTCTT | 105 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(102): Show |
112 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.233+6895_233+6896i others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785539 | ||||||
| chr4:15785539 | C | CTTTCTTT | 21 | a0001c0001t0002g0074 a0001c0001t0002g0196 a0001c0001t0004g0065 others(18): Show |
21 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.233+6895_233+6896i others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785539 | ||||||
| chr4:15785543 | T | C | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+6896T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785543 | |||||||
| chr4:15785591 | T | C | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+6944T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785591 | |||||||
| chr4:15785651 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.233+7004G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785651 | |||||||
| chr4:15785750 | T | C | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+7103T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785750 | |||||||
| chr4:15785819 | T | C | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+7172T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785819 | |||||||
| chr4:15785853 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.233+7206A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785853 | |||||||
| chr4:15785897 | C | T | 1 | a0001c0001t0043g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.233+7250C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785897 | |||||||
| chr4:15785905 | C | T | 13 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+7258C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785905 | |||||||
| chr4:15785991 | G | A | 2 | a0001c0001t0019g0159 a0001c0001t0042g0082 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.233+7344G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785991 | |||||||
| chr4:15785993 | G | A | 1 | a0001c0001t0002g0308 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.233+7346G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785993 | |||||||
| chr4:15785993 | GTCTGGAG others(16): Show |
G | 4 | a0001c0001t0001g0284 a0001c0001t0003g0212 a0001c0001t0003g0213 others(1): Show |
4 | HG03927.hp2 NA19079.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+7368_233+7390d others(25): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785993 | ||||||
| chr4:15786007 | G | C | 18 | a0001c0001t0001g0297 a0001c0001t0003g0023 a0001c0001t0003g0287 others(15): Show |
19 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.233+7360G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786007 | |||||||
| chr4:15786061 | G | C | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+7414G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786061 | |||||||
| chr4:15786088 | T | C | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+7441T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786088 | |||||||
| chr4:15786175 | T | A | 125 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(122): Show |
132 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.233+7528T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786175 | |||||||
| chr4:15786203 | G | A | 1 | a0001c0001t0043g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.233+7556G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786203 | |||||||
| chr4:15786284 | C | A | 2 | a0001c0001t0014g0210 a0001c0001t0072g0198 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.233+7637C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786284 | |||||||
| chr4:15786284 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.233+7637C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786284 | |||||||
| chr4:15786332 | C | T | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+7685C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786332 | |||||||
| chr4:15786367 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.233+7720C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786367 | |||||||
| chr4:15786557 | C | G | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+7910C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786557 | |||||||
| chr4:15786633 | C | T | 1 | a0001c0001t0033g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+7986C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786633 | |||||||
| chr4:15786700 | C | G | 2 | a0001c0001t0056g0303 a0001c0001t0058g0302 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.233+8053C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786700 | |||||||
| chr4:15786700 | C | T | 17 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(14): Show |
17 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.233+8053C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786700 | |||||||
| chr4:15786733 | G | A | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.233+8086G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786733 | |||||||
| chr4:15786756 | G | T | 1 | a0001c0002t0005g0098 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.233+8109G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786756 | |||||||
| chr4:15786780 | G | A | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+8133G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786780 | |||||||
| chr4:15786781 | C | T | 36 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(33): Show |
38 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.233+8134C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786781 | |||||||
| chr4:15786782 | G | A | 2 | a0001c0001t0008g0114 a0001c0001t0008g0168 |
2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.233+8135G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786782 | |||||||
| chr4:15786848 | C | T | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+8201C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786848 | |||||||
| chr4:15786860 | C | T | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+8213C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786860 | |||||||
| chr4:15786889 | C | T | 1 | a0001c0001t0013g0281 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.233+8242C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786889 | |||||||
| chr4:15786916 | G | A | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+8269G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786916 | |||||||
| chr4:15786968 | G | C | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+8321G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786968 | |||||||
| chr4:15786985 | G | A | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+8338G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786985 | |||||||
| chr4:15786999 | G | A | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+8352G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786999 | |||||||
| chr4:15787018 | GGCCGCTC others(1): Show |
G | 10 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+8373_233+8380d others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15787018 | ||||||
| chr4:15787028 | A | T | 10 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+8381A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787028 | |||||||
| chr4:15787030 | T | A | 10 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+8383T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787030 | |||||||
| chr4:15787096 | C | A | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+8449C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787096 | |||||||
| chr4:15787102 | T | G | 226 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(223): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.233+8455T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787102 | |||||||
| chr4:15787202 | G | A | 55 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0002g0010 others(52): Show |
60 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.233+8555G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787202 | |||||||
| chr4:15787251 | G | T | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+8604G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787251 | |||||||
| chr4:15787262 | T | C | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+8615T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787262 | |||||||
| chr4:15787364 | G | A | 10 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+8717G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787364 | |||||||
| chr4:15787436 | C | G | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+8789C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787436 | |||||||
| chr4:15787508 | C | T | 2 | a0001c0001t0004g0036 a0001c0001t0033g0037 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.233+8861C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787508 | |||||||
| chr4:15787665 | T | C | 7 | a0001c0001t0003g0287 a0001c0001t0003g0289 a0001c0001t0003g0290 others(4): Show |
7 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+9018T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787665 | |||||||
| chr4:15787694 | C | T | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+9047C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787694 | |||||||
| chr4:15787767 | G | T | 1 | a0001c0001t0046g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.233+9120G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787767 | |||||||
| chr4:15787792 | A | G | 205 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(202): Show |
218 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.233+9145A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787792 | |||||||
| chr4:15787837 | G | A | 11 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(8): Show |
11 | HG01243.hp2 HG01891.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.233+9190G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787837 | |||||||
| chr4:15787857 | G | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(314): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.233+9210G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787857 | |||||||
| chr4:15787992 | C | T | 2 | a0001c0001t0003g0299 a0001c0001t0010g0298 |
2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.233+9345C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787992 | |||||||
| chr4:15788132 | C | T | 1 | a0001c0001t0014g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.233+9485C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788132 | |||||||
| chr4:15788485 | CCAAA | C | 25 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.233+9841_233+9844d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15788485 | ||||||
| chr4:15788530 | A | C | 1 | a0001c0001t0002g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233+9883A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788530 | |||||||
| chr4:15788530 | A | G | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+9883A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788530 | |||||||
| chr4:15788715 | A | T | 1 | a0001c0002t0005g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.233+10068A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788715 | |||||||
| chr4:15788746 | G | A | 1 | a0001c0002t0009g0085 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.233+10099G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788746 | |||||||
| chr4:15788823 | A | G | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+10176A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788823 | |||||||
| chr4:15788970 | A | G | 5 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(2): Show |
5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+10323A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788970 | |||||||
| chr4:15788991 | C | A | 130 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(127): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.233+10344C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788991 | |||||||
| chr4:15789022 | G | A | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+10375G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789022 | |||||||
| chr4:15789064 | G | A | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+10417G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789064 | |||||||
| chr4:15789151 | A | C | 1 | a0001c0001t0009g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.233+10504A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789151 | |||||||
| chr4:15789151 | A | G | 138 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(135): Show |
146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.233+10504A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789151 | |||||||
| chr4:15789252 | A | G | 13 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+10605A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789252 | |||||||
| chr4:15789376 | A | C | 14 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(11): Show |
14 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+10729A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789376 | |||||||
| chr4:15789798 | CCT | C | 27 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(24): Show |
29 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.233+11152_233+1115 others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789798 | |||||||
| chr4:15789841 | G | T | 126 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+11194G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789841 | |||||||
| chr4:15790103 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.233+11456C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790103 | |||||||
| chr4:15790104 | G | GCTCTCC | 6 | a0001c0001t0001g0284 a0001c0001t0001g0297 a0001c0001t0002g0142 others(3): Show |
6 | HG00621.hp1 HG01081.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+11507_233+1151 others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790104 | ||||||
| chr4:15790104 | GCTCTCC | G | 9 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0220 others(6): Show |
9 | HG01261.hp2 HG01978.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.233+11507_233+1151 others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790104 | ||||||
| chr4:15790104 | GCTCTCCC others(5): Show |
G | 1 | a0001c0001t0003g0290 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.233+11501_233+1151 others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790104 | ||||||
| chr4:15790104 | GCTCTCCC others(23): Show |
G | 1 | a0001c0001t0014g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233+11483_233+1151 others(34): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790104 | ||||||
| chr4:15790118 | TCTCCCTC others(47): Show |
T | 4 | a0001c0001t0017g0058 a0001c0001t0060g0055 a0001c0001t0061g0054 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+11477_233+1153 others(58): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790118 | ||||||
| chr4:15790124 | TCTCCCTC others(41): Show |
T | 118 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(115): Show |
125 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.233+11483_233+1153 others(52): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790124 | ||||||
| chr4:15790125 | C | CTCCCTT | 60 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(57): Show |
63 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.233+11483_233+1148 others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790125 | ||||||
| chr4:15790125 | C | T | 2 | a0001c0001t0002g0140 a0001c0001t0006g0150 |
2 | NA19054.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.233+11478C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790125 | |||||||
| chr4:15790127 | CCCTCTCC others(40): Show |
C | 2 | a0001c0001t0002g0026 a0001c0001t0005g0025 |
2 | HG03927.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.233+11483_233+1152 others(51): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790127 | ||||||
| chr4:15790131 | C | T | 4 | a0001c0001t0006g0117 a0001c0001t0006g0141 a0001c0001t0008g0004 others(1): Show |
6 | NA18942.hp1 NA18945.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.233+11484C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790131 | |||||||
| chr4:15790140 | CCTCTCCC others(17): Show |
C | 13 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+11495_233+1151 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790140 | ||||||
| chr4:15790142 | TCTCCCTC others(17): Show |
T | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+11501_233+1152 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790142 | ||||||
| chr4:15790154 | TCTCCCCC others(11): Show |
T | 1 | a0001c0001t0014g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233+11517_233+1153 others(22): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790154 | ||||||
| chr4:15790178 | C | T | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+11531C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790178 | |||||||
| chr4:15790194 | T | C | 13 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+11547T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790194 | |||||||
| chr4:15790214 | G | A | 1 | a0001c0001t0073g0183 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.233+11567G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790214 | |||||||
| chr4:15790244 | A | G | 23 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(20): Show |
25 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.233+11597A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790244 | |||||||
| chr4:15790293 | C | T | 1 | a0001c0001t0033g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+11646C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790293 | |||||||
| chr4:15790308 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.233+11661G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790308 | |||||||
| chr4:15790312 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.233+11665G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790312 | |||||||
| chr4:15790325 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+11678G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790325 | |||||||
| chr4:15790345 | G | GT | 28 | a0001c0001t0001g0220 a0001c0001t0001g0271 a0001c0001t0001g0272 others(25): Show |
30 | HG00438.hp1 HG01192.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.233+11710dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790345 | ||||||
| chr4:15790359 | G | A | 1 | a0001c0001t0033g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+11712G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790359 | |||||||
| chr4:15790421 | G | C | 36 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(33): Show |
39 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+11774G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790421 | |||||||
| chr4:15790424 | G | A | 16 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+11777G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790424 | |||||||
| chr4:15790430 | G | A | 1 | a0001c0001t0003g0186 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.233+11783G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790430 | |||||||
| chr4:15790466 | G | A | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.233+11819G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790466 | |||||||
| chr4:15790493 | G | A | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+11846G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790493 | |||||||
| chr4:15790508 | C | T | 1 | a0001c0001t0055g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233+11861C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790508 | |||||||
| chr4:15790553 | T | C | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+11906T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790553 | |||||||
| chr4:15790560 | C | G | 35 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(32): Show |
37 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.233+11913C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790560 | |||||||
| chr4:15790596 | A | AC | 5 | a0001c0001t0001g0223 a0001c0001t0002g0121 a0001c0001t0002g0169 others(2): Show |
5 | HG01243.hp1 HG01952.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+11953dupC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790596 | ||||||
| chr4:15790600 | C | T | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+11953C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790600 | |||||||
| chr4:15790640 | G | C | 1 | a0001c0001t0001g0224 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.233+11993G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790640 | |||||||
| chr4:15790690 | G | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0177 |
3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.233+12043G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790690 | |||||||
| chr4:15790734 | C | G | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+12087C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790734 | |||||||
| chr4:15790745 | C | T | 2 | a0001c0001t0019g0159 a0001c0001t0042g0082 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.233+12098C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790745 | |||||||
| chr4:15790748 | C | T | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+12101C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790748 | |||||||
| chr4:15790814 | A | G | 139 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(136): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+12167A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790814 | |||||||
| chr4:15790844 | G | A | 1 | a0001c0002t0004g0079 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.233+12197G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790844 | |||||||
| chr4:15790890 | T | C | 139 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(136): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+12243T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790890 | |||||||
| chr4:15790909 | C | T | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+12262C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790909 | |||||||
| chr4:15790977 | C | T | 1 | a0001c0001t0055g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233+12330C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790977 | |||||||
| chr4:15790981 | G | A | 64 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(61): Show |
69 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.233+12334G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790981 | |||||||
| chr4:15791013 | C | T | 36 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(33): Show |
39 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+12366C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791013 | |||||||
| chr4:15791014 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.233+12367G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791014 | |||||||
| chr4:15791018 | G | A | 2 | a0001c0001t0004g0293 a0001c0001t0010g0300 |
2 | HG02071.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.233+12371G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791018 | |||||||
| chr4:15791038 | G | A | 1 | a0001c0001t0016g0077 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.233+12391G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791038 | |||||||
| chr4:15791044 | T | TG | 39 | a0001c0001t0001g0024 a0001c0001t0001g0167 a0001c0001t0001g0228 others(36): Show |
41 | HG00408.hp1 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.233+12406dupG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791044 | ||||||
| chr4:15791051 | G | A | 1 | a0001c0001t0003g0304 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.233+12404G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791051 | |||||||
| chr4:15791051 | G | T | 2 | a0001c0001t0021g0056 a0001c0001t0025g0057 |
2 | NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.233+12404G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791051 | |||||||
| chr4:15791075 | T | C | 92 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(89): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.233+12428T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791075 | |||||||
| chr4:15791108 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.233+12461C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791108 | |||||||
| chr4:15791159 | G | A | 3 | a0001c0002t0003g0003 a0001c0002t0003g0087 a0001c0002t0010g0088 |
5 | HG02083.hp1 HG02135.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+12512G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791159 | |||||||
| chr4:15791177 | GGGGTCAG others(620): Show |
G | 1 | a0001c0001t0002g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.233+12560_233+1318 others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791177 | ||||||
| chr4:15791194 | C | T | 16 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+12547C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791194 | |||||||
| chr4:15791207 | A | C | 1 | a0001c0001t0004g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12560A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791207 | |||||||
| chr4:15791207 | A | T | 33 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(30): Show |
35 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.233+12560A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791207 | |||||||
| chr4:15791207 | AGTCCGGG others(71): Show |
A | 86 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(83): Show |
91 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.233+12571_233+1264 others(82): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791207 | ||||||
| chr4:15791208 | G | A | 33 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(30): Show |
35 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.233+12561G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791208 | |||||||
| chr4:15791211 | C | CGGGA | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12567_233+1257 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791211 | ||||||
| chr4:15791212 | G | A | 33 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(30): Show |
35 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.233+12565G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791212 | |||||||
| chr4:15791217 | GT | G | 4 | a0001c0001t0002g0027 a0001c0001t0004g0078 a0001c0001t0017g0058 others(1): Show |
4 | HG00408.hp1 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+12571delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791217 | |||||||
| chr4:15791220 | A | G | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12573A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791220 | |||||||
| chr4:15791223 | G | T | 4 | a0001c0001t0002g0027 a0001c0001t0004g0078 a0001c0001t0017g0058 others(1): Show |
4 | HG00408.hp1 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+12576G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791223 | |||||||
| chr4:15791224 | GCGCCTCT others(17): Show |
G | 3 | a0001c0001t0004g0078 a0001c0001t0017g0058 a0002c0003t0012g0106 |
3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12578_233+1260 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791224 | |||||||
| chr4:15791224 | GCGCCTCT others(69): Show |
G | 1 | a0001c0001t0002g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.233+12578_233+1265 others(80): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791224 | |||||||
| chr4:15791226 | G | C | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12579G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791226 | |||||||
| chr4:15791228 | C | G | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12581C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791228 | |||||||
| chr4:15791229 | T | C | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12582T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791229 | |||||||
| chr4:15791232 | G | C | 1 | a0001c0001t0004g0126 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.233+12585G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791232 | |||||||
| chr4:15791233 | C | G | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12586C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791233 | |||||||
| chr4:15791236 | G | A | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12589G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791236 | |||||||
| chr4:15791238 | C | G | 3 | a0001c0001t0002g0016 a0001c0001t0002g0192 a0001c0001t0002g0196 |
3 | NA18943.hp2 NA18966.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.233+12591C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791238 | |||||||
| chr4:15791243 | C | CA | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12596_233+1259 others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791243 | |||||||
| chr4:15791244 | G | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(226): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.233+12597G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791244 | |||||||
| chr4:15791246 | A | C | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12599A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791246 | |||||||
| chr4:15791247 | C | CGGG | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12600_233+1260 others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791247 | |||||||
| chr4:15791248 | T | A | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12601T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791248 | |||||||
| chr4:15791252 | A | G | 3 | a0001c0001t0004g0078 a0001c0001t0017g0058 a0002c0003t0012g0106 |
3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12605A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791252 | |||||||
| chr4:15791253 | A | G | 6 | a0001c0001t0004g0078 a0001c0001t0017g0058 a0001c0001t0060g0055 others(3): Show |
6 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+12606A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791253 | |||||||
| chr4:15791256 | G | C | 3 | a0001c0001t0004g0078 a0001c0001t0017g0058 a0002c0003t0012g0106 |
3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12609G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791256 | |||||||
| chr4:15791257 | A | G | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12610A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791257 | |||||||
| chr4:15791258 | GGAGC | G | 3 | a0001c0001t0004g0078 a0001c0001t0017g0058 a0002c0003t0012g0106 |
3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12612_233+1261 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791258 | |||||||
| chr4:15791262 | CCCCTCTG others(493): Show |
C | 33 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(30): Show |
35 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.233+12634_233+1313 others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791262 | ||||||
| chr4:15791265 | CT | C | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12619delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791265 | |||||||
| chr4:15791266 | T | C | 3 | a0001c0001t0004g0078 a0001c0001t0017g0058 a0002c0003t0012g0106 |
3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12619T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791266 | |||||||
| chr4:15791268 | T | C | 6 | a0001c0001t0004g0078 a0001c0001t0017g0058 a0001c0001t0060g0055 others(3): Show |
6 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+12621T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791268 | |||||||
| chr4:15791272 | C | T | 2 | a0001c0001t0056g0303 a0001c0001t0058g0302 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.233+12625C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791272 | |||||||
| chr4:15791273 | G | T | 3 | a0001c0001t0002g0144 a0001c0001t0002g0152 a0001c0001t0019g0145 |
3 | HG02451.hp1 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.233+12626G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791273 | |||||||
| chr4:15791281 | A | G | 6 | a0001c0001t0004g0078 a0001c0001t0017g0058 a0001c0001t0060g0055 others(3): Show |
6 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+12634A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791281 | |||||||
| chr4:15791285 | C | A | 2 | a0001c0001t0017g0058 a0002c0003t0012g0106 |
2 | HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12638C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791285 | |||||||
| chr4:15791297 | G | A | 91 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(88): Show |
96 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.233+12650G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791297 | |||||||
| chr4:15791299 | G | T | 1 | a0001c0001t0004g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12652G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791299 | |||||||
| chr4:15791300 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0004g0078 |
2 | HG01975.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.233+12653A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791300 | |||||||
| chr4:15791300 | A | T | 91 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(88): Show |
96 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.233+12653A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791300 | |||||||
| chr4:15791304 | G | T | 1 | a0001c0001t0053g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.233+12657G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791304 | |||||||
| chr4:15791307 | G | A | 1 | a0002c0003t0012g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.233+12660G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791307 | |||||||
| chr4:15791317 | T | C | 93 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(90): Show |
98 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.233+12670T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791317 | |||||||
| chr4:15791321 | C | T | 14 | a0001c0001t0004g0036 a0001c0001t0020g0154 a0001c0001t0020g0179 others(11): Show |
14 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+12674C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791321 | |||||||
| chr4:15791332 | C | T | 1 | a0001c0005t0007g0029 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.233+12685C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791332 | |||||||
| chr4:15791334 | C | A | 87 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(84): Show |
92 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.233+12687C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791334 | |||||||
| chr4:15791334 | C | T | 1 | a0001c0001t0004g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12687C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791334 | |||||||
| chr4:15791335 | G | A | 1 | a0001c0001t0003g0283 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.233+12688G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791335 | |||||||
| chr4:15791344 | G | A | 5 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(2): Show |
5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+12697G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791344 | |||||||
| chr4:15791351 | GT | G | 91 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0002g0005 others(88): Show |
96 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.233+12705delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791351 | |||||||
| chr4:15791352 | T | G | 2 | a0001c0001t0001g0035 a0002c0003t0012g0106 |
2 | HG03831.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12705T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791352 | |||||||
| chr4:15791357 | G | A | 53 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+12710G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791357 | |||||||
| chr4:15791366 | CCGCCCGG others(69): Show |
C | 1 | a0001c0001t0002g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.233+12721_233+1279 others(80): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791366 | ||||||
| chr4:15791367 | CGCCCGGC others(70): Show |
C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(17): Show |
22 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.233+12729_233+1280 others(81): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791367 | ||||||
| chr4:15791371 | C | T | 2 | a0001c0001t0004g0078 a0001c0001t0063g0059 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.233+12724C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791371 | |||||||
| chr4:15791376 | G | A | 84 | a0001c0001t0002g0074 a0001c0001t0004g0036 a0001c0001t0004g0063 others(81): Show |
88 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.233+12729G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791376 | |||||||
| chr4:15791382 | C | T | 1 | a0001c0001t0004g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12735C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791382 | |||||||
| chr4:15791384 | C | A | 9 | a0001c0001t0004g0036 a0001c0001t0030g0040 a0001c0001t0033g0037 others(6): Show |
9 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.233+12737C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791384 | |||||||
| chr4:15791389 | G | A | 1 | a0001c0001t0033g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+12742G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791389 | |||||||
| chr4:15791394 | GT | G | 71 | a0001c0001t0002g0074 a0001c0001t0004g0036 a0001c0001t0004g0065 others(68): Show |
74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12748delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791394 | |||||||
| chr4:15791400 | G | T | 71 | a0001c0001t0002g0074 a0001c0001t0004g0036 a0001c0001t0004g0065 others(68): Show |
74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12753G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791400 | |||||||
| chr4:15791401 | GCGCCTCT others(17): Show |
G | 71 | a0001c0001t0002g0074 a0001c0001t0004g0036 a0001c0001t0004g0065 others(68): Show |
74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12755_233+1277 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791401 | |||||||
| chr4:15791414 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(194): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.233+12767T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791414 | |||||||
| chr4:15791421 | G | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(194): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.233+12774G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791421 | |||||||
| chr4:15791425 | T | C | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+12778T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791425 | |||||||
| chr4:15791429 | A | G | 71 | a0001c0001t0002g0074 a0001c0001t0004g0036 a0001c0001t0004g0065 others(68): Show |
74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12782A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791429 | |||||||
| chr4:15791430 | A | G | 71 | a0001c0001t0002g0074 a0001c0001t0004g0036 a0001c0001t0004g0065 others(68): Show |
74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12783A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791430 | |||||||
| chr4:15791433 | G | C | 71 | a0001c0001t0002g0074 a0001c0001t0004g0036 a0001c0001t0004g0065 others(68): Show |
74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12786G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791433 | |||||||
| chr4:15791435 | GGAC | G | 71 | a0001c0001t0002g0074 a0001c0001t0004g0036 a0001c0001t0004g0065 others(68): Show |
74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12789_233+1279 others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791435 | |||||||
| chr4:15791438 | C | T | 1 | a0001c0001t0004g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12791C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791438 | |||||||
| chr4:15791439 | C | T | 1 | a0001c0001t0006g0117 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.233+12792C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791439 | |||||||
| chr4:15791442 | T | C | 71 | a0001c0001t0002g0074 a0001c0001t0004g0036 a0001c0001t0004g0065 others(68): Show |
74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12795T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791442 | |||||||
| chr4:15791444 | T | C | 72 | a0001c0001t0002g0027 a0001c0001t0002g0074 a0001c0001t0004g0036 others(69): Show |
75 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.233+12797T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791444 | |||||||
| chr4:15791461 | C | A | 1 | a0001c0001t0017g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+12814C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791461 | |||||||
| chr4:15791462 | G | A | 21 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(18): Show |
23 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.233+12815G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791462 | |||||||
| chr4:15791465 | C | A | 3 | a0001c0001t0031g0147 a0001c0001t0031g0148 a0001c0001t0032g0175 |
3 | HG00438.hp1 NA18981.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.233+12818C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791465 | |||||||
| chr4:15791476 | T | C | 1 | a0001c0001t0005g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.233+12829T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791476 | |||||||
| chr4:15791476 | T | TG | 20 | a0001c0001t0001g0020 a0001c0001t0001g0216 a0001c0001t0001g0229 others(17): Show |
20 | HG01099.hp1 HG01192.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.233+12838dupG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791476 | ||||||
| chr4:15791476 | TG | T | 80 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(77): Show |
85 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.233+12838delG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791476 | ||||||
| chr4:15791483 | GGGTCAGC others(191): Show |
G | 1 | a0001c0001t0004g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12837_233+1303 others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791483 | |||||||
| chr4:15791499 | C | T | 2 | a0001c0001t0019g0159 a0001c0001t0042g0082 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.233+12852C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791499 | |||||||
| chr4:15791500 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.233+12853G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791500 | |||||||
| chr4:15791512 | A | C | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0042g0082 others(3): Show |
6 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+12865A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791512 | |||||||
| chr4:15791512 | A | T | 88 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(85): Show |
93 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.233+12865A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791512 | |||||||
| chr4:15791534 | A | G | 4 | a0001c0001t0017g0058 a0001c0001t0060g0055 a0001c0001t0061g0054 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+12887A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791534 | |||||||
| chr4:15791548 | C | T | 89 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(86): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12901C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791548 | |||||||
| chr4:15791559 | C | T | 88 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(85): Show |
93 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.233+12912C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791559 | |||||||
| chr4:15791561 | C | T | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12914C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791561 | |||||||
| chr4:15791565 | CGGGA | C | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12925_233+1292 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791565 | ||||||
| chr4:15791578 | G | A | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12931G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791578 | |||||||
| chr4:15791582 | GGTCA | G | 89 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(86): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12937_233+1294 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791582 | ||||||
| chr4:15791583 | G | A | 13 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+12936G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791583 | |||||||
| chr4:15791587 | G | C | 89 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(86): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12940G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791587 | |||||||
| chr4:15791588 | C | G | 89 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(86): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12941C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791588 | |||||||
| chr4:15791589 | C | G | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12942C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791589 | |||||||
| chr4:15791591 | C | T | 89 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(86): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12944C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791591 | |||||||
| chr4:15791592 | C | T | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12945C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791592 | |||||||
| chr4:15791593 | C | T | 89 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(86): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12946C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791593 | |||||||
| chr4:15791594 | G | T | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12947G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791594 | |||||||
| chr4:15791595 | C | G | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12948C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791595 | |||||||
| chr4:15791597 | C | T | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12950C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791597 | |||||||
| chr4:15791598 | G | T | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12951G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791598 | |||||||
| chr4:15791598 | GGCCA | G | 89 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(86): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12955_233+1295 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791598 | ||||||
| chr4:15791608 | C | T | 3 | a0001c0001t0060g0055 a0001c0001t0061g0054 a0001c0001t0063g0059 |
3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12961C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791608 | |||||||
| chr4:15791610 | C | T | 1 | a0001c0001t0017g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+12963C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791610 | |||||||
| chr4:15791611 | G | GTCCGGGA others(70): Show |
1 | a0001c0001t0046g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.233+12973_233+1297 others(81): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791611 | ||||||
| chr4:15791611 | G | T | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12964G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791611 | |||||||
| chr4:15791612 | T | A | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12965T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791612 | |||||||
| chr4:15791613 | CCGGG | C | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12967_233+1297 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791613 | |||||||
| chr4:15791618 | A | T | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12971A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791618 | |||||||
| chr4:15791620 | G | GT | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12973_233+1297 others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791620 | |||||||
| chr4:15791623 | G | A | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12976G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791623 | |||||||
| chr4:15791625 | T | G | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12978T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791625 | |||||||
| chr4:15791626 | G | GCGCCTCT others(17): Show |
12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12979_233+1298 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791626 | |||||||
| chr4:15791627 | G | A | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12980G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791627 | |||||||
| chr4:15791629 | GGGGTC | G | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12983_233+1298 others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791629 | |||||||
| chr4:15791630 | G | A | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12983G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791630 | |||||||
| chr4:15791631 | G | A | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12984G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791631 | |||||||
| chr4:15791632 | G | A | 1 | a0001c0001t0017g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+12985G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791632 | |||||||
| chr4:15791634 | C | G | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12987C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791634 | |||||||
| chr4:15791636 | G | GGAT | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12989_233+1299 others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791636 | |||||||
| chr4:15791636 | G | T | 90 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12989G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791636 | |||||||
| chr4:15791640 | C | CCCGCCTG others(70): Show |
1 | a0001c0001t0017g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+12994_233+1299 others(81): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791640 | ||||||
| chr4:15791640 | C | T | 102 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(99): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.233+12993C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791640 | |||||||
| chr4:15791642 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0003g0266 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.233+12995T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791642 | |||||||
| chr4:15791660 | G | A | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+13013G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791660 | |||||||
| chr4:15791681 | A | G | 104 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(101): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.233+13034A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791681 | |||||||
| chr4:15791692 | G | A | 2 | a0001c0001t0002g0172 a0001c0001t0018g0011 |
3 | HG00733.hp2 HG01069.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.233+13045G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791692 | |||||||
| chr4:15791695 | T | C | 105 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(102): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13048T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791695 | |||||||
| chr4:15791703 | C | A | 1 | a0001c0001t0063g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.233+13056C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791703 | |||||||
| chr4:15791708 | C | T | 105 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(102): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13061C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791708 | |||||||
| chr4:15791709 | G | A | 105 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(102): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13062G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791709 | |||||||
| chr4:15791713 | G | A | 105 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(102): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13066G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791713 | |||||||
| chr4:15791713 | GGGAGGTG others(119): Show |
G | 1 | a0001c0001t0001g0280 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.233+13115_233+1324 others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791713 | ||||||
| chr4:15791727 | G | A | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+13080G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791727 | |||||||
| chr4:15791761 | A | AG | 105 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(102): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13114_233+1311 others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791761 | |||||||
| chr4:15791762 | T | C | 105 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(102): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13115T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791762 | |||||||
| chr4:15791772 | C | T | 138 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(135): Show |
146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.233+13125C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791772 | |||||||
| chr4:15791780 | C | T | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+13133C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791780 | |||||||
| chr4:15791785 | C | T | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+13138C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791785 | |||||||
| chr4:15791786 | G | A | 125 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(122): Show |
132 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.233+13139G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791786 | |||||||
| chr4:15791789 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.233+13142C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791789 | |||||||
| chr4:15791797 | A | T | 138 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(135): Show |
146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.233+13150A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791797 | |||||||
| chr4:15791804 | A | G | 138 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(135): Show |
146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.233+13157A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791804 | |||||||
| chr4:15791809 | C | T | 138 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(135): Show |
146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.233+13162C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791809 | |||||||
| chr4:15791811 | G | GC | 67 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0001g0137 others(64): Show |
72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.233+13170dupC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791811 | ||||||
| chr4:15791834 | T | C | 138 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(135): Show |
146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.233+13187T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791834 | |||||||
| chr4:15791839 | A | G | 138 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(135): Show |
146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.233+13192A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791839 | |||||||
| chr4:15791855 | C | T | 138 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(135): Show |
146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.233+13208C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791855 | |||||||
| chr4:15791905 | G | C | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13258G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791905 | |||||||
| chr4:15791906 | G | C | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13259G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791906 | |||||||
| chr4:15791911 | C | G | 12 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+13264C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791911 | |||||||
| chr4:15791925 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13278G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791925 | |||||||
| chr4:15791930 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13283G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791930 | |||||||
| chr4:15791932 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13285G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791932 | |||||||
| chr4:15791941 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13294G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791941 | |||||||
| chr4:15791942 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0177 |
3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.233+13295G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791942 | |||||||
| chr4:15791943 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13296G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791943 | |||||||
| chr4:15791945 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13298T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791945 | |||||||
| chr4:15791985 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13338C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791985 | |||||||
| chr4:15791991 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13344G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791991 | |||||||
| chr4:15792003 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13356A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792003 | |||||||
| chr4:15792026 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13379G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792026 | |||||||
| chr4:15792027 | G | T | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13380G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792027 | |||||||
| chr4:15792036 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13389G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792036 | |||||||
| chr4:15792039 | T | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13392T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792039 | |||||||
| chr4:15792075 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13428T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792075 | |||||||
| chr4:15792131 | C | T | 127 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(124): Show |
134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+13484C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792131 | |||||||
| chr4:15792185 | G | A | 6 | a0001c0001t0006g0117 a0001c0001t0006g0141 a0001c0001t0008g0004 others(3): Show |
8 | NA18942.hp1 NA18945.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+13538G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792185 | |||||||
| chr4:15792239 | G | A | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+13592G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792239 | |||||||
| chr4:15792284 | C | G | 1 | a0001c0001t0001g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233+13637C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792284 | |||||||
| chr4:15792339 | G | C | 5 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(2): Show |
5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+13692G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792339 | |||||||
| chr4:15792358 | C | G | 1 | a0001c0001t0055g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233+13711C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792358 | |||||||
| chr4:15792427 | T | A | 205 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(202): Show |
218 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.233+13780T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792427 | |||||||
| chr4:15792432 | T | A | 1 | a0001c0001t0004g0126 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.233+13785T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792432 | |||||||
| chr4:15792432 | T | TA | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.233+13789dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15792432 | ||||||
| chr4:15792437 | T | A | 225 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(222): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.233+13790T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792437 | |||||||
| chr4:15792446 | G | A | 282 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0022 others(279): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.233+13799G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792446 | |||||||
| chr4:15792458 | G | GA | 7 | a0001c0001t0017g0058 a0001c0001t0030g0040 a0001c0001t0034g0112 others(4): Show |
7 | HG02257.hp2 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+13820dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15792458 | ||||||
| chr4:15792463 | A | G | 64 | a0001c0001t0001g0137 a0001c0001t0001g0167 a0001c0001t0002g0010 others(61): Show |
69 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.233+13816A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792463 | |||||||
| chr4:15792467 | AG | A | 3 | a0001c0001t0006g0041 a0001c0001t0009g0178 a0001c0002t0005g0089 |
3 | NA19009.hp2 NA19043.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.233+13821delG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792467 | |||||||
| chr4:15792468 | G | A | 136 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(133): Show |
144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.233+13821G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792468 | |||||||
| chr4:15792486 | G | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0206 |
2 | HG00642.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.233+13839G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792486 | |||||||
| chr4:15792523 | A | C | 1 | a0001c0001t0002g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.233+13876A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792523 | |||||||
| chr4:15792524 | A | C | 1 | a0001c0001t0017g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+13877A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792524 | |||||||
| chr4:15792663 | G | A | 127 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(124): Show |
134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+14016G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792663 | |||||||
| chr4:15792817 | C | T | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.233+14170C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792817 | |||||||
| chr4:15792912 | G | T | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+14265G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792912 | |||||||
| chr4:15792989 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0006g0041 |
2 | NA19057.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.233+14342G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792989 | |||||||
| chr4:15793323 | A | T | 2 | a0001c0001t0003g0268 a0001c0001t0004g0269 |
2 | HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.233+14676A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793323 | |||||||
| chr4:15793369 | C | T | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.233+14722C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793369 | |||||||
| chr4:15793518 | T | A | 1 | a0001c0001t0003g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.233+14871T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793518 | |||||||
| chr4:15793746 | A | T | 3 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0036g0160 |
3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.233+15099A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793746 | |||||||
| chr4:15793859 | C | T | 63 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(60): Show |
68 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.233+15212C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793859 | |||||||
| chr4:15793937 | G | A | 66 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(63): Show |
71 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.233+15290G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793937 | |||||||
| chr4:15793942 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.233+15295T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793942 | |||||||
| chr4:15794020 | T | C | 1 | a0001c0001t0002g0161 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.233+15373T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794020 | |||||||
| chr4:15794140 | G | T | 15 | a0001c0001t0004g0063 a0001c0001t0009g0178 a0001c0001t0011g0002 others(12): Show |
16 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+15493G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794140 | |||||||
| chr4:15794263 | T | A | 36 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(33): Show |
39 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+15616T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794263 | |||||||
| chr4:15794295 | T | G | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+15648T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794295 | |||||||
| chr4:15794345 | C | A | 1 | a0001c0001t0017g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.233+15698C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794345 | |||||||
| chr4:15794358 | C | G | 25 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.233+15711C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794358 | |||||||
| chr4:15794364 | T | G | 2 | a0001c0001t0060g0055 a0001c0001t0061g0054 |
2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+15717T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794364 | |||||||
| chr4:15794403 | A | G | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.233+15756A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794403 | |||||||
| chr4:15794465 | C | T | 18 | a0001c0001t0001g0297 a0001c0001t0003g0023 a0001c0001t0003g0287 others(15): Show |
19 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.233+15818C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794465 | |||||||
| chr4:15794570 | C | G | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.233+15923C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794570 | |||||||
| chr4:15794656 | G | C | 1 | a0001c0001t0018g0011 | 2 | HG00733.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.233+16009G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794656 | |||||||
| chr4:15794710 | A | G | 226 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(223): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.233+16063A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794710 | |||||||
| chr4:15794775 | GA | G | 70 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(67): Show |
75 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.233+16135delA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15794775 | ||||||
| chr4:15795070 | C | A | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+16423C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795070 | |||||||
| chr4:15795218 | C | CGT | 8 | a0001c0001t0002g0026 a0001c0001t0006g0252 a0001c0001t0009g0139 others(5): Show |
8 | HG02145.hp2 HG02559.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+16588_233+1658 others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15795218 | ||||||
| chr4:15795572 | A | G | 1 | a0001c0001t0034g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+16925A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795572 | |||||||
| chr4:15795640 | A | C | 25 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.233+16993A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795640 | |||||||
| chr4:15795712 | A | G | 130 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(127): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.233+17065A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795712 | |||||||
| chr4:15795739 | A | G | 2 | a0001c0001t0056g0303 a0001c0001t0058g0302 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.233+17092A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795739 | |||||||
| chr4:15796081 | T | G | 130 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(127): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.233+17434T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796081 | |||||||
| chr4:15796146 | A | C | 1 | a0001c0001t0041g0292 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.233+17499A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796146 | |||||||
| chr4:15796212 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.233+17565C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796212 | |||||||
| chr4:15796383 | T | C | 130 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(127): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.233+17736T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796383 | |||||||
| chr4:15796399 | A | G | 1 | a0001c0001t0028g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.233+17752A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796399 | |||||||
| chr4:15796448 | T | C | 120 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(117): Show |
127 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.233+17801T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796448 | |||||||
| chr4:15796641 | A | G | 36 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(33): Show |
39 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+17994A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796641 | |||||||
| chr4:15796645 | T | C | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+17998T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796645 | |||||||
| chr4:15796762 | C | T | 124 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(121): Show |
131 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.233+18115C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796762 | |||||||
| chr4:15797064 | T | C | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.233+18417T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797064 | |||||||
| chr4:15797122 | A | G | 124 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(121): Show |
131 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.233+18475A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797122 | |||||||
| chr4:15797320 | A | G | 124 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(121): Show |
131 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.233+18673A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797320 | |||||||
| chr4:15797407 | T | C | 2 | a0001c0001t0008g0114 a0001c0001t0008g0168 |
2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.233+18760T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797407 | |||||||
| chr4:15797584 | C | T | 127 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(124): Show |
134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.234-18927C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797584 | |||||||
| chr4:15797585 | G | A | 1 | a0001c0001t0055g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.234-18926G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797585 | |||||||
| chr4:15797842 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.234-18669G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797842 | |||||||
| chr4:15797910 | T | C | 1 | a0001c0001t0008g0128 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.234-18601T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797910 | |||||||
| chr4:15797927 | G | T | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-18584G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797927 | |||||||
| chr4:15797963 | G | T | 1 | a0001c0001t0024g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.234-18548G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797963 | |||||||
| chr4:15798018 | T | C | 1 | a0001c0001t0070g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234-18493T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798018 | |||||||
| chr4:15798070 | A | C | 25 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.234-18441A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798070 | |||||||
| chr4:15798087 | G | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0177 |
3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.234-18424G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798087 | |||||||
| chr4:15798166 | G | A | 2 | a0001c0001t0035g0155 a0001c0001t0039g0156 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.234-18345G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798166 | |||||||
| chr4:15798218 | C | T | 2 | a0001c0004t0001g0249 a0001c0004t0001g0250 |
2 | HG00423.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.234-18293C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798218 | |||||||
| chr4:15798255 | C | T | 21 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(18): Show |
23 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-18256C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798255 | |||||||
| chr4:15798278 | C | T | 63 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(60): Show |
68 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.234-18233C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798278 | |||||||
| chr4:15798365 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.234-18146T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798365 | |||||||
| chr4:15798540 | G | A | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-17971G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798540 | |||||||
| chr4:15798645 | G | A | 139 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(136): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.234-17866G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798645 | |||||||
| chr4:15798731 | C | T | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-17780C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798731 | |||||||
| chr4:15798895 | T | G | 1 | a0001c0001t0001g0277 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.234-17616T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798895 | |||||||
| chr4:15798961 | C | T | 3 | a0001c0001t0003g0287 a0001c0001t0003g0289 a0001c0001t0010g0288 |
3 | HG01256.hp2 HG01258.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.234-17550C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798961 | |||||||
| chr4:15799167 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.234-17344C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799167 | |||||||
| chr4:15799231 | T | C | 1 | a0001c0001t0003g0304 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.234-17280T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799231 | |||||||
| chr4:15799267 | A | T | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-17244A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799267 | |||||||
| chr4:15799414 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.234-17097T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799414 | |||||||
| chr4:15799588 | A | ATTGGG | 4 | a0001c0001t0002g0016 a0001c0001t0002g0192 a0001c0001t0002g0195 others(1): Show |
5 | NA18943.hp2 NA18954.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-16921_234-1691 others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15799588 | ||||||
| chr4:15799678 | G | T | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-16833G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799678 | |||||||
| chr4:15799713 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.234-16798T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799713 | |||||||
| chr4:15799869 | C | G | 2 | a0001c0001t0035g0155 a0001c0001t0039g0156 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.234-16642C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799869 | |||||||
| chr4:15799888 | G | A | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-16623G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799888 | |||||||
| chr4:15799925 | C | T | 1 | a0001c0001t0070g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234-16586C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799925 | |||||||
| chr4:15800295 | T | G | 61 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(58): Show |
64 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.234-16216T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800295 | |||||||
| chr4:15800311 | G | T | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-16200G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800311 | |||||||
| chr4:15800333 | A | T | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-16178A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800333 | |||||||
| chr4:15800359 | A | G | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-16152A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800359 | |||||||
| chr4:15800590 | T | C | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-15921T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800590 | |||||||
| chr4:15800681 | T | C | 2 | a0001c0002t0029g0163 a0001c0002t0029g0164 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.234-15830T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800681 | |||||||
| chr4:15800912 | C | T | 2 | a0001c0001t0031g0147 a0001c0001t0031g0148 |
2 | NA18981.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.234-15599C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800912 | |||||||
| chr4:15800921 | C | T | 1 | a0001c0001t0053g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.234-15590C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800921 | |||||||
| chr4:15801047 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.234-15464C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801047 | |||||||
| chr4:15801144 | T | TA | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-15366dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15801144 | ||||||
| chr4:15801240 | G | A | 66 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(63): Show |
71 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.234-15271G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801240 | |||||||
| chr4:15801642 | T | C | 130 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(127): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.234-14869T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801642 | |||||||
| chr4:15801664 | A | G | 4 | a0001c0001t0004g0070 a0001c0002t0001g0009 a0001c0002t0001g0096 others(1): Show |
5 | NA18522.hp2 NA18942.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-14847A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801664 | |||||||
| chr4:15801872 | C | G | 1 | a0001c0001t0004g0269 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.234-14639C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801872 | |||||||
| chr4:15801880 | T | C | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-14631T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801880 | |||||||
| chr4:15801915 | G | C | 130 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(127): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.234-14596G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801915 | |||||||
| chr4:15802038 | C | T | 139 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(136): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.234-14473C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802038 | |||||||
| chr4:15802303 | G | T | 1 | a0001c0001t0009g0314 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.234-14208G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802303 | |||||||
| chr4:15802491 | G | GTTTTA | 66 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(63): Show |
70 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.234-13961_234-1395 others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | G | GTTTTATT others(3): Show |
33 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0224 others(30): Show |
33 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.234-13966_234-1395 others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | G | GTTTTATT others(8): Show |
15 | a0001c0001t0001g0137 a0001c0001t0001g0220 a0001c0001t0001g0228 others(12): Show |
15 | HG00642.hp1 HG00741.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.234-13971_234-1395 others(19): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | G | GTTTTATT others(13): Show |
3 | a0001c0001t0001g0223 a0001c0001t0004g0267 a0001c0001t0052g0218 |
3 | HG02523.hp2 HG04115.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.234-13976_234-1395 others(24): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | G | GTTTTATT others(23): Show |
1 | a0001c0001t0002g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.234-13986_234-1395 others(34): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | GTTTTA | G | 45 | a0001c0001t0001g0167 a0001c0001t0002g0010 a0001c0001t0002g0125 others(42): Show |
50 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.234-13961_234-1395 others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | GTTTTATT others(3): Show |
G | 25 | a0001c0001t0002g0015 a0001c0001t0002g0188 a0001c0001t0002g0191 others(22): Show |
26 | HG00099.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.234-13966_234-1395 others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | GTTTTATT others(8): Show |
G | 41 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0187 others(38): Show |
43 | HG00642.hp2 HG00741.hp2 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.234-13971_234-1395 others(19): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | GTTTTATT others(13): Show |
G | 32 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(29): Show |
34 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.234-13976_234-1395 others(24): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | GTTTTATT others(18): Show |
G | 7 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(4): Show |
7 | HG02622.hp2 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-13981_234-1395 others(29): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802491 | GTTTTATT others(33): Show |
G | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-13996_234-1395 others(44): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | ||||||
| chr4:15802774 | A | T | 1 | a0001c0001t0013g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.234-13737A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802774 | |||||||
| chr4:15802817 | T | C | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-13694T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802817 | |||||||
| chr4:15802864 | C | A | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-13647C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802864 | |||||||
| chr4:15803052 | C | T | 21 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(18): Show |
23 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-13459C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803052 | |||||||
| chr4:15803317 | G | A | 1 | a0001c0001t0060g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.234-13194G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803317 | |||||||
| chr4:15803352 | A | C | 3 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0036g0160 |
3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.234-13159A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803352 | |||||||
| chr4:15803414 | G | C | 3 | a0001c0001t0009g0178 a0001c0001t0019g0159 a0001c0001t0042g0082 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-13097G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803414 | |||||||
| chr4:15803445 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.234-13066T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803445 | |||||||
| chr4:15803583 | C | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0142 a0001c0001t0002g0169 others(1): Show |
5 | HG01081.hp2 HG01361.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-12928C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803583 | |||||||
| chr4:15803656 | T | G | 1 | a0001c0001t0004g0256 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.234-12855T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803656 | |||||||
| chr4:15803722 | G | T | 1 | a0001c0001t0002g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.234-12789G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803722 | |||||||
| chr4:15803759 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.234-12752G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803759 | |||||||
| chr4:15803901 | T | C | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-12610T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803901 | |||||||
| chr4:15804011 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.234-12500T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804011 | |||||||
| chr4:15804025 | A | G | 130 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(127): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.234-12486A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804025 | |||||||
| chr4:15804259 | TG | T | 25 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.234-12251delG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804259 | |||||||
| chr4:15804451 | T | C | 62 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(59): Show |
65 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.234-12060T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804451 | |||||||
| chr4:15804636 | A | G | 1 | a0001c0001t0009g0314 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.234-11875A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804636 | |||||||
| chr4:15804717 | G | T | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.234-11794G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804717 | |||||||
| chr4:15804848 | A | G | 1 | a0001c0004t0001g0250 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.234-11663A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804848 | |||||||
| chr4:15804920 | G | A | 1 | a0001c0001t0033g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234-11591G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804920 | |||||||
| chr4:15805097 | G | A | 61 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(58): Show |
64 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.234-11414G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805097 | |||||||
| chr4:15805101 | C | T | 2 | a0001c0002t0029g0163 a0001c0002t0029g0164 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.234-11410C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805101 | |||||||
| chr4:15805148 | A | C | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-11363A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805148 | |||||||
| chr4:15805337 | T | TC | 131 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(128): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-11172dupC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15805337 | ||||||
| chr4:15805346 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.234-11165C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805346 | |||||||
| chr4:15805410 | C | T | 65 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.234-11101C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805410 | |||||||
| chr4:15805477 | A | G | 61 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(58): Show |
64 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.234-11034A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805477 | |||||||
| chr4:15805496 | C | T | 131 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(128): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-11015C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805496 | |||||||
| chr4:15805498 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.234-11013T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805498 | |||||||
| chr4:15805545 | T | C | 2 | a0001c0001t0015g0068 a0001c0001t0023g0067 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234-10966T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805545 | |||||||
| chr4:15805555 | G | A | 1 | a0001c0002t0030g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.234-10956G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805555 | |||||||
| chr4:15805644 | A | G | 1 | a0001c0001t0002g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.234-10867A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805644 | |||||||
| chr4:15805801 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.234-10710T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805801 | |||||||
| chr4:15805933 | C | T | 12 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(9): Show |
13 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.234-10578C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805933 | |||||||
| chr4:15805989 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.234-10522G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805989 | |||||||
| chr4:15805994 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.234-10517T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805994 | |||||||
| chr4:15806133 | C | A | 129 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(126): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.234-10378C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806133 | |||||||
| chr4:15806134 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.234-10377G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806134 | |||||||
| chr4:15806224 | C | G | 6 | a0001c0001t0002g0129 a0001c0001t0002g0140 a0001c0001t0008g0124 others(3): Show |
6 | HG02074.hp1 HG02129.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.234-10287C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806224 | |||||||
| chr4:15806469 | G | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0177 |
3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.234-10042G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806469 | |||||||
| chr4:15806574 | T | C | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.234-9937T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806574 | |||||||
| chr4:15806817 | G | A | 3 | a0001c0001t0002g0172 a0001c0001t0003g0290 a0001c0001t0009g0139 |
3 | HG01081.hp1 HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.234-9694G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806817 | |||||||
| chr4:15806823 | G | A | 2 | a0001c0001t0056g0303 a0001c0001t0058g0302 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.234-9688G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806823 | |||||||
| chr4:15806832 | C | T | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.234-9679C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806832 | |||||||
| chr4:15806971 | C | A | 1 | a0001c0001t0039g0156 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.234-9540C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806971 | |||||||
| chr4:15807105 | G | A | 131 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(128): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-9406G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807105 | |||||||
| chr4:15807113 | T | G | 1 | a0001c0001t0009g0314 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.234-9398T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807113 | |||||||
| chr4:15807228 | T | C | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.234-9283T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807228 | |||||||
| chr4:15807445 | G | A | 49 | a0001c0001t0009g0178 a0001c0001t0017g0058 a0001c0001t0020g0154 others(46): Show |
52 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.234-9066G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807445 | |||||||
| chr4:15807539 | C | G | 47 | a0001c0001t0017g0058 a0001c0001t0020g0154 a0001c0001t0020g0179 others(44): Show |
50 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.234-8972C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807539 | |||||||
| chr4:15807540 | CTGAG | C | 47 | a0001c0001t0017g0058 a0001c0001t0020g0154 a0001c0001t0020g0179 others(44): Show |
50 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.234-8968_234-8965d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15807540 | ||||||
| chr4:15807551 | G | A | 5 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(2): Show |
5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-8960G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807551 | |||||||
| chr4:15807551 | G | C | 82 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(79): Show |
86 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.234-8960G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807551 | |||||||
| chr4:15807555 | G | C | 1 | a0001c0001t0050g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234-8956G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807555 | |||||||
| chr4:15808124 | G | A | 2 | a0001c0001t0009g0178 a0001c0001t0042g0082 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-8387G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808124 | |||||||
| chr4:15808231 | T | G | 49 | a0001c0001t0009g0178 a0001c0001t0017g0058 a0001c0001t0020g0154 others(46): Show |
52 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.234-8280T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808231 | |||||||
| chr4:15808351 | A | G | 131 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(128): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-8160A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808351 | |||||||
| chr4:15808399 | T | C | 27 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(24): Show |
29 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.234-8112T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808399 | |||||||
| chr4:15808585 | A | G | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-7926A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808585 | |||||||
| chr4:15808664 | A | G | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.234-7847A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808664 | |||||||
| chr4:15808765 | A | G | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-7746A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808765 | |||||||
| chr4:15808797 | G | T | 6 | a0001c0001t0001g0024 a0001c0001t0002g0026 a0001c0001t0005g0025 others(3): Show |
6 | HG02027.hp1 HG03927.hp1 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.234-7714G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808797 | |||||||
| chr4:15809004 | T | G | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-7507T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809004 | |||||||
| chr4:15809156 | G | T | 49 | a0001c0001t0009g0178 a0001c0001t0017g0058 a0001c0001t0020g0154 others(46): Show |
52 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.234-7355G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809156 | |||||||
| chr4:15809272 | A | G | 1 | a0001c0001t0054g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.234-7239A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809272 | |||||||
| chr4:15809368 | C | T | 3 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0036g0160 |
3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.234-7143C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809368 | |||||||
| chr4:15809545 | G | T | 2 | a0001c0001t0007g0031 a0001c0001t0007g0045 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.234-6966G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809545 | |||||||
| chr4:15809653 | C | A | 131 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(128): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-6858C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809653 | |||||||
| chr4:15809734 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.234-6777C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809734 | |||||||
| chr4:15809750 | T | C | 129 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(126): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.234-6761T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809750 | |||||||
| chr4:15809819 | T | G | 49 | a0001c0001t0009g0178 a0001c0001t0017g0058 a0001c0001t0020g0154 others(46): Show |
52 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.234-6692T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809819 | |||||||
| chr4:15809909 | C | T | 129 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(126): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.234-6602C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809909 | |||||||
| chr4:15810124 | T | C | 3 | a0001c0001t0001g0233 a0001c0001t0009g0232 a0001c0001t0009g0314 |
3 | NA18982.hp1 NA19006.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.234-6387T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810124 | |||||||
| chr4:15810139 | C | T | 13 | a0001c0001t0009g0178 a0001c0001t0017g0058 a0001c0001t0020g0154 others(10): Show |
13 | HG02559.hp2 HG02572.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.234-6372C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810139 | |||||||
| chr4:15810272 | C | T | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-6239C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810272 | |||||||
| chr4:15810333 | G | A | 1 | a0001c0002t0030g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.234-6178G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810333 | |||||||
| chr4:15810467 | G | A | 2 | a0001c0001t0056g0303 a0001c0001t0058g0302 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.234-6044G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810467 | |||||||
| chr4:15810793 | C | T | 9 | a0001c0001t0017g0058 a0001c0001t0020g0154 a0001c0001t0020g0179 others(6): Show |
9 | HG02965.hp2 HG02970.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.234-5718C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810793 | |||||||
| chr4:15810796 | G | C | 2 | a0001c0001t0002g0074 a0001c0001t0028g0076 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.234-5715G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810796 | |||||||
| chr4:15810808 | C | T | 1 | a0001c0001t0072g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.234-5703C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810808 | |||||||
| chr4:15810834 | G | T | 118 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(115): Show |
125 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.234-5677G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810834 | |||||||
| chr4:15810995 | C | G | 129 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(126): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.234-5516C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810995 | |||||||
| chr4:15811044 | G | A | 129 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(126): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.234-5467G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811044 | |||||||
| chr4:15811232 | C | T | 1 | a0001c0001t0070g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234-5279C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811232 | |||||||
| chr4:15811254 | C | T | 68 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0167 others(65): Show |
73 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.234-5257C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811254 | |||||||
| chr4:15811255 | G | A | 11 | a0001c0001t0009g0178 a0001c0001t0017g0058 a0001c0001t0020g0154 others(8): Show |
11 | HG02572.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-5256G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811255 | |||||||
| chr4:15811266 | AT | A | 80 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(77): Show |
84 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.234-5241delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15811266 | ||||||
| chr4:15811336 | A | G | 11 | a0001c0001t0009g0178 a0001c0001t0017g0058 a0001c0001t0020g0154 others(8): Show |
11 | HG02572.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-5175A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811336 | |||||||
| chr4:15811510 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.234-5001C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811510 | |||||||
| chr4:15811668 | CAGAT | C | 117 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(114): Show |
124 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.234-4840_234-4837d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15811668 | ||||||
| chr4:15811984 | T | G | 173 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(170): Show |
184 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.234-4527T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811984 | |||||||
| chr4:15812008 | A | T | 1 | a0001c0001t0004g0256 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.234-4503A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812008 | |||||||
| chr4:15812087 | A | G | 11 | a0001c0001t0009g0178 a0001c0001t0017g0058 a0001c0001t0019g0159 others(8): Show |
11 | HG02647.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-4424A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812087 | |||||||
| chr4:15812100 | T | A | 173 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(170): Show |
184 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.234-4411T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812100 | |||||||
| chr4:15812322 | C | T | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-4189C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812322 | |||||||
| chr4:15812365 | G | T | 6 | a0001c0001t0002g0129 a0001c0001t0002g0140 a0001c0001t0008g0124 others(3): Show |
6 | HG02074.hp1 HG02129.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.234-4146G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812365 | |||||||
| chr4:15812466 | G | C | 84 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(81): Show |
89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.234-4045G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812466 | |||||||
| chr4:15812479 | C | T | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.234-4032C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812479 | |||||||
| chr4:15812525 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.234-3986G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812525 | |||||||
| chr4:15812684 | G | A | 1 | a0001c0001t0004g0256 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.234-3827G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812684 | |||||||
| chr4:15812686 | C | T | 11 | a0001c0001t0009g0178 a0001c0001t0017g0058 a0001c0001t0019g0159 others(8): Show |
11 | HG02647.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-3825C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812686 | |||||||
| chr4:15812723 | A | G | 30 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0187 others(27): Show |
32 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.234-3788A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812723 | |||||||
| chr4:15812795 | T | A | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-3716T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812795 | |||||||
| chr4:15812956 | C | T | 95 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(92): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.234-3555C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812956 | |||||||
| chr4:15812965 | T | G | 1 | a0001c0001t0031g0147 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.234-3546T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812965 | |||||||
| chr4:15812970 | C | T | 1 | a0001c0001t0043g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.234-3541C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812970 | |||||||
| chr4:15812998 | G | A | 65 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0002g0010 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.234-3513G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812998 | |||||||
| chr4:15813191 | T | C | 81 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(78): Show |
86 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.234-3320T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813191 | |||||||
| chr4:15813299 | C | T | 95 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(92): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.234-3212C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813299 | |||||||
| chr4:15813308 | G | GT | 84 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(81): Show |
89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.234-3196dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15813308 | ||||||
| chr4:15813337 | T | C | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-3174T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813337 | |||||||
| chr4:15813439 | T | A | 1 | a0001c0001t0026g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.234-3072T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813439 | |||||||
| chr4:15813440 | A | T | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-3071A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813440 | |||||||
| chr4:15813623 | G | A | 15 | a0001c0001t0001g0137 a0001c0001t0002g0062 a0001c0001t0002g0121 others(12): Show |
15 | HG01071.hp2 HG01433.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.234-2888G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813623 | |||||||
| chr4:15813658 | C | T | 5 | a0001c0001t0002g0074 a0001c0001t0004g0078 a0001c0001t0022g0047 others(2): Show |
5 | HG01243.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-2853C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813658 | |||||||
| chr4:15813672 | C | T | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-2839C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813672 | |||||||
| chr4:15813690 | G | C | 96 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(93): Show |
101 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.234-2821G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813690 | |||||||
| chr4:15813791 | T | C | 56 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.234-2720T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813791 | |||||||
| chr4:15814168 | C | G | 2 | a0001c0001t0056g0303 a0001c0001t0058g0302 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.234-2343C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814168 | |||||||
| chr4:15814258 | A | G | 86 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(83): Show |
91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.234-2253A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814258 | |||||||
| chr4:15814408 | G | A | 86 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(83): Show |
91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.234-2103G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814408 | |||||||
| chr4:15814618 | T | C | 16 | a0001c0001t0002g0074 a0001c0001t0004g0065 a0001c0001t0004g0070 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.234-1893T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814618 | |||||||
| chr4:15814785 | GTTTTTGT | G | 81 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(78): Show |
86 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.234-1699_234-1693d others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15814785 | ||||||
| chr4:15814812 | GT | G | 10 | a0001c0001t0001g0251 a0001c0001t0017g0058 a0001c0001t0019g0159 others(7): Show |
10 | HG02647.hp2 HG02735.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1687delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15814812 | ||||||
| chr4:15814819 | T | G | 11 | a0001c0001t0001g0228 a0001c0001t0003g0266 a0001c0001t0004g0063 others(8): Show |
12 | HG00741.hp1 HG01106.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-1692T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814819 | |||||||
| chr4:15814838 | G | A | 1 | a0001c0001t0033g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234-1673G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814838 | |||||||
| chr4:15814845 | T | C | 84 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(81): Show |
89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.234-1666T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814845 | |||||||
| chr4:15814876 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.234-1635G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814876 | |||||||
| chr4:15815047 | T | C | 105 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(102): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.234-1464T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815047 | |||||||
| chr4:15815049 | C | T | 84 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(81): Show |
89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.234-1462C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815049 | |||||||
| chr4:15815113 | C | T | 1 | a0001c0001t0023g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.234-1398C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815113 | |||||||
| chr4:15815181 | A | G | 22 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
24 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.234-1330A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815181 | |||||||
| chr4:15815232 | A | T | 19 | a0001c0001t0001g0297 a0001c0001t0003g0023 a0001c0001t0003g0186 others(16): Show |
20 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.234-1279A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815232 | |||||||
| chr4:15815335 | T | C | 1 | a0001c0001t0007g0061 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.234-1176T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815335 | |||||||
| chr4:15815410 | T | G | 5 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1101T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815410 | |||||||
| chr4:15815694 | T | A | 1 | a0001c0001t0004g0309 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.234-817T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815694 | |||||||
| chr4:15815701 | A | G | 105 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(102): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.234-810A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815701 | |||||||
| chr4:15815806 | C | T | 172 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(169): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.234-705C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815806 | |||||||
| chr4:15815833 | T | C | 1 | a0001c0001t0003g0234 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.234-678T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815833 | |||||||
| chr4:15815889 | G | T | 1 | a0001c0001t0015g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.234-622G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815889 | |||||||
| chr4:15815940 | C | T | 2 | a0001c0001t0056g0303 a0001c0001t0058g0302 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.234-571C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815940 | |||||||
| chr4:15816273 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.234-238C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816273 | |||||||
| chr4:15816278 | T | A | 2 | a0001c0001t0001g0217 a0001c0001t0003g0234 |
2 | NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.234-233T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816278 | |||||||
| chr4:15816299 | C | T | 65 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0002g0010 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.234-212C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816299 | |||||||
| chr4:15816355 | G | A | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-156G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816355 | |||||||
| chr4:15816382 | G | A | 1 | a0001c0001t0033g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234-129G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816382 | |||||||
| chr4:15816719 | A | G | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.363+79A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816719 | |||||||
| chr4:15816743 | A | C | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.363+103A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816743 | |||||||
| chr4:15816768 | G | A | 66 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0002g0010 others(63): Show |
71 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.363+128G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816768 | |||||||
| chr4:15816925 | G | A | 58 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(55): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.363+285G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816925 | |||||||
| chr4:15816962 | C | A | 5 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(2): Show |
5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+322C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816962 | |||||||
| chr4:15816973 | C | T | 2 | a0001c0002t0029g0163 a0001c0002t0029g0164 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+333C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816973 | |||||||
| chr4:15817101 | T | A | 1 | a0001c0001t0002g0172 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.363+461T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817101 | |||||||
| chr4:15817216 | G | C | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.363+576G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817216 | |||||||
| chr4:15817229 | T | C | 1 | a0001c0001t0005g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.363+589T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817229 | |||||||
| chr4:15817240 | C | T | 68 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0002g0010 others(65): Show |
73 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.363+600C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817240 | |||||||
| chr4:15817293 | A | G | 67 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0002g0010 others(64): Show |
72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.363+653A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817293 | |||||||
| chr4:15817365 | C | T | 67 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0002g0010 others(64): Show |
72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.363+725C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817365 | |||||||
| chr4:15817510 | A | G | 1 | a0001c0001t0041g0292 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.363+870A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817510 | |||||||
| chr4:15817614 | T | C | 1 | a0001c0001t0009g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.363+974T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817614 | |||||||
| chr4:15817691 | G | A | 1 | a0001c0001t0006g0120 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.363+1051G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817691 | |||||||
| chr4:15817697 | A | T | 5 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1057A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817697 | |||||||
| chr4:15817742 | C | A | 2 | a0001c0001t0014g0149 a0001c0001t0014g0176 |
2 | HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.363+1102C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817742 | |||||||
| chr4:15818084 | A | G | 40 | a0001c0001t0013g0281 a0001c0001t0046g0053 a0001c0001t0065g0104 others(37): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.363+1444A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818084 | |||||||
| chr4:15818103 | G | T | 8 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(5): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+1463G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818103 | |||||||
| chr4:15818155 | G | C | 3 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0158 |
4 | NA18942.hp2 NA18947.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1515G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818155 | |||||||
| chr4:15818227 | G | C | 5 | a0001c0001t0002g0074 a0001c0001t0002g0144 a0001c0001t0002g0152 others(2): Show |
5 | HG02451.hp1 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1587G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818227 | |||||||
| chr4:15818228 | G | A | 46 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(43): Show |
49 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.363+1588G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818228 | |||||||
| chr4:15818279 | T | G | 1 | a0001c0001t0001g0229 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.363+1639T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818279 | |||||||
| chr4:15818293 | C | T | 14 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0004g0078 others(11): Show |
14 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.363+1653C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818293 | |||||||
| chr4:15818557 | A | G | 171 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(168): Show |
182 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.363+1917A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818557 | |||||||
| chr4:15818676 | G | C | 1 | a0001c0002t0006g0102 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.363+2036G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818676 | |||||||
| chr4:15818693 | C | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.363+2053C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818693 | |||||||
| chr4:15818697 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.363+2057A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818697 | |||||||
| chr4:15818747 | C | T | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+2107C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818747 | |||||||
| chr4:15818987 | T | C | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.363+2347T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818987 | |||||||
| chr4:15819035 | A | G | 5 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+2395A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819035 | |||||||
| chr4:15819051 | C | T | 1 | a0001c0001t0013g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.363+2411C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819051 | |||||||
| chr4:15819109 | TCTCA | T | 19 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0189 others(16): Show |
21 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.363+2474_363+2477d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15819109 | ||||||
| chr4:15819118 | T | C | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.363+2478T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819118 | |||||||
| chr4:15819238 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.363+2598C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819238 | |||||||
| chr4:15819305 | A | C | 4 | a0001c0002t0003g0083 a0001c0002t0009g0085 a0001c0002t0016g0108 others(1): Show |
4 | HG01106.hp2 HG01192.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+2665A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819305 | |||||||
| chr4:15819482 | G | A | 1 | a0001c0001t0013g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.363+2842G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819482 | |||||||
| chr4:15819520 | T | A | 1 | a0001c0001t0003g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.363+2880T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819520 | |||||||
| chr4:15819870 | A | G | 1 | a0001c0001t0036g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.363+3230A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819870 | |||||||
| chr4:15819885 | A | T | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.363+3245A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819885 | |||||||
| chr4:15819927 | C | T | 2 | a0001c0001t0065g0104 a0001c0001t0067g0075 |
2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.363+3287C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819927 | |||||||
| chr4:15820008 | C | A | 1 | a0001c0001t0007g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+3368C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820008 | |||||||
| chr4:15820155 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.363+3515G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820155 | |||||||
| chr4:15820410 | T | C | 7 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(4): Show |
7 | HG01358.hp2 HG02965.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+3770T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820410 | |||||||
| chr4:15820675 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.363+4035C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820675 | |||||||
| chr4:15820765 | T | A | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.364-4116T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820765 | |||||||
| chr4:15820839 | C | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.364-4042C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820839 | |||||||
| chr4:15820858 | G | A | 1 | a0001c0001t0043g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.364-4023G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820858 | |||||||
| chr4:15820883 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0230 a0001c0001t0001g0236 others(5): Show |
9 | HG02735.hp1 NA18951.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.364-3998T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820883 | |||||||
| chr4:15821005 | C | T | 67 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(64): Show |
72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.364-3876C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821005 | |||||||
| chr4:15821049 | G | A | 47 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(44): Show |
49 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.364-3832G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821049 | |||||||
| chr4:15821149 | A | G | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-3732A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821149 | |||||||
| chr4:15821220 | G | A | 67 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(64): Show |
72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.364-3661G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821220 | |||||||
| chr4:15821365 | C | A | 1 | a0001c0001t0001g0312 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.364-3516C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821365 | |||||||
| chr4:15821380 | C | CA | 15 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0254 others(12): Show |
18 | HG00140.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.364-3492dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15821380 | ||||||
| chr4:15821439 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.364-3442C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821439 | |||||||
| chr4:15821491 | A | G | 40 | a0001c0001t0013g0281 a0001c0002t0001g0009 a0001c0002t0001g0096 others(37): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.364-3390A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821491 | |||||||
| chr4:15821635 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.364-3246T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821635 | |||||||
| chr4:15821689 | C | T | 1 | a0001c0001t0067g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.364-3192C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821689 | |||||||
| chr4:15821694 | CA | C | 73 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(70): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.364-3169delA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15821694 | ||||||
| chr4:15821694 | CAA | C | 29 | a0001c0001t0004g0063 a0001c0001t0004g0065 a0001c0001t0004g0070 others(26): Show |
30 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.364-3170_364-3169d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15821694 | ||||||
| chr4:15821698 | A | C | 1 | a0001c0001t0039g0156 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.364-3183A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821698 | |||||||
| chr4:15821717 | A | G | 1 | a0001c0001t0067g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.364-3164A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821717 | |||||||
| chr4:15821800 | T | C | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.364-3081T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821800 | |||||||
| chr4:15821821 | C | G | 1 | a0001c0001t0002g0136 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.364-3060C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821821 | |||||||
| chr4:15822270 | T | G | 14 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0004g0078 others(11): Show |
14 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.364-2611T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822270 | |||||||
| chr4:15822341 | G | A | 69 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(66): Show |
74 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.364-2540G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822341 | |||||||
| chr4:15822444 | G | C | 171 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(168): Show |
182 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.364-2437G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822444 | |||||||
| chr4:15822479 | G | A | 2 | a0001c0002t0001g0009 a0001c0002t0001g0158 |
3 | NA18942.hp2 NA18947.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.364-2402G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822479 | |||||||
| chr4:15822532 | T | C | 2 | a0001c0001t0004g0065 a0001c0001t0004g0070 |
2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.364-2349T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822532 | |||||||
| chr4:15822545 | A | G | 2 | a0001c0002t0029g0163 a0001c0002t0029g0164 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-2336A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822545 | |||||||
| chr4:15822630 | A | C | 24 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(21): Show |
26 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.364-2251A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822630 | |||||||
| chr4:15822725 | G | A | 1 | a0001c0004t0001g0250 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.364-2156G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822725 | |||||||
| chr4:15822973 | C | T | 2 | a0001c0001t0002g0172 a0001c0001t0009g0139 |
2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.364-1908C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822973 | |||||||
| chr4:15823053 | G | A | 162 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(159): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.364-1828G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823053 | |||||||
| chr4:15823119 | C | T | 5 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(2): Show |
5 | HG01168.hp2 HG01257.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-1762C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823119 | |||||||
| chr4:15823351 | C | T | 67 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(64): Show |
72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.364-1530C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823351 | |||||||
| chr4:15823408 | T | G | 1 | a0001c0005t0007g0029 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.364-1473T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823408 | |||||||
| chr4:15823417 | C | T | 20 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
22 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.364-1464C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823417 | |||||||
| chr4:15823612 | A | T | 1 | a0001c0001t0001g0312 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.364-1269A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823612 | |||||||
| chr4:15823737 | T | C | 7 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(4): Show |
7 | HG01358.hp2 HG02965.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-1144T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823737 | |||||||
| chr4:15823787 | G | A | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-1094G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823787 | |||||||
| chr4:15823835 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.364-1046A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823835 | |||||||
| chr4:15823899 | A | T | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.364-982A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823899 | |||||||
| chr4:15824005 | A | T | 1 | a0001c0001t0009g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.364-876A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824005 | |||||||
| chr4:15824007 | A | C | 1 | a0001c0001t0001g0312 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.364-874A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824007 | |||||||
| chr4:15824143 | G | A | 1 | a0001c0001t0035g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.364-738G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824143 | |||||||
| chr4:15824228 | G | A | 1 | a0001c0002t0005g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.364-653G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824228 | |||||||
| chr4:15824421 | A | T | 1 | a0001c0001t0046g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.364-460A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824421 | |||||||
| chr4:15824443 | G | C | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-438G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824443 | |||||||
| chr4:15824504 | A | C | 1 | a0001c0001t0062g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.364-377A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824504 | |||||||
| chr4:15824517 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.364-364T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824517 | |||||||
| chr4:15824549 | C | G | 5 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-332C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824549 | |||||||
| chr4:15824561 | G | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0028 a0001c0001t0002g0032 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-320G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824561 | |||||||
| chr4:15824681 | A | AAC | 4 | a0001c0001t0014g0210 a0001c0001t0047g0200 a0001c0001t0056g0303 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-181_364-180dup others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15824681 | ||||||
| chr4:15824681 | AAC | A | 120 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(117): Show |
129 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.364-181_364-180del others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15824681 | ||||||
| chr4:15824681 | AACAC | A | 47 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(44): Show |
49 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.364-183_364-180del others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15824681 | ||||||
| chr4:15824711 | G | A | 1 | a0001c0002t0007g0101 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.364-170G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824711 | |||||||
| chr4:15824739 | A | T | 57 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(54): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.364-142A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824739 | |||||||
| chr4:15824750 | A | C | 1 | a0001c0001t0008g0170 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.364-131A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824750 | |||||||
| chr4:15824760 | C | T | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.364-121C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824760 | |||||||
| chr4:15824792 | G | GT | 58 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(55): Show |
61 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.364-79dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15824792 | ||||||
| chr4:15824842 | A | C | 1 | a0001c0001t0004g0293 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.364-39A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824842 | |||||||
| chr4:15825231 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.499+215G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825231 | |||||||
| chr4:15825264 | A | G | 3 | a0001c0002t0005g0103 a0001c0002t0006g0102 a0001c0002t0007g0101 |
3 | HG03491.hp2 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.499+248A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825264 | |||||||
| chr4:15825561 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.499+545T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825561 | |||||||
| chr4:15825592 | T | C | 1 | a0001c0005t0007g0029 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.499+576T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825592 | |||||||
| chr4:15825878 | C | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.499+862C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825878 | |||||||
| chr4:15825993 | T | C | 24 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(21): Show |
26 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.499+977T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825993 | |||||||
| chr4:15826183 | C | T | 1 | a0001c0001t0010g0300 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.499+1167C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826183 | |||||||
| chr4:15826300 | G | A | 18 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(15): Show |
20 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.499+1284G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826300 | |||||||
| chr4:15826307 | T | C | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.499+1291T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826307 | |||||||
| chr4:15826450 | CTT | C | 70 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(67): Show |
75 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.499+1437_499+1438d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826450 | ||||||
| chr4:15826453 | T | G | 4 | a0001c0001t0002g0028 a0001c0001t0002g0144 a0001c0001t0014g0176 others(1): Show |
4 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1437T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826453 | |||||||
| chr4:15826456 | T | C | 4 | a0001c0001t0002g0028 a0001c0001t0002g0144 a0001c0001t0014g0176 others(1): Show |
4 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1440T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826456 | |||||||
| chr4:15826456 | T | TGCGCAC | 8 | a0001c0002t0001g0158 a0001c0002t0004g0079 a0001c0002t0005g0093 others(5): Show |
8 | HG00423.hp2 HG01106.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+1441_499+1446d others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826456 | ||||||
| chr4:15826457 | G | GCGCA | 8 | a0001c0001t0007g0061 a0001c0001t0009g0178 a0001c0001t0013g0281 others(5): Show |
8 | HG02027.hp1 HG02622.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+1443_499+1446d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826457 | ||||||
| chr4:15826459 | G | A | 4 | a0001c0001t0002g0028 a0001c0001t0002g0144 a0001c0001t0014g0176 others(1): Show |
4 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1443G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826459 | |||||||
| chr4:15826459 | G | GCA | 24 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0188 others(21): Show |
26 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.499+1481_499+1482d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | G | GCACA | 10 | a0001c0001t0002g0189 a0001c0001t0002g0193 a0001c0001t0002g0203 others(7): Show |
10 | HG00609.hp2 HG00642.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.499+1479_499+1482d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | G | GCACGCA | 19 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(16): Show |
21 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | G | GCACGCAC others(1): Show |
9 | a0001c0001t0002g0044 a0001c0001t0004g0078 a0001c0001t0007g0031 others(6): Show |
9 | HG01168.hp1 HG01891.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | G | GCACGCAC others(3): Show |
3 | a0001c0001t0002g0032 a0001c0001t0004g0065 a0001c0001t0022g0047 |
3 | HG01255.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.499+1446_499+1447i others(12): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | G | GCACGCAC others(5): Show |
1 | a0001c0001t0017g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.499+1446_499+1447i others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | G | GCACGCGC others(1): Show |
16 | a0001c0002t0001g0099 a0001c0002t0003g0003 a0001c0002t0005g0008 others(13): Show |
18 | HG00621.hp2 HG01192.hp2 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | G | GCACGCGC others(3): Show |
8 | a0001c0002t0001g0096 a0001c0002t0002g0091 a0001c0002t0003g0087 others(5): Show |
8 | HG02074.hp2 HG02083.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(12): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | G | GCACGCGC others(5): Show |
2 | a0001c0002t0004g0007 a0001c0002t0012g0007 |
2 | HG00408.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.499+1446_499+1447i others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | GCA | G | 27 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0255 others(24): Show |
27 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.499+1481_499+1482d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | GCACA | G | 67 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0113 others(64): Show |
74 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(71): Show |
intron_variant | MODIFIER | c.499+1479_499+1482d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826459 | GCACACA | G | 4 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+1477_499+1482d others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | ||||||
| chr4:15826461 | A | ACG | 10 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(7): Show |
11 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826461 | ||||||
| chr4:15826461 | A | ACGCG | 4 | a0001c0002t0001g0009 a0001c0002t0003g0083 a0001c0002t0005g0081 others(1): Show |
4 | HG01928.hp2 HG03139.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826461 | ||||||
| chr4:15826461 | A | G | 4 | a0001c0001t0001g0272 a0001c0001t0002g0144 a0001c0001t0014g0176 others(1): Show |
4 | HG02451.hp1 HG02738.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1445A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826461 | |||||||
| chr4:15826463 | A | G | 12 | a0001c0001t0002g0074 a0001c0001t0002g0123 a0001c0001t0002g0151 others(9): Show |
12 | HG00099.hp1 HG00438.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+1447A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826463 | |||||||
| chr4:15826465 | A | G | 5 | a0001c0001t0002g0143 a0001c0001t0008g0133 a0001c0001t0014g0149 others(2): Show |
5 | HG01934.hp1 HG02922.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+1449A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826465 | |||||||
| chr4:15826467 | A | G | 56 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(53): Show |
61 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.499+1451A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826467 | |||||||
| chr4:15826469 | A | G | 4 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+1453A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826469 | |||||||
| chr4:15826645 | C | A | 1 | a0001c0001t0004g0269 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.499+1629C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826645 | |||||||
| chr4:15826758 | G | GA | 73 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(70): Show |
78 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.499+1751dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826758 | ||||||
| chr4:15826918 | G | T | 1 | a0001c0001t0033g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.499+1902G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826918 | |||||||
| chr4:15826946 | G | T | 1 | a0001c0001t0004g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.499+1930G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826946 | |||||||
| chr4:15827069 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.499+2053C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827069 | |||||||
| chr4:15827303 | C | T | 4 | a0001c0001t0007g0031 a0001c0001t0007g0045 a0001c0001t0011g0051 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+2287C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827303 | |||||||
| chr4:15827336 | ATGCAGAA others(8): Show |
A | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.499+2323_499+2337d others(17): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15827336 | ||||||
| chr4:15827579 | A | G | 1 | a0001c0002t0037g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.499+2563A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827579 | |||||||
| chr4:15827582 | T | G | 64 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(61): Show |
69 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.499+2566T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827582 | |||||||
| chr4:15827606 | T | C | 1 | a0001c0001t0011g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.499+2590T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827606 | |||||||
| chr4:15827748 | C | T | 1 | a0001c0001t0006g0132 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.499+2732C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827748 | |||||||
| chr4:15827989 | A | G | 223 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0113 others(220): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.499+2973A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827989 | |||||||
| chr4:15828164 | G | A | 2 | a0001c0002t0029g0163 a0001c0002t0029g0164 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.499+3148G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828164 | |||||||
| chr4:15828311 | C | T | 37 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(34): Show |
40 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.499+3295C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828311 | |||||||
| chr4:15828375 | A | G | 1 | a0001c0001t0007g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.499+3359A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828375 | |||||||
| chr4:15828692 | T | C | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.499+3676T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828692 | |||||||
| chr4:15828771 | A | G | 2 | a0001c0001t0026g0071 a0001c0001t0026g0072 |
2 | HG01433.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.499+3755A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828771 | |||||||
| chr4:15828979 | G | A | 1 | a0001c0002t0030g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.499+3963G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828979 | |||||||
| chr4:15829239 | G | A | 2 | a0001c0001t0065g0104 a0001c0001t0067g0075 |
2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.499+4223G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829239 | |||||||
| chr4:15829273 | A | G | 39 | a0001c0001t0013g0281 a0001c0002t0001g0009 a0001c0002t0001g0096 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.499+4257A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829273 | |||||||
| chr4:15829400 | C | T | 18 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(15): Show |
20 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.499+4384C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829400 | |||||||
| chr4:15829412 | A | G | 1 | a0001c0001t0008g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.499+4396A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829412 | |||||||
| chr4:15829497 | G | T | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.499+4481G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829497 | |||||||
| chr4:15829508 | G | A | 1 | a0001c0001t0006g0226 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.499+4492G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829508 | |||||||
| chr4:15829705 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.500-4512T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829705 | |||||||
| chr4:15829725 | C | T | 1 | a0001c0001t0043g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.500-4492C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829725 | |||||||
| chr4:15830045 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.500-4172A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830045 | |||||||
| chr4:15830130 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.500-4087A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830130 | |||||||
| chr4:15830184 | G | T | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.500-4033G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830184 | |||||||
| chr4:15830349 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.500-3868T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830349 | |||||||
| chr4:15830440 | T | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-3777T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830440 | |||||||
| chr4:15830523 | T | C | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.500-3694T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830523 | |||||||
| chr4:15830575 | A | G | 40 | a0001c0001t0013g0281 a0001c0002t0001g0009 a0001c0002t0001g0096 others(37): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.500-3642A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830575 | |||||||
| chr4:15830870 | C | T | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.500-3347C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830870 | |||||||
| chr4:15830881 | T | C | 1 | a0001c0001t0072g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.500-3336T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830881 | |||||||
| chr4:15830948 | T | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-3269T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830948 | |||||||
| chr4:15831299 | C | A | 1 | a0001c0002t0005g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.500-2918C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831299 | |||||||
| chr4:15831302 | G | A | 1 | a0001c0001t0009g0139 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.500-2915G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831302 | |||||||
| chr4:15831319 | T | G | 1 | a0001c0001t0004g0257 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.500-2898T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831319 | |||||||
| chr4:15831568 | CT | C | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-2639delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15831568 | ||||||
| chr4:15831611 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.500-2606C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831611 | |||||||
| chr4:15831909 | A | G | 223 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0113 others(220): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.500-2308A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831909 | |||||||
| chr4:15832016 | C | T | 1 | a0001c0001t0003g0299 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.500-2201C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832016 | |||||||
| chr4:15832172 | C | T | 40 | a0001c0001t0013g0281 a0001c0002t0001g0009 a0001c0002t0001g0096 others(37): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.500-2045C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832172 | |||||||
| chr4:15832229 | T | C | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-1988T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832229 | |||||||
| chr4:15832241 | A | G | 4 | a0001c0002t0003g0083 a0001c0002t0009g0085 a0001c0002t0016g0108 others(1): Show |
4 | HG01106.hp2 HG01192.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-1976A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832241 | |||||||
| chr4:15832243 | C | T | 1 | a0001c0001t0060g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.500-1974C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832243 | |||||||
| chr4:15832340 | C | T | 40 | a0001c0001t0013g0281 a0001c0002t0001g0009 a0001c0002t0001g0096 others(37): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.500-1877C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832340 | |||||||
| chr4:15832380 | CCTGTTTG others(2): Show |
C | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.500-1834_500-1826d others(11): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15832380 | ||||||
| chr4:15832435 | T | A | 1 | a0001c0001t0025g0240 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.500-1782T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832435 | |||||||
| chr4:15832472 | A | C | 40 | a0001c0001t0013g0281 a0001c0002t0001g0009 a0001c0002t0001g0096 others(37): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.500-1745A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832472 | |||||||
| chr4:15832482 | A | G | 1 | a0001c0001t0019g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.500-1735A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832482 | |||||||
| chr4:15832607 | T | A | 2 | a0001c0001t0016g0064 a0001c0001t0049g0069 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.500-1610T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832607 | |||||||
| chr4:15832665 | T | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-1552T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832665 | |||||||
| chr4:15832737 | T | A | 2 | a0001c0001t0065g0104 a0001c0001t0067g0075 |
2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.500-1480T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832737 | |||||||
| chr4:15832872 | A | G | 1 | a0001c0001t0004g0267 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.500-1345A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832872 | |||||||
| chr4:15832983 | A | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-1234A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832983 | |||||||
| chr4:15833129 | TC | T | 6 | a0001c0001t0006g0226 a0001c0001t0006g0243 a0001c0001t0006g0245 others(3): Show |
6 | HG02055.hp2 NA18945.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-1084delC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15833129 | ||||||
| chr4:15833163 | T | A | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-1054T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833163 | |||||||
| chr4:15833576 | A | G | 1 | a0001c0001t0059g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.500-641A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833576 | |||||||
| chr4:15833582 | T | C | 1 | a0001c0001t0003g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.500-635T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833582 | |||||||
| chr4:15833742 | T | C | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-475T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833742 | |||||||
| chr4:15833831 | A | T | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-386A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833831 | |||||||
| chr4:15833863 | G | T | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.500-354G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833863 | |||||||
| chr4:15833912 | C | T | 2 | a0001c0001t0002g0203 a0001c0001t0002g0204 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.500-305C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833912 | |||||||
| chr4:15834083 | G | A | 5 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-134G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15834083 | |||||||
| chr4:15834360 | C | T | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+58C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834360 | |||||||
| chr4:15834408 | G | T | 2 | a0001c0001t0004g0036 a0001c0001t0033g0037 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.585+106G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834408 | |||||||
| chr4:15834449 | T | C | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+147T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834449 | |||||||
| chr4:15834512 | G | A | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+210G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834512 | |||||||
| chr4:15834542 | A | C | 1 | a0001c0001t0001g0237 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.585+240A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834542 | |||||||
| chr4:15834614 | G | A | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+312G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834614 | |||||||
| chr4:15834688 | A | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+386A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834688 | |||||||
| chr4:15834829 | C | A | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.585+527C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834829 | |||||||
| chr4:15834894 | A | AT | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+600dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15834894 | ||||||
| chr4:15834902 | T | A | 1 | a0001c0001t0002g0028 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.585+600T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834902 | |||||||
| chr4:15834903 | A | T | 43 | a0001c0001t0001g0217 a0001c0001t0001g0229 a0001c0001t0003g0234 others(40): Show |
46 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.585+601A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834903 | |||||||
| chr4:15834904 | A | T | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+602A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834904 | |||||||
| chr4:15835260 | T | C | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+958T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835260 | |||||||
| chr4:15835268 | T | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+966T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835268 | |||||||
| chr4:15835290 | A | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+988A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835290 | |||||||
| chr4:15835363 | CT | C | 93 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(90): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.585+1093delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | ||||||
| chr4:15835363 | CTT | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0022 others(68): Show |
74 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.585+1092_585+1093d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | ||||||
| chr4:15835363 | CTTT | C | 54 | a0001c0001t0001g0113 a0001c0001t0001g0312 a0001c0001t0002g0062 others(51): Show |
58 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.585+1091_585+1093d others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | ||||||
| chr4:15835363 | CTTTTT | C | 15 | a0001c0002t0001g0099 a0001c0002t0002g0091 a0001c0002t0005g0008 others(12): Show |
15 | HG00423.hp2 HG00621.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.585+1089_585+1093d others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | ||||||
| chr4:15835363 | CTTTTTT | C | 26 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(23): Show |
30 | HG00408.hp2 HG01891.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.585+1088_585+1093d others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | ||||||
| chr4:15835363 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0129 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.585+1081_585+1093d others(15): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | ||||||
| chr4:15835363 | CTTTTTTT others(7): Show |
C | 16 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0004g0078 others(13): Show |
16 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.585+1080_585+1093d others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | ||||||
| chr4:15835363 | CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0009g0178 a0001c0001t0026g0071 a0001c0001t0026g0072 others(2): Show |
5 | HG01243.hp2 HG01433.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.585+1079_585+1093d others(17): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | ||||||
| chr4:15835363 | CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0062g0110 |
3 | HG02647.hp2 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.585+1078_585+1093d others(18): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | ||||||
| chr4:15835382 | T | C | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+1080T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835382 | |||||||
| chr4:15835444 | C | T | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+1142C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835444 | |||||||
| chr4:15835452 | C | A | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1150C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835452 | |||||||
| chr4:15835567 | G | A | 3 | a0001c0001t0069g0043 a0001c0001t0070g0039 a0001c0001t0071g0180 |
3 | HG02622.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.585+1265G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835567 | |||||||
| chr4:15835647 | A | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1345A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835647 | |||||||
| chr4:15835657 | C | T | 2 | a0001c0001t0056g0303 a0001c0001t0058g0302 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.585+1355C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835657 | |||||||
| chr4:15835674 | G | A | 1 | a0001c0002t0016g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.585+1372G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835674 | |||||||
| chr4:15835754 | T | C | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1452T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835754 | |||||||
| chr4:15835759 | A | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1457A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835759 | |||||||
| chr4:15835763 | T | C | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1461T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835763 | |||||||
| chr4:15835777 | T | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1475T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835777 | |||||||
| chr4:15835964 | G | A | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1662G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835964 | |||||||
| chr4:15835995 | A | G | 1 | a0001c0001t0043g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.585+1693A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835995 | |||||||
| chr4:15836008 | A | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1706A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836008 | |||||||
| chr4:15836015 | T | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1713T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836015 | |||||||
| chr4:15836110 | T | C | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.585+1808T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836110 | |||||||
| chr4:15836228 | T | G | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-1864T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836228 | |||||||
| chr4:15836250 | T | C | 1 | a0001c0002t0007g0101 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.586-1842T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836250 | |||||||
| chr4:15836296 | G | C | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.586-1796G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836296 | |||||||
| chr4:15836321 | G | C | 1 | a0001c0002t0030g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.586-1771G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836321 | |||||||
| chr4:15836915 | T | C | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-1177T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836915 | |||||||
| chr4:15836927 | G | A | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.586-1165G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836927 | |||||||
| chr4:15837098 | G | A | 1 | a0001c0001t0004g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.586-994G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837098 | |||||||
| chr4:15837186 | A | C | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-906A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837186 | |||||||
| chr4:15837206 | C | T | 1 | a0001c0001t0006g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.586-886C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837206 | |||||||
| chr4:15837223 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.586-869G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837223 | |||||||
| chr4:15837339 | C | T | 67 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(64): Show |
72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.586-753C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837339 | |||||||
| chr4:15837340 | A | G | 160 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(157): Show |
170 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.586-752A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837340 | |||||||
| chr4:15837748 | T | C | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-344T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837748 | |||||||
| chr4:15837846 | C | T | 1 | a0001c0001t0067g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.586-246C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837846 | |||||||
| chr4:15838021 | G | T | 1 | a0001c0001t0003g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.586-71G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15838021 | |||||||
| chr4:15838170 | A | G | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.659+5A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838170 | |||||||
| chr4:15838185 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.659+20C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838185 | |||||||
| chr4:15838197 | T | C | 1 | a0001c0001t0002g0015 | 2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.659+32T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838197 | |||||||
| chr4:15838456 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.659+291G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838456 | |||||||
| chr4:15838568 | C | T | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.659+403C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838568 | |||||||
| chr4:15838620 | A | G | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.659+455A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838620 | |||||||
| chr4:15838644 | A | C | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.659+479A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838644 | |||||||
| chr4:15838659 | T | C | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.659+494T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838659 | |||||||
| chr4:15838808 | G | C | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.659+643G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838808 | |||||||
| chr4:15838821 | T | G | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.659+656T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838821 | |||||||
| chr4:15838856 | T | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0274 a0001c0006t0001g0022 |
3 | NA18969.hp2 NA18970.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.659+691T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838856 | |||||||
| chr4:15839000 | G | T | 5 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.659+835G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839000 | |||||||
| chr4:15839158 | G | A | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.660-868G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839158 | |||||||
| chr4:15839216 | A | G | 223 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0113 others(220): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.660-810A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839216 | |||||||
| chr4:15839244 | G | A | 1 | a0001c0001t0059g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.660-782G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839244 | |||||||
| chr4:15839281 | G | A | 1 | a0001c0001t0007g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.660-745G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839281 | |||||||
| chr4:15839415 | C | CT | 15 | a0001c0001t0001g0034 a0001c0001t0001g0231 a0001c0001t0001g0236 others(12): Show |
15 | HG01261.hp2 HG02257.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.660-585dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 15839415 | ||||||
| chr4:15839415 | CT | C | 49 | a0001c0001t0001g0035 a0001c0001t0001g0229 a0001c0001t0001g0280 others(46): Show |
52 | HG00408.hp2 HG00423.hp2 HG01168.hp2 others(49): Show |
intron_variant | MODIFIER | c.660-585delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 15839415 | ||||||
| chr4:15839415 | CTT | C | 9 | a0001c0001t0011g0002 a0001c0001t0011g0048 a0001c0001t0011g0049 others(6): Show |
10 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.660-586_660-585del others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 15839415 | ||||||
| chr4:15839415 | CTTTTTTT | C | 63 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(60): Show |
68 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.660-591_660-585del others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 15839415 | ||||||
| chr4:15839419 | T | C | 1 | a0001c0001t0013g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.660-607T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839419 | |||||||
| chr4:15839450 | G | A | 1 | a0001c0001t0055g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.660-576G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839450 | |||||||
| chr4:15839524 | C | T | 1 | a0001c0001t0047g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.660-502C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839524 | |||||||
| chr4:15839688 | G | C | 1 | a0001c0001t0007g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.660-338G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839688 | |||||||
| chr4:15840164 | C | T | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.752+46C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840164 | |||||||
| chr4:15840187 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.752+69A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840187 | |||||||
| chr4:15840224 | C | G | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.752+106C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840224 | |||||||
| chr4:15840268 | C | A | 17 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0004g0078 others(14): Show |
17 | HG01433.hp2 HG01891.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.752+150C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840268 | |||||||
| chr4:15840280 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.752+162T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840280 | |||||||
| chr4:15840369 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.753-83C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840369 | |||||||
| chr4:15840662 | C | T | 5 | a0001c0001t0015g0181 a0001c0001t0017g0201 a0001c0001t0024g0185 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.839+124C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15840662 | |||||||
| chr4:15840674 | T | C | 3 | a0001c0001t0030g0040 a0001c0001t0034g0112 a0001c0001t0064g0038 |
3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.839+136T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15840674 | |||||||
| chr4:15841001 | C | T | 1 | a0001c0001t0004g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.839+463C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841001 | |||||||
| chr4:15841242 | G | A | 1 | a0001c0001t0067g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.839+704G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841242 | |||||||
| chr4:15841532 | TAAAAGCA others(6080): Show |
T | 6 | a0001c0001t0017g0058 a0001c0001t0019g0159 a0001c0001t0060g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.839+1009_840-906de others(1): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15841532 | ||||||
| chr4:15841584 | G | A | 1 | a0001c0001t0005g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.839+1046G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841584 | |||||||
| chr4:15841620 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.839+1082G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841620 | |||||||
| chr4:15841650 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.839+1112G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841650 | |||||||
| chr4:15841703 | A | G | 4 | a0001c0001t0006g0012 a0001c0001t0006g0120 a0001c0001t0006g0130 others(1): Show |
5 | HG00408.hp2 NA18970.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.839+1165A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841703 | |||||||
| chr4:15841719 | G | A | 38 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(35): Show |
41 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.839+1181G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841719 | |||||||
| chr4:15841729 | G | A | 1 | a0001c0001t0015g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.839+1191G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841729 | |||||||
| chr4:15841873 | G | A | 161 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(158): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.839+1335G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841873 | |||||||
| chr4:15841916 | C | T | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+1378C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841916 | |||||||
| chr4:15841917 | G | T | 1 | a0001c0001t0010g0305 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.839+1379G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841917 | |||||||
| chr4:15841966 | G | A | 2 | a0001c0001t0008g0114 a0001c0001t0008g0168 |
2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.839+1428G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841966 | |||||||
| chr4:15841972 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.839+1434G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841972 | |||||||
| chr4:15842005 | G | C | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.839+1467G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842005 | |||||||
| chr4:15842030 | A | G | 6 | a0001c0001t0002g0123 a0001c0001t0002g0136 a0001c0001t0002g0161 others(3): Show |
6 | NA18956.hp2 NA18966.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.839+1492A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842030 | |||||||
| chr4:15842062 | C | G | 1 | a0001c0001t0002g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.839+1524C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842062 | |||||||
| chr4:15842204 | T | G | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.839+1666T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842204 | |||||||
| chr4:15842233 | T | C | 146 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(143): Show |
156 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.839+1695T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842233 | |||||||
| chr4:15842258 | C | A | 2 | a0001c0001t0005g0025 a0001c0001t0005g0042 |
2 | NA19068.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.839+1720C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842258 | |||||||
| chr4:15842314 | T | C | 1 | a0001c0001t0004g0269 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.839+1776T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842314 | |||||||
| chr4:15842320 | A | G | 1 | a0001c0001t0004g0269 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.839+1782A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842320 | |||||||
| chr4:15842321 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.839+1783G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842321 | |||||||
| chr4:15842376 | C | A | 1 | a0001c0001t0003g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.839+1838C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842376 | |||||||
| chr4:15842390 | T | C | 1 | a0001c0001t0003g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.839+1852T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842390 | |||||||
| chr4:15842396 | G | A | 1 | a0001c0001t0003g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.839+1858G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842396 | |||||||
| chr4:15842443 | A | T | 1 | a0001c0001t0003g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.839+1905A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842443 | |||||||
| chr4:15842501 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.839+1963G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842501 | |||||||
| chr4:15842522 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.839+1984C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842522 | |||||||
| chr4:15842523 | G | A | 1 | a0001c0001t0004g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.839+1985G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842523 | |||||||
| chr4:15842542 | A | G | 2 | a0001c0001t0003g0023 a0001c0001t0003g0307 |
3 | HG00738.hp2 HG01099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.839+2004A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842542 | |||||||
| chr4:15842572 | C | T | 1 | a0001c0002t0030g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.839+2034C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842572 | |||||||
| chr4:15842842 | A | C | 1 | a0001c0001t0010g0298 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.839+2304A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842842 | |||||||
| chr4:15842879 | G | C | 1 | a0001c0001t0022g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.839+2341G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842879 | |||||||
| chr4:15842899 | A | G | 1 | a0001c0001t0033g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.839+2361A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842899 | |||||||
| chr4:15842917 | A | G | 1 | a0001c0001t0022g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.839+2379A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842917 | |||||||
| chr4:15842927 | C | T | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.839+2389C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842927 | |||||||
| chr4:15843061 | G | A | 20 | a0001c0001t0001g0297 a0001c0001t0003g0023 a0001c0001t0003g0186 others(17): Show |
21 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.839+2523G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843061 | |||||||
| chr4:15843078 | C | T | 1 | a0001c0001t0067g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.839+2540C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843078 | |||||||
| chr4:15843080 | A | G | 7 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0035g0155 others(4): Show |
7 | HG01358.hp2 HG02965.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.839+2542A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843080 | |||||||
| chr4:15843101 | A | G | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+2563A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843101 | |||||||
| chr4:15843168 | A | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0270 |
2 | HG00140.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.839+2630A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843168 | |||||||
| chr4:15843184 | A | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0270 |
2 | HG00140.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.839+2646A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843184 | |||||||
| chr4:15843213 | C | A | 1 | a0001c0002t0004g0007 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.839+2675C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843213 | |||||||
| chr4:15843248 | C | T | 1 | a0001c0002t0007g0101 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.839+2710C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843248 | |||||||
| chr4:15843288 | A | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0270 |
2 | HG00140.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.839+2750A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843288 | |||||||
| chr4:15843295 | A | C | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+2757A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843295 | |||||||
| chr4:15843478 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.839+2940G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843478 | |||||||
| chr4:15843575 | A | G | 1 | a0001c0001t0069g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.839+3037A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843575 | |||||||
| chr4:15843627 | A | C | 1 | a0001c0001t0007g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.839+3089A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843627 | |||||||
| chr4:15843772 | T | A | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+3234T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843772 | |||||||
| chr4:15843818 | C | A | 39 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+3280C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843818 | |||||||
| chr4:15843919 | C | G | 4 | a0001c0001t0031g0147 a0001c0001t0031g0148 a0001c0001t0032g0175 others(1): Show |
4 | HG00438.hp1 NA18968.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.839+3381C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843919 | |||||||
| chr4:15844325 | G | A | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.839+3787G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844325 | |||||||
| chr4:15844660 | G | A | 1 | a0001c0001t0067g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.840-3879G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844660 | |||||||
| chr4:15844684 | A | G | 2 | a0001c0001t0003g0023 a0001c0001t0003g0307 |
3 | HG00738.hp2 HG01099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.840-3855A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844684 | |||||||
| chr4:15844737 | C | T | 1 | a0001c0001t0003g0291 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.840-3802C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844737 | |||||||
| chr4:15844739 | G | A | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.840-3800G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844739 | |||||||
| chr4:15844783 | C | T | 22 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(19): Show |
24 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.840-3756C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844783 | |||||||
| chr4:15844813 | A | G | 1 | a0001c0002t0001g0158 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.840-3726A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844813 | |||||||
| chr4:15844824 | C | A | 40 | a0001c0001t0065g0104 a0001c0002t0001g0009 a0001c0002t0001g0096 others(37): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.840-3715C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844824 | |||||||
| chr4:15844868 | G | C | 1 | a0001c0001t0038g0014 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.840-3671G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844868 | |||||||
| chr4:15844883 | A | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0254 others(1): Show |
6 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.840-3656A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844883 | |||||||
| chr4:15845050 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0003g0266 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.840-3489T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845050 | |||||||
| chr4:15845160 | T | C | 1 | a0001c0001t0002g0015 | 2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.840-3379T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845160 | |||||||
| chr4:15845234 | C | T | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-3305C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845234 | |||||||
| chr4:15845261 | C | T | 2 | a0001c0001t0030g0040 a0001c0001t0064g0038 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.840-3278C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845261 | |||||||
| chr4:15845289 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0003g0266 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.840-3250T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845289 | |||||||
| chr4:15845333 | G | T | 1 | a0001c0001t0001g0297 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.840-3206G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845333 | |||||||
| chr4:15845360 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.840-3179C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845360 | |||||||
| chr4:15845364 | G | C | 158 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0113 others(155): Show |
168 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.840-3175G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845364 | |||||||
| chr4:15845365 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.840-3174C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845365 | |||||||
| chr4:15845406 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.840-3133C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845406 | |||||||
| chr4:15845407 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0003g0266 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.840-3132G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845407 | |||||||
| chr4:15845434 | T | C | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-3105T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845434 | |||||||
| chr4:15845448 | C | G | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-3091C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845448 | |||||||
| chr4:15845502 | C | G | 65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-3037C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845502 | |||||||
| chr4:15845575 | G | A | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.840-2964G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845575 | |||||||
| chr4:15845774 | C | G | 9 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.840-2765C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845774 | |||||||
| chr4:15845935 | C | CATTCCA | 162 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(159): Show |
173 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.840-2604_840-2603i others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845935 | |||||||
| chr4:15845954 | A | T | 38 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(35): Show |
41 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.840-2585A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845954 | |||||||
| chr4:15845963 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.840-2576G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845963 | |||||||
| chr4:15846016 | C | G | 1 | a0001c0001t0042g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.840-2523C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846016 | |||||||
| chr4:15846076 | C | T | 38 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(35): Show |
41 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.840-2463C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846076 | |||||||
| chr4:15846090 | G | A | 1 | a0001c0001t0008g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.840-2449G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846090 | |||||||
| chr4:15846094 | T | C | 8 | a0001c0001t0011g0002 a0001c0001t0011g0048 a0001c0001t0011g0049 others(5): Show |
9 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.840-2445T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846094 | |||||||
| chr4:15846170 | C | A | 214 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0113 others(211): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.840-2369C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846170 | |||||||
| chr4:15846197 | T | C | 20 | a0001c0001t0001g0297 a0001c0001t0003g0023 a0001c0001t0003g0186 others(17): Show |
21 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.840-2342T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846197 | |||||||
| chr4:15846270 | T | C | 1 | a0001c0001t0004g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.840-2269T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846270 | |||||||
| chr4:15846295 | C | G | 1 | a0001c0001t0067g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.840-2244C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846295 | |||||||
| chr4:15846301 | A | C | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-2238A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846301 | |||||||
| chr4:15846305 | G | A | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.840-2234G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846305 | |||||||
| chr4:15846394 | T | C | 1 | a0001c0001t0003g0291 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.840-2145T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846394 | |||||||
| chr4:15846413 | T | G | 1 | a0001c0001t0002g0161 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.840-2126T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846413 | |||||||
| chr4:15846456 | T | C | 1 | a0001c0001t0043g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.840-2083T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846456 | |||||||
| chr4:15846494 | G | A | 19 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(16): Show |
21 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.840-2045G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846494 | |||||||
| chr4:15846510 | T | C | 9 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0004g0078 others(6): Show |
9 | HG01891.hp2 HG02572.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.840-2029T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846510 | |||||||
| chr4:15846578 | A | G | 38 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(35): Show |
41 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.840-1961A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846578 | |||||||
| chr4:15846629 | A | G | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-1910A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846629 | |||||||
| chr4:15846630 | C | A | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-1909C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846630 | |||||||
| chr4:15846640 | A | C | 1 | a0001c0001t0006g0243 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.840-1899A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846640 | |||||||
| chr4:15846646 | C | T | 162 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(159): Show |
173 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.840-1893C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846646 | |||||||
| chr4:15846740 | T | C | 1 | a0001c0001t0010g0305 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.840-1799T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846740 | |||||||
| chr4:15846887 | A | G | 14 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0004g0078 others(11): Show |
14 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.840-1652A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846887 | |||||||
| chr4:15846928 | C | T | 89 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(86): Show |
96 | HG00408.hp1 HG00438.hp1 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.840-1611C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846928 | |||||||
| chr4:15846984 | T | G | 2 | a0001c0001t0004g0078 a0001c0001t0022g0047 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.840-1555T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846984 | |||||||
| chr4:15847066 | A | C | 163 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(160): Show |
174 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.840-1473A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847066 | |||||||
| chr4:15847109 | C | T | 1 | a0001c0001t0055g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.840-1430C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847109 | |||||||
| chr4:15847122 | C | A | 1 | a0001c0002t0003g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.840-1417C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847122 | |||||||
| chr4:15847122 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0009g0232 a0001c0001t0009g0314 |
3 | NA18982.hp1 NA19006.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.840-1417C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847122 | |||||||
| chr4:15847123 | G | A | 24 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(21): Show |
26 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.840-1416G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847123 | |||||||
| chr4:15847350 | A | G | 1 | a0001c0001t0006g0252 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.840-1189A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847350 | |||||||
| chr4:15847560 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0067g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.840-972_840-971ins others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847560 | ||||||
| chr4:15847564 | A | AAAAAAAT others(10): Show |
1 | a0001c0002t0006g0102 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.840-972_840-971ins others(17): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847564 | ||||||
| chr4:15847564 | A | AAAAAATA others(3): Show |
3 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0036g0160 |
3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.840-972_840-971ins others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847564 | ||||||
| chr4:15847565 | A | AAAAAATA others(9): Show |
32 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(29): Show |
35 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.840-972_840-971ins others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847565 | ||||||
| chr4:15847565 | A | AAAAATAA others(8): Show |
2 | a0001c0002t0003g0157 a0001c0002t0030g0073 |
2 | HG02074.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.840-972_840-971ins others(15): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847565 | ||||||
| chr4:15847568 | T | A | 40 | a0001c0001t0035g0155 a0001c0001t0038g0014 a0001c0001t0039g0156 others(37): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.840-971T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847568 | |||||||
| chr4:15847570 | A | AAAAAT | 3 | a0001c0001t0020g0154 a0001c0001t0020g0179 a0001c0001t0036g0160 |
3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.840-964_840-960dup others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847570 | ||||||
| chr4:15847570 | A | AATAAATA others(10): Show |
65 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(62): Show |
70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-968_840-967ins others(17): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847570 | ||||||
| chr4:15847570 | A | ATAAATAA others(9): Show |
4 | a0001c0001t0035g0155 a0001c0001t0038g0014 a0001c0001t0039g0156 others(1): Show |
4 | HG01358.hp2 HG02965.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.840-969_840-968ins others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847570 | |||||||
| chr4:15847595 | C | CA | 54 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(51): Show |
56 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.840-916dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAA | 17 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0167 others(14): Show |
18 | HG00423.hp1 HG01243.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.840-917_840-916dup others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAAAA | 12 | a0001c0001t0001g0034 a0001c0001t0002g0005 a0001c0001t0002g0006 others(9): Show |
13 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.840-919_840-916dup others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAAAAA | 10 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0027 others(7): Show |
10 | HG00408.hp1 HG01109.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.840-920_840-916dup others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0004g0078 a0001c0001t0015g0068 a0001c0001t0022g0047 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.840-925_840-916dup others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0009g0178 a0001c0001t0026g0071 a0001c0001t0026g0072 others(3): Show |
6 | HG01433.hp2 HG02257.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.840-926_840-916dup others(11): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAAAAAAA others(5): Show |
11 | a0001c0001t0004g0070 a0001c0001t0034g0112 a0001c0002t0001g0009 others(8): Show |
11 | HG00408.hp2 HG01928.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.840-927_840-916dup others(12): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAAAAAAA others(6): Show |
14 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(11): Show |
16 | HG00423.hp2 HG00621.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.840-928_840-916dup others(13): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAAAAAAA others(7): Show |
5 | a0001c0002t0002g0091 a0001c0002t0003g0087 a0001c0002t0005g0008 others(2): Show |
5 | HG02083.hp1 HG03491.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.840-929_840-916dup others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAAAAAAA others(9): Show |
1 | a0001c0002t0005g0092 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.840-931_840-916dup others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | C | CAAAAAAA others(11): Show |
1 | a0001c0002t0005g0089 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.840-933_840-916dup others(18): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | CA | C | 12 | a0001c0001t0002g0308 a0001c0001t0003g0023 a0001c0001t0003g0287 others(9): Show |
13 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.840-916delA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | CAAAAAA | C | 6 | a0001c0001t0016g0064 a0001c0001t0017g0066 a0001c0001t0020g0154 others(3): Show |
6 | HG01891.hp2 HG03130.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.840-921_840-916del others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | CAAAAAAA | C | 31 | a0001c0001t0001g0035 a0001c0001t0002g0015 a0001c0001t0002g0016 others(28): Show |
33 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.840-922_840-916del others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0002g0205 a0001c0001t0004g0267 a0001c0001t0006g0012 others(4): Show |
7 | HG01168.hp2 HG01358.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.840-923_840-916del others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | CAAAAAAA others(2): Show |
C | 8 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0003g0186 others(5): Show |
10 | HG00438.hp1 HG03669.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.840-924_840-916del others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | CAAAAAAA others(3): Show |
C | 56 | a0001c0001t0001g0113 a0001c0001t0002g0010 a0001c0001t0002g0062 others(53): Show |
58 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.840-925_840-916del others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0006g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.840-926_840-916del others(11): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0299 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.840-927_840-916del others(12): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847595 | CAAAAAAA others(7): Show |
C | 13 | a0001c0001t0004g0063 a0001c0001t0011g0002 a0001c0001t0011g0048 others(10): Show |
14 | HG01106.hp2 HG01192.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.840-929_840-916del others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | ||||||
| chr4:15847645 | G | C | 168 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(165): Show |
179 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.840-894G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847645 | |||||||
| chr4:15847685 | G | A | 35 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(32): Show |
38 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.840-854G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847685 | |||||||
| chr4:15847752 | T | C | 35 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(32): Show |
38 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.840-787T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847752 | |||||||
| chr4:15847763 | G | A | 8 | a0001c0001t0011g0002 a0001c0001t0011g0048 a0001c0001t0011g0049 others(5): Show |
9 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.840-776G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847763 | |||||||
| chr4:15847798 | A | T | 1 | a0001c0002t0037g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.840-741A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847798 | |||||||
| chr4:15847965 | C | G | 35 | a0001c0002t0001g0009 a0001c0002t0001g0096 a0001c0002t0001g0099 others(32): Show |
38 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.840-574C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847965 | |||||||
| chr4:15847977 | C | T | 2 | a0001c0001t0030g0040 a0001c0001t0064g0038 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.840-562C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847977 | |||||||
| chr4:15848106 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.840-433C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848106 | |||||||
| chr4:15848140 | T | A | 21 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0004g0078 others(18): Show |
21 | HG01433.hp2 HG01891.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.840-399T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848140 | |||||||
| chr4:15848178 | T | C | 13 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0004g0078 others(10): Show |
13 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.840-361T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848178 | |||||||
| chr4:15848248 | C | G | 1 | a0001c0001t0002g0308 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.840-291C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848248 | |||||||
| chr4:15848363 | G | T | 168 | a0001c0001t0001g0034 a0001c0001t0001g0113 a0001c0001t0002g0005 others(165): Show |
179 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.840-176G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848363 | |||||||
| chr4:15848367 | G | A | 1 | a0001c0001t0004g0257 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.840-172G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848367 | |||||||
| chr4:15848425 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.840-114C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848425 | |||||||
| chr4:15848487 | G | A | 14 | a0001c0001t0004g0065 a0001c0001t0004g0070 a0001c0001t0004g0078 others(11): Show |
14 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.840-52G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848487 | |||||||
| chr4:15848503 | G | A | 1 | a0001c0001t0065g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-36G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848503 | |||||||
| chr4:15848511 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.840-28G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848511 |