Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 222194 |
| ensemblid | ENSG00000187257.16 |
| hgncid | 24765 |
| symbol | RSBN1L |
| name | round spermatid basic protein 1 like |
| refseq_nuc | NM_198467.3 |
| refseq_prot | NP_940869.2 |
| ensembl_nuc | ENST00000334955.13 |
| ensembl_prot | ENSP00000334040.7 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 77696459 |
| end | 77783022 |
| strand | + |
| ver | v1.2 |
| region | chr7:77696459-77783022 |
| region5000 | chr7:77691459-77788022 |
| regionname0 | RSBN1L_chr7_77696459_77783022 |
| regionname5000 | RSBN1L_chr7_77691459_77788022 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 846 | 321 | 79 | 63 | 114 | 18 | 45 | 89 | RSBN1L_chr7_77691459_77788022 | RSBN1L | MAEPP others(841): Show |
chr7 | 77691459 | 77788022 |
| a0002 | 0/0 | 846 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | MAEPP others(841): Show |
chr7 | 77691459 | 77788022 |
| a0003 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | MAEPP others(841): Show |
chr7 | 77691459 | 77788022 |
| a0004 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | MAEPP others(841): Show |
chr7 | 77691459 | 77788022 |
| a0005 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | MAELP others(841): Show |
chr7 | 77691459 | 77788022 |
| a0006 | 0/0 | 846 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | MAEPP others(841): Show |
chr7 | 77691459 | 77788022 |
| a0007 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | MAEPP others(841): Show |
chr7 | 77691459 | 77788022 |
| a0008 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | MAEPP others(841): Show |
chr7 | 77691459 | 77788022 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2538 | 200 | 70 | 30 | 64 | 12 | 23 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0001c0002 | 1/0 | 2538 | 115 | 8 | 29 | 50 | 6 | 21 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0001c0004 | 0/0 | 2538 | 4 | 0 | 4 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0001c0005 | 0/0 | 2538 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0001c0009 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0002c0003 | 0/0 | 2538 | 9 | 8 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0003c0008 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0004c0010 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0005c0012 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0006c0007 | 0/0 | 2538 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0007c0011 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 | ||
| a0008c0006 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | ATGGC others(2533): Show |
chr7 | 77691459 | 77788022 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 6407 | 50 | 4 | 10 | 28 | 1 | 6 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0003 | 0/0 | 6404 | 40 | 3 | 5 | 22 | 1 | 9 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6399): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0004 | 0/0 | 6406 | 30 | 7 | 4 | 10 | 8 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0005 | 0/0 | 6404 | 18 | 13 | 3 | 0 | 0 | 2 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6399): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0007 | 0/0 | 6407 | 5 | 4 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0008 | 0/0 | 6404 | 7 | 7 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6399): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0009 | 0/0 | 6407 | 6 | 6 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0010 | 0/0 | 6408 | 5 | 0 | 1 | 2 | 0 | 2 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6403): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0011 | 0/0 | 6408 | 5 | 5 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6403): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0012 | 0/0 | 6405 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6400): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0013 | 0/0 | 6409 | 4 | 3 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6404): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0014 | 0/0 | 6406 | 3 | 1 | 1 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0015 | 0/0 | 6408 | 3 | 0 | 1 | 0 | 1 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6403): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0016 | 0/0 | 6408 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6403): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0018 | 0/0 | 6407 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0019 | 0/0 | 6405 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6400): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0020 | 0/0 | 6404 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6399): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0022 | 0/0 | 6406 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0023 | 0/0 | 6404 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6399): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0024 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6404): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0025 | 0/0 | 6407 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0026 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0027 | 0/0 | 6404 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6399): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0029 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0030 | 0/0 | 6407 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0031 | 0/0 | 6404 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6399): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0032 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0033 | 0/0 | 6407 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0034 | 0/0 | 6406 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0001t0035 | 0/0 | 6405 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6400): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0001 | 1/0 | 6406 | 95 | 6 | 20 | 47 | 4 | 17 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0006 | 0/0 | 6407 | 8 | 1 | 3 | 2 | 1 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0016 | 0/0 | 6408 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6403): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0017 | 0/0 | 6408 | 3 | 0 | 1 | 0 | 1 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6403): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0021 | 0/0 | 6406 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0036 | 0/0 | 6406 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0037 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6403): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0038 | 0/0 | 6407 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0039 | 0/0 | 6408 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6403): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0041 | 0/0 | 6406 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0002t0042 | 0/0 | 6408 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6403): Show |
chr7 | 77691459 | 77788022 |
| a0001c0004t0005 | 0/0 | 6404 | 4 | 0 | 4 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6399): Show |
chr7 | 77691459 | 77788022 |
| a0001c0005t0040 | 0/0 | 6406 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0001c0009t0003 | 0/0 | 6404 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6399): Show |
chr7 | 77691459 | 77788022 |
| a0002c0003t0004 | 0/0 | 6406 | 7 | 7 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0002c0003t0007 | 0/0 | 6407 | 2 | 1 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0003c0008t0001 | 0/0 | 6406 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0004c0010t0028 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| a0005c0012t0012 | 0/0 | 6405 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6400): Show |
chr7 | 77691459 | 77788022 |
| a0006c0007t0006 | 0/0 | 6407 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6402): Show |
chr7 | 77691459 | 77788022 |
| a0007c0011t0012 | 0/0 | 6405 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6400): Show |
chr7 | 77691459 | 77788022 |
| a0008c0006t0001 | 0/0 | 6406 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | AGGAG others(6401): Show |
chr7 | 77691459 | 77788022 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0010g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0010g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0011g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0012g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0013g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0013g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0013g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0013g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0014g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0014g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0015g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0015g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0015g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0016g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0016g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0018g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0018g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0019g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0019g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0020g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0020g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0022g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0022g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0023g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0024g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0025g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0026g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0027g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0029g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0030g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0031g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0032g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0033g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0034g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0001t0035g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0006g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0006g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0006g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0016g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0017g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0017g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0017g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0021g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0021g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0036g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0037g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0038g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0039g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0041g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0002t0042g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0004t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0004t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0004t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0004t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0005t0040g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0001c0009t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0002c0003t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0002c0003t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0002c0003t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0002c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0002c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0002c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0002c0003t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0002c0003t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0002c0003t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0003c0008t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0004c0010t0028g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0005c0012t0012g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0006c0007t0006g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0007c0011t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| a0008c0006t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | GBR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00099 | hp2 | a0001 | c0002 | t0017 | g0235 | EUR | GBR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00140 | hp1 | a0001 | c0001 | t0015 | g0030 | EUR | GBR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00140 | hp2 | a0001 | c0002 | t0006 | g0264 | EUR | GBR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0108 | EUR | FIN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0140 | EUR | FIN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0229 | EUR | FIN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0107 | EUR | FIN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | CHS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | CHS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00639 | hp1 | a0001 | c0001 | t0013 | g0122 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0050 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0316 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01070 | hp1 | a0001 | c0004 | t0005 | g0208 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01070 | hp2 | a0001 | c0002 | t0041 | g0239 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01071 | hp1 | a0001 | c0004 | t0005 | g0209 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01071 | hp2 | a0001 | c0002 | t0021 | g0242 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01074 | hp2 | a0001 | c0002 | t0021 | g0241 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0315 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0198 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01109 | hp1 | a0001 | c0001 | t0025 | g0113 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01109 | hp2 | a0001 | c0002 | t0017 | g0237 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01169 | hp1 | a0001 | c0002 | t0006 | g0266 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01175 | hp1 | a0001 | c0002 | t0039 | g0291 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0150 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01192 | hp1 | a0002 | c0003 | t0007 | g0105 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01192 | hp2 | a0001 | c0004 | t0005 | g0194 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01256 | hp1 | a0001 | c0001 | t0015 | g0028 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01256 | hp2 | a0001 | c0001 | t0016 | g0006 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0309 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01258 | hp1 | a0001 | c0001 | t0016 | g0015 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01261 | hp1 | a0001 | c0002 | t0042 | g0245 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0205 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0299 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0300 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0267 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0274 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0287 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0141 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0135 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0074 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01891 | hp1 | a0001 | c0001 | t0031 | g0216 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01891 | hp2 | a0001 | c0001 | t0022 | g0041 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0319 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01975 | hp1 | a0001 | c0001 | t0014 | g0078 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0282 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01981 | hp2 | a0001 | c0002 | t0006 | g0280 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0293 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02027 | hp1 | a0001 | c0002 | t0037 | g0324 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0025 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02074 | hp2 | a0003 | c0008 | t0001 | g0317 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0334 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02145 | hp1 | a0002 | c0003 | t0004 | g0047 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02145 | hp2 | a0001 | c0001 | t0018 | g0138 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | CDX | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | CDX | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0313 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0199 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02258 | hp2 | a0001 | c0001 | t0018 | g0128 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02280 | hp1 | a0004 | c0010 | t0028 | g0143 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02293 | hp2 | a0001 | c0004 | t0005 | g0210 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0129 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02451 | hp2 | a0001 | c0001 | t0035 | g0037 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0095 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0215 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02615 | hp1 | a0001 | c0009 | t0003 | g0179 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02622 | hp1 | a0002 | c0003 | t0004 | g0116 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02622 | hp2 | a0001 | c0002 | t0006 | g0254 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0124 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02647 | hp1 | a0001 | c0001 | t0029 | g0145 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02683 | hp2 | a0001 | c0002 | t0006 | g0246 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0252 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02723 | hp2 | a0001 | c0001 | t0013 | g0123 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0272 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02735 | hp2 | a0001 | c0002 | t0036 | g0275 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0331 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02818 | hp1 | a0001 | c0001 | t0027 | g0072 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02886 | hp1 | a0002 | c0003 | t0004 | g0045 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0132 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0040 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02965 | hp1 | a0002 | c0003 | t0004 | g0046 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02965 | hp2 | a0001 | c0001 | t0020 | g0212 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02970 | hp1 | a0001 | c0001 | t0012 | g0189 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02976 | hp1 | a0001 | c0001 | t0032 | g0033 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0159 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03041 | hp1 | a0002 | c0003 | t0007 | g0042 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03041 | hp2 | a0001 | c0002 | t0016 | g0265 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0085 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03130 | hp2 | a0005 | c0012 | t0012 | g0207 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0136 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0057 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0240 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03239 | hp2 | a0001 | c0001 | t0015 | g0029 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0055 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0271 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0257 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0032 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0195 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0089 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03579 | hp2 | a0001 | c0001 | t0024 | g0056 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03654 | hp2 | a0001 | c0001 | t0010 | g0048 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0330 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0306 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03704 | hp1 | a0001 | c0001 | t0023 | g0112 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03704 | hp2 | a0001 | c0002 | t0017 | g0236 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03710 | hp1 | a0001 | c0005 | t0040 | g0259 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0197 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0333 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0214 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03927 | hp2 | a0001 | c0001 | t0010 | g0121 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0192 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04115 | hp2 | a0006 | c0007 | t0006 | g0281 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0276 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0305 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0278 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04204 | hp1 | a0001 | c0002 | t0038 | g0297 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG04228 | hp2 | a0001 | c0001 | t0034 | g0173 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | CHB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | CHB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CHB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | CHB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0092 | AFR | YRI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18906 | hp2 | a0007 | c0011 | t0012 | g0190 | AFR | YRI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18949 | hp1 | a0001 | c0001 | t0010 | g0106 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18974 | hp2 | a0001 | c0002 | t0006 | g0220 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18980 | hp2 | a0001 | c0001 | t0010 | g0079 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19056 | hp1 | a0008 | c0006 | t0001 | g0263 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19062 | hp2 | a0001 | c0002 | t0006 | g0302 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19063 | hp2 | a0001 | c0001 | t0014 | g0094 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0049 | AFR | YRI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | YRI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ASW | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20129 | hp2 | a0001 | c0001 | t0026 | g0114 | AFR | ASW | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0161 | EUR | TSI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | TSI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20805 | hp1 | a0001 | c0001 | t0030 | g0027 | EUR | TSI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0142 | EUR | TSI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0255 | SAS | GIH | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | GIH | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01123 | hp1 | a0001 | c0001 | t0033 | g0149 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG01123 | hp2 | a0001 | c0002 | t0006 | g0290 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02109 | hp1 | a0002 | c0003 | t0004 | g0044 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0134 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02486 | hp1 | a0002 | c0003 | t0004 | g0115 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02486 | hp2 | a0001 | c0001 | t0013 | g0125 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG02559 | hp2 | a0001 | c0001 | t0019 | g0031 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG06807 | hp1 | a0001 | c0001 | t0012 | g0158 | AFR | USA | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | USA | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20300 | hp1 | a0002 | c0003 | t0004 | g0043 | AFR | USA | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | USA | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0038 | REF | REF | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0243 | REF | REF | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77696480 | C | T | 1 | a0005 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.11C>T | p.Pro4Leu | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 22/6406 | 11/2541 | 4/846 | chr7 | 77696480 | |||
| chr7:77696602 | G | A | 1 | a0002 | 9 | HG01192.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
missense_variant | MODERATE | c.133G>A | p.Val45Ile | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 144/6406 | 133/2541 | 45/846 | chr7 | 77696602 | |||
| chr7:77696810 | C | T | 1 | a0007 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.341C>T | p.Ser114Phe | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 352/6406 | 341/2541 | 114/846 | chr7 | 77696810 | |||
| chr7:77749523 | G | A | 1 | a0008 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.803G>A | p.Arg268His | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/8 | 814/6406 | 803/2541 | 268/846 | chr7 | 77749523 | |||
| chr7:77749526 | C | T | 1 | a0004 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.806C>T | p.Pro269Leu | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/8 | 817/6406 | 806/2541 | 269/846 | chr7 | 77749526 | |||
| chr7:77749861 | G | A | 1 | a0006 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1141G>A | p.Ala381Thr | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/8 | 1152/6406 | 1141/2541 | 381/846 | chr7 | 77749861 | |||
| chr7:77778896 | A | G | 1 | a0003 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.2269A>G | p.Ile757Val | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2280/6406 | 2269/2541 | 757/846 | chr7 | 77778896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77696601 | G | A | 1 | a0001c0005 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.132G>A | p.Lys44Lys | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 143/6406 | 132/2541 | 44/846 | chr7 | 77696601 | |||
| chr7:77696757 | C | T | 1 | a0001c0004 | 4 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(1): Show |
synonymous_variant | LOW | c.288C>T | p.Ser96Ser | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 299/6406 | 288/2541 | 96/846 | chr7 | 77696757 | |||
| chr7:77736453 | A | G | 7 | a0001c0001 a0001c0004 a0001c0009 others(4): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
synonymous_variant | LOW | c.630A>G | p.Glu210Glu | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/8 | 641/6406 | 630/2541 | 210/846 | chr7 | 77736453 | |||
| chr7:77765605 | C | T | 1 | a0001c0009 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.1455C>T | p.Asp485Asp | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/8 | 1466/6406 | 1455/2541 | 485/846 | chr7 | 77765605 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77779334 | C | T | 1 | a0001c0001t0022 | 2 | HG01891.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*166C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 166 | chr7 | 77779334 | ||||||
| chr7:77779432 | G | A | 1 | a0001c0001t0018 | 2 | HG02145.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*264G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 264 | chr7 | 77779432 | ||||||
| chr7:77779443 | C | CAT | 2 | a0001c0002t0017 a0001c0002t0042 |
4 | HG00099.hp2 HG01109.hp2 HG01261.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*291_*292dupTA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 293 | INFO_REALIGN_3_PRIME | chr7 | 77779443 | |||||
| chr7:77779443 | CAT | C | 33 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(30): Show |
202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*291_*292delTA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 291 | INFO_REALIGN_3_PRIME | chr7 | 77779443 | |||||
| chr7:77779924 | G | A | 1 | a0001c0001t0013 | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*756G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 756 | chr7 | 77779924 | ||||||
| chr7:77780037 | G | A | 1 | a0001c0002t0036 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*869G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 869 | chr7 | 77780037 | ||||||
| chr7:77780065 | T | C | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*897T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 897 | chr7 | 77780065 | ||||||
| chr7:77780122 | G | A | 8 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(5): Show |
70 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*954G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 954 | chr7 | 77780122 | ||||||
| chr7:77780224 | T | C | 22 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(19): Show |
131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1056T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1056 | chr7 | 77780224 | ||||||
| chr7:77780273 | A | G | 4 | a0001c0001t0003 a0001c0001t0033 a0001c0001t0034 others(1): Show |
43 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1105A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1105 | chr7 | 77780273 | ||||||
| chr7:77780531 | T | C | 1 | a0001c0001t0019 | 2 | HG02559.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1363T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1363 | chr7 | 77780531 | ||||||
| chr7:77780805 | A | G | 1 | a0001c0002t0041 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1637A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1637 | chr7 | 77780805 | ||||||
| chr7:77780817 | C | T | 1 | a0001c0005t0040 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1649C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1649 | chr7 | 77780817 | ||||||
| chr7:77780942 | T | A | 1 | a0001c0002t0038 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1774T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1774 | chr7 | 77780942 | ||||||
| chr7:77780984 | A | G | 1 | a0001c0001t0029 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1816A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1816 | chr7 | 77780984 | ||||||
| chr7:77780997 | G | C | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*1829G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1829 | chr7 | 77780997 | ||||||
| chr7:77781138 | A | G | 1 | a0001c0002t0042 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1970A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1970 | chr7 | 77781138 | ||||||
| chr7:77781146 | A | T | 2 | a0001c0001t0011 a0001c0001t0024 |
6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1978A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1978 | chr7 | 77781146 | ||||||
| chr7:77781335 | G | C | 1 | a0001c0001t0008 | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2167G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2167 | chr7 | 77781335 | ||||||
| chr7:77781530 | G | A | 2 | a0001c0001t0015 a0001c0001t0030 |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2362G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2362 | chr7 | 77781530 | ||||||
| chr7:77781946 | C | G | 1 | a0001c0002t0042 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2778C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2778 | chr7 | 77781946 | ||||||
| chr7:77781950 | C | T | 3 | a0001c0001t0009 a0001c0001t0018 a0004c0010t0028 |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2782C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2782 | chr7 | 77781950 | ||||||
| chr7:77781963 | C | T | 1 | a0001c0001t0032 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2795C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2795 | chr7 | 77781963 | ||||||
| chr7:77781972 | C | CA | 11 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0015 others(8): Show |
28 | HG00140.hp1 HG00140.hp2 HG01123.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2824dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2825 | INFO_REALIGN_3_PRIME | chr7 | 77781972 | |||||
| chr7:77781972 | C | CAA | 13 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(10): Show |
52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2823_*2824dupAA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2825 | INFO_REALIGN_3_PRIME | chr7 | 77781972 | |||||
| chr7:77781972 | C | CAAA | 7 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(4): Show |
67 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2822_*2824dupAAA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2825 | INFO_REALIGN_3_PRIME | chr7 | 77781972 | |||||
| chr7:77781972 | C | CAAAA | 2 | a0001c0001t0010 a0001c0001t0024 |
6 | HG00642.hp1 HG03579.hp2 HG03654.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2821_*2824dupAAAA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2825 | INFO_REALIGN_3_PRIME | chr7 | 77781972 | |||||
| chr7:77782116 | A | G | 2 | a0001c0001t0025 a0001c0001t0026 |
2 | HG01109.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2948A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2948 | chr7 | 77782116 | ||||||
| chr7:77782231 | C | T | 1 | a0001c0001t0032 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3063C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3063 | chr7 | 77782231 | ||||||
| chr7:77782247 | C | T | 2 | a0001c0001t0015 a0001c0001t0030 |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3079C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3079 | chr7 | 77782247 | ||||||
| chr7:77782372 | A | AG | 2 | a0001c0001t0011 a0001c0001t0024 |
6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3206dupG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3207 | INFO_REALIGN_3_PRIME | chr7 | 77782372 | |||||
| chr7:77782409 | C | A | 9 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0012 others(6): Show |
69 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*3241C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3241 | chr7 | 77782409 | ||||||
| chr7:77782635 | T | C | 1 | a0001c0001t0031 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3467T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3467 | chr7 | 77782635 | ||||||
| chr7:77782716 | A | AGTG | 2 | a0001c0001t0015 a0001c0001t0030 |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3554_*3556dupGGT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3557 | INFO_REALIGN_3_PRIME | chr7 | 77782716 | |||||
| chr7:77782791 | G | A | 1 | a0001c0001t0027 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3623G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3623 | chr7 | 77782791 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77697093 | T | C | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.586+38T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77697093 | |||||||
| chr7:77697431 | G | T | 68 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(65): Show |
68 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.586+376G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77697431 | |||||||
| chr7:77697865 | C | A | 1 | a0001c0001t0004g0003 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.586+810C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77697865 | |||||||
| chr7:77697885 | T | C | 1 | a0001c0002t0001g0218 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.586+830T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77697885 | |||||||
| chr7:77698016 | G | A | 17 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(14): Show |
17 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.586+961G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698016 | |||||||
| chr7:77698032 | CTT | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+981_586+982del others(2): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77698032 | ||||||
| chr7:77698077 | C | T | 1 | a0001c0001t0033g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.586+1022C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698077 | |||||||
| chr7:77698176 | T | G | 1 | a0001c0001t0005g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.586+1121T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698176 | |||||||
| chr7:77698756 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.586+1701A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698756 | |||||||
| chr7:77698783 | A | C | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.586+1728A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698783 | |||||||
| chr7:77698786 | T | C | 1 | a0001c0001t0030g0027 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.586+1731T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698786 | |||||||
| chr7:77699012 | A | C | 38 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(35): Show |
39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.586+1957A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699012 | |||||||
| chr7:77699071 | T | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+2016T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699071 | |||||||
| chr7:77699266 | A | C | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.586+2211A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699266 | |||||||
| chr7:77699325 | CGAAA | C | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+2273_586+2276d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77699325 | ||||||
| chr7:77699376 | T | G | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+2321T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699376 | |||||||
| chr7:77699796 | A | AT | 21 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(18): Show |
21 | HG00140.hp1 HG01256.hp1 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.586+2757dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77699796 | ||||||
| chr7:77699901 | A | G | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.586+2846A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699901 | |||||||
| chr7:77699922 | G | A | 81 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(78): Show |
81 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.586+2867G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699922 | |||||||
| chr7:77700075 | G | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+3020G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700075 | |||||||
| chr7:77700426 | C | T | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.586+3371C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700426 | |||||||
| chr7:77700436 | G | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+3381G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700436 | |||||||
| chr7:77700526 | G | A | 47 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(44): Show |
47 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.586+3471G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700526 | |||||||
| chr7:77700653 | A | G | 1 | a0001c0002t0001g0329 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.586+3598A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700653 | |||||||
| chr7:77700852 | G | T | 1 | a0001c0002t0001g0328 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.586+3797G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700852 | |||||||
| chr7:77700879 | G | A | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.586+3824G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700879 | |||||||
| chr7:77701057 | C | T | 1 | a0001c0001t0031g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.586+4002C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701057 | |||||||
| chr7:77701091 | ACAGTAAG others(1): Show |
A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+4037_586+4044d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701091 | |||||||
| chr7:77701112 | AC | A | 140 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(137): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.586+4058delC | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701112 | |||||||
| chr7:77701151 | C | CA | 27 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(24): Show |
27 | HG00323.hp1 HG01192.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.586+4115dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701151 | ||||||
| chr7:77701155 | A | C | 7 | a0001c0001t0002g0111 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.586+4100A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701155 | |||||||
| chr7:77701159 | A | C | 2 | a0001c0001t0002g0111 a0001c0001t0023g0112 |
2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.586+4104A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701159 | |||||||
| chr7:77701166 | AAAAACAA others(1): Show |
A | 8 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(5): Show |
8 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+4114_586+4121d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701166 | ||||||
| chr7:77701168 | A | C | 2 | a0001c0002t0001g0314 a0001c0002t0037g0324 |
2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.586+4113A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701168 | |||||||
| chr7:77701169 | AACAACAA others(1): Show |
A | 110 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(107): Show |
111 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.586+4116_586+4123d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701169 | ||||||
| chr7:77701170 | AC | A | 7 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(4): Show |
7 | HG00140.hp1 HG01256.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+4116delC | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701170 | |||||||
| chr7:77701170 | ACAACAAC | A | 14 | a0001c0001t0002g0039 a0001c0001t0002g0064 a0001c0001t0002g0076 others(11): Show |
14 | HG00438.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.586+4116_586+4122d others(9): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701170 | |||||||
| chr7:77701171 | C | A | 67 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(64): Show |
67 | HG00639.hp2 HG00741.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.586+4116C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701171 | |||||||
| chr7:77701180 | C | A | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.586+4125C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701180 | |||||||
| chr7:77701189 | C | A | 1 | a0001c0002t0001g0229 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.586+4134C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701189 | |||||||
| chr7:77701189 | C | CA | 11 | a0001c0001t0003g0157 a0001c0001t0003g0186 a0001c0001t0005g0195 others(8): Show |
11 | HG01433.hp1 HG02074.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+4143dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701189 | ||||||
| chr7:77701192 | A | C | 2 | a0001c0002t0001g0326 a0001c0002t0001g0327 |
2 | NA18972.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.586+4137A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701192 | |||||||
| chr7:77701196 | A | G | 1 | a0001c0001t0020g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.586+4141A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701196 | |||||||
| chr7:77701199 | C | T | 1 | a0001c0002t0001g0327 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.586+4144C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701199 | |||||||
| chr7:77701514 | C | T | 1 | a0001c0002t0001g0325 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.586+4459C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701514 | |||||||
| chr7:77701515 | G | A | 1 | a0001c0001t0002g0039 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.586+4460G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701515 | |||||||
| chr7:77701653 | CT | C | 211 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(208): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.586+4614delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701653 | ||||||
| chr7:77701734 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0214 |
2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.586+4679C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701734 | |||||||
| chr7:77701755 | A | G | 2 | a0001c0001t0005g0196 a0001c0001t0005g0213 |
2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.586+4700A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701755 | |||||||
| chr7:77701792 | C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+4737C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701792 | |||||||
| chr7:77701862 | G | A | 136 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(133): Show |
137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.586+4807G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701862 | |||||||
| chr7:77701924 | G | A | 5 | a0001c0002t0001g0219 a0001c0002t0001g0231 a0001c0002t0001g0232 others(2): Show |
5 | HG00423.hp1 NA19054.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+4869G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701924 | |||||||
| chr7:77702025 | A | G | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+4970A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702025 | |||||||
| chr7:77702050 | C | A | 9 | a0001c0001t0002g0111 a0001c0001t0004g0107 a0001c0001t0004g0108 others(6): Show |
9 | HG00280.hp1 HG00323.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.586+4995C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702050 | |||||||
| chr7:77702168 | G | A | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.586+5113G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702168 | |||||||
| chr7:77702417 | A | G | 2 | a0001c0001t0004g0146 a0001c0001t0004g0147 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.586+5362A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702417 | |||||||
| chr7:77702741 | G | C | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.586+5686G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702741 | |||||||
| chr7:77702743 | G | C | 58 | a0001c0001t0002g0111 a0001c0001t0004g0001 a0001c0001t0004g0003 others(55): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.586+5688G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702743 | |||||||
| chr7:77703013 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.586+5958C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703013 | |||||||
| chr7:77703079 | G | A | 1 | a0001c0001t0010g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.586+6024G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703079 | |||||||
| chr7:77703087 | G | A | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+6032G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703087 | |||||||
| chr7:77703146 | G | T | 1 | a0001c0002t0001g0230 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.586+6091G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703146 | |||||||
| chr7:77703290 | G | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6235G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703290 | |||||||
| chr7:77703438 | C | T | 1 | a0001c0001t0005g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.586+6383C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703438 | |||||||
| chr7:77703477 | G | GT | 54 | a0001c0001t0002g0111 a0001c0001t0004g0110 a0001c0001t0004g0130 others(51): Show |
54 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.586+6452dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | G | GTT | 45 | a0001c0001t0004g0001 a0001c0001t0004g0137 a0001c0001t0004g0139 others(42): Show |
47 | HG00280.hp2 HG00738.hp2 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.586+6451_586+6452d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | G | GTTT | 22 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0146 others(19): Show |
22 | HG00323.hp1 HG00733.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.586+6450_586+6452d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | G | GTTTT | 11 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0010 others(8): Show |
11 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+6449_586+6452d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | G | GTTTTT | 6 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0009g0144 others(3): Show |
6 | HG01258.hp1 HG02071.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+6448_586+6452d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | GT | G | 32 | a0001c0001t0003g0157 a0001c0001t0003g0181 a0001c0001t0003g0182 others(29): Show |
32 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.586+6452delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | GTT | G | 45 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(42): Show |
45 | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.586+6451_586+6452d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | GTTT | G | 8 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(5): Show |
8 | HG01952.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+6450_586+6452d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | GTTTT | G | 15 | a0001c0001t0002g0039 a0001c0001t0002g0090 a0001c0001t0002g0091 others(12): Show |
15 | HG00639.hp1 HG01258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.586+6449_586+6452d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | GTTTTT | G | 48 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(45): Show |
48 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.586+6448_586+6452d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0004g0004 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.586+6443_586+6452d others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703477 | GTTTTTTT others(6): Show |
G | 1 | a0001c0002t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.586+6440_586+6452d others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | ||||||
| chr7:77703530 | C | A | 1 | a0001c0001t0002g0117 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.586+6475C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703530 | |||||||
| chr7:77703779 | C | T | 136 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(133): Show |
137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.586+6724C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703779 | |||||||
| chr7:77703850 | C | T | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+6795C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703850 | |||||||
| chr7:77703872 | C | T | 2 | a0001c0001t0004g0146 a0001c0001t0004g0147 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.586+6817C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703872 | |||||||
| chr7:77703950 | G | A | 67 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(64): Show |
67 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.586+6895G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703950 | |||||||
| chr7:77703990 | A | T | 1 | a0005c0012t0012g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.586+6935A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703990 | |||||||
| chr7:77704191 | G | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7136G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704191 | |||||||
| chr7:77704273 | A | G | 2 | a0001c0001t0004g0146 a0001c0001t0004g0147 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.586+7218A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704273 | |||||||
| chr7:77704461 | T | C | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+7406T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704461 | |||||||
| chr7:77704556 | C | T | 1 | a0001c0002t0001g0258 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.586+7501C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704556 | |||||||
| chr7:77704657 | C | T | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+7602C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704657 | |||||||
| chr7:77704844 | C | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7789C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704844 | |||||||
| chr7:77704923 | G | A | 1 | a0001c0005t0040g0259 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.586+7868G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704923 | |||||||
| chr7:77704937 | A | G | 1 | a0001c0001t0007g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.586+7882A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704937 | |||||||
| chr7:77704950 | C | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7895C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704950 | |||||||
| chr7:77704990 | G | A | 1 | a0001c0001t0008g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+7935G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704990 | |||||||
| chr7:77704991 | T | G | 1 | a0001c0001t0008g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+7936T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704991 | |||||||
| chr7:77704991 | T | TTG | 207 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(204): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.586+7950_586+7951d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77704991 | ||||||
| chr7:77704991 | TTGTG | T | 6 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(3): Show |
6 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+7948_586+7951d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77704991 | ||||||
| chr7:77705043 | C | T | 4 | a0001c0001t0004g0001 a0001c0001t0004g0140 a0001c0001t0004g0141 others(1): Show |
5 | HG00280.hp2 HG01515.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+7988C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705043 | |||||||
| chr7:77705076 | T | G | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+8021T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705076 | |||||||
| chr7:77705124 | C | T | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.586+8069C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705124 | |||||||
| chr7:77705144 | T | G | 1 | a0001c0002t0001g0282 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.586+8089T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705144 | |||||||
| chr7:77705427 | A | T | 1 | a0001c0001t0004g0005 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.586+8372A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705427 | |||||||
| chr7:77705502 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.586+8447T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705502 | |||||||
| chr7:77705510 | G | GT | 17 | a0001c0002t0001g0228 a0001c0002t0001g0229 a0001c0002t0001g0256 others(14): Show |
17 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.586+8474dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | ||||||
| chr7:77705510 | G | GTTT | 54 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(51): Show |
54 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.586+8472_586+8474d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | ||||||
| chr7:77705510 | G | GTTTT | 108 | a0001c0001t0002g0039 a0001c0001t0002g0075 a0001c0001t0002g0076 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.586+8471_586+8474d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | ||||||
| chr7:77705510 | G | GTTTTT | 42 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(39): Show |
43 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.586+8470_586+8474d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | ||||||
| chr7:77705510 | G | GTTTTTT | 7 | a0001c0001t0008g0022 a0001c0001t0008g0023 a0001c0001t0008g0024 others(4): Show |
7 | HG02055.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.586+8469_586+8474d others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | ||||||
| chr7:77705510 | G | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+8455G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705510 | |||||||
| chr7:77705736 | T | C | 1 | a0001c0001t0020g0212 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+8681T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705736 | |||||||
| chr7:77705961 | T | C | 1 | a0001c0002t0001g0258 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.586+8906T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705961 | |||||||
| chr7:77706003 | C | T | 1 | a0001c0001t0013g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.586+8948C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706003 | |||||||
| chr7:77706080 | G | GT | 8 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(5): Show |
8 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+9038dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77706080 | ||||||
| chr7:77706356 | C | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.586+9301C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706356 | |||||||
| chr7:77706432 | A | G | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+9377A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706432 | |||||||
| chr7:77706433 | A | G | 58 | a0001c0001t0002g0111 a0001c0001t0004g0001 a0001c0001t0004g0003 others(55): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.586+9378A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706433 | |||||||
| chr7:77706625 | G | T | 1 | a0001c0001t0008g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+9570G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706625 | |||||||
| chr7:77706832 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0140 a0001c0001t0004g0141 others(8): Show |
12 | HG00280.hp2 HG01515.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.586+9777A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706832 | |||||||
| chr7:77707022 | A | AT | 75 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(72): Show |
75 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.586+9986dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77707022 | ||||||
| chr7:77707086 | C | T | 2 | a0001c0001t0007g0085 a0001c0001t0027g0072 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.586+10031C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707086 | |||||||
| chr7:77707216 | G | C | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+10161G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707216 | |||||||
| chr7:77707251 | C | T | 1 | a0001c0001t0004g0004 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.586+10196C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707251 | |||||||
| chr7:77707756 | A | G | 1 | a0001c0001t0034g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.586+10701A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707756 | |||||||
| chr7:77707879 | G | C | 1 | a0005c0012t0012g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.586+10824G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707879 | |||||||
| chr7:77707931 | T | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+10876T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707931 | |||||||
| chr7:77708072 | T | G | 1 | a0001c0002t0001g0238 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.586+11017T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708072 | |||||||
| chr7:77708119 | C | T | 69 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(66): Show |
69 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.586+11064C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708119 | |||||||
| chr7:77708356 | G | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+11301G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708356 | |||||||
| chr7:77708364 | T | G | 1 | a0005c0012t0012g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.586+11309T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708364 | |||||||
| chr7:77708385 | A | AT | 207 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(204): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.586+11345dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77708385 | ||||||
| chr7:77708385 | A | ATT | 8 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0083 others(5): Show |
8 | HG01109.hp1 HG01261.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+11344_586+1134 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77708385 | ||||||
| chr7:77708467 | C | T | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.586+11412C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708467 | |||||||
| chr7:77708512 | G | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+11457G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708512 | |||||||
| chr7:77708530 | C | T | 210 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(207): Show |
211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.586+11475C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708530 | |||||||
| chr7:77708538 | C | T | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.586+11483C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708538 | |||||||
| chr7:77708670 | C | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+11615C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708670 | |||||||
| chr7:77708681 | C | T | 2 | a0001c0001t0009g0134 a0001c0001t0009g0135 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.586+11626C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708681 | |||||||
| chr7:77708865 | A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+11810A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708865 | |||||||
| chr7:77708989 | G | A | 2 | a0001c0001t0002g0083 a0001c0001t0002g0098 |
2 | NA18998.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.586+11934G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708989 | |||||||
| chr7:77709039 | G | A | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+11984G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709039 | |||||||
| chr7:77709152 | TTG | T | 8 | a0001c0002t0001g0240 a0001c0002t0001g0260 a0001c0002t0001g0268 others(5): Show |
8 | HG01071.hp2 HG01074.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+12141_586+1214 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | ||||||
| chr7:77709152 | TTGTG | T | 19 | a0001c0002t0001g0221 a0001c0002t0001g0222 a0001c0002t0001g0227 others(16): Show |
19 | HG01243.hp2 HG01255.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.586+12139_586+1214 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | ||||||
| chr7:77709152 | TTGTGTG | T | 81 | a0001c0002t0001g0002 a0001c0002t0001g0218 a0001c0002t0001g0219 others(78): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.586+12137_586+1214 others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | ||||||
| chr7:77709152 | TTGTGTGT others(1): Show |
T | 5 | a0001c0002t0001g0319 a0001c0002t0001g0330 a0001c0002t0006g0266 others(2): Show |
5 | HG01123.hp2 HG01169.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.586+12135_586+1214 others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | ||||||
| chr7:77709152 | TTGTGTGT others(3): Show |
T | 3 | a0001c0002t0001g0253 a0001c0002t0001g0334 a0001c0002t0006g0254 |
3 | HG02132.hp1 HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.586+12133_586+1214 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | ||||||
| chr7:77709152 | TTGTGTGT others(5): Show |
T | 3 | a0001c0001t0002g0071 a0001c0001t0002g0083 a0001c0001t0002g0098 |
3 | NA18998.hp1 NA19066.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.586+12131_586+1214 others(16): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | ||||||
| chr7:77709170 | G | A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+12115G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709170 | |||||||
| chr7:77709174 | G | A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+12119G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709174 | |||||||
| chr7:77709180 | G | A | 6 | a0001c0001t0012g0158 a0001c0001t0012g0189 a0001c0001t0019g0031 others(3): Show |
6 | HG02559.hp2 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+12125G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709180 | |||||||
| chr7:77709182 | G | A | 8 | a0001c0001t0002g0070 a0001c0001t0002g0086 a0001c0001t0002g0117 others(5): Show |
8 | HG02738.hp2 HG02818.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+12127G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709182 | |||||||
| chr7:77709184 | G | A | 6 | a0001c0001t0008g0022 a0001c0001t0010g0050 a0001c0001t0011g0074 others(3): Show |
6 | HG00642.hp1 HG01884.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+12129G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709184 | |||||||
| chr7:77709186 | G | A | 68 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(65): Show |
68 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.586+12131G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709186 | |||||||
| chr7:77709188 | G | A | 15 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0087 others(12): Show |
15 | HG00280.hp2 HG00642.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.586+12133G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709188 | |||||||
| chr7:77709188 | G | GTA | 38 | a0001c0001t0003g0034 a0001c0001t0003g0151 a0001c0001t0003g0153 others(35): Show |
38 | HG00639.hp2 HG00741.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.586+12134_586+1213 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709188 | ||||||
| chr7:77709188 | GTGTGTGT others(3): Show |
G | 11 | a0001c0001t0002g0070 a0001c0001t0002g0086 a0001c0001t0002g0117 others(8): Show |
11 | HG02559.hp2 HG02738.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.586+12137_586+1214 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709188 | ||||||
| chr7:77709190 | G | A | 93 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(90): Show |
94 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.586+12135G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709190 | |||||||
| chr7:77709190 | G | GTATGTA | 12 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0152 others(9): Show |
12 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.586+12136_586+1213 others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709190 | ||||||
| chr7:77709190 | GTGTGTGT others(1): Show |
G | 3 | a0001c0001t0008g0022 a0001c0001t0010g0050 a0001c0001t0011g0074 |
3 | HG00642.hp1 HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.586+12139_586+1214 others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709190 | ||||||
| chr7:77709192 | G | A | 75 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0087 others(72): Show |
75 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.586+12137G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709192 | |||||||
| chr7:77709192 | GTGTGTA | G | 58 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(55): Show |
58 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.586+12141_586+1214 others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709192 | ||||||
| chr7:77709194 | G | A | 46 | a0001c0001t0002g0088 a0001c0001t0004g0001 a0001c0001t0004g0003 others(43): Show |
47 | HG00280.hp1 HG00323.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.586+12139G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709194 | |||||||
| chr7:77709194 | G | GTA | 4 | a0001c0001t0009g0133 a0001c0001t0022g0040 a0001c0001t0022g0041 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+12140_586+1214 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709194 | ||||||
| chr7:77709194 | GTGTA | G | 8 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0087 others(5): Show |
8 | HG00280.hp2 HG01255.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+12147_586+1215 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709194 | ||||||
| chr7:77709196 | G | A | 39 | a0001c0001t0002g0111 a0001c0001t0003g0035 a0001c0001t0003g0036 others(36): Show |
39 | HG00140.hp1 HG00733.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.586+12141G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709196 | |||||||
| chr7:77709196 | GTA | G | 33 | a0001c0001t0002g0088 a0001c0001t0004g0001 a0001c0001t0004g0003 others(30): Show |
34 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.586+12143_586+1214 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709196 | ||||||
| chr7:77709198 | A | ATG | 57 | a0001c0001t0003g0034 a0001c0001t0003g0151 a0001c0001t0003g0153 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.586+12145_586+1214 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709198 | ||||||
| chr7:77709198 | A | G | 39 | a0001c0001t0002g0111 a0001c0001t0003g0035 a0001c0001t0003g0036 others(36): Show |
39 | HG00140.hp1 HG00733.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.586+12143A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709198 | |||||||
| chr7:77709299 | T | G | 4 | a0001c0001t0004g0011 a0001c0001t0004g0016 a0001c0001t0004g0017 others(1): Show |
4 | HG02071.hp2 NA18612.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+12244T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709299 | |||||||
| chr7:77709324 | G | C | 1 | a0002c0003t0007g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.586+12269G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709324 | |||||||
| chr7:77709447 | G | C | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+12392G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709447 | |||||||
| chr7:77709526 | G | A | 2 | a0001c0001t0018g0128 a0001c0001t0018g0138 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.586+12471G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709526 | |||||||
| chr7:77709679 | C | G | 2 | a0001c0002t0001g0253 a0001c0002t0006g0254 |
2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.586+12624C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709679 | |||||||
| chr7:77709782 | G | C | 4 | a0001c0001t0005g0150 a0001c0001t0012g0158 a0001c0001t0012g0189 others(1): Show |
4 | HG01175.hp2 HG02970.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+12727G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709782 | |||||||
| chr7:77709816 | A | G | 1 | a0001c0002t0001g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.586+12761A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709816 | |||||||
| chr7:77709893 | C | A | 1 | a0001c0001t0034g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.586+12838C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709893 | |||||||
| chr7:77709976 | T | C | 2 | a0001c0001t0005g0193 a0001c0001t0005g0198 |
2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.586+12921T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709976 | |||||||
| chr7:77710456 | C | G | 1 | a0005c0012t0012g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.586+13401C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710456 | |||||||
| chr7:77710528 | A | G | 1 | a0001c0001t0005g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.586+13473A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710528 | |||||||
| chr7:77710592 | T | C | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+13537T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710592 | |||||||
| chr7:77710650 | T | G | 18 | a0001c0001t0002g0111 a0001c0001t0004g0107 a0001c0001t0004g0108 others(15): Show |
18 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.586+13595T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710650 | |||||||
| chr7:77710702 | T | G | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.586+13647T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710702 | |||||||
| chr7:77710758 | G | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+13703G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710758 | |||||||
| chr7:77711081 | A | G | 2 | a0001c0002t0001g0326 a0001c0002t0001g0327 |
2 | NA18972.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.586+14026A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711081 | |||||||
| chr7:77711257 | A | G | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+14202A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711257 | |||||||
| chr7:77711293 | A | G | 1 | a0001c0002t0001g0226 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.586+14238A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711293 | |||||||
| chr7:77711322 | A | AT | 6 | a0001c0001t0004g0017 a0001c0002t0001g0233 a0001c0002t0001g0252 others(3): Show |
6 | HG02071.hp2 HG02698.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+14288dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77711322 | ||||||
| chr7:77711322 | AT | A | 45 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.586+14288delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77711322 | ||||||
| chr7:77711322 | ATT | A | 128 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(125): Show |
128 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.586+14287_586+1428 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77711322 | ||||||
| chr7:77711322 | ATTT | A | 6 | a0001c0001t0002g0093 a0001c0001t0002g0104 a0001c0001t0003g0151 others(3): Show |
6 | HG02004.hp2 HG02572.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+14286_586+1428 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77711322 | ||||||
| chr7:77711346 | C | T | 6 | a0001c0001t0005g0199 a0001c0001t0005g0200 a0001c0001t0005g0201 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+14291C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711346 | |||||||
| chr7:77711424 | C | T | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+14369C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711424 | |||||||
| chr7:77711504 | T | A | 71 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(68): Show |
71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.586+14449T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711504 | |||||||
| chr7:77711544 | T | C | 2 | a0001c0002t0001g0253 a0001c0002t0006g0254 |
2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.586+14489T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711544 | |||||||
| chr7:77711557 | G | T | 2 | a0001c0001t0022g0040 a0001c0001t0022g0041 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.586+14502G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711557 | |||||||
| chr7:77711578 | G | A | 1 | a0001c0001t0003g0175 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.586+14523G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711578 | |||||||
| chr7:77711631 | A | G | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+14576A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711631 | |||||||
| chr7:77711915 | A | C | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+14860A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711915 | |||||||
| chr7:77712058 | GT | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.586+15011delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77712058 | ||||||
| chr7:77712215 | G | GTA | 58 | a0001c0001t0002g0111 a0001c0001t0004g0001 a0001c0001t0004g0003 others(55): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.586+15165_586+1516 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77712215 | ||||||
| chr7:77712278 | A | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+15223A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712278 | |||||||
| chr7:77712287 | A | T | 38 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(35): Show |
39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.586+15232A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712287 | |||||||
| chr7:77712422 | A | T | 58 | a0001c0001t0002g0111 a0001c0001t0004g0001 a0001c0001t0004g0003 others(55): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.586+15367A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712422 | |||||||
| chr7:77712436 | A | G | 1 | a0001c0002t0001g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.586+15381A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712436 | |||||||
| chr7:77712530 | C | T | 1 | a0001c0002t0001g0301 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.586+15475C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712530 | |||||||
| chr7:77712780 | T | TA | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+15726dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77712780 | ||||||
| chr7:77712819 | C | CTT | 322 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(319): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.586+15764_586+1576 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712819 | |||||||
| chr7:77712882 | G | T | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.586+15827G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712882 | |||||||
| chr7:77712971 | A | G | 1 | a0001c0001t0004g0008 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.586+15916A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712971 | |||||||
| chr7:77713254 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+16199A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713254 | |||||||
| chr7:77713268 | T | C | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.586+16213T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713268 | |||||||
| chr7:77713302 | T | C | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.586+16247T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713302 | |||||||
| chr7:77713311 | C | A | 1 | a0001c0002t0001g0310 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.586+16256C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713311 | |||||||
| chr7:77713356 | T | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+16301T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713356 | |||||||
| chr7:77713385 | C | T | 4 | a0001c0004t0005g0194 a0001c0004t0005g0208 a0001c0004t0005g0209 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+16330C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713385 | |||||||
| chr7:77713391 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.586+16336C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713391 | |||||||
| chr7:77713482 | G | A | 1 | a0001c0002t0001g0226 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.586+16427G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713482 | |||||||
| chr7:77713484 | G | A | 1 | a0001c0002t0001g0226 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.586+16429G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713484 | |||||||
| chr7:77713524 | T | G | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+16469T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713524 | |||||||
| chr7:77713546 | C | T | 17 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(14): Show |
17 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.586+16491C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713546 | |||||||
| chr7:77713665 | C | CT | 74 | a0001c0001t0002g0103 a0001c0001t0003g0034 a0001c0001t0003g0035 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.586+16624dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77713665 | ||||||
| chr7:77713679 | T | A | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+16624T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713679 | |||||||
| chr7:77713680 | A | T | 67 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(64): Show |
67 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.586+16625A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713680 | |||||||
| chr7:77713807 | C | G | 1 | a0001c0001t0009g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586+16752C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713807 | |||||||
| chr7:77713885 | A | G | 1 | a0001c0001t0007g0013 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.586+16830A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713885 | |||||||
| chr7:77713951 | A | C | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.586+16896A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713951 | |||||||
| chr7:77714340 | G | A | 1 | a0001c0001t0003g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.586+17285G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714340 | |||||||
| chr7:77714381 | T | C | 16 | a0001c0001t0002g0111 a0001c0001t0004g0107 a0001c0001t0004g0108 others(13): Show |
16 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.586+17326T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714381 | |||||||
| chr7:77714467 | C | T | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+17412C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714467 | |||||||
| chr7:77714581 | A | G | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+17526A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714581 | |||||||
| chr7:77714685 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.586+17630G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714685 | |||||||
| chr7:77714744 | C | T | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.586+17689C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714744 | |||||||
| chr7:77714843 | G | A | 1 | a0001c0001t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586+17788G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714843 | |||||||
| chr7:77714957 | T | C | 4 | a0001c0002t0001g0002 a0001c0002t0001g0283 a0001c0002t0001g0311 others(1): Show |
5 | NA18747.hp2 NA18946.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+17902T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714957 | |||||||
| chr7:77714958 | C | CA | 7 | a0001c0002t0001g0228 a0001c0002t0001g0253 a0001c0002t0001g0301 others(4): Show |
7 | HG01981.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.586+17924dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77714958 | ||||||
| chr7:77714958 | CA | C | 203 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(200): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.586+17924delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77714958 | ||||||
| chr7:77714958 | CAA | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+17923_586+1792 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77714958 | ||||||
| chr7:77714975 | A | G | 2 | a0001c0002t0001g0300 a0001c0002t0001g0320 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.586+17920A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714975 | |||||||
| chr7:77715117 | C | A | 1 | a0004c0010t0028g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+18062C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715117 | |||||||
| chr7:77715139 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.586+18084G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715139 | |||||||
| chr7:77715267 | C | T | 2 | a0001c0001t0009g0132 a0001c0001t0009g0144 |
2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.586+18212C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715267 | |||||||
| chr7:77715330 | AGTGGGAT others(21): Show |
A | 1 | a0001c0002t0001g0326 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.586+18276_586+1830 others(32): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715330 | |||||||
| chr7:77715425 | C | T | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+18370C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715425 | |||||||
| chr7:77715462 | A | G | 3 | a0001c0002t0001g0282 a0001c0002t0001g0299 a0001c0002t0001g0328 |
3 | HG01496.hp1 HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.586+18407A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715462 | |||||||
| chr7:77715465 | C | T | 3 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0080 |
3 | NA19056.hp2 NA19079.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.586+18410C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715465 | |||||||
| chr7:77715977 | A | G | 71 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(68): Show |
71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.586+18922A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715977 | |||||||
| chr7:77715991 | ACTC | A | 6 | a0001c0001t0005g0197 a0001c0001t0005g0214 a0001c0004t0005g0194 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+18939_586+1894 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77715991 | ||||||
| chr7:77716018 | A | G | 1 | a0001c0001t0005g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.586+18963A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716018 | |||||||
| chr7:77716260 | C | T | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.586+19205C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716260 | |||||||
| chr7:77716456 | C | CT | 208 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(205): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.586+19414dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77716456 | ||||||
| chr7:77716469 | T | C | 1 | a0001c0002t0041g0239 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.586+19414T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716469 | |||||||
| chr7:77716610 | A | G | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+19555A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716610 | |||||||
| chr7:77716618 | C | G | 1 | a0004c0010t0028g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+19563C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716618 | |||||||
| chr7:77716624 | C | CT | 58 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0053 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.586+19595dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77716624 | ||||||
| chr7:77716624 | C | CTT | 18 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(15): Show |
18 | HG01943.hp1 HG01952.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.586+19594_586+1959 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77716624 | ||||||
| chr7:77716624 | CT | C | 64 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(61): Show |
64 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.586+19595delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77716624 | ||||||
| chr7:77716650 | T | TTA | 6 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0099 others(3): Show |
6 | NA18978.hp1 NA18981.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+19595_586+1959 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716650 | |||||||
| chr7:77716654 | C | T | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.586+19599C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716654 | |||||||
| chr7:77716717 | C | T | 4 | a0001c0001t0005g0150 a0001c0001t0012g0158 a0001c0001t0012g0189 others(1): Show |
4 | HG01175.hp2 HG02970.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+19662C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716717 | |||||||
| chr7:77716763 | C | G | 1 | a0001c0001t0011g0074 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.587-19647C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716763 | |||||||
| chr7:77716777 | G | A | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.587-19633G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716777 | |||||||
| chr7:77716780 | C | T | 38 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(35): Show |
39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.587-19630C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716780 | |||||||
| chr7:77716781 | A | G | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-19629A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716781 | |||||||
| chr7:77716783 | C | T | 4 | a0001c0001t0005g0199 a0001c0001t0005g0200 a0001c0001t0005g0201 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-19627C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716783 | |||||||
| chr7:77717152 | T | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-19258T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717152 | |||||||
| chr7:77717177 | A | G | 1 | a0001c0001t0034g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.587-19233A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717177 | |||||||
| chr7:77717431 | T | C | 2 | a0001c0001t0004g0130 a0001c0001t0014g0129 |
2 | HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.587-18979T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717431 | |||||||
| chr7:77717477 | T | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-18933T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717477 | |||||||
| chr7:77717552 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.587-18858G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717552 | |||||||
| chr7:77717669 | A | G | 12 | a0001c0002t0001g0221 a0001c0002t0001g0223 a0001c0002t0001g0224 others(9): Show |
12 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-18741A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717669 | |||||||
| chr7:77717828 | G | A | 1 | a0001c0005t0040g0259 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.587-18582G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717828 | |||||||
| chr7:77717864 | T | A | 5 | a0001c0001t0002g0053 a0001c0001t0002g0060 a0001c0001t0002g0065 others(2): Show |
5 | HG00438.hp1 HG02071.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-18546T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717864 | |||||||
| chr7:77717992 | C | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-18418C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717992 | |||||||
| chr7:77718256 | C | A | 1 | a0001c0001t0002g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-18154C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718256 | |||||||
| chr7:77718278 | C | A | 2 | a0001c0001t0022g0040 a0001c0001t0022g0041 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.587-18132C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718278 | |||||||
| chr7:77718380 | T | G | 58 | a0001c0001t0002g0111 a0001c0001t0004g0001 a0001c0001t0004g0003 others(55): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.587-18030T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718380 | |||||||
| chr7:77718846 | T | C | 1 | a0001c0001t0005g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.587-17564T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718846 | |||||||
| chr7:77718993 | G | A | 1 | a0001c0002t0001g0231 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.587-17417G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718993 | |||||||
| chr7:77718999 | T | C | 2 | a0001c0001t0013g0122 a0001c0001t0013g0124 |
2 | HG00639.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.587-17411T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718999 | |||||||
| chr7:77719129 | A | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-17281A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719129 | |||||||
| chr7:77719285 | TTTAA | T | 3 | a0001c0002t0001g0230 a0001c0002t0001g0272 a0001c0002t0001g0284 |
3 | HG02735.hp1 NA18945.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.587-17122_587-1711 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77719285 | ||||||
| chr7:77719448 | G | A | 1 | a0001c0002t0001g0301 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.587-16962G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719448 | |||||||
| chr7:77719582 | A | G | 3 | a0001c0002t0001g0298 a0001c0002t0001g0304 a0001c0002t0001g0318 |
3 | NA18995.hp1 NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.587-16828A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719582 | |||||||
| chr7:77719911 | C | T | 1 | a0001c0002t0001g0273 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.587-16499C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719911 | |||||||
| chr7:77719920 | G | A | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-16490G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719920 | |||||||
| chr7:77720073 | C | T | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-16337C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720073 | |||||||
| chr7:77720392 | G | A | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.587-16018G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720392 | |||||||
| chr7:77720484 | G | A | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.587-15926G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720484 | |||||||
| chr7:77720499 | C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-15911C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720499 | |||||||
| chr7:77720520 | T | C | 1 | a0001c0001t0005g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.587-15890T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720520 | |||||||
| chr7:77720619 | C | G | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.587-15791C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720619 | |||||||
| chr7:77720630 | A | G | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.587-15780A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720630 | |||||||
| chr7:77720763 | C | CT | 13 | a0001c0001t0003g0152 a0001c0001t0005g0197 a0001c0001t0005g0213 others(10): Show |
13 | HG02717.hp1 HG02818.hp2 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.587-15627dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77720763 | ||||||
| chr7:77720763 | CT | C | 123 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0053 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.587-15627delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77720763 | ||||||
| chr7:77720763 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.587-15636_587-1562 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77720763 | ||||||
| chr7:77720772 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.587-15638T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720772 | |||||||
| chr7:77720881 | T | C | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-15529T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720881 | |||||||
| chr7:77721009 | TG | T | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-15398delG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77721009 | ||||||
| chr7:77721021 | G | A | 1 | a0001c0002t0001g0325 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.587-15389G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721021 | |||||||
| chr7:77721032 | G | A | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.587-15378G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721032 | |||||||
| chr7:77721045 | T | G | 1 | a0001c0001t0034g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.587-15365T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721045 | |||||||
| chr7:77721086 | G | A | 1 | a0001c0002t0001g0301 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.587-15324G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721086 | |||||||
| chr7:77721148 | G | T | 71 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(68): Show |
71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.587-15262G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721148 | |||||||
| chr7:77721226 | G | GT | 30 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(27): Show |
30 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.587-15172dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77721226 | ||||||
| chr7:77721238 | T | C | 1 | a0001c0002t0001g0226 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.587-15172T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721238 | |||||||
| chr7:77721276 | A | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-15134A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721276 | |||||||
| chr7:77721283 | A | G | 2 | a0001c0001t0003g0192 a0001c0001t0034g0173 |
2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.587-15127A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721283 | |||||||
| chr7:77721508 | T | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-14902T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721508 | |||||||
| chr7:77721516 | C | T | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-14894C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721516 | |||||||
| chr7:77721729 | A | G | 1 | a0001c0002t0036g0275 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587-14681A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721729 | |||||||
| chr7:77721767 | A | C | 58 | a0001c0001t0002g0111 a0001c0001t0004g0001 a0001c0001t0004g0003 others(55): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.587-14643A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721767 | |||||||
| chr7:77721767 | A | G | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-14643A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721767 | |||||||
| chr7:77721925 | C | T | 1 | a0001c0002t0001g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-14485C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721925 | |||||||
| chr7:77721971 | A | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-14439A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721971 | |||||||
| chr7:77722023 | C | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-14387C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722023 | |||||||
| chr7:77722147 | C | T | 3 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0014 |
3 | HG00735.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.587-14263C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722147 | |||||||
| chr7:77722232 | T | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-14178T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722232 | |||||||
| chr7:77722326 | G | T | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-14084G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722326 | |||||||
| chr7:77722388 | G | T | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-14022G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722388 | |||||||
| chr7:77722410 | T | C | 1 | a0001c0001t0009g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.587-14000T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722410 | |||||||
| chr7:77722440 | A | T | 1 | a0001c0002t0001g0326 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.587-13970A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722440 | |||||||
| chr7:77722474 | C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-13936C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722474 | |||||||
| chr7:77722600 | C | T | 1 | a0001c0002t0001g0272 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.587-13810C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722600 | |||||||
| chr7:77722624 | T | A | 1 | a0001c0002t0001g0326 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.587-13786T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722624 | |||||||
| chr7:77722968 | C | CT | 121 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
122 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.587-13425dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77722968 | ||||||
| chr7:77722968 | CT | C | 88 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(85): Show |
88 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.587-13425delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77722968 | ||||||
| chr7:77722998 | C | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-13412C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722998 | |||||||
| chr7:77723037 | G | A | 1 | a0001c0002t0001g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-13373G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723037 | |||||||
| chr7:77723071 | G | T | 5 | a0001c0002t0001g0271 a0001c0002t0001g0276 a0001c0002t0001g0278 others(2): Show |
5 | HG03491.hp1 HG04115.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-13339G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723071 | |||||||
| chr7:77723112 | A | G | 38 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(35): Show |
39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.587-13298A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723112 | |||||||
| chr7:77723216 | T | G | 6 | a0001c0001t0011g0055 a0001c0001t0011g0057 a0001c0001t0011g0074 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-13194T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723216 | |||||||
| chr7:77723310 | A | G | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.587-13100A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723310 | |||||||
| chr7:77723383 | A | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-13027A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723383 | |||||||
| chr7:77723384 | G | A | 5 | a0001c0001t0003g0152 a0001c0001t0003g0162 a0001c0001t0003g0163 others(2): Show |
5 | NA18943.hp1 NA18954.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-13026G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723384 | |||||||
| chr7:77723407 | A | G | 1 | a0001c0002t0006g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.587-13003A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723407 | |||||||
| chr7:77723502 | C | T | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.587-12908C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723502 | |||||||
| chr7:77723846 | A | G | 1 | a0001c0001t0003g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.587-12564A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723846 | |||||||
| chr7:77723921 | T | C | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.587-12489T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723921 | |||||||
| chr7:77723944 | A | T | 1 | a0001c0002t0001g0224 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.587-12466A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723944 | |||||||
| chr7:77723944 | AT | A | 213 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(210): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.587-12453delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77723944 | ||||||
| chr7:77723946 | T | A | 53 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(50): Show |
54 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.587-12464T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723946 | |||||||
| chr7:77723976 | CTGTGTTG others(14): Show |
C | 1 | a0001c0002t0001g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-12433_587-1241 others(25): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723976 | |||||||
| chr7:77724113 | C | T | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-12297C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724113 | |||||||
| chr7:77724216 | A | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-12194A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724216 | |||||||
| chr7:77724287 | CCTT | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-12120_587-1211 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77724287 | ||||||
| chr7:77724476 | A | C | 1 | a0001c0002t0001g0285 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.587-11934A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724476 | |||||||
| chr7:77724592 | A | C | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-11818A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724592 | |||||||
| chr7:77724711 | C | G | 1 | a0001c0002t0001g0326 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.587-11699C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724711 | |||||||
| chr7:77724711 | C | T | 210 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(207): Show |
211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.587-11699C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724711 | |||||||
| chr7:77724865 | G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-11545G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724865 | |||||||
| chr7:77725243 | A | AATTTTTT others(22): Show |
2 | a0001c0001t0005g0200 a0005c0012t0012g0207 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.587-11167_587-1116 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725243 | |||||||
| chr7:77725243 | A | AATTTTTT others(24): Show |
2 | a0001c0001t0005g0201 a0001c0001t0005g0202 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.587-11167_587-1116 others(35): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725243 | |||||||
| chr7:77725243 | A | AATTTTTT others(26): Show |
1 | a0001c0001t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.587-11167_587-1116 others(37): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725243 | |||||||
| chr7:77725244 | C | CT | 33 | a0001c0001t0002g0111 a0001c0001t0004g0107 a0001c0001t0004g0108 others(30): Show |
33 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.587-11145dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTT | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-11146_587-1114 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(3): Show |
14 | a0001c0001t0003g0151 a0001c0001t0003g0156 a0001c0001t0003g0157 others(11): Show |
14 | HG02074.hp1 HG02647.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.587-11154_587-1114 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0003g0167 a0001c0001t0003g0183 a0001c0001t0020g0212 others(2): Show |
5 | HG02129.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-11155_587-1114 others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(5): Show |
19 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(16): Show |
19 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.587-11156_587-1114 others(16): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(6): Show |
26 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(23): Show |
26 | HG00639.hp1 HG01074.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.587-11157_587-1114 others(17): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(7): Show |
28 | a0001c0001t0002g0058 a0001c0001t0002g0061 a0001c0001t0002g0062 others(25): Show |
28 | HG00438.hp1 HG01167.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.587-11158_587-1114 others(18): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(8): Show |
20 | a0001c0001t0002g0059 a0001c0001t0002g0077 a0001c0001t0002g0090 others(17): Show |
21 | HG00280.hp2 HG00423.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.587-11159_587-1114 others(19): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(9): Show |
12 | a0001c0001t0002g0096 a0001c0001t0003g0187 a0001c0001t0004g0003 others(9): Show |
12 | HG00735.hp2 HG01123.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.587-11160_587-1114 others(20): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(10): Show |
8 | a0001c0001t0002g0101 a0001c0001t0004g0004 a0001c0001t0004g0012 others(5): Show |
8 | HG02071.hp2 HG02080.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-11161_587-1114 others(21): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0004g0011 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.587-11162_587-1114 others(22): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0080 others(1): Show |
4 | NA19043.hp2 NA19056.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-11163_587-1114 others(23): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0004g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.587-11164_587-1114 others(24): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0005g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(27): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0005g0195 a0001c0001t0005g0205 a0001c0001t0005g0211 |
3 | HG01433.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.587-11145_587-1114 others(28): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(18): Show |
3 | a0001c0001t0003g0162 a0001c0001t0003g0170 a0001c0001t0003g0185 |
3 | HG02559.hp1 NA18747.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.587-11145_587-1114 others(29): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(19): Show |
5 | a0001c0001t0003g0163 a0001c0001t0003g0186 a0001c0001t0004g0147 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-11145_587-1114 others(30): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(20): Show |
4 | a0001c0001t0003g0175 a0001c0001t0034g0173 a0001c0004t0005g0194 others(1): Show |
4 | HG01192.hp2 HG02293.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-11145_587-1114 others(31): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(21): Show |
3 | a0001c0001t0003g0034 a0001c0001t0003g0174 a0001c0009t0003g0179 |
3 | HG02615.hp1 NA19066.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.587-11145_587-1114 others(32): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0005g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.587-11145_587-1114 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(34): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(24): Show |
5 | a0001c0001t0003g0036 a0001c0001t0003g0171 a0001c0001t0003g0176 others(2): Show |
5 | HG03492.hp1 HG03710.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-11145_587-1114 others(35): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0003g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(36): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0003g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(37): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(28): Show |
2 | a0001c0001t0003g0155 a0001c0001t0005g0206 |
2 | HG03540.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.587-11145_587-1114 others(39): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | CTTTTTTT others(32): Show |
1 | a0001c0001t0005g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(43): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725244 | C | T | 6 | a0001c0001t0005g0199 a0001c0001t0005g0200 a0001c0001t0005g0201 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-11166C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725244 | |||||||
| chr7:77725244 | CT | C | 11 | a0001c0001t0003g0164 a0001c0001t0005g0193 a0001c0001t0005g0198 others(8): Show |
11 | HG00639.hp2 HG01099.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.587-11145delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | ||||||
| chr7:77725381 | T | TG | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-11027dupG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725381 | ||||||
| chr7:77725397 | G | A | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-11013G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725397 | |||||||
| chr7:77725398 | C | T | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-11012C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725398 | |||||||
| chr7:77725409 | G | A | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-11001G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725409 | |||||||
| chr7:77725414 | A | ATTTTGTA others(51): Show |
214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-10980_587-1097 others(62): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725414 | ||||||
| chr7:77725543 | G | A | 2 | a0001c0001t0003g0165 a0001c0001t0003g0177 |
2 | NA18975.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.587-10867G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725543 | |||||||
| chr7:77725583 | T | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10827T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725583 | |||||||
| chr7:77725833 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.587-10577G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725833 | |||||||
| chr7:77725947 | G | T | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-10463G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725947 | |||||||
| chr7:77725948 | C | T | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-10462C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725948 | |||||||
| chr7:77726002 | A | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10408A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726002 | |||||||
| chr7:77726040 | A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-10370A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726040 | |||||||
| chr7:77726087 | T | C | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-10323T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726087 | |||||||
| chr7:77726282 | G | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10128G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726282 | |||||||
| chr7:77726303 | A | G | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.587-10107A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726303 | |||||||
| chr7:77726361 | T | C | 2 | a0001c0001t0005g0193 a0001c0001t0005g0198 |
2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.587-10049T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726361 | |||||||
| chr7:77726388 | T | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10022T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726388 | |||||||
| chr7:77726466 | G | A | 1 | a0001c0002t0001g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.587-9944G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726466 | |||||||
| chr7:77726547 | A | G | 4 | a0002c0003t0004g0043 a0002c0003t0004g0044 a0002c0003t0004g0046 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-9863A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726547 | |||||||
| chr7:77726776 | A | AT | 148 | a0001c0001t0002g0099 a0001c0001t0002g0111 a0001c0001t0003g0034 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.587-9613dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77726776 | ||||||
| chr7:77726776 | A | ATT | 71 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(68): Show |
71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.587-9614_587-9613d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77726776 | ||||||
| chr7:77726776 | A | ATTT | 6 | a0001c0001t0002g0096 a0001c0001t0002g0098 a0001c0001t0002g0103 others(3): Show |
6 | HG01884.hp2 HG02738.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-9615_587-9613d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77726776 | ||||||
| chr7:77726776 | ATT | A | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-9614_587-9613d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77726776 | ||||||
| chr7:77726872 | C | T | 2 | a0001c0001t0004g0146 a0001c0001t0004g0147 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.587-9538C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726872 | |||||||
| chr7:77727000 | C | T | 3 | a0001c0002t0001g0227 a0001c0002t0001g0296 a0001c0002t0001g0323 |
3 | NA18983.hp1 NA19009.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.587-9410C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727000 | |||||||
| chr7:77727002 | C | T | 16 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(13): Show |
16 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.587-9408C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727002 | |||||||
| chr7:77727033 | G | T | 3 | a0001c0001t0004g0131 a0001c0001t0004g0137 a0001c0001t0004g0139 |
3 | HG02615.hp2 HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.587-9377G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727033 | |||||||
| chr7:77727089 | C | CT | 60 | a0001c0001t0002g0111 a0001c0001t0003g0186 a0001c0001t0004g0001 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.587-9306dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77727089 | ||||||
| chr7:77727245 | G | A | 1 | a0001c0001t0034g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.587-9165G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727245 | |||||||
| chr7:77727276 | G | A | 6 | a0001c0002t0001g0224 a0001c0002t0001g0247 a0001c0002t0001g0256 others(3): Show |
6 | HG01358.hp1 HG01516.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-9134G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727276 | |||||||
| chr7:77727379 | G | A | 1 | a0001c0001t0003g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.587-9031G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727379 | |||||||
| chr7:77727442 | T | A | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-8968T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727442 | |||||||
| chr7:77727600 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.587-8810C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727600 | |||||||
| chr7:77727625 | A | AT | 11 | a0001c0001t0007g0049 a0001c0001t0007g0073 a0001c0001t0008g0020 others(8): Show |
11 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.587-8769dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77727625 | ||||||
| chr7:77727626 | T | A | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.587-8784T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727626 | |||||||
| chr7:77727643 | C | T | 1 | a0001c0002t0001g0231 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.587-8767C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727643 | |||||||
| chr7:77727716 | T | A | 1 | a0001c0001t0003g0188 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.587-8694T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727716 | |||||||
| chr7:77727729 | G | A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-8681G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727729 | |||||||
| chr7:77727752 | C | T | 2 | a0001c0001t0018g0128 a0001c0001t0018g0138 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.587-8658C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727752 | |||||||
| chr7:77727957 | C | T | 71 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(68): Show |
71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.587-8453C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727957 | |||||||
| chr7:77728052 | C | T | 1 | a0007c0011t0012g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.587-8358C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728052 | |||||||
| chr7:77728074 | A | G | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.587-8336A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728074 | |||||||
| chr7:77728246 | T | A | 67 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(64): Show |
67 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.587-8164T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728246 | |||||||
| chr7:77728355 | T | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-8055T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728355 | |||||||
| chr7:77728431 | A | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-7979A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728431 | |||||||
| chr7:77728546 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.587-7864C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728546 | |||||||
| chr7:77728715 | A | T | 4 | a0001c0002t0001g0282 a0001c0002t0001g0299 a0001c0002t0001g0328 others(1): Show |
4 | HG01496.hp1 HG01952.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-7695A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728715 | |||||||
| chr7:77728755 | A | G | 71 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(68): Show |
71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.587-7655A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728755 | |||||||
| chr7:77728784 | T | C | 1 | a0001c0001t0007g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.587-7626T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728784 | |||||||
| chr7:77728830 | C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-7580C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728830 | |||||||
| chr7:77728959 | G | A | 1 | a0001c0002t0001g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.587-7451G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728959 | |||||||
| chr7:77729168 | A | T | 1 | a0001c0001t0004g0001 | 2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.587-7242A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77729168 | |||||||
| chr7:77729489 | G | C | 1 | a0001c0001t0013g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.587-6921G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77729489 | |||||||
| chr7:77729666 | T | C | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.587-6744T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77729666 | |||||||
| chr7:77729766 | C | T | 1 | a0001c0001t0029g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.587-6644C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77729766 | |||||||
| chr7:77730080 | T | A | 1 | a0002c0003t0004g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.587-6330T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77730080 | |||||||
| chr7:77730089 | G | C | 1 | a0005c0012t0012g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.587-6321G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77730089 | |||||||
| chr7:77730228 | C | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-6182C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77730228 | |||||||
| chr7:77730526 | T | TAAAAATC others(349): Show |
1 | a0001c0002t0001g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-5870_587-5869i others(358): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77730526 | ||||||
| chr7:77730620 | T | C | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.587-5790T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77730620 | |||||||
| chr7:77731014 | G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-5396G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731014 | |||||||
| chr7:77731092 | A | G | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.587-5318A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731092 | |||||||
| chr7:77731116 | T | G | 1 | a0001c0002t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.587-5294T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731116 | |||||||
| chr7:77731290 | T | G | 1 | a0001c0001t0003g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.587-5120T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731290 | |||||||
| chr7:77731306 | T | C | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-5104T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731306 | |||||||
| chr7:77731410 | A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-5000A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731410 | |||||||
| chr7:77731423 | A | G | 1 | a0001c0002t0001g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.587-4987A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731423 | |||||||
| chr7:77731534 | C | T | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.587-4876C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731534 | |||||||
| chr7:77731568 | T | C | 1 | a0001c0002t0006g0264 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.587-4842T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731568 | |||||||
| chr7:77731584 | A | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-4826A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731584 | |||||||
| chr7:77731772 | T | A | 1 | a0001c0001t0002g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.587-4638T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731772 | |||||||
| chr7:77731826 | C | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0214 |
2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.587-4584C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731826 | |||||||
| chr7:77731983 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.587-4427G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731983 | |||||||
| chr7:77732189 | T | A | 1 | a0001c0001t0002g0063 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.587-4221T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732189 | |||||||
| chr7:77732210 | A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-4200A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732210 | |||||||
| chr7:77732629 | C | G | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.587-3781C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732629 | |||||||
| chr7:77732675 | T | C | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587-3735T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732675 | |||||||
| chr7:77732763 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-3647A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732763 | |||||||
| chr7:77732955 | T | C | 1 | a0001c0001t0019g0032 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.587-3455T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732955 | |||||||
| chr7:77733091 | C | T | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.587-3319C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733091 | |||||||
| chr7:77733172 | G | C | 75 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(72): Show |
75 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.587-3238G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733172 | |||||||
| chr7:77733187 | A | G | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.587-3223A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733187 | |||||||
| chr7:77733368 | C | T | 1 | a0001c0001t0011g0074 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.587-3042C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733368 | |||||||
| chr7:77733376 | A | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-3034A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733376 | |||||||
| chr7:77733430 | C | T | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-2980C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733430 | |||||||
| chr7:77733812 | G | A | 211 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(208): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.587-2598G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733812 | |||||||
| chr7:77734140 | A | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-2270A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77734140 | |||||||
| chr7:77734570 | C | T | 6 | a0001c0001t0003g0152 a0001c0001t0003g0180 a0001c0002t0017g0235 others(3): Show |
6 | HG00099.hp2 HG01109.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-1840C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77734570 | |||||||
| chr7:77734654 | A | C | 1 | a0001c0002t0001g0329 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.587-1756A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77734654 | |||||||
| chr7:77734916 | T | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-1494T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77734916 | |||||||
| chr7:77735054 | G | GA | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-1345dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77735054 | ||||||
| chr7:77735065 | A | C | 3 | a0001c0002t0001g0238 a0001c0002t0001g0251 a0001c0002t0001g0277 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.587-1345A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735065 | |||||||
| chr7:77735068 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-1342A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735068 | |||||||
| chr7:77735211 | T | C | 1 | a0001c0002t0001g0253 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.587-1199T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735211 | |||||||
| chr7:77735219 | A | C | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-1191A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735219 | |||||||
| chr7:77735709 | A | G | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.587-701A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735709 | |||||||
| chr7:77735762 | T | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-648T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735762 | |||||||
| chr7:77735779 | TG | T | 3 | a0001c0002t0001g0238 a0001c0002t0001g0251 a0001c0002t0001g0277 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.587-630delG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735779 | |||||||
| chr7:77735917 | T | A | 38 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(35): Show |
39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.587-493T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735917 | |||||||
| chr7:77735974 | T | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-436T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735974 | |||||||
| chr7:77736048 | T | C | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.587-362T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77736048 | |||||||
| chr7:77736095 | C | A | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.587-315C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77736095 | |||||||
| chr7:77736165 | C | T | 1 | a0001c0002t0001g0252 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.587-245C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77736165 | |||||||
| chr7:77736213 | A | G | 1 | a0001c0002t0001g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-197A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77736213 | |||||||
| chr7:77736585 | G | A | 3 | a0001c0004t0005g0194 a0001c0004t0005g0208 a0001c0004t0005g0209 |
3 | HG01070.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.703+59G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736585 | |||||||
| chr7:77736664 | A | G | 1 | a0001c0002t0001g0279 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.703+138A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736664 | |||||||
| chr7:77736740 | G | C | 5 | a0001c0002t0001g0219 a0001c0002t0001g0231 a0001c0002t0001g0232 others(2): Show |
5 | HG00423.hp1 NA19054.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+214G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736740 | |||||||
| chr7:77736751 | G | A | 38 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(35): Show |
39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.703+225G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736751 | |||||||
| chr7:77736828 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+302A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736828 | |||||||
| chr7:77736860 | A | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.703+334A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736860 | |||||||
| chr7:77736941 | T | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+415T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736941 | |||||||
| chr7:77736983 | C | T | 1 | a0001c0002t0001g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.703+457C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736983 | |||||||
| chr7:77736994 | T | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+468T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736994 | |||||||
| chr7:77737034 | T | G | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.703+508T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737034 | |||||||
| chr7:77737558 | G | T | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+1032G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737558 | |||||||
| chr7:77737671 | G | A | 1 | a0001c0002t0017g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703+1145G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737671 | |||||||
| chr7:77737782 | G | T | 2 | a0001c0001t0007g0049 a0001c0001t0007g0073 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.703+1256G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737782 | |||||||
| chr7:77737830 | C | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+1304C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737830 | |||||||
| chr7:77737835 | C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+1309C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737835 | |||||||
| chr7:77737851 | C | T | 2 | a0001c0001t0005g0193 a0001c0001t0005g0198 |
2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.703+1325C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737851 | |||||||
| chr7:77737947 | G | A | 1 | a0001c0001t0008g0022 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.703+1421G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737947 | |||||||
| chr7:77738041 | G | T | 1 | a0001c0001t0014g0094 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.703+1515G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738041 | |||||||
| chr7:77738089 | A | AT | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+1572dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77738089 | ||||||
| chr7:77738098 | T | C | 1 | a0001c0002t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.703+1572T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738098 | |||||||
| chr7:77738212 | T | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+1686T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738212 | |||||||
| chr7:77738316 | A | T | 2 | a0001c0001t0005g0193 a0001c0001t0005g0198 |
2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.703+1790A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738316 | |||||||
| chr7:77738351 | A | G | 2 | a0001c0001t0022g0040 a0001c0001t0022g0041 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.703+1825A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738351 | |||||||
| chr7:77738728 | A | C | 1 | a0001c0002t0001g0276 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.703+2202A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738728 | |||||||
| chr7:77738763 | G | C | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.703+2237G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738763 | |||||||
| chr7:77738811 | T | A | 1 | a0001c0002t0001g0289 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.703+2285T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738811 | |||||||
| chr7:77738853 | C | T | 72 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(69): Show |
72 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.703+2327C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738853 | |||||||
| chr7:77738867 | A | G | 1 | a0001c0001t0005g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703+2341A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738867 | |||||||
| chr7:77739066 | A | G | 2 | a0001c0001t0019g0031 a0001c0001t0019g0032 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.703+2540A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739066 | |||||||
| chr7:77739100 | A | G | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703+2574A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739100 | |||||||
| chr7:77739533 | T | G | 1 | a0001c0001t0011g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703+3007T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739533 | |||||||
| chr7:77739574 | G | A | 2 | a0001c0001t0019g0031 a0001c0001t0019g0032 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.703+3048G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739574 | |||||||
| chr7:77739711 | G | GA | 67 | a0001c0001t0002g0053 a0001c0001t0002g0059 a0001c0001t0002g0065 others(64): Show |
67 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.703+3207dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | ||||||
| chr7:77739711 | G | GAA | 9 | a0001c0001t0002g0096 a0001c0001t0033g0149 a0001c0002t0001g0221 others(6): Show |
9 | HG00642.hp2 HG01123.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3206_703+3207d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | ||||||
| chr7:77739711 | GA | G | 91 | a0001c0001t0002g0086 a0001c0001t0003g0034 a0001c0001t0003g0035 others(88): Show |
92 | HG00280.hp2 HG00639.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.703+3207delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | ||||||
| chr7:77739711 | GAA | G | 8 | a0001c0001t0009g0134 a0001c0001t0009g0135 a0001c0001t0015g0028 others(5): Show |
8 | HG00140.hp1 HG01256.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+3206_703+3207d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | ||||||
| chr7:77739711 | GAAAAAA | G | 15 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(12): Show |
15 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.703+3202_703+3207d others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | ||||||
| chr7:77739739 | C | CT | 58 | a0001c0001t0005g0172 a0001c0001t0005g0204 a0001c0001t0005g0206 others(55): Show |
59 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.703+3242dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTT | 52 | a0001c0001t0005g0195 a0001c0001t0005g0197 a0001c0001t0005g0198 others(49): Show |
52 | HG00438.hp2 HG00738.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.703+3241_703+3242d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTT | 16 | a0001c0001t0005g0150 a0001c0001t0005g0193 a0001c0001t0005g0199 others(13): Show |
16 | HG00140.hp2 HG00423.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.703+3240_703+3242d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTTT | 12 | a0001c0001t0003g0035 a0001c0001t0003g0164 a0001c0001t0003g0168 others(9): Show |
12 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.703+3239_703+3242d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTTTT | 19 | a0001c0001t0003g0036 a0001c0001t0003g0152 a0001c0001t0003g0154 others(16): Show |
19 | HG00733.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.703+3238_703+3242d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTTTTT | 16 | a0001c0001t0003g0034 a0001c0001t0003g0163 a0001c0001t0003g0175 others(13): Show |
16 | HG00735.hp2 HG01884.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+3237_703+3242d others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTTTTTT | 8 | a0001c0001t0003g0155 a0001c0001t0004g0011 a0001c0001t0004g0019 others(5): Show |
8 | HG02647.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+3236_703+3242d others(9): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTTTTTT others(1): Show |
9 | a0001c0001t0003g0153 a0001c0001t0003g0156 a0001c0001t0003g0178 others(6): Show |
9 | HG01256.hp2 HG01258.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3235_703+3242d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0003g0151 a0001c0001t0003g0157 a0001c0001t0003g0160 others(6): Show |
9 | HG02055.hp1 HG02074.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3234_703+3242d others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0003g0166 a0001c0001t0004g0001 a0001c0001t0004g0140 others(2): Show |
6 | HG00280.hp2 HG01515.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+3233_703+3242d others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0004g0141 a0001c0001t0025g0113 a0001c0001t0026g0114 |
3 | HG01109.hp1 HG01517.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.703+3232_703+3242d others(13): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0188 a0001c0001t0018g0138 |
2 | HG02145.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.703+3231_703+3242d others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | CTTTTTTT | C | 12 | a0001c0001t0002g0039 a0001c0001t0002g0065 a0001c0001t0002g0075 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.703+3236_703+3242d others(9): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | CTTTTTTT others(1): Show |
C | 66 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(63): Show |
66 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.703+3235_703+3242d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739739 | CTTTTTTT others(4): Show |
C | 16 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(13): Show |
16 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+3232_703+3242d others(13): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | ||||||
| chr7:77739813 | G | A | 1 | a0001c0001t0002g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.703+3287G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739813 | |||||||
| chr7:77739849 | A | G | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.703+3323A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739849 | |||||||
| chr7:77739894 | C | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+3368C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739894 | |||||||
| chr7:77739899 | G | A | 1 | a0001c0001t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703+3373G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739899 | |||||||
| chr7:77740003 | C | T | 1 | a0001c0001t0007g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.703+3477C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740003 | |||||||
| chr7:77740004 | G | A | 6 | a0001c0001t0005g0195 a0001c0001t0005g0203 a0001c0001t0005g0204 others(3): Show |
6 | HG01433.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+3478G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740004 | |||||||
| chr7:77740119 | C | A | 67 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(64): Show |
67 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.703+3593C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740119 | |||||||
| chr7:77740237 | A | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+3711A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740237 | |||||||
| chr7:77740320 | CAT | C | 4 | a0001c0001t0004g0001 a0001c0001t0004g0140 a0001c0001t0004g0141 others(1): Show |
5 | HG00280.hp2 HG01515.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+3795_703+3796d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740320 | |||||||
| chr7:77740353 | A | G | 4 | a0001c0001t0005g0199 a0001c0001t0005g0200 a0001c0001t0005g0201 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+3827A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740353 | |||||||
| chr7:77740454 | C | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+3928C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740454 | |||||||
| chr7:77740662 | A | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+4136A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740662 | |||||||
| chr7:77740666 | G | A | 73 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(70): Show |
73 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.703+4140G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740666 | |||||||
| chr7:77740777 | G | A | 1 | a0001c0002t0001g0288 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.703+4251G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740777 | |||||||
| chr7:77740981 | TTTTC | T | 24 | a0001c0001t0003g0160 a0001c0001t0005g0150 a0001c0001t0005g0193 others(21): Show |
24 | HG01070.hp1 HG01071.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.703+4459_703+4462d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77740981 | ||||||
| chr7:77740982 | TTTC | T | 44 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(41): Show |
44 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.703+4459_703+4461d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77740982 | ||||||
| chr7:77740985 | C | CT | 7 | a0001c0001t0002g0064 a0001c0001t0002g0084 a0001c0001t0004g0003 others(4): Show |
7 | HG01981.hp1 HG02055.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+4478dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77740985 | ||||||
| chr7:77740985 | CT | C | 14 | a0001c0001t0002g0087 a0001c0001t0014g0129 a0001c0001t0026g0114 others(11): Show |
14 | HG00323.hp1 HG01192.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.703+4478delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77740985 | ||||||
| chr7:77740990 | T | C | 2 | a0001c0001t0002g0054 a0001c0001t0032g0033 |
2 | HG02015.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.703+4464T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740990 | |||||||
| chr7:77741041 | C | T | 1 | a0001c0001t0019g0032 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.703+4515C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741041 | |||||||
| chr7:77741080 | G | A | 1 | a0001c0002t0001g0312 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.703+4554G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741080 | |||||||
| chr7:77741094 | C | A | 5 | a0001c0001t0005g0199 a0001c0001t0005g0200 a0001c0001t0005g0201 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+4568C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741094 | |||||||
| chr7:77741111 | C | T | 2 | a0001c0001t0019g0031 a0001c0001t0019g0032 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.703+4585C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741111 | |||||||
| chr7:77741135 | C | T | 2 | a0001c0001t0005g0193 a0001c0001t0005g0198 |
2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.703+4609C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741135 | |||||||
| chr7:77741161 | G | A | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.703+4635G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741161 | |||||||
| chr7:77741199 | C | T | 4 | a0001c0002t0001g0271 a0001c0002t0001g0278 a0001c0002t0038g0297 others(1): Show |
4 | HG03491.hp1 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+4673C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741199 | |||||||
| chr7:77741230 | A | G | 1 | a0001c0001t0003g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.703+4704A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741230 | |||||||
| chr7:77741345 | A | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.703+4819A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741345 | |||||||
| chr7:77741477 | G | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+4951G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741477 | |||||||
| chr7:77741552 | C | T | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.703+5026C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741552 | |||||||
| chr7:77741691 | C | CA | 44 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(41): Show |
45 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.703+5180dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77741691 | ||||||
| chr7:77741691 | C | CAA | 6 | a0001c0001t0011g0055 a0001c0001t0011g0057 a0001c0001t0011g0074 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+5179_703+5180d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77741691 | ||||||
| chr7:77741691 | CA | C | 10 | a0001c0001t0002g0081 a0001c0001t0002g0117 a0001c0001t0003g0159 others(7): Show |
10 | HG01257.hp2 HG01433.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+5180delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77741691 | ||||||
| chr7:77741773 | G | A | 7 | a0001c0002t0001g0293 a0001c0002t0001g0295 a0001c0002t0001g0300 others(4): Show |
7 | HG01099.hp1 HG01433.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+5247G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741773 | |||||||
| chr7:77741999 | G | T | 1 | a0001c0001t0002g0100 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.703+5473G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741999 | |||||||
| chr7:77742038 | T | C | 1 | a0001c0002t0001g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.703+5512T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742038 | |||||||
| chr7:77742164 | TA | T | 18 | a0001c0001t0004g0004 a0001c0001t0004g0007 a0001c0001t0004g0009 others(15): Show |
18 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.703+5655delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742164 | ||||||
| chr7:77742179 | AAATACAC others(2): Show |
A | 7 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0093 others(4): Show |
7 | NA18946.hp1 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+5655_703+5663d others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742179 | ||||||
| chr7:77742179 | AAATACAC others(12): Show |
A | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+5655_703+5673d others(21): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742179 | ||||||
| chr7:77742180 | A | AT | 27 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0005 others(24): Show |
28 | HG01099.hp2 HG01175.hp2 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(3): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | |||||||
| chr7:77742180 | A | ATAC | 13 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0140 others(10): Show |
13 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | |||||||
| chr7:77742180 | A | ATACAC | 34 | a0001c0001t0002g0039 a0001c0001t0002g0068 a0001c0001t0002g0069 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | |||||||
| chr7:77742180 | A | ATACACAC | 65 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0058 others(62): Show |
65 | HG00423.hp2 HG00733.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(9): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | |||||||
| chr7:77742180 | A | ATACACAC others(2): Show |
33 | a0001c0001t0002g0053 a0001c0001t0002g0060 a0001c0001t0002g0063 others(30): Show |
33 | HG00438.hp1 HG01255.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | |||||||
| chr7:77742180 | A | ATACACAC others(4): Show |
5 | a0001c0001t0002g0065 a0001c0001t0002g0117 a0001c0001t0002g0126 others(2): Show |
5 | HG02071.hp1 HG02738.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(13): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | |||||||
| chr7:77742180 | A | ATACACAC others(6): Show |
2 | a0001c0001t0007g0085 a0001c0001t0025g0113 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.703+5654_703+5655i others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | |||||||
| chr7:77742180 | A | ATACACAC others(8): Show |
1 | a0002c0003t0004g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.703+5654_703+5655i others(17): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | |||||||
| chr7:77742180 | A | C | 5 | a0001c0001t0002g0054 a0001c0001t0003g0153 a0001c0001t0003g0161 others(2): Show |
5 | HG02015.hp1 HG03490.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+5654A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | |||||||
| chr7:77742182 | T | C | 186 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(183): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.703+5656T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742182 | |||||||
| chr7:77742182 | T | TAC | 24 | a0001c0002t0001g0221 a0001c0002t0001g0223 a0001c0002t0001g0224 others(21): Show |
24 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.703+5691_703+5692d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742182 | ||||||
| chr7:77742182 | T | TACAC | 11 | a0001c0002t0001g0219 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG00423.hp1 HG00438.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.703+5689_703+5692d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742182 | ||||||
| chr7:77742182 | TACACACA others(7): Show |
T | 2 | a0001c0002t0001g0260 a0001c0002t0001g0268 |
2 | NA18960.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.703+5679_703+5692d others(16): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742182 | ||||||
| chr7:77742184 | C | T | 1 | a0004c0010t0028g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.703+5658C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742184 | |||||||
| chr7:77742190 | C | T | 7 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0093 others(4): Show |
7 | NA18946.hp1 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+5664C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742190 | |||||||
| chr7:77742200 | C | T | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+5674C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742200 | |||||||
| chr7:77742463 | G | C | 10 | a0001c0001t0004g0146 a0001c0001t0004g0147 a0002c0003t0004g0043 others(7): Show |
10 | HG01192.hp1 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.703+5937G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742463 | |||||||
| chr7:77742512 | A | G | 15 | a0001c0002t0001g0221 a0001c0002t0001g0223 a0001c0002t0001g0224 others(12): Show |
15 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+5986A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742512 | |||||||
| chr7:77742674 | C | G | 2 | a0001c0002t0001g0250 a0001c0002t0001g0258 |
2 | HG01167.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.703+6148C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742674 | |||||||
| chr7:77742737 | C | A | 2 | a0001c0002t0001g0233 a0001c0002t0001g0289 |
2 | NA18970.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.703+6211C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742737 | |||||||
| chr7:77742789 | G | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+6263G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742789 | |||||||
| chr7:77742816 | C | A | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+6290C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742816 | |||||||
| chr7:77742829 | C | A | 1 | a0001c0001t0004g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.703+6303C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742829 | |||||||
| chr7:77742956 | T | G | 1 | a0001c0002t0001g0218 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.703+6430T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742956 | |||||||
| chr7:77743059 | A | AT | 213 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(210): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.704-6354dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743059 | ||||||
| chr7:77743285 | T | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-6139T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743285 | |||||||
| chr7:77743311 | T | A | 2 | a0001c0001t0003g0160 a0001c0001t0003g0183 |
2 | HG02129.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.704-6113T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743311 | |||||||
| chr7:77743460 | TTTTG | T | 8 | a0001c0001t0005g0172 a0001c0001t0008g0020 a0001c0001t0008g0021 others(5): Show |
8 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-5960_704-5957d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743460 | ||||||
| chr7:77743461 | TTTG | T | 47 | a0001c0001t0002g0054 a0001c0001t0003g0034 a0001c0001t0003g0035 others(44): Show |
47 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.704-5960_704-5958d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743461 | ||||||
| chr7:77743462 | TTG | T | 151 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.704-5960_704-5959d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743462 | ||||||
| chr7:77743463 | TG | T | 8 | a0001c0001t0002g0075 a0001c0001t0002g0086 a0001c0001t0005g0193 others(5): Show |
8 | HG01099.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-5960delG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743463 | |||||||
| chr7:77743464 | G | T | 1 | a0001c0002t0001g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.704-5960G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743464 | |||||||
| chr7:77743480 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.704-5944A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743480 | |||||||
| chr7:77743490 | CT | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-5932delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743490 | ||||||
| chr7:77743589 | C | T | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-5835C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743589 | |||||||
| chr7:77743683 | CAAAT | C | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.704-5740_704-5737d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743683 | |||||||
| chr7:77743717 | G | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0077 |
2 | HG00423.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.704-5707G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743717 | |||||||
| chr7:77743845 | G | T | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.704-5579G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743845 | |||||||
| chr7:77744120 | C | T | 3 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0331 |
3 | HG02738.hp1 HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-5304C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744120 | |||||||
| chr7:77744201 | A | T | 1 | a0001c0001t0020g0212 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.704-5223A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744201 | |||||||
| chr7:77744344 | G | A | 5 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(2): Show |
5 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-5080G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744344 | |||||||
| chr7:77744420 | G | A | 1 | a0001c0001t0011g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.704-5004G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744420 | |||||||
| chr7:77744526 | G | T | 1 | a0001c0001t0003g0166 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.704-4898G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744526 | |||||||
| chr7:77744637 | C | T | 1 | a0001c0002t0006g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.704-4787C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744637 | |||||||
| chr7:77745116 | C | T | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.704-4308C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745116 | |||||||
| chr7:77745119 | G | T | 13 | a0001c0001t0003g0151 a0001c0001t0003g0153 a0001c0001t0003g0156 others(10): Show |
13 | HG02074.hp1 HG02129.hp2 NA18953.hp2 others(10): Show |
intron_variant | MODIFIER | c.704-4305G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745119 | |||||||
| chr7:77745180 | G | A | 1 | a0001c0001t0013g0124 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.704-4244G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745180 | |||||||
| chr7:77745192 | C | T | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.704-4232C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745192 | |||||||
| chr7:77745262 | CA | C | 55 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(52): Show |
55 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.704-4146delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77745262 | ||||||
| chr7:77745291 | GA | G | 14 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0002t0001g0288 others(11): Show |
14 | HG01099.hp1 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.704-4131delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77745291 | ||||||
| chr7:77745310 | A | G | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.704-4114A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745310 | |||||||
| chr7:77745396 | A | G | 2 | a0001c0002t0001g0238 a0001c0002t0001g0251 |
2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.704-4028A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745396 | |||||||
| chr7:77745447 | T | C | 130 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(127): Show |
131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.704-3977T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745447 | |||||||
| chr7:77745487 | A | G | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-3937A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745487 | |||||||
| chr7:77745529 | C | T | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-3895C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745529 | |||||||
| chr7:77745697 | C | T | 1 | a0001c0001t0014g0094 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.704-3727C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745697 | |||||||
| chr7:77745866 | G | A | 1 | a0001c0001t0004g0141 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.704-3558G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745866 | |||||||
| chr7:77745994 | A | G | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-3430A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745994 | |||||||
| chr7:77746020 | A | C | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.704-3404A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746020 | |||||||
| chr7:77746079 | A | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.704-3345A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746079 | |||||||
| chr7:77746151 | C | T | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.704-3273C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746151 | |||||||
| chr7:77746208 | T | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.704-3216T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746208 | |||||||
| chr7:77746261 | G | C | 1 | a0001c0001t0003g0188 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.704-3163G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746261 | |||||||
| chr7:77746320 | C | T | 1 | a0001c0004t0005g0210 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.704-3104C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746320 | |||||||
| chr7:77746327 | C | T | 1 | a0001c0001t0022g0040 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.704-3097C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746327 | |||||||
| chr7:77746388 | A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.704-3036A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746388 | |||||||
| chr7:77746463 | C | T | 1 | a0001c0002t0001g0328 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.704-2961C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746463 | |||||||
| chr7:77746493 | C | T | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-2931C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746493 | |||||||
| chr7:77746494 | G | A | 1 | a0001c0001t0004g0131 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.704-2930G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746494 | |||||||
| chr7:77746517 | C | G | 1 | a0001c0002t0001g0285 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.704-2907C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746517 | |||||||
| chr7:77746688 | T | C | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-2736T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746688 | |||||||
| chr7:77746827 | C | T | 1 | a0001c0001t0003g0169 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.704-2597C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746827 | |||||||
| chr7:77746828 | G | A | 2 | a0001c0002t0001g0300 a0001c0002t0001g0320 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.704-2596G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746828 | |||||||
| chr7:77746913 | C | G | 54 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(51): Show |
55 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.704-2511C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746913 | |||||||
| chr7:77746961 | G | T | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.704-2463G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746961 | |||||||
| chr7:77747004 | G | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-2420G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747004 | |||||||
| chr7:77747005 | G | T | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-2419G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747005 | |||||||
| chr7:77747097 | C | A | 8 | a0001c0001t0004g0005 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
8 | HG02071.hp2 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-2327C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747097 | |||||||
| chr7:77747150 | C | T | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.704-2274C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747150 | |||||||
| chr7:77747324 | A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.704-2100A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747324 | |||||||
| chr7:77747358 | G | A | 2 | a0001c0001t0004g0146 a0001c0001t0004g0147 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.704-2066G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747358 | |||||||
| chr7:77747689 | G | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.704-1735G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747689 | |||||||
| chr7:77747749 | G | A | 1 | a0001c0002t0001g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.704-1675G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747749 | |||||||
| chr7:77747793 | C | T | 4 | a0001c0001t0009g0132 a0001c0001t0009g0134 a0001c0001t0009g0135 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1631C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747793 | |||||||
| chr7:77747797 | T | C | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.704-1627T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747797 | |||||||
| chr7:77747914 | G | A | 2 | a0001c0001t0005g0193 a0001c0001t0005g0198 |
2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.704-1510G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747914 | |||||||
| chr7:77747914 | G | C | 1 | a0001c0002t0001g0222 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.704-1510G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747914 | |||||||
| chr7:77747916 | G | C | 36 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(33): Show |
37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.704-1508G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747916 | |||||||
| chr7:77747919 | A | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.704-1505A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747919 | |||||||
| chr7:77747987 | A | G | 1 | a0001c0002t0001g0285 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.704-1437A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747987 | |||||||
| chr7:77748074 | A | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1350A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748074 | |||||||
| chr7:77748115 | G | T | 1 | a0001c0002t0001g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.704-1309G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748115 | |||||||
| chr7:77748378 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-1046A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748378 | |||||||
| chr7:77748492 | A | C | 1 | a0001c0001t0003g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.704-932A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748492 | |||||||
| chr7:77748536 | G | A | 71 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(68): Show |
71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.704-888G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748536 | |||||||
| chr7:77748631 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.704-793C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748631 | |||||||
| chr7:77748806 | T | C | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-618T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748806 | |||||||
| chr7:77748838 | G | A | 16 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(13): Show |
16 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.704-586G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748838 | |||||||
| chr7:77748896 | CGTCT | C | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.704-511_704-508del others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77748896 | ||||||
| chr7:77749124 | C | T | 1 | a0001c0001t0004g0140 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.704-300C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77749124 | |||||||
| chr7:77749236 | A | G | 1 | a0005c0012t0012g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.704-188A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77749236 | |||||||
| chr7:77750199 | A | G | 1 | a0001c0002t0001g0252 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1344+135A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750199 | |||||||
| chr7:77750211 | G | A | 1 | a0002c0003t0004g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1344+147G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750211 | |||||||
| chr7:77750280 | ATAAT | A | 73 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(70): Show |
73 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.1344+220_1344+223d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750280 | ||||||
| chr7:77750296 | G | GT | 23 | a0001c0001t0002g0039 a0001c0001t0002g0059 a0001c0001t0002g0060 others(20): Show |
23 | HG00423.hp2 HG00733.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1344+257dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | ||||||
| chr7:77750296 | G | GTT | 7 | a0001c0001t0002g0062 a0001c0001t0010g0079 a0001c0001t0011g0095 others(4): Show |
7 | HG01256.hp1 HG02572.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344+256_1344+257d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | ||||||
| chr7:77750296 | G | GTTT | 10 | a0001c0001t0002g0117 a0001c0001t0004g0107 a0001c0001t0004g0108 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+255_1344+257d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | ||||||
| chr7:77750296 | G | GTTTT | 6 | a0001c0001t0022g0041 a0002c0003t0004g0044 a0002c0003t0004g0045 others(3): Show |
6 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+254_1344+257d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | ||||||
| chr7:77750296 | GT | G | 133 | a0001c0001t0002g0069 a0001c0001t0003g0035 a0001c0001t0003g0036 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1344+257delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | ||||||
| chr7:77750296 | GTTTT | G | 33 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(30): Show |
34 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.1344+254_1344+257d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | ||||||
| chr7:77750296 | GTTTTTTT others(1): Show |
G | 10 | a0001c0001t0005g0195 a0001c0001t0005g0196 a0001c0001t0005g0204 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+250_1344+257d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | ||||||
| chr7:77750296 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0003g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1344+248_1344+257d others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | ||||||
| chr7:77750302 | T | G | 1 | a0001c0002t0001g0244 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1344+238T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750302 | |||||||
| chr7:77750413 | G | T | 67 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(64): Show |
67 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.1344+349G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750413 | |||||||
| chr7:77750420 | A | G | 2 | a0002c0003t0007g0042 a0002c0003t0007g0105 |
2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1344+356A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750420 | |||||||
| chr7:77750439 | G | A | 73 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(70): Show |
73 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1344+375G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750439 | |||||||
| chr7:77750563 | G | A | 14 | a0001c0001t0005g0195 a0001c0001t0005g0196 a0001c0001t0005g0197 others(11): Show |
14 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1344+499G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750563 | |||||||
| chr7:77750600 | G | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+536G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750600 | |||||||
| chr7:77751092 | G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1344+1028G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751092 | |||||||
| chr7:77751151 | TTTTTTTG | T | 128 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(125): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1344+1102_1344+110 others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77751151 | ||||||
| chr7:77751289 | A | ATCACCAT others(4): Show |
1 | a0001c0001t0004g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1344+1225_1344+122 others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751289 | |||||||
| chr7:77751290 | C | CCACCATG others(4): Show |
53 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(50): Show |
54 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1344+1227_1344+123 others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77751290 | ||||||
| chr7:77751290 | C | G | 1 | a0001c0001t0004g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1344+1226C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751290 | |||||||
| chr7:77751328 | CAG | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0283 a0001c0002t0001g0311 |
4 | NA18946.hp2 NA18949.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+1265_1344+126 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751328 | |||||||
| chr7:77751448 | A | T | 73 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(70): Show |
73 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.1344+1384A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751448 | |||||||
| chr7:77751604 | C | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1344+1540C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751604 | |||||||
| chr7:77751674 | G | A | 2 | a0001c0001t0003g0166 a0001c0001t0003g0178 |
2 | NA18988.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1344+1610G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751674 | |||||||
| chr7:77751716 | A | G | 1 | a0001c0001t0005g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1344+1652A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751716 | |||||||
| chr7:77751744 | G | C | 14 | a0001c0001t0005g0195 a0001c0001t0005g0196 a0001c0001t0005g0197 others(11): Show |
14 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1344+1680G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751744 | |||||||
| chr7:77751844 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1344+1780C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751844 | |||||||
| chr7:77751858 | G | T | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+1794G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751858 | |||||||
| chr7:77751860 | C | T | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1344+1796C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751860 | |||||||
| chr7:77751862 | C | T | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1344+1798C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751862 | |||||||
| chr7:77751878 | G | A | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+1814G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751878 | |||||||
| chr7:77752055 | C | G | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1344+1991C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752055 | |||||||
| chr7:77752275 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+2211A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752275 | |||||||
| chr7:77752415 | T | TATC | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1344+2353_1344+235 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77752415 | ||||||
| chr7:77752448 | A | T | 4 | a0001c0001t0003g0034 a0001c0001t0003g0170 a0001c0001t0003g0175 others(1): Show |
4 | HG02135.hp2 NA18747.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+2384A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752448 | |||||||
| chr7:77752478 | G | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+2414G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752478 | |||||||
| chr7:77752725 | C | A | 3 | a0001c0002t0001g0309 a0001c0002t0001g0316 a0001c0002t0001g0319 |
3 | HG00738.hp1 HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1344+2661C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752725 | |||||||
| chr7:77752946 | C | T | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1344+2882C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752946 | |||||||
| chr7:77752971 | G | A | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1344+2907G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752971 | |||||||
| chr7:77753006 | T | G | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1344+2942T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753006 | |||||||
| chr7:77753017 | T | C | 2 | a0001c0001t0019g0031 a0001c0001t0019g0032 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1344+2953T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753017 | |||||||
| chr7:77753033 | T | C | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1344+2969T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753033 | |||||||
| chr7:77753106 | A | C | 1 | a0001c0001t0004g0016 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1344+3042A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753106 | |||||||
| chr7:77753419 | A | G | 42 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(39): Show |
42 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1344+3355A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753419 | |||||||
| chr7:77753427 | T | C | 13 | a0001c0002t0001g0261 a0001c0002t0001g0288 a0001c0002t0001g0293 others(10): Show |
13 | HG01099.hp1 HG01433.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1344+3363T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753427 | |||||||
| chr7:77753619 | A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1344+3555A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753619 | |||||||
| chr7:77753938 | A | G | 69 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(66): Show |
69 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1344+3874A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753938 | |||||||
| chr7:77753980 | G | T | 1 | a0001c0001t0031g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1344+3916G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753980 | |||||||
| chr7:77754231 | G | A | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+4167G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754231 | |||||||
| chr7:77754523 | C | T | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1344+4459C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754523 | |||||||
| chr7:77754614 | A | G | 1 | a0001c0002t0001g0252 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1344+4550A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754614 | |||||||
| chr7:77754720 | C | G | 1 | a0001c0001t0002g0075 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1344+4656C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754720 | |||||||
| chr7:77754833 | C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1344+4769C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754833 | |||||||
| chr7:77754986 | C | CTA | 69 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(66): Show |
69 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1344+4932_1344+493 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77754986 | ||||||
| chr7:77755013 | A | T | 1 | a0001c0002t0001g0269 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1344+4949A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755013 | |||||||
| chr7:77755031 | G | C | 69 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(66): Show |
69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1344+4967G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755031 | |||||||
| chr7:77755250 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+5186A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755250 | |||||||
| chr7:77755391 | G | A | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1344+5327G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755391 | |||||||
| chr7:77755391 | G | T | 1 | a0001c0001t0009g0136 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1344+5327G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755391 | |||||||
| chr7:77755671 | CAAAACA | C | 208 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(205): Show |
209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1344+5618_1344+562 others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77755671 | ||||||
| chr7:77755679 | AAACAAAA others(3): Show |
A | 1 | a0001c0001t0002g0083 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1344+5618_1344+562 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77755679 | ||||||
| chr7:77755933 | C | T | 4 | a0001c0002t0001g0270 a0001c0002t0001g0286 a0001c0002t0001g0307 others(1): Show |
4 | HG00438.hp2 HG02015.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+5869C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755933 | |||||||
| chr7:77756008 | A | C | 80 | a0001c0001t0002g0096 a0001c0001t0004g0148 a0001c0002t0001g0002 others(77): Show |
81 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1344+5944A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756008 | |||||||
| chr7:77756050 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+5986A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756050 | |||||||
| chr7:77756154 | C | G | 47 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(44): Show |
47 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.1344+6090C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756154 | |||||||
| chr7:77756185 | G | A | 6 | a0001c0002t0001g0234 a0001c0002t0001g0309 a0001c0002t0001g0314 others(3): Show |
6 | HG00738.hp1 HG01257.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344+6121G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756185 | |||||||
| chr7:77756279 | G | A | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+6215G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756279 | |||||||
| chr7:77756322 | G | A | 1 | a0001c0001t0003g0151 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1344+6258G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756322 | |||||||
| chr7:77756323 | G | T | 1 | a0001c0001t0003g0151 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1344+6259G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756323 | |||||||
| chr7:77756377 | C | G | 2 | a0001c0001t0003g0161 a0001c0001t0003g0182 |
2 | HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1344+6313C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756377 | |||||||
| chr7:77756774 | G | A | 2 | a0001c0002t0001g0233 a0001c0002t0001g0289 |
2 | NA18970.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1344+6710G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756774 | |||||||
| chr7:77756864 | T | TAATG | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1344+6801_1344+680 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77756864 | ||||||
| chr7:77756876 | T | C | 1 | a0001c0001t0031g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1344+6812T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756876 | |||||||
| chr7:77756894 | A | G | 1 | a0001c0001t0007g0085 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1344+6830A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756894 | |||||||
| chr7:77757102 | A | G | 2 | a0001c0001t0002g0111 a0001c0001t0023g0112 |
2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1344+7038A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77757102 | |||||||
| chr7:77757107 | C | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+7043C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77757107 | |||||||
| chr7:77757280 | C | T | 42 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(39): Show |
42 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1344+7216C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77757280 | |||||||
| chr7:77757714 | T | C | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1344+7650T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77757714 | |||||||
| chr7:77757990 | CAG | C | 36 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(33): Show |
37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1345-7502_1345-750 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77757990 | ||||||
| chr7:77758174 | T | G | 36 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(33): Show |
37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1345-7321T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758174 | |||||||
| chr7:77758177 | T | C | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1345-7318T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758177 | |||||||
| chr7:77758201 | C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1345-7294C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758201 | |||||||
| chr7:77758397 | A | G | 7 | a0001c0001t0005g0193 a0001c0001t0005g0198 a0001c0001t0019g0031 others(4): Show |
7 | HG01099.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-7098A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758397 | |||||||
| chr7:77758402 | A | G | 1 | a0001c0002t0001g0285 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1345-7093A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758402 | |||||||
| chr7:77758477 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1345-7018C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758477 | |||||||
| chr7:77758494 | A | G | 2 | a0001c0001t0018g0128 a0001c0001t0018g0138 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1345-7001A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758494 | |||||||
| chr7:77758645 | A | G | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1345-6850A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758645 | |||||||
| chr7:77758827 | T | C | 1 | a0001c0001t0008g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1345-6668T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758827 | |||||||
| chr7:77758851 | G | A | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-6644G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758851 | |||||||
| chr7:77758978 | T | G | 36 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(33): Show |
37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1345-6517T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758978 | |||||||
| chr7:77759088 | G | A | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1345-6407G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759088 | |||||||
| chr7:77759151 | C | A | 21 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(18): Show |
21 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1345-6344C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759151 | |||||||
| chr7:77759228 | C | A | 6 | a0001c0001t0011g0055 a0001c0001t0011g0057 a0001c0001t0011g0074 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-6267C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759228 | |||||||
| chr7:77759364 | A | G | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345-6131A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759364 | |||||||
| chr7:77759392 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1345-6103C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759392 | |||||||
| chr7:77759423 | G | A | 1 | a0001c0001t0009g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1345-6072G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759423 | |||||||
| chr7:77759551 | A | G | 1 | a0001c0002t0001g0222 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1345-5944A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759551 | |||||||
| chr7:77759647 | A | G | 3 | a0001c0002t0001g0227 a0001c0002t0001g0296 a0001c0002t0001g0323 |
3 | NA18983.hp1 NA19009.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1345-5848A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759647 | |||||||
| chr7:77759684 | C | T | 1 | a0001c0001t0003g0151 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1345-5811C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759684 | |||||||
| chr7:77759835 | G | A | 3 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0148 |
3 | HG02135.hp1 NA18990.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1345-5660G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759835 | |||||||
| chr7:77760002 | G | A | 2 | a0001c0001t0009g0134 a0001c0001t0009g0135 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1345-5493G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760002 | |||||||
| chr7:77760149 | T | A | 1 | a0001c0001t0003g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1345-5346T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760149 | |||||||
| chr7:77760234 | T | G | 3 | a0001c0001t0007g0049 a0001c0001t0007g0073 a0001c0001t0007g0089 |
3 | HG02970.hp2 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1345-5261T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760234 | |||||||
| chr7:77760664 | A | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-4831A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760664 | |||||||
| chr7:77760722 | T | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-4773T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760722 | |||||||
| chr7:77760736 | A | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-4759A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760736 | |||||||
| chr7:77760786 | C | T | 3 | a0001c0002t0001g0238 a0001c0002t0001g0251 a0001c0002t0001g0277 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1345-4709C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760786 | |||||||
| chr7:77760852 | T | C | 2 | a0001c0001t0005g0201 a0001c0001t0005g0202 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1345-4643T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760852 | |||||||
| chr7:77761063 | A | T | 73 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(70): Show |
73 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1345-4432A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761063 | |||||||
| chr7:77761139 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | HG00741.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1345-4356T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761139 | |||||||
| chr7:77761204 | A | G | 2 | a0001c0001t0004g0107 a0001c0001t0004g0108 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.1345-4291A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761204 | |||||||
| chr7:77761712 | A | G | 7 | a0001c0001t0005g0193 a0001c0001t0005g0198 a0001c0001t0019g0031 others(4): Show |
7 | HG01099.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-3783A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761712 | |||||||
| chr7:77761967 | G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1345-3528G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761967 | |||||||
| chr7:77762152 | A | G | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1345-3343A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762152 | |||||||
| chr7:77762364 | A | C | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1345-3131A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762364 | |||||||
| chr7:77762414 | A | G | 1 | a0001c0001t0002g0096 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1345-3081A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762414 | |||||||
| chr7:77762663 | A | C | 38 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(35): Show |
39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.1345-2832A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762663 | |||||||
| chr7:77762697 | A | G | 2 | a0001c0001t0009g0132 a0001c0001t0009g0144 |
2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1345-2798A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762697 | |||||||
| chr7:77762699 | G | T | 38 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(35): Show |
39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.1345-2796G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762699 | |||||||
| chr7:77762799 | C | G | 1 | a0001c0002t0006g0264 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1345-2696C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762799 | |||||||
| chr7:77762945 | C | G | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-2550C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762945 | |||||||
| chr7:77762950 | G | C | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1345-2545G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762950 | |||||||
| chr7:77763015 | C | A | 1 | a0001c0002t0001g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1345-2480C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763015 | |||||||
| chr7:77763148 | A | C | 1 | a0001c0002t0001g0331 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1345-2347A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763148 | |||||||
| chr7:77763149 | C | CT | 83 | a0001c0001t0003g0170 a0001c0001t0004g0001 a0001c0001t0004g0003 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1345-2326dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77763149 | ||||||
| chr7:77763149 | C | CTT | 53 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(50): Show |
53 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1345-2327_1345-232 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77763149 | ||||||
| chr7:77763149 | CTTTTTTT | C | 72 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(69): Show |
72 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1345-2332_1345-232 others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77763149 | ||||||
| chr7:77763220 | C | T | 2 | a0001c0001t0002g0111 a0001c0001t0023g0112 |
2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1345-2275C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763220 | |||||||
| chr7:77763295 | G | C | 4 | a0001c0001t0013g0122 a0001c0001t0013g0123 a0001c0001t0013g0124 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-2200G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763295 | |||||||
| chr7:77763392 | C | T | 1 | a0001c0001t0004g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1345-2103C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763392 | |||||||
| chr7:77763768 | C | T | 4 | a0001c0001t0005g0193 a0001c0001t0005g0198 a0001c0001t0020g0212 others(1): Show |
4 | HG01099.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-1727C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763768 | |||||||
| chr7:77763798 | T | C | 6 | a0001c0001t0011g0055 a0001c0001t0011g0057 a0001c0001t0011g0074 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-1697T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763798 | |||||||
| chr7:77764013 | A | C | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345-1482A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764013 | |||||||
| chr7:77764052 | T | C | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1345-1443T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764052 | |||||||
| chr7:77764187 | C | G | 2 | a0001c0001t0005g0199 a0001c0001t0005g0200 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1345-1308C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764187 | |||||||
| chr7:77764422 | T | C | 67 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(64): Show |
67 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.1345-1073T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764422 | |||||||
| chr7:77764499 | A | G | 1 | a0001c0001t0003g0180 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1345-996A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764499 | |||||||
| chr7:77764631 | CT | C | 7 | a0001c0001t0002g0053 a0001c0001t0002g0060 a0001c0001t0002g0065 others(4): Show |
7 | HG00438.hp1 HG01256.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345-851delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77764631 | ||||||
| chr7:77764779 | G | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-716G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764779 | |||||||
| chr7:77765267 | A | G | 36 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(33): Show |
37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1345-228A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77765267 | |||||||
| chr7:77765362 | T | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-133T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77765362 | |||||||
| chr7:77765446 | C | A | 1 | a0001c0002t0041g0239 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1345-49C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77765446 | |||||||
| chr7:77765458 | A | T | 6 | a0001c0001t0005g0197 a0001c0001t0005g0214 a0001c0004t0005g0194 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345-37A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77765458 | |||||||
| chr7:77765671 | T | A | 18 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(15): Show |
18 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1482+39T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765671 | |||||||
| chr7:77765672 | A | T | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1482+40A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765672 | |||||||
| chr7:77765698 | G | A | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1482+66G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765698 | |||||||
| chr7:77765705 | A | T | 2 | a0001c0001t0022g0040 a0001c0001t0022g0041 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1482+73A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765705 | |||||||
| chr7:77765769 | C | T | 1 | a0001c0002t0001g0285 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1482+137C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765769 | |||||||
| chr7:77765848 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1482+216C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765848 | |||||||
| chr7:77765855 | T | C | 1 | a0001c0001t0003g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1482+223T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765855 | |||||||
| chr7:77766263 | A | G | 5 | a0001c0001t0002g0053 a0001c0001t0002g0060 a0001c0001t0002g0065 others(2): Show |
5 | HG00438.hp1 HG02071.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1482+631A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77766263 | |||||||
| chr7:77766520 | C | CT | 14 | a0001c0001t0005g0214 a0001c0001t0013g0122 a0001c0001t0013g0123 others(11): Show |
14 | HG00639.hp1 HG01192.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1482+902dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77766520 | ||||||
| chr7:77766520 | CT | C | 6 | a0001c0001t0002g0087 a0001c0001t0020g0212 a0001c0002t0001g0218 others(3): Show |
6 | HG01070.hp1 HG01975.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+902delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77766520 | ||||||
| chr7:77766599 | G | A | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1482+967G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77766599 | |||||||
| chr7:77766654 | A | G | 2 | a0001c0001t0015g0030 a0001c0001t0031g0216 |
2 | HG00140.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1482+1022A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77766654 | |||||||
| chr7:77766918 | G | A | 212 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(209): Show |
213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1482+1286G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77766918 | |||||||
| chr7:77767008 | TCCTTTCC others(22): Show |
T | 2 | a0001c0001t0005g0193 a0001c0001t0005g0198 |
2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1482+1381_1482+140 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767008 | ||||||
| chr7:77767013 | T | TCCTTCCC others(22): Show |
7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482+1436_1482+146 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767013 | ||||||
| chr7:77767013 | TCCTTCCC others(22): Show |
T | 2 | a0001c0001t0022g0040 a0001c0001t0022g0041 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1482+1436_1482+146 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767013 | ||||||
| chr7:77767120 | G | A | 1 | a0001c0001t0030g0027 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1482+1488G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767120 | |||||||
| chr7:77767290 | AT | A | 319 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(316): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1483-1357delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767290 | ||||||
| chr7:77767290 | ATT | A | 11 | a0001c0001t0003g0035 a0001c0001t0009g0132 a0001c0001t0009g0133 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1483-1358_1483-135 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767290 | ||||||
| chr7:77767405 | G | A | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-1256G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767405 | |||||||
| chr7:77767499 | G | A | 1 | a0001c0002t0001g0279 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1483-1162G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767499 | |||||||
| chr7:77767726 | GCCTCC | G | 58 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0005 others(55): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1483-917_1483-913d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767726 | ||||||
| chr7:77767731 | C | G | 1 | a0001c0001t0002g0067 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1483-930C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767731 | |||||||
| chr7:77767743 | C | T | 1 | a0001c0001t0004g0019 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1483-918C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767743 | |||||||
| chr7:77767744 | T | C | 1 | a0001c0001t0004g0019 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1483-917T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767744 | |||||||
| chr7:77767750 | C | CT | 3 | a0001c0001t0010g0106 a0001c0001t0019g0032 a0001c0004t0005g0210 |
3 | HG02293.hp2 HG03516.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1483-906dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767750 | ||||||
| chr7:77767755 | T | C | 1 | a0001c0001t0003g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1483-906T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767755 | |||||||
| chr7:77767776 | T | TC | 8 | a0001c0001t0002g0127 a0001c0001t0003g0035 a0001c0001t0008g0025 others(5): Show |
8 | HG02055.hp2 HG03209.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.1483-879dupC | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767776 | ||||||
| chr7:77767825 | C | T | 1 | a0001c0002t0001g0292 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1483-836C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767825 | |||||||
| chr7:77767834 | T | TC | 12 | a0001c0001t0002g0076 a0001c0001t0002g0101 a0001c0001t0002g0127 others(9): Show |
12 | HG00438.hp1 HG01192.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1483-821dupC | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767834 | ||||||
| chr7:77767843 | C | T | 128 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(125): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1483-818C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767843 | |||||||
| chr7:77767942 | C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1483-719C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767942 | |||||||
| chr7:77767998 | G | A | 1 | a0001c0001t0010g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1483-663G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767998 | |||||||
| chr7:77768062 | C | T | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1483-599C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768062 | |||||||
| chr7:77768097 | C | T | 2 | a0001c0002t0001g0267 a0001c0002t0001g0287 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1483-564C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768097 | |||||||
| chr7:77768320 | A | G | 25 | a0001c0002t0001g0221 a0001c0002t0001g0223 a0001c0002t0001g0224 others(22): Show |
25 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1483-341A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768320 | |||||||
| chr7:77768373 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1483-288A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768373 | |||||||
| chr7:77768417 | T | C | 1 | a0001c0001t0003g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1483-244T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768417 | |||||||
| chr7:77768525 | A | C | 1 | a0001c0001t0009g0136 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1483-136A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768525 | |||||||
| chr7:77768531 | T | C | 5 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0087 others(2): Show |
5 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483-130T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768531 | |||||||
| chr7:77768589 | ATAT | A | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1483-63_1483-61del others(3): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77768589 | ||||||
| chr7:77768841 | G | A | 1 | a0001c0002t0001g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1625+38G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77768841 | |||||||
| chr7:77768864 | T | C | 1 | a0001c0002t0001g0321 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1625+61T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77768864 | |||||||
| chr7:77768874 | A | G | 1 | a0001c0002t0001g0258 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1625+71A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77768874 | |||||||
| chr7:77769122 | G | C | 1 | a0001c0001t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1625+319G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769122 | |||||||
| chr7:77769147 | T | C | 1 | a0001c0001t0005g0205 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1625+344T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769147 | |||||||
| chr7:77769432 | G | T | 1 | a0002c0003t0007g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1625+629G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769432 | |||||||
| chr7:77769464 | G | A | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1625+661G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769464 | |||||||
| chr7:77769631 | A | C | 9 | a0001c0001t0009g0132 a0001c0001t0009g0133 a0001c0001t0009g0134 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1625+828A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769631 | |||||||
| chr7:77769688 | A | C | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1625+885A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769688 | |||||||
| chr7:77769898 | A | G | 1 | a0001c0001t0010g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1625+1095A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769898 | |||||||
| chr7:77769940 | C | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1625+1137C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769940 | |||||||
| chr7:77770077 | G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1625+1274G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770077 | |||||||
| chr7:77770182 | T | A | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1625+1379T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770182 | |||||||
| chr7:77770348 | C | T | 1 | a0005c0012t0012g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1625+1545C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770348 | |||||||
| chr7:77770483 | G | C | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1625+1680G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770483 | |||||||
| chr7:77770518 | A | G | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1625+1715A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770518 | |||||||
| chr7:77770525 | A | T | 211 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(208): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1625+1722A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770525 | |||||||
| chr7:77770559 | C | T | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1625+1756C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770559 | |||||||
| chr7:77770600 | G | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1625+1797G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770600 | |||||||
| chr7:77770719 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1625+1916A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770719 | |||||||
| chr7:77771034 | C | T | 2 | a0001c0001t0019g0031 a0001c0001t0019g0032 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1626-2113C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771034 | |||||||
| chr7:77771068 | A | T | 1 | a0001c0001t0002g0071 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1626-2079A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771068 | |||||||
| chr7:77771148 | G | A | 2 | a0001c0002t0001g0253 a0001c0002t0006g0254 |
2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1626-1999G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771148 | |||||||
| chr7:77771176 | G | A | 4 | a0001c0001t0005g0195 a0001c0001t0005g0204 a0001c0001t0005g0205 others(1): Show |
4 | HG01433.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626-1971G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771176 | |||||||
| chr7:77771207 | C | A | 214 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1626-1940C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771207 | |||||||
| chr7:77771228 | C | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626-1919C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771228 | |||||||
| chr7:77771270 | G | C | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1626-1877G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771270 | |||||||
| chr7:77771272 | T | G | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1626-1875T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771272 | |||||||
| chr7:77771506 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0086 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1626-1641C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771506 | |||||||
| chr7:77771511 | C | CT | 92 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0151 others(89): Show |
92 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1626-1620dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771511 | ||||||
| chr7:77771511 | C | CTT | 74 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(71): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1626-1621_1626-162 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771511 | ||||||
| chr7:77771511 | C | CTTT | 58 | a0001c0001t0002g0039 a0001c0001t0004g0001 a0001c0001t0004g0003 others(55): Show |
59 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.1626-1622_1626-162 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771511 | ||||||
| chr7:77771565 | A | G | 1 | a0001c0001t0002g0118 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1626-1582A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771565 | |||||||
| chr7:77771789 | C | T | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1626-1358C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771789 | |||||||
| chr7:77771826 | A | AT | 209 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(206): Show |
210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1626-1312dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771826 | ||||||
| chr7:77771826 | A | ATT | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1626-1313_1626-131 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771826 | ||||||
| chr7:77771990 | T | C | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1626-1157T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771990 | |||||||
| chr7:77772221 | C | G | 9 | a0001c0001t0009g0132 a0001c0001t0009g0133 a0001c0001t0009g0134 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626-926C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77772221 | |||||||
| chr7:77772331 | T | C | 163 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(160): Show |
164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1626-816T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77772331 | |||||||
| chr7:77772731 | TTAGA | T | 9 | a0001c0001t0009g0132 a0001c0001t0009g0133 a0001c0001t0009g0134 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626-412_1626-409d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77772731 | ||||||
| chr7:77772780 | G | A | 2 | a0001c0002t0001g0250 a0001c0002t0001g0258 |
2 | HG01167.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1626-367G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77772780 | |||||||
| chr7:77772874 | A | T | 9 | a0001c0001t0009g0132 a0001c0001t0009g0133 a0001c0001t0009g0134 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626-273A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77772874 | |||||||
| chr7:77773082 | T | G | 3 | a0001c0002t0001g0226 a0001c0002t0001g0292 a0001c0002t0001g0301 |
3 | HG02293.hp1 NA18943.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1626-65T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77773082 | |||||||
| chr7:77773355 | G | A | 1 | a0001c0001t0013g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1793+41G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773355 | |||||||
| chr7:77773378 | A | C | 1 | a0001c0001t0004g0008 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1793+64A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773378 | |||||||
| chr7:77773429 | A | G | 130 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(127): Show |
131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1793+115A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773429 | |||||||
| chr7:77773460 | A | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+146A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773460 | |||||||
| chr7:77773624 | G | A | 2 | a0001c0001t0025g0113 a0001c0001t0026g0114 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1793+310G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773624 | |||||||
| chr7:77773680 | T | G | 1 | a0001c0001t0003g0174 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1793+366T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773680 | |||||||
| chr7:77773685 | C | T | 1 | a0001c0002t0001g0301 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1793+371C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773685 | |||||||
| chr7:77773718 | G | A | 3 | a0001c0001t0003g0162 a0001c0001t0003g0163 a0001c0001t0003g0176 |
3 | NA18969.hp1 NA19062.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1793+404G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773718 | |||||||
| chr7:77773841 | C | T | 49 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(46): Show |
50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1793+527C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773841 | |||||||
| chr7:77773961 | C | T | 6 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1793+647C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773961 | |||||||
| chr7:77774433 | CA | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+1124delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77774433 | ||||||
| chr7:77774746 | A | C | 16 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1793+1432A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774746 | |||||||
| chr7:77774803 | A | G | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+1489A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774803 | |||||||
| chr7:77774862 | A | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+1548A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774862 | |||||||
| chr7:77774885 | A | G | 2 | a0002c0003t0004g0115 a0002c0003t0004g0116 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1793+1571A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774885 | |||||||
| chr7:77774943 | C | G | 70 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(67): Show |
70 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1793+1629C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774943 | |||||||
| chr7:77774959 | TCAAG | T | 3 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0148 |
3 | HG02135.hp1 NA18990.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1793+1651_1793+165 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77774959 | ||||||
| chr7:77775048 | T | G | 2 | a0001c0001t0020g0212 a0001c0001t0020g0215 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1793+1734T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775048 | |||||||
| chr7:77775080 | C | T | 1 | a0001c0002t0006g0280 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1793+1766C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775080 | |||||||
| chr7:77775122 | T | C | 7 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0022 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+1808T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775122 | |||||||
| chr7:77775237 | A | T | 2 | a0001c0002t0006g0266 a0001c0002t0039g0291 |
2 | HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1793+1923A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775237 | |||||||
| chr7:77775539 | T | C | 1 | a0001c0002t0006g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1793+2225T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775539 | |||||||
| chr7:77775573 | T | A | 1 | a0001c0001t0005g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1793+2259T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775573 | |||||||
| chr7:77775608 | G | A | 1 | a0001c0002t0001g0316 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1793+2294G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775608 | |||||||
| chr7:77775701 | A | T | 4 | a0001c0001t0015g0028 a0001c0001t0015g0029 a0001c0001t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1793+2387A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775701 | |||||||
| chr7:77775776 | C | T | 49 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(46): Show |
50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1793+2462C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775776 | |||||||
| chr7:77775826 | C | T | 4 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 others(1): Show |
4 | HG02559.hp2 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793+2512C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775826 | |||||||
| chr7:77775885 | A | T | 1 | a0001c0002t0006g0220 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1794-2453A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775885 | |||||||
| chr7:77775949 | G | A | 4 | a0001c0001t0005g0199 a0001c0001t0005g0200 a0001c0001t0005g0201 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794-2389G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775949 | |||||||
| chr7:77776056 | C | CA | 211 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(208): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1794-2272dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77776056 | ||||||
| chr7:77776145 | G | A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1794-2193G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776145 | |||||||
| chr7:77776180 | G | A | 1 | a0001c0001t0004g0003 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1794-2158G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776180 | |||||||
| chr7:77776232 | T | A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0032 a0001c0001t0032g0033 |
3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1794-2106T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776232 | |||||||
| chr7:77776250 | T | TTC | 216 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(213): Show |
217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1794-2087_1794-208 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77776250 | ||||||
| chr7:77776304 | A | G | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1794-2034A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776304 | |||||||
| chr7:77776424 | T | C | 215 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1794-1914T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776424 | |||||||
| chr7:77776526 | G | A | 1 | a0001c0002t0001g0233 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1794-1812G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776526 | |||||||
| chr7:77776581 | A | G | 74 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(71): Show |
74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1794-1757A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776581 | |||||||
| chr7:77776727 | CT | C | 12 | a0001c0001t0002g0039 a0001c0001t0002g0066 a0001c0001t0002g0067 others(9): Show |
12 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1794-1609delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77776727 | ||||||
| chr7:77776796 | A | C | 62 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(59): Show |
63 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1794-1542A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776796 | |||||||
| chr7:77776827 | T | C | 4 | a0001c0002t0001g0270 a0001c0002t0001g0286 a0001c0002t0001g0307 others(1): Show |
4 | HG00438.hp2 HG02015.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1794-1511T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776827 | |||||||
| chr7:77776925 | G | T | 77 | a0001c0002t0001g0002 a0001c0002t0001g0218 a0001c0002t0001g0219 others(74): Show |
78 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1794-1413G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776925 | |||||||
| chr7:77777087 | C | T | 129 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1794-1251C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777087 | |||||||
| chr7:77777171 | C | A | 67 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(64): Show |
67 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1794-1167C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777171 | |||||||
| chr7:77777224 | G | A | 75 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(72): Show |
75 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.1794-1114G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777224 | |||||||
| chr7:77777249 | T | C | 1 | a0001c0002t0001g0306 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1794-1089T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777249 | |||||||
| chr7:77777422 | G | A | 187 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(184): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1794-916G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777422 | |||||||
| chr7:77777430 | G | A | 67 | a0001c0001t0002g0039 a0001c0001t0002g0051 a0001c0001t0002g0052 others(64): Show |
67 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1794-908G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777430 | |||||||
| chr7:77777642 | T | C | 1 | a0001c0002t0001g0228 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1794-696T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777642 | |||||||
| chr7:77777677 | T | C | 1 | a0001c0001t0011g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1794-661T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777677 | |||||||
| chr7:77777732 | A | G | 5 | a0001c0002t0001g0271 a0001c0002t0001g0276 a0001c0002t0001g0278 others(2): Show |
5 | HG03491.hp1 HG04115.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1794-606A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777732 | |||||||
| chr7:77778063 | A | G | 70 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(67): Show |
70 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.1794-275A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77778063 | |||||||
| chr7:77778089 | A | G | 1 | a0001c0001t0011g0074 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1794-249A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77778089 | |||||||
| chr7:77778239 | A | G | 62 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(59): Show |
63 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1794-99A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77778239 |