Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1620 |
| ensemblid | ENSG00000078725.13 |
| hgncid | 2687 |
| symbol | BRINP1 |
| name | BMP/retinoic acid inducible neural specific 1 |
| refseq_nuc | NM_014618.3 |
| refseq_prot | NP_055433.2 |
| ensembl_nuc | ENST00000265922.8 |
| ensembl_prot | ENSP00000265922.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 119166629 |
| end | 119369435 |
| strand | - |
| ver | v1.2 |
| region | chr9:119166629-119369435 |
| region5000 | chr9:119161629-119374435 |
| regionname0 | BRINP1_chr9_119166629_119369435 |
| regionname5000 | BRINP1_chr9_119161629_119374435 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 761 | 231 | 78 | 57 | 56 | 12 | 26 | 34 | BRINP1_chr9_119161629_119374435 | BRINP1 | MNWRF others(756): Show |
chr9 | 119161629 | 119374435 |
| a0002 | 0/0 | 761 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | MNWRF others(756): Show |
chr9 | 119161629 | 119374435 |
| a0003 | 0/0 | 761 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | MNWRF others(756): Show |
chr9 | 119161629 | 119374435 |
| a0004 | 0/0 | 761 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | MNWRF others(756): Show |
chr9 | 119161629 | 119374435 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2283 | 88 | 17 | 20 | 27 | 6 | 16 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0002 | 0/0 | 2283 | 70 | 7 | 21 | 27 | 5 | 10 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0003 | 0/0 | 2283 | 45 | 37 | 7 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0004 | 0/0 | 2283 | 10 | 7 | 3 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0005 | 0/0 | 2283 | 5 | 5 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0006 | 0/0 | 2283 | 5 | 4 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0007 | 0/0 | 2283 | 4 | 0 | 4 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0009 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0010 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0014 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0001c0015 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0002c0012 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0002c0013 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0003c0008 | 0/0 | 2283 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 | ||
| a0004c0011 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATGAA others(2278): Show |
chr9 | 119161629 | 119374435 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3171 | 75 | 12 | 18 | 24 | 6 | 15 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0001t0002 | 1/0 | 3171 | 6 | 5 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0001t0003 | 0/0 | 3171 | 3 | 0 | 2 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0001t0004 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0001t0005 | 0/0 | 3171 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0001t0009 | 0/1 | 3171 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0002t0001 | 0/0 | 3171 | 58 | 4 | 16 | 24 | 4 | 10 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0002t0002 | 0/0 | 3171 | 2 | 2 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0002t0003 | 0/0 | 3171 | 7 | 1 | 5 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0002t0004 | 0/0 | 3171 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0002t0006 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0003t0001 | 0/0 | 3171 | 36 | 29 | 6 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0003t0002 | 0/0 | 3171 | 7 | 6 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0003t0007 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0003t0008 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3196): Show |
chr9 | 119161629 | 119374435 |
| a0001c0004t0001 | 0/0 | 3171 | 9 | 6 | 3 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0004t0002 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0005t0001 | 0/0 | 3171 | 4 | 4 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0005t0002 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0006t0001 | 0/0 | 3171 | 4 | 3 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0006t0002 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0007t0001 | 0/0 | 3171 | 4 | 0 | 4 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0009t0001 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0010t0001 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0014t0003 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0001c0015t0001 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0002c0012t0001 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0002c0013t0003 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0003c0008t0001 | 0/0 | 3171 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| a0004c0011t0001 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | ATTCG others(3166): Show |
chr9 | 119161629 | 119374435 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0009g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0007t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0007t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0007t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0007t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0009t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0010t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0014t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0015t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0002c0012t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0002c0013t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0003c0008t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0003c0008t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0004c0011t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0012 | EUR | GBR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0028 | EUR | GBR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0103 | EUR | FIN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0116 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0180 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00738 | hp1 | a0001 | c0014 | t0003 | g0004 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0142 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0025 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0027 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01074 | hp2 | a0002 | c0012 | t0001 | g0062 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0030 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01099 | hp2 | a0001 | c0007 | t0001 | g0081 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01109 | hp1 | a0001 | c0003 | t0002 | g0232 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01169 | hp1 | a0001 | c0007 | t0001 | g0080 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0162 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01175 | hp2 | a0001 | c0007 | t0001 | g0051 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0181 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01255 | hp1 | a0001 | c0007 | t0001 | g0037 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01256 | hp1 | a0004 | c0011 | t0001 | g0123 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0205 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0164 | EUR | IBS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | IBS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0050 | EUR | IBS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01884 | hp1 | a0001 | c0003 | t0008 | g0212 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0206 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01891 | hp2 | a0001 | c0003 | t0007 | g0183 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0173 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0059 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02293 | hp1 | a0002 | c0013 | t0003 | g0006 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02523 | hp1 | a0001 | c0010 | t0001 | g0096 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0019 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0229 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0185 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0196 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02622 | hp1 | a0001 | c0006 | t0001 | g0017 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0208 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0207 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0186 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02886 | hp2 | a0001 | c0005 | t0002 | g0235 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0040 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02897 | hp1 | a0001 | c0006 | t0002 | g0224 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0039 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0226 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0083 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0044 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02970 | hp2 | a0001 | c0006 | t0001 | g0018 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02976 | hp1 | a0001 | c0004 | t0002 | g0231 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0188 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0120 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0041 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03195 | hp2 | a0001 | c0009 | t0001 | g0189 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0209 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0190 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03453 | hp2 | a0001 | c0005 | t0001 | g0197 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0073 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0211 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0222 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0199 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0092 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0167 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0225 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18612 | hp2 | a0003 | c0008 | t0001 | g0172 | EAS | CHB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | CHB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18747 | hp2 | a0003 | c0008 | t0001 | g0089 | EAS | CHB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19002 | hp1 | a0001 | c0002 | t0006 | g0013 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0221 | AFR | LWK | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0175 | AFR | LWK | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19070 | hp2 | a0001 | c0015 | t0001 | g0131 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0072 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0184 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0105 | AFR | ASW | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ASW | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01123 | hp1 | a0001 | c0006 | t0001 | g0020 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0191 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0071 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0227 | AFR | USA | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0149 | AFR | USA | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20300 | hp2 | a0001 | c0006 | t0001 | g0016 | AFR | USA | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | LWK | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0236 | REF | REF | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0223 | REF | REF | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:119208791 | C | T | 1 | a0002 | 2 | HG01074.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.1073G>A | p.Arg358His | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/8 | 1503/3171 | 1073/2286 | 358/761 | chr9 | 119208791 | |||
| chr9:119214069 | A | T | 1 | a0004 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.772T>A | p.Tyr258Asn | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/8 | 1202/3171 | 772/2286 | 258/761 | chr9 | 119214069 | |||
| chr9:119242167 | C | A | 1 | a0003 | 2 | NA18612.hp2 NA18747.hp2 |
missense_variant | MODERATE | c.459G>T | p.Lys153Asn | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/8 | 889/3171 | 459/2286 | 153/761 | chr9 | 119242167 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:119167297 | T | C | 4 | a0001c0003 a0001c0004 a0001c0009 others(1): Show |
57 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(54): Show |
synonymous_variant | LOW | c.2073A>G | p.Ser691Ser | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 2503/3171 | 2073/2286 | 691/761 | chr9 | 119167297 | |||
| chr9:119168029 | G | A | 2 | a0001c0007 a0001c0014 |
5 | HG00738.hp1 HG01099.hp2 HG01169.hp1 others(2): Show |
synonymous_variant | LOW | c.1341C>T | p.Cys447Cys | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 1771/3171 | 1341/2286 | 447/761 | chr9 | 119168029 | |||
| chr9:119168110 | C | T | 2 | a0001c0005 a0001c0006 |
10 | HG01123.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
synonymous_variant | LOW | c.1260G>A | p.Thr420Thr | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 1690/3171 | 1260/2286 | 420/761 | chr9 | 119168110 | |||
| chr9:119238677 | C | T | 1 | a0001c0010 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.663G>A | p.Thr221Thr | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/8 | 1093/3171 | 663/2286 | 221/761 | chr9 | 119238677 | |||
| chr9:119238722 | G | A | 7 | a0001c0002 a0001c0004 a0001c0006 others(4): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
synonymous_variant | LOW | c.618C>T | p.Ser206Ser | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/8 | 1048/3171 | 618/2286 | 206/761 | chr9 | 119238722 | |||
| chr9:119248994 | G | A | 1 | a0001c0015 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.375C>T | p.Tyr125Tyr | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/8 | 805/3171 | 375/2286 | 125/761 | chr9 | 119248994 | |||
| chr9:119249072 | C | T | 1 | a0001c0009 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.297G>A | p.Pro99Pro | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/8 | 727/3171 | 297/2286 | 99/761 | chr9 | 119249072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:119166650 | T | G | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0002t0004 |
5 | HG00423.hp1 HG02523.hp2 NA18969.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*434A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 434 | chr9 | 119166650 | ||||||
| chr9:119166767 | T | TTACAATT others(23): Show |
1 | a0001c0003t0008 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287_*316dupGAAGGG others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 316 | chr9 | 119166767 | ||||||
| chr9:119166783 | A | G | 1 | a0001c0003t0007 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 301 | chr9 | 119166783 | ||||||
| chr9:119167079 | C | T | 1 | a0001c0001t0005 | 2 | NA18993.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 5 | chr9 | 119167079 | ||||||
| chr9:119369093 | A | C | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
5_prime_UTR_variant | MODIFIER | c.-88T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/8 | 55738 | chr9 | 119369093 | ||||||
| chr9:119369203 | C | T | 1 | a0001c0002t0006 | 1 | NA19002.hp1 | 5_prime_UTR_variant | MODIFIER | c.-198G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/8 | 55848 | chr9 | 119369203 | ||||||
| chr9:119369328 | C | G | 4 | a0001c0001t0003 a0001c0002t0003 a0001c0014t0003 others(1): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-323G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/8 | 55973 | chr9 | 119369328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:119168303 | G | A | 40 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(37): Show |
40 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1146-79C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168303 | |||||||
| chr9:119168413 | C | G | 1 | a0001c0002t0001g0035 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1146-189G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168413 | |||||||
| chr9:119168495 | T | TG | 47 | a0001c0003t0001g0021 a0001c0003t0001g0030 a0001c0003t0001g0039 others(44): Show |
47 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1146-272dupC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168495 | |||||||
| chr9:119168600 | A | ATTGTAAA others(52): Show |
32 | a0001c0001t0001g0036 a0001c0001t0001g0066 a0001c0001t0001g0085 others(29): Show |
32 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.1146-435_1146-377d others(61): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168600 | |||||||
| chr9:119168742 | C | T | 3 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 |
3 | HG01243.hp1 HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1146-518G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168742 | |||||||
| chr9:119168892 | A | G | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-668T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168892 | |||||||
| chr9:119168924 | C | T | 1 | a0001c0002t0001g0216 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1146-700G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168924 | |||||||
| chr9:119168936 | G | T | 8 | a0001c0003t0001g0044 a0001c0003t0001g0046 a0001c0003t0001g0083 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1146-712C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168936 | |||||||
| chr9:119169120 | G | A | 6 | a0001c0003t0001g0030 a0001c0003t0001g0142 a0001c0003t0001g0164 others(3): Show |
6 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146-896C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169120 | |||||||
| chr9:119169150 | C | T | 1 | a0001c0003t0001g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1146-926G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169150 | |||||||
| chr9:119169154 | A | G | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-930T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169154 | |||||||
| chr9:119169191 | T | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0004c0011t0001g0123 |
3 | HG01256.hp1 HG01258.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1146-967A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169191 | |||||||
| chr9:119169254 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1146-1030C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169254 | |||||||
| chr9:119169277 | G | T | 1 | a0001c0004t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1146-1053C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169277 | |||||||
| chr9:119169351 | A | T | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1127T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169351 | |||||||
| chr9:119169363 | G | T | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1139C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169363 | |||||||
| chr9:119169368 | T | C | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1144A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169368 | |||||||
| chr9:119169371 | C | T | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1147G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169371 | |||||||
| chr9:119169398 | C | CCT | 32 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(29): Show |
32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-1175_1146-117 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169398 | |||||||
| chr9:119169400 | A | C | 32 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(29): Show |
32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-1176T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169400 | |||||||
| chr9:119169470 | C | G | 1 | a0001c0006t0002g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1146-1246G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169470 | |||||||
| chr9:119169471 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1146-1247C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169471 | |||||||
| chr9:119169510 | G | A | 159 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1146-1286C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169510 | |||||||
| chr9:119169543 | C | T | 33 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1146-1319G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169543 | |||||||
| chr9:119169560 | G | A | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1336C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169560 | |||||||
| chr9:119169600 | C | T | 1 | a0001c0002t0001g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1146-1376G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169600 | |||||||
| chr9:119169672 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1146-1448C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169672 | |||||||
| chr9:119169789 | C | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-1565G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169789 | |||||||
| chr9:119169858 | G | C | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1634C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169858 | |||||||
| chr9:119169864 | AG | A | 3 | a0001c0003t0001g0044 a0001c0003t0001g0046 a0001c0003t0001g0211 |
3 | HG02451.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1146-1641delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169864 | |||||||
| chr9:119169880 | G | C | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1656C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169880 | |||||||
| chr9:119169906 | T | C | 35 | a0001c0001t0002g0233 a0001c0003t0001g0021 a0001c0003t0001g0041 others(32): Show |
35 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1146-1682A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169906 | |||||||
| chr9:119169923 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1146-1699T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169923 | |||||||
| chr9:119169927 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1146-1703C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169927 | |||||||
| chr9:119169937 | AAACT | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-1717_1146-171 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169937 | |||||||
| chr9:119170064 | A | T | 33 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0045 others(30): Show |
33 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1146-1840T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170064 | |||||||
| chr9:119170074 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1146-1850G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170074 | |||||||
| chr9:119170113 | G | A | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-1889C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170113 | |||||||
| chr9:119170169 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1146-1945C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170169 | |||||||
| chr9:119170231 | A | G | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-2007T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170231 | |||||||
| chr9:119170246 | G | T | 1 | a0001c0002t0001g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1146-2022C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170246 | |||||||
| chr9:119170344 | C | G | 1 | a0001c0003t0007g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1146-2120G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170344 | |||||||
| chr9:119170351 | C | T | 32 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(29): Show |
32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-2127G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170351 | |||||||
| chr9:119170352 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0202 |
2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1146-2128C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170352 | |||||||
| chr9:119170357 | G | A | 1 | a0001c0003t0007g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1146-2133C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170357 | |||||||
| chr9:119170472 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-2248C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170472 | |||||||
| chr9:119170499 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1146-2275T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170499 | |||||||
| chr9:119170500 | T | C | 1 | a0002c0013t0003g0006 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1146-2276A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170500 | |||||||
| chr9:119170569 | C | T | 109 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1146-2345G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170569 | |||||||
| chr9:119170649 | T | C | 56 | a0001c0001t0001g0022 a0001c0001t0001g0052 a0001c0001t0001g0079 others(53): Show |
56 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1146-2425A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170649 | |||||||
| chr9:119170776 | A | G | 147 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1146-2552T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170776 | |||||||
| chr9:119170777 | G | A | 145 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1146-2553C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170777 | |||||||
| chr9:119170784 | C | T | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1146-2560G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170784 | |||||||
| chr9:119170785 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0003g0009 |
3 | HG00741.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1146-2561C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170785 | |||||||
| chr9:119170883 | G | A | 14 | a0001c0003t0001g0019 a0001c0003t0001g0039 a0001c0003t0001g0040 others(11): Show |
14 | HG01169.hp2 HG01243.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146-2659C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170883 | |||||||
| chr9:119170917 | A | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-2693T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170917 | |||||||
| chr9:119170934 | G | C | 2 | a0001c0001t0001g0144 a0001c0002t0001g0167 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1146-2710C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170934 | |||||||
| chr9:119170935 | A | C | 2 | a0001c0001t0001g0144 a0001c0002t0001g0167 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1146-2711T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170935 | |||||||
| chr9:119171005 | C | T | 10 | a0001c0003t0001g0019 a0001c0003t0001g0039 a0001c0003t0001g0040 others(7): Show |
10 | HG01169.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1146-2781G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171005 | |||||||
| chr9:119171006 | G | A | 32 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(29): Show |
32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-2782C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171006 | |||||||
| chr9:119171049 | A | G | 34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-2825T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171049 | |||||||
| chr9:119171052 | A | ACTAGAAA others(1): Show |
34 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-2836_1146-282 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171052 | |||||||
| chr9:119171078 | G | A | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1146-2854C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171078 | |||||||
| chr9:119171083 | A | G | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-2859T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171083 | |||||||
| chr9:119171087 | A | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0124 |
2 | HG01346.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1146-2863T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171087 | |||||||
| chr9:119171243 | T | C | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1146-3019A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171243 | |||||||
| chr9:119171489 | C | T | 6 | a0001c0003t0001g0030 a0001c0003t0001g0142 a0001c0003t0001g0164 others(3): Show |
6 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146-3265G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171489 | |||||||
| chr9:119171561 | T | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0170 a0001c0001t0001g0193 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146-3337A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171561 | |||||||
| chr9:119171614 | G | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0146 a0001c0001t0001g0150 others(1): Show |
4 | HG01975.hp1 HG01978.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-3390C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171614 | |||||||
| chr9:119171644 | T | G | 1 | a0001c0002t0002g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1146-3420A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171644 | |||||||
| chr9:119171736 | A | C | 29 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(26): Show |
29 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1146-3512T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171736 | |||||||
| chr9:119171738 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0136 |
2 | HG00423.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1146-3514G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171738 | |||||||
| chr9:119171799 | A | T | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-3575T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171799 | |||||||
| chr9:119171839 | T | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-3615A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171839 | |||||||
| chr9:119171981 | C | G | 1 | a0001c0002t0001g0166 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1146-3757G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171981 | |||||||
| chr9:119171986 | T | G | 3 | a0001c0002t0001g0166 a0001c0003t0001g0179 a0001c0003t0001g0180 |
3 | HG00639.hp2 HG00735.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1146-3762A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171986 | |||||||
| chr9:119171988 | C | T | 49 | a0001c0002t0001g0166 a0001c0003t0001g0019 a0001c0003t0001g0021 others(46): Show |
49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-3764G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171988 | |||||||
| chr9:119172013 | C | G | 170 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1146-3789G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172013 | |||||||
| chr9:119172049 | A | C | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1146-3825T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172049 | |||||||
| chr9:119172274 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0148 a0001c0002t0006g0013 |
3 | HG00438.hp2 HG01934.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1146-4050G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172274 | |||||||
| chr9:119172276 | CAATAAAA | C | 4 | a0001c0003t0001g0059 a0001c0003t0001g0072 a0001c0003t0001g0120 others(1): Show |
4 | HG02258.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-4059_1146-405 others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172276 | |||||||
| chr9:119172326 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4102T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172326 | |||||||
| chr9:119172349 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4125T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172349 | |||||||
| chr9:119172389 | G | T | 1 | a0001c0003t0001g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1146-4165C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172389 | |||||||
| chr9:119172476 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1146-4252C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172476 | |||||||
| chr9:119172610 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4386T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172610 | |||||||
| chr9:119172610 | A | T | 9 | a0001c0003t0001g0030 a0001c0003t0001g0142 a0001c0003t0001g0164 others(6): Show |
9 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1146-4386T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172610 | |||||||
| chr9:119172613 | C | T | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4389G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172613 | |||||||
| chr9:119172630 | A | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4406T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172630 | |||||||
| chr9:119172635 | G | A | 8 | a0001c0003t0001g0030 a0001c0003t0001g0142 a0001c0003t0001g0164 others(5): Show |
8 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1146-4411C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172635 | |||||||
| chr9:119172661 | A | G | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1146-4437T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172661 | |||||||
| chr9:119172718 | T | C | 44 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0021 others(41): Show |
44 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1146-4494A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172718 | |||||||
| chr9:119172784 | C | T | 3 | a0001c0003t0001g0178 a0001c0003t0001g0179 a0001c0003t0001g0180 |
3 | HG00639.hp2 HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1146-4560G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172784 | |||||||
| chr9:119172806 | C | G | 3 | a0001c0003t0001g0021 a0001c0003t0001g0179 a0001c0003t0001g0180 |
3 | HG00639.hp2 HG00735.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1146-4582G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172806 | |||||||
| chr9:119172807 | A | G | 49 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0021 others(46): Show |
49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-4583T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172807 | |||||||
| chr9:119172861 | A | AGGGAAC | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4638_1146-463 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172861 | |||||||
| chr9:119172864 | G | A | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4640C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172864 | |||||||
| chr9:119172865 | A | T | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4641T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172865 | |||||||
| chr9:119172871 | A | AACAAT | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4648_1146-464 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172871 | |||||||
| chr9:119172895 | C | A | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4671G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172895 | |||||||
| chr9:119172902 | G | A | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4678C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172902 | |||||||
| chr9:119172910 | A | G | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4686T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172910 | |||||||
| chr9:119172930 | C | A | 9 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0001g0179 others(6): Show |
9 | HG00639.hp2 HG00735.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1146-4706G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172930 | |||||||
| chr9:119172932 | C | T | 3 | a0001c0003t0001g0019 a0001c0004t0001g0162 a0001c0004t0001g0175 |
3 | HG01169.hp2 HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1146-4708G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172932 | |||||||
| chr9:119172933 | C | G | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4709G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172933 | |||||||
| chr9:119172935 | T | G | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1146-4711A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172935 | |||||||
| chr9:119172942 | T | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4718A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172942 | |||||||
| chr9:119172980 | T | C | 10 | a0001c0003t0001g0019 a0001c0003t0001g0039 a0001c0003t0001g0040 others(7): Show |
10 | HG01169.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1146-4756A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172980 | |||||||
| chr9:119172997 | C | T | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4773G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172997 | |||||||
| chr9:119173000 | C | T | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4776G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173000 | |||||||
| chr9:119173019 | G | A | 153 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1146-4795C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173019 | |||||||
| chr9:119173290 | G | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5066C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173290 | |||||||
| chr9:119173336 | C | T | 5 | a0001c0003t0001g0092 a0001c0003t0001g0184 a0001c0003t0002g0225 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146-5112G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173336 | |||||||
| chr9:119173454 | C | T | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5230G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173454 | |||||||
| chr9:119173471 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1146-5247A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173471 | |||||||
| chr9:119173538 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5314T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173538 | |||||||
| chr9:119173570 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1146-5346C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173570 | |||||||
| chr9:119173651 | C | A | 165 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1146-5427G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173651 | |||||||
| chr9:119173668 | G | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5444C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173668 | |||||||
| chr9:119173679 | G | A | 3 | a0001c0001t0001g0161 a0001c0003t0001g0179 a0001c0003t0001g0180 |
3 | HG00639.hp2 HG00735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1146-5455C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173679 | |||||||
| chr9:119173713 | G | T | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5489C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173713 | |||||||
| chr9:119173837 | G | A | 10 | a0001c0005t0001g0190 a0001c0005t0001g0197 a0001c0005t0001g0199 others(7): Show |
10 | HG01123.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1146-5613C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173837 | |||||||
| chr9:119173903 | A | G | 21 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0063 others(18): Show |
21 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1146-5679T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173903 | |||||||
| chr9:119173906 | T | TAATA | 70 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0043 others(67): Show |
70 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1146-5683_1146-568 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173906 | |||||||
| chr9:119173913 | G | T | 1 | a0001c0007t0001g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1146-5689C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173913 | |||||||
| chr9:119173967 | C | T | 4 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(1): Show |
4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-5743G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173967 | |||||||
| chr9:119174008 | A | C | 6 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146-5784T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174008 | |||||||
| chr9:119174010 | C | T | 7 | a0001c0001t0001g0156 a0001c0002t0001g0200 a0001c0002t0001g0201 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1146-5786G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174010 | |||||||
| chr9:119174017 | C | CCTAAAAC others(15): Show |
127 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0036 others(124): Show |
127 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1146-5794_1146-579 others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174017 | |||||||
| chr9:119174052 | G | A | 4 | a0001c0001t0002g0218 a0001c0001t0002g0228 a0001c0003t0001g0179 others(1): Show |
4 | HG00639.hp2 HG00735.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-5828C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174052 | |||||||
| chr9:119174096 | T | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5872A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174096 | |||||||
| chr9:119174110 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5886T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174110 | |||||||
| chr9:119174121 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1146-5897G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174121 | |||||||
| chr9:119174347 | C | T | 17 | a0001c0003t0001g0041 a0001c0003t0001g0059 a0001c0003t0001g0072 others(14): Show |
17 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1146-6123G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174347 | |||||||
| chr9:119174358 | A | G | 49 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0021 others(46): Show |
49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-6134T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174358 | |||||||
| chr9:119174550 | G | T | 232 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(229): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1146-6326C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174550 | |||||||
| chr9:119174560 | A | G | 49 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0021 others(46): Show |
49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-6336T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174560 | |||||||
| chr9:119174647 | G | T | 34 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0045 others(31): Show |
34 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.1146-6423C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174647 | |||||||
| chr9:119174680 | C | T | 3 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0009t0001g0189 |
3 | HG02809.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1146-6456G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174680 | |||||||
| chr9:119174739 | T | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-6515A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174739 | |||||||
| chr9:119174835 | G | T | 57 | a0001c0001t0001g0043 a0001c0001t0002g0218 a0001c0001t0002g0228 others(54): Show |
57 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.1146-6611C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174835 | |||||||
| chr9:119174853 | C | A | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-6629G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174853 | |||||||
| chr9:119174861 | G | A | 3 | a0001c0003t0001g0191 a0001c0003t0002g0222 a0001c0004t0001g0014 |
3 | HG02109.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1146-6637C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174861 | |||||||
| chr9:119174861 | G | T | 3 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0009t0001g0189 |
3 | HG02809.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1146-6637C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174861 | |||||||
| chr9:119174884 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1146-6660C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174884 | |||||||
| chr9:119175005 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-6781T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175005 | |||||||
| chr9:119175049 | A | G | 49 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0021 others(46): Show |
49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-6825T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175049 | |||||||
| chr9:119175106 | TTAAAG | T | 80 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0036 others(77): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1146-6887_1146-688 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175106 | |||||||
| chr9:119175111 | G | A | 2 | a0001c0001t0005g0213 a0001c0001t0005g0215 |
2 | NA18993.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1146-6887C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175111 | |||||||
| chr9:119175113 | AAAG | A | 4 | a0001c0002t0006g0013 a0001c0003t0001g0176 a0001c0003t0002g0221 others(1): Show |
4 | HG06807.hp1 NA18906.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-6892_1146-689 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175113 | |||||||
| chr9:119175114 | A | T | 13 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0039 others(10): Show |
13 | HG01169.hp2 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1146-6890T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175114 | |||||||
| chr9:119175115 | AGTAT | A | 13 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0039 others(10): Show |
13 | HG01169.hp2 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1146-6895_1146-689 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175115 | |||||||
| chr9:119175119 | T | A | 5 | a0001c0003t0001g0176 a0001c0003t0002g0221 a0001c0003t0002g0227 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146-6895A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175119 | |||||||
| chr9:119175119 | T | TA | 31 | a0001c0003t0001g0021 a0001c0003t0001g0044 a0001c0003t0001g0046 others(28): Show |
31 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1146-6896dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175119 | |||||||
| chr9:119175119 | TA | T | 7 | a0001c0003t0001g0030 a0001c0003t0001g0142 a0001c0003t0001g0164 others(4): Show |
7 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-6896delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175119 | |||||||
| chr9:119175120 | A | AGTAT | 2 | a0001c0004t0001g0025 a0001c0004t0001g0027 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1146-6897_1146-689 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175120 | |||||||
| chr9:119175121 | AAAAAAAA others(7): Show |
A | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-6911_1146-689 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175121 | |||||||
| chr9:119175135 | C | CA | 11 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0002t0001g0023 others(8): Show |
11 | HG00280.hp1 HG01169.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1146-6912dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175135 | |||||||
| chr9:119175217 | C | G | 47 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0021 others(44): Show |
47 | HG01109.hp1 HG01169.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1146-6993G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175217 | |||||||
| chr9:119175228 | T | G | 46 | a0001c0003t0001g0019 a0001c0003t0001g0021 a0001c0003t0001g0039 others(43): Show |
46 | HG01109.hp1 HG01169.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.1146-7004A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175228 | |||||||
| chr9:119175237 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-7013T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175237 | |||||||
| chr9:119175472 | TAACA | T | 2 | a0001c0003t0001g0030 a0001c0003t0002g0227 |
2 | HG01099.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1146-7252_1146-724 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175472 | |||||||
| chr9:119175493 | A | T | 32 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(29): Show |
32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-7269T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175493 | |||||||
| chr9:119175712 | C | A | 6 | a0001c0003t0001g0030 a0001c0003t0001g0142 a0001c0003t0001g0164 others(3): Show |
6 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146-7488G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175712 | |||||||
| chr9:119176103 | T | C | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-7879A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119176103 | |||||||
| chr9:119176857 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1146-8633G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119176857 | |||||||
| chr9:119176893 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1146-8669T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119176893 | |||||||
| chr9:119177163 | T | C | 1 | a0001c0002t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1146-8939A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177163 | |||||||
| chr9:119177321 | G | A | 2 | a0001c0002t0001g0153 a0001c0002t0003g0003 |
2 | HG01070.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1146-9097C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177321 | |||||||
| chr9:119177393 | G | A | 9 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0002t0001g0153 others(6): Show |
9 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1146-9169C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177393 | |||||||
| chr9:119177549 | A | C | 1 | a0001c0002t0001g0152 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1146-9325T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177549 | |||||||
| chr9:119177564 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1146-9340C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177564 | |||||||
| chr9:119177750 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1146-9526G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177750 | |||||||
| chr9:119177935 | T | C | 32 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(29): Show |
32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-9711A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177935 | |||||||
| chr9:119178212 | G | T | 173 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1146-9988C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178212 | |||||||
| chr9:119178318 | G | A | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1146-10094C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178318 | |||||||
| chr9:119178399 | G | T | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-10175C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178399 | |||||||
| chr9:119178425 | T | TTG | 3 | a0001c0002t0001g0143 a0001c0002t0001g0147 a0001c0002t0001g0216 |
3 | NA18948.hp2 NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1146-10203_1146-10 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178425 | |||||||
| chr9:119178538 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-10314T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178538 | |||||||
| chr9:119178785 | G | C | 42 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0044 others(39): Show |
42 | HG01109.hp1 HG01123.hp1 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.1146-10561C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178785 | |||||||
| chr9:119178885 | G | GAAAT | 4 | a0001c0003t0001g0059 a0001c0003t0001g0072 a0001c0003t0001g0120 others(1): Show |
4 | HG02258.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-10665_1146-10 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178885 | |||||||
| chr9:119179251 | C | T | 1 | a0001c0003t0002g0227 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1146-11027G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179251 | |||||||
| chr9:119179332 | G | A | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1146-11108C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179332 | |||||||
| chr9:119179343 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-11119C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179343 | |||||||
| chr9:119179356 | G | A | 4 | a0001c0003t0001g0059 a0001c0003t0001g0072 a0001c0003t0001g0120 others(1): Show |
4 | HG02258.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-11132C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179356 | |||||||
| chr9:119179366 | G | A | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1146-11142C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179366 | |||||||
| chr9:119179542 | G | C | 1 | a0001c0003t0001g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1146-11318C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179542 | |||||||
| chr9:119180132 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1146-11908C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180132 | |||||||
| chr9:119180247 | A | C | 3 | a0001c0003t0001g0059 a0001c0003t0001g0072 a0001c0003t0001g0120 |
3 | HG02258.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1146-12023T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180247 | |||||||
| chr9:119180364 | C | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0198 others(1): Show |
4 | HG02145.hp1 HG02486.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-12140G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180364 | |||||||
| chr9:119180441 | CTGTTCTT others(6): Show |
C | 1 | a0001c0002t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1146-12230_1146-12 others(19): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180441 | |||||||
| chr9:119180473 | CTGTGCAT others(1): Show |
C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-12257_1146-12 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180473 | |||||||
| chr9:119180478 | CATGTGTG others(1): Show |
C | 4 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(1): Show |
4 | HG01169.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-12262_1146-12 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180478 | |||||||
| chr9:119180478 | CATGTGTG others(3): Show |
C | 17 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0030 others(14): Show |
17 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1146-12264_1146-12 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180478 | |||||||
| chr9:119180478 | CATGTGTG others(5): Show |
C | 29 | a0001c0003t0001g0021 a0001c0003t0001g0041 a0001c0003t0001g0059 others(26): Show |
29 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1146-12266_1146-12 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180478 | |||||||
| chr9:119180479 | A | ATG | 7 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0106 others(4): Show |
7 | HG00280.hp1 HG01175.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1146-12257_1146-12 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | |||||||
| chr9:119180479 | ATG | A | 25 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(22): Show |
25 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1146-12257_1146-12 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | |||||||
| chr9:119180479 | ATGTG | A | 60 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0047 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1146-12259_1146-12 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | |||||||
| chr9:119180479 | ATGTGTG | A | 12 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0054 others(9): Show |
12 | HG00280.hp2 HG01255.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1146-12261_1146-12 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | |||||||
| chr9:119180479 | ATGTGTGT others(1): Show |
A | 4 | a0001c0001t0002g0218 a0001c0001t0002g0228 a0001c0002t0001g0035 others(1): Show |
4 | HG01358.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-12263_1146-12 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | |||||||
| chr9:119180479 | ATGTGTGT others(3): Show |
A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0198 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1146-12265_1146-12 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | |||||||
| chr9:119180479 | ATGTGTGT others(5): Show |
A | 10 | a0001c0001t0001g0151 a0001c0005t0001g0190 a0001c0005t0001g0199 others(7): Show |
10 | HG01123.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1146-12267_1146-12 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | |||||||
| chr9:119180482 | T | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-12258A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180482 | |||||||
| chr9:119180545 | T | C | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1146-12321A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180545 | |||||||
| chr9:119180581 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1146-12357G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180581 | |||||||
| chr9:119180647 | C | A | 1 | a0001c0007t0001g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1146-12423G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180647 | |||||||
| chr9:119180712 | C | T | 5 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(2): Show |
5 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146-12488G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180712 | |||||||
| chr9:119181122 | C | T | 1 | a0001c0002t0001g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1146-12898G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181122 | |||||||
| chr9:119181156 | C | T | 1 | a0001c0003t0002g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1146-12932G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181156 | |||||||
| chr9:119181192 | G | A | 1 | a0001c0003t0002g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1146-12968C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181192 | |||||||
| chr9:119181209 | A | G | 1 | a0002c0013t0003g0006 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1146-12985T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181209 | |||||||
| chr9:119181358 | G | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-13134C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181358 | |||||||
| chr9:119181495 | C | T | 1 | a0001c0003t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1146-13271G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181495 | |||||||
| chr9:119181714 | C | T | 7 | a0001c0003t0001g0019 a0001c0003t0001g0176 a0001c0003t0002g0221 others(4): Show |
7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-13490G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181714 | |||||||
| chr9:119182292 | G | A | 4 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0003t0001g0030 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-14068C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182292 | |||||||
| chr9:119182500 | G | T | 3 | a0001c0003t0001g0191 a0001c0003t0002g0222 a0001c0004t0001g0014 |
3 | HG02109.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1146-14276C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182500 | |||||||
| chr9:119182529 | G | A | 1 | a0001c0003t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1146-14305C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182529 | |||||||
| chr9:119182562 | T | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-14338A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182562 | |||||||
| chr9:119182747 | T | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-14523A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182747 | |||||||
| chr9:119182795 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1146-14571G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182795 | |||||||
| chr9:119182970 | C | G | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-14746G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182970 | |||||||
| chr9:119183037 | G | A | 2 | a0001c0003t0002g0222 a0001c0004t0001g0014 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1146-14813C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183037 | |||||||
| chr9:119183228 | T | A | 1 | a0001c0001t0001g0151 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1146-15004A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183228 | |||||||
| chr9:119183339 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1146-15115T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183339 | |||||||
| chr9:119183497 | C | T | 2 | a0001c0001t0001g0168 a0001c0002t0001g0112 |
2 | HG00544.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1146-15273G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183497 | |||||||
| chr9:119183615 | C | G | 1 | a0001c0010t0001g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1146-15391G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183615 | |||||||
| chr9:119183730 | A | G | 2 | a0001c0003t0001g0184 a0001c0003t0002g0232 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1146-15506T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183730 | |||||||
| chr9:119183745 | T | A | 1 | a0001c0004t0001g0162 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1146-15521A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183745 | |||||||
| chr9:119183912 | T | C | 1 | a0001c0002t0001g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1146-15688A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183912 | |||||||
| chr9:119184159 | A | G | 8 | a0001c0002t0001g0078 a0001c0003t0001g0030 a0001c0003t0001g0164 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1146-15935T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184159 | |||||||
| chr9:119184189 | T | A | 4 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-15965A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184189 | |||||||
| chr9:119184232 | G | C | 64 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0066 others(61): Show |
64 | HG00140.hp1 HG00544.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1146-16008C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184232 | |||||||
| chr9:119184382 | G | A | 3 | a0001c0003t0001g0207 a0001c0004t0001g0015 a0001c0004t0002g0231 |
3 | HG02717.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1146-16158C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184382 | |||||||
| chr9:119184387 | G | A | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-16163C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184387 | |||||||
| chr9:119184458 | G | A | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1146-16234C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184458 | |||||||
| chr9:119184537 | A | G | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1146-16313T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184537 | |||||||
| chr9:119184736 | A | G | 14 | a0001c0001t0002g0218 a0001c0001t0002g0228 a0001c0003t0001g0041 others(11): Show |
14 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146-16512T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184736 | |||||||
| chr9:119184749 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1146-16525A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184749 | |||||||
| chr9:119184765 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-16541T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184765 | |||||||
| chr9:119184936 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1146-16712G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184936 | |||||||
| chr9:119184944 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1146-16720T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184944 | |||||||
| chr9:119184984 | G | T | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-16760C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184984 | |||||||
| chr9:119185085 | G | A | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1146-16861C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185085 | |||||||
| chr9:119185190 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-16966T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185190 | |||||||
| chr9:119185345 | T | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-17121A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185345 | |||||||
| chr9:119185447 | G | A | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-17223C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185447 | |||||||
| chr9:119185585 | C | T | 2 | a0001c0001t0001g0165 a0001c0002t0001g0056 |
2 | HG02683.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1146-17361G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185585 | |||||||
| chr9:119185700 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1146-17476C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185700 | |||||||
| chr9:119185708 | T | A | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-17484A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185708 | |||||||
| chr9:119185766 | C | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0054 others(11): Show |
14 | HG00099.hp1 HG01074.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1146-17542G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185766 | |||||||
| chr9:119185773 | T | C | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-17549A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185773 | |||||||
| chr9:119185841 | C | T | 4 | a0001c0003t0001g0187 a0001c0003t0001g0191 a0001c0003t0001g0195 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-17617G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185841 | |||||||
| chr9:119185963 | T | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-17739A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185963 | |||||||
| chr9:119186506 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1146-18282G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119186506 | |||||||
| chr9:119186846 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1146-18622G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119186846 | |||||||
| chr9:119186853 | G | A | 1 | a0001c0002t0001g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1146-18629C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119186853 | |||||||
| chr9:119186859 | G | T | 2 | a0001c0003t0001g0164 a0001c0010t0001g0096 |
2 | HG01515.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1146-18635C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119186859 | |||||||
| chr9:119187029 | T | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0054 others(11): Show |
14 | HG00099.hp1 HG01074.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1146-18805A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187029 | |||||||
| chr9:119187062 | G | C | 1 | a0001c0010t0001g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1146-18838C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187062 | |||||||
| chr9:119187117 | T | G | 4 | a0001c0003t0001g0187 a0001c0003t0001g0191 a0001c0003t0001g0195 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-18893A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187117 | |||||||
| chr9:119187144 | G | A | 1 | a0001c0003t0002g0227 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1146-18920C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187144 | |||||||
| chr9:119187483 | T | C | 1 | a0001c0003t0001g0092 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1146-19259A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187483 | |||||||
| chr9:119187566 | CTT | C | 25 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0198 others(22): Show |
25 | HG01109.hp1 HG01169.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.1146-19344_1146-19 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187566 | |||||||
| chr9:119187627 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0107 |
2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1146-19403A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187627 | |||||||
| chr9:119187949 | T | A | 2 | a0001c0003t0001g0191 a0001c0003t0001g0209 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1146-19725A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187949 | |||||||
| chr9:119188137 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1146-19913C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188137 | |||||||
| chr9:119188189 | AC | A | 37 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0053 others(34): Show |
37 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1146-19966delG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188189 | |||||||
| chr9:119188196 | C | T | 1 | a0001c0001t0002g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1146-19972G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188196 | |||||||
| chr9:119188242 | A | G | 3 | a0001c0003t0001g0207 a0001c0005t0001g0190 a0001c0005t0001g0208 |
3 | HG02622.hp2 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1146-20018T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188242 | |||||||
| chr9:119188300 | T | A | 1 | a0001c0002t0001g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1146-20076A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188300 | |||||||
| chr9:119188443 | T | G | 5 | a0001c0003t0001g0187 a0001c0003t0001g0191 a0001c0003t0001g0195 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146-20219A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188443 | |||||||
| chr9:119188771 | G | A | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1145+19948C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188771 | |||||||
| chr9:119189072 | A | G | 5 | a0001c0003t0001g0187 a0001c0003t0001g0191 a0001c0003t0001g0195 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1145+19647T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189072 | |||||||
| chr9:119189100 | A | G | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1145+19619T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189100 | |||||||
| chr9:119189214 | C | T | 83 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0042 others(80): Show |
83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+19505G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189214 | |||||||
| chr9:119189341 | A | G | 180 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1145+19378T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189341 | |||||||
| chr9:119189374 | G | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0107 |
3 | HG00735.hp1 HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1145+19345C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189374 | |||||||
| chr9:119189691 | A | C | 1 | a0001c0002t0001g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1145+19028T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189691 | |||||||
| chr9:119189735 | C | T | 83 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0042 others(80): Show |
83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+18984G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189735 | |||||||
| chr9:119190058 | T | C | 31 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0198 others(28): Show |
31 | HG01109.hp1 HG01169.hp2 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.1145+18661A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190058 | |||||||
| chr9:119190143 | A | T | 7 | a0001c0003t0001g0207 a0001c0005t0001g0190 a0001c0005t0001g0197 others(4): Show |
7 | HG02622.hp2 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145+18576T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190143 | |||||||
| chr9:119190185 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1145+18534C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190185 | |||||||
| chr9:119190412 | T | TA | 8 | a0001c0003t0001g0041 a0001c0003t0001g0059 a0001c0003t0001g0072 others(5): Show |
8 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1145+18306dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190412 | |||||||
| chr9:119190412 | TA | T | 51 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0045 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1145+18306delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190412 | |||||||
| chr9:119190427 | T | A | 8 | a0001c0003t0001g0041 a0001c0003t0001g0059 a0001c0003t0001g0072 others(5): Show |
8 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1145+18292A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190427 | |||||||
| chr9:119190568 | C | A | 1 | a0001c0003t0001g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1145+18151G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190568 | |||||||
| chr9:119190649 | A | C | 1 | a0001c0003t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1145+18070T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190649 | |||||||
| chr9:119191154 | A | G | 1 | a0001c0003t0002g0227 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1145+17565T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191154 | |||||||
| chr9:119191294 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1145+17425G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191294 | |||||||
| chr9:119191323 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1145+17396A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191323 | |||||||
| chr9:119191349 | C | G | 1 | a0001c0002t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1145+17370G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191349 | |||||||
| chr9:119191491 | C | A | 5 | a0001c0003t0001g0187 a0001c0003t0001g0191 a0001c0003t0001g0195 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1145+17228G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191491 | |||||||
| chr9:119191561 | G | A | 1 | a0001c0003t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1145+17158C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191561 | |||||||
| chr9:119191668 | T | G | 1 | a0001c0002t0004g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1145+17051A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191668 | |||||||
| chr9:119191786 | G | A | 26 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0198 others(23): Show |
26 | HG01109.hp1 HG01169.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.1145+16933C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191786 | |||||||
| chr9:119191800 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1145+16919C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191800 | |||||||
| chr9:119191922 | C | G | 8 | a0001c0003t0001g0083 a0001c0003t0001g0179 a0001c0003t0001g0180 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1145+16797G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191922 | |||||||
| chr9:119192140 | C | A | 3 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0009t0001g0189 |
3 | HG02809.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1145+16579G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192140 | |||||||
| chr9:119192145 | A | G | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1145+16574T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192145 | |||||||
| chr9:119192176 | C | T | 2 | a0001c0002t0001g0147 a0001c0002t0001g0216 |
2 | NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1145+16543G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192176 | |||||||
| chr9:119192193 | G | T | 7 | a0001c0003t0001g0092 a0001c0003t0001g0184 a0001c0003t0002g0225 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145+16526C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192193 | |||||||
| chr9:119192410 | C | T | 83 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0042 others(80): Show |
83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+16309G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192410 | |||||||
| chr9:119192415 | C | T | 16 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0198 others(13): Show |
16 | HG01109.hp1 HG01169.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1145+16304G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192415 | |||||||
| chr9:119192616 | G | A | 83 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0042 others(80): Show |
83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+16103C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192616 | |||||||
| chr9:119192640 | A | T | 83 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0042 others(80): Show |
83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+16079T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192640 | |||||||
| chr9:119192676 | A | G | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1145+16043T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192676 | |||||||
| chr9:119192837 | G | A | 1 | a0001c0014t0003g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1145+15882C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192837 | |||||||
| chr9:119192933 | C | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1145+15786G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192933 | |||||||
| chr9:119193044 | A | C | 1 | a0001c0002t0001g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1145+15675T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193044 | |||||||
| chr9:119193052 | T | C | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1145+15667A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193052 | |||||||
| chr9:119193147 | A | T | 5 | a0001c0003t0001g0187 a0001c0003t0001g0191 a0001c0003t0001g0195 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1145+15572T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193147 | |||||||
| chr9:119193296 | T | C | 7 | a0001c0001t0001g0210 a0001c0002t0001g0200 a0001c0002t0001g0201 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145+15423A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193296 | |||||||
| chr9:119193566 | G | A | 81 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0042 others(78): Show |
81 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1145+15153C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193566 | |||||||
| chr9:119193653 | T | C | 1 | a0001c0002t0001g0024 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1145+15066A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193653 | |||||||
| chr9:119193731 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1145+14988C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193731 | |||||||
| chr9:119193798 | G | A | 81 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0042 others(78): Show |
81 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1145+14921C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193798 | |||||||
| chr9:119194271 | A | G | 31 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0053 others(28): Show |
31 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1145+14448T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194271 | |||||||
| chr9:119194557 | G | A | 1 | a0001c0003t0002g0226 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1145+14162C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194557 | |||||||
| chr9:119194709 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1145+14010G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194709 | |||||||
| chr9:119194761 | T | C | 3 | a0001c0002t0001g0023 a0001c0002t0001g0074 a0001c0002t0001g0125 |
3 | HG02698.hp1 HG03239.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1145+13958A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194761 | |||||||
| chr9:119194809 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1145+13910G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194809 | |||||||
| chr9:119194851 | C | T | 1 | a0001c0003t0002g0227 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1145+13868G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194851 | |||||||
| chr9:119195067 | T | A | 1 | a0001c0002t0004g0029 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1145+13652A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119195067 | |||||||
| chr9:119195169 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1145+13550C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119195169 | |||||||
| chr9:119195328 | T | G | 24 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0198 others(21): Show |
24 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1145+13391A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119195328 | |||||||
| chr9:119195702 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1145+13017G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119195702 | |||||||
| chr9:119196164 | A | G | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0003t0001g0209 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145+12555T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119196164 | |||||||
| chr9:119196639 | C | G | 51 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0031 others(48): Show |
51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+12080G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119196639 | |||||||
| chr9:119196882 | G | A | 2 | a0001c0003t0001g0105 a0001c0003t0001g0137 |
2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1145+11837C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119196882 | |||||||
| chr9:119197088 | G | A | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1145+11631C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197088 | |||||||
| chr9:119197262 | G | A | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1145+11457C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197262 | |||||||
| chr9:119197292 | C | T | 3 | a0001c0004t0001g0025 a0001c0004t0001g0027 a0001c0004t0001g0071 |
3 | HG01069.hp1 HG01071.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1145+11427G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197292 | |||||||
| chr9:119197473 | A | G | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1145+11246T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197473 | |||||||
| chr9:119197710 | C | CAT | 197 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(194): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1145+11008_1145+11 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197710 | |||||||
| chr9:119197759 | G | A | 5 | a0001c0001t0002g0234 a0001c0003t0001g0041 a0001c0003t0001g0059 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+10960C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197759 | |||||||
| chr9:119197785 | G | A | 7 | a0001c0003t0001g0207 a0001c0003t0002g0221 a0001c0003t0008g0212 others(4): Show |
7 | HG01884.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145+10934C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197785 | |||||||
| chr9:119198236 | G | A | 1 | a0001c0003t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1145+10483C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198236 | |||||||
| chr9:119198382 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1145+10337G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198382 | |||||||
| chr9:119198473 | T | C | 1 | a0001c0003t0002g0232 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1145+10246A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198473 | |||||||
| chr9:119198484 | A | G | 6 | a0001c0002t0001g0091 a0001c0004t0001g0014 a0001c0004t0001g0015 others(3): Show |
6 | HG01169.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145+10235T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198484 | |||||||
| chr9:119198556 | G | A | 1 | a0001c0003t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1145+10163C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198556 | |||||||
| chr9:119198579 | A | C | 7 | a0001c0003t0001g0207 a0001c0003t0002g0221 a0001c0003t0008g0212 others(4): Show |
7 | HG01884.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145+10140T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198579 | |||||||
| chr9:119198672 | ATT | A | 154 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0060 others(151): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1145+10045_1145+10 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198672 | |||||||
| chr9:119198672 | ATTT | A | 35 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(32): Show |
35 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1145+10044_1145+10 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198672 | |||||||
| chr9:119198681 | T | A | 51 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0031 others(48): Show |
51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+10038A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198681 | |||||||
| chr9:119198721 | G | C | 1 | a0001c0002t0001g0200 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1145+9998C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198721 | |||||||
| chr9:119198806 | G | A | 1 | a0001c0003t0002g0232 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1145+9913C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198806 | |||||||
| chr9:119198893 | G | T | 32 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(29): Show |
32 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1145+9826C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198893 | |||||||
| chr9:119198961 | C | T | 1 | a0001c0002t0001g0194 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1145+9758G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198961 | |||||||
| chr9:119199346 | C | T | 38 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(35): Show |
38 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.1145+9373G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199346 | |||||||
| chr9:119199618 | G | A | 25 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0198 others(22): Show |
25 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1145+9101C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199618 | |||||||
| chr9:119199749 | G | A | 2 | a0003c0008t0001g0089 a0003c0008t0001g0172 |
2 | NA18612.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1145+8970C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199749 | |||||||
| chr9:119199762 | T | C | 34 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(31): Show |
34 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1145+8957A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199762 | |||||||
| chr9:119199796 | T | C | 19 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1145+8923A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199796 | |||||||
| chr9:119199800 | C | CT | 185 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1145+8918dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199800 | |||||||
| chr9:119199800 | C | CTT | 8 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(5): Show |
8 | HG01884.hp1 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1145+8917_1145+891 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199800 | |||||||
| chr9:119200241 | G | A | 1 | a0001c0003t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1145+8478C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200241 | |||||||
| chr9:119200292 | C | T | 44 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(41): Show |
44 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1145+8427G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200292 | |||||||
| chr9:119200389 | A | C | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1145+8330T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200389 | |||||||
| chr9:119200612 | G | A | 145 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1145+8107C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200612 | |||||||
| chr9:119200620 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1145+8099G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200620 | |||||||
| chr9:119200636 | G | GA | 93 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1145+8082dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200636 | |||||||
| chr9:119200636 | GA | G | 25 | a0001c0001t0001g0170 a0001c0001t0001g0193 a0001c0001t0001g0202 others(22): Show |
25 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1145+8082delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200636 | |||||||
| chr9:119200648 | AAAG | A | 5 | a0001c0001t0002g0234 a0001c0003t0001g0041 a0001c0003t0001g0059 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+8068_1145+807 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200648 | |||||||
| chr9:119200710 | T | C | 2 | a0001c0002t0001g0074 a0001c0002t0001g0125 |
2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1145+8009A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200710 | |||||||
| chr9:119200731 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1145+7988C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200731 | |||||||
| chr9:119200918 | G | A | 6 | a0001c0002t0001g0091 a0001c0004t0001g0014 a0001c0004t0001g0015 others(3): Show |
6 | HG01169.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145+7801C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200918 | |||||||
| chr9:119200921 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1145+7798T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200921 | |||||||
| chr9:119200936 | A | G | 194 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1145+7783T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200936 | |||||||
| chr9:119201244 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1145+7475G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119201244 | |||||||
| chr9:119201304 | A | G | 1 | a0001c0002t0001g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1145+7415T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119201304 | |||||||
| chr9:119202136 | A | G | 7 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(4): Show |
7 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145+6583T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202136 | |||||||
| chr9:119202196 | G | T | 10 | a0001c0001t0002g0218 a0001c0001t0002g0228 a0001c0003t0001g0207 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1145+6523C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202196 | |||||||
| chr9:119202413 | A | G | 2 | a0001c0003t0001g0072 a0001c0003t0001g0120 |
2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1145+6306T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202413 | |||||||
| chr9:119202572 | T | C | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1145+6147A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202572 | |||||||
| chr9:119202574 | C | A | 2 | a0001c0001t0002g0233 a0001c0003t0002g0227 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1145+6145G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202574 | |||||||
| chr9:119202670 | G | A | 23 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(20): Show |
23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+6049C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202670 | |||||||
| chr9:119202751 | C | T | 51 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0031 others(48): Show |
51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+5968G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202751 | |||||||
| chr9:119202791 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1145+5928G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202791 | |||||||
| chr9:119202962 | G | A | 23 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(20): Show |
23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+5757C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202962 | |||||||
| chr9:119203093 | C | T | 63 | a0001c0001t0001g0043 a0001c0001t0001g0097 a0001c0001t0001g0098 others(60): Show |
63 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1145+5626G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119203093 | |||||||
| chr9:119203427 | G | T | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1145+5292C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119203427 | |||||||
| chr9:119203894 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1145+4825G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119203894 | |||||||
| chr9:119204204 | T | C | 3 | a0001c0002t0001g0024 a0001c0002t0001g0095 a0001c0002t0001g0217 |
3 | HG02135.hp2 NA18961.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1145+4515A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119204204 | |||||||
| chr9:119204357 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0171 |
3 | HG03017.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1145+4362G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119204357 | |||||||
| chr9:119204457 | AATAAATT others(3): Show |
A | 28 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(25): Show |
28 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1145+4252_1145+426 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119204457 | |||||||
| chr9:119204547 | G | A | 39 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.1145+4172C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119204547 | |||||||
| chr9:119205176 | G | A | 193 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1145+3543C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205176 | |||||||
| chr9:119205267 | C | T | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1145+3452G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205267 | |||||||
| chr9:119205319 | A | C | 36 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(33): Show |
36 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1145+3400T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205319 | |||||||
| chr9:119205484 | A | T | 35 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(32): Show |
35 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1145+3235T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205484 | |||||||
| chr9:119205567 | A | G | 1 | a0001c0002t0001g0157 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1145+3152T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205567 | |||||||
| chr9:119205626 | C | A | 23 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(20): Show |
23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+3093G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205626 | |||||||
| chr9:119205645 | A | G | 127 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1145+3074T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205645 | |||||||
| chr9:119205679 | G | A | 104 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.1145+3040C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205679 | |||||||
| chr9:119205827 | G | T | 51 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0031 others(48): Show |
51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+2892C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205827 | |||||||
| chr9:119205858 | CATG | C | 23 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(20): Show |
23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+2858_1145+286 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205858 | |||||||
| chr9:119205859 | A | G | 166 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1145+2860T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205859 | |||||||
| chr9:119205917 | T | C | 127 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1145+2802A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205917 | |||||||
| chr9:119205995 | T | TA | 23 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(20): Show |
23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+2723dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205995 | |||||||
| chr9:119206102 | A | G | 1 | a0001c0002t0001g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1145+2617T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206102 | |||||||
| chr9:119206110 | TATCCTCT others(24): Show |
T | 1 | a0001c0001t0001g0055 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1145+2578_1145+260 others(35): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206110 | |||||||
| chr9:119206121 | G | A | 52 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(49): Show |
52 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.1145+2598C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206121 | |||||||
| chr9:119206233 | C | T | 14 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1145+2486G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206233 | |||||||
| chr9:119206334 | C | T | 2 | a0001c0001t0002g0233 a0001c0003t0002g0227 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1145+2385G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206334 | |||||||
| chr9:119206383 | G | A | 7 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(4): Show |
7 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145+2336C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206383 | |||||||
| chr9:119206419 | C | CA | 34 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0170 others(31): Show |
34 | HG00140.hp2 HG00741.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1145+2299dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | |||||||
| chr9:119206419 | C | CAA | 24 | a0001c0001t0001g0043 a0001c0001t0002g0218 a0001c0001t0002g0228 others(21): Show |
24 | HG00741.hp1 HG01169.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1145+2298_1145+229 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | |||||||
| chr9:119206419 | CA | C | 6 | a0001c0001t0001g0066 a0001c0001t0002g0230 a0001c0002t0001g0031 others(3): Show |
6 | HG01069.hp2 HG01070.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145+2299delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | |||||||
| chr9:119206419 | CAA | C | 22 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(19): Show |
22 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1145+2298_1145+229 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | |||||||
| chr9:119206419 | CAAAAAAA others(5): Show |
C | 53 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1145+2288_1145+229 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | |||||||
| chr9:119206491 | C | T | 5 | a0001c0001t0002g0234 a0001c0003t0001g0041 a0001c0003t0001g0059 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+2228G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206491 | |||||||
| chr9:119206492 | G | A | 1 | a0001c0002t0001g0114 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1145+2227C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206492 | |||||||
| chr9:119206684 | T | A | 1 | a0001c0002t0001g0028 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1145+2035A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206684 | |||||||
| chr9:119206785 | A | G | 127 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1145+1934T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206785 | |||||||
| chr9:119206837 | T | C | 5 | a0001c0001t0002g0234 a0001c0003t0001g0041 a0001c0003t0001g0059 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+1882A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206837 | |||||||
| chr9:119206842 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0202 |
2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1145+1877C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206842 | |||||||
| chr9:119207032 | G | A | 51 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0031 others(48): Show |
51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+1687C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207032 | |||||||
| chr9:119207072 | G | T | 39 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.1145+1647C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207072 | |||||||
| chr9:119207235 | A | G | 1 | a0001c0002t0001g0114 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1145+1484T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207235 | |||||||
| chr9:119207395 | G | A | 3 | a0001c0004t0001g0025 a0001c0004t0001g0027 a0001c0004t0001g0071 |
3 | HG01069.hp1 HG01071.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1145+1324C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207395 | |||||||
| chr9:119207887 | C | A | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1145+832G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207887 | |||||||
| chr9:119207983 | G | A | 2 | a0001c0003t0001g0105 a0001c0003t0001g0137 |
2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1145+736C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207983 | |||||||
| chr9:119208020 | G | A | 1 | a0001c0002t0003g0011 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1145+699C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208020 | |||||||
| chr9:119208141 | T | C | 140 | a0001c0001t0001g0043 a0001c0001t0001g0097 a0001c0001t0001g0098 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1145+578A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208141 | |||||||
| chr9:119208225 | C | T | 63 | a0001c0001t0001g0043 a0001c0001t0001g0097 a0001c0001t0001g0098 others(60): Show |
63 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1145+494G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208225 | |||||||
| chr9:119208314 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1145+405G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208314 | |||||||
| chr9:119208414 | T | A | 192 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1145+305A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208414 | |||||||
| chr9:119208601 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1145+118C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208601 | |||||||
| chr9:119208967 | G | T | 15 | a0001c0001t0001g0043 a0001c0001t0002g0218 a0001c0001t0002g0228 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.923-26C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119208967 | |||||||
| chr9:119209152 | C | T | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.923-211G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209152 | |||||||
| chr9:119209219 | C | T | 4 | a0001c0001t0001g0154 a0001c0003t0001g0083 a0001c0003t0001g0196 others(1): Show |
4 | HG01884.hp2 HG02165.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.923-278G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209219 | |||||||
| chr9:119209359 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0158 |
3 | HG00280.hp2 HG01517.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.923-418G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209359 | |||||||
| chr9:119209492 | C | T | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.923-551G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209492 | |||||||
| chr9:119209500 | A | C | 1 | a0001c0009t0001g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.923-559T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209500 | |||||||
| chr9:119209501 | G | C | 1 | a0001c0009t0001g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.923-560C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209501 | |||||||
| chr9:119209575 | T | TA | 15 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(12): Show |
15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.923-635dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209575 | |||||||
| chr9:119209577 | A | AAAAAAAA others(338): Show |
5 | a0001c0001t0002g0234 a0001c0003t0001g0041 a0001c0003t0001g0059 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.923-637_923-636ins others(345): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209577 | |||||||
| chr9:119209668 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.923-727C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209668 | |||||||
| chr9:119209758 | C | A | 136 | a0001c0001t0001g0043 a0001c0001t0001g0097 a0001c0001t0001g0098 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.923-817G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209758 | |||||||
| chr9:119209826 | G | T | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.923-885C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209826 | |||||||
| chr9:119209891 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0168 |
2 | HG00544.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.923-950A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209891 | |||||||
| chr9:119209906 | G | C | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.923-965C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209906 | |||||||
| chr9:119210082 | C | T | 68 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(65): Show |
68 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.923-1141G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210082 | |||||||
| chr9:119210147 | C | T | 3 | a0001c0002t0001g0028 a0001c0002t0001g0049 a0001c0002t0001g0050 |
3 | HG00140.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.923-1206G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210147 | |||||||
| chr9:119210148 | T | C | 14 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.923-1207A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210148 | |||||||
| chr9:119210362 | T | C | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.923-1421A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210362 | |||||||
| chr9:119210393 | T | C | 5 | a0001c0001t0002g0234 a0001c0003t0001g0041 a0001c0003t0001g0059 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.923-1452A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210393 | |||||||
| chr9:119210395 | G | T | 28 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(25): Show |
28 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.923-1454C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210395 | |||||||
| chr9:119210592 | A | G | 1 | a0001c0004t0001g0073 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.923-1651T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210592 | |||||||
| chr9:119210631 | G | A | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.923-1690C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210631 | |||||||
| chr9:119210631 | G | C | 53 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0031 others(50): Show |
53 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.923-1690C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210631 | |||||||
| chr9:119210646 | AG | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.923-1706delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210646 | |||||||
| chr9:119210937 | G | T | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.923-1996C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210937 | |||||||
| chr9:119211138 | T | C | 15 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(12): Show |
15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.923-2197A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211138 | |||||||
| chr9:119211149 | A | C | 52 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0031 others(49): Show |
52 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.923-2208T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211149 | |||||||
| chr9:119211164 | C | CTTTA | 18 | a0001c0001t0001g0038 a0001c0001t0001g0060 a0001c0001t0001g0088 others(15): Show |
18 | HG00738.hp2 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.923-2227_923-2224d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211164 | |||||||
| chr9:119211164 | CTTTA | C | 74 | a0001c0001t0001g0042 a0001c0001t0001g0052 a0001c0001t0001g0054 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.923-2227_923-2224d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211164 | |||||||
| chr9:119211164 | CTTTATTT others(1): Show |
C | 5 | a0001c0001t0001g0144 a0001c0003t0001g0021 a0001c0003t0001g0173 others(2): Show |
5 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.923-2231_923-2224d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211164 | |||||||
| chr9:119211164 | CTTTATTT others(9): Show |
C | 15 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(12): Show |
15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.923-2239_923-2224d others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211164 | |||||||
| chr9:119211212 | T | A | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.923-2271A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211212 | |||||||
| chr9:119211470 | T | TAC | 15 | a0001c0001t0001g0043 a0001c0001t0002g0218 a0001c0001t0002g0228 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.922+2447_922+2448d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211470 | |||||||
| chr9:119211564 | A | G | 67 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(64): Show |
67 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.922+2355T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211564 | |||||||
| chr9:119211713 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.922+2206G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211713 | |||||||
| chr9:119211740 | C | T | 67 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(64): Show |
67 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.922+2179G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211740 | |||||||
| chr9:119212170 | A | G | 189 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.922+1749T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212170 | |||||||
| chr9:119212425 | A | T | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.922+1494T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212425 | |||||||
| chr9:119212487 | T | A | 1 | a0004c0011t0001g0123 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.922+1432A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212487 | |||||||
| chr9:119212577 | A | T | 1 | a0004c0011t0001g0123 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.922+1342T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212577 | |||||||
| chr9:119212792 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.922+1127A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212792 | |||||||
| chr9:119212929 | C | T | 68 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(65): Show |
68 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.922+990G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212929 | |||||||
| chr9:119213024 | AC | A | 15 | a0001c0001t0001g0043 a0001c0001t0002g0218 a0001c0001t0002g0228 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.922+894delG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213024 | |||||||
| chr9:119213128 | C | G | 14 | a0001c0001t0001g0043 a0001c0001t0002g0218 a0001c0001t0002g0228 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.922+791G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213128 | |||||||
| chr9:119213206 | C | A | 7 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(4): Show |
7 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.922+713G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213206 | |||||||
| chr9:119213231 | T | A | 29 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(26): Show |
29 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.922+688A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213231 | |||||||
| chr9:119213369 | A | G | 15 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(12): Show |
15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.922+550T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213369 | |||||||
| chr9:119213438 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.922+481T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213438 | |||||||
| chr9:119213569 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0002g0218 a0001c0001t0002g0228 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.922+350G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213569 | |||||||
| chr9:119213589 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.922+330G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213589 | |||||||
| chr9:119213766 | G | A | 15 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(12): Show |
15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.922+153C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213766 | |||||||
| chr9:119213796 | C | A | 1 | a0004c0011t0001g0123 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.922+123G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213796 | |||||||
| chr9:119213797 | A | C | 1 | a0004c0011t0001g0123 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.922+122T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213797 | |||||||
| chr9:119214162 | G | A | 2 | a0003c0008t0001g0089 a0003c0008t0001g0172 |
2 | NA18612.hp2 NA18747.hp2 |
splice_region_variant&intron_variant | LOW | c.686-7C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214162 | |||||||
| chr9:119214167 | T | C | 1 | a0001c0002t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.686-12A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214167 | |||||||
| chr9:119214373 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0107 |
2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.686-218C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214373 | |||||||
| chr9:119214580 | G | A | 66 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(63): Show |
66 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.686-425C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214580 | |||||||
| chr9:119214587 | T | TA | 6 | a0001c0001t0002g0218 a0001c0005t0001g0208 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.686-433dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214587 | |||||||
| chr9:119214587 | T | TAA | 55 | a0001c0001t0001g0043 a0001c0001t0001g0097 a0001c0001t0001g0098 others(52): Show |
55 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.686-434_686-433dup others(2): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214587 | |||||||
| chr9:119214587 | T | TAAA | 13 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(10): Show |
13 | HG01109.hp2 HG01169.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.686-435_686-433dup others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214587 | |||||||
| chr9:119214587 | TA | T | 54 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0002t0001g0023 others(51): Show |
54 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.686-433delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214587 | |||||||
| chr9:119214646 | T | C | 199 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.686-491A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214646 | |||||||
| chr9:119214918 | G | A | 2 | a0001c0002t0001g0074 a0001c0002t0001g0125 |
2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.686-763C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214918 | |||||||
| chr9:119215011 | T | C | 4 | a0001c0001t0002g0234 a0001c0003t0001g0059 a0001c0003t0001g0072 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-856A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215011 | |||||||
| chr9:119215317 | G | A | 2 | a0001c0001t0002g0233 a0001c0003t0002g0227 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.686-1162C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215317 | |||||||
| chr9:119215484 | T | C | 30 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(27): Show |
30 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.686-1329A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215484 | |||||||
| chr9:119215536 | A | G | 4 | a0001c0002t0001g0024 a0001c0002t0001g0095 a0001c0002t0001g0163 others(1): Show |
4 | HG02135.hp2 HG03927.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-1381T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215536 | |||||||
| chr9:119215838 | GAAACCTG others(29): Show |
G | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.686-1719_686-1684d others(38): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215838 | |||||||
| chr9:119216084 | T | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0168 |
2 | HG00544.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.686-1929A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216084 | |||||||
| chr9:119216373 | C | G | 1 | a0001c0002t0001g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.686-2218G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216373 | |||||||
| chr9:119216397 | C | T | 1 | a0001c0002t0002g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.686-2242G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216397 | |||||||
| chr9:119216502 | A | C | 80 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(77): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.686-2347T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216502 | |||||||
| chr9:119216614 | C | T | 3 | a0001c0002t0001g0102 a0001c0002t0001g0110 a0001c0002t0001g0152 |
3 | HG02074.hp2 HG02129.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.686-2459G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216614 | |||||||
| chr9:119216774 | A | G | 4 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(1): Show |
4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-2619T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216774 | |||||||
| chr9:119216875 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.686-2720C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216875 | |||||||
| chr9:119216903 | T | G | 37 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(34): Show |
37 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.686-2748A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216903 | |||||||
| chr9:119216926 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.686-2771T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216926 | |||||||
| chr9:119217314 | AACACACA others(1): Show |
A | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.686-3167_686-3160d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217314 | |||||||
| chr9:119217330 | G | GAC | 19 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-3177_686-3176d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217330 | |||||||
| chr9:119217330 | GAC | G | 37 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(34): Show |
37 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.686-3177_686-3176d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217330 | |||||||
| chr9:119217345 | A | G | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-3190T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217345 | |||||||
| chr9:119217352 | G | C | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.686-3197C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217352 | |||||||
| chr9:119217521 | C | T | 118 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.686-3366G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217521 | |||||||
| chr9:119217527 | A | G | 1 | a0001c0003t0001g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.686-3372T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217527 | |||||||
| chr9:119217581 | GA | G | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.686-3427delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217581 | |||||||
| chr9:119217676 | G | A | 19 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-3521C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217676 | |||||||
| chr9:119217710 | T | G | 20 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(17): Show |
20 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.686-3555A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217710 | |||||||
| chr9:119217865 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.686-3710C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217865 | |||||||
| chr9:119218055 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0005g0213 a0001c0001t0005g0215 |
3 | HG00423.hp2 NA18993.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.686-3900C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218055 | |||||||
| chr9:119218064 | C | T | 21 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(18): Show |
21 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.686-3909G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218064 | |||||||
| chr9:119218069 | A | C | 118 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.686-3914T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218069 | |||||||
| chr9:119218167 | T | A | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-4012A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218167 | |||||||
| chr9:119218204 | AT | A | 67 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0043 others(64): Show |
67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.686-4050delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218204 | |||||||
| chr9:119218204 | ATT | A | 112 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0097 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.686-4051_686-4050d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218204 | |||||||
| chr9:119218204 | ATTT | A | 8 | a0001c0001t0002g0234 a0001c0002t0001g0067 a0001c0002t0001g0129 others(5): Show |
8 | HG01169.hp1 HG01243.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.686-4052_686-4050d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218204 | |||||||
| chr9:119218297 | C | T | 20 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(17): Show |
20 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.686-4142G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218297 | |||||||
| chr9:119218308 | G | A | 74 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0026 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.686-4153C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218308 | |||||||
| chr9:119218395 | G | A | 20 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(17): Show |
20 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.686-4240C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218395 | |||||||
| chr9:119218511 | C | T | 5 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(2): Show |
5 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-4356G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218511 | |||||||
| chr9:119218652 | G | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0079 |
2 | HG00738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.686-4497C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218652 | |||||||
| chr9:119218746 | A | AT | 67 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(64): Show |
67 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.686-4592dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218746 | |||||||
| chr9:119218746 | A | ATT | 11 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.686-4593_686-4592d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218746 | |||||||
| chr9:119218746 | A | ATTT | 21 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0130 others(18): Show |
21 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.686-4594_686-4592d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218746 | |||||||
| chr9:119218746 | AT | A | 77 | a0001c0001t0001g0132 a0001c0002t0001g0023 a0001c0002t0001g0024 others(74): Show |
77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.686-4592delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218746 | |||||||
| chr9:119218933 | C | T | 2 | a0001c0003t0001g0196 a0001c0003t0001g0206 |
2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.686-4778G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218933 | |||||||
| chr9:119219640 | G | C | 1 | a0001c0004t0001g0162 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.686-5485C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219640 | |||||||
| chr9:119219646 | T | TGA | 3 | a0001c0001t0001g0118 a0001c0001t0001g0144 a0001c0001t0002g0230 |
3 | HG03942.hp1 NA18522.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.686-5493_686-5492d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | T | TGAGA | 5 | a0001c0001t0001g0148 a0001c0001t0001g0192 a0001c0003t0002g0226 others(2): Show |
5 | HG00438.hp2 HG01109.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-5495_686-5492d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | T | TGAGAGA | 3 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0002t0001g0141 |
3 | HG01175.hp1 HG01261.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.686-5497_686-5492d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | T | TGAGAGAG others(9): Show |
1 | a0001c0003t0001g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.686-5507_686-5492d others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGA | T | 25 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0052 others(22): Show |
25 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.686-5493_686-5492d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGA | T | 27 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0053 others(24): Show |
27 | HG01069.hp2 HG01255.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.686-5495_686-5492d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGAGA | T | 11 | a0001c0001t0001g0038 a0001c0001t0001g0085 a0001c0001t0001g0146 others(8): Show |
11 | HG01346.hp1 HG01975.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.686-5497_686-5492d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGAGAG others(1): Show |
T | 16 | a0001c0001t0001g0075 a0001c0001t0001g0115 a0001c0001t0001g0119 others(13): Show |
16 | HG01106.hp2 HG01123.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.686-5499_686-5492d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGAGAG others(3): Show |
T | 16 | a0001c0001t0001g0043 a0001c0001t0001g0193 a0001c0002t0001g0103 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.686-5501_686-5492d others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGAGAG others(5): Show |
T | 49 | a0001c0001t0002g0218 a0001c0001t0002g0228 a0001c0002t0001g0023 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.686-5503_686-5492d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGAGAG others(7): Show |
T | 8 | a0001c0001t0001g0198 a0001c0001t0003g0008 a0001c0003t0001g0092 others(5): Show |
8 | HG01891.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.686-5505_686-5492d others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGAGAG others(11): Show |
T | 10 | a0001c0001t0001g0130 a0001c0001t0001g0210 a0001c0001t0003g0009 others(7): Show |
10 | HG00741.hp1 HG00741.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.686-5509_686-5492d others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGAGAG others(13): Show |
T | 15 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(12): Show |
15 | HG01109.hp2 HG01169.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.686-5511_686-5492d others(22): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGAGAG others(15): Show |
T | 16 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.686-5513_686-5492d others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219646 | TGAGAGAG others(17): Show |
T | 3 | a0001c0003t0001g0191 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.686-5515_686-5492d others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | |||||||
| chr9:119219675 | GAGAGAGA others(14): Show |
G | 1 | a0001c0003t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.686-5541_686-5521d others(23): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219675 | |||||||
| chr9:119219696 | A | AG | 3 | a0001c0001t0001g0047 a0001c0001t0001g0165 a0001c0001t0005g0213 |
3 | HG02683.hp1 HG03927.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.686-5542_686-5541i others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219696 | |||||||
| chr9:119219737 | A | G | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-5582T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219737 | |||||||
| chr9:119219766 | A | C | 2 | a0001c0002t0001g0090 a0001c0002t0001g0108 |
2 | NA18994.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.686-5611T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219766 | |||||||
| chr9:119219838 | G | T | 3 | a0001c0002t0001g0031 a0001c0002t0001g0112 a0001c0002t0001g0177 |
3 | HG03669.hp1 NA18940.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.686-5683C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219838 | |||||||
| chr9:119220092 | G | A | 24 | a0001c0002t0001g0026 a0001c0002t0001g0028 a0001c0002t0001g0035 others(21): Show |
24 | HG00140.hp2 HG01074.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.686-5937C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220092 | |||||||
| chr9:119220121 | C | A | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.686-5966G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220121 | |||||||
| chr9:119220274 | C | A | 19 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-6119G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220274 | |||||||
| chr9:119220303 | C | T | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-6148G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220303 | |||||||
| chr9:119220617 | C | CAA | 19 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-6464_686-6463d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220617 | |||||||
| chr9:119220617 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0107 |
2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.686-6462G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220617 | |||||||
| chr9:119220627 | A | G | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-6472T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220627 | |||||||
| chr9:119220731 | T | C | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-6576A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220731 | |||||||
| chr9:119220830 | A | T | 19 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-6675T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220830 | |||||||
| chr9:119220866 | G | T | 5 | a0001c0003t0001g0092 a0001c0003t0001g0149 a0001c0003t0001g0184 others(2): Show |
5 | HG01891.hp2 HG03579.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.686-6711C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220866 | |||||||
| chr9:119220875 | AT | A | 2 | a0001c0003t0001g0196 a0001c0003t0001g0206 |
2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.686-6721delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220875 | |||||||
| chr9:119221503 | C | A | 1 | a0001c0003t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.686-7348G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119221503 | |||||||
| chr9:119221836 | TAGC | T | 14 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.686-7684_686-7682d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119221836 | |||||||
| chr9:119221986 | C | T | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.686-7831G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119221986 | |||||||
| chr9:119222029 | C | G | 40 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.686-7874G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222029 | |||||||
| chr9:119222069 | C | T | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.686-7914G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222069 | |||||||
| chr9:119222275 | A | G | 40 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.686-8120T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222275 | |||||||
| chr9:119222395 | C | T | 188 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.686-8240G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222395 | |||||||
| chr9:119222588 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.686-8433C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222588 | |||||||
| chr9:119222615 | A | ACAAGGAA others(10): Show |
18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-8461_686-8460i others(19): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222615 | |||||||
| chr9:119222667 | T | C | 1 | a0001c0007t0001g0080 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.686-8512A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222667 | |||||||
| chr9:119222690 | CA | C | 7 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(4): Show |
7 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.686-8536delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222690 | |||||||
| chr9:119222822 | G | A | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-8667C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222822 | |||||||
| chr9:119222858 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.686-8703T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222858 | |||||||
| chr9:119223199 | T | C | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-9044A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223199 | |||||||
| chr9:119223520 | C | A | 3 | a0001c0003t0001g0083 a0001c0005t0001g0190 a0001c0005t0002g0235 |
3 | HG02886.hp2 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.686-9365G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223520 | |||||||
| chr9:119223562 | T | C | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-9407A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223562 | |||||||
| chr9:119223570 | C | T | 58 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.686-9415G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223570 | |||||||
| chr9:119223642 | G | A | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-9487C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223642 | |||||||
| chr9:119223722 | T | G | 13 | a0001c0001t0001g0043 a0001c0003t0001g0083 a0001c0003t0001g0178 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.686-9567A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223722 | |||||||
| chr9:119223790 | G | A | 3 | a0001c0001t0002g0218 a0001c0001t0002g0228 a0001c0005t0001g0208 |
3 | HG02622.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.686-9635C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223790 | |||||||
| chr9:119223827 | C | T | 118 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.686-9672G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223827 | |||||||
| chr9:119223929 | T | C | 1 | a0001c0002t0002g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.686-9774A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223929 | |||||||
| chr9:119223941 | TATAG | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(3): Show |
6 | HG01261.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.686-9790_686-9787d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223941 | |||||||
| chr9:119223955 | C | T | 3 | a0001c0001t0002g0218 a0001c0001t0002g0228 a0001c0005t0001g0208 |
3 | HG02622.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.686-9800G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223955 | |||||||
| chr9:119224106 | A | G | 41 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(38): Show |
41 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.686-9951T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119224106 | |||||||
| chr9:119224548 | T | A | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-10393A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119224548 | |||||||
| chr9:119224778 | C | G | 93 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0026 others(90): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.686-10623G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119224778 | |||||||
| chr9:119224873 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.686-10718G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119224873 | |||||||
| chr9:119225104 | T | A | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-10949A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225104 | |||||||
| chr9:119225142 | C | T | 150 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(147): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.686-10987G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225142 | |||||||
| chr9:119225209 | C | T | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.686-11054G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225209 | |||||||
| chr9:119225266 | A | G | 128 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.686-11111T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225266 | |||||||
| chr9:119225370 | A | G | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.686-11215T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225370 | |||||||
| chr9:119225441 | G | A | 3 | a0001c0001t0002g0218 a0001c0001t0002g0228 a0001c0005t0001g0208 |
3 | HG02622.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.686-11286C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225441 | |||||||
| chr9:119225709 | T | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.686-11554A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225709 | |||||||
| chr9:119225896 | TAAAC | T | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-11745_686-1174 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225896 | |||||||
| chr9:119225922 | G | A | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-11767C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225922 | |||||||
| chr9:119225965 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.686-11810C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225965 | |||||||
| chr9:119226009 | T | C | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.686-11854A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226009 | |||||||
| chr9:119226072 | C | T | 191 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(188): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.686-11917G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226072 | |||||||
| chr9:119226085 | A | G | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-11930T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226085 | |||||||
| chr9:119226090 | TAAGAC | T | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-11940_686-1193 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226090 | |||||||
| chr9:119226250 | G | A | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-12095C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226250 | |||||||
| chr9:119226437 | T | A | 191 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(188): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.685+12218A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226437 | |||||||
| chr9:119226621 | T | G | 93 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0026 others(90): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.685+12034A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226621 | |||||||
| chr9:119226668 | GT | G | 189 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.685+11986delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226668 | |||||||
| chr9:119226669 | T | G | 1 | a0001c0003t0002g0232 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.685+11986A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226669 | |||||||
| chr9:119226686 | C | T | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.685+11969G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226686 | |||||||
| chr9:119226812 | G | A | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.685+11843C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226812 | |||||||
| chr9:119227074 | A | G | 38 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(35): Show |
38 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.685+11581T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227074 | |||||||
| chr9:119227083 | CA | C | 4 | a0001c0001t0002g0234 a0001c0003t0001g0059 a0001c0003t0001g0072 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.685+11571delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227083 | |||||||
| chr9:119227278 | C | A | 1 | a0001c0001t0002g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.685+11377G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227278 | |||||||
| chr9:119227361 | T | C | 5 | a0001c0001t0002g0234 a0001c0003t0001g0041 a0001c0003t0001g0059 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.685+11294A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227361 | |||||||
| chr9:119227533 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.685+11122G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227533 | |||||||
| chr9:119227625 | G | C | 2 | a0001c0002t0001g0074 a0001c0002t0001g0125 |
2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.685+11030C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227625 | |||||||
| chr9:119227741 | T | C | 1 | a0001c0002t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.685+10914A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227741 | |||||||
| chr9:119227771 | C | T | 1 | a0001c0007t0001g0051 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.685+10884G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227771 | |||||||
| chr9:119227890 | T | A | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.685+10765A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227890 | |||||||
| chr9:119228034 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.685+10621G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228034 | |||||||
| chr9:119228036 | C | T | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.685+10619G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228036 | |||||||
| chr9:119228076 | G | A | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.685+10579C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228076 | |||||||
| chr9:119228212 | T | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+10443A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228212 | |||||||
| chr9:119228223 | A | T | 127 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.685+10432T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228223 | |||||||
| chr9:119228224 | T | A | 127 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.685+10431A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228224 | |||||||
| chr9:119228231 | C | T | 1 | a0001c0003t0002g0226 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.685+10424G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228231 | |||||||
| chr9:119228299 | C | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+10356G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228299 | |||||||
| chr9:119228307 | C | A | 1 | a0001c0002t0003g0012 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.685+10348G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228307 | |||||||
| chr9:119228398 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0107 |
2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.685+10257A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228398 | |||||||
| chr9:119228483 | TA | T | 57 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.685+10171delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228483 | |||||||
| chr9:119228576 | T | C | 71 | a0001c0001t0003g0001 a0001c0002t0001g0023 a0001c0002t0001g0024 others(68): Show |
71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.685+10079A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228576 | |||||||
| chr9:119228625 | A | G | 6 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.685+10030T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228625 | |||||||
| chr9:119228932 | T | C | 13 | a0001c0001t0001g0043 a0001c0003t0001g0083 a0001c0003t0001g0178 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.685+9723A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228932 | |||||||
| chr9:119229198 | A | G | 39 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.685+9457T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229198 | |||||||
| chr9:119229482 | C | T | 1 | a0001c0002t0001g0159 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.685+9173G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229482 | |||||||
| chr9:119229668 | C | CA | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.685+8986dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229668 | |||||||
| chr9:119229673 | A | G | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.685+8982T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229673 | |||||||
| chr9:119229863 | C | T | 126 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.685+8792G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229863 | |||||||
| chr9:119229996 | T | C | 39 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.685+8659A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229996 | |||||||
| chr9:119230072 | TGAGAGAG others(19): Show |
T | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.685+8557_685+8582d others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230072 | |||||||
| chr9:119230081 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.685+8574A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230081 | |||||||
| chr9:119230186 | A | G | 18 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.685+8469T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230186 | |||||||
| chr9:119230271 | C | T | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.685+8384G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230271 | |||||||
| chr9:119230408 | G | A | 125 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.685+8247C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230408 | |||||||
| chr9:119230469 | G | A | 184 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(181): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.685+8186C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230469 | |||||||
| chr9:119230480 | A | G | 188 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.685+8175T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230480 | |||||||
| chr9:119230683 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.685+7972C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230683 | |||||||
| chr9:119231230 | T | C | 114 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0121 others(111): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.685+7425A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119231230 | |||||||
| chr9:119231641 | C | A | 129 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.685+7014G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119231641 | |||||||
| chr9:119231689 | G | A | 19 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(16): Show |
19 | HG01109.hp2 HG01123.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.685+6966C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119231689 | |||||||
| chr9:119231996 | T | A | 2 | a0001c0001t0001g0132 a0004c0011t0001g0123 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.685+6659A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119231996 | |||||||
| chr9:119232010 | G | A | 1 | a0001c0004t0002g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.685+6645C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232010 | |||||||
| chr9:119232042 | A | T | 39 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.685+6613T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232042 | |||||||
| chr9:119232144 | T | C | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.685+6511A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232144 | |||||||
| chr9:119232225 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.685+6430G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232225 | |||||||
| chr9:119232435 | T | C | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+6220A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232435 | |||||||
| chr9:119232622 | T | C | 128 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.685+6033A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232622 | |||||||
| chr9:119232851 | A | G | 40 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.685+5804T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232851 | |||||||
| chr9:119232873 | G | A | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.685+5782C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232873 | |||||||
| chr9:119232908 | GCCATTAG others(10): Show |
G | 1 | a0001c0002t0001g0095 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.685+5730_685+5746d others(19): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232908 | |||||||
| chr9:119233012 | C | A | 1 | a0001c0002t0001g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.685+5643G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233012 | |||||||
| chr9:119233022 | C | CT | 127 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.685+5632dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233022 | |||||||
| chr9:119233146 | C | A | 2 | a0001c0003t0001g0207 a0001c0003t0002g0221 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.685+5509G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233146 | |||||||
| chr9:119233339 | T | A | 12 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.685+5316A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233339 | |||||||
| chr9:119233427 | A | G | 1 | a0001c0004t0001g0162 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.685+5228T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233427 | |||||||
| chr9:119233737 | A | G | 2 | a0001c0001t0001g0132 a0004c0011t0001g0123 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.685+4918T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233737 | |||||||
| chr9:119234188 | C | T | 178 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.685+4467G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234188 | |||||||
| chr9:119234371 | G | A | 1 | a0001c0003t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.685+4284C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234371 | |||||||
| chr9:119234435 | TTTCA | T | 25 | a0001c0001t0001g0043 a0001c0001t0001g0193 a0001c0001t0001g0198 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.685+4216_685+4219d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234435 | |||||||
| chr9:119234582 | T | C | 1 | a0001c0002t0001g0035 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.685+4073A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234582 | |||||||
| chr9:119234590 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.685+4065A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234590 | |||||||
| chr9:119234630 | G | A | 12 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.685+4025C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234630 | |||||||
| chr9:119234655 | C | A | 12 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.685+4000G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234655 | |||||||
| chr9:119234676 | C | T | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.685+3979G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234676 | |||||||
| chr9:119234988 | A | G | 1 | a0001c0002t0001g0026 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.685+3667T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234988 | |||||||
| chr9:119235560 | C | T | 14 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.685+3095G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119235560 | |||||||
| chr9:119235568 | T | C | 13 | a0001c0001t0001g0043 a0001c0003t0001g0083 a0001c0003t0001g0178 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.685+3087A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119235568 | |||||||
| chr9:119235585 | C | T | 39 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.685+3070G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119235585 | |||||||
| chr9:119235730 | G | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0128 a0001c0001t0001g0154 others(1): Show |
4 | HG00544.hp2 HG02135.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.685+2925C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119235730 | |||||||
| chr9:119236036 | A | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+2619T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236036 | |||||||
| chr9:119236257 | C | A | 1 | a0001c0003t0001g0164 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.685+2398G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236257 | |||||||
| chr9:119236484 | T | G | 2 | a0002c0012t0001g0062 a0002c0013t0003g0006 |
2 | HG01074.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.685+2171A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236484 | |||||||
| chr9:119236673 | C | G | 1 | a0001c0003t0002g0232 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.685+1982G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236673 | |||||||
| chr9:119236788 | T | C | 19 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(16): Show |
19 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.685+1867A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236788 | |||||||
| chr9:119236910 | A | C | 1 | a0001c0002t0001g0157 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.685+1745T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236910 | |||||||
| chr9:119237049 | T | C | 3 | a0001c0002t0001g0102 a0001c0002t0001g0110 a0001c0002t0001g0152 |
3 | HG02074.hp2 HG02129.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.685+1606A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237049 | |||||||
| chr9:119237289 | G | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.685+1366C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237289 | |||||||
| chr9:119237315 | T | G | 1 | a0003c0008t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.685+1340A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237315 | |||||||
| chr9:119237346 | C | CATTATT | 6 | a0001c0002t0001g0155 a0001c0003t0001g0039 a0001c0003t0001g0040 others(3): Show |
6 | HG01884.hp2 HG02129.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.685+1303_685+1308d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | |||||||
| chr9:119237346 | C | CATTATTA others(2): Show |
6 | a0001c0002t0004g0029 a0001c0002t0004g0116 a0001c0003t0001g0149 others(3): Show |
6 | HG00423.hp1 HG01891.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.685+1300_685+1308d others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | |||||||
| chr9:119237346 | C | CATTATTA others(5): Show |
14 | a0001c0002t0001g0160 a0001c0002t0001g0194 a0001c0002t0002g0219 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.685+1297_685+1308d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | |||||||
| chr9:119237346 | C | CATTATTA others(8): Show |
51 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0182 others(48): Show |
51 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.685+1294_685+1308d others(17): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | |||||||
| chr9:119237346 | C | CATTATTA others(11): Show |
27 | a0001c0001t0001g0198 a0001c0001t0001g0210 a0001c0001t0002g0234 others(24): Show |
27 | HG01070.hp2 HG01123.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.685+1291_685+1308d others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | |||||||
| chr9:119237346 | C | CATTATTA others(14): Show |
3 | a0001c0001t0001g0082 a0001c0003t0001g0187 a0001c0006t0001g0018 |
3 | HG01261.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.685+1288_685+1308d others(23): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | |||||||
| chr9:119237346 | CATT | C | 40 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.685+1306_685+1308d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | |||||||
| chr9:119237346 | CATTATT | C | 26 | a0001c0002t0001g0026 a0001c0002t0001g0028 a0001c0002t0001g0035 others(23): Show |
26 | HG00140.hp2 HG01074.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.685+1303_685+1308d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | |||||||
| chr9:119237375 | T | TTATTATT others(4): Show |
3 | a0001c0002t0001g0095 a0001c0002t0001g0140 a0001c0015t0001g0131 |
3 | NA18961.hp2 NA19070.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.685+1279_685+1280i others(13): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237375 | |||||||
| chr9:119237376 | T | TATTATTA others(6): Show |
1 | a0001c0005t0002g0235 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.685+1278_685+1279i others(15): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237376 | |||||||
| chr9:119237378 | T | A | 3 | a0001c0002t0001g0095 a0001c0002t0001g0140 a0001c0015t0001g0131 |
3 | NA18961.hp2 NA19070.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.685+1277A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237378 | |||||||
| chr9:119237487 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0003g0009 a0001c0003t0001g0142 |
3 | HG00741.hp1 HG00741.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+1168G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237487 | |||||||
| chr9:119237566 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.685+1089C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237566 | |||||||
| chr9:119237738 | T | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0097 others(2): Show |
5 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.685+917A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237738 | |||||||
| chr9:119237764 | C | T | 4 | a0001c0002t0001g0091 a0001c0004t0001g0014 a0001c0004t0001g0162 others(1): Show |
4 | HG01169.hp2 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.685+891G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237764 | |||||||
| chr9:119237796 | G | A | 2 | a0001c0003t0001g0184 a0001c0003t0007g0183 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.685+859C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237796 | |||||||
| chr9:119238031 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.685+624A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238031 | |||||||
| chr9:119238060 | G | C | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.685+595C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238060 | |||||||
| chr9:119238185 | TA | T | 89 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0026 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.685+469delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238185 | |||||||
| chr9:119238334 | C | T | 2 | a0001c0003t0001g0196 a0001c0003t0001g0206 |
2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.685+321G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238334 | |||||||
| chr9:119238339 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.685+316G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238339 | |||||||
| chr9:119238410 | CCTTA | C | 89 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0026 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.685+241_685+244del others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238410 | |||||||
| chr9:119238553 | TC | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+101delG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238553 | |||||||
| chr9:119238584 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 |
3 | HG01261.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.685+71T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238584 | |||||||
| chr9:119238776 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0107 |
2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.580-16T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119238776 | |||||||
| chr9:119238868 | G | A | 12 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-108C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119238868 | |||||||
| chr9:119238951 | G | C | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.580-191C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119238951 | |||||||
| chr9:119239006 | G | A | 12 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-246C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239006 | |||||||
| chr9:119239217 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.580-457G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239217 | |||||||
| chr9:119239436 | G | A | 177 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.580-676C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239436 | |||||||
| chr9:119239551 | T | C | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.580-791A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239551 | |||||||
| chr9:119239777 | C | T | 14 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-1017G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239777 | |||||||
| chr9:119239956 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.580-1196C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239956 | |||||||
| chr9:119239998 | C | T | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.580-1238G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239998 | |||||||
| chr9:119240105 | C | T | 53 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.580-1345G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119240105 | |||||||
| chr9:119240140 | G | A | 2 | a0003c0008t0001g0089 a0003c0008t0001g0172 |
2 | NA18612.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.580-1380C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119240140 | |||||||
| chr9:119240612 | A | T | 13 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(10): Show |
13 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.579+1435T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119240612 | |||||||
| chr9:119240891 | T | G | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.579+1156A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119240891 | |||||||
| chr9:119241025 | G | A | 4 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(1): Show |
4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+1022C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241025 | |||||||
| chr9:119241141 | T | C | 12 | a0001c0001t0001g0043 a0001c0003t0001g0083 a0001c0003t0001g0178 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+906A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241141 | |||||||
| chr9:119241289 | C | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.579+758G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241289 | |||||||
| chr9:119241364 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.579+683G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241364 | |||||||
| chr9:119241516 | G | C | 2 | a0001c0003t0001g0196 a0001c0003t0001g0206 |
2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.579+531C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241516 | |||||||
| chr9:119241669 | G | A | 2 | a0001c0002t0001g0147 a0001c0002t0001g0216 |
2 | NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.579+378C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241669 | |||||||
| chr9:119241750 | A | G | 39 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(36): Show |
39 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.579+297T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241750 | |||||||
| chr9:119241798 | T | C | 2 | a0001c0004t0001g0186 a0001c0006t0002g0224 |
2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.579+249A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241798 | |||||||
| chr9:119241877 | T | C | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+170A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241877 | |||||||
| chr9:119241894 | G | A | 12 | a0001c0001t0001g0043 a0001c0003t0001g0083 a0001c0003t0001g0178 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+153C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241894 | |||||||
| chr9:119242267 | GAGGACAG others(4): Show |
G | 72 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0026 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.410-62_410-52delAT others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242267 | |||||||
| chr9:119242538 | C | T | 41 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(38): Show |
41 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.410-322G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242538 | |||||||
| chr9:119242560 | A | G | 20 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(17): Show |
20 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.410-344T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242560 | |||||||
| chr9:119242684 | CT | C | 19 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(16): Show |
19 | HG01109.hp2 HG01123.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.410-469delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242684 | |||||||
| chr9:119242786 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.410-570C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242786 | |||||||
| chr9:119242799 | T | G | 3 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0009t0001g0189 |
3 | HG02809.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.410-583A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242799 | |||||||
| chr9:119242866 | T | G | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.410-650A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242866 | |||||||
| chr9:119242979 | CT | C | 145 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.410-764delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242979 | |||||||
| chr9:119242982 | T | C | 20 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0198 others(17): Show |
20 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.410-766A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242982 | |||||||
| chr9:119242983 | T | C | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.410-767A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242983 | |||||||
| chr9:119243242 | G | T | 15 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.410-1026C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119243242 | |||||||
| chr9:119243484 | T | A | 70 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0026 others(67): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.410-1268A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119243484 | |||||||
| chr9:119243682 | C | T | 114 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.410-1466G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119243682 | |||||||
| chr9:119244225 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.410-2009C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244225 | |||||||
| chr9:119244391 | T | A | 1 | a0001c0003t0002g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.410-2175A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244391 | |||||||
| chr9:119244515 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.410-2299C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244515 | |||||||
| chr9:119244626 | G | C | 11 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.410-2410C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244626 | |||||||
| chr9:119244696 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.410-2480T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244696 | |||||||
| chr9:119244757 | T | C | 1 | a0001c0003t0001g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.410-2541A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244757 | |||||||
| chr9:119244793 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.410-2577G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244793 | |||||||
| chr9:119245194 | T | TAC | 4 | a0001c0001t0001g0174 a0001c0003t0001g0187 a0001c0003t0001g0195 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-2980_410-2979d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245194 | |||||||
| chr9:119245210 | CACAT | C | 75 | a0001c0001t0001g0022 a0001c0001t0001g0161 a0001c0001t0003g0001 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.410-2998_410-2995d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245210 | |||||||
| chr9:119245212 | CAT | C | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.410-2998_410-2997d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245212 | |||||||
| chr9:119245437 | G | A | 16 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(13): Show |
16 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.410-3221C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245437 | |||||||
| chr9:119245481 | G | A | 1 | a0001c0002t0001g0216 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.410-3265C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245481 | |||||||
| chr9:119245485 | T | C | 2 | a0001c0003t0001g0196 a0001c0003t0001g0206 |
2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.410-3269A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245485 | |||||||
| chr9:119245532 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0104 |
2 | NA18970.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.410-3316G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245532 | |||||||
| chr9:119245616 | AT | A | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.409+3343delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245616 | |||||||
| chr9:119245750 | G | C | 1 | a0001c0003t0002g0232 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.409+3210C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245750 | |||||||
| chr9:119245782 | G | A | 137 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(134): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.409+3178C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245782 | |||||||
| chr9:119246069 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.409+2891T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246069 | |||||||
| chr9:119246417 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.409+2543G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246417 | |||||||
| chr9:119246456 | A | G | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.409+2504T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246456 | |||||||
| chr9:119246533 | G | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.409+2427C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246533 | |||||||
| chr9:119246627 | C | T | 1 | a0001c0002t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.409+2333G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246627 | |||||||
| chr9:119246895 | G | A | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+2065C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246895 | |||||||
| chr9:119247302 | C | CTGGT | 163 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.409+1654_409+1657d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247302 | |||||||
| chr9:119247454 | C | G | 1 | a0001c0003t0001g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.409+1506G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247454 | |||||||
| chr9:119247487 | T | TA | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.409+1472dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247487 | |||||||
| chr9:119247496 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.409+1464T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247496 | |||||||
| chr9:119247527 | C | T | 5 | a0001c0003t0001g0092 a0001c0003t0001g0149 a0001c0003t0001g0184 others(2): Show |
5 | HG01891.hp2 HG02886.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.409+1433G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247527 | |||||||
| chr9:119247528 | G | C | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.409+1432C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247528 | |||||||
| chr9:119247578 | C | A | 42 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(39): Show |
42 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.409+1382G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247578 | |||||||
| chr9:119247657 | CA | C | 16 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(13): Show |
16 | HG00741.hp1 HG01515.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.409+1302delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | |||||||
| chr9:119247657 | CAA | C | 29 | a0001c0001t0001g0161 a0001c0001t0002g0234 a0001c0002t0001g0026 others(26): Show |
29 | HG01074.hp1 HG01099.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.409+1301_409+1302d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | |||||||
| chr9:119247657 | CAAA | C | 30 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0082 others(27): Show |
30 | HG00140.hp2 HG00280.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.409+1300_409+1302d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | |||||||
| chr9:119247657 | CAAAA | C | 92 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0034 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.409+1299_409+1302d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | |||||||
| chr9:119247657 | CAAAAA | C | 43 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(40): Show |
43 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.409+1298_409+1302d others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | |||||||
| chr9:119247657 | CAAAAAA | C | 16 | a0001c0001t0001g0043 a0001c0002t0004g0029 a0001c0003t0001g0178 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.409+1297_409+1302d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | |||||||
| chr9:119247698 | T | C | 7 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.409+1262A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247698 | |||||||
| chr9:119247741 | C | T | 2 | a0001c0002t0001g0143 a0001c0015t0001g0131 |
2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.409+1219G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247741 | |||||||
| chr9:119247842 | A | G | 230 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(227): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.409+1118T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247842 | |||||||
| chr9:119247981 | C | T | 230 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(227): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.409+979G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247981 | |||||||
| chr9:119248081 | T | C | 1 | a0001c0002t0001g0035 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.409+879A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119248081 | |||||||
| chr9:119248088 | T | G | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.409+872A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119248088 | |||||||
| chr9:119248099 | T | C | 14 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.409+861A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119248099 | |||||||
| chr9:119249278 | G | C | 14 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.219-128C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249278 | |||||||
| chr9:119249751 | A | C | 166 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.219-601T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249751 | |||||||
| chr9:119249770 | G | A | 1 | a0001c0014t0003g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.219-620C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249770 | |||||||
| chr9:119249787 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0151 |
2 | HG00544.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.219-637C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249787 | |||||||
| chr9:119249805 | T | TGGAA | 62 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0052 others(59): Show |
62 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.219-659_219-656dup others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | |||||||
| chr9:119249805 | T | TGGAAGGA others(1): Show |
58 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0060 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(55): Show |
intron_variant | MODIFIER | c.219-663_219-656dup others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | |||||||
| chr9:119249805 | T | TGGAAGGA others(5): Show |
27 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0063 others(24): Show |
27 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.219-667_219-656dup others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | |||||||
| chr9:119249805 | T | TGGAAGGA others(9): Show |
10 | a0001c0001t0001g0054 a0001c0001t0001g0104 a0001c0001t0001g0158 others(7): Show |
10 | HG01109.hp2 HG01169.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.219-671_219-656dup others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | |||||||
| chr9:119249805 | TGGAAGGA others(5): Show |
T | 1 | a0001c0003t0002g0232 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.219-667_219-656del others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | |||||||
| chr9:119249839 | G | GAAGGAAG others(5): Show |
2 | a0001c0001t0001g0193 a0001c0001t0001g0202 |
2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.219-690_219-689ins others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249839 | |||||||
| chr9:119249839 | G | GAAGGAAG others(17): Show |
1 | a0001c0001t0001g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.219-690_219-689ins others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249839 | |||||||
| chr9:119249848 | A | G | 1 | a0001c0009t0001g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.219-698T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249848 | |||||||
| chr9:119249852 | A | AAGGAAGG others(9): Show |
2 | a0001c0001t0001g0045 a0001c0001t0001g0192 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.219-703_219-702ins others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | |||||||
| chr9:119249852 | A | AAGGAAGG others(1): Show |
2 | a0001c0003t0001g0059 a0001c0007t0001g0051 |
2 | HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.219-703_219-702ins others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | |||||||
| chr9:119249852 | A | G | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-702T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | |||||||
| chr9:119249852 | AAGGG | A | 18 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0107 others(15): Show |
18 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.219-706_219-703del others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | |||||||
| chr9:119249852 | AAGGGAGG others(1): Show |
A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0118 a0001c0001t0002g0228 |
3 | HG02135.hp1 HG03098.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.219-710_219-703del others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | |||||||
| chr9:119249853 | A | AGGAAGGA others(34): Show |
1 | a0001c0003t0001g0188 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.219-704_219-703ins others(41): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | |||||||
| chr9:119249853 | A | AGGAAGGA others(30): Show |
1 | a0001c0005t0001g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.219-704_219-703ins others(37): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | |||||||
| chr9:119249853 | A | AGGAAGGA others(34): Show |
1 | a0001c0003t0001g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-704_219-703ins others(41): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | |||||||
| chr9:119249853 | A | AGGAAGGA others(26): Show |
3 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0008g0212 |
3 | HG01884.hp1 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.219-704_219-703ins others(33): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | |||||||
| chr9:119249853 | A | AGGAAGGA others(30): Show |
1 | a0001c0005t0001g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219-704_219-703ins others(37): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | |||||||
| chr9:119249853 | A | AGGAAGGA others(22): Show |
2 | a0001c0003t0001g0207 a0001c0003t0002g0222 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.219-704_219-703ins others(29): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | |||||||
| chr9:119249856 | G | A | 110 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0038 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.219-706C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249856 | |||||||
| chr9:119249860 | G | A | 114 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.219-710C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249860 | |||||||
| chr9:119249860 | G | GAGGGAGG others(6): Show |
3 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 |
3 | HG02809.hp1 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.219-723_219-711dup others(13): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249860 | |||||||
| chr9:119249864 | G | A | 1 | a0001c0002t0001g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.219-714C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249864 | |||||||
| chr9:119249871 | G | A | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-721C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249871 | |||||||
| chr9:119249876 | GA | G | 9 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-727delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249876 | |||||||
| chr9:119249877 | A | AGGG | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-728_219-727ins others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249877 | |||||||
| chr9:119249877 | A | AGGGAGGG others(21): Show |
1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-728_219-727ins others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249877 | |||||||
| chr9:119249913 | G | A | 114 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.219-763C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249913 | |||||||
| chr9:119249916 | T | TGAAGGGA others(65): Show |
3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-838_219-767dup others(72): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249916 | |||||||
| chr9:119249938 | A | AAGGGAAG others(69): Show |
2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-864_219-789dup others(76): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249938 | |||||||
| chr9:119250049 | A | G | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-899T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250049 | |||||||
| chr9:119250071 | A | C | 2 | a0001c0002t0001g0091 a0001c0004t0001g0014 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.219-921T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250071 | |||||||
| chr9:119250081 | A | G | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-931T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250081 | |||||||
| chr9:119250082 | A | G | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-932T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250082 | |||||||
| chr9:119250085 | G | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-935C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250085 | |||||||
| chr9:119250086 | A | G | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-936T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250086 | |||||||
| chr9:119250090 | A | G | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-940T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250090 | |||||||
| chr9:119250092 | GGAAGGA | G | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-948_219-943del others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250092 | |||||||
| chr9:119250102 | A | G | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-952T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250102 | |||||||
| chr9:119250104 | A | AGGAAGGA others(9): Show |
1 | a0001c0003t0001g0176 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.219-970_219-955dup others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250104 | |||||||
| chr9:119250104 | AGGAAGG | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-960_219-955del others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250104 | |||||||
| chr9:119250124 | AGGAG | A | 3 | a0001c0002t0001g0147 a0001c0004t0001g0015 a0001c0004t0002g0231 |
3 | HG02976.hp1 HG03195.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.219-978_219-975del others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250124 | |||||||
| chr9:119250168 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.219-1018C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250168 | |||||||
| chr9:119250365 | T | C | 117 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.219-1215A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250365 | |||||||
| chr9:119250494 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.219-1344T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250494 | |||||||
| chr9:119250502 | T | A | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-1352A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250502 | |||||||
| chr9:119250679 | C | T | 1 | a0001c0003t0001g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.219-1529G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250679 | |||||||
| chr9:119250978 | G | A | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-1828C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250978 | |||||||
| chr9:119251244 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.219-2094G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251244 | |||||||
| chr9:119251361 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.219-2211G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251361 | |||||||
| chr9:119251476 | T | C | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-2326A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251476 | |||||||
| chr9:119251544 | T | A | 170 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.219-2394A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251544 | |||||||
| chr9:119251613 | C | CA | 24 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0055 others(21): Show |
24 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.219-2464dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251613 | |||||||
| chr9:119251665 | G | A | 10 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-2515C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251665 | |||||||
| chr9:119251669 | A | C | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-2519T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251669 | |||||||
| chr9:119251670 | C | G | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-2520G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251670 | |||||||
| chr9:119251671 | A | G | 180 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.219-2521T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251671 | |||||||
| chr9:119251671 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-2521T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251671 | |||||||
| chr9:119251672 | T | TTA | 170 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.219-2523_219-2522i others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251672 | |||||||
| chr9:119251692 | T | G | 49 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(46): Show |
49 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.219-2542A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251692 | |||||||
| chr9:119251693 | AG | A | 172 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.219-2544delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251693 | |||||||
| chr9:119251693 | AGGGG | A | 10 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-2547_219-2544d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251693 | |||||||
| chr9:119251749 | T | C | 182 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(179): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.219-2599A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251749 | |||||||
| chr9:119251750 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-2600C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251750 | |||||||
| chr9:119251968 | C | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.219-2818G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251968 | |||||||
| chr9:119252033 | C | T | 3 | a0001c0003t0001g0083 a0001c0003t0001g0196 a0001c0003t0001g0206 |
3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.219-2883G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252033 | |||||||
| chr9:119252059 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.219-2909G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252059 | |||||||
| chr9:119252061 | C | T | 171 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.219-2911G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252061 | |||||||
| chr9:119252161 | G | A | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-3011C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252161 | |||||||
| chr9:119252477 | T | C | 1 | a0001c0003t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.219-3327A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252477 | |||||||
| chr9:119252488 | TTA | T | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-3340_219-3339d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252488 | |||||||
| chr9:119252553 | C | T | 49 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(46): Show |
49 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.219-3403G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252553 | |||||||
| chr9:119252553 | CGT | C | 28 | a0001c0001t0001g0161 a0001c0001t0002g0233 a0001c0001t0002g0234 others(25): Show |
28 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.219-3405_219-3404d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252553 | |||||||
| chr9:119252574 | A | T | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-3424T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252574 | |||||||
| chr9:119252862 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-3712A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252862 | |||||||
| chr9:119252890 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.219-3740C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252890 | |||||||
| chr9:119252944 | C | T | 2 | a0001c0003t0001g0191 a0001c0003t0001g0209 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-3794G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252944 | |||||||
| chr9:119253110 | G | C | 2 | a0001c0001t0001g0047 a0001c0001t0003g0009 |
2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.219-3960C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253110 | |||||||
| chr9:119253137 | G | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.219-3987C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253137 | |||||||
| chr9:119253548 | A | T | 1 | a0001c0002t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.219-4398T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253548 | |||||||
| chr9:119253864 | A | G | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.219-4714T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253864 | |||||||
| chr9:119253906 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-4756A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253906 | |||||||
| chr9:119253955 | T | C | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-4805A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253955 | |||||||
| chr9:119253983 | T | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0156 |
2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.219-4833A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253983 | |||||||
| chr9:119254013 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.219-4863A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254013 | |||||||
| chr9:119254030 | A | C | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.219-4880T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254030 | |||||||
| chr9:119254166 | A | G | 1 | a0001c0002t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-5016T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254166 | |||||||
| chr9:119254315 | A | G | 29 | a0001c0001t0001g0121 a0001c0001t0001g0161 a0001c0001t0002g0233 others(26): Show |
29 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.219-5165T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254315 | |||||||
| chr9:119254378 | C | T | 40 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(37): Show |
40 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.219-5228G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254378 | |||||||
| chr9:119254407 | G | A | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-5257C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254407 | |||||||
| chr9:119254474 | T | C | 1 | a0001c0002t0001g0114 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.219-5324A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254474 | |||||||
| chr9:119254680 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.219-5530C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254680 | |||||||
| chr9:119254689 | G | A | 6 | a0001c0001t0001g0047 a0001c0001t0001g0210 a0001c0001t0003g0008 others(3): Show |
6 | HG00741.hp1 HG01515.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-5539C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254689 | |||||||
| chr9:119254811 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.219-5661A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254811 | |||||||
| chr9:119254812 | G | A | 28 | a0001c0001t0001g0161 a0001c0001t0002g0233 a0001c0001t0002g0234 others(25): Show |
28 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.219-5662C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254812 | |||||||
| chr9:119254950 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.219-5800C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254950 | |||||||
| chr9:119255080 | T | TA | 5 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(2): Show |
5 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-5931dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255080 | |||||||
| chr9:119255184 | G | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(6): Show |
9 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-6034C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255184 | |||||||
| chr9:119255512 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.219-6362G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255512 | |||||||
| chr9:119255513 | G | A | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-6363C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255513 | |||||||
| chr9:119255596 | G | C | 17 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(14): Show |
17 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-6446C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255596 | |||||||
| chr9:119255615 | G | T | 213 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.219-6465C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255615 | |||||||
| chr9:119255656 | C | T | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.219-6506G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255656 | |||||||
| chr9:119255687 | C | G | 1 | a0001c0002t0001g0102 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.219-6537G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255687 | |||||||
| chr9:119255782 | C | G | 34 | a0001c0001t0001g0043 a0001c0002t0001g0091 a0001c0002t0001g0200 others(31): Show |
34 | HG01109.hp2 HG01123.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.219-6632G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255782 | |||||||
| chr9:119255815 | C | T | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-6665G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255815 | |||||||
| chr9:119255835 | G | C | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-6685C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255835 | |||||||
| chr9:119255897 | G | C | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-6747C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255897 | |||||||
| chr9:119255904 | G | A | 14 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.219-6754C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255904 | |||||||
| chr9:119255909 | C | T | 132 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(129): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.219-6759G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255909 | |||||||
| chr9:119255912 | G | A | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-6762C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255912 | |||||||
| chr9:119255954 | C | CA | 7 | a0001c0001t0001g0047 a0001c0001t0001g0193 a0001c0001t0003g0009 others(4): Show |
7 | HG00741.hp1 HG01515.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-6805dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | |||||||
| chr9:119255954 | CA | C | 24 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0066 others(21): Show |
24 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.219-6805delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | |||||||
| chr9:119255954 | CAA | C | 83 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.219-6806_219-6805d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | |||||||
| chr9:119255954 | CAAA | C | 84 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0052 others(81): Show |
84 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.219-6807_219-6805d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | |||||||
| chr9:119255954 | CAAAAAA | C | 10 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-6810_219-6805d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | |||||||
| chr9:119256013 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.219-6863C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256013 | |||||||
| chr9:119256047 | G | A | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-6897C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256047 | |||||||
| chr9:119256192 | C | T | 2 | a0001c0003t0001g0191 a0001c0003t0001g0209 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-7042G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256192 | |||||||
| chr9:119256310 | T | C | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-7160A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256310 | |||||||
| chr9:119256413 | G | A | 2 | a0001c0001t0001g0130 a0001c0003t0001g0142 |
2 | HG00741.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.219-7263C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256413 | |||||||
| chr9:119256518 | C | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0068 a0001c0002t0001g0194 |
3 | HG00099.hp2 HG00280.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.219-7368G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256518 | |||||||
| chr9:119256526 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.219-7376T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256526 | |||||||
| chr9:119256588 | T | G | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-7438A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256588 | |||||||
| chr9:119256819 | TAATC | T | 2 | a0001c0002t0001g0069 a0001c0002t0001g0169 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.219-7673_219-7670d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256819 | |||||||
| chr9:119256941 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.219-7791G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256941 | |||||||
| chr9:119257060 | T | C | 17 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(14): Show |
17 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-7910A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257060 | |||||||
| chr9:119257156 | A | T | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-8006T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257156 | |||||||
| chr9:119257217 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.219-8067T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257217 | |||||||
| chr9:119257248 | A | G | 13 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(10): Show |
13 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-8098T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257248 | |||||||
| chr9:119257302 | G | C | 2 | a0001c0001t0001g0170 a0001c0003t0002g0225 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.219-8152C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257302 | |||||||
| chr9:119257631 | A | C | 20 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(17): Show |
20 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.219-8481T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257631 | |||||||
| chr9:119257781 | C | T | 17 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(14): Show |
17 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-8631G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257781 | |||||||
| chr9:119257782 | G | A | 1 | a0001c0002t0001g0028 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.219-8632C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257782 | |||||||
| chr9:119257867 | A | G | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-8717T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257867 | |||||||
| chr9:119257902 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0146 |
3 | HG01346.hp1 HG01975.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.219-8752G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257902 | |||||||
| chr9:119257918 | G | C | 1 | a0001c0001t0002g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.219-8768C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257918 | |||||||
| chr9:119257923 | A | T | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-8773T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257923 | |||||||
| chr9:119258401 | G | C | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.219-9251C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258401 | |||||||
| chr9:119258417 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0003g0009 |
2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.219-9267G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258417 | |||||||
| chr9:119258420 | T | C | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-9270A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258420 | |||||||
| chr9:119258506 | T | A | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-9356A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258506 | |||||||
| chr9:119258507 | G | T | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-9357C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258507 | |||||||
| chr9:119258604 | G | A | 30 | a0001c0001t0001g0043 a0001c0002t0001g0091 a0001c0002t0001g0200 others(27): Show |
30 | HG01109.hp2 HG01123.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.219-9454C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258604 | |||||||
| chr9:119258615 | C | T | 43 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(40): Show |
43 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.219-9465G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258615 | |||||||
| chr9:119258618 | A | G | 2 | a0001c0003t0001g0105 a0001c0003t0001g0137 |
2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.219-9468T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258618 | |||||||
| chr9:119258654 | T | C | 1 | a0001c0002t0001g0095 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.219-9504A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258654 | |||||||
| chr9:119258667 | G | T | 10 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-9517C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258667 | |||||||
| chr9:119258681 | G | C | 1 | a0001c0002t0001g0076 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.219-9531C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258681 | |||||||
| chr9:119258923 | T | G | 1 | a0001c0003t0001g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219-9773A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258923 | |||||||
| chr9:119259610 | G | A | 1 | a0001c0004t0002g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219-10460C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119259610 | |||||||
| chr9:119259847 | T | G | 3 | a0001c0003t0001g0044 a0001c0003t0001g0046 a0001c0003t0001g0211 |
3 | HG02451.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.219-10697A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119259847 | |||||||
| chr9:119260250 | C | T | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-11100G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260250 | |||||||
| chr9:119260540 | G | A | 1 | a0001c0006t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219-11390C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260540 | |||||||
| chr9:119260574 | T | G | 21 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(18): Show |
21 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.219-11424A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260574 | |||||||
| chr9:119260581 | A | G | 2 | a0001c0003t0001g0173 a0001c0003t0001g0205 |
2 | HG01496.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.219-11431T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260581 | |||||||
| chr9:119260838 | G | A | 5 | a0001c0001t0001g0047 a0001c0001t0003g0008 a0001c0001t0003g0009 others(2): Show |
5 | HG00741.hp1 HG01515.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-11688C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260838 | |||||||
| chr9:119260893 | G | A | 1 | a0001c0002t0001g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.219-11743C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260893 | |||||||
| chr9:119260967 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.219-11817A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260967 | |||||||
| chr9:119261221 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.219-12071C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261221 | |||||||
| chr9:119261258 | G | A | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-12108C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261258 | |||||||
| chr9:119261283 | G | T | 2 | a0001c0003t0001g0191 a0001c0003t0001g0209 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-12133C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261283 | |||||||
| chr9:119261296 | T | C | 211 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.219-12146A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261296 | |||||||
| chr9:119261380 | T | C | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-12230A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261380 | |||||||
| chr9:119261516 | A | C | 18 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(15): Show |
18 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-12366T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261516 | |||||||
| chr9:119261517 | G | C | 18 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(15): Show |
18 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-12367C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261517 | |||||||
| chr9:119261544 | C | T | 1 | a0001c0002t0001g0102 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.219-12394G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261544 | |||||||
| chr9:119261788 | T | C | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-12638A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261788 | |||||||
| chr9:119261861 | C | T | 10 | a0001c0001t0001g0043 a0001c0003t0001g0083 a0001c0003t0001g0178 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-12711G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261861 | |||||||
| chr9:119261943 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0156 |
2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.219-12793A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261943 | |||||||
| chr9:119261945 | G | A | 1 | a0001c0002t0001g0102 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.219-12795C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261945 | |||||||
| chr9:119262083 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.219-12933T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262083 | |||||||
| chr9:119262179 | A | G | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-13029T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262179 | |||||||
| chr9:119262521 | C | T | 1 | a0001c0003t0007g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.219-13371G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262521 | |||||||
| chr9:119262621 | G | C | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.219-13471C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262621 | |||||||
| chr9:119262632 | C | A | 1 | a0001c0003t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.219-13482G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262632 | |||||||
| chr9:119262645 | C | CA | 6 | a0001c0001t0001g0202 a0001c0001t0001g0210 a0001c0001t0002g0228 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-13496dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262645 | |||||||
| chr9:119262645 | CA | C | 176 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.219-13496delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262645 | |||||||
| chr9:119262689 | C | A | 2 | a0001c0003t0001g0196 a0001c0003t0001g0206 |
2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.219-13539G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262689 | |||||||
| chr9:119262957 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.219-13807T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262957 | |||||||
| chr9:119262971 | C | G | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-13821G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262971 | |||||||
| chr9:119262981 | A | G | 18 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(15): Show |
18 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-13831T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262981 | |||||||
| chr9:119263106 | G | T | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-13956C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263106 | |||||||
| chr9:119263158 | G | A | 13 | a0001c0001t0003g0001 a0001c0002t0001g0069 a0001c0002t0001g0160 others(10): Show |
13 | HG00140.hp1 HG00738.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.219-14008C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263158 | |||||||
| chr9:119263180 | C | G | 211 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.219-14030G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263180 | |||||||
| chr9:119263472 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.219-14322C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263472 | |||||||
| chr9:119263525 | T | C | 25 | a0001c0002t0001g0091 a0001c0002t0001g0200 a0001c0002t0001g0201 others(22): Show |
25 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.219-14375A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263525 | |||||||
| chr9:119263544 | A | G | 36 | a0001c0001t0001g0043 a0001c0002t0001g0091 a0001c0002t0001g0200 others(33): Show |
36 | HG01109.hp2 HG01123.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.219-14394T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263544 | |||||||
| chr9:119263567 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.219-14417A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263567 | |||||||
| chr9:119263601 | C | CT | 5 | a0001c0001t0001g0047 a0001c0001t0001g0202 a0001c0003t0001g0184 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-14452dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | |||||||
| chr9:119263601 | C | CTTT | 94 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0038 others(91): Show |
94 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.219-14454_219-1445 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | |||||||
| chr9:119263601 | C | CTTTT | 76 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0042 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.219-14455_219-1445 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | |||||||
| chr9:119263601 | C | CTTTTT | 25 | a0001c0001t0001g0022 a0001c0001t0002g0228 a0001c0002t0001g0056 others(22): Show |
25 | HG00423.hp1 HG00738.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.219-14456_219-1445 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | |||||||
| chr9:119263601 | C | CTTTTTT | 9 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0002g0219 others(6): Show |
9 | HG01106.hp1 HG01109.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-14457_219-1445 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | |||||||
| chr9:119263708 | C | T | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-14558G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263708 | |||||||
| chr9:119263764 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.219-14614G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263764 | |||||||
| chr9:119263845 | T | C | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-14695A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263845 | |||||||
| chr9:119263854 | C | A | 44 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(41): Show |
44 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.219-14704G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263854 | |||||||
| chr9:119264085 | A | T | 1 | a0001c0003t0002g0227 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.219-14935T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264085 | |||||||
| chr9:119264125 | T | A | 171 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.219-14975A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264125 | |||||||
| chr9:119264247 | C | A | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-15097G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264247 | |||||||
| chr9:119264421 | A | T | 10 | a0001c0001t0001g0043 a0001c0003t0001g0083 a0001c0003t0001g0178 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-15271T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264421 | |||||||
| chr9:119264717 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.219-15567G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264717 | |||||||
| chr9:119264878 | G | A | 1 | a0001c0002t0003g0005 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.219-15728C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264878 | |||||||
| chr9:119265016 | C | T | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-15866G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265016 | |||||||
| chr9:119265034 | T | C | 3 | a0001c0002t0001g0069 a0001c0002t0001g0169 a0001c0002t0003g0002 |
3 | HG01106.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.219-15884A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265034 | |||||||
| chr9:119265065 | T | C | 3 | a0001c0004t0001g0025 a0001c0004t0001g0027 a0001c0004t0001g0071 |
3 | HG01069.hp1 HG01071.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.219-15915A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265065 | |||||||
| chr9:119265350 | G | A | 211 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.219-16200C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265350 | |||||||
| chr9:119265443 | A | AT | 2 | a0001c0001t0001g0045 a0001c0001t0001g0192 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.219-16294dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265443 | |||||||
| chr9:119265445 | A | T | 170 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.219-16295T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265445 | |||||||
| chr9:119265446 | A | T | 1 | a0001c0002t0001g0147 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.219-16296T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265446 | |||||||
| chr9:119265591 | C | T | 3 | a0001c0001t0002g0230 a0001c0003t0002g0232 a0001c0005t0002g0235 |
3 | HG01109.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.219-16441G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265591 | |||||||
| chr9:119265720 | A | G | 2 | a0001c0003t0001g0191 a0001c0003t0001g0209 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-16570T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265720 | |||||||
| chr9:119265733 | A | T | 214 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.219-16583T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265733 | |||||||
| chr9:119265808 | G | A | 1 | a0001c0002t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-16658C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265808 | |||||||
| chr9:119265869 | C | T | 10 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-16719G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265869 | |||||||
| chr9:119265882 | G | A | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-16732C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265882 | |||||||
| chr9:119266266 | C | T | 2 | a0001c0003t0001g0191 a0001c0003t0001g0209 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-17116G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266266 | |||||||
| chr9:119266345 | G | A | 1 | a0001c0002t0004g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.219-17195C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266345 | |||||||
| chr9:119266511 | G | T | 13 | a0001c0001t0003g0001 a0001c0002t0001g0069 a0001c0002t0001g0160 others(10): Show |
13 | HG00140.hp1 HG00738.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.219-17361C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266511 | |||||||
| chr9:119266674 | C | T | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-17524G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266674 | |||||||
| chr9:119266681 | C | T | 79 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(76): Show |
79 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.219-17531G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266681 | |||||||
| chr9:119266810 | T | A | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-17660A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266810 | |||||||
| chr9:119267095 | T | C | 1 | a0001c0002t0003g0005 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.219-17945A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267095 | |||||||
| chr9:119267382 | C | A | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-18232G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267382 | |||||||
| chr9:119267402 | A | G | 52 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(49): Show |
52 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.219-18252T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267402 | |||||||
| chr9:119267428 | T | A | 52 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(49): Show |
52 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.219-18278A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267428 | |||||||
| chr9:119267445 | G | A | 1 | a0001c0003t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.219-18295C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267445 | |||||||
| chr9:119267584 | C | T | 1 | a0003c0008t0001g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.219-18434G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267584 | |||||||
| chr9:119267601 | A | T | 1 | a0001c0003t0002g0227 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.219-18451T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267601 | |||||||
| chr9:119267612 | G | A | 9 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-18462C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267612 | |||||||
| chr9:119267636 | C | CAATA | 50 | a0001c0001t0001g0022 a0001c0001t0001g0079 a0001c0001t0001g0088 others(47): Show |
50 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.219-18490_219-1848 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | |||||||
| chr9:119267636 | C | CAATAAAT others(1): Show |
22 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0151 others(19): Show |
22 | HG00544.hp2 HG01109.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.219-18494_219-1848 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | |||||||
| chr9:119267636 | C | CAATAAAT others(5): Show |
1 | a0001c0015t0001g0131 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.219-18498_219-1848 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | |||||||
| chr9:119267636 | CAATA | C | 26 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0052 others(23): Show |
26 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.219-18490_219-1848 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | |||||||
| chr9:119267636 | CAATAAAT others(1): Show |
C | 19 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(16): Show |
19 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-18494_219-1848 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | |||||||
| chr9:119267636 | CAATAAAT others(5): Show |
C | 3 | a0001c0004t0001g0015 a0001c0004t0002g0231 a0001c0006t0001g0016 |
3 | HG02976.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.219-18498_219-1848 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | |||||||
| chr9:119267636 | CAATAAAT others(17): Show |
C | 46 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(43): Show |
46 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.219-18510_219-1848 others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | |||||||
| chr9:119267733 | A | G | 1 | a0001c0002t0001g0102 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.219-18583T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267733 | |||||||
| chr9:119267786 | G | A | 26 | a0001c0001t0001g0150 a0001c0001t0001g0161 a0001c0002t0001g0026 others(23): Show |
26 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.219-18636C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267786 | |||||||
| chr9:119267798 | C | T | 46 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(43): Show |
46 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.219-18648G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267798 | |||||||
| chr9:119267900 | G | C | 46 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(43): Show |
46 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.219-18750C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267900 | |||||||
| chr9:119267989 | T | C | 17 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(14): Show |
17 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-18839A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267989 | |||||||
| chr9:119268052 | A | G | 218 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.219-18902T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268052 | |||||||
| chr9:119268088 | C | A | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-18938G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268088 | |||||||
| chr9:119268199 | C | T | 1 | a0001c0005t0002g0235 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219-19049G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268199 | |||||||
| chr9:119268201 | T | C | 208 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(205): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.219-19051A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268201 | |||||||
| chr9:119268243 | A | AATATAGA others(3): Show |
1 | a0001c0001t0001g0122 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.219-19094_219-1909 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268243 | |||||||
| chr9:119268243 | A | AATATAGA others(7): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0101 |
2 | HG03834.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.219-19094_219-1909 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268243 | |||||||
| chr9:119268247 | A | AATAG | 3 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0004t0002g0231 |
3 | HG00738.hp2 HG01106.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.219-19101_219-1909 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | |||||||
| chr9:119268247 | A | G | 5 | a0001c0001t0001g0053 a0001c0001t0001g0101 a0001c0001t0001g0122 others(2): Show |
5 | HG00639.hp1 HG02698.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-19097T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | |||||||
| chr9:119268247 | AATAG | A | 66 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0043 others(63): Show |
66 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.219-19101_219-1909 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | |||||||
| chr9:119268247 | AATAGATA others(1): Show |
A | 21 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0055 others(18): Show |
21 | HG00438.hp2 HG00735.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.219-19105_219-1909 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | |||||||
| chr9:119268247 | AATAGATA others(5): Show |
A | 2 | a0001c0001t0001g0066 a0001c0003t0002g0226 |
2 | HG01069.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.219-19109_219-1909 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | |||||||
| chr9:119268285 | T | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0101 a0001c0001t0001g0161 |
3 | HG03017.hp1 HG03834.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.219-19135A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | |||||||
| chr9:119268285 | T | TAGAC | 4 | a0001c0001t0001g0130 a0001c0002t0001g0026 a0001c0002t0001g0067 others(1): Show |
4 | HG01243.hp2 HG04184.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | |||||||
| chr9:119268285 | T | TAGATAGA others(1): Show |
9 | a0001c0001t0001g0038 a0001c0001t0001g0100 a0001c0001t0001g0146 others(6): Show |
9 | HG00280.hp1 HG01255.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | |||||||
| chr9:119268285 | T | TAGATAGA others(5): Show |
72 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0052 others(69): Show |
72 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | |||||||
| chr9:119268285 | T | TAGATAGA others(9): Show |
21 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0088 others(18): Show |
21 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | |||||||
| chr9:119268285 | T | TAGATAGA others(13): Show |
1 | a0001c0002t0003g0012 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.219-19136_219-1913 others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | |||||||
| chr9:119268285 | T | TAGATAGA others(13): Show |
6 | a0001c0001t0001g0151 a0001c0002t0001g0069 a0001c0002t0001g0108 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | |||||||
| chr9:119268285 | T | TAGATAGA others(17): Show |
2 | a0001c0002t0001g0086 a0001c0002t0001g0129 |
2 | NA18747.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.219-19136_219-1913 others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | |||||||
| chr9:119268289 | T | C | 1 | a0001c0002t0003g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.219-19139A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268289 | |||||||
| chr9:119268289 | T | TAGATAGA others(5): Show |
2 | a0001c0001t0001g0168 a0001c0003t0001g0196 |
2 | HG00544.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.219-19140_219-1913 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268289 | |||||||
| chr9:119268289 | T | TAGATAGA others(9): Show |
2 | a0001c0003t0001g0206 a0001c0014t0003g0004 |
2 | HG00738.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.219-19140_219-1913 others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268289 | |||||||
| chr9:119268345 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.219-19195G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268345 | |||||||
| chr9:119268495 | G | T | 1 | a0001c0002t0001g0076 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.219-19345C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268495 | |||||||
| chr9:119268538 | A | C | 52 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(49): Show |
52 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.219-19388T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268538 | |||||||
| chr9:119268693 | G | A | 2 | a0001c0004t0001g0015 a0001c0004t0002g0231 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-19543C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268693 | |||||||
| chr9:119268705 | G | A | 156 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(153): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.219-19555C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268705 | |||||||
| chr9:119269090 | C | G | 4 | a0001c0001t0002g0230 a0001c0003t0001g0209 a0001c0003t0002g0232 others(1): Show |
4 | HG01109.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-19940G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269090 | |||||||
| chr9:119269159 | A | G | 4 | a0001c0001t0002g0230 a0001c0003t0001g0209 a0001c0003t0002g0232 others(1): Show |
4 | HG01109.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-20009T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269159 | |||||||
| chr9:119269224 | TCACTATT others(7): Show |
T | 1 | a0001c0004t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.219-20088_219-2007 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269224 | |||||||
| chr9:119269225 | C | T | 207 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(204): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.219-20075G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269225 | |||||||
| chr9:119269239 | C | T | 1 | a0001c0004t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.219-20089G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269239 | |||||||
| chr9:119269270 | A | C | 1 | a0001c0002t0001g0166 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.219-20120T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269270 | |||||||
| chr9:119269325 | T | C | 52 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(49): Show |
52 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.219-20175A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269325 | |||||||
| chr9:119269399 | T | C | 2 | a0003c0008t0001g0089 a0003c0008t0001g0172 |
2 | NA18612.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.219-20249A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269399 | |||||||
| chr9:119269443 | T | C | 3 | a0001c0002t0001g0112 a0001c0003t0001g0039 a0001c0003t0001g0040 |
3 | HG02896.hp1 HG02897.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.219-20293A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269443 | |||||||
| chr9:119269449 | T | A | 1 | a0001c0002t0001g0166 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.219-20299A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269449 | |||||||
| chr9:119269503 | T | C | 9 | a0001c0001t0001g0043 a0001c0003t0001g0083 a0001c0003t0001g0178 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-20353A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269503 | |||||||
| chr9:119269625 | A | C | 1 | a0001c0003t0001g0176 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.219-20475T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269625 | |||||||
| chr9:119269752 | C | T | 4 | a0001c0001t0002g0230 a0001c0003t0001g0209 a0001c0003t0002g0232 others(1): Show |
4 | HG01109.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-20602G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269752 | |||||||
| chr9:119269822 | G | A | 6 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0004t0001g0015 others(3): Show |
6 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-20672C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269822 | |||||||
| chr9:119269824 | A | G | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-20674T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269824 | |||||||
| chr9:119269837 | T | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.219-20687A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269837 | |||||||
| chr9:119269868 | A | AC | 208 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(205): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.219-20719_219-2071 others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269868 | |||||||
| chr9:119270108 | G | A | 6 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0004t0001g0015 others(3): Show |
6 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-20958C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270108 | |||||||
| chr9:119270205 | T | C | 206 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.219-21055A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270205 | |||||||
| chr9:119270206 | G | A | 6 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0004t0001g0015 others(3): Show |
6 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-21056C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270206 | |||||||
| chr9:119270324 | C | T | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-21174G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270324 | |||||||
| chr9:119270329 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.219-21179G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270329 | |||||||
| chr9:119270397 | T | A | 6 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0004t0001g0015 others(3): Show |
6 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-21247A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270397 | |||||||
| chr9:119270449 | T | C | 47 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(44): Show |
47 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.219-21299A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270449 | |||||||
| chr9:119270658 | A | G | 208 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(205): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.219-21508T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270658 | |||||||
| chr9:119270666 | T | C | 150 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(147): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.219-21516A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270666 | |||||||
| chr9:119270804 | A | G | 3 | a0001c0001t0002g0230 a0001c0003t0002g0232 a0001c0005t0002g0235 |
3 | HG01109.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.219-21654T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270804 | |||||||
| chr9:119270896 | A | C | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-21746T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270896 | |||||||
| chr9:119271029 | A | G | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-21879T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271029 | |||||||
| chr9:119271188 | C | T | 149 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(146): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.219-22038G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271188 | |||||||
| chr9:119271276 | G | C | 202 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(199): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.219-22126C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271276 | |||||||
| chr9:119271324 | C | CA | 179 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.219-22175dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271324 | |||||||
| chr9:119271324 | C | CAA | 17 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0079 others(14): Show |
17 | HG00423.hp1 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-22176_219-2217 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271324 | |||||||
| chr9:119271388 | A | G | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-22238T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271388 | |||||||
| chr9:119271541 | C | A | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-22391G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271541 | |||||||
| chr9:119271695 | G | A | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-22545C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271695 | |||||||
| chr9:119271728 | G | A | 149 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(146): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.219-22578C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271728 | |||||||
| chr9:119271989 | G | T | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-22839C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271989 | |||||||
| chr9:119271993 | C | G | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-22843G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271993 | |||||||
| chr9:119272049 | G | A | 154 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(151): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.219-22899C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272049 | |||||||
| chr9:119272052 | A | G | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-22902T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272052 | |||||||
| chr9:119272091 | C | CA | 6 | a0001c0001t0002g0234 a0001c0003t0001g0059 a0001c0003t0001g0072 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-22942dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272091 | |||||||
| chr9:119272091 | CA | C | 153 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.219-22942delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272091 | |||||||
| chr9:119272091 | CAA | C | 25 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(22): Show |
25 | HG01109.hp2 HG01123.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.219-22943_219-2294 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272091 | |||||||
| chr9:119272091 | CAAA | C | 9 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-22944_219-2294 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272091 | |||||||
| chr9:119272142 | G | T | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-22992C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272142 | |||||||
| chr9:119272165 | G | A | 9 | a0001c0001t0001g0043 a0001c0003t0001g0178 a0001c0003t0001g0181 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-23015C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272165 | |||||||
| chr9:119272206 | G | GA | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-23057dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272206 | |||||||
| chr9:119272378 | C | T | 6 | a0001c0001t0001g0064 a0001c0001t0002g0234 a0001c0002t0001g0166 others(3): Show |
6 | HG01943.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-23228G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272378 | |||||||
| chr9:119272411 | T | C | 149 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(146): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.219-23261A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272411 | |||||||
| chr9:119272448 | A | G | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-23298T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272448 | |||||||
| chr9:119272563 | C | G | 5 | a0001c0001t0002g0230 a0001c0003t0001g0191 a0001c0003t0001g0209 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-23413G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272563 | |||||||
| chr9:119272575 | C | A | 151 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(148): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.219-23425G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272575 | |||||||
| chr9:119272760 | C | T | 146 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(143): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.219-23610G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272760 | |||||||
| chr9:119272795 | C | T | 150 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(147): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.219-23645G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272795 | |||||||
| chr9:119272816 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.219-23666G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272816 | |||||||
| chr9:119272954 | T | C | 11 | a0001c0001t0002g0230 a0001c0003t0001g0187 a0001c0003t0001g0191 others(8): Show |
11 | HG01109.hp1 HG02109.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.219-23804A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272954 | |||||||
| chr9:119273096 | A | G | 11 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.219-23946T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273096 | |||||||
| chr9:119273178 | A | C | 1 | a0001c0002t0001g0152 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.219-24028T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273178 | |||||||
| chr9:119273322 | T | C | 3 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0185 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-24172A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273322 | |||||||
| chr9:119273421 | G | C | 8 | a0001c0001t0001g0043 a0001c0001t0001g0210 a0001c0003t0001g0105 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-24271C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273421 | |||||||
| chr9:119273601 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.219-24451T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273601 | |||||||
| chr9:119273693 | T | C | 10 | a0001c0001t0001g0043 a0001c0001t0001g0210 a0001c0003t0001g0105 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-24543A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273693 | |||||||
| chr9:119273714 | A | G | 70 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0064 others(67): Show |
70 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.219-24564T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273714 | |||||||
| chr9:119273857 | A | G | 82 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.219-24707T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273857 | |||||||
| chr9:119274100 | T | C | 12 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(9): Show |
12 | HG00639.hp2 HG00735.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-24950A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274100 | |||||||
| chr9:119274179 | T | G | 14 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(11): Show |
14 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-25029A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274179 | |||||||
| chr9:119274180 | C | A | 3 | a0001c0001t0002g0234 a0001c0003t0001g0059 a0001c0003t0001g0072 |
3 | HG02258.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.219-25030G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274180 | |||||||
| chr9:119274396 | G | C | 24 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0202 others(21): Show |
24 | HG00639.hp2 HG00735.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.219-25246C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274396 | |||||||
| chr9:119274715 | C | T | 43 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0055 others(40): Show |
43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.219-25565G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274715 | |||||||
| chr9:119274809 | G | C | 1 | a0001c0001t0003g0009 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.219-25659C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274809 | |||||||
| chr9:119274848 | G | T | 43 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0055 others(40): Show |
43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.219-25698C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274848 | |||||||
| chr9:119275018 | C | T | 43 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0055 others(40): Show |
43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.219-25868G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275018 | |||||||
| chr9:119275073 | C | T | 3 | a0001c0001t0001g0122 a0001c0002t0001g0093 a0001c0002t0001g0102 |
3 | HG02074.hp1 NA18946.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.219-25923G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275073 | |||||||
| chr9:119275148 | T | C | 2 | a0001c0001t0001g0170 a0001c0003t0002g0225 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.219-25998A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275148 | |||||||
| chr9:119275188 | A | G | 2 | a0001c0005t0001g0197 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.219-26038T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275188 | |||||||
| chr9:119275266 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.219-26116A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275266 | |||||||
| chr9:119275390 | G | A | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-26240C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275390 | |||||||
| chr9:119275400 | C | G | 43 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0055 others(40): Show |
43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.219-26250G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275400 | |||||||
| chr9:119275569 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.219-26419G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275569 | |||||||
| chr9:119275607 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.219-26457T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275607 | |||||||
| chr9:119275679 | G | C | 9 | a0001c0001t0001g0043 a0001c0001t0001g0210 a0001c0003t0001g0105 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-26529C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275679 | |||||||
| chr9:119275807 | C | T | 2 | a0001c0002t0001g0108 a0001c0002t0001g0129 |
2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.219-26657G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275807 | |||||||
| chr9:119275856 | C | T | 2 | a0001c0003t0001g0191 a0001c0003t0001g0211 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219-26706G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275856 | |||||||
| chr9:119275897 | G | A | 5 | a0001c0003t0001g0021 a0001c0006t0001g0016 a0001c0006t0001g0017 others(2): Show |
5 | HG01123.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-26747C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275897 | |||||||
| chr9:119275899 | G | A | 41 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0055 others(38): Show |
41 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.219-26749C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275899 | |||||||
| chr9:119275945 | C | A | 2 | a0001c0001t0001g0064 a0001c0002t0001g0166 |
2 | HG01943.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.219-26795G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275945 | |||||||
| chr9:119276216 | A | G | 66 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(63): Show |
66 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.219-27066T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276216 | |||||||
| chr9:119276229 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0156 |
2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.219-27079A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276229 | |||||||
| chr9:119276272 | C | T | 6 | a0001c0001t0001g0193 a0001c0001t0001g0202 a0001c0003t0001g0083 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-27122G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276272 | |||||||
| chr9:119276582 | G | A | 96 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
96 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.219-27432C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276582 | |||||||
| chr9:119276691 | G | A | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-27541C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276691 | |||||||
| chr9:119276801 | G | A | 33 | a0001c0001t0001g0043 a0001c0001t0001g0193 a0001c0001t0001g0198 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.219-27651C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276801 | |||||||
| chr9:119277119 | G | A | 42 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0055 others(39): Show |
42 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.219-27969C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277119 | |||||||
| chr9:119277229 | G | C | 63 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(60): Show |
63 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.219-28079C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277229 | |||||||
| chr9:119277286 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-28136C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277286 | |||||||
| chr9:119277291 | A | G | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-28141T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277291 | |||||||
| chr9:119277298 | G | A | 139 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.219-28148C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277298 | |||||||
| chr9:119277322 | G | A | 12 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(9): Show |
12 | HG00639.hp2 HG00735.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-28172C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277322 | |||||||
| chr9:119277369 | G | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0182 others(3): Show |
6 | HG01261.hp1 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-28219C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277369 | |||||||
| chr9:119277426 | A | G | 63 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(60): Show |
63 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.219-28276T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277426 | |||||||
| chr9:119277495 | G | T | 33 | a0001c0001t0001g0043 a0001c0001t0001g0193 a0001c0001t0001g0198 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.219-28345C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277495 | |||||||
| chr9:119277556 | C | A | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-28406G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277556 | |||||||
| chr9:119277584 | G | A | 42 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0055 others(39): Show |
42 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.219-28434C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277584 | |||||||
| chr9:119277688 | T | C | 1 | a0001c0004t0002g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219-28538A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277688 | |||||||
| chr9:119277826 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.219-28676C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277826 | |||||||
| chr9:119277969 | T | A | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.219-28819A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277969 | |||||||
| chr9:119278310 | C | CA | 7 | a0001c0001t0001g0043 a0001c0001t0001g0210 a0001c0003t0001g0105 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-29161_219-2916 others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278310 | |||||||
| chr9:119278342 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.219-29192G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278342 | |||||||
| chr9:119278611 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0202 |
2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.219-29461A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278611 | |||||||
| chr9:119278616 | G | A | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-29466C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278616 | |||||||
| chr9:119278626 | G | A | 42 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0055 others(39): Show |
42 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.219-29476C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278626 | |||||||
| chr9:119278628 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.219-29478C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278628 | |||||||
| chr9:119278974 | C | G | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.219-29824G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278974 | |||||||
| chr9:119279079 | A | G | 4 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-29929T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279079 | |||||||
| chr9:119279182 | C | T | 132 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.219-30032G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279182 | |||||||
| chr9:119279298 | C | T | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-30148G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279298 | |||||||
| chr9:119279363 | C | T | 126 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.219-30213G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279363 | |||||||
| chr9:119279419 | C | T | 1 | a0001c0002t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.219-30269G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279419 | |||||||
| chr9:119279888 | G | C | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.219-30738C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279888 | |||||||
| chr9:119279892 | C | A | 1 | a0001c0003t0001g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219-30742G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279892 | |||||||
| chr9:119280028 | G | GA | 6 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-30879dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280028 | |||||||
| chr9:119280233 | G | C | 38 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(35): Show |
38 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.219-31083C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280233 | |||||||
| chr9:119280246 | C | CT | 109 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0045 others(106): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.219-31097dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280246 | |||||||
| chr9:119280260 | T | A | 124 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.219-31110A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280260 | |||||||
| chr9:119280301 | C | T | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-31151G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280301 | |||||||
| chr9:119280302 | G | A | 19 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(16): Show |
19 | HG01109.hp1 HG01109.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-31152C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280302 | |||||||
| chr9:119280342 | C | A | 1 | a0001c0003t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.219-31192G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280342 | |||||||
| chr9:119280404 | A | AT | 5 | a0001c0001t0001g0135 a0001c0001t0001g0168 a0001c0003t0001g0176 others(2): Show |
5 | HG00544.hp2 HG02698.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-31255dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280404 | |||||||
| chr9:119280404 | A | ATT | 65 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0055 others(62): Show |
65 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.219-31256_219-3125 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280404 | |||||||
| chr9:119280404 | A | T | 1 | a0001c0002t0001g0166 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.219-31254T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280404 | |||||||
| chr9:119280445 | C | T | 14 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(11): Show |
14 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-31295G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280445 | |||||||
| chr9:119280486 | C | T | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-31336G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280486 | |||||||
| chr9:119280531 | A | G | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219-31381T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280531 | |||||||
| chr9:119280650 | C | T | 14 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(11): Show |
14 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-31500G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280650 | |||||||
| chr9:119280705 | G | A | 1 | a0001c0004t0001g0186 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.219-31555C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280705 | |||||||
| chr9:119280718 | T | G | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.219-31568A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280718 | |||||||
| chr9:119280842 | TTTATTTA others(8): Show |
T | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.219-31707_219-3169 others(19): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280842 | |||||||
| chr9:119280906 | C | T | 14 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(11): Show |
14 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-31756G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280906 | |||||||
| chr9:119280942 | G | A | 18 | a0001c0001t0001g0182 a0001c0001t0002g0230 a0001c0002t0001g0200 others(15): Show |
18 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-31792C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280942 | |||||||
| chr9:119281222 | T | C | 1 | a0001c0002t0001g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.218+31916A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281222 | |||||||
| chr9:119281268 | C | A | 4 | a0001c0001t0001g0182 a0001c0001t0002g0230 a0001c0003t0001g0209 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+31870G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281268 | |||||||
| chr9:119281278 | T | C | 36 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.218+31860A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281278 | |||||||
| chr9:119281317 | A | G | 4 | a0001c0003t0001g0176 a0001c0004t0001g0014 a0001c0004t0001g0175 others(1): Show |
4 | HG02965.hp2 HG03453.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+31821T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281317 | |||||||
| chr9:119281542 | A | G | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.218+31596T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281542 | |||||||
| chr9:119281594 | G | A | 1 | a0001c0002t0003g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218+31544C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281594 | |||||||
| chr9:119281677 | TATATAA | T | 129 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.218+31455_218+3146 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281677 | |||||||
| chr9:119281743 | ATGATG | A | 2 | a0001c0003t0008g0212 a0001c0005t0001g0199 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.218+31390_218+3139 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281743 | |||||||
| chr9:119281806 | T | G | 1 | a0001c0002t0001g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218+31332A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281806 | |||||||
| chr9:119281915 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.218+31223G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281915 | |||||||
| chr9:119282115 | T | G | 2 | a0001c0002t0001g0087 a0001c0002t0001g0090 |
2 | NA18977.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.218+31023A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282115 | |||||||
| chr9:119282143 | T | C | 46 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0055 others(43): Show |
46 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.218+30995A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282143 | |||||||
| chr9:119282183 | C | T | 126 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.218+30955G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282183 | |||||||
| chr9:119282296 | C | G | 2 | a0001c0003t0008g0212 a0001c0005t0001g0199 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.218+30842G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282296 | |||||||
| chr9:119282356 | G | A | 3 | a0001c0003t0001g0179 a0001c0003t0001g0180 a0001c0005t0001g0197 |
3 | HG00639.hp2 HG00735.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.218+30782C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282356 | |||||||
| chr9:119282365 | C | T | 42 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0064 others(39): Show |
42 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.218+30773G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282365 | |||||||
| chr9:119282383 | G | A | 3 | a0001c0003t0001g0179 a0001c0003t0001g0180 a0001c0005t0001g0197 |
3 | HG00639.hp2 HG00735.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.218+30755C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282383 | |||||||
| chr9:119282709 | A | G | 2 | a0001c0001t0003g0008 a0001c0010t0001g0096 |
2 | HG02523.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.218+30429T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282709 | |||||||
| chr9:119282872 | T | G | 7 | a0001c0001t0001g0210 a0001c0003t0001g0105 a0001c0003t0001g0137 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+30266A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282872 | |||||||
| chr9:119282951 | A | G | 109 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.218+30187T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282951 | |||||||
| chr9:119283085 | G | C | 3 | a0001c0001t0002g0230 a0001c0003t0001g0173 a0001c0003t0001g0205 |
3 | HG01496.hp1 HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.218+30053C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283085 | |||||||
| chr9:119283121 | G | A | 135 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.218+30017C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283121 | |||||||
| chr9:119283237 | A | AGCCTCAG others(2): Show |
37 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(34): Show |
37 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.218+29900_218+2990 others(13): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283237 | |||||||
| chr9:119283240 | T | C | 41 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(38): Show |
41 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.218+29898A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283240 | |||||||
| chr9:119283462 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0151 a0001c0002t0001g0114 |
3 | HG00544.hp1 NA18977.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.218+29676T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283462 | |||||||
| chr9:119283491 | T | C | 36 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.218+29647A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283491 | |||||||
| chr9:119283548 | T | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+29590A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283548 | |||||||
| chr9:119283827 | C | T | 57 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+29311G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283827 | |||||||
| chr9:119283832 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.218+29306G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283832 | |||||||
| chr9:119283878 | T | A | 1 | a0001c0001t0002g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.218+29260A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283878 | |||||||
| chr9:119283915 | T | A | 106 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0045 others(103): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.218+29223A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283915 | |||||||
| chr9:119283949 | C | T | 3 | a0001c0001t0001g0082 a0001c0003t0001g0083 a0001c0004t0001g0186 |
3 | HG01261.hp1 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.218+29189G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283949 | |||||||
| chr9:119284159 | C | T | 3 | a0001c0001t0002g0230 a0001c0003t0001g0173 a0001c0003t0001g0205 |
3 | HG01496.hp1 HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.218+28979G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284159 | |||||||
| chr9:119284271 | T | A | 205 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.218+28867A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284271 | |||||||
| chr9:119284597 | C | G | 131 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.218+28541G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284597 | |||||||
| chr9:119284806 | A | G | 2 | a0001c0003t0001g0184 a0001c0003t0001g0196 |
2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218+28332T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284806 | |||||||
| chr9:119284818 | T | C | 3 | a0001c0001t0001g0210 a0001c0003t0001g0176 a0001c0004t0001g0175 |
3 | HG02258.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.218+28320A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284818 | |||||||
| chr9:119284850 | G | A | 1 | a0001c0015t0001g0131 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.218+28288C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284850 | |||||||
| chr9:119285021 | C | T | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+28117G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285021 | |||||||
| chr9:119285069 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+28069G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285069 | |||||||
| chr9:119285070 | G | C | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+28068C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285070 | |||||||
| chr9:119285103 | G | A | 57 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+28035C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285103 | |||||||
| chr9:119285169 | C | T | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+27969G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285169 | |||||||
| chr9:119285174 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.218+27964C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285174 | |||||||
| chr9:119285201 | C | CA | 25 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0161 others(22): Show |
25 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.218+27936dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | |||||||
| chr9:119285201 | CA | C | 34 | a0001c0001t0001g0038 a0001c0001t0001g0064 a0001c0001t0001g0088 others(31): Show |
34 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.218+27936delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | |||||||
| chr9:119285201 | CAA | C | 19 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0119 others(16): Show |
19 | HG00423.hp2 HG01256.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.218+27935_218+2793 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | |||||||
| chr9:119285201 | CAAA | C | 12 | a0001c0001t0001g0036 a0001c0001t0001g0101 a0001c0001t0001g0198 others(9): Show |
12 | HG01891.hp2 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+27934_218+2793 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | |||||||
| chr9:119285201 | CAAAAAAA | C | 60 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(57): Show |
60 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.218+27930_218+2793 others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | |||||||
| chr9:119285219 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+27919T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285219 | |||||||
| chr9:119285395 | C | G | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+27743G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285395 | |||||||
| chr9:119285402 | T | C | 5 | a0001c0003t0002g0221 a0001c0003t0002g0227 a0001c0003t0002g0232 others(2): Show |
5 | HG01109.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+27736A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285402 | |||||||
| chr9:119285672 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+27466A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285672 | |||||||
| chr9:119285697 | C | A | 1 | a0001c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.218+27441G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285697 | |||||||
| chr9:119285698 | G | A | 80 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.218+27440C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285698 | |||||||
| chr9:119285767 | C | T | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.218+27371G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285767 | |||||||
| chr9:119285771 | G | T | 1 | a0001c0002t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.218+27367C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285771 | |||||||
| chr9:119285819 | A | G | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+27319T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285819 | |||||||
| chr9:119285831 | G | A | 6 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(3): Show |
6 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+27307C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285831 | |||||||
| chr9:119285894 | A | G | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+27244T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285894 | |||||||
| chr9:119285908 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+27230G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285908 | |||||||
| chr9:119285954 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.218+27184G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285954 | |||||||
| chr9:119285973 | C | G | 1 | a0001c0003t0002g0222 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.218+27165G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285973 | |||||||
| chr9:119286179 | A | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.218+26959T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286179 | |||||||
| chr9:119286211 | G | A | 4 | a0001c0001t0001g0210 a0001c0001t0002g0230 a0001c0003t0001g0176 others(1): Show |
4 | HG02258.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26927C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286211 | |||||||
| chr9:119286238 | C | CT | 99 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.218+26899dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286238 | |||||||
| chr9:119286343 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+26795G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286343 | |||||||
| chr9:119286344 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+26794A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286344 | |||||||
| chr9:119286345 | C | G | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26793G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286345 | |||||||
| chr9:119286389 | C | T | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26749G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286389 | |||||||
| chr9:119286428 | G | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26710C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286428 | |||||||
| chr9:119286476 | C | T | 3 | a0001c0001t0001g0057 a0001c0003t0001g0019 a0001c0005t0001g0197 |
3 | HG02572.hp1 HG03239.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.218+26662G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286476 | |||||||
| chr9:119286492 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+26646G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286492 | |||||||
| chr9:119286523 | T | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26615A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286523 | |||||||
| chr9:119286529 | C | T | 1 | a0001c0003t0007g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218+26609G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286529 | |||||||
| chr9:119286785 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+26353T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286785 | |||||||
| chr9:119286831 | C | T | 2 | a0001c0001t0001g0174 a0001c0002t0001g0163 |
2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.218+26307G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286831 | |||||||
| chr9:119286846 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+26292T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286846 | |||||||
| chr9:119286849 | C | T | 3 | a0001c0001t0001g0082 a0001c0003t0001g0083 a0001c0004t0001g0186 |
3 | HG01261.hp1 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.218+26289G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286849 | |||||||
| chr9:119287044 | T | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26094A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287044 | |||||||
| chr9:119287060 | GA | G | 27 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0099 others(24): Show |
27 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.218+26077delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287060 | |||||||
| chr9:119287188 | T | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25950A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287188 | |||||||
| chr9:119287226 | C | T | 63 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0054 others(60): Show |
63 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.218+25912G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287226 | |||||||
| chr9:119287377 | T | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25761A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287377 | |||||||
| chr9:119287391 | T | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25747A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287391 | |||||||
| chr9:119287536 | G | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25602C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287536 | |||||||
| chr9:119287586 | A | C | 1 | a0001c0003t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218+25552T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287586 | |||||||
| chr9:119288003 | G | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25135C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288003 | |||||||
| chr9:119288140 | T | A | 2 | a0001c0007t0001g0080 a0001c0007t0001g0081 |
2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.218+24998A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288140 | |||||||
| chr9:119288328 | G | C | 1 | a0001c0001t0002g0228 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+24810C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288328 | |||||||
| chr9:119288350 | A | AT | 59 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(56): Show |
59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+24787dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288350 | |||||||
| chr9:119288417 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+24721A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288417 | |||||||
| chr9:119288497 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.218+24641C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288497 | |||||||
| chr9:119288538 | CT | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24599delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288538 | |||||||
| chr9:119288644 | G | A | 1 | a0001c0004t0002g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.218+24494C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288644 | |||||||
| chr9:119288769 | G | T | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24369C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288769 | |||||||
| chr9:119288798 | G | GT | 5 | a0001c0001t0001g0210 a0001c0001t0002g0230 a0001c0003t0001g0176 others(2): Show |
5 | HG02258.hp1 NA18522.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+24339dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288798 | |||||||
| chr9:119288803 | T | G | 77 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(74): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.218+24335A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288803 | |||||||
| chr9:119288821 | C | T | 2 | a0001c0001t0001g0132 a0004c0011t0001g0123 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.218+24317G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288821 | |||||||
| chr9:119288823 | C | T | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24315G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288823 | |||||||
| chr9:119288846 | T | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24292A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288846 | |||||||
| chr9:119288901 | T | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24237A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288901 | |||||||
| chr9:119288903 | C | T | 2 | a0001c0003t0002g0221 a0001c0004t0001g0015 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218+24235G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288903 | |||||||
| chr9:119288952 | C | T | 2 | a0001c0001t0003g0008 a0001c0010t0001g0096 |
2 | HG02523.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.218+24186G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288952 | |||||||
| chr9:119289017 | C | T | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24121G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289017 | |||||||
| chr9:119289061 | A | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24077T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289061 | |||||||
| chr9:119289080 | G | A | 3 | a0001c0002t0001g0070 a0001c0002t0001g0139 a0001c0002t0001g0153 |
3 | HG01123.hp2 HG01257.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.218+24058C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289080 | |||||||
| chr9:119289095 | C | T | 10 | a0001c0001t0001g0054 a0001c0001t0001g0158 a0001c0002t0001g0026 others(7): Show |
10 | HG01123.hp2 HG01169.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.218+24043G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289095 | |||||||
| chr9:119289114 | C | T | 63 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0054 others(60): Show |
63 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.218+24024G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289114 | |||||||
| chr9:119289132 | G | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24006C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289132 | |||||||
| chr9:119289151 | C | T | 18 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0101 others(15): Show |
18 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+23987G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289151 | |||||||
| chr9:119289275 | G | T | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+23863C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289275 | |||||||
| chr9:119289419 | T | C | 4 | a0001c0001t0001g0210 a0001c0001t0002g0230 a0001c0003t0001g0176 others(1): Show |
4 | HG02258.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+23719A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289419 | |||||||
| chr9:119289428 | T | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+23710A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289428 | |||||||
| chr9:119289429 | C | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+23709G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289429 | |||||||
| chr9:119289474 | A | T | 1 | a0001c0003t0001g0030 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.218+23664T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289474 | |||||||
| chr9:119289709 | C | T | 1 | a0001c0002t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.218+23429G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289709 | |||||||
| chr9:119289713 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+23425A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289713 | |||||||
| chr9:119289826 | A | C | 1 | a0001c0002t0001g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.218+23312T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289826 | |||||||
| chr9:119289870 | G | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+23268C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289870 | |||||||
| chr9:119289874 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+23264C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289874 | |||||||
| chr9:119289899 | T | A | 71 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(68): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.218+23239A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289899 | |||||||
| chr9:119290090 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.218+23048G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290090 | |||||||
| chr9:119290236 | C | T | 16 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0003t0001g0021 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.218+22902G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290236 | |||||||
| chr9:119290246 | A | G | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+22892T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290246 | |||||||
| chr9:119290519 | C | G | 134 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.218+22619G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290519 | |||||||
| chr9:119290858 | C | T | 1 | a0001c0003t0001g0176 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+22280G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290858 | |||||||
| chr9:119290889 | G | A | 18 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0101 others(15): Show |
18 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+22249C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290889 | |||||||
| chr9:119291041 | T | A | 2 | a0001c0003t0001g0195 a0001c0009t0001g0189 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.218+22097A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291041 | |||||||
| chr9:119291058 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.218+22080C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291058 | |||||||
| chr9:119291122 | C | CA | 53 | a0001c0001t0001g0036 a0001c0001t0001g0082 a0001c0001t0001g0088 others(50): Show |
53 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.218+22015dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291122 | |||||||
| chr9:119291122 | CA | C | 58 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0052 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+22015delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291122 | |||||||
| chr9:119291258 | G | C | 134 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.218+21880C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291258 | |||||||
| chr9:119291924 | T | G | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+21214A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291924 | |||||||
| chr9:119291977 | A | C | 1 | a0001c0003t0001g0092 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+21161T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291977 | |||||||
| chr9:119291993 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.218+21145T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291993 | |||||||
| chr9:119292526 | G | A | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+20612C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292526 | |||||||
| chr9:119292588 | T | C | 8 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(5): Show |
8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+20550A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292588 | |||||||
| chr9:119292601 | C | G | 8 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(5): Show |
8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+20537G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292601 | |||||||
| chr9:119292870 | A | G | 57 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+20268T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292870 | |||||||
| chr9:119292993 | T | C | 1 | a0001c0002t0001g0090 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.218+20145A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292993 | |||||||
| chr9:119293010 | T | C | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+20128A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119293010 | |||||||
| chr9:119293412 | G | A | 1 | a0001c0006t0002g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.218+19726C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119293412 | |||||||
| chr9:119293697 | T | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0202 |
2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.218+19441A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119293697 | |||||||
| chr9:119293922 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.218+19216A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119293922 | |||||||
| chr9:119294156 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.218+18982G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294156 | |||||||
| chr9:119294157 | C | T | 1 | a0001c0003t0001g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+18981G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294157 | |||||||
| chr9:119294182 | T | C | 3 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 |
3 | HG01243.hp1 HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.218+18956A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294182 | |||||||
| chr9:119294285 | C | T | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+18853G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294285 | |||||||
| chr9:119294297 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.218+18841C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294297 | |||||||
| chr9:119294378 | C | T | 63 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(60): Show |
63 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.218+18760G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294378 | |||||||
| chr9:119294695 | A | G | 1 | a0001c0002t0001g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.218+18443T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294695 | |||||||
| chr9:119294704 | A | G | 1 | a0001c0002t0001g0114 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.218+18434T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294704 | |||||||
| chr9:119294817 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+18321G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294817 | |||||||
| chr9:119294850 | C | T | 71 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(68): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.218+18288G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294850 | |||||||
| chr9:119294853 | T | TA | 21 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0003t0001g0021 others(18): Show |
21 | HG01123.hp1 HG01884.hp1 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.218+18284dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294853 | |||||||
| chr9:119294853 | T | TAAAAAA | 5 | a0001c0001t0001g0060 a0001c0001t0001g0135 a0001c0002t0001g0114 others(2): Show |
5 | HG00738.hp2 HG01243.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+18279_218+1828 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294853 | |||||||
| chr9:119294853 | T | TAAAAAAA | 54 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(51): Show |
54 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.218+18278_218+1828 others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294853 | |||||||
| chr9:119294853 | TA | T | 6 | a0001c0001t0002g0233 a0001c0002t0001g0125 a0001c0002t0001g0140 others(3): Show |
6 | HG01496.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+18284delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294853 | |||||||
| chr9:119294974 | C | CA | 133 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.218+18163dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294974 | |||||||
| chr9:119295063 | T | A | 5 | a0001c0003t0002g0221 a0001c0003t0002g0227 a0001c0003t0002g0232 others(2): Show |
5 | HG01109.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+18075A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295063 | |||||||
| chr9:119295077 | C | T | 63 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(60): Show |
63 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.218+18061G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295077 | |||||||
| chr9:119295085 | T | A | 4 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(1): Show |
4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+18053A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295085 | |||||||
| chr9:119295160 | AT | A | 32 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0101 others(29): Show |
32 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.218+17977delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295160 | |||||||
| chr9:119295393 | A | T | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+17745T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295393 | |||||||
| chr9:119295498 | T | C | 6 | a0001c0003t0001g0137 a0001c0003t0002g0221 a0001c0003t0002g0227 others(3): Show |
6 | HG01109.hp1 HG02886.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+17640A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295498 | |||||||
| chr9:119295523 | A | C | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+17615T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295523 | |||||||
| chr9:119295580 | A | C | 133 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.218+17558T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295580 | |||||||
| chr9:119295664 | A | AGTAT | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+17470_218+1747 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295664 | |||||||
| chr9:119295784 | G | T | 11 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0003t0001g0021 others(8): Show |
11 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+17354C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295784 | |||||||
| chr9:119295786 | G | A | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+17352C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295786 | |||||||
| chr9:119295868 | G | C | 133 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.218+17270C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295868 | |||||||
| chr9:119295895 | G | A | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+17243C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295895 | |||||||
| chr9:119296354 | G | C | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+16784C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296354 | |||||||
| chr9:119296550 | G | C | 1 | a0001c0002t0001g0147 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.218+16588C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296550 | |||||||
| chr9:119296679 | A | G | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+16459T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296679 | |||||||
| chr9:119296757 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.218+16381C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296757 | |||||||
| chr9:119296892 | TACGA | T | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+16242_218+1624 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296892 | |||||||
| chr9:119296901 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+16237T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296901 | |||||||
| chr9:119296963 | T | A | 1 | a0001c0003t0001g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.218+16175A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296963 | |||||||
| chr9:119296964 | A | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG00099.hp1 HG01099.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+16174T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296964 | |||||||
| chr9:119297037 | G | A | 133 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.218+16101C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297037 | |||||||
| chr9:119297121 | A | G | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+16017T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297121 | |||||||
| chr9:119297266 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.218+15872A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297266 | |||||||
| chr9:119297431 | T | C | 133 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.218+15707A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297431 | |||||||
| chr9:119297503 | G | A | 16 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0003t0001g0021 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.218+15635C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297503 | |||||||
| chr9:119297689 | G | A | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+15449C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297689 | |||||||
| chr9:119297746 | T | A | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+15392A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297746 | |||||||
| chr9:119297836 | A | ATAAT | 60 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(57): Show |
60 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.218+15301_218+1530 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297836 | |||||||
| chr9:119297836 | A | ATAATAAT | 3 | a0001c0001t0001g0171 a0001c0003t0001g0211 a0001c0005t0001g0208 |
3 | HG02622.hp2 HG03017.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+15301_218+1530 others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297836 | |||||||
| chr9:119297842 | T | C | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+15296A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297842 | |||||||
| chr9:119298079 | C | T | 26 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
26 | HG00099.hp1 HG00544.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.218+15059G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298079 | |||||||
| chr9:119298232 | C | A | 1 | a0001c0003t0001g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+14906G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298232 | |||||||
| chr9:119298474 | C | A | 2 | a0001c0002t0001g0108 a0001c0002t0001g0129 |
2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+14664G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298474 | |||||||
| chr9:119298596 | T | A | 2 | a0001c0002t0001g0155 a0001c0002t0001g0217 |
2 | HG02129.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.218+14542A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298596 | |||||||
| chr9:119298781 | A | C | 1 | a0001c0004t0002g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.218+14357T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298781 | |||||||
| chr9:119298909 | CAATACTT others(21): Show |
C | 1 | a0001c0001t0005g0215 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.218+14201_218+1422 others(32): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298909 | |||||||
| chr9:119299015 | T | C | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+14123A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299015 | |||||||
| chr9:119299036 | T | C | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+14102A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299036 | |||||||
| chr9:119299157 | T | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0148 others(1): Show |
4 | HG00423.hp1 HG00438.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+13981A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299157 | |||||||
| chr9:119299228 | C | G | 1 | a0001c0015t0001g0131 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.218+13910G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299228 | |||||||
| chr9:119299306 | T | A | 130 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.218+13832A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299306 | |||||||
| chr9:119299315 | A | G | 1 | a0001c0002t0002g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.218+13823T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299315 | |||||||
| chr9:119299342 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.218+13796C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299342 | |||||||
| chr9:119299443 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+13695C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299443 | |||||||
| chr9:119299612 | C | CA | 5 | a0001c0001t0001g0202 a0001c0002t0001g0048 a0001c0002t0001g0108 others(2): Show |
5 | HG01175.hp2 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+13525dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299612 | |||||||
| chr9:119299621 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0151 |
2 | HG00544.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.218+13517T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299621 | |||||||
| chr9:119299670 | C | T | 131 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.218+13468G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299670 | |||||||
| chr9:119299946 | T | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0003t0001g0021 others(14): Show |
17 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.218+13192A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299946 | |||||||
| chr9:119300046 | T | G | 2 | a0001c0002t0001g0108 a0001c0002t0001g0129 |
2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+13092A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300046 | |||||||
| chr9:119300047 | T | G | 2 | a0001c0002t0001g0108 a0001c0002t0001g0129 |
2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+13091A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300047 | |||||||
| chr9:119300049 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+13089C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300049 | |||||||
| chr9:119300050 | T | G | 2 | a0001c0002t0001g0108 a0001c0002t0001g0129 |
2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+13088A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300050 | |||||||
| chr9:119300051 | T | TAC | 2 | a0001c0002t0001g0108 a0001c0002t0001g0129 |
2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+13086_218+1308 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300051 | |||||||
| chr9:119300365 | T | C | 2 | a0001c0002t0003g0012 a0001c0007t0001g0037 |
2 | HG00140.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.218+12773A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300365 | |||||||
| chr9:119300536 | A | T | 13 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0003t0001g0021 others(10): Show |
13 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+12602T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300536 | |||||||
| chr9:119300662 | C | T | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+12476G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300662 | |||||||
| chr9:119300848 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.218+12290C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300848 | |||||||
| chr9:119300882 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.218+12256A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300882 | |||||||
| chr9:119301252 | A | G | 18 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0101 others(15): Show |
18 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+11886T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119301252 | |||||||
| chr9:119301875 | C | T | 11 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0003t0001g0021 others(8): Show |
11 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+11263G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119301875 | |||||||
| chr9:119302132 | A | C | 58 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+11006T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302132 | |||||||
| chr9:119302220 | T | G | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+10918A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302220 | |||||||
| chr9:119302388 | T | A | 1 | a0001c0001t0005g0215 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.218+10750A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302388 | |||||||
| chr9:119302401 | T | TAGCCACT others(16): Show |
1 | a0001c0001t0005g0215 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.218+10714_218+1073 others(27): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302401 | |||||||
| chr9:119302487 | TG | T | 7 | a0001c0003t0001g0021 a0001c0003t0001g0120 a0001c0004t0001g0073 others(4): Show |
7 | HG01123.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+10650delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302487 | |||||||
| chr9:119302540 | T | C | 1 | a0001c0002t0001g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.218+10598A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302540 | |||||||
| chr9:119302595 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.218+10543A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302595 | |||||||
| chr9:119302828 | C | T | 8 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(5): Show |
8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+10310G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302828 | |||||||
| chr9:119302959 | C | A | 39 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0088 others(36): Show |
39 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.218+10179G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302959 | |||||||
| chr9:119303052 | GGGAGACT others(6): Show |
G | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.218+10073_218+1008 others(17): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303052 | |||||||
| chr9:119303191 | C | T | 1 | a0001c0003t0007g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218+9947G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303191 | |||||||
| chr9:119303232 | C | T | 58 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+9906G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303232 | |||||||
| chr9:119303264 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+9874T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303264 | |||||||
| chr9:119303291 | G | GAC | 67 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0052 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.218+9845_218+9846d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | |||||||
| chr9:119303291 | G | GACAC | 17 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0099 others(14): Show |
17 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+9843_218+9846d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | |||||||
| chr9:119303291 | G | GACACAC | 11 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0210 others(8): Show |
11 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+9841_218+9846d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | |||||||
| chr9:119303291 | G | GACACACA others(1): Show |
4 | a0001c0002t0001g0200 a0001c0003t0001g0178 a0001c0003t0001g0181 others(1): Show |
4 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+9839_218+9846d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | |||||||
| chr9:119303291 | G | GACACACA others(3): Show |
5 | a0001c0002t0001g0201 a0001c0002t0001g0203 a0001c0002t0001g0204 others(2): Show |
5 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+9837_218+9846d others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | |||||||
| chr9:119303291 | GAC | G | 6 | a0001c0002t0001g0160 a0001c0003t0001g0041 a0001c0003t0001g0184 others(3): Show |
6 | HG01891.hp2 HG01934.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+9845_218+9846d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | |||||||
| chr9:119303291 | GACAC | G | 2 | a0001c0003t0001g0137 a0001c0004t0001g0015 |
2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.218+9843_218+9846d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | |||||||
| chr9:119303303 | C | G | 1 | a0001c0003t0008g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.218+9835G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303303 | |||||||
| chr9:119303425 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+9713C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303425 | |||||||
| chr9:119303427 | C | T | 58 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+9711G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303427 | |||||||
| chr9:119303520 | G | A | 2 | a0001c0003t0002g0221 a0001c0004t0001g0015 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218+9618C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303520 | |||||||
| chr9:119303523 | G | A | 8 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(5): Show |
8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+9615C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303523 | |||||||
| chr9:119303572 | G | C | 2 | a0001c0003t0001g0173 a0001c0003t0001g0205 |
2 | HG01496.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.218+9566C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303572 | |||||||
| chr9:119303875 | CT | C | 129 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.218+9262delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303875 | |||||||
| chr9:119303950 | G | T | 1 | a0001c0003t0001g0176 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+9188C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303950 | |||||||
| chr9:119304069 | G | T | 1 | a0001c0001t0002g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.218+9069C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304069 | |||||||
| chr9:119304094 | G | A | 18 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0101 others(15): Show |
18 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+9044C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304094 | |||||||
| chr9:119304175 | C | T | 1 | a0001c0003t0002g0229 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.218+8963G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304175 | |||||||
| chr9:119304191 | T | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0003t0001g0021 others(14): Show |
17 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.218+8947A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304191 | |||||||
| chr9:119304192 | C | T | 1 | a0001c0003t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+8946G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304192 | |||||||
| chr9:119304287 | C | T | 6 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+8851G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304287 | |||||||
| chr9:119304941 | A | C | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.218+8197T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304941 | |||||||
| chr9:119304957 | A | G | 4 | a0001c0001t0001g0130 a0001c0002t0001g0048 a0001c0002t0001g0078 others(1): Show |
4 | HG00741.hp2 HG03942.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+8181T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304957 | |||||||
| chr9:119304963 | T | C | 58 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+8175A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304963 | |||||||
| chr9:119305071 | G | A | 1 | a0001c0002t0001g0112 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.218+8067C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305071 | |||||||
| chr9:119305089 | G | A | 8 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(5): Show |
8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+8049C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305089 | |||||||
| chr9:119305092 | T | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0148 others(1): Show |
4 | HG00423.hp1 HG00438.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+8046A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305092 | |||||||
| chr9:119305193 | G | C | 1 | a0001c0002t0001g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.218+7945C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305193 | |||||||
| chr9:119305245 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.218+7893C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305245 | |||||||
| chr9:119305257 | G | C | 4 | a0001c0002t0001g0070 a0001c0002t0001g0139 a0001c0002t0001g0153 others(1): Show |
4 | HG01123.hp2 HG01257.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+7881C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305257 | |||||||
| chr9:119305401 | C | T | 58 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+7737G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305401 | |||||||
| chr9:119305509 | A | G | 16 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0101 others(13): Show |
16 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.218+7629T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305509 | |||||||
| chr9:119305684 | G | A | 37 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0088 others(34): Show |
37 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.218+7454C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305684 | |||||||
| chr9:119305810 | T | C | 27 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0002t0001g0200 others(24): Show |
27 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.218+7328A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305810 | |||||||
| chr9:119305916 | A | G | 1 | a0001c0003t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.218+7222T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305916 | |||||||
| chr9:119306029 | C | T | 1 | a0001c0003t0007g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218+7109G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306029 | |||||||
| chr9:119306230 | C | T | 128 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.218+6908G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306230 | |||||||
| chr9:119306557 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.218+6581C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306557 | |||||||
| chr9:119306603 | C | T | 37 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0088 others(34): Show |
37 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.218+6535G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306603 | |||||||
| chr9:119306604 | G | A | 1 | a0001c0003t0002g0227 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.218+6534C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306604 | |||||||
| chr9:119306625 | T | C | 27 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0002t0001g0200 others(24): Show |
27 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.218+6513A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306625 | |||||||
| chr9:119306749 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.218+6389A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306749 | |||||||
| chr9:119306804 | A | T | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+6334T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306804 | |||||||
| chr9:119307113 | G | A | 8 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(5): Show |
8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+6025C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307113 | |||||||
| chr9:119307186 | A | G | 131 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.218+5952T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307186 | |||||||
| chr9:119307374 | T | C | 131 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.218+5764A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307374 | |||||||
| chr9:119307557 | T | G | 34 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0002t0001g0200 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.218+5581A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307557 | |||||||
| chr9:119307629 | C | A | 4 | a0001c0001t0001g0210 a0001c0001t0002g0230 a0001c0003t0001g0176 others(1): Show |
4 | HG02258.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+5509G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307629 | |||||||
| chr9:119307701 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.218+5437A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307701 | |||||||
| chr9:119307706 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.218+5432G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307706 | |||||||
| chr9:119307980 | G | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+5158C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307980 | |||||||
| chr9:119308170 | G | T | 1 | a0001c0002t0001g0141 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.218+4968C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308170 | |||||||
| chr9:119308551 | C | T | 30 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0101 others(27): Show |
30 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.218+4587G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308551 | |||||||
| chr9:119308827 | G | A | 131 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.218+4311C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308827 | |||||||
| chr9:119308918 | C | A | 1 | a0001c0002t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.218+4220G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308918 | |||||||
| chr9:119308973 | G | GA | 10 | a0001c0002t0001g0093 a0001c0002t0006g0013 a0001c0003t0001g0164 others(7): Show |
10 | HG01109.hp1 HG01515.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+4164dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308973 | |||||||
| chr9:119308973 | G | GAA | 29 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0002t0001g0200 others(26): Show |
29 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.218+4163_218+4164d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308973 | |||||||
| chr9:119308973 | GA | G | 95 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.218+4164delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308973 | |||||||
| chr9:119309116 | C | T | 95 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.218+4022G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309116 | |||||||
| chr9:119309361 | T | C | 37 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0088 others(34): Show |
37 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.218+3777A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309361 | |||||||
| chr9:119309478 | C | T | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.218+3660G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309478 | |||||||
| chr9:119309735 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.218+3403A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309735 | |||||||
| chr9:119309736 | C | A | 95 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.218+3402G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309736 | |||||||
| chr9:119309841 | G | A | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0188 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+3297C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309841 | |||||||
| chr9:119309867 | C | T | 1 | a0001c0003t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+3271G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309867 | |||||||
| chr9:119310063 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.218+3075A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310063 | |||||||
| chr9:119310250 | G | A | 4 | a0001c0001t0001g0022 a0001c0002t0001g0028 a0001c0004t0001g0025 others(1): Show |
4 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+2888C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310250 | |||||||
| chr9:119310403 | G | A | 14 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0101 others(11): Show |
14 | HG00423.hp2 HG01256.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+2735C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310403 | |||||||
| chr9:119310648 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.218+2490C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310648 | |||||||
| chr9:119310739 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.218+2399T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310739 | |||||||
| chr9:119310776 | A | G | 2 | a0001c0001t0001g0132 a0004c0011t0001g0123 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.218+2362T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310776 | |||||||
| chr9:119310929 | G | C | 97 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.218+2209C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310929 | |||||||
| chr9:119311147 | T | C | 1 | a0001c0003t0001g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+1991A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311147 | |||||||
| chr9:119311189 | T | C | 1 | a0001c0001t0002g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.218+1949A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311189 | |||||||
| chr9:119311396 | A | C | 13 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(10): Show |
13 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+1742T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311396 | |||||||
| chr9:119311621 | C | T | 114 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.218+1517G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311621 | |||||||
| chr9:119311761 | T | C | 52 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(49): Show |
52 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.218+1377A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311761 | |||||||
| chr9:119311781 | G | A | 11 | a0001c0003t0001g0021 a0001c0003t0001g0092 a0001c0003t0001g0179 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+1357C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311781 | |||||||
| chr9:119312035 | T | G | 1 | a0001c0010t0001g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.218+1103A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119312035 | |||||||
| chr9:119312446 | G | C | 1 | a0001c0002t0001g0114 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.218+692C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119312446 | |||||||
| chr9:119312576 | G | A | 4 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+562C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119312576 | |||||||
| chr9:119312996 | A | T | 118 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.218+142T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119312996 | |||||||
| chr9:119313433 | A | G | 1 | a0001c0003t0002g0229 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-50-28T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119313433 | |||||||
| chr9:119313700 | T | C | 96 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-50-295A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119313700 | |||||||
| chr9:119313734 | G | C | 7 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-329C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119313734 | |||||||
| chr9:119314100 | A | G | 4 | a0001c0003t0001g0105 a0001c0003t0001g0137 a0001c0003t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02717.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-695T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314100 | |||||||
| chr9:119314296 | A | T | 223 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-50-891T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314296 | |||||||
| chr9:119314352 | A | G | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-947T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314352 | |||||||
| chr9:119314357 | C | T | 96 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-50-952G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314357 | |||||||
| chr9:119314388 | C | T | 96 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-50-983G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314388 | |||||||
| chr9:119314425 | G | A | 96 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-50-1020C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314425 | |||||||
| chr9:119314801 | T | C | 52 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(49): Show |
52 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-50-1396A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314801 | |||||||
| chr9:119314836 | C | T | 52 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(49): Show |
52 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-50-1431G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314836 | |||||||
| chr9:119314888 | T | G | 96 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-50-1483A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314888 | |||||||
| chr9:119314941 | A | G | 1 | a0001c0002t0001g0024 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-50-1536T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314941 | |||||||
| chr9:119315274 | G | A | 96 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-50-1869C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315274 | |||||||
| chr9:119315286 | T | C | 96 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-50-1881A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315286 | |||||||
| chr9:119315336 | T | A | 15 | a0001c0001t0002g0230 a0001c0003t0001g0021 a0001c0003t0001g0179 others(12): Show |
15 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50-1931A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315336 | |||||||
| chr9:119315345 | T | C | 1 | a0001c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50-1940A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315345 | |||||||
| chr9:119315346 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-50-1941C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315346 | |||||||
| chr9:119315454 | C | G | 111 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-50-2049G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315454 | |||||||
| chr9:119315928 | G | A | 22 | a0001c0001t0001g0182 a0001c0001t0002g0230 a0001c0003t0001g0021 others(19): Show |
22 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-2523C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315928 | |||||||
| chr9:119316115 | C | G | 22 | a0001c0001t0001g0182 a0001c0001t0002g0230 a0001c0003t0001g0021 others(19): Show |
22 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-2710G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316115 | |||||||
| chr9:119316119 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50-2714G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316119 | |||||||
| chr9:119316126 | G | A | 1 | a0001c0003t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-50-2721C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316126 | |||||||
| chr9:119316136 | G | A | 1 | a0001c0002t0001g0194 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-50-2731C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316136 | |||||||
| chr9:119316254 | T | G | 1 | a0001c0003t0001g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-50-2849A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316254 | |||||||
| chr9:119316355 | T | C | 3 | a0001c0003t0001g0041 a0001c0003t0007g0183 a0001c0004t0001g0175 |
3 | HG01891.hp2 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-50-2950A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316355 | |||||||
| chr9:119316445 | T | C | 44 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(41): Show |
44 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-50-3040A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316445 | |||||||
| chr9:119316448 | T | C | 7 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-3043A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316448 | |||||||
| chr9:119316504 | G | A | 3 | a0001c0001t0001g0045 a0001c0003t0001g0044 a0001c0003t0001g0046 |
3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-50-3099C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316504 | |||||||
| chr9:119316614 | A | G | 1 | a0001c0002t0001g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-50-3209T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316614 | |||||||
| chr9:119316877 | G | A | 1 | a0001c0002t0004g0029 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-50-3472C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316877 | |||||||
| chr9:119316892 | ACTATCCT others(259): Show |
A | 7 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-3753_-50-3488d others(2): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316892 | |||||||
| chr9:119316920 | G | T | 52 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(49): Show |
52 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-50-3515C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316920 | |||||||
| chr9:119317048 | A | G | 111 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-50-3643T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317048 | |||||||
| chr9:119317071 | C | T | 3 | a0001c0001t0003g0001 a0001c0002t0003g0005 a0002c0013t0003g0006 |
3 | HG01074.hp1 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-50-3666G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317071 | |||||||
| chr9:119317781 | A | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-50-4376T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317781 | |||||||
| chr9:119317902 | T | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-50-4497A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317902 | |||||||
| chr9:119317948 | G | A | 1 | a0001c0003t0001g0188 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-50-4543C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317948 | |||||||
| chr9:119318145 | C | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0168 a0001c0002t0001g0086 |
3 | HG00544.hp2 HG02165.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.-50-4740G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318145 | |||||||
| chr9:119318253 | C | T | 1 | a0001c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50-4848G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318253 | |||||||
| chr9:119318290 | G | T | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-4885C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318290 | |||||||
| chr9:119318547 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-50-5142G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318547 | |||||||
| chr9:119318734 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0003g0009 |
2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-50-5329C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318734 | |||||||
| chr9:119318841 | T | TG | 6 | a0001c0001t0001g0115 a0001c0002t0001g0194 a0001c0003t0001g0041 others(3): Show |
6 | HG00639.hp1 HG02809.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50-5437dupC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318841 | |||||||
| chr9:119318841 | T | TGG | 44 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0066 others(41): Show |
44 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.-50-5438_-50-5437d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318841 | |||||||
| chr9:119318843 | G | T | 1 | a0001c0003t0002g0227 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-50-5438C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318843 | |||||||
| chr9:119318844 | G | GGGGGT | 15 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(12): Show |
15 | HG00099.hp1 HG01099.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50-5440_-50-5439i others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318844 | G | GGGGT | 8 | a0001c0001t0001g0055 a0001c0001t0001g0100 a0001c0001t0001g0104 others(5): Show |
8 | HG00735.hp1 HG01934.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50-5440_-50-5439i others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318844 | G | GGGTGT | 4 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0003t0001g0206 others(1): Show |
4 | HG01261.hp2 HG01884.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-5440_-50-5439i others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318844 | G | GGT | 24 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0063 others(21): Show |
24 | HG01074.hp2 HG01109.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50-5441_-50-5440d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318844 | G | GGTGT | 7 | a0001c0001t0003g0008 a0001c0003t0001g0178 a0001c0003t0001g0179 others(4): Show |
7 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-5443_-50-5440d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318844 | G | GT | 2 | a0001c0002t0001g0035 a0001c0002t0001g0061 |
2 | HG01358.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-50-5440_-50-5439i others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318844 | G | T | 1 | a0001c0007t0001g0037 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-50-5439C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318844 | GGT | G | 7 | a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0002t0001g0048 others(4): Show |
7 | HG02572.hp1 HG02698.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-5441_-50-5440d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318844 | GGTGT | G | 28 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0054 others(25): Show |
28 | HG01099.hp2 HG01123.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.-50-5443_-50-5440d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318844 | GGTGTGT | G | 28 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0121 others(25): Show |
28 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.-50-5445_-50-5440d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | |||||||
| chr9:119318846 | T | G | 17 | a0001c0001t0001g0115 a0001c0001t0001g0145 a0001c0001t0001g0192 others(14): Show |
17 | HG01891.hp1 HG02071.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50-5441A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318846 | |||||||
| chr9:119318848 | T | G | 12 | a0001c0001t0001g0057 a0001c0001t0001g0198 a0001c0003t0001g0039 others(9): Show |
12 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-5443A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318848 | |||||||
| chr9:119318850 | T | G | 5 | a0001c0001t0001g0038 a0001c0003t0001g0187 a0001c0003t0001g0195 others(2): Show |
5 | HG01346.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50-5445A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318850 | |||||||
| chr9:119318852 | T | G | 2 | a0001c0002t0001g0167 a0001c0009t0001g0189 |
2 | HG03195.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-50-5447A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318852 | |||||||
| chr9:119318966 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-50-5561G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318966 | |||||||
| chr9:119318984 | C | G | 1 | a0001c0002t0001g0152 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-50-5579G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318984 | |||||||
| chr9:119319161 | T | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0130 a0001c0002t0001g0048 others(2): Show |
5 | HG00741.hp2 HG03669.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50-5756A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319161 | |||||||
| chr9:119319255 | T | C | 1 | a0001c0003t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50-5850A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319255 | |||||||
| chr9:119319391 | G | A | 4 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-5986C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319391 | |||||||
| chr9:119319400 | C | T | 1 | a0003c0008t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-50-5995G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319400 | |||||||
| chr9:119319540 | A | G | 44 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(41): Show |
44 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-50-6135T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319540 | |||||||
| chr9:119319597 | T | C | 103 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-50-6192A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319597 | |||||||
| chr9:119319746 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-50-6341C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319746 | |||||||
| chr9:119319762 | A | G | 1 | a0001c0002t0001g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-50-6357T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319762 | |||||||
| chr9:119319766 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0202 |
2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-50-6361G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319766 | |||||||
| chr9:119319854 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0146 a0001c0001t0001g0150 |
3 | HG01346.hp1 HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-50-6449G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319854 | |||||||
| chr9:119320074 | G | GT | 5 | a0001c0001t0002g0230 a0001c0003t0002g0221 a0001c0003t0002g0227 others(2): Show |
5 | HG01109.hp1 HG02886.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50-6670_-50-6669i others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320074 | |||||||
| chr9:119320075 | A | C | 5 | a0001c0001t0002g0230 a0001c0003t0002g0221 a0001c0003t0002g0227 others(2): Show |
5 | HG01109.hp1 HG02886.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50-6670T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320075 | |||||||
| chr9:119320250 | G | A | 1 | a0001c0002t0003g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-50-6845C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320250 | |||||||
| chr9:119320281 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-50-6876G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320281 | |||||||
| chr9:119320446 | C | G | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-7041G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320446 | |||||||
| chr9:119320991 | C | T | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-50-7586G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320991 | |||||||
| chr9:119321062 | C | T | 1 | a0001c0002t0001g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-50-7657G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321062 | |||||||
| chr9:119321133 | G | A | 14 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(11): Show |
14 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50-7728C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321133 | |||||||
| chr9:119321223 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50-7818T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321223 | |||||||
| chr9:119321226 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50-7821G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321226 | |||||||
| chr9:119321274 | T | C | 1 | a0003c0008t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-50-7869A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321274 | |||||||
| chr9:119321342 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0002t0001g0058 others(1): Show |
4 | HG01943.hp1 HG01943.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-7937A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321342 | |||||||
| chr9:119321496 | A | G | 49 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(46): Show |
49 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-50-8091T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321496 | |||||||
| chr9:119321500 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-50-8095A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321500 | |||||||
| chr9:119321700 | C | T | 18 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(15): Show |
18 | HG00639.hp2 HG00735.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.-50-8295G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321700 | |||||||
| chr9:119321757 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-50-8352A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321757 | |||||||
| chr9:119321861 | C | G | 1 | a0001c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50-8456G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321861 | |||||||
| chr9:119321977 | A | G | 12 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(9): Show |
12 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-8572T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321977 | |||||||
| chr9:119322166 | C | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0158 a0001c0002t0001g0056 others(1): Show |
4 | HG01169.hp2 HG01517.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-8761G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119322166 | |||||||
| chr9:119322375 | C | T | 4 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-8970G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119322375 | |||||||
| chr9:119322578 | T | C | 53 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-50-9173A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119322578 | |||||||
| chr9:119323660 | A | C | 51 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(48): Show |
51 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-50-10255T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119323660 | |||||||
| chr9:119323919 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-50-10514G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119323919 | |||||||
| chr9:119323948 | AC | A | 51 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(48): Show |
51 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-50-10544delG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119323948 | |||||||
| chr9:119324027 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50-10622C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119324027 | |||||||
| chr9:119324225 | C | A | 1 | a0001c0003t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-50-10820G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119324225 | |||||||
| chr9:119324357 | G | T | 1 | a0001c0002t0001g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-50-10952C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119324357 | |||||||
| chr9:119324869 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-50-11464C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119324869 | |||||||
| chr9:119325335 | T | A | 1 | a0001c0003t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-50-11930A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119325335 | |||||||
| chr9:119325379 | T | C | 51 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(48): Show |
51 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-50-11974A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119325379 | |||||||
| chr9:119325555 | C | T | 1 | a0001c0003t0002g0222 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-50-12150G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119325555 | |||||||
| chr9:119325863 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-50-12458C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119325863 | |||||||
| chr9:119326253 | G | C | 51 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(48): Show |
51 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-50-12848C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119326253 | |||||||
| chr9:119326254 | G | T | 1 | a0001c0001t0002g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50-12849C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119326254 | |||||||
| chr9:119326913 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50-13508T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119326913 | |||||||
| chr9:119327269 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-50-13864G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119327269 | |||||||
| chr9:119327476 | A | T | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-14071T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119327476 | |||||||
| chr9:119327555 | A | G | 1 | a0001c0002t0001g0026 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-50-14150T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119327555 | |||||||
| chr9:119327676 | ATTAGCAA others(3): Show |
A | 1 | a0001c0007t0001g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-50-14281_-50-1427 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119327676 | |||||||
| chr9:119328026 | A | T | 22 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(19): Show |
22 | HG00099.hp1 HG00423.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-14621T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328026 | |||||||
| chr9:119328117 | C | T | 1 | a0001c0001t0002g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-50-14712G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328117 | |||||||
| chr9:119328190 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-50-14785C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328190 | |||||||
| chr9:119328192 | T | C | 53 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-50-14787A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328192 | |||||||
| chr9:119328208 | C | T | 1 | a0001c0003t0008g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-50-14803G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328208 | |||||||
| chr9:119328737 | A | G | 19 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(16): Show |
19 | HG00099.hp1 HG00423.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50-15332T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328737 | |||||||
| chr9:119328843 | A | C | 4 | a0001c0001t0001g0053 a0001c0002t0001g0117 a0001c0002t0001g0141 others(1): Show |
4 | HG01074.hp2 HG01175.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-15438T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328843 | |||||||
| chr9:119329187 | A | C | 2 | a0001c0003t0001g0059 a0001c0004t0001g0073 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-50-15782T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329187 | |||||||
| chr9:119329193 | T | C | 22 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(19): Show |
22 | HG00099.hp1 HG00423.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-15788A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329193 | |||||||
| chr9:119329203 | A | G | 7 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-15798T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329203 | |||||||
| chr9:119329453 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-50-16048C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329453 | |||||||
| chr9:119329513 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-50-16108A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329513 | |||||||
| chr9:119329735 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-50-16330T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329735 | |||||||
| chr9:119330141 | T | G | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-50-16736A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330141 | |||||||
| chr9:119330206 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-50-16801G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330206 | |||||||
| chr9:119330482 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0130 a0001c0002t0001g0048 others(2): Show |
5 | HG00741.hp2 HG03669.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50-17077G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330482 | |||||||
| chr9:119330557 | T | A | 1 | a0001c0015t0001g0131 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-50-17152A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330557 | |||||||
| chr9:119330651 | C | T | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-17246G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330651 | |||||||
| chr9:119330798 | CG | C | 7 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-17394delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330798 | |||||||
| chr9:119330970 | C | T | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-50-17565G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330970 | |||||||
| chr9:119330983 | T | C | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-17578A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330983 | |||||||
| chr9:119331086 | T | C | 1 | a0001c0002t0001g0028 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-50-17681A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331086 | |||||||
| chr9:119331193 | A | T | 22 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(19): Show |
22 | HG00099.hp1 HG00423.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-17788T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331193 | |||||||
| chr9:119331460 | G | C | 1 | a0001c0003t0001g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-50-18055C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331460 | |||||||
| chr9:119331513 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-50-18108G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331513 | |||||||
| chr9:119331874 | G | A | 47 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(44): Show |
47 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-50-18469C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331874 | |||||||
| chr9:119331895 | A | G | 14 | a0001c0001t0003g0001 a0001c0002t0001g0069 a0001c0002t0001g0070 others(11): Show |
14 | HG00140.hp1 HG00738.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-50-18490T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331895 | |||||||
| chr9:119331936 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50-18531C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331936 | |||||||
| chr9:119331970 | T | G | 9 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0002t0001g0200 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50-18565A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331970 | |||||||
| chr9:119332524 | T | C | 15 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(12): Show |
15 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50-19119A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119332524 | |||||||
| chr9:119332694 | G | A | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-50-19289C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119332694 | |||||||
| chr9:119333010 | A | T | 1 | a0001c0002t0001g0112 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-50-19605T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333010 | |||||||
| chr9:119333336 | G | A | 1 | a0001c0003t0001g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-50-19931C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333336 | |||||||
| chr9:119333456 | T | C | 113 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-50-20051A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333456 | |||||||
| chr9:119333462 | C | CA | 8 | a0001c0001t0001g0052 a0001c0001t0001g0068 a0001c0001t0001g0079 others(5): Show |
8 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50-20058dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333462 | |||||||
| chr9:119333462 | CA | C | 43 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(40): Show |
43 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.-50-20058delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333462 | |||||||
| chr9:119333462 | CAA | C | 13 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(10): Show |
13 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-20059_-50-2005 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333462 | |||||||
| chr9:119333555 | T | C | 58 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(55): Show |
58 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-50-20150A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333555 | |||||||
| chr9:119333667 | G | A | 1 | a0001c0003t0001g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-50-20262C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333667 | |||||||
| chr9:119333878 | T | G | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-50-20473A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333878 | |||||||
| chr9:119333925 | A | C | 1 | a0001c0003t0002g0226 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-50-20520T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333925 | |||||||
| chr9:119334141 | G | C | 1 | a0001c0003t0001g0030 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-50-20736C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334141 | |||||||
| chr9:119334254 | C | A | 57 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0054 others(54): Show |
57 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-50-20849G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334254 | |||||||
| chr9:119334308 | G | T | 2 | a0001c0003t0001g0092 a0001c0003t0001g0149 |
2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-50-20903C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334308 | |||||||
| chr9:119334343 | T | C | 2 | a0001c0001t0001g0113 a0001c0002t0001g0157 |
2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.-50-20938A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334343 | |||||||
| chr9:119334355 | C | T | 7 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-20950G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334355 | |||||||
| chr9:119334461 | C | A | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-50-21056G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334461 | |||||||
| chr9:119334493 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50-21088T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334493 | |||||||
| chr9:119334795 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-50-21390A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334795 | |||||||
| chr9:119334861 | A | G | 3 | a0001c0001t0001g0045 a0001c0003t0001g0044 a0001c0003t0001g0046 |
3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-50-21456T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334861 | |||||||
| chr9:119334981 | A | C | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-21576T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334981 | |||||||
| chr9:119335038 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-50-21633C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335038 | |||||||
| chr9:119335080 | G | A | 7 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-21675C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335080 | |||||||
| chr9:119335126 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-50-21721T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335126 | |||||||
| chr9:119335927 | T | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0063 others(26): Show |
29 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50-22522A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335927 | |||||||
| chr9:119335942 | A | G | 7 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-22537T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335942 | |||||||
| chr9:119336273 | A | C | 1 | a0001c0004t0002g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-50-22868T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119336273 | |||||||
| chr9:119336494 | A | G | 110 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-50-23089T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119336494 | |||||||
| chr9:119336567 | A | T | 14 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(11): Show |
14 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50-23162T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119336567 | |||||||
| chr9:119337196 | C | T | 2 | a0001c0001t0003g0008 a0001c0010t0001g0096 |
2 | HG02523.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-50-23791G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337196 | |||||||
| chr9:119337207 | C | A | 47 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(44): Show |
47 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.-50-23802G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337207 | |||||||
| chr9:119337252 | C | T | 7 | a0001c0001t0001g0182 a0001c0003t0001g0178 a0001c0003t0001g0181 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-23847G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337252 | |||||||
| chr9:119337351 | T | C | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-23946A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337351 | |||||||
| chr9:119337639 | T | G | 47 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(44): Show |
47 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.-50-24234A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337639 | |||||||
| chr9:119337687 | G | A | 53 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-50-24282C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337687 | |||||||
| chr9:119337790 | G | A | 1 | a0003c0008t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-50-24385C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337790 | |||||||
| chr9:119338246 | C | CT | 47 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(44): Show |
47 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.-50-24842dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338246 | |||||||
| chr9:119338246 | CT | C | 173 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(170): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-50-24842delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338246 | |||||||
| chr9:119338261 | T | A | 1 | a0001c0003t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50-24856A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338261 | |||||||
| chr9:119338469 | G | A | 2 | a0001c0002t0001g0095 a0001c0002t0001g0166 |
2 | NA18953.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-50-25064C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338469 | |||||||
| chr9:119338716 | C | CA | 48 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(45): Show |
48 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-50-25312dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338716 | |||||||
| chr9:119338716 | C | CAAA | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25314_-50-2531 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338716 | |||||||
| chr9:119338810 | A | G | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25405T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338810 | |||||||
| chr9:119338840 | A | ACAC | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25438_-50-2543 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338840 | |||||||
| chr9:119338847 | C | T | 14 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(11): Show |
14 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50-25442G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338847 | |||||||
| chr9:119338900 | CA | C | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25496delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338900 | |||||||
| chr9:119339201 | T | G | 4 | a0001c0003t0001g0187 a0001c0003t0001g0195 a0001c0005t0001g0190 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-25796A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339201 | |||||||
| chr9:119339341 | C | T | 175 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(172): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-50-25936G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339341 | |||||||
| chr9:119339368 | T | TA | 47 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(44): Show |
47 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.-50-25964dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339368 | |||||||
| chr9:119339389 | A | G | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25984T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339389 | |||||||
| chr9:119339465 | G | C | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-26060C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339465 | |||||||
| chr9:119339906 | A | G | 7 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0004t0002g0231 others(4): Show |
7 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-26501T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339906 | |||||||
| chr9:119340096 | T | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0101 others(6): Show |
9 | HG02135.hp1 NA18940.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50-26691A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340096 | |||||||
| chr9:119340264 | C | T | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-26859G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340264 | |||||||
| chr9:119340310 | A | T | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-26905T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340310 | |||||||
| chr9:119340375 | A | C | 1 | a0001c0003t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-50-26970T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340375 | |||||||
| chr9:119340413 | G | GA | 7 | a0001c0003t0001g0021 a0001c0003t0001g0211 a0001c0003t0002g0229 others(4): Show |
7 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-27009dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340413 | |||||||
| chr9:119340612 | T | C | 1 | a0001c0002t0004g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-50-27207A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340612 | |||||||
| chr9:119340679 | G | A | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-27274C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340679 | |||||||
| chr9:119340728 | C | T | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-50-27323G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340728 | |||||||
| chr9:119340965 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-50-27560G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340965 | |||||||
| chr9:119341035 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-50-27630G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341035 | |||||||
| chr9:119341404 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0005g0213 a0001c0001t0005g0215 |
3 | NA18993.hp1 NA18993.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-51+27652T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341404 | |||||||
| chr9:119341408 | G | A | 56 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(53): Show |
56 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.-51+27648C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341408 | |||||||
| chr9:119341452 | G | C | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+27604C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341452 | |||||||
| chr9:119341762 | GTAT | G | 6 | a0001c0001t0001g0101 a0001c0001t0001g0115 a0001c0001t0001g0119 others(3): Show |
6 | NA18940.hp1 NA18948.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+27291_-51+2729 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341762 | |||||||
| chr9:119341786 | C | T | 1 | a0001c0003t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+27270G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341786 | |||||||
| chr9:119341866 | C | T | 2 | a0001c0001t0001g0060 a0001c0002t0001g0061 |
2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-51+27190G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341866 | |||||||
| chr9:119341912 | C | T | 9 | a0001c0001t0001g0082 a0001c0003t0001g0021 a0001c0003t0001g0083 others(6): Show |
9 | HG01123.hp1 HG01261.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+27144G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341912 | |||||||
| chr9:119342100 | T | TAAAGATC others(316): Show |
6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+26955_-51+2695 others(327): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342100 | |||||||
| chr9:119342250 | T | C | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+26806A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342250 | |||||||
| chr9:119342356 | G | A | 2 | a0001c0001t0001g0170 a0001c0003t0002g0225 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+26700C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342356 | |||||||
| chr9:119342849 | G | C | 1 | a0001c0003t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+26207C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342849 | |||||||
| chr9:119342883 | C | T | 12 | a0001c0001t0001g0053 a0001c0001t0001g0063 a0001c0001t0001g0064 others(9): Show |
12 | HG01074.hp2 HG01175.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+26173G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342883 | |||||||
| chr9:119343152 | A | G | 47 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(44): Show |
47 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.-51+25904T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343152 | |||||||
| chr9:119343427 | G | A | 1 | a0001c0002t0001g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-51+25629C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343427 | |||||||
| chr9:119343520 | A | G | 10 | a0001c0001t0001g0182 a0001c0003t0001g0021 a0001c0003t0001g0178 others(7): Show |
10 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+25536T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343520 | |||||||
| chr9:119343680 | T | G | 10 | a0001c0001t0001g0182 a0001c0003t0001g0021 a0001c0003t0001g0178 others(7): Show |
10 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+25376A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343680 | |||||||
| chr9:119343837 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-51+25219T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343837 | |||||||
| chr9:119344001 | C | A | 2 | a0001c0002t0001g0155 a0001c0002t0001g0217 |
2 | HG02129.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-51+25055G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344001 | |||||||
| chr9:119344025 | G | T | 1 | a0001c0003t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+25031C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344025 | |||||||
| chr9:119344199 | A | G | 58 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(55): Show |
58 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-51+24857T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344199 | |||||||
| chr9:119344429 | A | T | 1 | a0001c0007t0001g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-51+24627T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344429 | |||||||
| chr9:119344917 | T | C | 1 | a0001c0007t0001g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-51+24139A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344917 | |||||||
| chr9:119344998 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-51+24058A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344998 | |||||||
| chr9:119345083 | C | T | 46 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(43): Show |
46 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-51+23973G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119345083 | |||||||
| chr9:119345109 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-51+23947G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119345109 | |||||||
| chr9:119345607 | C | T | 1 | a0001c0003t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+23449G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119345607 | |||||||
| chr9:119345766 | C | T | 53 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-51+23290G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119345766 | |||||||
| chr9:119346179 | A | C | 47 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(44): Show |
47 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.-51+22877T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119346179 | |||||||
| chr9:119346568 | C | T | 1 | a0001c0002t0001g0152 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-51+22488G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119346568 | |||||||
| chr9:119347260 | T | C | 10 | a0001c0001t0001g0182 a0001c0003t0001g0021 a0001c0003t0001g0178 others(7): Show |
10 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+21796A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347260 | |||||||
| chr9:119347344 | G | A | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-51+21712C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347344 | |||||||
| chr9:119347614 | C | T | 1 | a0001c0003t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-51+21442G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347614 | |||||||
| chr9:119347809 | T | C | 1 | a0001c0004t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51+21247A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347809 | |||||||
| chr9:119347871 | T | C | 4 | a0001c0001t0001g0022 a0001c0002t0001g0028 a0001c0004t0001g0025 others(1): Show |
4 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+21185A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347871 | |||||||
| chr9:119348314 | G | C | 1 | a0001c0002t0003g0012 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-51+20742C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348314 | |||||||
| chr9:119348513 | T | G | 2 | a0001c0001t0001g0121 a0001c0002t0001g0177 |
2 | HG03669.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-51+20543A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348513 | |||||||
| chr9:119348528 | C | T | 1 | a0001c0003t0001g0092 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51+20528G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348528 | |||||||
| chr9:119348616 | C | G | 1 | a0001c0003t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+20440G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348616 | |||||||
| chr9:119348968 | T | C | 3 | a0001c0001t0001g0045 a0001c0003t0001g0044 a0001c0003t0001g0046 |
3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+20088A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348968 | |||||||
| chr9:119349144 | C | T | 3 | a0001c0001t0001g0045 a0001c0003t0001g0044 a0001c0003t0001g0046 |
3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+19912G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349144 | |||||||
| chr9:119349178 | C | A | 46 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(43): Show |
46 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-51+19878G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349178 | |||||||
| chr9:119349481 | A | C | 2 | a0001c0001t0001g0047 a0001c0001t0003g0009 |
2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-51+19575T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349481 | |||||||
| chr9:119349495 | T | A | 110 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-51+19561A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349495 | |||||||
| chr9:119349737 | T | C | 1 | a0001c0003t0001g0195 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-51+19319A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349737 | |||||||
| chr9:119349790 | G | GGGGAAAA others(9): Show |
1 | a0001c0002t0001g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-51+19250_-51+1926 others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349790 | |||||||
| chr9:119350115 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51+18941A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119350115 | |||||||
| chr9:119350285 | C | T | 47 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(44): Show |
47 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-51+18771G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119350285 | |||||||
| chr9:119350901 | T | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-51+18155A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119350901 | |||||||
| chr9:119350902 | C | CT | 53 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-51+18153dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119350902 | |||||||
| chr9:119351399 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51+17657G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351399 | |||||||
| chr9:119351545 | G | A | 28 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0063 others(25): Show |
28 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-51+17511C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351545 | |||||||
| chr9:119351624 | T | G | 47 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(44): Show |
47 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.-51+17432A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351624 | |||||||
| chr9:119351686 | G | T | 1 | a0001c0002t0003g0005 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-51+17370C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351686 | |||||||
| chr9:119351818 | A | T | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+17238T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351818 | |||||||
| chr9:119351818 | AT | A | 102 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-51+17237delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351818 | |||||||
| chr9:119351819 | T | A | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+17237A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351819 | |||||||
| chr9:119351865 | G | A | 6 | a0001c0003t0001g0021 a0001c0003t0002g0229 a0001c0006t0001g0016 others(3): Show |
6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+17191C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351865 | |||||||
| chr9:119351886 | G | C | 5 | a0001c0001t0001g0079 a0001c0001t0001g0130 a0001c0002t0001g0048 others(2): Show |
5 | HG00741.hp2 HG03669.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+17170C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351886 | |||||||
| chr9:119351982 | G | C | 3 | a0001c0001t0001g0045 a0001c0003t0001g0044 a0001c0003t0001g0046 |
3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+17074C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351982 | |||||||
| chr9:119352018 | G | A | 1 | a0001c0015t0001g0131 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-51+17038C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352018 | |||||||
| chr9:119352052 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-51+17004G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352052 | |||||||
| chr9:119352201 | G | A | 2 | a0001c0001t0001g0036 a0001c0002t0001g0031 |
2 | NA18946.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-51+16855C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352201 | |||||||
| chr9:119352801 | T | C | 1 | a0001c0002t0001g0167 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-51+16255A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352801 | |||||||
| chr9:119352821 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-51+16235G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352821 | |||||||
| chr9:119353020 | C | A | 46 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(43): Show |
46 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.-51+16036G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353020 | |||||||
| chr9:119353061 | GCTCCAAT others(3): Show |
G | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-51+15985_-51+1599 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353061 | |||||||
| chr9:119353368 | T | A | 1 | a0001c0001t0003g0009 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-51+15688A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353368 | |||||||
| chr9:119353411 | G | C | 114 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-51+15645C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353411 | |||||||
| chr9:119353479 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-51+15577G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353479 | |||||||
| chr9:119353511 | C | T | 107 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-51+15545G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353511 | |||||||
| chr9:119353781 | T | G | 1 | a0001c0002t0001g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-51+15275A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353781 | |||||||
| chr9:119353822 | C | CT | 9 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0168 others(6): Show |
9 | HG00544.hp2 HG00741.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+15233dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | |||||||
| chr9:119353822 | CT | C | 64 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0043 others(61): Show |
64 | HG00140.hp1 HG00438.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.-51+15233delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | |||||||
| chr9:119353822 | CTT | C | 24 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0111 others(21): Show |
24 | HG00438.hp2 HG00544.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-51+15232_-51+1523 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | |||||||
| chr9:119353822 | CTTT | C | 37 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0066 others(34): Show |
37 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-51+15231_-51+1523 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | |||||||
| chr9:119353822 | CTTTT | C | 26 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
26 | HG00099.hp1 HG01070.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51+15230_-51+1523 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | |||||||
| chr9:119353822 | CTTTTT | C | 13 | a0001c0001t0001g0198 a0001c0003t0001g0039 a0001c0003t0001g0040 others(10): Show |
13 | HG01891.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+15229_-51+1523 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | |||||||
| chr9:119353880 | T | C | 1 | a0001c0003t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-51+15176A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353880 | |||||||
| chr9:119354685 | A | C | 110 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-51+14371T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354685 | |||||||
| chr9:119354686 | C | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0150 |
2 | HG01346.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-51+14370G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354686 | |||||||
| chr9:119354695 | TA | T | 107 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-51+14360delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354695 | |||||||
| chr9:119354703 | A | G | 3 | a0001c0003t0001g0105 a0001c0003t0001g0206 a0001c0003t0001g0207 |
3 | HG01884.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-51+14353T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354703 | |||||||
| chr9:119354704 | A | T | 3 | a0001c0001t0001g0045 a0001c0003t0001g0044 a0001c0003t0001g0046 |
3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+14352T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354704 | |||||||
| chr9:119354789 | A | G | 1 | a0001c0003t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-51+14267T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354789 | |||||||
| chr9:119354837 | C | G | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-51+14219G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354837 | |||||||
| chr9:119354909 | G | A | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51+14147C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354909 | |||||||
| chr9:119354928 | T | C | 3 | a0001c0001t0001g0045 a0001c0003t0001g0044 a0001c0003t0001g0046 |
3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+14128A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354928 | |||||||
| chr9:119354996 | A | G | 9 | a0001c0001t0001g0202 a0001c0001t0002g0234 a0001c0002t0001g0200 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+14060T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354996 | |||||||
| chr9:119355137 | T | C | 3 | a0001c0001t0001g0193 a0001c0003t0002g0222 a0001c0004t0001g0015 |
3 | HG02486.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-51+13919A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355137 | |||||||
| chr9:119355258 | C | A | 1 | a0001c0001t0004g0094 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-51+13798G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355258 | |||||||
| chr9:119355373 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-51+13683G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355373 | |||||||
| chr9:119355446 | C | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0210 a0001c0003t0001g0191 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+13610G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355446 | |||||||
| chr9:119355447 | G | A | 1 | a0001c0002t0001g0166 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-51+13609C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355447 | |||||||
| chr9:119355451 | G | A | 2 | a0001c0003t0001g0206 a0001c0003t0001g0207 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-51+13605C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355451 | |||||||
| chr9:119355455 | A | G | 37 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0055 others(34): Show |
37 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.-51+13601T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355455 | |||||||
| chr9:119355456 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-51+13600G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355456 | |||||||
| chr9:119355467 | G | A | 3 | a0001c0003t0001g0191 a0001c0003t0001g0209 a0001c0005t0001g0208 |
3 | HG02109.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-51+13589C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355467 | |||||||
| chr9:119355485 | T | C | 13 | a0001c0001t0001g0047 a0001c0001t0001g0075 a0001c0001t0001g0079 others(10): Show |
13 | HG00741.hp2 HG01074.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51+13571A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355485 | |||||||
| chr9:119355524 | T | C | 11 | a0001c0001t0001g0047 a0001c0001t0001g0075 a0001c0001t0001g0079 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51+13532A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355524 | |||||||
| chr9:119355556 | A | G | 1 | a0001c0005t0001g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-51+13500T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355556 | |||||||
| chr9:119355558 | C | G | 2 | a0001c0001t0001g0036 a0001c0002t0001g0031 |
2 | NA18946.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-51+13498G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355558 | |||||||
| chr9:119355589 | C | A | 1 | a0001c0003t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-51+13467G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355589 | |||||||
| chr9:119355601 | T | C | 1 | a0001c0001t0004g0094 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-51+13455A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355601 | |||||||
| chr9:119355642 | T | C | 35 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(32): Show |
35 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-51+13414A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355642 | |||||||
| chr9:119355665 | C | G | 1 | a0001c0003t0002g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-51+13391G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355665 | |||||||
| chr9:119355723 | C | T | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-51+13333G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355723 | |||||||
| chr9:119355728 | C | CA | 45 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
45 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.-51+13327dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355728 | |||||||
| chr9:119355836 | C | T | 136 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0047 others(133): Show |
136 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-51+13220G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355836 | |||||||
| chr9:119355883 | T | C | 8 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0002t0001g0194 others(5): Show |
8 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51+13173A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355883 | |||||||
| chr9:119356033 | G | A | 3 | a0001c0003t0001g0179 a0001c0003t0001g0180 a0001c0003t0001g0205 |
3 | HG00639.hp2 HG00735.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-51+13023C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356033 | |||||||
| chr9:119356130 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-51+12926T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356130 | |||||||
| chr9:119356253 | C | G | 4 | a0001c0001t0001g0210 a0001c0003t0001g0209 a0001c0003t0001g0211 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+12803G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356253 | |||||||
| chr9:119356343 | C | G | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+12713G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356343 | |||||||
| chr9:119356423 | T | C | 1 | a0001c0003t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-51+12633A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356423 | |||||||
| chr9:119356676 | G | A | 1 | a0001c0003t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-51+12380C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356676 | |||||||
| chr9:119356800 | G | A | 29 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-51+12256C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356800 | |||||||
| chr9:119356804 | C | CA | 97 | a0001c0001t0001g0047 a0001c0001t0001g0075 a0001c0001t0001g0084 others(94): Show |
97 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-51+12251dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356804 | |||||||
| chr9:119356923 | T | C | 2 | a0001c0001t0001g0107 a0001c0003t0001g0164 |
2 | HG01256.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-51+12133A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356923 | |||||||
| chr9:119357029 | T | A | 175 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(172): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-51+12027A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357029 | |||||||
| chr9:119357053 | C | T | 2 | a0001c0003t0001g0059 a0001c0004t0001g0073 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-51+12003G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357053 | |||||||
| chr9:119357123 | A | G | 2 | a0001c0001t0001g0082 a0001c0003t0001g0083 |
2 | HG01261.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-51+11933T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357123 | |||||||
| chr9:119357168 | G | A | 2 | a0001c0003t0001g0059 a0001c0004t0001g0073 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-51+11888C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357168 | |||||||
| chr9:119357243 | G | A | 1 | a0001c0001t0003g0009 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-51+11813C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357243 | |||||||
| chr9:119357254 | C | CAT | 2 | a0001c0001t0001g0107 a0001c0003t0001g0164 |
2 | HG01256.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-51+11800_-51+1180 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357254 | |||||||
| chr9:119357385 | T | C | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51+11671A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357385 | |||||||
| chr9:119357411 | C | T | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+11645G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357411 | |||||||
| chr9:119357433 | CT | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0174 a0001c0002t0001g0177 others(4): Show |
7 | HG01261.hp1 HG01884.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+11622delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357433 | |||||||
| chr9:119357736 | G | C | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+11320C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357736 | |||||||
| chr9:119357748 | A | G | 3 | a0001c0001t0001g0045 a0001c0003t0001g0044 a0001c0003t0001g0046 |
3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+11308T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357748 | |||||||
| chr9:119357831 | T | G | 180 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(177): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-51+11225A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357831 | |||||||
| chr9:119357838 | A | G | 1 | a0001c0002t0001g0024 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-51+11218T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357838 | |||||||
| chr9:119357919 | T | G | 180 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(177): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-51+11137A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357919 | |||||||
| chr9:119358277 | C | A | 155 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(152): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-51+10779G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358277 | |||||||
| chr9:119358331 | G | A | 12 | a0001c0001t0001g0082 a0001c0001t0001g0174 a0001c0002t0001g0177 others(9): Show |
12 | HG01123.hp1 HG01261.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-51+10725C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358331 | |||||||
| chr9:119358384 | T | C | 3 | a0001c0002t0001g0091 a0001c0003t0001g0105 a0001c0003t0001g0137 |
3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-51+10672A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358384 | |||||||
| chr9:119358387 | TA | T | 43 | a0001c0001t0001g0088 a0001c0001t0001g0100 a0001c0001t0001g0101 others(40): Show |
43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-51+10668delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358387 | |||||||
| chr9:119358387 | TAA | T | 122 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(119): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-51+10667_-51+1066 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358387 | |||||||
| chr9:119358387 | TAAA | T | 15 | a0001c0001t0001g0170 a0001c0001t0003g0001 a0001c0001t0003g0008 others(12): Show |
15 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51+10666_-51+1066 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358387 | |||||||
| chr9:119358416 | A | G | 221 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-51+10640T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358416 | |||||||
| chr9:119358464 | T | C | 211 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-51+10592A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358464 | |||||||
| chr9:119358481 | G | A | 31 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(28): Show |
31 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-51+10575C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358481 | |||||||
| chr9:119358537 | A | G | 97 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0075 others(94): Show |
97 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-51+10519T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358537 | |||||||
| chr9:119358550 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0002g0218 others(4): Show |
7 | HG02886.hp1 HG02976.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+10506G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358550 | |||||||
| chr9:119358551 | G | T | 1 | a0003c0008t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-51+10505C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358551 | |||||||
| chr9:119358559 | C | T | 2 | a0001c0001t0001g0124 a0001c0002t0001g0167 |
2 | HG01346.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-51+10497G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358559 | |||||||
| chr9:119358560 | G | T | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+10496C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358560 | |||||||
| chr9:119358563 | G | A | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+10493C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358563 | |||||||
| chr9:119358714 | A | G | 97 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0075 others(94): Show |
97 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-51+10342T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358714 | |||||||
| chr9:119358730 | C | G | 21 | a0001c0001t0001g0082 a0001c0001t0001g0107 a0001c0001t0001g0174 others(18): Show |
21 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-51+10326G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358730 | |||||||
| chr9:119358811 | C | T | 1 | a0001c0006t0002g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-51+10245G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358811 | |||||||
| chr9:119358861 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0174 a0001c0002t0001g0177 others(2): Show |
5 | HG01261.hp1 HG02965.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+10195C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358861 | |||||||
| chr9:119358871 | G | A | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+10185C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358871 | |||||||
| chr9:119358878 | T | C | 21 | a0001c0001t0001g0082 a0001c0001t0001g0107 a0001c0001t0001g0174 others(18): Show |
21 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-51+10178A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358878 | |||||||
| chr9:119359852 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0174 a0001c0002t0001g0177 others(2): Show |
5 | HG01261.hp1 HG02965.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+9204C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119359852 | |||||||
| chr9:119359906 | A | G | 1 | a0001c0003t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+9150T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119359906 | |||||||
| chr9:119359998 | G | C | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+9058C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119359998 | |||||||
| chr9:119360006 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-51+9050C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360006 | |||||||
| chr9:119360009 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0174 a0001c0002t0001g0177 others(2): Show |
5 | HG01261.hp1 HG02965.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+9047G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360009 | |||||||
| chr9:119360063 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0075 a0001c0002t0001g0074 |
3 | HG01106.hp2 HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-51+8993C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360063 | |||||||
| chr9:119360488 | C | G | 1 | a0001c0002t0001g0157 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-51+8568G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360488 | |||||||
| chr9:119360518 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-51+8538C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360518 | |||||||
| chr9:119360527 | G | GAC | 96 | a0001c0001t0001g0053 a0001c0001t0001g0084 a0001c0001t0001g0085 others(93): Show |
96 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-51+8527_-51+8528d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360527 | |||||||
| chr9:119360636 | T | C | 9 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0002t0001g0194 others(6): Show |
9 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+8420A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360636 | |||||||
| chr9:119360946 | G | T | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51+8110C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360946 | |||||||
| chr9:119361013 | C | T | 177 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(174): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-51+8043G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361013 | |||||||
| chr9:119361087 | G | A | 7 | a0001c0001t0001g0082 a0001c0001t0001g0174 a0001c0002t0001g0177 others(4): Show |
7 | HG01261.hp1 HG01884.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+7969C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361087 | |||||||
| chr9:119361515 | C | G | 177 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(174): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-51+7541G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361515 | |||||||
| chr9:119361608 | ATTC | A | 46 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(43): Show |
46 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.-51+7445_-51+7447d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361608 | |||||||
| chr9:119361797 | A | AT | 31 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0054 others(28): Show |
31 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.-51+7258dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361797 | |||||||
| chr9:119361797 | AT | A | 106 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(103): Show |
106 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-51+7258delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361797 | |||||||
| chr9:119362047 | A | AC | 10 | a0001c0001t0001g0047 a0001c0001t0001g0077 a0001c0001t0003g0001 others(7): Show |
10 | HG00423.hp1 HG00741.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+7008dupG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362047 | |||||||
| chr9:119362098 | G | T | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-51+6958C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362098 | |||||||
| chr9:119362223 | T | C | 1 | a0001c0002t0001g0194 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-51+6833A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362223 | |||||||
| chr9:119362342 | T | C | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+6714A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362342 | |||||||
| chr9:119362372 | T | A | 4 | a0001c0001t0001g0106 a0001c0002t0001g0095 a0001c0002t0001g0114 others(1): Show |
4 | HG02071.hp1 NA18747.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+6684A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362372 | |||||||
| chr9:119362509 | T | C | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+6547A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362509 | |||||||
| chr9:119362511 | G | A | 93 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(90): Show |
93 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-51+6545C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362511 | |||||||
| chr9:119362542 | T | C | 3 | a0001c0001t0001g0210 a0001c0003t0001g0209 a0001c0003t0001g0211 |
3 | HG02258.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+6514A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362542 | |||||||
| chr9:119362576 | C | T | 1 | a0001c0004t0002g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-51+6480G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362576 | |||||||
| chr9:119362624 | G | T | 9 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0002t0001g0194 others(6): Show |
9 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+6432C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362624 | |||||||
| chr9:119362705 | C | A | 34 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0054 others(31): Show |
34 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-51+6351G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362705 | |||||||
| chr9:119363066 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-51+5990C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363066 | |||||||
| chr9:119363076 | G | A | 19 | a0001c0001t0001g0082 a0001c0001t0001g0174 a0001c0001t0003g0001 others(16): Show |
19 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+5980C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363076 | |||||||
| chr9:119363263 | T | A | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+5793A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363263 | |||||||
| chr9:119363323 | A | G | 44 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(41): Show |
44 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-51+5733T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363323 | |||||||
| chr9:119363326 | A | G | 3 | a0001c0002t0001g0091 a0001c0003t0001g0105 a0001c0003t0001g0137 |
3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-51+5730T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363326 | |||||||
| chr9:119363335 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0174 a0001c0002t0001g0177 others(2): Show |
5 | HG01261.hp1 HG02965.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5721G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363335 | |||||||
| chr9:119363341 | A | T | 2 | a0001c0001t0001g0082 a0001c0003t0001g0083 |
2 | HG01261.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-51+5715T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363341 | |||||||
| chr9:119363398 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-51+5658C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363398 | |||||||
| chr9:119363881 | G | A | 1 | a0001c0003t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+5175C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363881 | |||||||
| chr9:119363935 | G | A | 2 | a0001c0003t0001g0179 a0001c0003t0001g0180 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-51+5121C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363935 | |||||||
| chr9:119363974 | A | G | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+5082T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363974 | |||||||
| chr9:119364018 | CT | C | 18 | a0001c0001t0001g0042 a0001c0001t0003g0001 a0001c0001t0003g0008 others(15): Show |
18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-51+5037delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364018 | |||||||
| chr9:119364018 | CTT | C | 100 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0088 others(97): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-51+5036_-51+5037d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364018 | |||||||
| chr9:119364018 | CTTT | C | 60 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.-51+5035_-51+5037d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364018 | |||||||
| chr9:119364048 | G | A | 95 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(92): Show |
95 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-51+5008C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364048 | |||||||
| chr9:119364200 | A | G | 176 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(173): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-51+4856T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364200 | |||||||
| chr9:119364387 | C | T | 3 | a0001c0001t0001g0210 a0001c0003t0001g0209 a0001c0003t0001g0211 |
3 | HG02258.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+4669G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364387 | |||||||
| chr9:119364416 | C | T | 1 | a0001c0005t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+4640G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364416 | |||||||
| chr9:119364445 | C | T | 176 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(173): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-51+4611G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364445 | |||||||
| chr9:119364655 | G | A | 3 | a0001c0001t0001g0132 a0001c0002t0001g0133 a0004c0011t0001g0123 |
3 | HG01256.hp1 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-51+4401C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364655 | |||||||
| chr9:119364893 | C | T | 1 | a0001c0003t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-51+4163G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364893 | |||||||
| chr9:119364917 | A | G | 1 | a0001c0003t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+4139T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364917 | |||||||
| chr9:119364964 | T | A | 1 | a0001c0003t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+4092A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364964 | |||||||
| chr9:119365098 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-51+3958A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365098 | |||||||
| chr9:119365210 | G | A | 2 | a0001c0003t0001g0206 a0001c0003t0001g0207 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-51+3846C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365210 | |||||||
| chr9:119365284 | G | T | 7 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0115 others(4): Show |
7 | HG00423.hp2 HG00438.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+3772C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365284 | |||||||
| chr9:119365330 | GA | G | 3 | a0001c0001t0001g0210 a0001c0003t0001g0209 a0001c0003t0001g0211 |
3 | HG02258.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+3725delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365330 | |||||||
| chr9:119365468 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0119 |
2 | NA18940.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-51+3588C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365468 | |||||||
| chr9:119365752 | C | A | 1 | a0001c0001t0002g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-51+3304G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365752 | |||||||
| chr9:119365816 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-51+3240G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365816 | |||||||
| chr9:119365996 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0075 a0001c0002t0001g0074 |
3 | HG01106.hp2 HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-51+3060G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365996 | |||||||
| chr9:119366052 | C | T | 9 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0002t0001g0194 others(6): Show |
9 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+3004G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366052 | |||||||
| chr9:119366336 | C | T | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+2720G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366336 | |||||||
| chr9:119366498 | A | G | 222 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.-51+2558T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366498 | |||||||
| chr9:119366503 | C | CGT | 2 | a0001c0001t0001g0202 a0001c0007t0001g0080 |
2 | HG01169.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-51+2551_-51+2552d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | C | CGTGT | 2 | a0001c0002t0001g0200 a0001c0002t0001g0201 |
2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+2549_-51+2552d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGT | C | 9 | a0001c0001t0001g0084 a0001c0002t0001g0024 a0001c0002t0001g0026 others(6): Show |
9 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+2551_-51+2552d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGT | C | 12 | a0001c0001t0001g0052 a0001c0001t0001g0165 a0001c0001t0003g0008 others(9): Show |
12 | HG00280.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-51+2549_-51+2552d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGTGT | C | 25 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(22): Show |
25 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-51+2547_-51+2552d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGTGTG others(1): Show |
C | 47 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0097 others(44): Show |
47 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.-51+2545_-51+2552d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGTGTG others(3): Show |
C | 103 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-51+2543_-51+2552d others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGTGTG others(5): Show |
C | 15 | a0001c0001t0001g0075 a0001c0001t0001g0144 a0001c0001t0001g0161 others(12): Show |
15 | HG00639.hp1 HG01106.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-51+2541_-51+2552d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGTGTG others(7): Show |
C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0156 a0001c0001t0001g0193 others(2): Show |
5 | HG01261.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+2539_-51+2552d others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGTGTG others(9): Show |
C | 2 | a0001c0003t0001g0187 a0001c0003t0001g0209 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-51+2537_-51+2552d others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGTGTG others(11): Show |
C | 2 | a0001c0001t0001g0210 a0001c0005t0002g0235 |
2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-51+2535_-51+2552d others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGTGTG others(13): Show |
C | 2 | a0001c0003t0001g0211 a0001c0005t0001g0208 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+2533_-51+2552d others(22): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366503 | CGTGTGTG others(21): Show |
C | 3 | a0001c0002t0001g0087 a0001c0002t0001g0090 a0001c0003t0001g0173 |
3 | HG02145.hp2 NA18977.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-51+2525_-51+2552d others(30): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | |||||||
| chr9:119366504 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-51+2552C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366504 | |||||||
| chr9:119366506 | G | A | 2 | a0001c0001t0001g0084 a0001c0003t0001g0149 |
2 | HG06807.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-51+2550C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366506 | |||||||
| chr9:119366508 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-51+2548C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366508 | |||||||
| chr9:119366510 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0146 a0001c0001t0001g0150 others(3): Show |
6 | HG01257.hp1 HG01952.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+2546C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366510 | |||||||
| chr9:119366512 | G | A | 16 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
16 | HG00423.hp2 HG00438.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.-51+2544C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366512 | |||||||
| chr9:119366514 | G | A | 61 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0100 others(58): Show |
61 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.-51+2542C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366514 | |||||||
| chr9:119366516 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0161 a0001c0002t0001g0141 others(1): Show |
4 | HG01169.hp2 HG01175.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+2540C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366516 | |||||||
| chr9:119366518 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-51+2538C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366518 | |||||||
| chr9:119366532 | G | A | 2 | a0001c0002t0001g0087 a0001c0002t0001g0090 |
2 | NA18977.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-51+2524C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366532 | |||||||
| chr9:119366741 | T | C | 176 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(173): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-51+2315A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366741 | |||||||
| chr9:119366833 | A | G | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+2223T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366833 | |||||||
| chr9:119367094 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-51+1962C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367094 | |||||||
| chr9:119367097 | T | C | 3 | a0001c0001t0001g0079 a0001c0002t0001g0048 a0001c0002t0001g0078 |
3 | HG03669.hp2 HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-51+1959A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367097 | |||||||
| chr9:119367177 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-51+1879G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367177 | |||||||
| chr9:119367193 | A | ATG | 11 | a0001c0001t0001g0082 a0001c0001t0001g0174 a0001c0002t0001g0177 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51+1861_-51+1862d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367193 | |||||||
| chr9:119367193 | A | ATGTG | 32 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(29): Show |
32 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-51+1859_-51+1862d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367193 | |||||||
| chr9:119367194 | T | C | 1 | a0001c0003t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-51+1862A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367194 | |||||||
| chr9:119367215 | G | GAT | 2 | a0001c0007t0001g0080 a0001c0007t0001g0081 |
2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-51+1840_-51+1841i others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367215 | |||||||
| chr9:119367217 | G | GTGTGATA others(1): Show |
2 | a0001c0002t0003g0011 a0001c0002t0003g0012 |
2 | HG00140.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATA others(5): Show |
3 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0002t0003g0010 |
3 | HG00741.hp1 HG02683.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATA others(7): Show |
4 | a0001c0002t0003g0005 a0001c0002t0003g0007 a0001c0014t0003g0004 others(1): Show |
4 | HG00738.hp1 HG01074.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATA others(9): Show |
5 | a0001c0001t0001g0198 a0001c0002t0003g0002 a0001c0002t0003g0003 others(2): Show |
5 | HG01070.hp2 HG01106.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATA others(11): Show |
2 | a0001c0001t0003g0001 a0001c0002t0001g0194 |
2 | HG00639.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATA others(13): Show |
1 | a0001c0001t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(22): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATA others(15): Show |
1 | a0001c0003t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATA others(17): Show |
2 | a0001c0003t0001g0184 a0001c0003t0007g0183 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATA others(23): Show |
1 | a0001c0003t0001g0176 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(32): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATT others(17): Show |
3 | a0001c0003t0001g0188 a0001c0005t0001g0190 a0001c0009t0001g0189 |
3 | HG03041.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATT others(21): Show |
3 | a0001c0001t0001g0182 a0001c0003t0001g0181 a0001c0004t0001g0014 |
3 | HG01243.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(30): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATT others(23): Show |
1 | a0001c0003t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(32): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATT others(27): Show |
1 | a0001c0004t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(36): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATT others(29): Show |
1 | a0001c0003t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(38): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGATT others(41): Show |
1 | a0003c0008t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(50): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGTGA others(17): Show |
1 | a0001c0001t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | G | GTGTGTGA others(19): Show |
2 | a0001c0003t0001g0187 a0001c0004t0001g0186 |
2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367217 | GAT | G | 3 | a0001c0001t0001g0170 a0001c0003t0001g0206 a0001c0003t0001g0207 |
3 | HG01884.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+1837_-51+1838d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | |||||||
| chr9:119367220 | T | A | 36 | a0001c0001t0001g0182 a0001c0001t0001g0192 a0001c0001t0001g0193 others(33): Show |
36 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-51+1836A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367220 | |||||||
| chr9:119367221 | G | GAT | 24 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(21): Show |
24 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-51+1833_-51+1834d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATAT | 33 | a0001c0001t0001g0022 a0001c0001t0001g0052 a0001c0001t0001g0053 others(30): Show |
33 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-51+1831_-51+1834d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATAT | 3 | a0001c0001t0001g0047 a0001c0001t0001g0168 a0001c0002t0001g0048 |
3 | HG00544.hp2 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-51+1829_-51+1834d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(1): Show |
10 | a0001c0001t0001g0082 a0001c0001t0001g0202 a0001c0002t0001g0167 others(7): Show |
10 | HG01109.hp2 HG01261.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51+1827_-51+1834d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(3): Show |
3 | a0001c0001t0001g0045 a0001c0003t0001g0044 a0001c0003t0001g0046 |
3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+1825_-51+1834d others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(5): Show |
3 | a0001c0001t0001g0165 a0001c0002t0001g0166 a0001c0005t0001g0199 |
3 | HG02683.hp1 HG03579.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-51+1823_-51+1834d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(7): Show |
3 | a0001c0002t0001g0163 a0001c0003t0001g0164 a0001c0003t0008g0212 |
3 | HG01515.hp1 HG01884.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-51+1821_-51+1834d others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(9): Show |
5 | a0001c0001t0001g0161 a0001c0002t0001g0159 a0001c0002t0001g0160 others(2): Show |
5 | HG00438.hp1 HG01169.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+1819_-51+1834d others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(11): Show |
2 | a0001c0001t0001g0158 a0001c0002t0001g0157 |
2 | HG01517.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.-51+1817_-51+1834d others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(13): Show |
5 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0153 others(2): Show |
5 | HG01952.hp2 HG02109.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+1815_-51+1834d others(22): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(15): Show |
5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0002t0001g0152 others(2): Show |
5 | HG01978.hp1 HG02074.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+1813_-51+1834d others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(17): Show |
9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(6): Show |
9 | HG00438.hp2 HG01975.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(19): Show |
4 | a0001c0001t0001g0144 a0001c0002t0001g0143 a0001c0003t0001g0179 others(1): Show |
4 | HG00639.hp2 HG00735.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(21): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0136 a0001c0001t0001g0138 others(6): Show |
9 | HG00423.hp2 HG00741.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(30): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(23): Show |
17 | a0001c0001t0001g0042 a0001c0001t0001g0121 a0001c0001t0001g0122 others(14): Show |
17 | HG01256.hp1 HG01258.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(32): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(25): Show |
6 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0174 others(3): Show |
6 | HG00423.hp1 HG03130.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(34): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(27): Show |
13 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0107 others(10): Show |
13 | HG00544.hp1 HG01256.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(36): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(29): Show |
9 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(6): Show |
9 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(38): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(31): Show |
5 | a0001c0001t0004g0094 a0001c0002t0001g0091 a0001c0002t0001g0093 others(2): Show |
5 | HG02074.hp1 HG02523.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(40): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(33): Show |
4 | a0001c0001t0001g0088 a0001c0002t0001g0090 a0001c0002t0006g0013 others(1): Show |
4 | HG02135.hp1 NA18747.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(42): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | GATATATA others(35): Show |
4 | a0001c0001t0001g0085 a0001c0001t0002g0218 a0001c0002t0001g0086 others(1): Show |
4 | HG02165.hp1 HG02886.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(44): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | G | T | 36 | a0001c0001t0001g0182 a0001c0001t0001g0192 a0001c0001t0001g0193 others(33): Show |
36 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-51+1835C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367221 | GATATATA others(5): Show |
G | 4 | a0001c0001t0001g0210 a0001c0003t0001g0209 a0001c0003t0001g0211 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+1823_-51+1834d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | |||||||
| chr9:119367224 | A | T | 3 | a0001c0001t0001g0170 a0001c0003t0001g0206 a0001c0003t0001g0207 |
3 | HG01884.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+1832T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367224 | |||||||
| chr9:119367225 | T | G | 3 | a0001c0001t0001g0170 a0001c0003t0001g0206 a0001c0003t0001g0207 |
3 | HG01884.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+1831A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367225 | |||||||
| chr9:119367238 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0084 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-51+1817_-51+1818i others(31): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367238 | |||||||
| chr9:119367245 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-51+1811A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367245 | |||||||
| chr9:119367297 | C | T | 94 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(91): Show |
94 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-51+1759G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367297 | |||||||
| chr9:119367318 | G | T | 2 | a0001c0001t0001g0082 a0001c0003t0001g0083 |
2 | HG01261.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-51+1738C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367318 | |||||||
| chr9:119367359 | G | A | 3 | a0001c0001t0001g0210 a0001c0003t0001g0209 a0001c0003t0001g0211 |
3 | HG02258.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+1697C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367359 | |||||||
| chr9:119367605 | T | G | 1 | a0001c0003t0008g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-51+1451A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367605 | |||||||
| chr9:119367815 | ACTCTCTC others(1): Show |
A | 4 | a0001c0001t0001g0214 a0001c0001t0005g0213 a0001c0001t0005g0215 others(1): Show |
4 | NA18966.hp1 NA18970.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1233_-51+1240d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367815 | |||||||
| chr9:119367933 | G | A | 176 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(173): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-51+1123C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367933 | |||||||
| chr9:119368004 | A | C | 12 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+1052T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368004 | |||||||
| chr9:119368410 | T | G | 1 | a0001c0002t0001g0217 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-51+646A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368410 | |||||||
| chr9:119368459 | A | G | 7 | a0001c0003t0001g0019 a0001c0003t0001g0021 a0001c0004t0001g0015 others(4): Show |
7 | HG01123.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51+597T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368459 | |||||||
| chr9:119368886 | C | T | 26 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
26 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51+170G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368886 | |||||||
| chr9:119368925 | G | T | 1 | a0001c0004t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51+131C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368925 |