Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 768211 |
| ensemblid | ENSG00000181826.10 |
| hgncid | 27379 |
| symbol | RELL1 |
| name | RELT like 1 |
| refseq_nuc | NM_001085400.2 |
| refseq_prot | NP_001078869.1 |
| ensembl_nuc | ENST00000454158.7 |
| ensembl_prot | ENSP00000398778.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 37610634 |
| end | 37686376 |
| strand | - |
| ver | v1.2 |
| region | chr4:37610634-37686376 |
| region5000 | chr4:37605634-37691376 |
| regionname0 | RELL1_chr4_37610634_37686376 |
| regionname5000 | RELL1_chr4_37605634_37691376 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 271 | 318 | 78 | 64 | 120 | 15 | 39 | 81 | RELL1_chr4_37605634_37691376 | RELL1 | MAPRA others(266): Show |
chr4 | 37605634 | 37691376 |
| a0002 | 0/0 | 271 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | MAPRA others(266): Show |
chr4 | 37605634 | 37691376 |
| a0003 | 0/0 | 271 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | MAPRA others(266): Show |
chr4 | 37605634 | 37691376 |
| a0004 | 0/0 | 271 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | MAPRA others(266): Show |
chr4 | 37605634 | 37691376 |
| a0005 | 0/0 | 271 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | MAPRA others(266): Show |
chr4 | 37605634 | 37691376 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 813 | 305 | 67 | 63 | 120 | 15 | 38 | RELL1_chr4_37605634_37691376 | RELL1 | ATGGC others(808): Show |
chr4 | 37605634 | 37691376 | ||
| a0001c0002 | 0/0 | 813 | 6 | 5 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ATGGC others(808): Show |
chr4 | 37605634 | 37691376 | ||
| a0001c0003 | 0/0 | 813 | 4 | 4 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ATGGC others(808): Show |
chr4 | 37605634 | 37691376 | ||
| a0001c0006 | 0/0 | 813 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ATGGC others(808): Show |
chr4 | 37605634 | 37691376 | ||
| a0001c0007 | 0/0 | 813 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | ATGGC others(808): Show |
chr4 | 37605634 | 37691376 | ||
| a0002c0004 | 0/0 | 813 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ATGGC others(808): Show |
chr4 | 37605634 | 37691376 | ||
| a0003c0005 | 0/0 | 813 | 2 | 0 | 0 | 1 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | ATGGC others(808): Show |
chr4 | 37605634 | 37691376 | ||
| a0004c0008 | 0/0 | 813 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ATGGC others(808): Show |
chr4 | 37605634 | 37691376 | ||
| a0005c0009 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ATGGC others(808): Show |
chr4 | 37605634 | 37691376 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3615 | 72 | 18 | 16 | 25 | 5 | 8 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0002 | 0/0 | 3615 | 53 | 17 | 8 | 26 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0003 | 0/0 | 3618 | 33 | 0 | 2 | 28 | 0 | 3 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0004 | 0/0 | 3617 | 30 | 3 | 12 | 0 | 6 | 9 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0005 | 0/0 | 3615 | 13 | 0 | 4 | 6 | 0 | 3 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0006 | 0/0 | 3616 | 8 | 2 | 1 | 1 | 2 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0007 | 0/0 | 3616 | 6 | 2 | 0 | 4 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0008 | 0/0 | 3618 | 4 | 0 | 0 | 4 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0010 | 0/0 | 3617 | 4 | 4 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0011 | 0/0 | 3617 | 4 | 0 | 3 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0012 | 0/0 | 3615 | 4 | 0 | 0 | 1 | 0 | 3 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0013 | 0/0 | 3619 | 4 | 0 | 2 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3614): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0014 | 0/0 | 3614 | 3 | 0 | 2 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3609): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0015 | 0/0 | 3617 | 3 | 1 | 0 | 0 | 1 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0016 | 0/0 | 3615 | 3 | 1 | 2 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0018 | 0/0 | 3617 | 3 | 3 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0019 | 0/0 | 3618 | 3 | 0 | 1 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0020 | 0/0 | 3616 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0021 | 0/0 | 3614 | 2 | 0 | 0 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3609): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0022 | 0/0 | 3616 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0024 | 0/0 | 3620 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3615): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0025 | 0/0 | 3617 | 2 | 1 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0026 | 0/0 | 3617 | 2 | 1 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0027 | 0/0 | 3618 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0028 | 0/0 | 3618 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0029 | 0/0 | 3617 | 2 | 0 | 0 | 1 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0030 | 0/0 | 3618 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0031 | 0/0 | 3616 | 2 | 0 | 0 | 1 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0032 | 0/0 | 3619 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3614): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0034 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3625): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0035 | 0/0 | 3632 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3627): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0036 | 0/0 | 3615 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0037 | 0/0 | 3615 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0038 | 0/0 | 3615 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0039 | 0/0 | 3618 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0040 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3614): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0042 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3609): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0043 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0045 | 1/0 | 3617 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0046 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0047 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0048 | 0/1 | 3613 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3608): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0049 | 0/0 | 3618 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0050 | 0/0 | 3616 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0051 | 0/0 | 3619 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3614): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0053 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3614): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0054 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0055 | 0/0 | 3621 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3616): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0056 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3614): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0057 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0058 | 0/0 | 3618 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0059 | 0/0 | 3614 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3609): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0060 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0061 | 0/0 | 3620 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3615): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0062 | 0/0 | 3620 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3615): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0063 | 0/0 | 3618 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0064 | 0/0 | 3617 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0065 | 0/0 | 3614 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3609): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0066 | 0/0 | 3616 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0067 | 0/0 | 3617 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0001t0068 | 0/0 | 3604 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3599): Show |
chr4 | 37605634 | 37691376 |
| a0001c0002t0002 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0002t0009 | 0/0 | 3617 | 4 | 3 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0001c0002t0044 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0003t0017 | 0/0 | 3615 | 3 | 3 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0003t0052 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3611): Show |
chr4 | 37605634 | 37691376 |
| a0001c0006t0023 | 0/0 | 3615 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0001c0007t0028 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0002c0004t0033 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3609): Show |
chr4 | 37605634 | 37691376 |
| a0002c0004t0041 | 0/0 | 3613 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3608): Show |
chr4 | 37605634 | 37691376 |
| a0003c0005t0002 | 0/0 | 3615 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| a0003c0005t0003 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3613): Show |
chr4 | 37605634 | 37691376 |
| a0004c0008t0004 | 0/0 | 3617 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3612): Show |
chr4 | 37605634 | 37691376 |
| a0005c0009t0002 | 0/0 | 3615 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | ACTCG others(3610): Show |
chr4 | 37605634 | 37691376 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0011g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0012g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0012g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0012g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0013g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0013g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0013g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0013g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0014g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0014g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0014g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0015g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0015g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0016g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0016g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0018g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0018g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0019g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0019g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0019g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0020g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0020g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0021g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0021g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0022g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0022g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0024g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0024g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0025g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0025g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0026g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0026g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0027g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0027g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0028g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0029g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0029g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0030g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0030g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0031g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0031g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0032g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0032g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0034g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0035g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0036g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0037g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0038g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0039g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0040g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0042g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0043g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0045g0287 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0046g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0047g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0048g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0049g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0050g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0051g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0053g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0054g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0055g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0056g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0057g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0058g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0059g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0060g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0061g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0062g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0063g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0064g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0065g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0066g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0067g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0068g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0009g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0009g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0044g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0003t0017g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0003t0017g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0003t0017g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0003t0052g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0006t0023g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0006t0023g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0007t0028g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0002c0004t0033g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0002c0004t0041g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0003c0005t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0003c0005t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0004c0008t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0005c0009t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0061 | g0056 | EUR | GBR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00140 | hp1 | a0004 | c0008 | t0004 | g0267 | EUR | GBR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0041 | EUR | FIN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0241 | EUR | FIN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00438 | hp2 | a0001 | c0001 | t0020 | g0217 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0141 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00558 | hp2 | a0001 | c0001 | t0036 | g0153 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00597 | hp1 | a0001 | c0001 | t0008 | g0137 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00642 | hp2 | a0001 | c0001 | t0019 | g0030 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0214 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00733 | hp2 | a0001 | c0001 | t0011 | g0053 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01069 | hp1 | a0001 | c0001 | t0038 | g0211 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01070 | hp1 | a0001 | c0001 | t0062 | g0077 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0231 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0076 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01074 | hp2 | a0001 | c0001 | t0066 | g0199 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01081 | hp2 | a0001 | c0001 | t0059 | g0144 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01106 | hp2 | a0001 | c0001 | t0028 | g0012 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01167 | hp2 | a0001 | c0001 | t0016 | g0002 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01168 | hp2 | a0001 | c0002 | t0009 | g0066 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01169 | hp1 | a0001 | c0001 | t0016 | g0002 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0227 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0215 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0250 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0205 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01257 | hp1 | a0001 | c0001 | t0014 | g0165 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0206 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01358 | hp1 | a0001 | c0001 | t0051 | g0120 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01358 | hp2 | a0001 | c0001 | t0039 | g0039 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01433 | hp2 | a0001 | c0001 | t0063 | g0177 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0059 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0221 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0031 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0038 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01884 | hp2 | a0001 | c0003 | t0052 | g0291 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01928 | hp2 | a0001 | c0001 | t0013 | g0072 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01943 | hp1 | a0001 | c0001 | t0050 | g0099 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01943 | hp2 | a0001 | c0001 | t0065 | g0133 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01952 | hp2 | a0001 | c0001 | t0014 | g0098 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02027 | hp1 | a0001 | c0001 | t0029 | g0147 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02027 | hp2 | a0001 | c0001 | t0024 | g0246 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02056 | hp1 | a0001 | c0001 | t0012 | g0293 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02074 | hp1 | a0001 | c0001 | t0056 | g0071 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02074 | hp2 | a0001 | c0001 | t0014 | g0170 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02129 | hp2 | a0005 | c0009 | t0002 | g0319 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02145 | hp2 | a0001 | c0001 | t0054 | g0285 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | CDX | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CDX | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02257 | hp2 | a0001 | c0001 | t0053 | g0051 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02258 | hp2 | a0001 | c0006 | t0023 | g0024 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02273 | hp1 | a0001 | c0001 | t0011 | g0075 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0234 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0245 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02451 | hp2 | a0001 | c0001 | t0043 | g0254 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02572 | hp1 | a0001 | c0001 | t0016 | g0026 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0134 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02602 | hp1 | a0001 | c0007 | t0028 | g0088 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02622 | hp2 | a0001 | c0001 | t0025 | g0013 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02647 | hp1 | a0001 | c0001 | t0060 | g0271 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02647 | hp2 | a0001 | c0001 | t0026 | g0011 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0294 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02698 | hp2 | a0001 | c0001 | t0015 | g0202 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02723 | hp2 | a0001 | c0003 | t0017 | g0249 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0004 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0313 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0140 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02809 | hp2 | a0001 | c0002 | t0009 | g0001 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02895 | hp1 | a0001 | c0001 | t0018 | g0028 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02922 | hp2 | a0001 | c0001 | t0018 | g0019 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02970 | hp1 | a0001 | c0001 | t0018 | g0020 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02970 | hp2 | a0002 | c0004 | t0041 | g0007 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02976 | hp2 | a0002 | c0004 | t0033 | g0006 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0083 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03139 | hp2 | a0001 | c0001 | t0042 | g0318 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03209 | hp1 | a0001 | c0001 | t0034 | g0292 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03225 | hp2 | a0001 | c0001 | t0047 | g0014 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03486 | hp2 | a0001 | c0006 | t0023 | g0251 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0194 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03491 | hp1 | a0001 | c0001 | t0021 | g0296 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0151 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03540 | hp2 | a0001 | c0002 | t0009 | g0001 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03579 | hp1 | a0001 | c0003 | t0017 | g0276 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03579 | hp2 | a0001 | c0001 | t0035 | g0253 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0156 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0311 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0079 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03688 | hp2 | a0001 | c0001 | t0031 | g0301 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0089 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03831 | hp1 | a0001 | c0001 | t0029 | g0086 | SAS | BEB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03831 | hp2 | a0003 | c0005 | t0003 | g0101 | SAS | BEB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03834 | hp1 | a0001 | c0001 | t0012 | g0152 | SAS | BEB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0299 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04199 | hp1 | a0001 | c0001 | t0019 | g0078 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0136 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04204 | hp1 | a0001 | c0001 | t0011 | g0117 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04204 | hp2 | a0001 | c0001 | t0021 | g0094 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0122 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18522 | hp2 | a0001 | c0003 | t0017 | g0091 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | CHB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18906 | hp2 | a0001 | c0001 | t0027 | g0289 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18939 | hp1 | a0001 | c0001 | t0049 | g0263 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18939 | hp2 | a0001 | c0001 | t0025 | g0270 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18942 | hp1 | a0001 | c0001 | t0064 | g0163 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18950 | hp1 | a0001 | c0001 | t0026 | g0262 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18954 | hp2 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18956 | hp1 | a0001 | c0001 | t0022 | g0166 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18956 | hp2 | a0001 | c0001 | t0058 | g0239 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18964 | hp1 | a0001 | c0001 | t0008 | g0148 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18967 | hp2 | a0001 | c0001 | t0013 | g0132 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18977 | hp1 | a0001 | c0001 | t0067 | g0045 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18977 | hp2 | a0001 | c0001 | t0024 | g0062 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18983 | hp1 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18988 | hp1 | a0001 | c0001 | t0068 | g0092 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18994 | hp1 | a0001 | c0001 | t0013 | g0142 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18995 | hp2 | a0001 | c0001 | t0030 | g0116 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19000 | hp2 | a0001 | c0001 | t0030 | g0096 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0160 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19001 | hp2 | a0001 | c0001 | t0006 | g0309 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19003 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19009 | hp2 | a0003 | c0005 | t0002 | g0185 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19010 | hp1 | a0001 | c0001 | t0022 | g0123 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19030 | hp1 | a0001 | c0001 | t0046 | g0255 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19030 | hp2 | a0001 | c0001 | t0027 | g0114 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19043 | hp1 | a0001 | c0002 | t0009 | g0068 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19054 | hp2 | a0001 | c0001 | t0020 | g0264 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19058 | hp1 | a0001 | c0001 | t0032 | g0181 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19067 | hp1 | a0001 | c0001 | t0032 | g0146 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19067 | hp2 | a0001 | c0001 | t0007 | g0302 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19083 | hp1 | a0001 | c0001 | t0037 | g0243 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19083 | hp2 | a0001 | c0001 | t0008 | g0064 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19087 | hp1 | a0001 | c0001 | t0031 | g0219 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0047 | EUR | TSI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20752 | hp2 | a0001 | c0001 | t0015 | g0061 | EUR | TSI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0244 | EUR | TSI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0164 | EUR | TSI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20905 | hp1 | a0001 | c0001 | t0012 | g0004 | SAS | GIH | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20905 | hp2 | a0001 | c0001 | t0019 | g0060 | SAS | GIH | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0103 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02486 | hp1 | a0001 | c0001 | t0040 | g0040 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02559 | hp1 | a0001 | c0001 | t0057 | g0288 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0290 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03471 | hp2 | a0001 | c0002 | t0044 | g0067 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | USA | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0050 | AFR | USA | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | USA | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA21309 | hp1 | a0001 | c0001 | t0055 | g0049 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0048 | g0121 | REF | REF | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0045 | g0287 | REF | REF | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37631404 | C | T | 1 | a0004 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.800G>A | p.Arg267His | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/7 | 889/3617 | 800/816 | 267/271 | chr4 | 37631404 | |||
| chr4:37649441 | C | T | 1 | a0003 | 2 | HG03831.hp2 NA19009.hp2 |
missense_variant | MODERATE | c.148G>A | p.Asp50Asn | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/7 | 237/3617 | 148/816 | 50/271 | chr4 | 37649441 | |||
| chr4:37686239 | A | G | 1 | a0002 | 2 | HG02970.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.49T>C | p.Phe17Leu | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/7 | 138/3617 | 49/816 | 17/271 | chr4 | 37686239 | |||
| chr4:37686260 | C | A | 1 | a0005 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.28G>T | p.Ala10Ser | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/7 | 117/3617 | 28/816 | 10/271 | chr4 | 37686260 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37631469 | C | T | 1 | a0001c0003 | 4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.735G>A | p.Leu245Leu | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/7 | 824/3617 | 735/816 | 245/271 | chr4 | 37631469 | |||
| chr4:37635021 | C | T | 1 | a0001c0006 | 2 | HG02258.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.546G>A | p.Thr182Thr | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/7 | 635/3617 | 546/816 | 182/271 | chr4 | 37635021 | |||
| chr4:37638458 | A | G | 1 | a0001c0002 | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
synonymous_variant | LOW | c.432T>C | p.Tyr144Tyr | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/7 | 521/3617 | 432/816 | 144/271 | chr4 | 37638458 | |||
| chr4:37638497 | A | G | 1 | a0001c0007 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.393T>C | p.Ala131Ala | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/7 | 482/3617 | 393/816 | 131/271 | chr4 | 37638497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37610728 | T | C | 1 | a0001c0001t0038 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2618A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20660 | chr4 | 37610728 | ||||||
| chr4:37610864 | T | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*2482A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20524 | chr4 | 37610864 | ||||||
| chr4:37610897 | G | A | 3 | a0001c0001t0015 a0001c0001t0039 a0001c0001t0040 |
5 | HG01358.hp2 HG02486.hp1 HG02698.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2449C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20491 | chr4 | 37610897 | ||||||
| chr4:37610904 | G | A | 10 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0018 others(7): Show |
43 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2442C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20484 | chr4 | 37610904 | ||||||
| chr4:37610945 | G | A | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2401C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20443 | chr4 | 37610945 | ||||||
| chr4:37610947 | A | G | 6 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0037 others(3): Show |
19 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2399T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20441 | chr4 | 37610947 | ||||||
| chr4:37611008 | G | A | 1 | a0001c0001t0050 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2338C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20380 | chr4 | 37611008 | ||||||
| chr4:37611110 | A | AAAG | 17 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 others(14): Show |
64 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2233_*2235dupCTT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20277 | chr4 | 37611110 | ||||||
| chr4:37611312 | T | G | 1 | a0001c0001t0012 | 4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2034A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20076 | chr4 | 37611312 | ||||||
| chr4:37611379 | AGT | A | 2 | a0001c0002t0009 a0001c0002t0044 |
5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1965_*1966delAC | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20007 | chr4 | 37611379 | ||||||
| chr4:37611630 | T | C | 1 | a0001c0001t0055 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1716A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19758 | chr4 | 37611630 | ||||||
| chr4:37611834 | A | G | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1512T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19554 | chr4 | 37611834 | ||||||
| chr4:37611854 | G | C | 1 | a0001c0001t0038 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1492C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19534 | chr4 | 37611854 | ||||||
| chr4:37611902 | G | A | 1 | a0001c0001t0010 | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1444C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19486 | chr4 | 37611902 | ||||||
| chr4:37611933 | T | C | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1413A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19455 | chr4 | 37611933 | ||||||
| chr4:37611960 | G | C | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1386C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19428 | chr4 | 37611960 | ||||||
| chr4:37611992 | G | A | 13 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0019 others(10): Show |
24 | HG00642.hp2 HG00733.hp2 HG01070.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1354C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19396 | chr4 | 37611992 | ||||||
| chr4:37612003 | G | T | 1 | a0001c0001t0036 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1343C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19385 | chr4 | 37612003 | ||||||
| chr4:37612176 | CA | C | 16 | a0001c0001t0008 a0001c0001t0020 a0001c0001t0022 others(13): Show |
24 | HG00438.hp2 HG00597.hp1 HG01074.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1169delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19211 | chr4 | 37612176 | ||||||
| chr4:37612176 | CAA | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*1168_*1169delTT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19210 | chr4 | 37612176 | ||||||
| chr4:37612176 | CAAA | C | 8 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0014 others(5): Show |
17 | HG00733.hp2 HG01071.hp2 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1167_*1169delTTT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19209 | chr4 | 37612176 | ||||||
| chr4:37612275 | T | A | 2 | a0001c0001t0046 a0001c0006t0023 |
3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1071A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19113 | chr4 | 37612275 | ||||||
| chr4:37612308 | G | A | 10 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0018 others(7): Show |
43 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1038C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19080 | chr4 | 37612308 | ||||||
| chr4:37612322 | T | TTA | 16 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0015 others(13): Show |
53 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1024insTA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19065 | chr4 | 37612322 | ||||||
| chr4:37612322 | T | TTAA | 2 | a0001c0001t0024 a0001c0001t0030 |
4 | HG02027.hp2 NA18977.hp2 NA18995.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1024insTTA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19065 | chr4 | 37612322 | ||||||
| chr4:37612322 | TAA | T | 6 | a0001c0001t0016 a0001c0001t0042 a0001c0003t0017 others(3): Show |
10 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1022_*1023delTT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19064 | chr4 | 37612322 | ||||||
| chr4:37612324 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0068 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1007_*1021delGTTT others(11): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612324 | ||||||
| chr4:37612327 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0012 | 4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1018delGTTT others(8): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612327 | ||||||
| chr4:37612328 | AAAAAAAA others(4): Show |
A | 5 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0065 others(2): Show |
18 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1017delGTTT others(7): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612328 | ||||||
| chr4:37612330 | AAAAAAAA others(2): Show |
A | 5 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0043 others(2): Show |
11 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1015delGTTT others(5): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612330 | ||||||
| chr4:37612333 | A | C | 1 | a0001c0001t0002 | 2 | NA18942.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1013T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19055 | chr4 | 37612333 | ||||||
| chr4:37612334 | A | C | 5 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0019 others(2): Show |
42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1012T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19054 | chr4 | 37612334 | ||||||
| chr4:37612334 | AAAAACAA others(8): Show |
A | 4 | a0001c0001t0053 a0001c0001t0055 a0001c0002t0009 others(1): Show |
7 | HG01168.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*997_*1011delGTTTT others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19039 | chr4 | 37612334 | ||||||
| chr4:37612336 | A | C | 9 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0021 others(6): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1010T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19052 | chr4 | 37612336 | ||||||
| chr4:37612337 | AAC | A | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(16): Show |
135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1008delGT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612337 | ||||||
| chr4:37612338 | AC | A | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0020 others(3): Show |
23 | HG00438.hp2 HG01243.hp1 HG01255.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1007delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612338 | ||||||
| chr4:37612339 | C | A | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(24): Show |
110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1007G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612339 | ||||||
| chr4:37612340 | A | C | 9 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0028 others(6): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1006T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19048 | chr4 | 37612340 | ||||||
| chr4:37612342 | A | C | 13 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0014 others(10): Show |
75 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1004T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19046 | chr4 | 37612342 | ||||||
| chr4:37612349 | C | A | 10 | a0001c0001t0011 a0001c0001t0025 a0001c0001t0030 others(7): Show |
15 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*997G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19039 | chr4 | 37612349 | ||||||
| chr4:37612402 | G | A | 8 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0019 others(5): Show |
47 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*944C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18986 | chr4 | 37612402 | ||||||
| chr4:37612416 | G | A | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*930C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18972 | chr4 | 37612416 | ||||||
| chr4:37612590 | T | G | 1 | a0001c0001t0049 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*756A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18798 | chr4 | 37612590 | ||||||
| chr4:37612624 | G | A | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0019 others(3): Show |
44 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*722C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18764 | chr4 | 37612624 | ||||||
| chr4:37612624 | G | T | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*722C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18764 | chr4 | 37612624 | ||||||
| chr4:37612636 | C | CA | 21 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0013 others(18): Show |
43 | HG00323.hp1 HG01106.hp2 HG01168.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*709dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18751 | chr4 | 37612636 | ||||||
| chr4:37612636 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0034 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*697_*709dupTTTTTT others(7): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18751 | chr4 | 37612636 | ||||||
| chr4:37612636 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0035 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*695_*709dupTTTTTT others(9): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18751 | chr4 | 37612636 | ||||||
| chr4:37612656 | C | A | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18732 | chr4 | 37612656 | ||||||
| chr4:37612657 | C | A | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*689G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18731 | chr4 | 37612657 | ||||||
| chr4:37612658 | T | A | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*688A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18730 | chr4 | 37612658 | ||||||
| chr4:37612659 | T | C | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*687A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18729 | chr4 | 37612659 | ||||||
| chr4:37612697 | T | C | 12 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 others(9): Show |
56 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*649A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18691 | chr4 | 37612697 | ||||||
| chr4:37612721 | T | C | 1 | a0001c0001t0060 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18667 | chr4 | 37612721 | ||||||
| chr4:37612781 | T | A | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*565A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18607 | chr4 | 37612781 | ||||||
| chr4:37612782 | C | T | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*564G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18606 | chr4 | 37612782 | ||||||
| chr4:37612938 | G | A | 4 | a0001c0001t0011 a0001c0001t0061 a0001c0001t0062 others(1): Show |
7 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*408C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18450 | chr4 | 37612938 | ||||||
| chr4:37612949 | C | T | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*397G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18439 | chr4 | 37612949 | ||||||
| chr4:37612967 | C | A | 2 | a0001c0001t0030 a0001c0001t0064 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*379G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18421 | chr4 | 37612967 | ||||||
| chr4:37613115 | C | A | 12 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0012 others(9): Show |
66 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18273 | chr4 | 37613115 | ||||||
| chr4:37686343 | C | G | 1 | a0002c0004t0033 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/7 | 56 | chr4 | 37686343 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37613429 | G | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(3): Show |
6 | HG01167.hp1 HG02258.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.*4-87C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613429 | |||||||
| chr4:37613442 | C | G | 1 | a0001c0001t0002g0126 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.*4-100G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613442 | |||||||
| chr4:37613513 | G | T | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-171C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613513 | |||||||
| chr4:37613577 | T | C | 316 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(313): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.*4-235A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613577 | |||||||
| chr4:37613611 | C | T | 2 | a0001c0001t0004g0079 a0001c0001t0004g0089 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-269G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613611 | |||||||
| chr4:37613642 | G | A | 3 | a0001c0001t0025g0013 a0001c0001t0025g0270 a0001c0001t0058g0239 |
3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*4-300C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613642 | |||||||
| chr4:37613668 | C | G | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-326G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613668 | |||||||
| chr4:37613701 | A | G | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-359T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613701 | |||||||
| chr4:37613829 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.*4-487C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613829 | |||||||
| chr4:37613952 | C | G | 228 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0025 others(225): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.*4-610G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613952 | |||||||
| chr4:37613989 | G | A | 52 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.*4-647C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613989 | |||||||
| chr4:37614057 | C | T | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-715G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614057 | |||||||
| chr4:37614069 | A | G | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-727T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614069 | |||||||
| chr4:37614086 | A | G | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.*4-744T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614086 | |||||||
| chr4:37614108 | C | T | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-766G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614108 | |||||||
| chr4:37614112 | G | A | 3 | a0001c0001t0025g0013 a0001c0001t0025g0270 a0001c0001t0058g0239 |
3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*4-770C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614112 | |||||||
| chr4:37614202 | T | C | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-860A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614202 | |||||||
| chr4:37614294 | A | G | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-952T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614294 | |||||||
| chr4:37614298 | T | C | 44 | a0001c0001t0003g0052 a0001c0001t0003g0073 a0001c0001t0003g0093 others(41): Show |
44 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.*4-956A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614298 | |||||||
| chr4:37614474 | C | A | 1 | a0001c0001t0019g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.*4-1132G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614474 | |||||||
| chr4:37614484 | A | G | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-1142T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614484 | |||||||
| chr4:37614670 | C | T | 17 | a0001c0001t0010g0035 a0001c0001t0010g0134 a0001c0001t0010g0140 others(14): Show |
18 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.*4-1328G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614670 | |||||||
| chr4:37614756 | A | G | 2 | a0001c0001t0004g0079 a0001c0001t0004g0089 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-1414T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614756 | |||||||
| chr4:37614764 | G | A | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-1422C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614764 | |||||||
| chr4:37614952 | T | G | 4 | a0001c0001t0018g0019 a0001c0001t0018g0020 a0001c0001t0018g0028 others(1): Show |
4 | HG02895.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-1610A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614952 | |||||||
| chr4:37615007 | G | A | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.*4-1665C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615007 | |||||||
| chr4:37615070 | G | C | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.*4-1728C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615070 | |||||||
| chr4:37615217 | T | C | 4 | a0001c0001t0002g0193 a0001c0001t0002g0260 a0001c0001t0002g0314 others(1): Show |
4 | HG02129.hp2 NA18988.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-1875A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615217 | |||||||
| chr4:37615353 | C | T | 46 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(43): Show |
46 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.*4-2011G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615353 | |||||||
| chr4:37615367 | A | G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0216 a0001c0001t0001g0220 others(3): Show |
6 | HG01256.hp1 HG01257.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-2025T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615367 | |||||||
| chr4:37615767 | A | G | 79 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(76): Show |
80 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.*4-2425T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615767 | |||||||
| chr4:37615796 | G | T | 1 | a0001c0002t0009g0066 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.*4-2454C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615796 | |||||||
| chr4:37615827 | T | C | 4 | a0001c0002t0009g0001 a0001c0002t0009g0066 a0001c0002t0009g0068 others(1): Show |
5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-2485A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615827 | |||||||
| chr4:37615957 | C | T | 4 | a0001c0001t0011g0053 a0001c0001t0011g0076 a0001c0001t0062g0077 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-2615G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615957 | |||||||
| chr4:37616023 | T | TAAGAAAC others(332): Show |
1 | a0001c0001t0002g0186 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*4-2682_*4-2681ins others(339): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616023 | |||||||
| chr4:37616069 | A | G | 1 | a0001c0001t0029g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*4-2727T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616069 | |||||||
| chr4:37616157 | G | T | 4 | a0001c0002t0009g0001 a0001c0002t0009g0066 a0001c0002t0009g0068 others(1): Show |
5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-2815C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616157 | |||||||
| chr4:37616158 | GTAC | G | 4 | a0001c0002t0009g0001 a0001c0002t0009g0066 a0001c0002t0009g0068 others(1): Show |
5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-2819_*4-2817del others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616158 | |||||||
| chr4:37616486 | G | A | 4 | a0001c0002t0009g0001 a0001c0002t0009g0066 a0001c0002t0009g0068 others(1): Show |
5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-3144C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616486 | |||||||
| chr4:37616646 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*4-3304G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616646 | |||||||
| chr4:37616678 | AAAAT | A | 76 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(73): Show |
77 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.*4-3340_*4-3337del others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616678 | |||||||
| chr4:37616693 | C | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-3351G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616693 | |||||||
| chr4:37616888 | G | A | 1 | a0001c0001t0039g0039 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.*4-3546C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616888 | |||||||
| chr4:37617227 | C | T | 2 | a0001c0001t0042g0318 a0002c0004t0033g0006 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.*4-3885G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617227 | |||||||
| chr4:37617280 | T | C | 4 | a0001c0001t0001g0303 a0001c0001t0025g0013 a0001c0001t0025g0270 others(1): Show |
4 | HG02622.hp2 HG03704.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-3938A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617280 | |||||||
| chr4:37617285 | G | A | 3 | a0001c0001t0046g0255 a0001c0006t0023g0024 a0001c0006t0023g0251 |
3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*4-3943C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617285 | |||||||
| chr4:37617302 | T | C | 2 | a0001c0001t0016g0002 a0001c0001t0016g0026 |
3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.*4-3960A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617302 | |||||||
| chr4:37617316 | A | G | 89 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(86): Show |
90 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.*4-3974T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617316 | |||||||
| chr4:37617361 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*4-4019G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617361 | |||||||
| chr4:37617801 | A | T | 1 | a0001c0001t0007g0029 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*4-4459T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617801 | |||||||
| chr4:37617873 | T | G | 4 | a0001c0001t0001g0303 a0001c0001t0025g0013 a0001c0001t0025g0270 others(1): Show |
4 | HG02622.hp2 HG03704.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-4531A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617873 | |||||||
| chr4:37618170 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*4-4828C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618170 | |||||||
| chr4:37618171 | T | G | 4 | a0001c0001t0010g0035 a0001c0001t0010g0134 a0001c0001t0010g0140 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-4829A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618171 | |||||||
| chr4:37618399 | T | A | 28 | a0001c0001t0005g0103 a0001c0001t0005g0141 a0001c0001t0005g0151 others(25): Show |
29 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.*4-5057A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618399 | |||||||
| chr4:37618494 | T | A | 1 | a0001c0001t0004g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*4-5152A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618494 | |||||||
| chr4:37618529 | C | A | 1 | a0001c0001t0028g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*4-5187G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618529 | |||||||
| chr4:37618547 | A | G | 22 | a0001c0001t0005g0103 a0001c0001t0005g0141 a0001c0001t0005g0151 others(19): Show |
23 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.*4-5205T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618547 | |||||||
| chr4:37618595 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*4-5253A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618595 | |||||||
| chr4:37618832 | T | C | 7 | a0001c0001t0008g0063 a0001c0001t0008g0064 a0001c0001t0008g0148 others(4): Show |
7 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.*4-5490A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618832 | |||||||
| chr4:37618866 | G | A | 4 | a0001c0001t0001g0303 a0001c0001t0025g0013 a0001c0001t0025g0270 others(1): Show |
4 | HG02622.hp2 HG03704.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-5524C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618866 | |||||||
| chr4:37618867 | T | TTTTTC | 59 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.*4-5530_*4-5526dup others(5): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618867 | |||||||
| chr4:37618867 | T | TTTTTCTT others(3): Show |
10 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0001g0266 others(7): Show |
10 | HG01175.hp2 HG02027.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.*4-5535_*4-5526dup others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618867 | |||||||
| chr4:37619042 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.*4-5700C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619042 | |||||||
| chr4:37619186 | C | G | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.*4-5844G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619186 | |||||||
| chr4:37619322 | A | G | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-5980T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619322 | |||||||
| chr4:37619342 | C | T | 6 | a0001c0001t0001g0044 a0001c0001t0001g0106 a0001c0001t0001g0191 others(3): Show |
6 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.*4-6000G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619342 | |||||||
| chr4:37619430 | G | T | 232 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0025 others(229): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.*4-6088C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619430 | |||||||
| chr4:37619470 | C | T | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-6128G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619470 | |||||||
| chr4:37619596 | C | T | 18 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0113 others(15): Show |
18 | HG00423.hp2 HG01106.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.*4-6254G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619596 | |||||||
| chr4:37619652 | C | T | 1 | a0003c0005t0002g0185 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.*4-6310G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619652 | |||||||
| chr4:37620268 | C | T | 1 | a0001c0001t0007g0302 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.*4-6926G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37620268 | |||||||
| chr4:37620547 | C | A | 1 | a0001c0001t0012g0293 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.*4-7205G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37620547 | |||||||
| chr4:37620943 | C | T | 3 | a0001c0001t0025g0013 a0001c0001t0025g0270 a0001c0001t0058g0239 |
3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*4-7601G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37620943 | |||||||
| chr4:37620963 | G | C | 1 | a0001c0001t0042g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*4-7621C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37620963 | |||||||
| chr4:37621138 | A | G | 51 | a0001c0001t0003g0052 a0001c0001t0003g0073 a0001c0001t0003g0093 others(48): Show |
51 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.*4-7796T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621138 | |||||||
| chr4:37621300 | C | CA | 4 | a0001c0003t0017g0091 a0001c0003t0017g0249 a0001c0003t0017g0276 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-7959dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621300 | |||||||
| chr4:37621330 | C | A | 3 | a0001c0001t0046g0255 a0001c0006t0023g0024 a0001c0006t0023g0251 |
3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*4-7988G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621330 | |||||||
| chr4:37621348 | C | T | 41 | a0001c0001t0003g0052 a0001c0001t0003g0073 a0001c0001t0003g0093 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.*4-8006G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621348 | |||||||
| chr4:37621563 | G | A | 3 | a0001c0001t0025g0013 a0001c0001t0025g0270 a0001c0001t0058g0239 |
3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*4-8221C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621563 | |||||||
| chr4:37621702 | A | T | 27 | a0001c0001t0001g0303 a0001c0001t0005g0103 a0001c0001t0005g0141 others(24): Show |
28 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.*4-8360T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621702 | |||||||
| chr4:37621811 | G | C | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8469C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621811 | |||||||
| chr4:37621851 | A | C | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8509T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621851 | |||||||
| chr4:37621880 | A | G | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8538T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621880 | |||||||
| chr4:37621948 | A | C | 4 | a0001c0001t0015g0050 a0001c0001t0015g0202 a0001c0001t0039g0039 others(1): Show |
4 | HG01358.hp2 HG02486.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-8606T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621948 | |||||||
| chr4:37622074 | A | G | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8732T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622074 | |||||||
| chr4:37622167 | G | T | 1 | a0001c0001t0002g0196 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.*4-8825C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622167 | |||||||
| chr4:37622215 | T | C | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8873A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622215 | |||||||
| chr4:37622583 | G | A | 1 | a0001c0001t0035g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.*3+8802C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622583 | |||||||
| chr4:37622696 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.*3+8689C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622696 | |||||||
| chr4:37622749 | A | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+8636T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622749 | |||||||
| chr4:37622797 | T | C | 1 | a0001c0001t0002g0021 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.*3+8588A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622797 | |||||||
| chr4:37622799 | C | CT | 12 | a0001c0001t0001g0145 a0001c0001t0002g0069 a0001c0001t0002g0224 others(9): Show |
12 | HG01175.hp2 HG02027.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.*3+8585dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622799 | |||||||
| chr4:37622799 | C | T | 26 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(23): Show |
26 | HG00642.hp1 HG01175.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.*3+8586G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622799 | |||||||
| chr4:37622819 | T | C | 2 | a0001c0001t0016g0002 a0001c0001t0016g0026 |
3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.*3+8566A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622819 | |||||||
| chr4:37623005 | G | A | 3 | a0001c0001t0003g0131 a0001c0001t0032g0146 a0001c0001t0068g0092 |
3 | HG02071.hp2 NA18988.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.*3+8380C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623005 | |||||||
| chr4:37623095 | A | G | 314 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.*3+8290T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623095 | |||||||
| chr4:37623099 | G | A | 4 | a0001c0002t0009g0001 a0001c0002t0009g0066 a0001c0002t0009g0068 others(1): Show |
5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*3+8286C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623099 | |||||||
| chr4:37623137 | A | C | 3 | a0001c0001t0046g0255 a0001c0006t0023g0024 a0001c0006t0023g0251 |
3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+8248T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623137 | |||||||
| chr4:37623582 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.*3+7803G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623582 | |||||||
| chr4:37623617 | G | A | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+7768C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623617 | |||||||
| chr4:37623649 | C | G | 4 | a0001c0003t0017g0091 a0001c0003t0017g0249 a0001c0003t0017g0276 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+7736G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623649 | |||||||
| chr4:37623671 | A | C | 4 | a0001c0003t0017g0091 a0001c0003t0017g0249 a0001c0003t0017g0276 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+7714T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623671 | |||||||
| chr4:37623710 | G | A | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+7675C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623710 | |||||||
| chr4:37623829 | G | A | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+7556C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623829 | |||||||
| chr4:37623953 | A | T | 7 | a0001c0001t0002g0095 a0001c0001t0002g0158 a0001c0001t0002g0161 others(4): Show |
7 | HG02080.hp1 NA18946.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.*3+7432T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623953 | |||||||
| chr4:37624035 | G | A | 1 | a0001c0001t0055g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*3+7350C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624035 | |||||||
| chr4:37624048 | G | T | 3 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 |
3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.*3+7337C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624048 | |||||||
| chr4:37624050 | C | A | 2 | a0001c0001t0001g0310 a0001c0001t0006g0309 |
2 | NA18969.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.*3+7335G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624050 | |||||||
| chr4:37624078 | CCA | C | 2 | a0001c0001t0012g0004 a0001c0001t0012g0152 |
3 | HG02735.hp1 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*3+7305_*3+7306del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624078 | |||||||
| chr4:37624184 | T | C | 1 | a0001c0001t0037g0243 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.*3+7201A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624184 | |||||||
| chr4:37624252 | G | A | 10 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 others(7): Show |
10 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.*3+7133C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624252 | |||||||
| chr4:37624393 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(4): Show |
7 | HG01167.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.*3+6992C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624393 | |||||||
| chr4:37624418 | C | CT | 25 | a0001c0001t0001g0259 a0001c0001t0005g0103 a0001c0001t0005g0141 others(22): Show |
26 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.*3+6966dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624418 | |||||||
| chr4:37624418 | C | T | 3 | a0001c0001t0046g0255 a0001c0006t0023g0024 a0001c0006t0023g0251 |
3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+6967G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624418 | |||||||
| chr4:37624418 | CT | C | 192 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(189): Show |
195 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.*3+6966delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624418 | |||||||
| chr4:37624418 | CTT | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(48): Show |
52 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+6965_*3+6966del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624418 | |||||||
| chr4:37624422 | T | C | 10 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 others(7): Show |
10 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.*3+6963A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624422 | |||||||
| chr4:37624573 | G | A | 2 | a0001c0001t0027g0114 a0001c0001t0027g0289 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.*3+6812C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624573 | |||||||
| chr4:37624580 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*3+6805G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624580 | |||||||
| chr4:37624614 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0184 |
2 | NA18945.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.*3+6771T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624614 | |||||||
| chr4:37624620 | G | A | 3 | a0001c0001t0046g0255 a0001c0006t0023g0024 a0001c0006t0023g0251 |
3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+6765C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624620 | |||||||
| chr4:37624849 | T | G | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+6536A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624849 | |||||||
| chr4:37624952 | G | A | 1 | a0001c0001t0042g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*3+6433C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624952 | |||||||
| chr4:37625003 | G | A | 4 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0074 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.*3+6382C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625003 | |||||||
| chr4:37625142 | C | T | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*3+6243G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625142 | |||||||
| chr4:37625231 | T | G | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+6154A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625231 | |||||||
| chr4:37625308 | G | GGACAATG others(339): Show |
1 | a0001c0001t0002g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.*3+6076_*3+6077ins others(346): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625308 | |||||||
| chr4:37625366 | A | T | 1 | a0001c0001t0055g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*3+6019T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625366 | |||||||
| chr4:37625673 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.*3+5712C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625673 | |||||||
| chr4:37625717 | A | C | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+5668T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625717 | |||||||
| chr4:37625909 | T | TA | 52 | a0001c0001t0003g0052 a0001c0001t0003g0073 a0001c0001t0003g0093 others(49): Show |
52 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+5475dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625909 | |||||||
| chr4:37625973 | C | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+5412G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625973 | |||||||
| chr4:37626048 | A | G | 7 | a0001c0001t0008g0063 a0001c0001t0008g0064 a0001c0001t0008g0148 others(4): Show |
7 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.*3+5337T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626048 | |||||||
| chr4:37626370 | C | T | 5 | a0001c0001t0015g0050 a0001c0001t0015g0061 a0001c0001t0015g0202 others(2): Show |
5 | HG01358.hp2 HG02486.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.*3+5015G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626370 | |||||||
| chr4:37626548 | G | C | 11 | a0001c0001t0004g0031 a0001c0001t0004g0079 a0001c0001t0004g0082 others(8): Show |
11 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.*3+4837C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626548 | |||||||
| chr4:37626614 | T | C | 1 | a0001c0001t0004g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.*3+4771A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626614 | |||||||
| chr4:37626698 | G | A | 3 | a0001c0001t0019g0030 a0001c0001t0019g0060 a0001c0001t0019g0078 |
3 | HG00642.hp2 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.*3+4687C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626698 | |||||||
| chr4:37626802 | G | A | 87 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0025 others(84): Show |
88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.*3+4583C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626802 | |||||||
| chr4:37626827 | A | G | 1 | a0001c0001t0003g0180 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.*3+4558T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626827 | |||||||
| chr4:37626863 | G | C | 1 | a0001c0001t0016g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.*3+4522C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626863 | |||||||
| chr4:37626937 | C | G | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+4448G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626937 | |||||||
| chr4:37626999 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*3+4386A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626999 | |||||||
| chr4:37627101 | C | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+4284G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627101 | |||||||
| chr4:37627377 | A | G | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+4008T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627377 | |||||||
| chr4:37627433 | A | G | 2 | a0001c0001t0016g0002 a0001c0001t0016g0026 |
3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.*3+3952T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627433 | |||||||
| chr4:37627441 | C | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+3944G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627441 | |||||||
| chr4:37627659 | T | C | 18 | a0001c0001t0005g0103 a0001c0001t0005g0141 a0001c0001t0005g0151 others(15): Show |
18 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.*3+3726A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627659 | |||||||
| chr4:37627722 | A | G | 1 | a0001c0001t0042g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*3+3663T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627722 | |||||||
| chr4:37628044 | T | C | 4 | a0001c0001t0001g0310 a0001c0001t0003g0258 a0001c0001t0003g0261 others(1): Show |
4 | HG00597.hp2 NA18969.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.*3+3341A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628044 | |||||||
| chr4:37628152 | A | G | 1 | a0001c0001t0029g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*3+3233T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628152 | |||||||
| chr4:37628208 | T | G | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+3177A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628208 | |||||||
| chr4:37628353 | G | T | 2 | a0001c0003t0017g0091 a0001c0003t0017g0276 |
2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.*3+3032C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628353 | |||||||
| chr4:37628381 | C | T | 3 | a0001c0001t0046g0255 a0001c0006t0023g0024 a0001c0006t0023g0251 |
3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+3004G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628381 | |||||||
| chr4:37628418 | C | T | 9 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.*3+2967G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628418 | |||||||
| chr4:37628516 | T | C | 4 | a0001c0001t0018g0019 a0001c0001t0018g0020 a0001c0001t0018g0028 others(1): Show |
4 | HG02895.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+2869A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628516 | |||||||
| chr4:37628673 | C | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+2712G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628673 | |||||||
| chr4:37628789 | G | A | 9 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.*3+2596C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628789 | |||||||
| chr4:37628830 | C | T | 4 | a0001c0003t0017g0091 a0001c0003t0017g0249 a0001c0003t0017g0276 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+2555G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628830 | |||||||
| chr4:37628953 | C | T | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.*3+2432G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628953 | |||||||
| chr4:37628954 | G | A | 1 | a0001c0001t0015g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*3+2431C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628954 | |||||||
| chr4:37629680 | GCTAA | G | 3 | a0001c0001t0025g0013 a0001c0001t0025g0270 a0001c0001t0058g0239 |
3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*3+1701_*3+1704del others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629680 | |||||||
| chr4:37629784 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.*3+1601C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629784 | |||||||
| chr4:37629901 | C | T | 6 | a0001c0001t0011g0053 a0001c0001t0011g0075 a0001c0001t0011g0076 others(3): Show |
6 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.*3+1484G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629901 | |||||||
| chr4:37629954 | C | G | 4 | a0001c0001t0001g0303 a0001c0001t0012g0004 a0001c0001t0012g0152 others(1): Show |
5 | HG02056.hp1 HG02735.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.*3+1431G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629954 | |||||||
| chr4:37629972 | A | G | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*3+1413T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629972 | |||||||
| chr4:37630252 | A | C | 20 | a0001c0001t0004g0047 a0001c0001t0004g0054 a0001c0001t0004g0055 others(17): Show |
20 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.*3+1133T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630252 | |||||||
| chr4:37630279 | G | A | 6 | a0001c0001t0011g0053 a0001c0001t0011g0075 a0001c0001t0011g0076 others(3): Show |
6 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.*3+1106C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630279 | |||||||
| chr4:37630356 | G | GT | 103 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0001t0001g0171 others(100): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.*3+1028dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | |||||||
| chr4:37630356 | G | GTT | 38 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0111 others(35): Show |
38 | HG00423.hp2 HG00597.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.*3+1027_*3+1028dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | |||||||
| chr4:37630356 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0002g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.*3+1019_*3+1028dup others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | |||||||
| chr4:37630356 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0002g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*3+1018_*3+1028dup others(11): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | |||||||
| chr4:37630356 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0002g0021 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.*3+1015_*3+1028dup others(14): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | |||||||
| chr4:37630356 | GT | G | 24 | a0001c0001t0001g0305 a0001c0001t0002g0284 a0001c0001t0003g0129 others(21): Show |
24 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.*3+1028delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | |||||||
| chr4:37630367 | T | G | 4 | a0001c0003t0017g0091 a0001c0003t0017g0249 a0001c0003t0017g0276 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+1018A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630367 | |||||||
| chr4:37630368 | T | G | 1 | a0001c0001t0003g0261 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.*3+1017A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630368 | |||||||
| chr4:37630368 | T | TG | 51 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(48): Show |
52 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+1016_*3+1017ins others(1): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630368 | |||||||
| chr4:37630388 | C | G | 1 | a0001c0001t0016g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.*3+997G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630388 | |||||||
| chr4:37630392 | T | A | 1 | a0001c0001t0010g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.*3+993A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630392 | |||||||
| chr4:37630465 | C | T | 1 | a0001c0001t0042g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*3+920G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630465 | |||||||
| chr4:37630598 | C | A | 53 | a0001c0001t0001g0172 a0001c0001t0001g0297 a0001c0001t0002g0043 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.*3+787G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630598 | |||||||
| chr4:37630614 | C | T | 3 | a0001c0001t0046g0255 a0001c0006t0023g0024 a0001c0006t0023g0251 |
3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+771G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630614 | |||||||
| chr4:37630616 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.*3+769G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630616 | |||||||
| chr4:37630688 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.*3+697A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630688 | |||||||
| chr4:37630941 | TA | T | 22 | a0001c0001t0001g0305 a0001c0001t0005g0103 a0001c0001t0005g0141 others(19): Show |
23 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.*3+443delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630941 | |||||||
| chr4:37631373 | A | G | 1 | a0001c0001t0004g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.*3+12T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37631373 | |||||||
| chr4:37631601 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.681-78T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37631601 | |||||||
| chr4:37631647 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.681-124C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37631647 | |||||||
| chr4:37631886 | A | C | 229 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0025 others(226): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.681-363T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37631886 | |||||||
| chr4:37631891 | G | A | 19 | a0001c0001t0001g0305 a0001c0001t0005g0103 a0001c0001t0005g0141 others(16): Show |
19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.681-368C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37631891 | |||||||
| chr4:37632051 | C | G | 1 | a0001c0001t0061g0056 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.681-528G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632051 | |||||||
| chr4:37632079 | A | G | 44 | a0001c0001t0003g0052 a0001c0001t0003g0073 a0001c0001t0003g0093 others(41): Show |
44 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.681-556T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632079 | |||||||
| chr4:37632084 | G | GA | 63 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0139 others(60): Show |
64 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.681-562dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632084 | |||||||
| chr4:37632084 | G | GAA | 105 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0172 others(102): Show |
107 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.681-563_681-562dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632084 | |||||||
| chr4:37632084 | G | GAAA | 61 | a0001c0001t0001g0009 a0001c0001t0001g0070 a0001c0001t0001g0208 others(58): Show |
62 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.681-564_681-562dup others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632084 | |||||||
| chr4:37632084 | GA | G | 22 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0111 others(19): Show |
22 | HG00642.hp1 HG01256.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.681-562delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632084 | |||||||
| chr4:37632114 | T | G | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.681-591A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632114 | |||||||
| chr4:37632125 | A | C | 1 | a0001c0001t0042g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681-602T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632125 | |||||||
| chr4:37632137 | C | T | 41 | a0001c0001t0003g0052 a0001c0001t0003g0073 a0001c0001t0003g0093 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.681-614G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632137 | |||||||
| chr4:37632150 | G | A | 1 | a0001c0001t0042g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681-627C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632150 | |||||||
| chr4:37632171 | T | TTTTG | 229 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0025 others(226): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.681-652_681-649dup others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632171 | |||||||
| chr4:37632241 | G | A | 3 | a0001c0001t0046g0255 a0001c0006t0023g0024 a0001c0006t0023g0251 |
3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.681-718C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632241 | |||||||
| chr4:37632342 | T | C | 1 | a0001c0001t0042g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681-819A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632342 | |||||||
| chr4:37632345 | AT | A | 80 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(77): Show |
81 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.681-823delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632345 | |||||||
| chr4:37632403 | C | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.681-880G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632403 | |||||||
| chr4:37632445 | T | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0025 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.681-922A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632445 | |||||||
| chr4:37632534 | C | T | 23 | a0001c0001t0001g0303 a0001c0001t0001g0305 a0001c0001t0005g0103 others(20): Show |
24 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.681-1011G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632534 | |||||||
| chr4:37632570 | C | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.681-1047G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632570 | |||||||
| chr4:37632572 | A | G | 1 | a0001c0001t0003g0261 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.681-1049T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632572 | |||||||
| chr4:37632626 | T | C | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.681-1103A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632626 | |||||||
| chr4:37632701 | T | TA | 25 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(22): Show |
25 | HG00642.hp1 HG01175.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.681-1179dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632701 | |||||||
| chr4:37632915 | T | G | 1 | a0001c0001t0004g0245 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.681-1392A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632915 | |||||||
| chr4:37632921 | C | G | 41 | a0001c0001t0003g0052 a0001c0001t0003g0073 a0001c0001t0003g0093 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.681-1398G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632921 | |||||||
| chr4:37633087 | A | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(51): Show |
55 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.681-1564T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633087 | |||||||
| chr4:37633136 | C | T | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.681-1613G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633136 | |||||||
| chr4:37633179 | C | G | 3 | a0001c0001t0002g0119 a0001c0001t0002g0196 a0001c0001t0014g0170 |
3 | HG02074.hp2 NA18942.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.681-1656G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633179 | |||||||
| chr4:37633183 | T | C | 314 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.681-1660A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633183 | |||||||
| chr4:37633382 | T | C | 53 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(50): Show |
54 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.680+1505A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633382 | |||||||
| chr4:37633408 | CAAA | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0149 a0001c0001t0001g0184 others(6): Show |
9 | HG01884.hp2 HG03579.hp1 NA18522.hp2 others(6): Show |
intron_variant | MODIFIER | c.680+1476_680+1478d others(5): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAA | C | 18 | a0001c0001t0001g0081 a0001c0001t0001g0108 a0001c0001t0001g0110 others(15): Show |
18 | HG01081.hp2 HG01516.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.680+1475_680+1478d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAAA | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(32): Show |
36 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.680+1474_680+1478d others(7): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAAAA | C | 18 | a0001c0001t0001g0111 a0001c0001t0001g0248 a0001c0001t0006g0240 others(15): Show |
18 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.680+1473_680+1478d others(8): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAAAAA | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0272 others(10): Show |
13 | HG01175.hp1 HG01515.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.680+1472_680+1478d others(9): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAAAAA others(1): Show |
C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0118 a0001c0001t0001g0171 others(11): Show |
14 | HG00642.hp1 HG01256.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.680+1471_680+1478d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAAAAA others(2): Show |
C | 30 | a0001c0001t0001g0303 a0001c0001t0002g0033 a0001c0001t0002g0036 others(27): Show |
31 | HG01123.hp1 HG01192.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.680+1470_680+1478d others(11): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAAAAA others(3): Show |
C | 68 | a0001c0001t0001g0305 a0001c0001t0002g0018 a0001c0001t0002g0257 others(65): Show |
70 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.680+1469_680+1478d others(12): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAAAAA others(4): Show |
C | 28 | a0001c0001t0004g0047 a0001c0001t0004g0054 a0001c0001t0004g0055 others(25): Show |
28 | HG00140.hp1 HG00323.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.680+1468_680+1478d others(13): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAAAAA others(16): Show |
C | 3 | a0001c0001t0007g0173 a0002c0004t0041g0007 a0003c0005t0002g0185 |
3 | HG02970.hp2 NA19003.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.680+1456_680+1478d others(25): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633408 | CAAAAAAA others(17): Show |
C | 78 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(75): Show |
79 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.680+1455_680+1478d others(26): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | |||||||
| chr4:37633451 | T | C | 125 | a0001c0001t0001g0303 a0001c0001t0001g0305 a0001c0001t0002g0018 others(122): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.680+1436A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633451 | |||||||
| chr4:37633506 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.680+1381C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633506 | |||||||
| chr4:37633975 | G | A | 2 | a0001c0001t0034g0292 a0001c0001t0035g0253 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.680+912C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633975 | |||||||
| chr4:37634014 | C | T | 4 | a0001c0001t0001g0303 a0001c0001t0012g0004 a0001c0001t0012g0152 others(1): Show |
5 | HG02056.hp1 HG02735.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.680+873G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634014 | |||||||
| chr4:37634068 | G | T | 1 | a0001c0001t0002g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.680+819C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634068 | |||||||
| chr4:37634135 | G | A | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.680+752C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634135 | |||||||
| chr4:37634188 | A | G | 183 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0025 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.680+699T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634188 | |||||||
| chr4:37634519 | G | A | 1 | a0001c0001t0004g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.680+368C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634519 | |||||||
| chr4:37634592 | A | G | 2 | a0001c0001t0002g0069 a0001c0001t0002g0224 |
2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.680+295T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634592 | |||||||
| chr4:37634627 | T | C | 4 | a0001c0001t0001g0303 a0001c0001t0025g0013 a0001c0001t0025g0270 others(1): Show |
4 | HG02622.hp2 HG03704.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+260A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634627 | |||||||
| chr4:37634719 | C | T | 48 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(45): Show |
49 | HG00140.hp1 HG00741.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.680+168G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634719 | |||||||
| chr4:37634739 | G | A | 19 | a0001c0001t0001g0305 a0001c0001t0005g0103 a0001c0001t0005g0141 others(16): Show |
19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.680+148C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634739 | |||||||
| chr4:37635128 | T | G | 173 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(170): Show |
176 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(173): Show |
splice_region_variant&intron_variant | LOW | c.444-5A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635128 | |||||||
| chr4:37635222 | GA | G | 8 | a0001c0001t0002g0286 a0001c0001t0010g0134 a0001c0001t0010g0140 others(5): Show |
8 | HG02258.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.444-100delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635222 | |||||||
| chr4:37635300 | C | A | 25 | a0001c0001t0001g0305 a0001c0001t0005g0103 a0001c0001t0005g0141 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.444-177G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635300 | |||||||
| chr4:37635525 | G | A | 9 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 others(6): Show |
10 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.444-402C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635525 | |||||||
| chr4:37635534 | G | A | 5 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0164 others(2): Show |
5 | HG01081.hp1 HG01346.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-411C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635534 | |||||||
| chr4:37635652 | C | G | 1 | a0001c0001t0002g0126 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.444-529G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635652 | |||||||
| chr4:37635764 | T | C | 2 | a0001c0001t0001g0297 a0001c0001t0021g0296 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.444-641A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635764 | |||||||
| chr4:37635853 | C | G | 2 | a0001c0001t0003g0115 a0001c0001t0003g0128 |
2 | NA18966.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.444-730G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635853 | |||||||
| chr4:37635954 | G | A | 29 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0004g0241 others(26): Show |
30 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.444-831C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635954 | |||||||
| chr4:37635968 | T | C | 63 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.444-845A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635968 | |||||||
| chr4:37636146 | C | T | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.444-1023G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636146 | |||||||
| chr4:37636163 | A | G | 1 | a0001c0001t0038g0211 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.444-1040T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636163 | |||||||
| chr4:37636205 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.444-1082G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636205 | |||||||
| chr4:37636260 | G | C | 33 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(30): Show |
33 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.444-1137C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636260 | |||||||
| chr4:37636287 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.444-1164G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636287 | |||||||
| chr4:37636361 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0192 a0001c0001t0001g0213 others(1): Show |
4 | HG00741.hp1 HG01081.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-1238G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636361 | |||||||
| chr4:37636413 | A | G | 102 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0172 others(99): Show |
105 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.444-1290T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636413 | |||||||
| chr4:37636479 | C | G | 1 | a0001c0001t0002g0257 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.444-1356G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636479 | |||||||
| chr4:37636522 | A | G | 171 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(168): Show |
174 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.444-1399T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636522 | |||||||
| chr4:37636526 | C | T | 56 | a0001c0001t0001g0191 a0001c0001t0001g0279 a0001c0001t0002g0010 others(53): Show |
56 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.444-1403G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636526 | |||||||
| chr4:37636554 | C | T | 19 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(16): Show |
19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.444-1431G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636554 | |||||||
| chr4:37636594 | C | CA | 9 | a0001c0001t0002g0015 a0001c0001t0022g0166 a0001c0001t0029g0086 others(6): Show |
9 | HG02027.hp1 HG03209.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.444-1472dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636594 | |||||||
| chr4:37636594 | CA | C | 68 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(65): Show |
69 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.444-1472delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636594 | |||||||
| chr4:37636677 | G | A | 2 | a0001c0001t0016g0002 a0001c0001t0016g0026 |
3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.444-1554C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636677 | |||||||
| chr4:37636683 | G | A | 1 | a0001c0001t0005g0175 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.444-1560C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636683 | |||||||
| chr4:37636790 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.443+1657G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636790 | |||||||
| chr4:37637298 | G | A | 26 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(23): Show |
27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.443+1149C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637298 | |||||||
| chr4:37637307 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0277 |
2 | NA18970.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.443+1140A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637307 | |||||||
| chr4:37637355 | C | A | 3 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0074 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.443+1092G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637355 | |||||||
| chr4:37637450 | A | C | 26 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(23): Show |
27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.443+997T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637450 | |||||||
| chr4:37637485 | G | T | 3 | a0001c0001t0012g0004 a0001c0001t0012g0152 a0001c0001t0012g0293 |
4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+962C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637485 | |||||||
| chr4:37637517 | C | T | 62 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(59): Show |
63 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.443+930G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637517 | |||||||
| chr4:37637705 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.443+742G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637705 | |||||||
| chr4:37637930 | T | C | 3 | a0001c0001t0004g0241 a0001c0001t0038g0211 a0001c0001t0057g0288 |
3 | HG00323.hp2 HG01069.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.443+517A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637930 | |||||||
| chr4:37637944 | C | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0070 a0001c0001t0053g0051 |
3 | HG01099.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.443+503G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637944 | |||||||
| chr4:37638338 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.443+109C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37638338 | |||||||
| chr4:37638381 | A | G | 2 | a0001c0001t0016g0002 a0001c0001t0016g0026 |
3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.443+66T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37638381 | |||||||
| chr4:37638418 | G | A | 1 | a0001c0001t0021g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.443+29C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37638418 | |||||||
| chr4:37638643 | G | A | 4 | a0001c0001t0011g0053 a0001c0001t0011g0076 a0001c0001t0062g0077 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-139C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638643 | |||||||
| chr4:37638670 | G | A | 19 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(16): Show |
19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.386-166C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638670 | |||||||
| chr4:37638706 | T | C | 3 | a0001c0001t0004g0241 a0001c0001t0038g0211 a0001c0001t0057g0288 |
3 | HG00323.hp2 HG01069.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.386-202A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638706 | |||||||
| chr4:37638740 | A | G | 4 | a0001c0003t0017g0091 a0001c0003t0017g0249 a0001c0003t0017g0276 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-236T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638740 | |||||||
| chr4:37638762 | G | A | 43 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(40): Show |
43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.386-258C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638762 | |||||||
| chr4:37638767 | T | C | 101 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0172 others(98): Show |
104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-263A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638767 | |||||||
| chr4:37638861 | C | A | 176 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(173): Show |
179 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.386-357G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638861 | |||||||
| chr4:37638905 | T | C | 1 | a0001c0001t0004g0245 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.386-401A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638905 | |||||||
| chr4:37638921 | A | G | 1 | a0001c0001t0005g0299 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.386-417T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638921 | |||||||
| chr4:37639012 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0248 a0001c0001t0001g0280 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-508C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639012 | |||||||
| chr4:37639208 | C | A | 26 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(23): Show |
27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.386-704G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639208 | |||||||
| chr4:37639315 | C | T | 17 | a0001c0001t0004g0241 a0001c0001t0010g0134 a0001c0001t0010g0140 others(14): Show |
19 | HG00323.hp2 HG01069.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.386-811G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639315 | |||||||
| chr4:37639340 | C | T | 133 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(130): Show |
133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.386-836G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639340 | |||||||
| chr4:37639354 | A | C | 1 | a0001c0001t0001g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.386-850T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639354 | |||||||
| chr4:37639362 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.386-858G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639362 | |||||||
| chr4:37639363 | G | A | 57 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(54): Show |
57 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.386-859C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639363 | |||||||
| chr4:37639383 | C | CA | 62 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0111 others(59): Show |
62 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.386-880dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | |||||||
| chr4:37639383 | C | CAA | 46 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0203 others(43): Show |
48 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.386-881_386-880dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | |||||||
| chr4:37639383 | C | CAAA | 6 | a0001c0001t0001g0118 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG00323.hp2 HG01361.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-882_386-880dup others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | |||||||
| chr4:37639383 | C | CAAAA | 7 | a0001c0001t0001g0016 a0001c0001t0005g0103 a0001c0001t0006g0130 others(4): Show |
7 | HG01123.hp1 HG01175.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-883_386-880dup others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | |||||||
| chr4:37639383 | CA | C | 46 | a0001c0001t0001g0044 a0001c0001t0001g0184 a0001c0001t0002g0090 others(43): Show |
47 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.386-880delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | |||||||
| chr4:37639383 | CAA | C | 8 | a0001c0001t0001g0108 a0001c0001t0003g0105 a0001c0001t0003g0115 others(5): Show |
8 | HG00408.hp1 HG02258.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-881_386-880del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | |||||||
| chr4:37639415 | G | T | 5 | a0001c0001t0016g0002 a0001c0001t0016g0026 a0001c0001t0046g0255 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-911C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639415 | |||||||
| chr4:37639448 | C | T | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.386-944G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639448 | |||||||
| chr4:37639521 | C | CA | 43 | a0001c0001t0001g0157 a0001c0001t0002g0018 a0001c0001t0002g0033 others(40): Show |
43 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.386-1018dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639521 | |||||||
| chr4:37639521 | C | CAA | 33 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(30): Show |
33 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.386-1019_386-1018d others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639521 | |||||||
| chr4:37639585 | C | T | 1 | a0001c0001t0004g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.386-1081G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639585 | |||||||
| chr4:37639766 | G | C | 1 | a0001c0001t0001g0265 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.386-1262C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639766 | |||||||
| chr4:37639816 | A | C | 176 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(173): Show |
179 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.386-1312T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639816 | |||||||
| chr4:37640017 | A | G | 1 | a0001c0001t0012g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.386-1513T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640017 | |||||||
| chr4:37640071 | G | GT | 14 | a0001c0001t0004g0031 a0001c0001t0004g0082 a0001c0001t0004g0122 others(11): Show |
14 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.386-1568dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640071 | |||||||
| chr4:37640072 | T | G | 4 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1568A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640072 | |||||||
| chr4:37640136 | G | C | 4 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-1632C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640136 | |||||||
| chr4:37640468 | C | T | 3 | a0001c0001t0012g0004 a0001c0001t0012g0152 a0001c0001t0012g0293 |
4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1964G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640468 | |||||||
| chr4:37640491 | T | C | 5 | a0001c0001t0042g0318 a0001c0003t0017g0091 a0001c0003t0017g0249 others(2): Show |
5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-1987A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640491 | |||||||
| chr4:37640715 | G | A | 1 | a0001c0001t0003g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.386-2211C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640715 | |||||||
| chr4:37640733 | G | A | 315 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(312): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.386-2229C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640733 | |||||||
| chr4:37640747 | AT | A | 105 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0172 others(102): Show |
108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.386-2244delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640747 | |||||||
| chr4:37640802 | T | A | 3 | a0001c0001t0004g0164 a0001c0001t0004g0206 a0001c0001t0051g0120 |
3 | HG01346.hp1 HG01358.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.386-2298A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640802 | |||||||
| chr4:37640812 | A | G | 1 | a0001c0006t0023g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.386-2308T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640812 | |||||||
| chr4:37640845 | C | T | 1 | a0001c0001t0034g0292 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386-2341G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640845 | |||||||
| chr4:37641124 | G | A | 3 | a0001c0001t0004g0241 a0001c0001t0038g0211 a0001c0001t0057g0288 |
3 | HG00323.hp2 HG01069.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.386-2620C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641124 | |||||||
| chr4:37641245 | A | C | 58 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(55): Show |
58 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.386-2741T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641245 | |||||||
| chr4:37641457 | G | T | 4 | a0001c0001t0011g0053 a0001c0001t0011g0076 a0001c0001t0062g0077 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-2953C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641457 | |||||||
| chr4:37641570 | A | G | 142 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0172 others(139): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.386-3066T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641570 | |||||||
| chr4:37641675 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.386-3171G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641675 | |||||||
| chr4:37641678 | T | C | 2 | a0001c0001t0004g0241 a0001c0001t0038g0211 |
2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.386-3174A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641678 | |||||||
| chr4:37641691 | G | A | 1 | a0001c0001t0034g0292 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386-3187C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641691 | |||||||
| chr4:37641854 | T | A | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.386-3350A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641854 | |||||||
| chr4:37641972 | G | A | 15 | a0001c0001t0004g0031 a0001c0001t0004g0082 a0001c0001t0004g0122 others(12): Show |
15 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.386-3468C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641972 | |||||||
| chr4:37641979 | C | T | 50 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(47): Show |
51 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.386-3475G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641979 | |||||||
| chr4:37642073 | A | G | 59 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(56): Show |
59 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.386-3569T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642073 | |||||||
| chr4:37642097 | G | A | 11 | a0001c0001t0004g0241 a0001c0001t0010g0134 a0001c0001t0010g0140 others(8): Show |
12 | HG00323.hp2 HG01069.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.386-3593C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642097 | |||||||
| chr4:37642163 | G | C | 26 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(23): Show |
27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.386-3659C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642163 | |||||||
| chr4:37642475 | C | T | 3 | a0001c0001t0012g0004 a0001c0001t0012g0152 a0001c0001t0012g0293 |
4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-3971G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642475 | |||||||
| chr4:37642530 | T | C | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.386-4026A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642530 | |||||||
| chr4:37642643 | C | T | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.386-4139G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642643 | |||||||
| chr4:37642685 | A | G | 316 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(313): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.386-4181T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642685 | |||||||
| chr4:37642929 | A | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0213 a0001c0001t0059g0144 |
3 | HG01081.hp2 HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.386-4425T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642929 | |||||||
| chr4:37643019 | T | C | 9 | a0001c0001t0004g0082 a0001c0001t0004g0122 a0001c0001t0004g0127 others(6): Show |
9 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.385+4349A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643019 | |||||||
| chr4:37643264 | CCAAA | C | 22 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(19): Show |
23 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.385+4100_385+4103d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643264 | |||||||
| chr4:37643393 | C | T | 2 | a0001c0001t0004g0241 a0001c0001t0038g0211 |
2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.385+3975G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643393 | |||||||
| chr4:37643630 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0248 a0001c0001t0001g0280 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+3738A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643630 | |||||||
| chr4:37643638 | T | C | 1 | a0001c0001t0002g0304 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.385+3730A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643638 | |||||||
| chr4:37643767 | C | T | 120 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(117): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.385+3601G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643767 | |||||||
| chr4:37643960 | T | C | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.385+3408A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643960 | |||||||
| chr4:37644017 | G | A | 38 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(35): Show |
38 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.385+3351C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644017 | |||||||
| chr4:37644078 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.385+3290C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644078 | |||||||
| chr4:37644094 | G | A | 33 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(30): Show |
33 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.385+3274C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644094 | |||||||
| chr4:37644172 | A | T | 7 | a0001c0001t0008g0063 a0001c0001t0008g0064 a0001c0001t0008g0148 others(4): Show |
7 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+3196T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644172 | |||||||
| chr4:37644200 | C | A | 67 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(64): Show |
67 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.385+3168G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644200 | |||||||
| chr4:37644420 | T | C | 3 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 |
3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+2948A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644420 | |||||||
| chr4:37644438 | T | TTTTA | 108 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0044 others(105): Show |
110 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.385+2926_385+2929d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | |||||||
| chr4:37644438 | T | TTTTATTT others(1): Show |
27 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0265 others(24): Show |
27 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.385+2922_385+2929d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | |||||||
| chr4:37644438 | T | TTTTATTT others(5): Show |
33 | a0001c0001t0001g0172 a0001c0001t0001g0266 a0001c0001t0001g0303 others(30): Show |
34 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.385+2918_385+2929d others(14): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | |||||||
| chr4:37644438 | T | TTTTATTT others(9): Show |
4 | a0001c0001t0001g0305 a0001c0001t0004g0206 a0001c0001t0011g0053 others(1): Show |
4 | HG00408.hp2 HG00733.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+2914_385+2929d others(18): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | |||||||
| chr4:37644438 | T | TTTTTTTT others(5): Show |
2 | a0001c0001t0005g0214 a0001c0001t0005g0215 |
2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.385+2929_385+2930i others(14): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | |||||||
| chr4:37644438 | TTTTA | T | 29 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.385+2926_385+2929d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | |||||||
| chr4:37644438 | TTTTATTT others(1): Show |
T | 3 | a0001c0001t0004g0143 a0001c0001t0016g0002 a0001c0001t0016g0026 |
4 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+2922_385+2929d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | |||||||
| chr4:37644438 | TTTTATTT others(5): Show |
T | 16 | a0001c0001t0001g0139 a0001c0001t0001g0232 a0001c0001t0001g0235 others(13): Show |
16 | HG02027.hp1 HG02027.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.385+2918_385+2929d others(14): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | |||||||
| chr4:37644438 | TTTTATTT others(9): Show |
T | 1 | a0001c0001t0002g0174 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385+2914_385+2929d others(18): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | |||||||
| chr4:37644487 | A | G | 1 | a0001c0001t0046g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.385+2881T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644487 | |||||||
| chr4:37644545 | G | C | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+2823C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644545 | |||||||
| chr4:37644649 | G | A | 5 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 others(2): Show |
5 | HG00140.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+2719C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644649 | |||||||
| chr4:37644662 | G | A | 25 | a0001c0001t0004g0082 a0001c0001t0004g0122 a0001c0001t0004g0127 others(22): Show |
26 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.385+2706C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644662 | |||||||
| chr4:37644672 | C | T | 35 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(32): Show |
36 | HG00642.hp1 HG01106.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.385+2696G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644672 | |||||||
| chr4:37644914 | G | A | 60 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(57): Show |
60 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.385+2454C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644914 | |||||||
| chr4:37645074 | C | T | 5 | a0001c0001t0042g0318 a0001c0003t0017g0091 a0001c0003t0017g0249 others(2): Show |
5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+2294G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645074 | |||||||
| chr4:37645105 | G | A | 1 | a0001c0001t0034g0292 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385+2263C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645105 | |||||||
| chr4:37645119 | C | T | 1 | a0001c0001t0004g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.385+2249G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645119 | |||||||
| chr4:37645137 | A | G | 19 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(16): Show |
19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.385+2231T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645137 | |||||||
| chr4:37645151 | G | A | 5 | a0001c0001t0018g0019 a0001c0001t0018g0020 a0001c0001t0018g0028 others(2): Show |
5 | HG02451.hp2 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+2217C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645151 | |||||||
| chr4:37645298 | GC | G | 5 | a0001c0001t0018g0019 a0001c0001t0018g0020 a0001c0001t0018g0028 others(2): Show |
5 | HG02451.hp2 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+2069delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645298 | |||||||
| chr4:37645299 | C | G | 311 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.385+2069G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645299 | |||||||
| chr4:37645471 | G | A | 47 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(44): Show |
48 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.385+1897C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645471 | |||||||
| chr4:37645518 | T | A | 3 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 |
3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+1850A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645518 | |||||||
| chr4:37645548 | T | C | 60 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(57): Show |
60 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.385+1820A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645548 | |||||||
| chr4:37645611 | C | A | 25 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.385+1757G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645611 | |||||||
| chr4:37645612 | G | A | 97 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.385+1756C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645612 | |||||||
| chr4:37645732 | C | A | 97 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.385+1636G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645732 | |||||||
| chr4:37645771 | C | T | 3 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 |
3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+1597G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645771 | |||||||
| chr4:37645842 | C | T | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.385+1526G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645842 | |||||||
| chr4:37646115 | T | C | 47 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(44): Show |
48 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.385+1253A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646115 | |||||||
| chr4:37646222 | T | C | 97 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.385+1146A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646222 | |||||||
| chr4:37646274 | G | T | 43 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(40): Show |
43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.385+1094C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646274 | |||||||
| chr4:37646341 | T | C | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.385+1027A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646341 | |||||||
| chr4:37646433 | G | C | 47 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(44): Show |
48 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.385+935C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646433 | |||||||
| chr4:37646456 | G | T | 38 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(35): Show |
38 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.385+912C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646456 | |||||||
| chr4:37646562 | G | C | 2 | a0001c0001t0002g0069 a0001c0001t0002g0224 |
2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.385+806C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646562 | |||||||
| chr4:37646709 | A | G | 3 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 |
3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+659T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646709 | |||||||
| chr4:37646792 | A | C | 97 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.385+576T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646792 | |||||||
| chr4:37646793 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.385+575A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646793 | |||||||
| chr4:37646887 | C | T | 25 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.385+481G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646887 | |||||||
| chr4:37647086 | A | G | 149 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(146): Show |
151 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.385+282T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647086 | |||||||
| chr4:37647191 | A | G | 174 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(171): Show |
177 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.385+177T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647191 | |||||||
| chr4:37647223 | G | A | 38 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(35): Show |
38 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.385+145C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647223 | |||||||
| chr4:37647305 | G | A | 1 | a0001c0001t0003g0138 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.385+63C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647305 | |||||||
| chr4:37647336 | T | G | 5 | a0001c0001t0042g0318 a0001c0003t0017g0091 a0001c0003t0017g0249 others(2): Show |
5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+32A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647336 | |||||||
| chr4:37647670 | A | C | 36 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(33): Show |
36 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.314-231T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647670 | |||||||
| chr4:37647711 | T | C | 149 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(146): Show |
151 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.314-272A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647711 | |||||||
| chr4:37647781 | G | T | 25 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.314-342C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647781 | |||||||
| chr4:37647833 | T | G | 1 | a0001c0001t0003g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.314-394A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647833 | |||||||
| chr4:37647835 | C | T | 96 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(93): Show |
97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.314-396G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647835 | |||||||
| chr4:37647844 | T | C | 35 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(32): Show |
35 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.314-405A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647844 | |||||||
| chr4:37648057 | C | T | 1 | a0001c0001t0043g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.314-618G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648057 | |||||||
| chr4:37648140 | C | T | 25 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.314-701G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648140 | |||||||
| chr4:37648397 | G | A | 1 | a0001c0001t0014g0165 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.313+879C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648397 | |||||||
| chr4:37648449 | A | G | 1 | a0001c0001t0003g0168 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.313+827T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648449 | |||||||
| chr4:37648516 | C | G | 1 | a0001c0001t0002g0126 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.313+760G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648516 | |||||||
| chr4:37648700 | T | A | 1 | a0001c0001t0004g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.313+576A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648700 | |||||||
| chr4:37648810 | C | T | 1 | a0001c0001t0035g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.313+466G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648810 | |||||||
| chr4:37648819 | T | C | 1 | a0001c0001t0002g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.313+457A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648819 | |||||||
| chr4:37649533 | A | G | 97 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.89-33T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37649533 | |||||||
| chr4:37650024 | T | A | 96 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(93): Show |
97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.89-524A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650024 | |||||||
| chr4:37650037 | T | C | 96 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(93): Show |
97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.89-537A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650037 | |||||||
| chr4:37650095 | G | A | 41 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(38): Show |
41 | HG01081.hp1 HG01099.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-595C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650095 | |||||||
| chr4:37650106 | C | G | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-606G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650106 | |||||||
| chr4:37650156 | T | G | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-656A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650156 | |||||||
| chr4:37650192 | G | A | 25 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.89-692C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650192 | |||||||
| chr4:37650229 | G | A | 7 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0015 others(4): Show |
8 | HG01255.hp1 HG02280.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-729C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650229 | |||||||
| chr4:37650258 | T | A | 96 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(93): Show |
97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.89-758A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650258 | |||||||
| chr4:37650441 | C | A | 22 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(19): Show |
23 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.89-941G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650441 | |||||||
| chr4:37650886 | C | A | 25 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.89-1386G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650886 | |||||||
| chr4:37650887 | C | G | 25 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.89-1387G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650887 | |||||||
| chr4:37650945 | G | C | 2 | a0001c0001t0003g0218 a0001c0001t0013g0132 |
2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.89-1445C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650945 | |||||||
| chr4:37650972 | T | C | 1 | a0001c0001t0002g0119 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-1472A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650972 | |||||||
| chr4:37650973 | T | C | 173 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(170): Show |
176 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.89-1473A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650973 | |||||||
| chr4:37651057 | C | CA | 10 | a0001c0001t0001g0048 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
10 | HG00741.hp1 HG03139.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-1558dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651057 | |||||||
| chr4:37651057 | CA | C | 28 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(25): Show |
29 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.89-1558delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651057 | |||||||
| chr4:37651057 | CAA | C | 12 | a0001c0001t0013g0132 a0001c0001t0018g0019 a0001c0001t0018g0020 others(9): Show |
12 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-1559_89-1558del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651057 | |||||||
| chr4:37651057 | CAAA | C | 132 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(129): Show |
134 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.89-1560_89-1558del others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651057 | |||||||
| chr4:37651076 | A | T | 105 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(102): Show |
107 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.89-1576T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651076 | |||||||
| chr4:37651122 | C | G | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-1622G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651122 | |||||||
| chr4:37651193 | T | C | 121 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(118): Show |
123 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.89-1693A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651193 | |||||||
| chr4:37651202 | T | A | 1 | a0001c0001t0004g0084 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.89-1702A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651202 | |||||||
| chr4:37651323 | C | A | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-1823G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651323 | |||||||
| chr4:37651406 | T | A | 49 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(46): Show |
49 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.89-1906A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651406 | |||||||
| chr4:37651439 | A | G | 96 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(93): Show |
97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.89-1939T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651439 | |||||||
| chr4:37651548 | T | C | 1 | a0001c0001t0011g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.89-2048A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651548 | |||||||
| chr4:37651658 | C | A | 1 | a0001c0001t0005g0306 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.89-2158G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651658 | |||||||
| chr4:37651685 | G | A | 1 | a0001c0001t0015g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.89-2185C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651685 | |||||||
| chr4:37651787 | T | A | 2 | a0001c0001t0004g0230 a0001c0001t0004g0231 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.89-2287A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651787 | |||||||
| chr4:37651866 | C | T | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-2366G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651866 | |||||||
| chr4:37651884 | G | A | 138 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(135): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.89-2384C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651884 | |||||||
| chr4:37651927 | T | G | 1 | a0001c0001t0002g0021 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.89-2427A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651927 | |||||||
| chr4:37652000 | G | A | 37 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(34): Show |
37 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.89-2500C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652000 | |||||||
| chr4:37652027 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.89-2527G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652027 | |||||||
| chr4:37652034 | G | A | 141 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(138): Show |
143 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.89-2534C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652034 | |||||||
| chr4:37652040 | A | C | 7 | a0001c0001t0008g0063 a0001c0001t0008g0064 a0001c0001t0008g0148 others(4): Show |
7 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2540T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652040 | |||||||
| chr4:37652089 | T | C | 30 | a0001c0001t0001g0106 a0001c0001t0003g0052 a0001c0001t0003g0073 others(27): Show |
30 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-2589A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652089 | |||||||
| chr4:37652234 | A | G | 1 | a0001c0001t0024g0246 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.89-2734T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652234 | |||||||
| chr4:37652284 | C | T | 18 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.89-2784G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652284 | |||||||
| chr4:37652318 | A | G | 191 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(188): Show |
194 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.89-2818T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652318 | |||||||
| chr4:37652382 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.89-2882T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652382 | |||||||
| chr4:37652391 | G | A | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-2891C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652391 | |||||||
| chr4:37652573 | T | A | 139 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(136): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.89-3073A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652573 | |||||||
| chr4:37652628 | G | A | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.89-3128C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652628 | |||||||
| chr4:37652738 | A | G | 10 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0008g0063 others(7): Show |
10 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-3238T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652738 | |||||||
| chr4:37652796 | C | T | 2 | a0001c0001t0004g0057 a0001c0001t0004g0058 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.89-3296G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652796 | |||||||
| chr4:37652858 | G | T | 33 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(30): Show |
34 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.89-3358C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652858 | |||||||
| chr4:37652959 | G | C | 3 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 |
3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.89-3459C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652959 | |||||||
| chr4:37653198 | C | T | 1 | a0001c0001t0011g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.89-3698G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653198 | |||||||
| chr4:37653235 | T | G | 1 | a0001c0001t0006g0130 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.89-3735A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653235 | |||||||
| chr4:37653313 | T | TGTATTGA others(13): Show |
5 | a0001c0001t0004g0241 a0001c0001t0010g0134 a0001c0001t0010g0140 others(2): Show |
5 | HG00323.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-3833_89-3814dup others(20): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653313 | |||||||
| chr4:37653317 | T | C | 1 | a0001c0001t0043g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.89-3817A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653317 | |||||||
| chr4:37653324 | CTCAATAC others(40): Show |
C | 4 | a0001c0001t0001g0312 a0001c0001t0006g0136 a0001c0001t0025g0013 others(1): Show |
4 | HG02622.hp2 HG03017.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-3871_89-3825del others(47): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653324 | |||||||
| chr4:37653344 | CTCAATAC others(20): Show |
C | 193 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(190): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.89-3871_89-3845del others(27): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653344 | |||||||
| chr4:37653344 | CTCAATAC others(47): Show |
C | 1 | a0001c0001t0003g0107 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.89-3898_89-3845del others(54): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653344 | |||||||
| chr4:37653364 | CTCAATAT | C | 64 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(61): Show |
64 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.89-3871_89-3865del others(7): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653364 | |||||||
| chr4:37653370 | A | ACAAGTAT others(6): Show |
39 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0057 others(36): Show |
42 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.89-3871_89-3870ins others(13): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653370 | |||||||
| chr4:37653370 | A | ACAAGTAT others(26): Show |
3 | a0001c0001t0004g0205 a0001c0001t0004g0227 a0004c0008t0004g0267 |
3 | HG00140.hp1 HG01192.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.89-3871_89-3870ins others(33): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653370 | |||||||
| chr4:37653371 | T | C | 42 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0057 others(39): Show |
45 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.89-3871A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653371 | |||||||
| chr4:37653375 | A | G | 1 | a0001c0001t0021g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.89-3875T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653375 | |||||||
| chr4:37653415 | A | AT | 3 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 |
3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.89-3916_89-3915ins others(1): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653415 | |||||||
| chr4:37653416 | A | T | 6 | a0001c0001t0042g0318 a0001c0001t0057g0288 a0001c0003t0017g0091 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3916T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653416 | |||||||
| chr4:37653417 | C | A | 6 | a0001c0001t0042g0318 a0001c0001t0057g0288 a0001c0003t0017g0091 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3917G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653417 | |||||||
| chr4:37653417 | C | CCTCAATA others(47): Show |
1 | a0001c0001t0046g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89-3918_89-3917ins others(54): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653417 | |||||||
| chr4:37653417 | C | CTCAATAT others(19): Show |
3 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 |
3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.89-3918_89-3917ins others(26): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653417 | |||||||
| chr4:37653493 | A | C | 3 | a0001c0001t0004g0085 a0001c0001t0019g0060 a0001c0001t0019g0078 |
3 | HG01081.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.89-3993T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653493 | |||||||
| chr4:37653675 | C | G | 1 | a0001c0001t0004g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-4175G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653675 | |||||||
| chr4:37653768 | A | T | 133 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.89-4268T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653768 | |||||||
| chr4:37653872 | C | T | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.89-4372G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653872 | |||||||
| chr4:37653921 | A | G | 1 | a0001c0001t0043g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.89-4421T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653921 | |||||||
| chr4:37654031 | T | A | 1 | a0001c0001t0005g0189 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.89-4531A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654031 | |||||||
| chr4:37654186 | T | C | 1 | a0001c0001t0004g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-4686A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654186 | |||||||
| chr4:37654573 | C | T | 1 | a0001c0003t0017g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.89-5073G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654573 | |||||||
| chr4:37654615 | G | T | 18 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.89-5115C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654615 | |||||||
| chr4:37654648 | T | C | 1 | a0001c0001t0003g0105 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.89-5148A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654648 | |||||||
| chr4:37654668 | A | T | 27 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(24): Show |
28 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.89-5168T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654668 | |||||||
| chr4:37654704 | G | A | 170 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(167): Show |
173 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.89-5204C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654704 | |||||||
| chr4:37654837 | T | G | 63 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.89-5337A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654837 | |||||||
| chr4:37654881 | G | A | 1 | a0001c0001t0046g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89-5381C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654881 | |||||||
| chr4:37655242 | A | AAT | 3 | a0001c0001t0002g0295 a0001c0001t0004g0164 a0001c0001t0051g0120 |
3 | HG01358.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.89-5744_89-5743dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655242 | |||||||
| chr4:37655242 | A | AATAT | 4 | a0001c0001t0001g0191 a0001c0001t0002g0315 a0001c0001t0003g0131 others(1): Show |
4 | HG00558.hp2 HG00621.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-5746_89-5743dup others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655242 | |||||||
| chr4:37655242 | AAT | A | 140 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(137): Show |
142 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.89-5744_89-5743del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655242 | |||||||
| chr4:37655262 | A | T | 1 | a0001c0001t0036g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.89-5762T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655262 | |||||||
| chr4:37655497 | C | T | 1 | a0001c0001t0018g0028 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.89-5997G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655497 | |||||||
| chr4:37655507 | C | A | 1 | a0001c0001t0002g0113 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.89-6007G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655507 | |||||||
| chr4:37655517 | C | A | 2 | a0001c0001t0007g0027 a0001c0001t0026g0011 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.89-6017G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655517 | |||||||
| chr4:37655602 | C | T | 3 | a0001c0001t0030g0096 a0001c0001t0030g0116 a0001c0001t0064g0163 |
3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.89-6102G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655602 | |||||||
| chr4:37655675 | C | T | 1 | a0001c0001t0046g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89-6175G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655675 | |||||||
| chr4:37655821 | G | C | 5 | a0001c0001t0042g0318 a0001c0003t0017g0091 a0001c0003t0017g0249 others(2): Show |
5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-6321C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655821 | |||||||
| chr4:37655921 | G | A | 2 | a0001c0006t0023g0024 a0001c0006t0023g0251 |
2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.89-6421C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655921 | |||||||
| chr4:37655952 | G | A | 35 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(32): Show |
36 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.89-6452C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655952 | |||||||
| chr4:37655975 | A | G | 2 | a0001c0001t0003g0179 a0001c0001t0013g0142 |
2 | NA18994.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.89-6475T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655975 | |||||||
| chr4:37656116 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0281 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-6616C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656116 | |||||||
| chr4:37656159 | T | A | 2 | a0001c0001t0001g0297 a0001c0001t0021g0296 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.89-6659A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656159 | |||||||
| chr4:37656164 | T | C | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-6664A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656164 | |||||||
| chr4:37656251 | C | T | 5 | a0001c0001t0001g0225 a0001c0001t0002g0003 a0001c0001t0002g0008 others(2): Show |
6 | HG01255.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-6751G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656251 | |||||||
| chr4:37656324 | T | G | 2 | a0001c0006t0023g0024 a0001c0006t0023g0251 |
2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.89-6824A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656324 | |||||||
| chr4:37656348 | G | A | 3 | a0001c0001t0003g0154 a0001c0001t0003g0218 a0001c0001t0013g0132 |
3 | HG02132.hp2 NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.89-6848C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656348 | |||||||
| chr4:37656366 | G | A | 3 | a0001c0001t0005g0156 a0001c0001t0005g0299 a0001c0001t0005g0306 |
3 | HG02129.hp1 HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.89-6866C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656366 | |||||||
| chr4:37656568 | C | A | 1 | a0001c0001t0004g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-7068G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656568 | |||||||
| chr4:37656583 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-7083C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656583 | |||||||
| chr4:37656601 | A | G | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-7101T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656601 | |||||||
| chr4:37656611 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.89-7111C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656611 | |||||||
| chr4:37656653 | G | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-7153C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656653 | |||||||
| chr4:37656752 | C | T | 1 | a0001c0001t0067g0045 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.89-7252G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656752 | |||||||
| chr4:37656753 | G | C | 1 | a0001c0001t0035g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.89-7253C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656753 | |||||||
| chr4:37656804 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.89-7304A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656804 | |||||||
| chr4:37656878 | A | G | 11 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(8): Show |
11 | HG00140.hp1 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-7378T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656878 | |||||||
| chr4:37657100 | T | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0256 a0001c0001t0027g0114 |
3 | HG02258.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.89-7600A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657100 | |||||||
| chr4:37657135 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.89-7635T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657135 | |||||||
| chr4:37657144 | A | C | 1 | a0001c0001t0004g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-7644T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657144 | |||||||
| chr4:37657317 | C | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-7817G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657317 | |||||||
| chr4:37657480 | G | T | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-7980C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657480 | |||||||
| chr4:37657526 | C | T | 1 | a0001c0001t0004g0205 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.89-8026G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657526 | |||||||
| chr4:37657616 | G | T | 39 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0057 others(36): Show |
41 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-8116C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657616 | |||||||
| chr4:37657635 | C | T | 35 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(32): Show |
36 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.89-8135G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657635 | |||||||
| chr4:37657754 | A | G | 11 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(8): Show |
11 | HG00140.hp1 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-8254T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657754 | |||||||
| chr4:37657885 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0005g0103 a0001c0001t0005g0234 |
3 | HG01123.hp1 HG01346.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.89-8385C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657885 | |||||||
| chr4:37657894 | G | C | 5 | a0001c0001t0042g0318 a0001c0003t0017g0091 a0001c0003t0017g0249 others(2): Show |
5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-8394C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657894 | |||||||
| chr4:37657998 | A | G | 1 | a0001c0001t0004g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.89-8498T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657998 | |||||||
| chr4:37658113 | G | A | 35 | a0001c0001t0001g0172 a0001c0001t0001g0305 a0001c0001t0005g0103 others(32): Show |
36 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.89-8613C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658113 | |||||||
| chr4:37658255 | C | A | 1 | a0001c0001t0001g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.89-8755G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658255 | |||||||
| chr4:37658356 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.89-8856G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658356 | |||||||
| chr4:37658386 | C | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-8886G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658386 | |||||||
| chr4:37658464 | C | T | 3 | a0001c0001t0012g0004 a0001c0001t0012g0152 a0001c0001t0012g0293 |
4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-8964G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658464 | |||||||
| chr4:37658601 | C | A | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-9101G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658601 | |||||||
| chr4:37658660 | C | T | 11 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0036 others(8): Show |
11 | HG00140.hp1 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-9160G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658660 | |||||||
| chr4:37658688 | G | A | 3 | a0001c0001t0010g0134 a0001c0001t0010g0140 a0001c0001t0010g0290 |
3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.89-9188C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658688 | |||||||
| chr4:37658782 | G | A | 32 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(29): Show |
32 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.89-9282C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658782 | |||||||
| chr4:37658993 | G | A | 94 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(91): Show |
96 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.89-9493C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658993 | |||||||
| chr4:37659154 | A | G | 22 | a0001c0001t0001g0305 a0001c0001t0003g0209 a0001c0001t0005g0141 others(19): Show |
23 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.89-9654T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659154 | |||||||
| chr4:37659172 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-9672G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659172 | |||||||
| chr4:37659211 | G | A | 53 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0034 others(50): Show |
55 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.89-9711C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659211 | |||||||
| chr4:37659220 | A | G | 316 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(313): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.89-9720T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659220 | |||||||
| chr4:37659278 | A | G | 5 | a0001c0002t0002g0065 a0001c0002t0009g0001 a0001c0002t0009g0066 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-9778T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659278 | |||||||
| chr4:37659310 | T | A | 1 | a0001c0001t0004g0084 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.89-9810A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659310 | |||||||
| chr4:37659452 | G | A | 21 | a0001c0001t0001g0305 a0001c0001t0005g0156 a0001c0001t0005g0175 others(18): Show |
22 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.89-9952C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659452 | |||||||
| chr4:37659461 | T | C | 1 | a0001c0001t0034g0292 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.89-9961A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659461 | |||||||
| chr4:37659479 | T | C | 7 | a0001c0001t0001g0248 a0001c0001t0002g0036 a0001c0001t0018g0019 others(4): Show |
7 | HG02486.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-9979A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659479 | |||||||
| chr4:37659518 | T | A | 1 | a0001c0001t0003g0107 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.89-10018A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659518 | |||||||
| chr4:37659609 | C | G | 3 | a0001c0001t0002g0015 a0001c0001t0002g0069 a0001c0001t0007g0029 |
3 | HG02280.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.89-10109G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659609 | |||||||
| chr4:37659737 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89-10237A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659737 | |||||||
| chr4:37659848 | G | A | 17 | a0001c0001t0001g0305 a0001c0001t0002g0090 a0001c0001t0002g0295 others(14): Show |
17 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.89-10348C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659848 | |||||||
| chr4:37660041 | TG | T | 6 | a0001c0001t0001g0025 a0001c0001t0002g0036 a0001c0001t0018g0019 others(3): Show |
6 | HG02723.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-10542delC | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660041 | |||||||
| chr4:37660104 | GC | G | 22 | a0001c0001t0001g0198 a0001c0001t0001g0269 a0001c0001t0001g0310 others(19): Show |
22 | HG00597.hp2 HG01074.hp2 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.89-10605delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660104 | |||||||
| chr4:37660145 | T | C | 21 | a0001c0001t0001g0198 a0001c0001t0001g0269 a0001c0001t0001g0310 others(18): Show |
21 | HG01074.hp2 HG01975.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.89-10645A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660145 | |||||||
| chr4:37660152 | G | C | 1 | a0001c0001t0005g0175 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.89-10652C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660152 | |||||||
| chr4:37660162 | A | T | 30 | a0001c0001t0001g0070 a0001c0001t0001g0248 a0001c0001t0001g0259 others(27): Show |
31 | HG00099.hp1 HG01081.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-10662T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660162 | |||||||
| chr4:37660232 | G | C | 1 | a0001c0001t0002g0135 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.89-10732C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660232 | |||||||
| chr4:37660265 | G | A | 2 | a0001c0001t0004g0054 a0001c0001t0004g0244 |
2 | HG03688.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.89-10765C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660265 | |||||||
| chr4:37660401 | C | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0080 others(7): Show |
10 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-10901G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660401 | |||||||
| chr4:37660669 | C | T | 9 | a0001c0001t0001g0272 a0001c0001t0001g0275 a0001c0001t0002g0182 others(6): Show |
10 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-11169G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660669 | |||||||
| chr4:37660678 | C | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0080 others(8): Show |
11 | HG00099.hp1 HG00642.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-11178G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660678 | |||||||
| chr4:37660754 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.89-11254C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660754 | |||||||
| chr4:37660758 | G | A | 294 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(291): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.89-11258C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660758 | |||||||
| chr4:37660766 | T | A | 66 | a0001c0001t0001g0048 a0001c0001t0001g0087 a0001c0001t0001g0106 others(63): Show |
67 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.89-11266A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660766 | |||||||
| chr4:37660769 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.89-11269G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660769 | |||||||
| chr4:37660797 | C | T | 1 | a0001c0001t0020g0217 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.89-11297G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660797 | |||||||
| chr4:37660798 | A | G | 2 | a0001c0001t0020g0217 a0001c0001t0055g0049 |
2 | HG00438.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.89-11298T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660798 | |||||||
| chr4:37660807 | A | G | 1 | a0001c0001t0020g0217 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.89-11307T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660807 | |||||||
| chr4:37660821 | G | A | 4 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0003g0313 others(1): Show |
4 | HG02071.hp1 HG02129.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-11321C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660821 | |||||||
| chr4:37660839 | G | A | 91 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0032 others(88): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.89-11339C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660839 | |||||||
| chr4:37660848 | G | A | 16 | a0001c0001t0001g0192 a0001c0001t0001g0213 a0001c0001t0001g0256 others(13): Show |
16 | HG00733.hp1 HG01081.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-11348C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660848 | |||||||
| chr4:37660899 | C | T | 169 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(166): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.89-11399G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660899 | |||||||
| chr4:37660904 | G | T | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.89-11404C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660904 | |||||||
| chr4:37660910 | T | A | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.89-11410A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660910 | |||||||
| chr4:37660956 | G | A | 1 | a0001c0001t0003g0176 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.89-11456C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660956 | |||||||
| chr4:37660974 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.89-11474A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660974 | |||||||
| chr4:37660979 | C | T | 42 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0025 others(39): Show |
43 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.89-11479G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660979 | |||||||
| chr4:37660980 | G | A | 3 | a0001c0001t0002g0069 a0001c0001t0004g0055 a0001c0001t0016g0002 |
4 | HG01167.hp2 HG01169.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-11480C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660980 | |||||||
| chr4:37661009 | T | C | 1 | a0001c0001t0003g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.89-11509A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661009 | |||||||
| chr4:37661025 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.89-11525A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661025 | |||||||
| chr4:37661030 | C | CA | 9 | a0001c0001t0001g0032 a0001c0001t0002g0008 a0001c0001t0002g0015 others(6): Show |
10 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-11531dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661030 | |||||||
| chr4:37661148 | C | A | 2 | a0001c0001t0002g0260 a0001c0001t0049g0263 |
2 | NA18939.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.89-11648G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661148 | |||||||
| chr4:37661181 | T | C | 2 | a0001c0001t0003g0229 a0001c0001t0005g0233 |
2 | NA18941.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.89-11681A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661181 | |||||||
| chr4:37661267 | C | CTGTT | 48 | a0001c0001t0001g0016 a0001c0001t0001g0171 a0001c0001t0001g0201 others(45): Show |
49 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.89-11771_89-11768d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661267 | |||||||
| chr4:37661267 | C | CTGTTTGT others(1): Show |
28 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(25): Show |
28 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.89-11775_89-11768d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661267 | |||||||
| chr4:37661267 | CTGTT | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(41): Show |
46 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.89-11771_89-11768d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661267 | |||||||
| chr4:37661324 | C | A | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.89-11824G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661324 | |||||||
| chr4:37661424 | C | T | 14 | a0001c0001t0001g0106 a0001c0001t0001g0269 a0001c0001t0002g0097 others(11): Show |
14 | HG00621.hp2 HG01257.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-11924G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661424 | |||||||
| chr4:37661517 | C | A | 1 | a0001c0001t0003g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.89-12017G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661517 | |||||||
| chr4:37661560 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0007g0029 |
2 | NA18970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.89-12060C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661560 | |||||||
| chr4:37662021 | G | C | 117 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(114): Show |
119 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.89-12521C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662021 | |||||||
| chr4:37662050 | T | A | 52 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.89-12550A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662050 | |||||||
| chr4:37662126 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.89-12626G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662126 | |||||||
| chr4:37662300 | A | G | 12 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(9): Show |
12 | HG00140.hp1 HG02040.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-12800T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662300 | |||||||
| chr4:37662488 | A | G | 38 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(35): Show |
39 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.89-12988T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662488 | |||||||
| chr4:37662520 | G | A | 52 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.89-13020C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662520 | |||||||
| chr4:37662578 | TA | T | 109 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(106): Show |
110 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.89-13079delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662578 | |||||||
| chr4:37662697 | G | A | 32 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(29): Show |
33 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-13197C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662697 | |||||||
| chr4:37662734 | A | C | 27 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(24): Show |
27 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-13234T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662734 | |||||||
| chr4:37662961 | G | T | 10 | a0001c0001t0001g0171 a0001c0001t0001g0272 a0001c0001t0001g0273 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-13461C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662961 | |||||||
| chr4:37663055 | A | G | 115 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(112): Show |
117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.89-13555T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663055 | |||||||
| chr4:37663095 | C | T | 65 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(62): Show |
66 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.89-13595G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663095 | |||||||
| chr4:37663115 | G | A | 3 | a0001c0001t0035g0253 a0001c0001t0043g0254 a0001c0001t0046g0255 |
3 | HG02451.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.89-13615C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663115 | |||||||
| chr4:37663175 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89-13675G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663175 | |||||||
| chr4:37663176 | T | C | 44 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.89-13676A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663176 | |||||||
| chr4:37663279 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-13779G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663279 | |||||||
| chr4:37663422 | A | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.89-13922T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663422 | |||||||
| chr4:37663422 | A | T | 1 | a0002c0004t0041g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-13922T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663422 | |||||||
| chr4:37663658 | C | T | 189 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0042 others(186): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.89-14158G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663658 | |||||||
| chr4:37663738 | C | T | 4 | a0001c0001t0001g0272 a0001c0001t0001g0275 a0001c0001t0060g0271 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-14238G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663738 | |||||||
| chr4:37663763 | T | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.89-14263A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663763 | |||||||
| chr4:37663861 | C | A | 65 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(62): Show |
66 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.89-14361G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663861 | |||||||
| chr4:37663950 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.89-14450A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663950 | |||||||
| chr4:37664046 | A | G | 1 | a0001c0001t0006g0240 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-14546T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664046 | |||||||
| chr4:37664095 | C | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0015 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.89-14595G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664095 | |||||||
| chr4:37664117 | C | G | 62 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(59): Show |
63 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.89-14617G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664117 | |||||||
| chr4:37664194 | G | T | 1 | a0001c0007t0028g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.89-14694C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664194 | |||||||
| chr4:37664348 | C | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(62): Show |
66 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.89-14848G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664348 | |||||||
| chr4:37664369 | T | C | 7 | a0001c0001t0001g0256 a0001c0001t0002g0252 a0001c0001t0035g0253 others(4): Show |
7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-14869A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664369 | |||||||
| chr4:37664372 | CA | C | 84 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
85 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.89-14873delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664372 | |||||||
| chr4:37664388 | T | C | 5 | a0001c0001t0002g0135 a0001c0001t0005g0189 a0001c0001t0008g0137 others(2): Show |
5 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-14888A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664388 | |||||||
| chr4:37664433 | G | T | 1 | a0001c0001t0019g0030 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.89-14933C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664433 | |||||||
| chr4:37664489 | T | C | 1 | a0001c0001t0002g0095 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.89-14989A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664489 | |||||||
| chr4:37664557 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-15057A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664557 | |||||||
| chr4:37664806 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-15306C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664806 | |||||||
| chr4:37664901 | G | A | 7 | a0001c0001t0001g0256 a0001c0001t0002g0252 a0001c0001t0035g0253 others(4): Show |
7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-15401C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664901 | |||||||
| chr4:37665006 | C | T | 1 | a0001c0001t0013g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.89-15506G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665006 | |||||||
| chr4:37665173 | T | G | 8 | a0001c0001t0001g0307 a0001c0001t0001g0310 a0001c0001t0002g0298 others(5): Show |
8 | HG00423.hp2 HG01106.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-15673A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665173 | |||||||
| chr4:37665354 | C | G | 58 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(55): Show |
59 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.89-15854G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665354 | |||||||
| chr4:37665369 | T | G | 116 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(113): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.89-15869A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665369 | |||||||
| chr4:37665374 | A | C | 27 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(24): Show |
27 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-15874T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665374 | |||||||
| chr4:37665470 | A | T | 6 | a0001c0001t0001g0198 a0001c0001t0002g0126 a0001c0001t0002g0200 others(3): Show |
6 | HG01074.hp2 NA18950.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-15970T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665470 | |||||||
| chr4:37665519 | C | T | 2 | a0001c0001t0034g0292 a0001c0001t0042g0318 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.89-16019G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665519 | |||||||
| chr4:37665607 | C | G | 4 | a0001c0001t0001g0272 a0001c0001t0001g0275 a0001c0001t0060g0271 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-16107G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665607 | |||||||
| chr4:37665674 | C | A | 23 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(20): Show |
23 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.89-16174G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665674 | |||||||
| chr4:37665722 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0167 |
2 | HG00621.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.89-16222G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665722 | |||||||
| chr4:37665747 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-16247C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665747 | |||||||
| chr4:37665806 | G | A | 102 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(99): Show |
104 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.89-16306C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665806 | |||||||
| chr4:37665819 | T | A | 2 | a0001c0001t0003g0218 a0001c0001t0013g0132 |
2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.89-16319A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665819 | |||||||
| chr4:37665895 | T | C | 42 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(39): Show |
43 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.89-16395A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665895 | |||||||
| chr4:37665901 | A | G | 60 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(57): Show |
61 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.89-16401T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665901 | |||||||
| chr4:37666205 | G | C | 37 | a0001c0001t0001g0256 a0001c0001t0001g0297 a0001c0001t0001g0303 others(34): Show |
37 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.89-16705C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666205 | |||||||
| chr4:37666242 | A | G | 39 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(36): Show |
40 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.89-16742T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666242 | |||||||
| chr4:37666287 | C | T | 15 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0172 others(12): Show |
15 | HG00673.hp1 HG01123.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-16787G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666287 | |||||||
| chr4:37666288 | G | A | 2 | a0001c0001t0034g0292 a0001c0001t0042g0318 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.89-16788C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666288 | |||||||
| chr4:37666362 | C | T | 1 | a0001c0001t0003g0313 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.89-16862G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666362 | |||||||
| chr4:37666541 | T | C | 23 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(20): Show |
23 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.89-17041A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666541 | |||||||
| chr4:37666853 | G | A | 2 | a0001c0001t0011g0076 a0001c0001t0062g0077 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.89-17353C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666853 | |||||||
| chr4:37666862 | A | G | 70 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(67): Show |
71 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.89-17362T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666862 | |||||||
| chr4:37666915 | G | A | 3 | a0001c0001t0005g0151 a0001c0001t0012g0004 a0001c0001t0012g0152 |
4 | HG02735.hp1 HG03491.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-17415C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666915 | |||||||
| chr4:37667008 | G | A | 8 | a0001c0001t0003g0052 a0001c0001t0003g0073 a0001c0001t0008g0063 others(5): Show |
8 | HG01928.hp2 HG01975.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-17508C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667008 | |||||||
| chr4:37667033 | A | T | 1 | a0001c0001t0003g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.89-17533T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667033 | |||||||
| chr4:37667044 | G | C | 3 | a0001c0001t0001g0316 a0001c0001t0002g0260 a0001c0001t0049g0263 |
3 | HG02040.hp1 NA18939.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.89-17544C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667044 | |||||||
| chr4:37667054 | G | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.89-17554C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667054 | |||||||
| chr4:37667090 | A | G | 1 | a0001c0001t0006g0309 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.89-17590T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667090 | |||||||
| chr4:37667125 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-17625G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667125 | |||||||
| chr4:37667126 | G | A | 20 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0004g0031 others(17): Show |
20 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.89-17626C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667126 | |||||||
| chr4:37667163 | A | C | 2 | a0001c0001t0013g0250 a0001c0006t0023g0251 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.89-17663T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667163 | |||||||
| chr4:37667221 | G | A | 1 | a0001c0001t0004g0059 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.89-17721C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667221 | |||||||
| chr4:37667275 | T | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0006t0023g0024 |
3 | HG01167.hp1 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.89-17775A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667275 | |||||||
| chr4:37667581 | G | A | 1 | a0002c0004t0033g0006 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.89-18081C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667581 | |||||||
| chr4:37667735 | CT | C | 33 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(30): Show |
34 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.89-18236delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667735 | |||||||
| chr4:37667875 | C | G | 102 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(99): Show |
104 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.88+18325G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667875 | |||||||
| chr4:37667951 | A | G | 70 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(67): Show |
71 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.88+18249T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667951 | |||||||
| chr4:37668076 | G | C | 2 | a0001c0001t0001g0256 a0001c0001t0002g0252 |
2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88+18124C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668076 | |||||||
| chr4:37668079 | AT | A | 34 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(31): Show |
35 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.88+18120delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668079 | |||||||
| chr4:37668213 | T | C | 1 | a0001c0001t0058g0239 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.88+17987A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668213 | |||||||
| chr4:37668227 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.88+17973A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668227 | |||||||
| chr4:37668261 | A | G | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.88+17939T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668261 | |||||||
| chr4:37668263 | C | A | 1 | a0001c0001t0002g0257 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+17937G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668263 | |||||||
| chr4:37668264 | G | C | 2 | a0001c0001t0001g0025 a0001c0001t0047g0014 |
2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.88+17936C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668264 | |||||||
| chr4:37668268 | C | G | 4 | a0001c0001t0011g0053 a0001c0001t0011g0075 a0001c0001t0011g0076 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+17932G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668268 | |||||||
| chr4:37668269 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.88+17931C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668269 | |||||||
| chr4:37668282 | A | C | 1 | a0001c0001t0010g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.88+17918T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668282 | |||||||
| chr4:37668450 | G | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17750C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668450 | |||||||
| chr4:37668460 | C | T | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0002g0090 others(2): Show |
5 | HG01516.hp2 HG01517.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+17740G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668460 | |||||||
| chr4:37668517 | G | C | 197 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0042 others(194): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.88+17683C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668517 | |||||||
| chr4:37668522 | A | G | 2 | a0001c0001t0013g0250 a0001c0006t0023g0251 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+17678T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668522 | |||||||
| chr4:37668551 | G | C | 1 | a0001c0001t0034g0292 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.88+17649C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668551 | |||||||
| chr4:37668565 | A | C | 2 | a0001c0001t0001g0297 a0001c0001t0021g0296 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.88+17635T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668565 | |||||||
| chr4:37668626 | C | G | 2 | a0001c0001t0002g0222 a0001c0001t0065g0133 |
2 | HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.88+17574G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668626 | |||||||
| chr4:37668636 | A | AC | 5 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0003g0178 others(2): Show |
5 | HG02080.hp1 HG02602.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+17563dupG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668636 | |||||||
| chr4:37668659 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.88+17541C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668659 | |||||||
| chr4:37668673 | G | A | 4 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0003g0313 others(1): Show |
4 | HG02071.hp1 HG02129.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+17527C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668673 | |||||||
| chr4:37668733 | G | A | 27 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(24): Show |
27 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.88+17467C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668733 | |||||||
| chr4:37668745 | G | C | 1 | a0001c0001t0002g0162 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.88+17455C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668745 | |||||||
| chr4:37668745 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.88+17455C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668745 | |||||||
| chr4:37668753 | TCCCATCT others(33): Show |
T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(30): Show |
34 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.88+17407_88+17446d others(42): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668753 | |||||||
| chr4:37668766 | G | A | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0002g0090 others(2): Show |
5 | HG01516.hp2 HG01517.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+17434C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668766 | |||||||
| chr4:37668793 | C | T | 279 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0032 others(276): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.88+17407G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668793 | |||||||
| chr4:37668800 | T | TA | 4 | a0001c0001t0001g0118 a0001c0001t0001g0220 a0001c0001t0001g0226 others(1): Show |
4 | HG01256.hp1 HG01361.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+17399dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668800 | |||||||
| chr4:37668813 | G | C | 4 | a0001c0001t0011g0053 a0001c0001t0011g0075 a0001c0001t0011g0076 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+17387C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668813 | |||||||
| chr4:37668838 | C | G | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17362G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668838 | |||||||
| chr4:37668845 | G | C | 3 | a0001c0001t0008g0063 a0001c0001t0008g0064 a0001c0001t0024g0062 |
3 | NA18977.hp2 NA18983.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.88+17355C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668845 | |||||||
| chr4:37668852 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+17348C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668852 | |||||||
| chr4:37668871 | T | C | 115 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(112): Show |
117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.88+17329A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668871 | |||||||
| chr4:37668873 | G | A | 2 | a0001c0001t0013g0250 a0001c0006t0023g0251 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+17327C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668873 | |||||||
| chr4:37668902 | G | C | 2 | a0001c0001t0002g0222 a0001c0001t0065g0133 |
2 | HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.88+17298C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668902 | |||||||
| chr4:37668958 | GGTGAGGA others(169): Show |
G | 5 | a0001c0001t0004g0054 a0001c0001t0004g0109 a0001c0001t0004g0122 others(2): Show |
5 | HG01361.hp1 HG03490.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+17066_88+17241d others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668958 | |||||||
| chr4:37668960 | T | C | 1 | a0001c0001t0013g0250 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.88+17240A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668960 | |||||||
| chr4:37668986 | G | T | 2 | a0001c0001t0013g0250 a0001c0006t0023g0251 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+17214C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668986 | |||||||
| chr4:37668991 | A | G | 100 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(97): Show |
102 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.88+17209T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668991 | |||||||
| chr4:37668995 | A | G | 100 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(97): Show |
102 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.88+17205T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668995 | |||||||
| chr4:37669006 | GGGGGGGT others(41): Show |
G | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17146_88+17193d others(50): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669006 | |||||||
| chr4:37669088 | C | T | 2 | a0001c0001t0004g0143 a0001c0001t0063g0177 |
2 | HG00741.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.88+17112G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669088 | |||||||
| chr4:37669092 | T | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17108A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669092 | |||||||
| chr4:37669106 | C | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17094G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669106 | |||||||
| chr4:37669107 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0002g0252 |
2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88+17093C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669107 | |||||||
| chr4:37669117 | G | A | 65 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(62): Show |
66 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.88+17083C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669117 | |||||||
| chr4:37669119 | C | A | 8 | a0001c0001t0004g0079 a0001c0001t0004g0082 a0001c0001t0004g0083 others(5): Show |
8 | HG01081.hp1 HG01358.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+17081G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669119 | |||||||
| chr4:37669121 | G | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17079C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669121 | |||||||
| chr4:37669121 | GCCCCTAC others(347): Show |
G | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.88+16725_88+17078d others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669121 | |||||||
| chr4:37669124 | C | T | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17076G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669124 | |||||||
| chr4:37669153 | CGGCCAGC others(46): Show |
C | 4 | a0001c0001t0001g0236 a0001c0001t0001g0256 a0001c0001t0002g0252 others(1): Show |
4 | HG01081.hp2 HG02055.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+16994_88+17046d others(55): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669153 | |||||||
| chr4:37669161 | C | G | 2 | a0001c0001t0013g0250 a0001c0006t0023g0251 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+17039G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669161 | |||||||
| chr4:37669166 | C | T | 1 | a0001c0001t0002g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+17034G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669166 | |||||||
| chr4:37669170 | C | A | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0002g0268 others(2): Show |
5 | NA18945.hp1 NA18950.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+17030G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669170 | |||||||
| chr4:37669170 | C | T | 2 | a0001c0001t0014g0165 a0001c0001t0050g0099 |
2 | HG01257.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.88+17030G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669170 | |||||||
| chr4:37669181 | TG | T | 196 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(193): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.88+17018delC | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669181 | |||||||
| chr4:37669181 | TGG | T | 62 | a0001c0001t0001g0016 a0001c0001t0001g0171 a0001c0001t0001g0272 others(59): Show |
63 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.88+17017_88+17018d others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669181 | |||||||
| chr4:37669186 | GGGGGGGT others(41): Show |
G | 1 | a0001c0001t0002g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.88+16966_88+17013d others(50): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669186 | |||||||
| chr4:37669187 | GGGGGGTC others(40): Show |
G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0025 others(12): Show |
15 | HG01243.hp1 HG01255.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+16966_88+17012d others(49): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669187 | |||||||
| chr4:37669188 | G | A | 1 | a0001c0001t0003g0237 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.88+17012C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669188 | |||||||
| chr4:37669188 | GGGGGTCA others(39): Show |
G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0010g0035 others(2): Show |
5 | HG01167.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+16966_88+17011d others(48): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669188 | |||||||
| chr4:37669189 | GGGGTCAG others(38): Show |
G | 4 | a0001c0001t0004g0074 a0001c0001t0011g0053 a0001c0001t0011g0076 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+16966_88+17010d others(47): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669189 | |||||||
| chr4:37669190 | G | T | 2 | a0001c0001t0010g0140 a0001c0001t0057g0288 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.88+17010C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669190 | |||||||
| chr4:37669190 | GGGTCAGC others(37): Show |
G | 4 | a0001c0001t0002g0008 a0001c0001t0002g0069 a0001c0001t0011g0075 others(1): Show |
4 | HG02257.hp2 HG02273.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+16966_88+17009d others(46): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669190 | |||||||
| chr4:37669191 | GGTCAGCC others(36): Show |
G | 1 | a0001c0001t0001g0070 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+16966_88+17008d others(45): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669191 | |||||||
| chr4:37669194 | C | A | 1 | a0001c0001t0001g0149 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.88+17006G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669194 | |||||||
| chr4:37669218 | C | T | 29 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(26): Show |
29 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.88+16982G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669218 | |||||||
| chr4:37669220 | GTCCGGGA others(40): Show |
G | 1 | a0001c0001t0016g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.88+16933_88+16979d others(49): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669220 | |||||||
| chr4:37669249 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0002g0069 a0001c0001t0053g0051 |
3 | HG02257.hp2 HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.88+16951G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669249 | |||||||
| chr4:37669253 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0002g0069 a0001c0001t0053g0051 |
3 | HG02257.hp2 HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.88+16947G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669253 | |||||||
| chr4:37669267 | A | G | 30 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(27): Show |
30 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.88+16933T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669267 | |||||||
| chr4:37669294 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.88+16906G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669294 | |||||||
| chr4:37669298 | C | G | 4 | a0001c0001t0001g0070 a0001c0001t0002g0069 a0001c0001t0016g0002 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16902G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669298 | |||||||
| chr4:37669327 | T | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(39): Show |
42 | HG00140.hp1 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.88+16873A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669327 | |||||||
| chr4:37669340 | G | T | 1 | a0001c0001t0005g0103 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.88+16860C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669340 | |||||||
| chr4:37669348 | C | T | 2 | a0001c0001t0034g0292 a0001c0001t0042g0318 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.88+16852G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669348 | |||||||
| chr4:37669349 | G | C | 1 | a0001c0001t0019g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.88+16851C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669349 | |||||||
| chr4:37669375 | C | T | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0002g0090 others(2): Show |
5 | HG01516.hp2 HG01517.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16825G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669375 | |||||||
| chr4:37669378 | C | A | 1 | a0001c0001t0006g0136 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.88+16822G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669378 | |||||||
| chr4:37669394 | G | A | 1 | a0001c0001t0004g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.88+16806C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669394 | |||||||
| chr4:37669409 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.88+16791C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669409 | |||||||
| chr4:37669430 | G | C | 4 | a0001c0001t0001g0070 a0001c0001t0002g0069 a0001c0001t0016g0002 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16770C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669430 | |||||||
| chr4:37669442 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+16758G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669442 | |||||||
| chr4:37669446 | C | T | 2 | a0001c0001t0034g0292 a0001c0001t0042g0318 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.88+16754G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669446 | |||||||
| chr4:37669461 | G | A | 4 | a0001c0001t0001g0070 a0001c0001t0002g0069 a0001c0001t0016g0002 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16739C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669461 | |||||||
| chr4:37669541 | G | A | 2 | a0001c0001t0013g0250 a0001c0006t0023g0251 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+16659C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669541 | |||||||
| chr4:37669561 | G | A | 38 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(35): Show |
39 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.88+16639C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669561 | |||||||
| chr4:37669573 | A | G | 4 | a0001c0001t0001g0225 a0001c0001t0002g0223 a0001c0001t0002g0224 others(1): Show |
4 | HG02572.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+16627T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669573 | |||||||
| chr4:37669575 | T | C | 4 | a0001c0001t0001g0225 a0001c0001t0002g0223 a0001c0001t0002g0224 others(1): Show |
4 | HG02572.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+16625A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669575 | |||||||
| chr4:37669596 | G | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+16604C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669596 | |||||||
| chr4:37669634 | G | A | 4 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0003g0313 others(1): Show |
4 | HG02071.hp1 HG02129.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+16566C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669634 | |||||||
| chr4:37669702 | A | G | 4 | a0001c0001t0001g0070 a0001c0001t0002g0069 a0001c0001t0016g0002 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16498T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669702 | |||||||
| chr4:37669706 | T | C | 69 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(66): Show |
70 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.88+16494A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669706 | |||||||
| chr4:37669827 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0002g0069 a0001c0001t0016g0002 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16373G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669827 | |||||||
| chr4:37669847 | G | A | 191 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0042 others(188): Show |
194 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.88+16353C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669847 | |||||||
| chr4:37669895 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+16305G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669895 | |||||||
| chr4:37669897 | A | C | 106 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(103): Show |
108 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.88+16303T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669897 | |||||||
| chr4:37669930 | A | G | 3 | a0001c0001t0010g0290 a0001c0001t0027g0289 a0001c0003t0052g0291 |
3 | HG01884.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.88+16270T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669930 | |||||||
| chr4:37669934 | A | G | 2 | a0001c0001t0039g0039 a0001c0001t0040g0040 |
2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.88+16266T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669934 | |||||||
| chr4:37669941 | T | C | 2 | a0001c0001t0034g0292 a0001c0001t0042g0318 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.88+16259A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669941 | |||||||
| chr4:37670056 | TA | T | 20 | a0001c0001t0001g0025 a0001c0001t0002g0010 a0001c0001t0002g0036 others(17): Show |
21 | HG02071.hp1 HG02129.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.88+16143delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670056 | |||||||
| chr4:37670061 | A | G | 1 | a0001c0001t0007g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.88+16139T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670061 | |||||||
| chr4:37670100 | A | T | 2 | a0001c0001t0006g0311 a0001c0001t0031g0301 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.88+16100T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670100 | |||||||
| chr4:37670210 | G | GT | 41 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0171 others(38): Show |
42 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.88+15989dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670210 | |||||||
| chr4:37670242 | G | A | 1 | a0001c0001t0004g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88+15958C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670242 | |||||||
| chr4:37670339 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.88+15861C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670339 | |||||||
| chr4:37670566 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.88+15634G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670566 | |||||||
| chr4:37670575 | C | CT | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0023 others(28): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+15624dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670575 | |||||||
| chr4:37670767 | T | A | 6 | a0001c0001t0001g0256 a0001c0001t0002g0252 a0001c0001t0043g0254 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+15433A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670767 | |||||||
| chr4:37670772 | C | T | 19 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0034 others(16): Show |
19 | HG01167.hp1 HG01243.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.88+15428G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670772 | |||||||
| chr4:37670789 | A | G | 288 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(285): Show |
293 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.88+15411T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670789 | |||||||
| chr4:37670818 | C | T | 1 | a0001c0001t0055g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+15382G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670818 | |||||||
| chr4:37671031 | C | G | 3 | a0001c0001t0001g0037 a0001c0001t0006g0038 a0001c0001t0006g0041 |
3 | HG00323.hp1 HG01123.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.88+15169G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671031 | |||||||
| chr4:37671058 | T | C | 5 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(2): Show |
5 | HG01243.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+15142A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671058 | |||||||
| chr4:37671082 | A | G | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.88+15118T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671082 | |||||||
| chr4:37671109 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.88+15091T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671109 | |||||||
| chr4:37671200 | T | C | 1 | a0001c0001t0002g0010 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.88+15000A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671200 | |||||||
| chr4:37671220 | C | G | 26 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0184 others(23): Show |
26 | HG00621.hp2 HG01257.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+14980G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671220 | |||||||
| chr4:37671253 | C | G | 228 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0042 others(225): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.88+14947G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671253 | |||||||
| chr4:37671259 | C | T | 224 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0042 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.88+14941G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671259 | |||||||
| chr4:37671272 | A | G | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.88+14928T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671272 | |||||||
| chr4:37671371 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.88+14829C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671371 | |||||||
| chr4:37671657 | T | C | 13 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(10): Show |
13 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+14543A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671657 | |||||||
| chr4:37671723 | G | GCTATGCC others(12): Show |
5 | a0001c0001t0001g0316 a0001c0001t0002g0314 a0001c0001t0002g0315 others(2): Show |
5 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14476_88+14477i others(21): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671723 | |||||||
| chr4:37671724 | G | A | 5 | a0001c0001t0001g0316 a0001c0001t0002g0314 a0001c0001t0002g0315 others(2): Show |
5 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14476C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671724 | |||||||
| chr4:37671726 | C | CTA | 5 | a0001c0001t0001g0316 a0001c0001t0002g0314 a0001c0001t0002g0315 others(2): Show |
5 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14473_88+14474i others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671726 | |||||||
| chr4:37671732 | T | C | 1 | a0001c0001t0002g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.88+14468A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671732 | |||||||
| chr4:37671773 | TC | T | 230 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0042 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.88+14426delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671773 | |||||||
| chr4:37671808 | T | G | 1 | a0001c0001t0008g0137 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.88+14392A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671808 | |||||||
| chr4:37671933 | T | C | 4 | a0001c0001t0001g0310 a0001c0001t0002g0298 a0001c0001t0002g0304 others(1): Show |
4 | HG01106.hp1 HG02273.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+14267A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671933 | |||||||
| chr4:37671934 | G | A | 2 | a0001c0001t0002g0298 a0001c0001t0002g0304 |
2 | HG01106.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.88+14266C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671934 | |||||||
| chr4:37671968 | G | T | 2 | a0001c0003t0017g0091 a0001c0003t0017g0249 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.88+14232C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671968 | |||||||
| chr4:37672004 | G | A | 216 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0042 others(213): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.88+14196C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672004 | |||||||
| chr4:37672264 | T | A | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.88+13936A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672264 | |||||||
| chr4:37672332 | G | A | 2 | a0001c0001t0013g0250 a0001c0006t0023g0251 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+13868C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672332 | |||||||
| chr4:37672344 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.88+13856A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672344 | |||||||
| chr4:37672541 | C | A | 3 | a0001c0001t0035g0253 a0001c0001t0043g0254 a0001c0001t0046g0255 |
3 | HG02451.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.88+13659G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672541 | |||||||
| chr4:37672686 | T | C | 1 | a0001c0001t0059g0144 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.88+13514A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672686 | |||||||
| chr4:37672732 | T | C | 1 | a0001c0001t0029g0147 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.88+13468A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672732 | |||||||
| chr4:37672755 | C | T | 26 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
26 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.88+13445G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672755 | |||||||
| chr4:37673048 | A | C | 1 | a0001c0001t0002g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.88+13152T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673048 | |||||||
| chr4:37673052 | G | T | 265 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(262): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.88+13148C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673052 | |||||||
| chr4:37673172 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0002g0252 |
2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88+13028A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673172 | |||||||
| chr4:37673175 | A | T | 2 | a0001c0001t0013g0250 a0001c0006t0023g0251 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+13025T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673175 | |||||||
| chr4:37673186 | C | CTT | 11 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(8): Show |
11 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+13012_88+13013d others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | |||||||
| chr4:37673186 | C | CTTTTTT | 168 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(165): Show |
171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.88+13008_88+13013d others(8): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | |||||||
| chr4:37673186 | C | CTTTTTTT | 79 | a0001c0001t0001g0087 a0001c0001t0001g0106 a0001c0001t0001g0108 others(76): Show |
80 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.88+13007_88+13013d others(9): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | |||||||
| chr4:37673186 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0002g0097 a0001c0001t0003g0100 a0001c0001t0005g0151 others(5): Show |
8 | HG01433.hp2 HG01928.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+13006_88+13013d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | |||||||
| chr4:37673186 | C | T | 1 | a0001c0001t0003g0138 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.88+13014G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | |||||||
| chr4:37673186 | CT | C | 9 | a0001c0001t0001g0312 a0001c0001t0002g0003 a0001c0001t0002g0295 others(6): Show |
10 | HG01070.hp1 HG01071.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+13013delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | |||||||
| chr4:37673190 | T | C | 7 | a0001c0001t0001g0256 a0001c0001t0002g0252 a0001c0001t0035g0253 others(4): Show |
7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+13010A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673190 | |||||||
| chr4:37673213 | A | G | 8 | a0001c0001t0001g0172 a0001c0001t0002g0104 a0001c0001t0002g0174 others(5): Show |
8 | HG00673.hp1 HG01123.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+12987T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673213 | |||||||
| chr4:37673218 | T | C | 305 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(302): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.88+12982A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673218 | |||||||
| chr4:37673253 | T | C | 273 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.88+12947A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673253 | |||||||
| chr4:37673264 | A | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
41 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+12936T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673264 | |||||||
| chr4:37673288 | T | C | 1 | a0001c0003t0017g0091 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.88+12912A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673288 | |||||||
| chr4:37673389 | G | C | 1 | a0001c0001t0003g0229 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.88+12811C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673389 | |||||||
| chr4:37673467 | C | T | 1 | a0001c0001t0057g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.88+12733G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673467 | |||||||
| chr4:37673559 | G | A | 18 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(15): Show |
18 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+12641C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673559 | |||||||
| chr4:37673766 | G | A | 191 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0042 others(188): Show |
194 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.88+12434C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673766 | |||||||
| chr4:37673822 | G | A | 14 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(11): Show |
14 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+12378C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673822 | |||||||
| chr4:37674071 | G | A | 7 | a0001c0001t0001g0256 a0001c0001t0002g0252 a0001c0001t0035g0253 others(4): Show |
7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+12129C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674071 | |||||||
| chr4:37674161 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.88+12039A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674161 | |||||||
| chr4:37674162 | A | C | 6 | a0001c0001t0010g0290 a0001c0001t0027g0289 a0001c0001t0034g0292 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+12038T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674162 | |||||||
| chr4:37674269 | C | T | 2 | a0001c0001t0003g0150 a0001c0001t0068g0092 |
2 | HG00558.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.88+11931G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674269 | |||||||
| chr4:37674319 | A | C | 273 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.88+11881T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674319 | |||||||
| chr4:37674540 | G | A | 273 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.88+11660C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674540 | |||||||
| chr4:37674556 | A | C | 273 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.88+11644T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674556 | |||||||
| chr4:37674629 | G | A | 6 | a0001c0001t0002g0003 a0001c0001t0004g0074 a0001c0001t0011g0053 others(3): Show |
7 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+11571C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674629 | |||||||
| chr4:37674746 | GC | G | 273 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.88+11453delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674746 | |||||||
| chr4:37674759 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.88+11441A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674759 | |||||||
| chr4:37675348 | T | C | 2 | a0001c0001t0004g0230 a0001c0001t0004g0231 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.88+10852A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675348 | |||||||
| chr4:37675471 | T | C | 59 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0265 others(56): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.88+10729A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675471 | |||||||
| chr4:37675705 | C | T | 8 | a0001c0001t0002g0102 a0001c0001t0003g0100 a0001c0001t0003g0167 others(5): Show |
8 | HG00621.hp2 HG02074.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+10495G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675705 | |||||||
| chr4:37675886 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0053g0051 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.88+10314A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675886 | |||||||
| chr4:37675932 | C | G | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.88+10268G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675932 | |||||||
| chr4:37675978 | T | C | 1 | a0001c0001t0056g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.88+10222A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675978 | |||||||
| chr4:37676196 | C | G | 1 | a0001c0001t0004g0084 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.88+10004G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676196 | |||||||
| chr4:37676357 | C | T | 38 | a0001c0001t0001g0256 a0001c0001t0001g0297 a0001c0001t0001g0303 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.88+9843G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676357 | |||||||
| chr4:37676442 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.88+9758C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676442 | |||||||
| chr4:37676516 | C | T | 58 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0265 others(55): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.88+9684G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676516 | |||||||
| chr4:37676846 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.88+9354G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676846 | |||||||
| chr4:37676872 | T | C | 32 | a0001c0001t0001g0256 a0001c0001t0001g0297 a0001c0001t0001g0303 others(29): Show |
32 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.88+9328A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676872 | |||||||
| chr4:37676885 | C | T | 32 | a0001c0001t0001g0256 a0001c0001t0001g0297 a0001c0001t0001g0303 others(29): Show |
32 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.88+9315G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676885 | |||||||
| chr4:37676919 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.88+9281C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676919 | |||||||
| chr4:37677005 | C | T | 1 | a0001c0001t0013g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.88+9195G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677005 | |||||||
| chr4:37677182 | A | T | 4 | a0001c0001t0002g0097 a0001c0001t0014g0098 a0001c0001t0014g0165 others(1): Show |
4 | HG01257.hp1 HG01928.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+9018T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677182 | |||||||
| chr4:37677268 | T | C | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.88+8932A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677268 | |||||||
| chr4:37677343 | C | T | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+8857G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677343 | |||||||
| chr4:37677650 | C | T | 52 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0265 others(49): Show |
52 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.88+8550G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677650 | |||||||
| chr4:37677832 | C | T | 1 | a0001c0001t0004g0164 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.88+8368G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677832 | |||||||
| chr4:37677921 | G | A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0232 a0001c0001t0003g0138 others(2): Show |
5 | NA18941.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+8279C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677921 | |||||||
| chr4:37678049 | G | A | 1 | a0001c0001t0005g0234 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.88+8151C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678049 | |||||||
| chr4:37678122 | AGAGGAGC others(8): Show |
A | 6 | a0001c0001t0001g0256 a0001c0001t0002g0252 a0001c0001t0035g0253 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+8063_88+8077del others(15): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678122 | |||||||
| chr4:37678135 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.88+8065G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678135 | |||||||
| chr4:37678145 | C | T | 2 | a0001c0001t0030g0096 a0001c0001t0064g0163 |
2 | NA18942.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.88+8055G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678145 | |||||||
| chr4:37678146 | G | A | 25 | a0001c0001t0001g0139 a0001c0001t0001g0235 a0001c0001t0001g0236 others(22): Show |
25 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.88+8054C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678146 | |||||||
| chr4:37678166 | G | C | 1 | a0001c0001t0015g0050 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.88+8034C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678166 | |||||||
| chr4:37678170 | G | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0004g0031 others(2): Show |
5 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+8030C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678170 | |||||||
| chr4:37678249 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.88+7951T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678249 | |||||||
| chr4:37678255 | C | T | 18 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(15): Show |
18 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+7945G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678255 | |||||||
| chr4:37678372 | A | G | 20 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(17): Show |
20 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+7828T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678372 | |||||||
| chr4:37678482 | A | G | 20 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(17): Show |
20 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+7718T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678482 | |||||||
| chr4:37678491 | T | G | 3 | a0001c0001t0001g0034 a0001c0001t0002g0033 a0001c0001t0025g0013 |
3 | HG01243.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.88+7709A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678491 | |||||||
| chr4:37678601 | A | T | 1 | a0001c0001t0004g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88+7599T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678601 | |||||||
| chr4:37678705 | T | A | 1 | a0001c0001t0047g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.88+7495A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678705 | |||||||
| chr4:37678707 | T | C | 1 | a0001c0001t0010g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+7493A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678707 | |||||||
| chr4:37678735 | C | G | 2 | a0001c0001t0002g0298 a0001c0001t0002g0304 |
2 | HG01106.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.88+7465G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678735 | |||||||
| chr4:37678762 | C | T | 260 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(257): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.88+7438G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678762 | |||||||
| chr4:37678933 | A | T | 6 | a0001c0001t0002g0095 a0001c0001t0002g0158 a0001c0001t0002g0161 others(3): Show |
6 | HG02080.hp1 NA18946.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+7267T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678933 | |||||||
| chr4:37679099 | A | G | 2 | a0001c0001t0005g0156 a0001c0001t0021g0094 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.88+7101T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679099 | |||||||
| chr4:37679171 | AAG | A | 3 | a0001c0001t0003g0052 a0001c0001t0003g0073 a0001c0001t0013g0072 |
3 | HG01928.hp2 HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.88+7027_88+7028del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679171 | |||||||
| chr4:37679240 | G | A | 18 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(15): Show |
18 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.88+6960C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679240 | |||||||
| chr4:37679307 | T | G | 1 | a0001c0001t0005g0141 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.88+6893A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679307 | |||||||
| chr4:37679466 | A | G | 1 | a0001c0006t0023g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.88+6734T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679466 | |||||||
| chr4:37679568 | A | G | 14 | a0001c0001t0001g0042 a0001c0001t0001g0080 a0001c0001t0001g0081 others(11): Show |
14 | HG00140.hp2 HG01081.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+6632T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679568 | |||||||
| chr4:37679574 | C | T | 3 | a0001c0001t0002g0295 a0001c0001t0004g0294 a0001c0001t0012g0293 |
3 | HG02056.hp1 HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.88+6626G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679574 | |||||||
| chr4:37679664 | C | G | 1 | a0001c0001t0026g0262 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.88+6536G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679664 | |||||||
| chr4:37679665 | A | T | 19 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(16): Show |
19 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+6535T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679665 | |||||||
| chr4:37679884 | G | A | 3 | a0001c0001t0035g0253 a0001c0001t0043g0254 a0001c0001t0046g0255 |
3 | HG02451.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.88+6316C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679884 | |||||||
| chr4:37679893 | A | T | 2 | a0001c0001t0001g0256 a0001c0001t0002g0252 |
2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88+6307T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679893 | |||||||
| chr4:37679972 | C | T | 4 | a0001c0001t0004g0083 a0001c0001t0010g0290 a0001c0001t0027g0289 others(1): Show |
4 | HG01884.hp2 HG03017.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+6228G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679972 | |||||||
| chr4:37680082 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.88+6118T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680082 | |||||||
| chr4:37680104 | A | T | 1 | a0001c0001t0002g0043 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.88+6096T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680104 | |||||||
| chr4:37680188 | C | T | 19 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(16): Show |
19 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+6012G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680188 | |||||||
| chr4:37680301 | C | G | 1 | a0001c0001t0005g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.88+5899G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680301 | |||||||
| chr4:37680457 | C | T | 25 | a0001c0001t0001g0070 a0001c0001t0001g0248 a0001c0001t0002g0069 others(22): Show |
27 | HG00099.hp1 HG01167.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.88+5743G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680457 | |||||||
| chr4:37680638 | G | A | 1 | a0001c0001t0058g0239 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.88+5562C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680638 | |||||||
| chr4:37680744 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.88+5456G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680744 | |||||||
| chr4:37680837 | C | T | 1 | a0001c0006t0023g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.88+5363G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680837 | |||||||
| chr4:37680843 | A | G | 18 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(15): Show |
18 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+5357T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680843 | |||||||
| chr4:37680848 | C | T | 1 | a0001c0001t0015g0050 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.88+5352G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680848 | |||||||
| chr4:37680886 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.88+5314G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680886 | |||||||
| chr4:37680931 | C | CA | 16 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0001g0242 others(13): Show |
16 | HG00323.hp2 HG00741.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+5268dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | |||||||
| chr4:37680931 | C | CAA | 17 | a0001c0001t0001g0305 a0001c0001t0001g0307 a0001c0001t0001g0310 others(14): Show |
17 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.88+5267_88+5268dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | |||||||
| chr4:37680931 | CA | C | 52 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0025 others(49): Show |
53 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.88+5268delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | |||||||
| chr4:37680931 | CAA | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0273 a0001c0001t0001g0274 others(13): Show |
16 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+5267_88+5268del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | |||||||
| chr4:37680931 | CAAA | C | 26 | a0001c0001t0001g0070 a0001c0001t0001g0248 a0001c0001t0002g0003 others(23): Show |
29 | HG00099.hp1 HG01167.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.88+5266_88+5268del others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | |||||||
| chr4:37680931 | CAAAA | C | 11 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(8): Show |
11 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+5265_88+5268del others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | |||||||
| chr4:37681142 | T | C | 19 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(16): Show |
19 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+5058A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681142 | |||||||
| chr4:37681377 | C | G | 2 | a0002c0004t0033g0006 a0002c0004t0041g0007 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.88+4823G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681377 | |||||||
| chr4:37681394 | A | G | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.88+4806T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681394 | |||||||
| chr4:37681400 | T | G | 2 | a0001c0001t0004g0054 a0001c0001t0004g0244 |
2 | HG03688.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.88+4800A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681400 | |||||||
| chr4:37681477 | G | A | 1 | a0001c0001t0004g0245 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.88+4723C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681477 | |||||||
| chr4:37681518 | GT | G | 167 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0023 others(164): Show |
171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.88+4681delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | |||||||
| chr4:37681518 | GTT | G | 20 | a0001c0001t0001g0087 a0001c0001t0001g0265 a0001c0001t0001g0266 others(17): Show |
20 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.88+4680_88+4681del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | |||||||
| chr4:37681518 | GTTT | G | 7 | a0001c0001t0001g0297 a0001c0001t0002g0298 a0001c0001t0002g0300 others(4): Show |
7 | HG00423.hp2 HG01106.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+4679_88+4681del others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | |||||||
| chr4:37681518 | GTTTT | G | 20 | a0001c0001t0001g0303 a0001c0001t0001g0305 a0001c0001t0001g0307 others(17): Show |
20 | HG00408.hp2 HG02055.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.88+4678_88+4681del others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | |||||||
| chr4:37681518 | GTTTTT | G | 7 | a0001c0001t0001g0256 a0001c0001t0001g0316 a0001c0001t0002g0314 others(4): Show |
7 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+4677_88+4681del others(5): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | |||||||
| chr4:37681522 | T | G | 5 | a0001c0001t0001g0297 a0001c0001t0002g0298 a0001c0001t0002g0300 others(2): Show |
5 | HG00423.hp2 HG01106.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+4678A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681522 | |||||||
| chr4:37681523 | T | G | 20 | a0001c0001t0001g0303 a0001c0001t0001g0305 a0001c0001t0001g0307 others(17): Show |
20 | HG00408.hp2 HG02055.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.88+4677A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681523 | |||||||
| chr4:37681524 | T | G | 7 | a0001c0001t0001g0256 a0001c0001t0001g0316 a0001c0001t0002g0314 others(4): Show |
7 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+4676A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681524 | |||||||
| chr4:37681533 | T | G | 5 | a0001c0001t0001g0316 a0001c0001t0002g0314 a0001c0001t0002g0315 others(2): Show |
5 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+4667A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681533 | |||||||
| chr4:37681688 | C | T | 26 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(23): Show |
26 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+4512G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681688 | |||||||
| chr4:37681991 | T | C | 1 | a0001c0001t0024g0246 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.88+4209A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681991 | |||||||
| chr4:37682133 | A | C | 312 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.88+4067T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682133 | |||||||
| chr4:37682663 | T | C | 1 | a0001c0001t0005g0317 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.88+3537A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682663 | |||||||
| chr4:37682704 | C | T | 23 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(20): Show |
23 | HG00140.hp1 HG00597.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.88+3496G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682704 | |||||||
| chr4:37682807 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.88+3393C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682807 | |||||||
| chr4:37682843 | A | C | 23 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(20): Show |
23 | HG00140.hp1 HG00597.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.88+3357T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682843 | |||||||
| chr4:37683224 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.88+2976C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683224 | |||||||
| chr4:37683248 | A | C | 6 | a0001c0001t0001g0256 a0001c0001t0002g0252 a0001c0001t0035g0253 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+2952T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683248 | |||||||
| chr4:37683274 | G | A | 169 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0044 others(166): Show |
171 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.88+2926C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683274 | |||||||
| chr4:37683446 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.88+2754A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683446 | |||||||
| chr4:37683856 | C | T | 1 | a0001c0001t0055g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+2344G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683856 | |||||||
| chr4:37683858 | G | T | 2 | a0001c0001t0001g0048 a0001c0001t0004g0047 |
2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.88+2342C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683858 | |||||||
| chr4:37683974 | T | G | 5 | a0001c0001t0010g0290 a0001c0001t0027g0289 a0001c0001t0034g0292 others(2): Show |
5 | HG01884.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+2226A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683974 | |||||||
| chr4:37684016 | G | A | 6 | a0001c0001t0010g0290 a0001c0001t0027g0289 a0001c0001t0034g0292 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+2184C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684016 | |||||||
| chr4:37684032 | C | T | 3 | a0001c0001t0002g0295 a0001c0001t0004g0294 a0001c0001t0012g0293 |
3 | HG02056.hp1 HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.88+2168G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684032 | |||||||
| chr4:37684055 | G | A | 46 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0265 others(43): Show |
46 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.88+2145C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684055 | |||||||
| chr4:37684349 | C | CAA | 8 | a0001c0001t0001g0256 a0001c0001t0002g0252 a0001c0001t0002g0257 others(5): Show |
8 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+1849_88+1850dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684349 | |||||||
| chr4:37684349 | C | CAAAA | 7 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
7 | HG02257.hp1 HG02523.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+1847_88+1850dup others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684349 | |||||||
| chr4:37684473 | C | T | 1 | a0001c0001t0002g0046 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.88+1727G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684473 | |||||||
| chr4:37684488 | T | C | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+1712A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684488 | |||||||
| chr4:37684647 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.88+1553C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684647 | |||||||
| chr4:37684654 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(10): Show |
13 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+1546C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684654 | |||||||
| chr4:37685264 | G | C | 306 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(303): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.88+936C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685264 | |||||||
| chr4:37685316 | A | G | 1 | a0001c0001t0067g0045 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.88+884T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685316 | |||||||
| chr4:37685473 | G | T | 2 | a0001c0001t0001g0272 a0001c0001t0060g0271 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.88+727C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685473 | |||||||
| chr4:37685508 | C | A | 13 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0266 others(10): Show |
13 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+692G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685508 | |||||||
| chr4:37685611 | G | A | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+589C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685611 | |||||||
| chr4:37685719 | A | C | 2 | a0001c0001t0001g0044 a0001c0001t0002g0043 |
2 | HG02080.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.88+481T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685719 | |||||||
| chr4:37685774 | A | C | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+426T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685774 | |||||||
| chr4:37685787 | AGC | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+411_88+412delGC | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685787 | |||||||
| chr4:37685887 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.88+313C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685887 | |||||||
| chr4:37685925 | C | T | 34 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
34 | HG00323.hp1 HG00642.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.88+275G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685925 | |||||||
| chr4:37685931 | T | A | 306 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(303): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.88+269A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685931 | |||||||
| chr4:37685938 | C | G | 306 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(303): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.88+262G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685938 | |||||||
| chr4:37686032 | C | A | 26 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0305 others(23): Show |
26 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+168G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37686032 | |||||||
| chr4:37686190 | G | A | 1 | a0001c0001t0042g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88+10C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37686190 |