Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57148 |
| ensemblid | ENSG00000170471.15 |
| hgncid | 29221 |
| symbol | RALGAPB |
| name | Ral GTPase activating protein non-catalytic subunit beta |
| refseq_nuc | NM_020336.4 |
| refseq_prot | NP_065069.1 |
| ensembl_nuc | ENST00000262879.11 |
| ensembl_prot | ENSP00000262879.6 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 38472843 |
| end | 38578858 |
| strand | + |
| ver | v1.2 |
| region | chr20:38472843-38578858 |
| region5000 | chr20:38467843-38583858 |
| regionname0 | RALGAPB_chr20_38472843_38578858 |
| regionname5000 | RALGAPB_chr20_38467843_38583858 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1494 | 210 | 80 | 40 | 61 | 6 | 21 | 51 | RALGAPB_chr20_38467843_38583858 | RALGAPB | MYSEW others(1489): Show |
chr20 | 38467843 | 38583858 |
| a0002 | 0/0 | 1494 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | MYSEW others(1489): Show |
chr20 | 38467843 | 38583858 |
| a0003 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | MYSEW others(1489): Show |
chr20 | 38467843 | 38583858 |
| a0004 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | MYSEW others(1489): Show |
chr20 | 38467843 | 38583858 |
| a0005 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | MYSEW others(1489): Show |
chr20 | 38467843 | 38583858 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4482 | 175 | 55 | 35 | 56 | 6 | 21 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0001c0002 | 0/0 | 4482 | 15 | 12 | 3 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0001c0003 | 0/0 | 4482 | 14 | 13 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0001c0005 | 0/0 | 4482 | 2 | 0 | 0 | 2 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0001c0007 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0001c0008 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0001c0009 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0001c0012 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0002c0004 | 0/0 | 4482 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0003c0006 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0004c0011 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 | ||
| a0005c0010 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | ATGTA others(4477): Show |
chr20 | 38467843 | 38583858 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8635 | 78 | 13 | 13 | 39 | 1 | 12 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0002 | 1/0 | 8633 | 28 | 4 | 8 | 8 | 3 | 4 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8628): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0003 | 0/0 | 8637 | 26 | 6 | 6 | 8 | 2 | 4 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8632): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0004 | 0/0 | 8627 | 11 | 10 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8622): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0006 | 0/0 | 8631 | 7 | 7 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8626): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0007 | 0/0 | 8631 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8626): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0008 | 0/0 | 8633 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8628): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0009 | 0/0 | 8641 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8636): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0011 | 0/0 | 8643 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8638): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0013 | 0/0 | 8635 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0014 | 0/0 | 8637 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8632): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0015 | 0/0 | 8635 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0016 | 0/0 | 8633 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8628): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0017 | 0/0 | 8633 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8628): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0018 | 0/0 | 8633 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8628): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0019 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8634): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0020 | 0/0 | 8643 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8638): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0021 | 0/0 | 8641 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8636): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0022 | 0/0 | 8627 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8622): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0023 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8634): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0024 | 0/0 | 8635 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0025 | 0/0 | 8635 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0026 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8634): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0027 | 0/0 | 8635 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0001t0028 | 0/1 | 8635 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0002t0002 | 0/0 | 8633 | 12 | 11 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8628): Show |
chr20 | 38467843 | 38583858 |
| a0001c0002t0007 | 0/0 | 8631 | 3 | 1 | 2 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8626): Show |
chr20 | 38467843 | 38583858 |
| a0001c0003t0005 | 0/0 | 8638 | 9 | 9 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8633): Show |
chr20 | 38467843 | 38583858 |
| a0001c0003t0010 | 0/0 | 8636 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8631): Show |
chr20 | 38467843 | 38583858 |
| a0001c0003t0012 | 0/0 | 8640 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8635): Show |
chr20 | 38467843 | 38583858 |
| a0001c0005t0001 | 0/0 | 8635 | 2 | 0 | 0 | 2 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0007t0003 | 0/0 | 8637 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8632): Show |
chr20 | 38467843 | 38583858 |
| a0001c0008t0001 | 0/0 | 8635 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0009t0001 | 0/0 | 8635 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0001c0012t0001 | 0/0 | 8635 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| a0002c0004t0029 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8634): Show |
chr20 | 38467843 | 38583858 |
| a0002c0004t0030 | 0/0 | 8637 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8632): Show |
chr20 | 38467843 | 38583858 |
| a0002c0004t0031 | 0/0 | 8633 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8628): Show |
chr20 | 38467843 | 38583858 |
| a0003c0006t0003 | 0/0 | 8637 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8632): Show |
chr20 | 38467843 | 38583858 |
| a0004c0011t0002 | 0/0 | 8633 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8628): Show |
chr20 | 38467843 | 38583858 |
| a0005c0010t0001 | 0/0 | 8635 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | AGTCG others(8630): Show |
chr20 | 38467843 | 38583858 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0011g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0013g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0014g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0015g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0016g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0017g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0018g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0019g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0020g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0021g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0022g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0023g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0024g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0025g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0026g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0027g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0028g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0007g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0012g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0007t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0008t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0012t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0002c0004t0029g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0002c0004t0030g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0002c0004t0031g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0003c0006t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0004c0011t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0005c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | FIN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0143 | EUR | FIN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00642 | hp2 | a0001 | c0002 | t0007 | g0004 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0163 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01081 | hp1 | a0001 | c0001 | t0014 | g0050 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01106 | hp1 | a0001 | c0008 | t0001 | g0049 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01106 | hp2 | a0001 | c0001 | t0027 | g0066 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01109 | hp1 | a0001 | c0003 | t0012 | g0006 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01243 | hp1 | a0001 | c0001 | t0024 | g0097 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0013 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01433 | hp2 | a0001 | c0002 | t0007 | g0004 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | IBS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0036 | EUR | IBS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | IBS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01884 | hp1 | a0001 | c0001 | t0022 | g0026 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01993 | hp2 | a0001 | c0001 | t0017 | g0151 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02027 | hp1 | a0001 | c0009 | t0001 | g0088 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02055 | hp1 | a0001 | c0001 | t0020 | g0023 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02145 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02258 | hp2 | a0002 | c0004 | t0029 | g0008 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02293 | hp1 | a0001 | c0001 | t0015 | g0043 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02451 | hp1 | a0001 | c0003 | t0005 | g0005 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02451 | hp2 | a0001 | c0001 | t0016 | g0175 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02622 | hp1 | a0001 | c0003 | t0010 | g0201 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02622 | hp2 | a0001 | c0001 | t0026 | g0121 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0129 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02723 | hp1 | a0001 | c0003 | t0010 | g0202 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02886 | hp1 | a0001 | c0001 | t0019 | g0039 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0171 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02896 | hp2 | a0001 | c0003 | t0005 | g0210 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0172 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02922 | hp2 | a0001 | c0003 | t0005 | g0205 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02970 | hp1 | a0001 | c0001 | t0023 | g0015 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02970 | hp2 | a0001 | c0003 | t0005 | g0203 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03139 | hp2 | a0001 | c0003 | t0005 | g0206 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03195 | hp1 | a0001 | c0003 | t0005 | g0207 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0123 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03579 | hp2 | a0001 | c0003 | t0012 | g0006 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03669 | hp2 | a0004 | c0011 | t0002 | g0160 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03688 | hp2 | a0001 | c0001 | t0025 | g0113 | SAS | STU | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18522 | hp2 | a0001 | c0003 | t0005 | g0005 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0173 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18954 | hp1 | a0001 | c0001 | t0013 | g0087 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18979 | hp1 | a0005 | c0010 | t0001 | g0111 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18999 | hp1 | a0001 | c0012 | t0001 | g0075 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19001 | hp1 | a0001 | c0007 | t0003 | g0067 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0194 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19030 | hp2 | a0001 | c0003 | t0010 | g0209 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19043 | hp2 | a0002 | c0004 | t0031 | g0009 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19059 | hp1 | a0001 | c0005 | t0001 | g0118 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19059 | hp2 | a0001 | c0005 | t0001 | g0117 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0131 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19240 | hp2 | a0001 | c0003 | t0005 | g0204 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02109 | hp1 | a0001 | c0002 | t0007 | g0134 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02109 | hp2 | a0001 | c0001 | t0021 | g0022 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02486 | hp1 | a0002 | c0004 | t0030 | g0007 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02486 | hp2 | a0003 | c0006 | t0003 | g0033 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | USA | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | USA | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | USA | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA21309 | hp2 | a0001 | c0003 | t0005 | g0208 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0028 | g0046 | REF | REF | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0157 | REF | REF | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38521596 | C | G | 1 | a0004 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1517C>G | p.Pro506Arg | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/30 | 1774/8633 | 1517/4485 | 506/1494 | chr20 | 38521596 | |||
| chr20:38532803 | C | T | 1 | a0002 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.2189C>T | p.Thr730Met | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/30 | 2446/8633 | 2189/4485 | 730/1494 | chr20 | 38532803 | |||
| chr20:38539810 | G | A | 1 | a0004 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2414G>A | p.Arg805Gln | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/30 | 2671/8633 | 2414/4485 | 805/1494 | chr20 | 38539810 | |||
| chr20:38551125 | T | G | 1 | a0003 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.3064T>G | p.Ser1022Ala | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/30 | 3321/8633 | 3064/4485 | 1022/1494 | chr20 | 38551125 | |||
| chr20:38574894 | G | A | 1 | a0005 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.4412G>A | p.Arg1471Gln | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 4669/8633 | 4412/4485 | 1471/1494 | chr20 | 38574894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38517867 | A | G | 1 | a0002c0004 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.1284A>G | p.Glu428Glu | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/30 | 1541/8633 | 1284/4485 | 428/1494 | chr20 | 38517867 | |||
| chr20:38517921 | C | G | 1 | a0001c0012 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.1338C>G | p.Leu446Leu | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/30 | 1595/8633 | 1338/4485 | 446/1494 | chr20 | 38517921 | |||
| chr20:38539826 | G | T | 1 | a0001c0003 | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.2430G>T | p.Val810Val | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/30 | 2687/8633 | 2430/4485 | 810/1494 | chr20 | 38539826 | |||
| chr20:38539877 | G | A | 1 | a0001c0005 | 2 | NA19059.hp1 NA19059.hp2 |
synonymous_variant | LOW | c.2481G>A | p.Arg827Arg | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/30 | 2738/8633 | 2481/4485 | 827/1494 | chr20 | 38539877 | |||
| chr20:38548780 | A | G | 1 | a0001c0002 | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
synonymous_variant | LOW | c.2994A>G | p.Ala998Ala | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/30 | 3251/8633 | 2994/4485 | 998/1494 | chr20 | 38548780 | |||
| chr20:38567130 | T | C | 1 | a0001c0007 | 1 | NA19001.hp1 | synonymous_variant | LOW | c.3852T>C | p.Asp1284Asp | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/30 | 4109/8633 | 3852/4485 | 1284/1494 | chr20 | 38567130 | |||
| chr20:38570800 | G | A | 1 | a0001c0008 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.4095G>A | p.Glu1365Glu | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/30 | 4352/8633 | 4095/4485 | 1365/1494 | chr20 | 38570800 | |||
| chr20:38574841 | T | C | 1 | a0001c0009 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.4359T>C | p.Ser1453Ser | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 4616/8633 | 4359/4485 | 1453/1494 | chr20 | 38574841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38575064 | C | T | 3 | a0002c0004t0029 a0002c0004t0030 a0002c0004t0031 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*97C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 97 | chr20 | 38575064 | ||||||
| chr20:38575177 | G | T | 1 | a0001c0001t0027 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 210 | chr20 | 38575177 | ||||||
| chr20:38575389 | A | G | 1 | a0001c0001t0026 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*422A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 422 | chr20 | 38575389 | ||||||
| chr20:38575527 | TAAG | T | 3 | a0001c0003t0005 a0001c0003t0010 a0001c0003t0012 |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*564_*566delAAG | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 564 | INFO_REALIGN_3_PRIME | chr20 | 38575527 | |||||
| chr20:38575800 | A | G | 1 | a0001c0001t0025 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 833 | chr20 | 38575800 | ||||||
| chr20:38576096 | T | G | 1 | a0001c0001t0013 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1129T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1129 | chr20 | 38576096 | ||||||
| chr20:38576188 | T | C | 1 | a0001c0001t0014 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1221 | chr20 | 38576188 | ||||||
| chr20:38576199 | C | T | 1 | a0001c0001t0024 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1232C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1232 | chr20 | 38576199 | ||||||
| chr20:38576864 | C | T | 8 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0011 others(5): Show |
32 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1897C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1897 | chr20 | 38576864 | ||||||
| chr20:38576919 | T | G | 1 | a0001c0001t0022 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1952T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1952 | chr20 | 38576919 | ||||||
| chr20:38577017 | T | C | 1 | a0001c0001t0015 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2050T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2050 | chr20 | 38577017 | ||||||
| chr20:38577185 | C | T | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02055.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2218C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2218 | chr20 | 38577185 | ||||||
| chr20:38577249 | T | C | 10 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0011 others(7): Show |
34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2282T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2282 | chr20 | 38577249 | ||||||
| chr20:38577391 | T | G | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02055.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2424T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2424 | chr20 | 38577391 | ||||||
| chr20:38577452 | G | T | 1 | a0001c0001t0019 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2485G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2485 | chr20 | 38577452 | ||||||
| chr20:38577484 | G | A | 1 | a0001c0001t0016 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2517G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2517 | chr20 | 38577484 | ||||||
| chr20:38577513 | C | T | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2546C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2546 | chr20 | 38577513 | ||||||
| chr20:38577698 | G | GAC | 12 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0013 others(9): Show |
96 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2764_*2765dupAC | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | |||||
| chr20:38577698 | G | GACAC | 5 | a0001c0001t0003 a0001c0001t0014 a0001c0007t0003 others(2): Show |
30 | HG00280.hp1 HG00738.hp1 HG01071.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2762_*2765dupACAC | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | |||||
| chr20:38577698 | G | GACACAC | 5 | a0001c0001t0019 a0001c0001t0023 a0001c0001t0026 others(2): Show |
7 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2760_*2765dupACAC others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | |||||
| chr20:38577698 | G | GACACACA others(1): Show |
3 | a0001c0001t0009 a0001c0001t0021 a0001c0003t0005 |
13 | HG02109.hp2 HG02451.hp1 HG02896.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2758_*2765dupACAC others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | |||||
| chr20:38577698 | G | GACACACA others(3): Show |
3 | a0001c0001t0011 a0001c0001t0020 a0001c0003t0012 |
5 | HG01109.hp1 HG01361.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2756_*2765dupACAC others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | |||||
| chr20:38577698 | GAC | G | 2 | a0001c0001t0007 a0001c0002t0007 |
4 | HG00642.hp2 HG00738.hp2 HG01433.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2764_*2765delAC | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2764 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | |||||
| chr20:38577698 | GACACAC | G | 2 | a0001c0001t0004 a0001c0001t0022 |
12 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2760_*2765delACAC others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2760 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | |||||
| chr20:38577726 | C | A | 1 | a0001c0001t0008 | 3 | HG02896.hp1 HG02897.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2759C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2759 | chr20 | 38577726 | ||||||
| chr20:38577776 | T | A | 7 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0011 others(4): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2809T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2809 | chr20 | 38577776 | ||||||
| chr20:38578046 | AAAAT | A | 1 | a0001c0001t0006 | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3098_*3101delATAA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 3098 | INFO_REALIGN_3_PRIME | chr20 | 38578046 | |||||
| chr20:38578341 | G | T | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3374G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 3374 | chr20 | 38578341 | ||||||
| chr20:38578601 | T | G | 1 | a0001c0001t0017 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3634T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 3634 | chr20 | 38578601 | ||||||
| chr20:38578738 | G | C | 1 | a0001c0001t0016 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3771G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 3771 | chr20 | 38578738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38473165 | C | T | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31+96C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473165 | |||||||
| chr20:38473182 | G | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-31+113G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473182 | |||||||
| chr20:38473277 | G | T | 1 | a0001c0001t0003g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-31+208G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473277 | |||||||
| chr20:38473325 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-31+256C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473325 | |||||||
| chr20:38473368 | T | G | 44 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 others(41): Show |
48 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(45): Show |
intron_variant | MODIFIER | c.-31+299T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473368 | |||||||
| chr20:38473950 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-31+881G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473950 | |||||||
| chr20:38474014 | G | C | 40 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(37): Show |
44 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.-31+945G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474014 | |||||||
| chr20:38474057 | C | A | 4 | a0001c0001t0001g0037 a0001c0001t0003g0035 a0001c0001t0003g0036 others(1): Show |
4 | HG01071.hp2 HG01081.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+988C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474057 | |||||||
| chr20:38474081 | G | C | 1 | a0001c0001t0019g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-31+1012G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474081 | |||||||
| chr20:38474164 | G | C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(148): Show |
157 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-31+1095G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474164 | |||||||
| chr20:38474243 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-31+1174G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474243 | |||||||
| chr20:38474269 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(37): Show |
44 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.-31+1200G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474269 | |||||||
| chr20:38474435 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-31+1366C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474435 | |||||||
| chr20:38474681 | C | A | 7 | a0001c0001t0006g0016 a0001c0001t0009g0010 a0001c0001t0009g0011 others(4): Show |
7 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+1612C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474681 | |||||||
| chr20:38474769 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-31+1700C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474769 | |||||||
| chr20:38474786 | T | G | 6 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(3): Show |
7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+1717T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474786 | |||||||
| chr20:38474885 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-31+1816C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474885 | |||||||
| chr20:38474955 | C | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+1886C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474955 | |||||||
| chr20:38475079 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+2010G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475079 | |||||||
| chr20:38475089 | G | A | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-31+2020G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475089 | |||||||
| chr20:38475108 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(37): Show |
44 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.-31+2039G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475108 | |||||||
| chr20:38475429 | A | G | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+2360A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475429 | |||||||
| chr20:38475642 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-31+2573T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475642 | |||||||
| chr20:38475717 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-31+2648C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475717 | |||||||
| chr20:38475813 | C | T | 1 | a0001c0001t0018g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-31+2744C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475813 | |||||||
| chr20:38475928 | C | A | 1 | a0001c0001t0003g0141 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-31+2859C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475928 | |||||||
| chr20:38476073 | G | T | 12 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(9): Show |
12 | NA18941.hp1 NA18949.hp1 NA18956.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+3004G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476073 | |||||||
| chr20:38476156 | G | A | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-31+3087G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476156 | |||||||
| chr20:38476243 | G | C | 1 | a0001c0001t0015g0043 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-31+3174G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476243 | |||||||
| chr20:38476385 | T | G | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-31+3316T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476385 | |||||||
| chr20:38476461 | C | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-31+3392C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476461 | |||||||
| chr20:38476472 | C | T | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-31+3403C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476472 | |||||||
| chr20:38476586 | T | C | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-31+3517T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476586 | |||||||
| chr20:38476765 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-31+3696G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476765 | |||||||
| chr20:38476783 | G | T | 1 | a0001c0001t0002g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-31+3714G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476783 | |||||||
| chr20:38477514 | C | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(123): Show |
131 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-31+4445C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38477514 | |||||||
| chr20:38477713 | T | C | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+4644T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38477713 | |||||||
| chr20:38477984 | G | A | 1 | a0001c0003t0010g0201 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-31+4915G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38477984 | |||||||
| chr20:38478113 | C | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-31+5044C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478113 | |||||||
| chr20:38478200 | C | T | 3 | a0001c0001t0001g0116 a0001c0005t0001g0117 a0001c0005t0001g0118 |
3 | NA19006.hp2 NA19059.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.-31+5131C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478200 | |||||||
| chr20:38478295 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 |
3 | HG00639.hp1 HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-31+5226G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478295 | |||||||
| chr20:38478397 | A | G | 1 | a0001c0001t0004g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-31+5328A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478397 | |||||||
| chr20:38478398 | A | T | 149 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(146): Show |
155 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.-31+5329A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478398 | |||||||
| chr20:38478429 | C | CT | 4 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
5 | HG00735.hp2 HG01517.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+5369dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38478429 | ||||||
| chr20:38478444 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-31+5375G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478444 | |||||||
| chr20:38478513 | C | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-31+5444C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478513 | |||||||
| chr20:38478531 | C | G | 1 | a0001c0001t0002g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-31+5462C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478531 | |||||||
| chr20:38478582 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(81): Show |
85 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.-31+5513G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478582 | |||||||
| chr20:38478640 | G | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31+5571G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478640 | |||||||
| chr20:38478678 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-31+5609G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478678 | |||||||
| chr20:38478683 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-31+5614C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478683 | |||||||
| chr20:38478773 | C | T | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+5704C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478773 | |||||||
| chr20:38478786 | T | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(86): Show |
90 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-31+5717T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478786 | |||||||
| chr20:38478843 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(4): Show |
7 | HG00741.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+5774C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478843 | |||||||
| chr20:38479003 | G | A | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-31+5934G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479003 | |||||||
| chr20:38479103 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-31+6034A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479103 | |||||||
| chr20:38479113 | C | CTACT | 2 | a0001c0001t0001g0112 a0005c0010t0001g0111 |
2 | HG02004.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-31+6045_-31+6048d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38479113 | ||||||
| chr20:38479737 | G | A | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6668G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479737 | |||||||
| chr20:38479738 | A | T | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6669A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479738 | |||||||
| chr20:38479739 | T | C | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6670T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479739 | |||||||
| chr20:38479935 | A | G | 11 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(8): Show |
13 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+6866A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479935 | |||||||
| chr20:38479994 | T | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6925T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479994 | |||||||
| chr20:38479996 | G | T | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6927G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479996 | |||||||
| chr20:38479998 | T | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6929T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479998 | |||||||
| chr20:38480011 | T | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-31+6942T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480011 | |||||||
| chr20:38480050 | T | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6981T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480050 | |||||||
| chr20:38480262 | C | T | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+7193C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480262 | |||||||
| chr20:38480277 | A | G | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31+7208A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480277 | |||||||
| chr20:38480321 | C | CT | 6 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
7 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+7265dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38480321 | ||||||
| chr20:38480321 | C | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+7252C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480321 | |||||||
| chr20:38480321 | CT | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(121): Show |
129 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-31+7265delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38480321 | ||||||
| chr20:38480322 | T | C | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+7253T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480322 | |||||||
| chr20:38480385 | CTTTTTTT others(2): Show |
C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-31+7327_-31+7335d others(11): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38480385 | ||||||
| chr20:38480389 | T | C | 1 | a0001c0003t0005g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-31+7320T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480389 | |||||||
| chr20:38480426 | A | C | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+7357A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480426 | |||||||
| chr20:38480427 | C | A | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+7358C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480427 | |||||||
| chr20:38480539 | A | C | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+7470A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480539 | |||||||
| chr20:38480636 | C | T | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31+7567C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480636 | |||||||
| chr20:38480735 | G | C | 1 | a0001c0001t0002g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-31+7666G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480735 | |||||||
| chr20:38480735 | G | GC | 30 | a0001c0001t0001g0041 a0001c0001t0001g0051 a0001c0001t0001g0054 others(27): Show |
30 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.-30-7660dupC | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38480735 | ||||||
| chr20:38480744 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0014g0050 a0001c0008t0001g0049 |
3 | HG01081.hp1 HG01106.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-30-7659T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480744 | |||||||
| chr20:38480760 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(85): Show |
89 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-30-7643C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480760 | |||||||
| chr20:38480761 | G | A | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-7642G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480761 | |||||||
| chr20:38480783 | G | A | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-7620G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480783 | |||||||
| chr20:38480841 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(82): Show |
86 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-30-7562C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480841 | |||||||
| chr20:38480878 | C | T | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-7525C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480878 | |||||||
| chr20:38480882 | C | T | 1 | a0001c0001t0023g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-30-7521C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480882 | |||||||
| chr20:38480884 | T | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(147): Show |
156 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.-30-7519T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480884 | |||||||
| chr20:38480885 | G | A | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-7518G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480885 | |||||||
| chr20:38480941 | C | T | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-30-7462C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480941 | |||||||
| chr20:38481159 | G | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0106 a0001c0001t0003g0107 others(3): Show |
6 | HG00639.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-7244G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481159 | |||||||
| chr20:38481279 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-30-7124G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481279 | |||||||
| chr20:38481431 | A | G | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30-6972A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481431 | |||||||
| chr20:38481459 | C | T | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-6944C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481459 | |||||||
| chr20:38481974 | T | A | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-6429T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481974 | |||||||
| chr20:38482014 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-30-6389A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38482014 | |||||||
| chr20:38482019 | T | TTCAAGTA others(308): Show |
3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-30-6371_-30-6370i others(317): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38482019 | ||||||
| chr20:38482158 | T | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(123): Show |
131 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-30-6245T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38482158 | |||||||
| chr20:38482426 | C | CT | 11 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0135 others(8): Show |
11 | HG00639.hp1 HG00741.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-5958dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38482426 | ||||||
| chr20:38482426 | C | CTT | 93 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0042 others(90): Show |
96 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-30-5959_-30-5958d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38482426 | ||||||
| chr20:38482426 | CT | C | 17 | a0001c0001t0001g0146 a0001c0001t0002g0145 a0001c0001t0004g0024 others(14): Show |
18 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30-5958delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38482426 | ||||||
| chr20:38482745 | T | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-5658T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38482745 | |||||||
| chr20:38483006 | C | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-5397C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483006 | |||||||
| chr20:38483032 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-30-5371G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483032 | |||||||
| chr20:38483153 | T | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-5250T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483153 | |||||||
| chr20:38483159 | G | T | 1 | a0001c0001t0025g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30-5244G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483159 | |||||||
| chr20:38483316 | C | G | 2 | a0001c0003t0005g0210 a0001c0003t0012g0006 |
3 | HG01109.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-30-5087C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483316 | |||||||
| chr20:38483413 | A | G | 3 | a0001c0001t0004g0025 a0001c0001t0004g0027 a0001c0001t0004g0028 |
3 | HG02055.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-30-4990A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483413 | |||||||
| chr20:38483440 | T | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-4963T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483440 | |||||||
| chr20:38483471 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(95): Show |
101 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.-30-4932T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483471 | |||||||
| chr20:38483575 | A | C | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-4828A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483575 | |||||||
| chr20:38483814 | G | A | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-30-4589G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483814 | |||||||
| chr20:38483975 | G | A | 8 | a0001c0001t0001g0065 a0001c0001t0001g0116 a0001c0001t0001g0138 others(5): Show |
8 | HG01106.hp2 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-4428G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483975 | |||||||
| chr20:38484052 | G | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-4351G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484052 | |||||||
| chr20:38484116 | C | G | 22 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(19): Show |
23 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.-30-4287C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484116 | |||||||
| chr20:38484135 | G | A | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-30-4268G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484135 | |||||||
| chr20:38484292 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(95): Show |
101 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.-30-4111A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484292 | |||||||
| chr20:38484319 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-30-4084G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484319 | |||||||
| chr20:38484604 | G | A | 2 | a0001c0003t0005g0210 a0001c0003t0012g0006 |
3 | HG01109.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-30-3799G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484604 | |||||||
| chr20:38485119 | A | G | 1 | a0001c0001t0025g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30-3284A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485119 | |||||||
| chr20:38485211 | T | G | 1 | a0001c0007t0003g0067 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-30-3192T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485211 | |||||||
| chr20:38485243 | G | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(86): Show |
90 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-30-3160G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485243 | |||||||
| chr20:38485320 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0103 |
2 | HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-30-3083A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485320 | |||||||
| chr20:38485320 | A | T | 1 | a0001c0001t0003g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-30-3083A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485320 | |||||||
| chr20:38485544 | G | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0069 others(3): Show |
6 | HG01361.hp2 HG02602.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-2859G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485544 | |||||||
| chr20:38485761 | G | A | 1 | a0001c0001t0019g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-30-2642G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485761 | |||||||
| chr20:38485966 | C | CT | 177 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(174): Show |
183 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(180): Show |
intron_variant | MODIFIER | c.-30-2417dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38485966 | ||||||
| chr20:38485966 | C | CTT | 7 | a0001c0001t0001g0047 a0001c0001t0003g0110 a0001c0001t0003g0192 others(4): Show |
7 | HG00741.hp1 HG01243.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-2418_-30-2417d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38485966 | ||||||
| chr20:38486008 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-30-2395C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486008 | |||||||
| chr20:38486026 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0003g0182 |
2 | NA18986.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-30-2377A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486026 | |||||||
| chr20:38486070 | C | T | 2 | a0001c0003t0005g0210 a0001c0003t0012g0006 |
3 | HG01109.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-30-2333C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486070 | |||||||
| chr20:38486264 | C | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30-2139C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486264 | |||||||
| chr20:38486792 | C | G | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-30-1611C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486792 | |||||||
| chr20:38486889 | A | G | 32 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(29): Show |
35 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.-30-1514A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486889 | |||||||
| chr20:38487242 | T | C | 3 | a0001c0001t0001g0077 a0001c0001t0003g0076 a0001c0012t0001g0075 |
3 | NA18977.hp1 NA18999.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-30-1161T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487242 | |||||||
| chr20:38487248 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-30-1155G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487248 | |||||||
| chr20:38487334 | A | AT | 127 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(124): Show |
132 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-30-1060dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38487334 | ||||||
| chr20:38487430 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0027g0066 |
2 | HG01106.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-30-973C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487430 | |||||||
| chr20:38487512 | G | A | 1 | a0001c0001t0019g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-30-891G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487512 | |||||||
| chr20:38487522 | T | C | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-30-881T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487522 | |||||||
| chr20:38487705 | A | C | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30-698A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487705 | |||||||
| chr20:38487755 | A | T | 1 | a0001c0001t0003g0061 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-30-648A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487755 | |||||||
| chr20:38487837 | C | T | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-566C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487837 | |||||||
| chr20:38487921 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(146): Show |
155 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.-30-482T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487921 | |||||||
| chr20:38487930 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-30-473G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487930 | |||||||
| chr20:38488067 | G | GA | 7 | a0001c0001t0006g0016 a0001c0001t0009g0010 a0001c0001t0009g0011 others(4): Show |
7 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-328dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38488067 | ||||||
| chr20:38488148 | C | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30-255C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38488148 | |||||||
| chr20:38488211 | C | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-30-192C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38488211 | |||||||
| chr20:38488279 | C | T | 12 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(9): Show |
13 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-30-124C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38488279 | |||||||
| chr20:38488758 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.186+140C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38488758 | |||||||
| chr20:38488928 | A | G | 1 | a0001c0001t0004g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.186+310A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38488928 | |||||||
| chr20:38489651 | A | G | 1 | a0001c0001t0004g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186+1033A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38489651 | |||||||
| chr20:38489815 | A | G | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+1197A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38489815 | |||||||
| chr20:38489837 | G | A | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.186+1219G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38489837 | |||||||
| chr20:38490011 | CT | C | 5 | a0001c0001t0001g0055 a0001c0001t0002g0161 a0001c0001t0002g0162 others(2): Show |
5 | HG02809.hp2 NA18974.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+1409delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr20 | 38490011 | ||||||
| chr20:38490033 | G | A | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.186+1415G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490033 | |||||||
| chr20:38490080 | G | A | 1 | a0001c0001t0007g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.186+1462G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490080 | |||||||
| chr20:38490100 | C | T | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+1482C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490100 | |||||||
| chr20:38490301 | C | T | 1 | a0001c0001t0019g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.186+1683C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490301 | |||||||
| chr20:38490334 | G | A | 1 | a0001c0001t0003g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.186+1716G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490334 | |||||||
| chr20:38490507 | C | G | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.186+1889C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490507 | |||||||
| chr20:38490511 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0047 |
2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.186+1893T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490511 | |||||||
| chr20:38490650 | GCATGCAC others(69): Show |
G | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+2034_186+2109d others(78): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr20 | 38490650 | ||||||
| chr20:38490803 | C | T | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.187-2127C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490803 | |||||||
| chr20:38491013 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.187-1917A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491013 | |||||||
| chr20:38491032 | C | G | 1 | a0004c0011t0002g0160 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.187-1898C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491032 | |||||||
| chr20:38491044 | C | G | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-1886C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491044 | |||||||
| chr20:38491324 | A | T | 3 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 |
3 | HG02257.hp1 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.187-1606A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491324 | |||||||
| chr20:38491333 | C | CT | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-1586dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr20 | 38491333 | ||||||
| chr20:38491333 | CT | C | 9 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0001t0002g0145 others(6): Show |
9 | HG00280.hp2 HG00735.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.187-1586delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr20 | 38491333 | ||||||
| chr20:38491539 | T | C | 1 | a0001c0001t0006g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.187-1391T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491539 | |||||||
| chr20:38491638 | G | T | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187-1292G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491638 | |||||||
| chr20:38491927 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.187-1003C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491927 | |||||||
| chr20:38492839 | G | T | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187-91G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38492839 | |||||||
| chr20:38493171 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.389+39A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38493171 | |||||||
| chr20:38493826 | G | T | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+694G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38493826 | |||||||
| chr20:38494144 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.389+1012C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494144 | |||||||
| chr20:38494220 | C | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0071 |
2 | NA18974.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.389+1088C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494220 | |||||||
| chr20:38494387 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.389+1255T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494387 | |||||||
| chr20:38494537 | AG | A | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.389+1407delG | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr20 | 38494537 | ||||||
| chr20:38494580 | G | A | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.389+1448G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494580 | |||||||
| chr20:38494585 | T | A | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.389+1453T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494585 | |||||||
| chr20:38494760 | A | G | 32 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(29): Show |
35 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.389+1628A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494760 | |||||||
| chr20:38494762 | G | T | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.389+1630G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494762 | |||||||
| chr20:38494809 | T | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.389+1677T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494809 | |||||||
| chr20:38495187 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0103 |
2 | HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.389+2055A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38495187 | |||||||
| chr20:38495466 | T | C | 8 | a0001c0001t0002g0147 a0001c0001t0002g0161 a0001c0001t0002g0162 others(5): Show |
8 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-1887T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38495466 | |||||||
| chr20:38495710 | G | T | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.390-1643G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38495710 | |||||||
| chr20:38495927 | T | C | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.390-1426T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38495927 | |||||||
| chr20:38496038 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.390-1315A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496038 | |||||||
| chr20:38496242 | G | C | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-1111G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496242 | |||||||
| chr20:38496265 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.390-1088C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496265 | |||||||
| chr20:38496736 | T | G | 1 | a0001c0001t0003g0058 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.390-617T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496736 | |||||||
| chr20:38496749 | A | G | 1 | a0001c0001t0003g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.390-604A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496749 | |||||||
| chr20:38496897 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0106 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.390-456T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496897 | |||||||
| chr20:38497197 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.390-156T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38497197 | |||||||
| chr20:38497214 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.390-139C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38497214 | |||||||
| chr20:38497802 | G | A | 5 | a0001c0001t0002g0147 a0001c0001t0002g0165 a0001c0001t0002g0166 others(2): Show |
5 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.553+286G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38497802 | |||||||
| chr20:38497889 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.553+373C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38497889 | |||||||
| chr20:38498069 | C | CA | 109 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(106): Show |
113 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.553+569dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 38498069 | ||||||
| chr20:38498069 | C | CAA | 5 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0109 others(2): Show |
5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.553+568_553+569dup others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 38498069 | ||||||
| chr20:38498083 | AAAG | A | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.553+570_553+572del others(3): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 38498083 | ||||||
| chr20:38498095 | CAATT | C | 8 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0038 others(5): Show |
8 | HG00280.hp1 HG00738.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.553+582_553+585del others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 38498095 | ||||||
| chr20:38498169 | G | A | 5 | a0001c0001t0001g0116 a0001c0001t0001g0139 a0001c0001t0027g0066 others(2): Show |
5 | HG01106.hp2 HG02071.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.553+653G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498169 | |||||||
| chr20:38498619 | C | T | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.554-828C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498619 | |||||||
| chr20:38498708 | C | T | 12 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(9): Show |
13 | HG00642.hp2 HG01433.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.554-739C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498708 | |||||||
| chr20:38498794 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.554-653A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498794 | |||||||
| chr20:38498812 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.554-635A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498812 | |||||||
| chr20:38499272 | G | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.554-175G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38499272 | |||||||
| chr20:38499437 | T | C | 17 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(14): Show |
20 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.554-10T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38499437 | |||||||
| chr20:38499641 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | splice_region_variant&intron_variant | LOW | c.740+8A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499641 | |||||||
| chr20:38499686 | T | A | 1 | a0001c0001t0006g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.740+53T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499686 | |||||||
| chr20:38499894 | A | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.740+261A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499894 | |||||||
| chr20:38499922 | G | C | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.740+289G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499922 | |||||||
| chr20:38499961 | A | G | 7 | a0001c0001t0001g0065 a0001c0001t0001g0116 a0001c0001t0001g0139 others(4): Show |
7 | HG01106.hp2 HG02056.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.740+328A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499961 | |||||||
| chr20:38500132 | T | G | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+499T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500132 | |||||||
| chr20:38500173 | C | A | 1 | a0002c0004t0030g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.740+540C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500173 | |||||||
| chr20:38500174 | G | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(123): Show |
131 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.740+541G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500174 | |||||||
| chr20:38500254 | T | C | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.740+621T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500254 | |||||||
| chr20:38500300 | G | C | 1 | a0001c0001t0003g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.740+667G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500300 | |||||||
| chr20:38500598 | G | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(118): Show |
125 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.740+965G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500598 | |||||||
| chr20:38500961 | G | C | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.740+1328G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500961 | |||||||
| chr20:38501023 | C | T | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.740+1390C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501023 | |||||||
| chr20:38501041 | A | G | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+1408A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501041 | |||||||
| chr20:38501103 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.740+1470C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501103 | |||||||
| chr20:38501105 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.740+1472A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501105 | |||||||
| chr20:38501338 | G | T | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+1705G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501338 | |||||||
| chr20:38501365 | A | G | 13 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(10): Show |
14 | HG00741.hp2 HG01884.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.740+1732A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501365 | |||||||
| chr20:38501430 | G | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.740+1797G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501430 | |||||||
| chr20:38501437 | G | C | 36 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(33): Show |
39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.740+1804G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501437 | |||||||
| chr20:38501488 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.740+1855C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501488 | |||||||
| chr20:38501683 | G | C | 1 | a0001c0001t0025g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.740+2050G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501683 | |||||||
| chr20:38501703 | C | T | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+2070C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501703 | |||||||
| chr20:38501958 | C | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(148): Show |
157 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.740+2325C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501958 | |||||||
| chr20:38501994 | A | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 |
4 | HG00735.hp2 HG01517.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.740+2361A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501994 | |||||||
| chr20:38502000 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.740+2367T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502000 | |||||||
| chr20:38502048 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0003g0076 a0001c0012t0001g0075 |
3 | NA18977.hp1 NA18999.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.740+2415G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502048 | |||||||
| chr20:38502171 | A | G | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+2538A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502171 | |||||||
| chr20:38502205 | G | A | 2 | a0001c0001t0001g0077 a0001c0012t0001g0075 |
2 | NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.740+2572G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502205 | |||||||
| chr20:38502208 | A | C | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.740+2575A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502208 | |||||||
| chr20:38502542 | A | G | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.740+2909A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502542 | |||||||
| chr20:38502592 | A | AT | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+2968dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38502592 | ||||||
| chr20:38502667 | C | T | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.740+3034C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502667 | |||||||
| chr20:38502848 | G | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.740+3215G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502848 | |||||||
| chr20:38502978 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.740+3345C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502978 | |||||||
| chr20:38503019 | C | T | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+3386C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503019 | |||||||
| chr20:38503078 | A | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.740+3445A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503078 | |||||||
| chr20:38503239 | A | C | 3 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0176 |
3 | NA18973.hp1 NA19012.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.740+3606A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503239 | |||||||
| chr20:38503409 | C | G | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.740+3776C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503409 | |||||||
| chr20:38503820 | A | AT | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+4192dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38503820 | ||||||
| chr20:38503961 | A | G | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+4328A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503961 | |||||||
| chr20:38504034 | G | A | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.740+4401G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504034 | |||||||
| chr20:38504194 | T | C | 1 | a0001c0001t0019g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.740+4561T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504194 | |||||||
| chr20:38504305 | CAG | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.740+4675_740+4676d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38504305 | ||||||
| chr20:38504319 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.740+4686A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504319 | |||||||
| chr20:38504340 | C | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.740+4707C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504340 | |||||||
| chr20:38504381 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.741-4696T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504381 | |||||||
| chr20:38504476 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.741-4601A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504476 | |||||||
| chr20:38504577 | A | G | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.741-4500A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504577 | |||||||
| chr20:38505049 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.741-4028A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505049 | |||||||
| chr20:38505185 | G | A | 1 | a0001c0001t0007g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.741-3892G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505185 | |||||||
| chr20:38505215 | G | A | 7 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(4): Show |
8 | HG02451.hp1 HG02922.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.741-3862G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505215 | |||||||
| chr20:38505228 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.741-3849A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505228 | |||||||
| chr20:38505505 | A | G | 1 | a0001c0001t0022g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.741-3572A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505505 | |||||||
| chr20:38505636 | AT | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.741-3436delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38505636 | ||||||
| chr20:38505661 | A | G | 1 | a0001c0001t0003g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.741-3416A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505661 | |||||||
| chr20:38505793 | G | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(4): Show |
7 | HG00741.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.741-3284G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505793 | |||||||
| chr20:38505942 | G | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.741-3135G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505942 | |||||||
| chr20:38505995 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.741-3082C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505995 | |||||||
| chr20:38506056 | ACTGC | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
154 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.741-3017_741-3014d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38506056 | ||||||
| chr20:38506248 | A | G | 3 | a0001c0001t0006g0016 a0001c0001t0020g0023 a0001c0001t0021g0022 |
3 | HG02055.hp1 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.741-2829A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38506248 | |||||||
| chr20:38506306 | T | G | 1 | a0001c0001t0001g0188 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.741-2771T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38506306 | |||||||
| chr20:38507294 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.741-1783C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507294 | |||||||
| chr20:38507614 | A | G | 7 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(4): Show |
8 | HG00642.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.741-1463A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507614 | |||||||
| chr20:38507682 | G | A | 1 | a0001c0001t0003g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.741-1395G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507682 | |||||||
| chr20:38507700 | T | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.741-1377T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507700 | |||||||
| chr20:38507706 | T | C | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.741-1371T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507706 | |||||||
| chr20:38508082 | CTT | C | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.741-992_741-991del others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38508082 | ||||||
| chr20:38508105 | A | G | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.741-972A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508105 | |||||||
| chr20:38508168 | C | T | 63 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(60): Show |
68 | HG00642.hp1 HG00642.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.741-909C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508168 | |||||||
| chr20:38508196 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.741-881A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508196 | |||||||
| chr20:38508242 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0002g0155 |
3 | HG03491.hp1 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.741-835T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508242 | |||||||
| chr20:38508326 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.741-751A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508326 | |||||||
| chr20:38508552 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.741-525A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508552 | |||||||
| chr20:38508601 | T | C | 4 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0027 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-476T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508601 | |||||||
| chr20:38508847 | A | T | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.741-230A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508847 | |||||||
| chr20:38509017 | C | A | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.741-60C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38509017 | |||||||
| chr20:38509379 | C | T | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.872+171C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509379 | |||||||
| chr20:38509456 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.872+248G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509456 | |||||||
| chr20:38509548 | C | T | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.872+340C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509548 | |||||||
| chr20:38509748 | T | C | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.872+540T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509748 | |||||||
| chr20:38509786 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.872+578T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509786 | |||||||
| chr20:38510131 | T | TAC | 7 | a0001c0001t0001g0034 a0001c0001t0001g0055 a0001c0001t0001g0140 others(4): Show |
7 | HG02015.hp2 HG02071.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.872+957_872+958dup others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | ||||||
| chr20:38510131 | TAC | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(50): Show |
54 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.872+957_872+958del others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | ||||||
| chr20:38510131 | TACAC | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0073 others(12): Show |
15 | HG00741.hp2 HG01255.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.872+955_872+958del others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | ||||||
| chr20:38510131 | TACACAC | T | 52 | a0001c0001t0001g0119 a0001c0001t0002g0095 a0001c0001t0002g0168 others(49): Show |
56 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.872+953_872+958del others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | ||||||
| chr20:38510131 | TACACACA others(7): Show |
T | 1 | a0001c0001t0019g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.872+945_872+958del others(14): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | ||||||
| chr20:38510131 | TACACACA others(9): Show |
T | 4 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.872+943_872+958del others(16): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | ||||||
| chr20:38510131 | TACACACA others(11): Show |
T | 1 | a0001c0001t0006g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.872+941_872+958del others(18): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | ||||||
| chr20:38510144 | A | G | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.872+936A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38510144 | |||||||
| chr20:38510165 | CAG | C | 3 | a0001c0001t0001g0072 a0001c0001t0001g0098 a0001c0001t0024g0097 |
3 | HG01243.hp1 HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.872+959_872+960del others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510165 | ||||||
| chr20:38510613 | TGAAAATC others(306): Show |
T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(37): Show |
44 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.872+1420_872+1732d others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510613 | ||||||
| chr20:38510638 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.872+1430C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38510638 | |||||||
| chr20:38510925 | A | C | 4 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0176 others(1): Show |
4 | HG03669.hp2 NA18973.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+1717A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38510925 | |||||||
| chr20:38510957 | C | T | 1 | a0001c0001t0003g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.872+1749C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38510957 | |||||||
| chr20:38511042 | T | C | 5 | a0001c0001t0002g0147 a0001c0001t0002g0165 a0001c0001t0002g0166 others(2): Show |
5 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1834T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511042 | |||||||
| chr20:38511082 | CAG | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.872+1879_872+1880d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38511082 | ||||||
| chr20:38511321 | CT | C | 18 | a0001c0001t0001g0056 a0001c0001t0001g0153 a0001c0001t0006g0030 others(15): Show |
19 | HG01069.hp1 HG01884.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.872+2127delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38511321 | ||||||
| chr20:38511385 | G | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.872+2177G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511385 | |||||||
| chr20:38511577 | A | G | 1 | a0001c0012t0001g0075 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.872+2369A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511577 | |||||||
| chr20:38511858 | C | CG | 4 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0004g0019 others(1): Show |
4 | HG00741.hp2 HG02004.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+2654dupG | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38511858 | ||||||
| chr20:38511867 | G | A | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.872+2659G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511867 | |||||||
| chr20:38511871 | G | T | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+2663G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511871 | |||||||
| chr20:38511903 | C | T | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+2695C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511903 | |||||||
| chr20:38512256 | C | T | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.872+3048C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512256 | |||||||
| chr20:38512319 | T | C | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.872+3111T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512319 | |||||||
| chr20:38512496 | A | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.872+3288A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512496 | |||||||
| chr20:38512623 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.872+3415G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512623 | |||||||
| chr20:38512782 | T | C | 37 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(34): Show |
41 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.873-3410T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512782 | |||||||
| chr20:38512791 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.873-3401G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512791 | |||||||
| chr20:38512935 | A | AT | 12 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
13 | HG00741.hp2 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.873-3251dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38512935 | ||||||
| chr20:38513055 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.873-3137C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513055 | |||||||
| chr20:38513137 | G | A | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.873-3055G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513137 | |||||||
| chr20:38513138 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.873-3054C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513138 | |||||||
| chr20:38513157 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.873-3035T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513157 | |||||||
| chr20:38513241 | C | T | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.873-2951C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513241 | |||||||
| chr20:38513268 | C | G | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.873-2924C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513268 | |||||||
| chr20:38513283 | C | T | 4 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 others(1): Show |
4 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-2909C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513283 | |||||||
| chr20:38513373 | A | G | 2 | a0001c0003t0010g0201 a0001c0003t0010g0209 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.873-2819A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513373 | |||||||
| chr20:38513453 | C | T | 1 | a0001c0001t0003g0092 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.873-2739C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513453 | |||||||
| chr20:38513482 | G | A | 4 | a0001c0001t0002g0147 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-2710G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513482 | |||||||
| chr20:38513482 | G | C | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.873-2710G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513482 | |||||||
| chr20:38513503 | T | C | 4 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0027 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.873-2689T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513503 | |||||||
| chr20:38513646 | CA | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.873-2530delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38513646 | ||||||
| chr20:38513703 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.873-2489C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513703 | |||||||
| chr20:38513799 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.873-2393C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513799 | |||||||
| chr20:38513822 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.873-2370T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513822 | |||||||
| chr20:38513878 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.873-2314A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513878 | |||||||
| chr20:38514010 | TTAGA | T | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.873-2178_873-2175d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38514010 | ||||||
| chr20:38514084 | A | T | 1 | a0001c0002t0002g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.873-2108A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514084 | |||||||
| chr20:38514198 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.873-1994C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514198 | |||||||
| chr20:38514432 | G | A | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.873-1760G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514432 | |||||||
| chr20:38514498 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.873-1694G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514498 | |||||||
| chr20:38514529 | C | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0027 a0001c0001t0004g0028 |
3 | HG02055.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.873-1663C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514529 | |||||||
| chr20:38514532 | C | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(204): Show |
213 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(210): Show |
intron_variant | MODIFIER | c.873-1660C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514532 | |||||||
| chr20:38515126 | C | T | 9 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(6): Show |
10 | HG02451.hp1 HG02622.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.873-1066C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515126 | |||||||
| chr20:38515164 | C | T | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.873-1028C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515164 | |||||||
| chr20:38515338 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.873-854T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515338 | |||||||
| chr20:38515507 | CTGTT | C | 3 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0109 |
3 | HG02895.hp1 HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.873-681_873-678del others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38515507 | ||||||
| chr20:38515546 | G | A | 1 | a0004c0011t0002g0160 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.873-646G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515546 | |||||||
| chr20:38515648 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.873-544G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515648 | |||||||
| chr20:38515717 | CTTTTTCT others(1): Show |
C | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.873-452_873-445del others(8): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38515717 | ||||||
| chr20:38515758 | A | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.873-434A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515758 | |||||||
| chr20:38515851 | A | C | 1 | a0001c0001t0004g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.873-341A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515851 | |||||||
| chr20:38515877 | G | T | 1 | a0001c0001t0003g0092 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.873-315G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515877 | |||||||
| chr20:38515884 | C | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.873-308C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515884 | |||||||
| chr20:38515984 | G | C | 2 | a0001c0001t0001g0077 a0001c0012t0001g0075 |
2 | NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.873-208G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515984 | |||||||
| chr20:38516053 | G | A | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.873-139G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38516053 | |||||||
| chr20:38516445 | T | C | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1051+75T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516445 | |||||||
| chr20:38516461 | G | A | 12 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(9): Show |
12 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1051+91G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516461 | |||||||
| chr20:38516495 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1051+125G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516495 | |||||||
| chr20:38516643 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1051+273T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516643 | |||||||
| chr20:38516677 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1051+307G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516677 | |||||||
| chr20:38516710 | T | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1051+340T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516710 | |||||||
| chr20:38516871 | T | C | 1 | a0001c0001t0004g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1051+501T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516871 | |||||||
| chr20:38516932 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0144 a0001c0001t0001g0170 others(1): Show |
4 | HG02015.hp2 NA18981.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051+562T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516932 | |||||||
| chr20:38517013 | T | C | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1052-493T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38517013 | |||||||
| chr20:38517319 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1052-187C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38517319 | |||||||
| chr20:38517732 | A | G | 35 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(32): Show |
38 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.1201-52A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 8/29 | chr20 | 38517732 | |||||||
| chr20:38518123 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1417+123A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518123 | |||||||
| chr20:38518375 | G | A | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1417+375G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518375 | |||||||
| chr20:38518402 | A | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(2): Show |
5 | HG00741.hp2 HG02280.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1417+402A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518402 | |||||||
| chr20:38518404 | A | G | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 others(5): Show |
9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1417+404A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518404 | |||||||
| chr20:38518514 | CTT | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1417+515_1417+516d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518514 | |||||||
| chr20:38518750 | T | G | 1 | a0001c0001t0004g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1417+750T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518750 | |||||||
| chr20:38518958 | C | G | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1417+958C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518958 | |||||||
| chr20:38519024 | A | G | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1417+1024A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519024 | |||||||
| chr20:38519076 | A | G | 4 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0038 others(1): Show |
4 | HG01071.hp2 HG01081.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1417+1076A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519076 | |||||||
| chr20:38519296 | C | T | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1417+1296C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519296 | |||||||
| chr20:38519452 | A | T | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1417+1452A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519452 | |||||||
| chr20:38519505 | T | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1417+1505T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519505 | |||||||
| chr20:38519588 | A | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1417+1588A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519588 | |||||||
| chr20:38520372 | T | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1418-1125T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38520372 | |||||||
| chr20:38520524 | C | CT | 37 | a0001c0001t0001g0146 a0001c0001t0001g0198 a0001c0001t0001g0199 others(34): Show |
40 | HG01109.hp1 HG01109.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.1418-951dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 38520524 | ||||||
| chr20:38520524 | C | CTT | 16 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(13): Show |
17 | HG00642.hp1 HG00741.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1418-952_1418-951d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 38520524 | ||||||
| chr20:38520524 | C | CTTT | 12 | a0001c0001t0004g0019 a0001c0002t0002g0122 a0001c0002t0002g0123 others(9): Show |
13 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1418-953_1418-951d others(5): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 38520524 | ||||||
| chr20:38520524 | CT | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0114 others(5): Show |
8 | HG01168.hp2 HG02896.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.1418-951delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 38520524 | ||||||
| chr20:38521066 | A | G | 1 | a0001c0001t0003g0192 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1418-431A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38521066 | |||||||
| chr20:38521396 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1418-101T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38521396 | |||||||
| chr20:38521922 | G | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1619+224G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38521922 | |||||||
| chr20:38521995 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1619+297T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38521995 | |||||||
| chr20:38522075 | G | A | 35 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(32): Show |
38 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.1619+377G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522075 | |||||||
| chr20:38522166 | C | T | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1619+468C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522166 | |||||||
| chr20:38522192 | C | T | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1619+494C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522192 | |||||||
| chr20:38522193 | A | G | 36 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(33): Show |
39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.1619+495A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522193 | |||||||
| chr20:38522198 | A | G | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1619+500A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522198 | |||||||
| chr20:38522387 | A | G | 3 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 |
3 | HG02809.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1619+689A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522387 | |||||||
| chr20:38522531 | C | T | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1619+833C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522531 | |||||||
| chr20:38522955 | T | C | 5 | a0001c0001t0002g0147 a0001c0001t0002g0165 a0001c0001t0002g0166 others(2): Show |
5 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619+1257T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522955 | |||||||
| chr20:38523153 | CA | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(4): Show |
8 | HG01884.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1619+1469delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr20 | 38523153 | ||||||
| chr20:38523246 | G | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(80): Show |
84 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1620-1532G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38523246 | |||||||
| chr20:38523362 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1620-1416A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38523362 | |||||||
| chr20:38524277 | A | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1620-501A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524277 | |||||||
| chr20:38524400 | G | A | 36 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(33): Show |
39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.1620-378G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524400 | |||||||
| chr20:38524491 | AT | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(84): Show |
88 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1620-276delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr20 | 38524491 | ||||||
| chr20:38524642 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1620-136T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524642 | |||||||
| chr20:38524647 | A | G | 1 | a0001c0001t0024g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1620-131A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524647 | |||||||
| chr20:38524745 | A | T | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1620-33A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524745 | |||||||
| chr20:38525583 | C | T | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1902+65C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 12/29 | chr20 | 38525583 | |||||||
| chr20:38525656 | A | C | 1 | a0001c0001t0003g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1902+138A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 12/29 | chr20 | 38525656 | |||||||
| chr20:38525802 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1903-93C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 12/29 | chr20 | 38525802 | |||||||
| chr20:38526247 | C | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2050+205C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38526247 | |||||||
| chr20:38526592 | T | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0106 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2050+550T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38526592 | |||||||
| chr20:38526906 | G | A | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2050+864G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38526906 | |||||||
| chr20:38527125 | C | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2050+1083C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527125 | |||||||
| chr20:38527265 | G | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2050+1223G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527265 | |||||||
| chr20:38527294 | A | G | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2050+1252A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527294 | |||||||
| chr20:38527317 | G | C | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2050+1275G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527317 | |||||||
| chr20:38527379 | T | A | 1 | a0001c0001t0003g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2050+1337T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527379 | |||||||
| chr20:38527491 | C | G | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2050+1449C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527491 | |||||||
| chr20:38527502 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2050+1460T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527502 | |||||||
| chr20:38527510 | T | C | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2050+1468T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527510 | |||||||
| chr20:38527644 | G | A | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.2050+1602G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527644 | |||||||
| chr20:38527725 | G | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0106 a0001c0001t0003g0107 others(3): Show |
6 | HG00639.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2050+1683G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527725 | |||||||
| chr20:38527855 | G | A | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2050+1813G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527855 | |||||||
| chr20:38528232 | A | G | 35 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(32): Show |
38 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.2050+2190A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528232 | |||||||
| chr20:38528333 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2050+2291C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528333 | |||||||
| chr20:38528345 | T | A | 1 | a0001c0002t0002g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050+2303T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528345 | |||||||
| chr20:38528345 | T | TTTTA | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp2 HG02280.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2050+2344_2050+234 others(8): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | ||||||
| chr20:38528345 | T | TTTTATTT others(1): Show |
5 | a0001c0001t0001g0199 a0001c0002t0002g0124 a0001c0002t0002g0125 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2050+2340_2050+234 others(12): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | ||||||
| chr20:38528345 | TTTTA | T | 16 | a0001c0001t0001g0034 a0001c0001t0001g0140 a0001c0001t0001g0144 others(13): Show |
16 | HG01256.hp1 HG01993.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.2050+2344_2050+234 others(8): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | ||||||
| chr20:38528345 | TTTTATTT others(1): Show |
T | 63 | a0001c0001t0001g0169 a0001c0001t0001g0183 a0001c0001t0001g0184 others(60): Show |
65 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.2050+2340_2050+234 others(12): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | ||||||
| chr20:38528345 | TTTTATTT others(5): Show |
T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(94): Show |
99 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.2050+2336_2050+234 others(16): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | ||||||
| chr20:38528345 | TTTTATTT others(17): Show |
T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2050+2324_2050+234 others(28): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | ||||||
| chr20:38528357 | A | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2050+2315A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528357 | |||||||
| chr20:38528396 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2050+2354A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528396 | |||||||
| chr20:38528613 | C | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 others(5): Show |
9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2051-2554C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528613 | |||||||
| chr20:38528711 | C | T | 9 | a0001c0001t0001g0062 a0001c0001t0001g0103 a0001c0001t0009g0010 others(6): Show |
9 | HG01361.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2051-2456C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528711 | |||||||
| chr20:38528723 | C | G | 1 | a0001c0001t0002g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2051-2444C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528723 | |||||||
| chr20:38528740 | G | A | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2051-2427G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528740 | |||||||
| chr20:38528827 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-2340C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528827 | |||||||
| chr20:38528853 | G | A | 7 | a0001c0001t0006g0016 a0001c0001t0009g0010 a0001c0001t0009g0011 others(4): Show |
7 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2051-2314G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528853 | |||||||
| chr20:38528912 | T | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2051-2255T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528912 | |||||||
| chr20:38528972 | G | A | 1 | a0001c0008t0001g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2051-2195G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528972 | |||||||
| chr20:38529170 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2051-1997A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529170 | |||||||
| chr20:38529203 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2051-1964A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529203 | |||||||
| chr20:38529310 | A | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(147): Show |
156 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.2051-1857A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529310 | |||||||
| chr20:38529517 | C | CA | 7 | a0001c0001t0001g0065 a0001c0001t0001g0116 a0001c0001t0001g0139 others(4): Show |
7 | HG01106.hp2 HG02071.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2051-1638dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38529517 | ||||||
| chr20:38529525 | A | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2051-1642A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529525 | |||||||
| chr20:38529530 | T | A | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2051-1637T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529530 | |||||||
| chr20:38529565 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2051-1602G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529565 | |||||||
| chr20:38529613 | A | C | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2051-1554A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529613 | |||||||
| chr20:38529645 | A | T | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2051-1522A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529645 | |||||||
| chr20:38529682 | A | G | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2051-1485A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529682 | |||||||
| chr20:38529701 | G | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0106 a0001c0001t0003g0107 others(3): Show |
6 | HG00639.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2051-1466G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529701 | |||||||
| chr20:38529715 | C | T | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2051-1452C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529715 | |||||||
| chr20:38529743 | G | A | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-1424G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529743 | |||||||
| chr20:38529791 | A | G | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-1376A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529791 | |||||||
| chr20:38530193 | T | C | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-974T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38530193 | |||||||
| chr20:38530303 | A | C | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2051-864A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38530303 | |||||||
| chr20:38530339 | A | G | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-828A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38530339 | |||||||
| chr20:38530393 | G | A | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2051-774G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38530393 | |||||||
| chr20:38530891 | A | AT | 85 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(82): Show |
86 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.2051-261dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38530891 | ||||||
| chr20:38531465 | A | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2115+234A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531465 | |||||||
| chr20:38531506 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2115+275A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531506 | |||||||
| chr20:38531805 | A | G | 41 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(38): Show |
45 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.2115+574A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531805 | |||||||
| chr20:38531843 | G | A | 1 | a0001c0001t0019g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2115+612G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531843 | |||||||
| chr20:38531878 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2115+647C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531878 | |||||||
| chr20:38531922 | T | C | 6 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(3): Show |
7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2115+691T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531922 | |||||||
| chr20:38532117 | G | A | 11 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(8): Show |
12 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2116-613G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532117 | |||||||
| chr20:38532206 | C | T | 2 | a0001c0002t0007g0004 a0001c0002t0007g0134 |
3 | HG00642.hp2 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2116-524C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532206 | |||||||
| chr20:38532325 | G | A | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2116-405G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532325 | |||||||
| chr20:38532363 | A | G | 6 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(3): Show |
7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2116-367A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532363 | |||||||
| chr20:38532486 | A | G | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2116-244A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532486 | |||||||
| chr20:38532974 | A | C | 1 | a0001c0001t0016g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2245+115A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38532974 | |||||||
| chr20:38533047 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2245+188A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533047 | |||||||
| chr20:38533067 | G | A | 1 | a0001c0001t0003g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2245+208G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533067 | |||||||
| chr20:38533069 | A | G | 1 | a0001c0001t0027g0066 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2245+210A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533069 | |||||||
| chr20:38533165 | C | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0112 a0001c0001t0003g0076 others(2): Show |
5 | HG02004.hp1 HG02293.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.2245+306C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533165 | |||||||
| chr20:38533271 | G | A | 1 | a0001c0001t0016g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2245+412G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533271 | |||||||
| chr20:38533360 | G | C | 35 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(32): Show |
38 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.2245+501G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533360 | |||||||
| chr20:38533612 | G | A | 4 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0109 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245+753G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533612 | |||||||
| chr20:38533777 | A | G | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2245+918A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533777 | |||||||
| chr20:38533890 | G | C | 1 | a0005c0010t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2245+1031G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533890 | |||||||
| chr20:38534138 | C | CA | 10 | a0001c0001t0001g0040 a0001c0001t0001g0060 a0001c0001t0001g0080 others(7): Show |
10 | HG00735.hp1 HG01255.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2246-918dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr20 | 38534138 | ||||||
| chr20:38534417 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2246-657T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534417 | |||||||
| chr20:38534504 | C | A | 1 | a0001c0001t0002g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2246-570C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534504 | |||||||
| chr20:38534724 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0144 |
2 | HG02015.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2246-350A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534724 | |||||||
| chr20:38534729 | A | G | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2246-345A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534729 | |||||||
| chr20:38534794 | C | T | 7 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0186 others(4): Show |
7 | NA18941.hp1 NA18956.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.2246-280C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534794 | |||||||
| chr20:38534963 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2246-111C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534963 | |||||||
| chr20:38535254 | G | C | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2379+47G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38535254 | |||||||
| chr20:38535356 | C | T | 3 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0176 |
3 | NA18973.hp1 NA19012.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2379+149C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38535356 | |||||||
| chr20:38535652 | G | A | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2379+445G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38535652 | |||||||
| chr20:38535910 | C | T | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2379+703C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38535910 | |||||||
| chr20:38536031 | T | C | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2379+824T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536031 | |||||||
| chr20:38536313 | C | T | 1 | a0001c0001t0003g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2379+1106C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536313 | |||||||
| chr20:38536437 | A | T | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2379+1230A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536437 | |||||||
| chr20:38536692 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2379+1485C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536692 | |||||||
| chr20:38536717 | C | G | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2379+1510C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536717 | |||||||
| chr20:38536903 | T | G | 2 | a0001c0001t0001g0139 a0001c0001t0027g0066 |
2 | HG01106.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2379+1696T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536903 | |||||||
| chr20:38537034 | C | T | 5 | a0001c0001t0002g0147 a0001c0001t0002g0165 a0001c0001t0002g0166 others(2): Show |
5 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.2379+1827C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537034 | |||||||
| chr20:38537175 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2379+1968A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537175 | |||||||
| chr20:38537176 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2379+1969T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537176 | |||||||
| chr20:38537180 | A | G | 13 | a0001c0001t0018g0194 a0001c0003t0005g0005 a0001c0003t0005g0203 others(10): Show |
15 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2379+1973A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537180 | |||||||
| chr20:38537282 | A | G | 36 | a0001c0001t0001g0034 a0001c0001t0001g0140 a0001c0001t0001g0144 others(33): Show |
36 | HG00738.hp2 HG02015.hp2 HG02027.hp2 others(33): Show |
intron_variant | MODIFIER | c.2379+2075A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537282 | |||||||
| chr20:38537295 | C | CA | 7 | a0001c0001t0003g0064 a0001c0001t0006g0002 a0001c0001t0006g0016 others(4): Show |
8 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2379+2096dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr20 | 38537295 | ||||||
| chr20:38537355 | C | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2379+2148C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537355 | |||||||
| chr20:38537505 | CAA | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2380-2270_2380-226 others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537505 | |||||||
| chr20:38537565 | C | T | 6 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(3): Show |
7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2380-2211C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537565 | |||||||
| chr20:38537683 | A | T | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2380-2093A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537683 | |||||||
| chr20:38537715 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(143): Show |
152 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.2380-2061G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537715 | |||||||
| chr20:38537918 | A | G | 1 | a0001c0001t0024g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2380-1858A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537918 | |||||||
| chr20:38538009 | T | C | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2380-1767T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538009 | |||||||
| chr20:38538288 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2380-1488G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538288 | |||||||
| chr20:38538331 | G | C | 1 | a0001c0001t0004g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2380-1445G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538331 | |||||||
| chr20:38538405 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 |
4 | HG00735.hp2 HG01517.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2380-1371G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538405 | |||||||
| chr20:38538406 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0003g0197 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2380-1370C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538406 | |||||||
| chr20:38538440 | A | G | 6 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(3): Show |
7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2380-1336A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538440 | |||||||
| chr20:38538500 | G | A | 6 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(3): Show |
7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2380-1276G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538500 | |||||||
| chr20:38538639 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2380-1137C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538639 | |||||||
| chr20:38539024 | A | G | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2380-752A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539024 | |||||||
| chr20:38539180 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2380-596A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539180 | |||||||
| chr20:38539378 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2380-398T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539378 | |||||||
| chr20:38539611 | C | T | 6 | a0001c0001t0001g0065 a0001c0001t0001g0116 a0001c0001t0001g0138 others(3): Show |
6 | HG01106.hp2 HG02056.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2380-165C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539611 | |||||||
| chr20:38539616 | C | T | 2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | NA18974.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2380-160C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539616 | |||||||
| chr20:38540291 | G | C | 14 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(11): Show |
14 | NA18941.hp1 NA18949.hp1 NA18956.hp1 others(11): Show |
intron_variant | MODIFIER | c.2562+333G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/29 | chr20 | 38540291 | |||||||
| chr20:38540749 | A | T | 204 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(201): Show |
210 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.2563-292A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/29 | chr20 | 38540749 | |||||||
| chr20:38541011 | T | C | 54 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(51): Show |
59 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.2563-30T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/29 | chr20 | 38541011 | |||||||
| chr20:38541335 | G | A | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2714+143G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38541335 | |||||||
| chr20:38541349 | A | G | 1 | a0001c0001t0003g0076 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2714+157A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38541349 | |||||||
| chr20:38542491 | TA | T | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2714+1308delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr20 | 38542491 | ||||||
| chr20:38542622 | A | G | 36 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(33): Show |
39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.2714+1430A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542622 | |||||||
| chr20:38542649 | G | A | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2714+1457G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542649 | |||||||
| chr20:38542704 | A | G | 36 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(33): Show |
39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.2714+1512A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542704 | |||||||
| chr20:38542780 | C | T | 1 | a0001c0001t0007g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2714+1588C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542780 | |||||||
| chr20:38542798 | C | T | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2714+1606C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542798 | |||||||
| chr20:38542814 | G | T | 1 | a0001c0008t0001g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2714+1622G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542814 | |||||||
| chr20:38542843 | A | G | 21 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(18): Show |
22 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2714+1651A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542843 | |||||||
| chr20:38542865 | G | GA | 15 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(12): Show |
17 | HG01109.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2714+1683dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr20 | 38542865 | ||||||
| chr20:38543468 | C | A | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2714+2276C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38543468 | |||||||
| chr20:38543473 | T | C | 4 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0027 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2714+2281T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38543473 | |||||||
| chr20:38543765 | A | G | 2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | NA18974.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2715-2478A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38543765 | |||||||
| chr20:38544014 | C | T | 1 | a0001c0001t0023g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2715-2229C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544014 | |||||||
| chr20:38544171 | C | T | 4 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0027 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2715-2072C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544171 | |||||||
| chr20:38544178 | A | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2715-2065A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544178 | |||||||
| chr20:38544232 | C | T | 1 | a0001c0002t0002g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2715-2011C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544232 | |||||||
| chr20:38544745 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2715-1498G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544745 | |||||||
| chr20:38544843 | G | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(34): Show |
38 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.2715-1400G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544843 | |||||||
| chr20:38545181 | A | G | 1 | a0001c0001t0019g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2715-1062A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545181 | |||||||
| chr20:38545245 | A | T | 1 | a0001c0001t0001g0189 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2715-998A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545245 | |||||||
| chr20:38545512 | A | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2715-731A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545512 | |||||||
| chr20:38545545 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2715-698A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545545 | |||||||
| chr20:38545551 | C | T | 1 | a0001c0001t0004g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2715-692C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545551 | |||||||
| chr20:38545673 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2715-570G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545673 | |||||||
| chr20:38545761 | A | G | 4 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0027 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2715-482A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545761 | |||||||
| chr20:38545917 | G | C | 7 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0038 others(4): Show |
7 | HG00280.hp1 HG01071.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2715-326G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545917 | |||||||
| chr20:38545944 | A | G | 2 | a0001c0001t0002g0142 a0001c0001t0002g0143 |
2 | HG00280.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2715-299A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545944 | |||||||
| chr20:38546070 | G | GA | 6 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(3): Show |
7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2715-172dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr20 | 38546070 | ||||||
| chr20:38546526 | T | A | 1 | a0001c0001t0019g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2902+96T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546526 | |||||||
| chr20:38546536 | G | A | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2902+106G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546536 | |||||||
| chr20:38546599 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2902+169T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546599 | |||||||
| chr20:38546611 | A | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(4): Show |
8 | HG01884.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2902+181A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546611 | |||||||
| chr20:38546708 | G | T | 13 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0027 others(10): Show |
13 | HG01361.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2902+278G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546708 | |||||||
| chr20:38546779 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2902+349G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546779 | |||||||
| chr20:38546838 | C | G | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2902+408C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546838 | |||||||
| chr20:38546873 | A | G | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2902+443A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546873 | |||||||
| chr20:38547007 | C | G | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2902+577C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38547007 | |||||||
| chr20:38547847 | C | T | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2903-842C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38547847 | |||||||
| chr20:38547888 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2903-801A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38547888 | |||||||
| chr20:38547916 | G | C | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2903-773G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38547916 | |||||||
| chr20:38548053 | G | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2903-636G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548053 | |||||||
| chr20:38548076 | C | T | 2 | a0001c0003t0005g0005 a0001c0003t0005g0207 |
3 | HG02451.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2903-613C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548076 | |||||||
| chr20:38548136 | TCCATCCT others(17): Show |
T | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2903-550_2903-527d others(26): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr20 | 38548136 | ||||||
| chr20:38548366 | G | A | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2903-323G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548366 | |||||||
| chr20:38548384 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2903-305G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548384 | |||||||
| chr20:38548532 | T | C | 37 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(34): Show |
41 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.2903-157T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548532 | |||||||
| chr20:38548984 | G | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(35): Show |
39 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.3009+189G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38548984 | |||||||
| chr20:38549288 | T | C | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3009+493T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549288 | |||||||
| chr20:38549295 | A | C | 1 | a0001c0001t0007g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3009+500A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549295 | |||||||
| chr20:38549533 | TA | T | 9 | a0001c0001t0001g0056 a0001c0001t0001g0065 a0001c0001t0001g0099 others(6): Show |
9 | HG01069.hp1 HG02622.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.3009+755delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549533 | ||||||
| chr20:38549543 | A | T | 4 | a0001c0001t0006g0002 a0001c0002t0002g0124 a0001c0002t0007g0004 others(1): Show |
6 | HG00642.hp2 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.3009+748A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549543 | |||||||
| chr20:38549545 | A | T | 25 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(22): Show |
28 | HG00642.hp2 HG00741.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+750A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549545 | |||||||
| chr20:38549547 | A | AT | 5 | a0001c0001t0002g0147 a0001c0001t0002g0159 a0001c0001t0002g0176 others(2): Show |
5 | HG01978.hp1 HG02109.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.3009+752_3009+753i others(3): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549547 | |||||||
| chr20:38549547 | A | T | 53 | a0001c0001t0001g0041 a0001c0001t0001g0063 a0001c0001t0001g0089 others(50): Show |
57 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3009+752A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549547 | |||||||
| chr20:38549549 | A | AT | 4 | a0001c0001t0001g0042 a0001c0001t0001g0084 a0001c0001t0002g0158 others(1): Show |
4 | HG03486.hp1 NA18973.hp1 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.3009+754_3009+755i others(3): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549549 | |||||||
| chr20:38549549 | A | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0041 others(159): Show |
168 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(165): Show |
intron_variant | MODIFIER | c.3009+754A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549549 | |||||||
| chr20:38549551 | T | A | 1 | a0001c0001t0003g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3009+756T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549551 | |||||||
| chr20:38549563 | T | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3009+768T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549563 | |||||||
| chr20:38549563 | T | TATAC | 7 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(4): Show |
8 | HG02451.hp1 HG02922.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3009+769_3009+770i others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549563 | ||||||
| chr20:38549575 | CACAT | C | 10 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3009+786_3009+789d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549575 | ||||||
| chr20:38549585 | T | TAC | 2 | a0001c0001t0026g0121 a0003c0006t0003g0033 |
2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3009+806_3009+807d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549585 | ||||||
| chr20:38549585 | TAC | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(78): Show |
82 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.3009+806_3009+807d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549585 | ||||||
| chr20:38549585 | TACAC | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0144 a0001c0005t0001g0117 others(1): Show |
4 | NA19001.hp1 NA19006.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.3009+804_3009+807d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549585 | ||||||
| chr20:38549720 | A | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3009+925A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549720 | |||||||
| chr20:38549738 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3009+943A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549738 | |||||||
| chr20:38549785 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0099 |
2 | NA18956.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.3009+990C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549785 | |||||||
| chr20:38549785 | CT | C | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3009+997delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549785 | ||||||
| chr20:38550038 | G | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3010-1033G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550038 | |||||||
| chr20:38550142 | T | G | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3010-929T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550142 | |||||||
| chr20:38550147 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3010-924G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550147 | |||||||
| chr20:38550153 | G | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3010-918G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550153 | |||||||
| chr20:38550312 | A | T | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3010-759A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550312 | |||||||
| chr20:38550323 | A | T | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3010-748A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550323 | |||||||
| chr20:38550384 | A | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3010-687A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550384 | |||||||
| chr20:38550612 | A | G | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3010-459A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550612 | |||||||
| chr20:38550856 | A | G | 5 | a0001c0001t0002g0148 a0001c0001t0002g0150 a0001c0001t0002g0152 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.3010-215A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550856 | |||||||
| chr20:38551336 | G | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0099 |
2 | NA18956.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.3162+113G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38551336 | |||||||
| chr20:38551657 | T | A | 6 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(3): Show |
7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3162+434T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38551657 | |||||||
| chr20:38551708 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3162+485A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38551708 | |||||||
| chr20:38551831 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0106 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3162+608C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38551831 | |||||||
| chr20:38552140 | A | AT | 82 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(79): Show |
83 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.3162+932dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38552140 | ||||||
| chr20:38552140 | AT | A | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 others(5): Show |
9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3162+932delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38552140 | ||||||
| chr20:38552253 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(82): Show |
86 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.3162+1030A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552253 | |||||||
| chr20:38552434 | C | T | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3162+1211C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552434 | |||||||
| chr20:38552475 | C | T | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3162+1252C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552475 | |||||||
| chr20:38552775 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(81): Show |
85 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.3163-1092G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552775 | |||||||
| chr20:38552798 | A | G | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 others(5): Show |
9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3163-1069A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552798 | |||||||
| chr20:38552824 | C | T | 1 | a0001c0003t0005g0207 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3163-1043C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552824 | |||||||
| chr20:38553264 | A | G | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3163-603A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553264 | |||||||
| chr20:38553364 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3163-503C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553364 | |||||||
| chr20:38553377 | A | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3163-490A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553377 | |||||||
| chr20:38553455 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3163-412A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553455 | |||||||
| chr20:38553525 | A | G | 36 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(33): Show |
39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.3163-342A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553525 | |||||||
| chr20:38553777 | C | CA | 13 | a0001c0001t0001g0144 a0001c0001t0001g0153 a0001c0001t0001g0154 others(10): Show |
13 | HG02027.hp2 HG02257.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.3163-66dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | ||||||
| chr20:38553777 | C | CAA | 68 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(65): Show |
70 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.3163-67_3163-66dup others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | ||||||
| chr20:38553777 | C | CAAA | 32 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0051 others(29): Show |
32 | HG00558.hp1 HG00735.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.3163-68_3163-66dup others(3): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | ||||||
| chr20:38553777 | CA | C | 16 | a0001c0001t0001g0186 a0001c0001t0002g0179 a0001c0001t0004g0025 others(13): Show |
17 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.3163-66delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | ||||||
| chr20:38553777 | CAA | C | 6 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(3): Show |
7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3163-67_3163-66del others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | ||||||
| chr20:38553777 | CAAAAAAA others(6): Show |
C | 12 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
13 | HG00741.hp2 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3163-78_3163-66del others(13): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | ||||||
| chr20:38554169 | T | TA | 26 | a0001c0001t0001g0144 a0001c0001t0003g0182 a0001c0001t0004g0001 others(23): Show |
27 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.3372+107dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr20 | 38554169 | ||||||
| chr20:38554169 | TA | T | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.3372+107delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr20 | 38554169 | ||||||
| chr20:38554181 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3372+105A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38554181 | |||||||
| chr20:38554736 | C | T | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3372+660C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38554736 | |||||||
| chr20:38554742 | A | T | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3372+666A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38554742 | |||||||
| chr20:38554961 | A | G | 1 | a0004c0011t0002g0160 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3372+885A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38554961 | |||||||
| chr20:38555162 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3372+1086A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38555162 | |||||||
| chr20:38555462 | G | A | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3372+1386G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38555462 | |||||||
| chr20:38555489 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0013g0087 |
2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.3372+1413T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38555489 | |||||||
| chr20:38555549 | C | G | 12 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
13 | HG00741.hp2 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3372+1473C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38555549 | |||||||
| chr20:38556015 | G | A | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3372+1939G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556015 | |||||||
| chr20:38556125 | A | T | 1 | a0001c0001t0003g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3372+2049A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556125 | |||||||
| chr20:38556247 | T | G | 4 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0038 others(1): Show |
4 | HG01071.hp2 HG01081.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.3373-2048T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556247 | |||||||
| chr20:38556322 | C | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 others(5): Show |
9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3373-1973C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556322 | |||||||
| chr20:38556323 | G | T | 2 | a0001c0001t0001g0116 a0001c0005t0001g0117 |
2 | NA19006.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.3373-1972G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556323 | |||||||
| chr20:38556327 | A | G | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 others(5): Show |
9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3373-1968A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556327 | |||||||
| chr20:38556434 | A | G | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3373-1861A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556434 | |||||||
| chr20:38556783 | A | G | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.3373-1512A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556783 | |||||||
| chr20:38556965 | A | T | 8 | a0001c0001t0002g0147 a0001c0001t0002g0161 a0001c0001t0002g0162 others(5): Show |
8 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.3373-1330A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556965 | |||||||
| chr20:38557155 | G | T | 1 | a0001c0001t0003g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3373-1140G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557155 | |||||||
| chr20:38557199 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3373-1096T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557199 | |||||||
| chr20:38557224 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0003g0192 |
2 | NA18956.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3373-1071A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557224 | |||||||
| chr20:38557342 | A | T | 2 | a0001c0002t0007g0004 a0001c0002t0007g0134 |
3 | HG00642.hp2 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.3373-953A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557342 | |||||||
| chr20:38557366 | C | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(133): Show |
142 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.3373-929C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557366 | |||||||
| chr20:38557508 | A | T | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3373-787A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557508 | |||||||
| chr20:38557667 | G | T | 1 | a0001c0003t0005g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3373-628G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557667 | |||||||
| chr20:38557674 | C | A | 1 | a0001c0001t0022g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3373-621C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557674 | |||||||
| chr20:38557809 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3373-486C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557809 | |||||||
| chr20:38557887 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0071 |
2 | NA18974.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.3373-408A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557887 | |||||||
| chr20:38557991 | G | T | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3373-304G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557991 | |||||||
| chr20:38558172 | T | C | 2 | a0001c0001t0001g0112 a0005c0010t0001g0111 |
2 | HG02004.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3373-123T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38558172 | |||||||
| chr20:38558467 | A | AT | 5 | a0001c0001t0001g0060 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG00280.hp1 HG00738.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.3531+26dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 38558467 | ||||||
| chr20:38558573 | G | T | 2 | a0001c0001t0001g0112 a0005c0010t0001g0111 |
2 | HG02004.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3531+120G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38558573 | |||||||
| chr20:38558989 | G | C | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3531+536G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38558989 | |||||||
| chr20:38559042 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3531+589T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559042 | |||||||
| chr20:38559460 | C | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3531+1007C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559460 | |||||||
| chr20:38559641 | C | A | 2 | a0001c0001t0001g0112 a0005c0010t0001g0111 |
2 | HG02004.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3531+1188C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559641 | |||||||
| chr20:38559672 | C | T | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3531+1219C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559672 | |||||||
| chr20:38559911 | G | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 |
3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3531+1458G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559911 | |||||||
| chr20:38560106 | G | GT | 17 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(14): Show |
18 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.3531+1665dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 38560106 | ||||||
| chr20:38560106 | GT | G | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3531+1665delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 38560106 | ||||||
| chr20:38560123 | T | C | 6 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(3): Show |
7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3531+1670T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560123 | |||||||
| chr20:38560235 | T | C | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3531+1782T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560235 | |||||||
| chr20:38560270 | T | C | 7 | a0001c0001t0006g0016 a0001c0001t0009g0010 a0001c0001t0009g0011 others(4): Show |
7 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.3531+1817T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560270 | |||||||
| chr20:38560484 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3531+2031G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560484 | |||||||
| chr20:38560524 | G | A | 1 | a0001c0001t0003g0192 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3532-2008G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560524 | |||||||
| chr20:38561257 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3532-1275G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561257 | |||||||
| chr20:38561569 | TAGA | T | 2 | a0001c0001t0002g0142 a0001c0001t0002g0143 |
2 | HG00280.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.3532-960_3532-958d others(5): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 38561569 | ||||||
| chr20:38561585 | G | A | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3532-947G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561585 | |||||||
| chr20:38561751 | C | A | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3532-781C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561751 | |||||||
| chr20:38561759 | C | T | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3532-773C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561759 | |||||||
| chr20:38561875 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3532-657T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561875 | |||||||
| chr20:38561983 | A | C | 14 | a0001c0002t0002g0122 a0001c0002t0002g0123 a0001c0002t0002g0124 others(11): Show |
15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.3532-549A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561983 | |||||||
| chr20:38561985 | G | A | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3532-547G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561985 | |||||||
| chr20:38562071 | C | T | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3532-461C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38562071 | |||||||
| chr20:38562269 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0047 |
2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.3532-263C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38562269 | |||||||
| chr20:38562748 | GT | G | 6 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(3): Show |
7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3697+62delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 38562748 | ||||||
| chr20:38562759 | T | C | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3697+62T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38562759 | |||||||
| chr20:38562812 | A | G | 33 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(30): Show |
36 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.3697+115A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38562812 | |||||||
| chr20:38563017 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3697+320A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563017 | |||||||
| chr20:38563135 | G | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3697+438G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563135 | |||||||
| chr20:38563144 | T | G | 32 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(29): Show |
35 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.3697+447T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563144 | |||||||
| chr20:38563194 | T | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3697+497T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563194 | |||||||
| chr20:38563267 | C | T | 32 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(29): Show |
35 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.3697+570C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563267 | |||||||
| chr20:38563357 | A | G | 6 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(3): Show |
7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3697+660A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563357 | |||||||
| chr20:38563447 | A | G | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3697+750A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563447 | |||||||
| chr20:38563848 | C | T | 2 | a0001c0002t0007g0004 a0001c0002t0007g0134 |
3 | HG00642.hp2 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.3697+1151C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563848 | |||||||
| chr20:38563867 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3697+1170C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563867 | |||||||
| chr20:38563965 | A | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3697+1268A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563965 | |||||||
| chr20:38564175 | A | G | 40 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(37): Show |
43 | HG00642.hp1 HG00741.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.3698-1184A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564175 | |||||||
| chr20:38564190 | C | A | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3698-1169C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564190 | |||||||
| chr20:38564234 | G | A | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3698-1125G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564234 | |||||||
| chr20:38564395 | ACCTCTTG others(9): Show |
A | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3698-963_3698-948d others(18): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564395 | |||||||
| chr20:38564412 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3698-947T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564412 | |||||||
| chr20:38564560 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3698-799G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564560 | |||||||
| chr20:38564686 | C | T | 1 | a0001c0007t0003g0067 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3698-673C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564686 | |||||||
| chr20:38564812 | A | AAT | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3698-546_3698-545i others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 38564812 | ||||||
| chr20:38564814 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3698-545C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564814 | |||||||
| chr20:38564877 | C | T | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3698-482C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564877 | |||||||
| chr20:38564883 | TTCC | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 |
4 | HG00735.hp2 HG01517.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.3698-467_3698-465d others(5): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 38564883 | ||||||
| chr20:38564961 | G | C | 1 | a0001c0002t0002g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3698-398G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564961 | |||||||
| chr20:38564961 | G | GTC | 3 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0003t0005g0204 |
3 | HG00280.hp2 HG02738.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3698-380_3698-379d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 38564961 | ||||||
| chr20:38565077 | C | G | 1 | a0001c0001t0004g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3698-282C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38565077 | |||||||
| chr20:38565117 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0106 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3698-242C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38565117 | |||||||
| chr20:38565206 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3698-153A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38565206 | |||||||
| chr20:38565329 | C | A | 1 | a0001c0001t0003g0061 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3698-30C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38565329 | |||||||
| chr20:38565611 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(80): Show |
84 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.3817+133G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38565611 | |||||||
| chr20:38565677 | C | T | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3817+199C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38565677 | |||||||
| chr20:38565740 | A | C | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3817+262A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38565740 | |||||||
| chr20:38565790 | C | T | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3817+312C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38565790 | |||||||
| chr20:38566471 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3818-625G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566471 | |||||||
| chr20:38566585 | G | A | 1 | a0001c0001t0022g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3818-511G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566585 | |||||||
| chr20:38566595 | T | C | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3818-501T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566595 | |||||||
| chr20:38566691 | A | G | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3818-405A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566691 | |||||||
| chr20:38566899 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3818-197G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566899 | |||||||
| chr20:38567001 | G | C | 1 | a0001c0001t0001g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3818-95G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38567001 | |||||||
| chr20:38567324 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3954+92A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38567324 | |||||||
| chr20:38567375 | T | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(17): Show |
21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3954+143T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38567375 | |||||||
| chr20:38567874 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3954+642G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38567874 | |||||||
| chr20:38568046 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3954+814A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38568046 | |||||||
| chr20:38568262 | CA | C | 31 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(28): Show |
34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.3954+1040delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 38568262 | ||||||
| chr20:38568517 | G | T | 2 | a0001c0001t0001g0037 a0001c0008t0001g0049 |
2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.3954+1285G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38568517 | |||||||
| chr20:38568758 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
154 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.3955-1130G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38568758 | |||||||
| chr20:38568841 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3955-1047T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38568841 | |||||||
| chr20:38569024 | T | C | 31 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(28): Show |
34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.3955-864T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569024 | |||||||
| chr20:38569058 | A | C | 65 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(62): Show |
70 | HG00642.hp1 HG00642.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.3955-830A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569058 | |||||||
| chr20:38569085 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 |
3 | HG00639.hp1 HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.3955-803A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569085 | |||||||
| chr20:38569108 | A | T | 1 | a0001c0001t0003g0109 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3955-780A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569108 | |||||||
| chr20:38569135 | T | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3955-753T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569135 | |||||||
| chr20:38569306 | T | C | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3955-582T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569306 | |||||||
| chr20:38569333 | TA | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(28): Show |
34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.3955-553delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 38569333 | ||||||
| chr20:38569337 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3955-551A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569337 | |||||||
| chr20:38569467 | T | C | 3 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 |
3 | HG02257.hp1 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3955-421T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569467 | |||||||
| chr20:38569503 | T | C | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3955-385T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569503 | |||||||
| chr20:38569513 | A | G | 1 | a0001c0001t0002g0158 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3955-375A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569513 | |||||||
| chr20:38569629 | A | C | 6 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(3): Show |
7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3955-259A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569629 | |||||||
| chr20:38569729 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3955-159C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569729 | |||||||
| chr20:38570070 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0013g0087 |
2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.4063+74T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570070 | |||||||
| chr20:38570200 | A | G | 11 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(8): Show |
13 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.4063+204A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570200 | |||||||
| chr20:38570215 | C | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(28): Show |
34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.4063+219C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570215 | |||||||
| chr20:38570280 | C | T | 6 | a0001c0001t0009g0010 a0001c0001t0009g0011 a0001c0001t0009g0012 others(3): Show |
6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.4063+284C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570280 | |||||||
| chr20:38570407 | A | G | 34 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(31): Show |
37 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.4064-362A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570407 | |||||||
| chr20:38570494 | G | C | 1 | a0001c0001t0027g0066 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4064-275G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570494 | |||||||
| chr20:38570596 | G | A | 1 | a0001c0009t0001g0088 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4064-173G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570596 | |||||||
| chr20:38570637 | A | G | 1 | a0001c0001t0026g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4064-132A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570637 | |||||||
| chr20:38570896 | T | C | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.4142+49T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38570896 | |||||||
| chr20:38571014 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4142+167T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571014 | |||||||
| chr20:38571418 | C | G | 1 | a0001c0001t0002g0162 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.4142+571C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571418 | |||||||
| chr20:38571679 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(82): Show |
86 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.4142+832A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571679 | |||||||
| chr20:38571891 | T | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4142+1044T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571891 | |||||||
| chr20:38571913 | G | A | 1 | a0001c0001t0003g0076 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4142+1066G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571913 | |||||||
| chr20:38571923 | A | C | 12 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(9): Show |
14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.4142+1076A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571923 | |||||||
| chr20:38571946 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4142+1099C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571946 | |||||||
| chr20:38571950 | A | C | 2 | a0001c0001t0011g0013 a0001c0001t0011g0014 |
2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.4142+1103A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571950 | |||||||
| chr20:38571954 | C | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(188): Show |
197 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(194): Show |
intron_variant | MODIFIER | c.4142+1107C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571954 | |||||||
| chr20:38572462 | T | C | 38 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(35): Show |
41 | HG00642.hp1 HG00741.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.4142+1615T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38572462 | |||||||
| chr20:38572887 | T | C | 2 | a0001c0001t0020g0023 a0001c0001t0021g0022 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.4143-1263T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38572887 | |||||||
| chr20:38573001 | G | C | 3 | a0002c0004t0029g0008 a0002c0004t0030g0007 a0002c0004t0031g0009 |
3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4143-1149G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573001 | |||||||
| chr20:38573184 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4143-966G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573184 | |||||||
| chr20:38573315 | C | CT | 12 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00741.hp2 HG01109.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.4143-824dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr20 | 38573315 | ||||||
| chr20:38573395 | A | G | 1 | a0001c0002t0002g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4143-755A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573395 | |||||||
| chr20:38573524 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.4143-626C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573524 | |||||||
| chr20:38573530 | T | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0040 others(146): Show |
155 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.4143-620T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573530 | |||||||
| chr20:38573567 | C | T | 9 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0197 others(6): Show |
10 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.4143-583C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573567 | |||||||
| chr20:38573752 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4143-398C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573752 | |||||||
| chr20:38574132 | C | A | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.4143-18C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38574132 | |||||||
| chr20:38574319 | C | T | 19 | a0001c0001t0004g0001 a0001c0001t0004g0017 a0001c0001t0004g0018 others(16): Show |
20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.4291+21C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 29/29 | chr20 | 38574319 | |||||||
| chr20:38574447 | T | C | 2 | a0001c0002t0007g0004 a0001c0002t0007g0134 |
3 | HG00642.hp2 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.4291+149T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 29/29 | chr20 | 38574447 | |||||||
| chr20:38574597 | G | T | 7 | a0001c0003t0005g0005 a0001c0003t0005g0203 a0001c0003t0005g0204 others(4): Show |
8 | HG02451.hp1 HG02922.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.4292-177G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 29/29 | chr20 | 38574597 | |||||||
| chr20:38574762 | T | A | 6 | a0001c0001t0006g0002 a0001c0001t0006g0016 a0001c0001t0006g0029 others(3): Show |
7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4292-12T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 29/29 | chr20 | 38574762 |