Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6461 |
| ensemblid | ENSG00000107338.10 |
| hgncid | 10838 |
| symbol | SHB |
| name | SH2 domain containing adaptor protein B |
| refseq_nuc | NM_003028.3 |
| refseq_prot | NP_003019.2 |
| ensembl_nuc | ENST00000377707.4 |
| ensembl_prot | ENSP00000366936.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 37915898 |
| end | 38069227 |
| strand | - |
| ver | v1.2 |
| region | chr9:37915898-38069227 |
| region5000 | chr9:37910898-38074227 |
| regionname0 | SHB_chr9_37915898_38069227 |
| regionname5000 | SHB_chr9_37910898_38074227 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 509 | 309 | 72 | 61 | 117 | 11 | 46 | 81 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0002 | 0/0 | 509 | 9 | 1 | 3 | 5 | 0 | 0 | 5 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0003 | 0/0 | 509 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0004 | 0/0 | 509 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0005 | 0/0 | 509 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0006 | 0/0 | 509 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0007 | 0/0 | 509 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0008 | 0/0 | 509 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0009 | 0/0 | 509 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0010 | 0/0 | 509 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| a0011 | 0/0 | 509 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | MAKWL others(504): Show |
chr9 | 37910898 | 38074227 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1527 | 115 | 16 | 17 | 64 | 3 | 14 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0002 | 0/0 | 1527 | 70 | 10 | 24 | 14 | 2 | 20 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0003 | 0/0 | 1527 | 37 | 13 | 6 | 14 | 1 | 3 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0004 | 0/0 | 1527 | 27 | 5 | 7 | 6 | 5 | 4 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0005 | 0/0 | 1527 | 22 | 9 | 0 | 12 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0006 | 0/0 | 1527 | 7 | 0 | 2 | 4 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0007 | 1/0 | 1527 | 7 | 0 | 3 | 1 | 0 | 2 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0008 | 0/0 | 1527 | 5 | 4 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0010 | 0/0 | 1527 | 4 | 3 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0011 | 0/0 | 1527 | 4 | 1 | 0 | 2 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0013 | 0/0 | 1527 | 3 | 3 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0015 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0016 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0017 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0023 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0001c0024 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0002c0009 | 0/0 | 1527 | 5 | 0 | 0 | 5 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0002c0012 | 0/0 | 1527 | 3 | 0 | 3 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0002c0020 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0003c0019 | 0/0 | 1527 | 2 | 0 | 0 | 0 | 1 | 1 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0004c0018 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0005c0014 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0006c0025 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0007c0022 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0008c0028 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0009c0021 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0010c0026 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 | ||
| a0011c0027 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | ATGGC others(1522): Show |
chr9 | 37910898 | 38074227 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6035 | 43 | 3 | 7 | 27 | 0 | 5 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0002 | 0/0 | 6033 | 49 | 4 | 8 | 31 | 2 | 4 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0013 | 0/0 | 6037 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6032): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0014 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5964): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0015 | 0/0 | 6033 | 3 | 0 | 0 | 0 | 0 | 3 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0020 | 0/0 | 6035 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0023 | 0/0 | 6034 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6029): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0038 | 0/0 | 6041 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6036): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0039 | 0/0 | 6035 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0043 | 0/0 | 6035 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0044 | 0/0 | 6035 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0045 | 0/0 | 6035 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0048 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5970): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0050 | 0/0 | 6035 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0051 | 0/0 | 6033 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0053 | 0/0 | 6034 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6029): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0060 | 0/0 | 6033 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0062 | 0/0 | 6035 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0063 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5970): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0064 | 0/0 | 6035 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0071 | 0/0 | 6034 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6029): Show |
chr9 | 37910898 | 38074227 |
| a0001c0001t0073 | 0/0 | 6035 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0001 | 0/0 | 6035 | 42 | 8 | 14 | 8 | 1 | 11 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0002 | 0/0 | 6033 | 5 | 0 | 3 | 1 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0004 | 0/0 | 5901 | 8 | 0 | 5 | 0 | 1 | 2 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5896): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0014 | 0/0 | 5969 | 2 | 0 | 0 | 2 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5964): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0019 | 0/0 | 5979 | 2 | 0 | 0 | 2 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5974): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0021 | 0/0 | 6035 | 2 | 0 | 1 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0022 | 0/0 | 5975 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5970): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0036 | 0/0 | 6107 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6102): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0040 | 0/0 | 6035 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0041 | 0/0 | 6035 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0057 | 0/0 | 5902 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5897): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0058 | 0/0 | 5901 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5896): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0059 | 0/0 | 6035 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0061 | 0/0 | 6021 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6016): Show |
chr9 | 37910898 | 38074227 |
| a0001c0002t0072 | 0/0 | 6033 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0003t0001 | 0/0 | 6035 | 19 | 0 | 5 | 11 | 1 | 2 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0003t0002 | 0/0 | 6033 | 10 | 6 | 0 | 3 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0003t0008 | 0/0 | 5974 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5969): Show |
chr9 | 37910898 | 38074227 |
| a0001c0003t0016 | 0/0 | 6035 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0003t0023 | 0/0 | 6034 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6029): Show |
chr9 | 37910898 | 38074227 |
| a0001c0003t0029 | 0/0 | 6033 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0003t0030 | 0/0 | 6035 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0003t0052 | 0/0 | 6033 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0001 | 0/0 | 6035 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0003 | 0/0 | 5975 | 15 | 1 | 5 | 2 | 4 | 3 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5970): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0007 | 0/0 | 6035 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0009 | 0/0 | 5975 | 4 | 0 | 2 | 0 | 1 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5970): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0028 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5964): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0035 | 0/0 | 5977 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5972): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0037 | 0/0 | 5977 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5972): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0049 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5964): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0054 | 0/0 | 5973 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5968): Show |
chr9 | 37910898 | 38074227 |
| a0001c0004t0068 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5970): Show |
chr9 | 37910898 | 38074227 |
| a0001c0005t0001 | 0/0 | 6035 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0005t0005 | 0/0 | 6041 | 6 | 0 | 0 | 6 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6036): Show |
chr9 | 37910898 | 38074227 |
| a0001c0005t0006 | 0/0 | 5982 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5977): Show |
chr9 | 37910898 | 38074227 |
| a0001c0005t0007 | 0/0 | 6035 | 4 | 4 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0005t0011 | 0/0 | 5980 | 4 | 0 | 0 | 4 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5975): Show |
chr9 | 37910898 | 38074227 |
| a0001c0005t0024 | 0/0 | 5980 | 2 | 0 | 0 | 1 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5975): Show |
chr9 | 37910898 | 38074227 |
| a0001c0005t0047 | 0/0 | 6035 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0005t0069 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5975): Show |
chr9 | 37910898 | 38074227 |
| a0001c0005t0070 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5973): Show |
chr9 | 37910898 | 38074227 |
| a0001c0006t0010 | 0/0 | 6041 | 4 | 0 | 2 | 2 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6036): Show |
chr9 | 37910898 | 38074227 |
| a0001c0006t0031 | 0/0 | 6041 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6036): Show |
chr9 | 37910898 | 38074227 |
| a0001c0006t0032 | 0/0 | 5973 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5968): Show |
chr9 | 37910898 | 38074227 |
| a0001c0006t0067 | 0/0 | 6041 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6036): Show |
chr9 | 37910898 | 38074227 |
| a0001c0007t0001 | 0/0 | 6035 | 6 | 0 | 3 | 1 | 0 | 2 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0007t0046 | 1/0 | 6035 | 1 | 0 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0008t0002 | 0/0 | 6033 | 3 | 2 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0008t0022 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5970): Show |
chr9 | 37910898 | 38074227 |
| a0001c0008t0055 | 0/0 | 6033 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0001c0010t0012 | 0/0 | 6035 | 3 | 3 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0001c0010t0027 | 0/0 | 6034 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6029): Show |
chr9 | 37910898 | 38074227 |
| a0001c0011t0003 | 0/0 | 5975 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5970): Show |
chr9 | 37910898 | 38074227 |
| a0001c0011t0005 | 0/0 | 6041 | 2 | 0 | 0 | 2 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6036): Show |
chr9 | 37910898 | 38074227 |
| a0001c0011t0056 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5902): Show |
chr9 | 37910898 | 38074227 |
| a0001c0013t0008 | 0/0 | 5974 | 3 | 3 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5969): Show |
chr9 | 37910898 | 38074227 |
| a0001c0015t0018 | 0/0 | 5969 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5964): Show |
chr9 | 37910898 | 38074227 |
| a0001c0016t0026 | 0/0 | 5977 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5972): Show |
chr9 | 37910898 | 38074227 |
| a0001c0017t0025 | 0/0 | 5950 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5945): Show |
chr9 | 37910898 | 38074227 |
| a0001c0023t0066 | 0/0 | 5973 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5968): Show |
chr9 | 37910898 | 38074227 |
| a0001c0024t0002 | 0/0 | 6033 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0002c0009t0006 | 0/0 | 5982 | 5 | 0 | 0 | 5 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5977): Show |
chr9 | 37910898 | 38074227 |
| a0002c0012t0001 | 0/0 | 6035 | 3 | 0 | 3 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0002c0020t0002 | 0/0 | 6033 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6028): Show |
chr9 | 37910898 | 38074227 |
| a0003c0019t0001 | 0/0 | 6035 | 2 | 0 | 0 | 0 | 1 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0004c0018t0017 | 0/0 | 5975 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5970): Show |
chr9 | 37910898 | 38074227 |
| a0005c0014t0013 | 0/0 | 6037 | 2 | 2 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6032): Show |
chr9 | 37910898 | 38074227 |
| a0006c0025t0042 | 0/0 | 6035 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0007c0022t0065 | 0/0 | 5973 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5968): Show |
chr9 | 37910898 | 38074227 |
| a0008c0028t0001 | 0/0 | 6035 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0009c0021t0034 | 0/0 | 6035 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0010c0026t0001 | 0/0 | 6035 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(6030): Show |
chr9 | 37910898 | 38074227 |
| a0011c0027t0033 | 0/0 | 6001 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | AGTGG others(5996): Show |
chr9 | 37910898 | 38074227 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0013g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0014g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0015g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0015g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0015g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0020g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0020g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0023g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0038g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0039g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0043g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0044g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0045g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0048g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0050g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0051g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0053g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0060g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0062g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0063g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0064g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0071g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0001t0073g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0014g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0014g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0019g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0019g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0021g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0021g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0022g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0036g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0040g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0041g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0057g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0058g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0059g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0061g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0002t0072g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0016g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0016g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0023g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0029g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0030g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0003t0052g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0009g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0009g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0009g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0028g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0035g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0037g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0049g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0054g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0004t0068g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0011g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0011g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0011g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0011g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0024g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0024g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0047g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0069g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0005t0070g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0006t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0006t0010g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0006t0010g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0006t0010g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0006t0031g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0006t0032g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0006t0067g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0007t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0007t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0007t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0007t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0007t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0007t0046g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0008t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0008t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0008t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0008t0022g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0008t0055g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0010t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0010t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0010t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0010t0027g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0011t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0011t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0011t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0011t0056g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0013t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0013t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0013t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0015t0018g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0015t0018g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0016t0026g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0016t0026g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0017t0025g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0017t0025g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0023t0066g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0001c0024t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0002c0009t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0002c0009t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0002c0009t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0002c0009t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0002c0009t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0002c0012t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0002c0012t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0002c0020t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0003c0019t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0003c0019t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0004c0018t0017g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0004c0018t0017g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0005c0014t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0005c0014t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0006c0025t0042g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0007c0022t0065g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0008c0028t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0009c0021t0034g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0010c0026t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| a0011c0027t0033g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0267 | EUR | GBR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00099 | hp2 | a0001 | c0002 | t0004 | g0129 | EUR | GBR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00140 | hp1 | a0003 | c0019 | t0001 | g0320 | EUR | GBR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00140 | hp2 | a0001 | c0004 | t0003 | g0109 | EUR | GBR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0057 | EUR | FIN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00323 | hp2 | a0001 | c0004 | t0003 | g0105 | EUR | FIN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00438 | hp1 | a0001 | c0004 | t0003 | g0171 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00438 | hp2 | a0001 | c0006 | t0010 | g0023 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00544 | hp2 | a0001 | c0002 | t0061 | g0061 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00597 | hp1 | a0001 | c0004 | t0037 | g0111 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0115 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00621 | hp2 | a0001 | c0002 | t0019 | g0165 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00642 | hp1 | a0001 | c0003 | t0052 | g0126 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0132 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00735 | hp1 | a0001 | c0004 | t0003 | g0177 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00735 | hp2 | a0001 | c0006 | t0010 | g0022 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0130 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG00741 | hp2 | a0001 | c0004 | t0003 | g0108 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0170 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0100 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0123 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01099 | hp2 | a0001 | c0006 | t0010 | g0020 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01106 | hp2 | a0001 | c0004 | t0003 | g0131 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0079 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01109 | hp2 | a0001 | c0010 | t0027 | g0011 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01168 | hp2 | a0001 | c0002 | t0021 | g0086 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01175 | hp1 | a0001 | c0004 | t0009 | g0009 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0121 | AMR | PUR | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01255 | hp1 | a0001 | c0008 | t0002 | g0026 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01256 | hp1 | a0001 | c0004 | t0003 | g0141 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01257 | hp1 | a0001 | c0007 | t0001 | g0227 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0085 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01496 | hp1 | a0001 | c0002 | t0040 | g0176 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01516 | hp1 | a0001 | c0004 | t0009 | g0008 | EUR | IBS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0259 | EUR | IBS | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0153 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01891 | hp2 | a0001 | c0008 | t0002 | g0027 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01928 | hp2 | a0002 | c0012 | t0001 | g0001 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01934 | hp1 | a0001 | c0004 | t0003 | g0138 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01934 | hp2 | a0002 | c0012 | t0001 | g0034 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01952 | hp1 | a0002 | c0012 | t0001 | g0001 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01981 | hp2 | a0001 | c0002 | t0004 | g0137 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02004 | hp1 | a0001 | c0007 | t0001 | g0226 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02015 | hp1 | a0001 | c0002 | t0014 | g0151 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02055 | hp1 | a0004 | c0018 | t0017 | g0249 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02080 | hp1 | a0001 | c0003 | t0002 | g0179 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0169 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02129 | hp1 | a0001 | c0002 | t0019 | g0157 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0117 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02148 | hp2 | a0001 | c0001 | t0062 | g0294 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02155 | hp1 | a0001 | c0001 | t0038 | g0262 | EAS | CDX | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CDX | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02165 | hp1 | a0001 | c0001 | t0044 | g0276 | EAS | CDX | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | CDX | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0146 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02258 | hp1 | a0001 | c0001 | t0050 | g0251 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02258 | hp2 | a0001 | c0005 | t0001 | g0076 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02273 | hp1 | a0001 | c0007 | t0001 | g0245 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02451 | hp1 | a0001 | c0005 | t0007 | g0041 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02451 | hp2 | a0001 | c0016 | t0026 | g0323 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0164 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02622 | hp1 | a0001 | c0015 | t0018 | g0192 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02630 | hp2 | a0001 | c0005 | t0070 | g0071 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02647 | hp1 | a0001 | c0013 | t0008 | g0190 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02647 | hp2 | a0001 | c0003 | t0030 | g0014 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02683 | hp1 | a0001 | c0001 | t0039 | g0278 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0134 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02717 | hp1 | a0001 | c0004 | t0049 | g0077 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02735 | hp2 | a0001 | c0004 | t0003 | g0113 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02738 | hp1 | a0003 | c0019 | t0001 | g0321 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02738 | hp2 | a0001 | c0002 | t0021 | g0095 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02809 | hp2 | a0001 | c0004 | t0003 | g0058 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02818 | hp1 | a0001 | c0023 | t0066 | g0183 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02818 | hp2 | a0001 | c0001 | t0014 | g0217 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02895 | hp1 | a0001 | c0003 | t0016 | g0016 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02895 | hp2 | a0001 | c0003 | t0008 | g0066 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02897 | hp1 | a0001 | c0003 | t0008 | g0065 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02897 | hp2 | a0001 | c0001 | t0073 | g0325 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02922 | hp1 | a0004 | c0018 | t0017 | g0248 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02922 | hp2 | a0001 | c0004 | t0068 | g0181 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02965 | hp1 | a0001 | c0015 | t0018 | g0193 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02970 | hp1 | a0001 | c0002 | t0072 | g0324 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02976 | hp1 | a0001 | c0003 | t0016 | g0017 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02976 | hp2 | a0001 | c0001 | t0063 | g0234 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0127 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03017 | hp2 | a0006 | c0025 | t0042 | g0187 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03041 | hp2 | a0001 | c0005 | t0007 | g0040 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03130 | hp1 | a0001 | c0005 | t0007 | g0042 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0142 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03139 | hp1 | a0001 | c0010 | t0012 | g0010 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03139 | hp2 | a0001 | c0003 | t0023 | g0168 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03195 | hp1 | a0001 | c0008 | t0002 | g0029 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03195 | hp2 | a0001 | c0003 | t0029 | g0015 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03209 | hp1 | a0001 | c0005 | t0069 | g0078 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03209 | hp2 | a0001 | c0003 | t0002 | g0167 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03239 | hp1 | a0001 | c0001 | t0064 | g0238 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03239 | hp2 | a0001 | c0007 | t0001 | g0253 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03453 | hp1 | a0001 | c0011 | t0056 | g0199 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03453 | hp2 | a0001 | c0004 | t0007 | g0039 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03486 | hp1 | a0001 | c0013 | t0008 | g0189 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0125 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03516 | hp1 | a0001 | c0010 | t0012 | g0013 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03516 | hp2 | a0001 | c0001 | t0023 | g0215 | AFR | ESN | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0145 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03540 | hp2 | a0005 | c0014 | t0013 | g0037 | AFR | GWD | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0069 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03579 | hp2 | a0001 | c0001 | t0020 | g0283 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03654 | hp2 | a0001 | c0002 | t0022 | g0098 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03669 | hp1 | a0001 | c0002 | t0041 | g0175 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03669 | hp2 | a0001 | c0004 | t0003 | g0114 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0096 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03688 | hp2 | a0001 | c0007 | t0001 | g0318 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03704 | hp2 | a0001 | c0011 | t0003 | g0198 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03831 | hp1 | a0001 | c0002 | t0057 | g0128 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03927 | hp2 | a0001 | c0004 | t0009 | g0006 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03942 | hp1 | a0001 | c0002 | t0036 | g0135 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03942 | hp2 | a0001 | c0001 | t0015 | g0246 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04115 | hp2 | a0001 | c0001 | t0015 | g0256 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04184 | hp2 | a0001 | c0005 | t0024 | g0067 | SAS | BEB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04199 | hp1 | a0001 | c0006 | t0067 | g0194 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04199 | hp2 | a0001 | c0004 | t0003 | g0110 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0172 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04204 | hp2 | a0001 | c0002 | t0058 | g0166 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04228 | hp1 | a0001 | c0001 | t0015 | g0255 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0154 | SAS | STU | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18522 | hp1 | a0001 | c0024 | t0002 | g0186 | AFR | YRI | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18522 | hp2 | a0007 | c0022 | t0065 | g0182 | AFR | YRI | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | CHB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CHB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18747 | hp1 | a0001 | c0004 | t0003 | g0082 | EAS | CHB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0122 | EAS | CHB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18943 | hp2 | a0001 | c0005 | t0024 | g0045 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18944 | hp1 | a0001 | c0005 | t0011 | g0046 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18945 | hp1 | a0001 | c0011 | t0005 | g0196 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18946 | hp2 | a0001 | c0005 | t0005 | g0044 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18948 | hp2 | a0001 | c0005 | t0006 | g0051 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18949 | hp1 | a0001 | c0004 | t0035 | g0106 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18950 | hp2 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18951 | hp1 | a0002 | c0009 | t0006 | g0035 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18951 | hp2 | a0001 | c0004 | t0054 | g0139 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18957 | hp1 | a0001 | c0005 | t0011 | g0056 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18960 | hp2 | a0001 | c0005 | t0011 | g0055 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18963 | hp1 | a0008 | c0028 | t0001 | g0319 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18968 | hp1 | a0002 | c0009 | t0006 | g0030 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18972 | hp1 | a0002 | c0009 | t0006 | g0032 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18972 | hp2 | a0001 | c0001 | t0060 | g0297 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18978 | hp1 | a0002 | c0009 | t0006 | g0031 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18979 | hp2 | a0001 | c0005 | t0005 | g0050 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18980 | hp1 | a0001 | c0007 | t0001 | g0244 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18986 | hp2 | a0001 | c0006 | t0031 | g0021 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18989 | hp2 | a0001 | c0005 | t0005 | g0047 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18995 | hp1 | a0001 | c0001 | t0051 | g0240 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18995 | hp2 | a0009 | c0021 | t0034 | g0184 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19000 | hp2 | a0001 | c0005 | t0005 | g0052 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19010 | hp2 | a0001 | c0001 | t0053 | g0247 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19011 | hp1 | a0001 | c0005 | t0005 | g0049 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19011 | hp2 | a0010 | c0026 | t0001 | g0188 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19012 | hp2 | a0001 | c0003 | t0002 | g0180 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19030 | hp1 | a0001 | c0016 | t0026 | g0322 | AFR | LWK | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0143 | AFR | LWK | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19043 | hp1 | a0001 | c0001 | t0020 | g0286 | AFR | LWK | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19043 | hp2 | a0001 | c0004 | t0028 | g0018 | AFR | LWK | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19056 | hp1 | a0001 | c0011 | t0005 | g0197 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19057 | hp1 | a0001 | c0005 | t0011 | g0054 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19070 | hp2 | a0001 | c0006 | t0032 | g0024 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19076 | hp1 | a0001 | c0001 | t0071 | g0243 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19076 | hp2 | a0011 | c0027 | t0033 | g0195 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19079 | hp2 | a0001 | c0006 | t0010 | g0019 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19086 | hp1 | a0001 | c0002 | t0014 | g0063 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19091 | hp2 | a0002 | c0009 | t0006 | g0033 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19240 | hp1 | a0001 | c0013 | t0008 | g0191 | AFR | YRI | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0144 | AFR | YRI | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA20752 | hp1 | a0001 | c0004 | t0003 | g0107 | EUR | TSI | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0088 | EUR | TSI | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA20805 | hp1 | a0001 | c0004 | t0003 | g0112 | EUR | TSI | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA20805 | hp2 | a0001 | c0001 | t0043 | g0242 | EUR | TSI | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | GIH | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA20905 | hp2 | a0001 | c0003 | t0002 | g0140 | SAS | GIH | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01123 | hp1 | a0001 | c0004 | t0009 | g0007 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG01123 | hp2 | a0001 | c0001 | t0013 | g0225 | AMR | CLM | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02109 | hp1 | a0001 | c0005 | t0047 | g0068 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02109 | hp2 | a0001 | c0002 | t0059 | g0070 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02486 | hp1 | a0001 | c0017 | t0025 | g0305 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02486 | hp2 | a0001 | c0010 | t0012 | g0012 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02559 | hp1 | a0001 | c0017 | t0025 | g0306 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG02559 | hp2 | a0001 | c0005 | t0007 | g0043 | AFR | ACB | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03471 | hp1 | a0001 | c0001 | t0045 | g0236 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG03471 | hp2 | a0001 | c0008 | t0055 | g0028 | AFR | MSL | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG06807 | hp1 | a0001 | c0008 | t0022 | g0025 | AFR | USA | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| HG06807 | hp2 | a0005 | c0014 | t0013 | g0038 | AFR | USA | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18955 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA18955 | hp2 | a0001 | c0005 | t0005 | g0048 | EAS | JPT | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA20300 | hp1 | a0002 | c0020 | t0002 | g0036 | AFR | USA | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA20300 | hp2 | a0001 | c0001 | t0048 | g0235 | AFR | USA | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | LWK | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | LWK | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0233 | REF | REF | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| homoSapiens | grch38p0 | a0001 | c0007 | t0046 | g0219 | REF | REF | SHB_chr9_37910898_38074227 | SHB | chr9 | 37910898 | 38074227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:37919880 | G | A | 1 | a0009 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.1471C>T | p.Pro491Ser | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2053/6035 | 1471/1530 | 491/509 | chr9 | 37919880 | |||
| chr9:37955902 | C | T | 1 | a0007 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1207G>A | p.Val403Ile | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/6 | 1789/6035 | 1207/1530 | 403/509 | chr9 | 37955902 | |||
| chr9:37956009 | G | A | 1 | a0004 | 2 | HG02055.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.1100C>T | p.Ser367Leu | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/6 | 1682/6035 | 1100/1530 | 367/509 | chr9 | 37956009 | |||
| chr9:38067964 | C | T | 1 | a0005 | 2 | HG03540.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.682G>A | p.Ala228Thr | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 1264/6035 | 682/1530 | 228/509 | chr9 | 38067964 | |||
| chr9:38068009 | T | C | 1 | a0008 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.637A>G | p.Thr213Ala | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 1219/6035 | 637/1530 | 213/509 | chr9 | 38068009 | |||
| chr9:38068165 | G | C | 1 | a0006 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.481C>G | p.Leu161Val | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 1063/6035 | 481/1530 | 161/509 | chr9 | 38068165 | |||
| chr9:38068182 | G | A | 1 | a0010 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.464C>T | p.Ser155Phe | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 1046/6035 | 464/1530 | 155/509 | chr9 | 38068182 | |||
| chr9:38068210 | C | T | 1 | a0002 | 9 | HG01928.hp2 HG01934.hp2 HG01952.hp1 others(6): Show |
missense_variant | MODERATE | c.436G>A | p.Ala146Thr | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 1018/6035 | 436/1530 | 146/509 | chr9 | 38068210 | |||
| chr9:38068333 | T | C | 1 | a0003 | 2 | HG00140.hp1 HG02738.hp1 |
missense_variant | MODERATE | c.313A>G | p.Lys105Glu | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 895/6035 | 313/1530 | 105/509 | chr9 | 38068333 | |||
| chr9:38068432 | C | G | 1 | a0011 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.214G>C | p.Asp72His | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 796/6035 | 214/1530 | 72/509 | chr9 | 38068432 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:37919842 | G | A | 3 | a0001c0017 a0001c0023 a0007c0022 |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.1509C>T | p.Pro503Pro | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2091/6035 | 1509/1530 | 503/509 | chr9 | 37919842 | |||
| chr9:37919929 | C | T | 2 | a0001c0023 a0007c0022 |
2 | HG02818.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.1422G>A | p.Pro474Pro | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2004/6035 | 1422/1530 | 474/509 | chr9 | 37919929 | |||
| chr9:37948727 | T | C | 8 | a0001c0004 a0001c0005 a0001c0006 others(5): Show |
71 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(68): Show |
synonymous_variant | LOW | c.1254A>G | p.Gly418Gly | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/6 | 1836/6035 | 1254/1530 | 418/509 | chr9 | 37948727 | |||
| chr9:37974746 | T | C | 18 | a0001c0001 a0001c0003 a0001c0004 others(15): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
synonymous_variant | LOW | c.930A>G | p.Ser310Ser | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/6 | 1512/6035 | 930/1530 | 310/509 | chr9 | 37974746 | |||
| chr9:38016045 | G | A | 1 | a0004c0018 | 2 | HG02055.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.804C>T | p.Tyr268Tyr | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/6 | 1386/6035 | 804/1530 | 268/509 | chr9 | 38016045 | |||
| chr9:38068115 | G | A | 1 | a0001c0024 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.531C>T | p.Arg177Arg | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 1113/6035 | 531/1530 | 177/509 | chr9 | 38068115 | |||
| chr9:38068373 | G | A | 2 | a0001c0013 a0001c0015 |
5 | HG02622.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.273C>T | p.Asp91Asp | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 855/6035 | 273/1530 | 91/509 | chr9 | 38068373 | |||
| chr9:38068454 | T | C | 3 | a0001c0006 a0001c0008 a0001c0010 |
16 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(13): Show |
synonymous_variant | LOW | c.192A>G | p.Ser64Ser | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 774/6035 | 192/1530 | 64/509 | chr9 | 38068454 | |||
| chr9:38068457 | G | A | 1 | a0001c0016 | 2 | HG02451.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.189C>T | p.Phe63Phe | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 771/6035 | 189/1530 | 63/509 | chr9 | 38068457 | |||
| chr9:38068532 | C | T | 2 | a0001c0008 a0001c0010 |
9 | HG01109.hp2 HG01255.hp1 HG01891.hp2 others(6): Show |
synonymous_variant | LOW | c.114G>A | p.Ser38Ser | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 696/6035 | 114/1530 | 38/509 | chr9 | 38068532 | |||
| chr9:38068535 | A | G | 20 | a0001c0002 a0001c0003 a0001c0004 others(17): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
synonymous_variant | LOW | c.111T>C | p.Pro37Pro | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 693/6035 | 111/1530 | 37/509 | chr9 | 38068535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:37916059 | GCCAAGGG others(17): Show |
G | 1 | a0001c0017t0025 | 2 | HG02486.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3738_*3761delTCCT others(20): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3738 | chr9 | 37916059 | ||||||
| chr9:37916110 | C | T | 8 | a0001c0002t0057 a0001c0004t0068 a0001c0005t0006 others(5): Show |
16 | HG02630.hp2 HG02922.hp2 HG03209.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3711G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3711 | chr9 | 37916110 | ||||||
| chr9:37916137 | C | T | 1 | a0001c0017t0025 | 2 | HG02486.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3684G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3684 | chr9 | 37916137 | ||||||
| chr9:37916167 | C | T | 6 | a0001c0004t0003 a0001c0004t0009 a0001c0004t0035 others(3): Show |
23 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3654G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3654 | chr9 | 37916167 | ||||||
| chr9:37916196 | G | A | 6 | a0001c0001t0043 a0001c0005t0005 a0001c0006t0010 others(3): Show |
15 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3625C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3625 | chr9 | 37916196 | ||||||
| chr9:37916308 | C | G | 1 | a0006c0025t0042 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3513G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3513 | chr9 | 37916308 | ||||||
| chr9:37916325 | C | T | 2 | a0001c0023t0066 a0007c0022t0065 |
2 | HG02818.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3496G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3496 | chr9 | 37916325 | ||||||
| chr9:37916353 | G | A | 3 | a0001c0001t0020 a0001c0001t0073 a0001c0003t0030 |
4 | HG02647.hp2 HG02897.hp2 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3468C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3468 | chr9 | 37916353 | ||||||
| chr9:37916411 | T | C | 28 | a0001c0001t0048 a0001c0001t0063 a0001c0002t0040 others(25): Show |
60 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3410A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3410 | chr9 | 37916411 | ||||||
| chr9:37916545 | T | C | 1 | a0001c0003t0052 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3276A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3276 | chr9 | 37916545 | ||||||
| chr9:37916596 | G | A | 1 | a0001c0002t0021 | 2 | HG01168.hp2 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3225C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3225 | chr9 | 37916596 | ||||||
| chr9:37916607 | G | A | 1 | a0001c0001t0044 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3214C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3214 | chr9 | 37916607 | ||||||
| chr9:37916734 | C | T | 6 | a0001c0004t0003 a0001c0004t0009 a0001c0004t0035 others(3): Show |
23 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3087G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 3087 | chr9 | 37916734 | ||||||
| chr9:37917008 | A | T | 1 | a0001c0004t0068 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2813T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2813 | chr9 | 37917008 | ||||||
| chr9:37917037 | G | GA | 12 | a0001c0001t0053 a0001c0001t0071 a0001c0002t0057 others(9): Show |
24 | HG02486.hp1 HG02559.hp1 HG02630.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2783dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2783 | chr9 | 37917037 | ||||||
| chr9:37917120 | G | A | 1 | a0001c0001t0045 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2701C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2701 | chr9 | 37917120 | ||||||
| chr9:37917161 | G | A | 1 | a0001c0002t0058 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2660C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2660 | chr9 | 37917161 | ||||||
| chr9:37917165 | C | G | 3 | a0001c0017t0025 a0001c0023t0066 a0007c0022t0065 |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2656G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2656 | chr9 | 37917165 | ||||||
| chr9:37917271 | C | T | 1 | a0001c0016t0026 | 2 | HG02451.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2550G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2550 | chr9 | 37917271 | ||||||
| chr9:37917385 | A | G | 3 | a0001c0017t0025 a0001c0023t0066 a0007c0022t0065 |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2436T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2436 | chr9 | 37917385 | ||||||
| chr9:37917448 | G | A | 1 | a0001c0002t0059 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2373C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2373 | chr9 | 37917448 | ||||||
| chr9:37917476 | G | A | 1 | a0001c0001t0063 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2345C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2345 | chr9 | 37917476 | ||||||
| chr9:37917605 | A | G | 23 | a0001c0002t0040 a0001c0002t0057 a0001c0004t0003 others(20): Show |
51 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2216T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2216 | chr9 | 37917605 | ||||||
| chr9:37917627 | C | T | 1 | a0001c0001t0051 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 2194 | chr9 | 37917627 | ||||||
| chr9:37917915 | AAGGGCAG others(27): Show |
A | 1 | a0011c0027t0033 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1872_*1905delGTGG others(30): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1872 | chr9 | 37917915 | ||||||
| chr9:37918045 | A | G | 1 | a0001c0003t0029 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1776T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1776 | chr9 | 37918045 | ||||||
| chr9:37918068 | C | A | 1 | a0001c0002t0059 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1753G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1753 | chr9 | 37918068 | ||||||
| chr9:37918112 | A | G | 92 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0013 others(89): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
3_prime_UTR_variant | MODIFIER | c.*1709T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1709 | chr9 | 37918112 | ||||||
| chr9:37918112 | A | T | 2 | a0001c0001t0048 a0001c0001t0063 |
2 | HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1709T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1709 | chr9 | 37918112 | ||||||
| chr9:37918201 | C | A | 1 | a0001c0005t0047 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1620G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1620 | chr9 | 37918201 | ||||||
| chr9:37918201 | C | T | 1 | a0001c0006t0067 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1620G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1620 | chr9 | 37918201 | ||||||
| chr9:37918222 | A | T | 13 | a0001c0002t0040 a0001c0002t0041 a0001c0004t0003 others(10): Show |
32 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1599T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1599 | chr9 | 37918222 | ||||||
| chr9:37918231 | A | T | 1 | a0001c0001t0039 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1590T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1590 | chr9 | 37918231 | ||||||
| chr9:37918374 | C | CGTGTGT | 6 | a0001c0001t0038 a0001c0005t0005 a0001c0006t0010 others(3): Show |
15 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1441_*1446dupACAC others(2): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1446 | chr9 | 37918374 | ||||||
| chr9:37918374 | CGTGTGTA others(53): Show |
C | 24 | a0001c0001t0048 a0001c0001t0063 a0001c0002t0019 others(21): Show |
56 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1387_*1446delACAC others(56): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1387 | chr9 | 37918374 | ||||||
| chr9:37918374 | CGTGTGTA others(57): Show |
C | 2 | a0001c0023t0066 a0007c0022t0065 |
2 | HG02818.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1383_*1446delACAC others(60): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1383 | chr9 | 37918374 | ||||||
| chr9:37918374 | CGTGTGTA others(59): Show |
C | 5 | a0001c0001t0014 a0001c0002t0014 a0001c0004t0028 others(2): Show |
7 | HG02015.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1381_*1446delACAC others(62): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1381 | chr9 | 37918374 | ||||||
| chr9:37918374 | CGTGTGTA others(121): Show |
C | 1 | a0001c0011t0056 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319_*1446del | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1319 | chr9 | 37918374 | ||||||
| chr9:37918374 | CGTGTGTA others(127): Show |
C | 3 | a0001c0002t0004 a0001c0002t0057 a0001c0002t0058 |
10 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1313_*1446del | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1313 | chr9 | 37918374 | ||||||
| chr9:37918421 | C | CTG | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0044 others(5): Show |
17 | HG01081.hp1 HG02040.hp2 HG02135.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1398_*1399dupCA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1399 | chr9 | 37918421 | ||||||
| chr9:37918421 | CTGTGTGT others(61): Show |
C | 13 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0039 others(10): Show |
45 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1332_*1399delCAGC others(64): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1332 | chr9 | 37918421 | ||||||
| chr9:37918456 | T | C | 1 | a0001c0001t0050 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1365A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1365 | chr9 | 37918456 | ||||||
| chr9:37918487 | C | CTG | 8 | a0001c0001t0013 a0001c0004t0035 a0001c0004t0037 others(5): Show |
10 | HG00597.hp1 HG01123.hp2 HG02451.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1332_*1333dupCA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1333 | chr9 | 37918487 | ||||||
| chr9:37918487 | C | CTGTG | 4 | a0001c0002t0019 a0001c0005t0011 a0001c0005t0024 others(1): Show |
9 | HG00621.hp2 HG02129.hp1 HG03209.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1330_*1333dupCACA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1333 | chr9 | 37918487 | ||||||
| chr9:37918487 | C | CTGTGTG | 2 | a0001c0005t0006 a0002c0009t0006 |
6 | NA18948.hp2 NA18951.hp1 NA18968.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1328_*1333dupCACA others(2): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1333 | chr9 | 37918487 | ||||||
| chr9:37918487 | C | CTGTGTGT others(65): Show |
1 | a0001c0002t0036 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333_*1334insCAGC others(68): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1333 | chr9 | 37918487 | ||||||
| chr9:37918487 | CTG | C | 27 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0038 others(24): Show |
105 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1332_*1333delCA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1332 | chr9 | 37918487 | ||||||
| chr9:37918489 | G | GTGTGTGT others(57): Show |
1 | a0001c0001t0001 | 2 | HG01070.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1331_*1332insGCCC others(60): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1331 | chr9 | 37918489 | ||||||
| chr9:37918489 | G | GTGTGTGT others(59): Show |
1 | a0001c0001t0001 | 4 | NA18994.hp1 NA19007.hp1 NA19009.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1266_*1331dupGCCC others(62): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1331 | chr9 | 37918489 | ||||||
| chr9:37918491 | G | C | 1 | a0001c0008t0055 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1330C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1330 | chr9 | 37918491 | ||||||
| chr9:37918507 | G | T | 1 | a0011c0027t0033 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1314C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1314 | chr9 | 37918507 | ||||||
| chr9:37918508 | T | C | 1 | a0001c0001t0015 | 3 | HG03942.hp2 HG04115.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1313A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1313 | chr9 | 37918508 | ||||||
| chr9:37918605 | C | T | 1 | a0001c0005t0069 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1216G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 1216 | chr9 | 37918605 | ||||||
| chr9:37918843 | TG | T | 3 | a0001c0001t0023 a0001c0003t0023 a0001c0010t0027 |
3 | HG01109.hp2 HG03139.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*977delC | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 977 | chr9 | 37918843 | ||||||
| chr9:37918846 | T | C | 7 | a0001c0001t0023 a0001c0002t0059 a0001c0002t0072 others(4): Show |
10 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*975A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 975 | chr9 | 37918846 | ||||||
| chr9:37918874 | C | T | 1 | a0001c0015t0018 | 2 | HG02622.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*947G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 947 | chr9 | 37918874 | ||||||
| chr9:37918890 | A | G | 1 | a0001c0004t0035 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*931T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 931 | chr9 | 37918890 | ||||||
| chr9:37919017 | C | T | 12 | a0001c0003t0030 a0001c0004t0068 a0001c0005t0005 others(9): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*804G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 804 | chr9 | 37919017 | ||||||
| chr9:37919058 | G | A | 1 | a0001c0001t0060 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*763C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 763 | chr9 | 37919058 | ||||||
| chr9:37919099 | C | T | 1 | a0009c0021t0034 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*722G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 722 | chr9 | 37919099 | ||||||
| chr9:37919247 | A | G | 2 | a0001c0023t0066 a0007c0022t0065 |
2 | HG02818.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*574T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 574 | chr9 | 37919247 | ||||||
| chr9:37919304 | CACACTCA others(5): Show |
C | 1 | a0001c0002t0061 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*505_*516delCTGTGT others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 505 | chr9 | 37919304 | ||||||
| chr9:37919423 | T | A | 1 | a0001c0001t0062 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 398 | chr9 | 37919423 | ||||||
| chr9:37919512 | G | A | 1 | a0001c0001t0063 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 309 | chr9 | 37919512 | ||||||
| chr9:37919645 | G | A | 1 | a0001c0001t0064 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 176 | chr9 | 37919645 | ||||||
| chr9:37919661 | G | A | 2 | a0001c0003t0008 a0001c0013t0008 |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*160C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 160 | chr9 | 37919661 | ||||||
| chr9:37919746 | T | C | 17 | a0001c0003t0030 a0001c0004t0068 a0001c0005t0005 others(14): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*75A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 75 | chr9 | 37919746 | ||||||
| chr9:37919750 | C | T | 1 | a0011c0027t0033 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 71 | chr9 | 37919750 | ||||||
| chr9:37919764 | G | A | 1 | a0001c0001t0071 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 6/6 | 57 | chr9 | 37919764 | ||||||
| chr9:38068708 | G | A | 1 | a0001c0016t0026 | 2 | HG02451.hp2 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-63C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 63 | chr9 | 38068708 | ||||||
| chr9:38068776 | A | C | 3 | a0001c0006t0010 a0001c0006t0031 a0001c0006t0032 |
6 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-131T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 131 | chr9 | 38068776 | ||||||
| chr9:38068860 | G | A | 1 | a0001c0002t0072 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-215C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 215 | chr9 | 38068860 | ||||||
| chr9:38068889 | C | G | 4 | a0001c0003t0016 a0001c0003t0029 a0001c0003t0030 others(1): Show |
5 | HG02647.hp2 HG02895.hp1 HG02976.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-244G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 244 | chr9 | 38068889 | ||||||
| chr9:38068924 | G | C | 1 | a0001c0001t0073 | 1 | HG02897.hp2 | 5_prime_UTR_variant | MODIFIER | c.-279C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 279 | chr9 | 38068924 | ||||||
| chr9:38068983 | G | T | 2 | a0001c0010t0012 a0001c0010t0027 |
4 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-338C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 338 | chr9 | 38068983 | ||||||
| chr9:38069201 | G | T | 1 | a0001c0004t0009 | 4 | HG01123.hp1 HG01175.hp1 HG01516.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-556C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/6 | 556 | chr9 | 38069201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:37920039 | C | CCCTGACA others(32): Show |
1 | a0001c0005t0005g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1347-74_1347-36dup others(39): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920039 | |||||||
| chr9:37920179 | G | A | 31 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(28): Show |
31 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1347-175C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920179 | |||||||
| chr9:37920179 | G | C | 18 | a0001c0001t0001g0314 a0001c0001t0002g0207 a0001c0001t0002g0258 others(15): Show |
18 | HG01070.hp1 HG01516.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.1347-175C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920179 | |||||||
| chr9:37920192 | C | T | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1347-188G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920192 | |||||||
| chr9:37920204 | C | T | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-200G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920204 | |||||||
| chr9:37920233 | A | G | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-229T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920233 | |||||||
| chr9:37920249 | C | T | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1347-245G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920249 | |||||||
| chr9:37920275 | A | AAAAAAAA others(3): Show |
2 | a0001c0004t0003g0109 a0001c0004t0003g0177 |
2 | HG00140.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1347-272_1347-271i others(12): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | A | AAAAAC | 21 | a0001c0001t0001g0200 a0001c0001t0001g0218 a0001c0001t0001g0232 others(18): Show |
21 | HG00140.hp1 HG00741.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1347-276_1347-272d others(7): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | A | AAAAACAA others(3): Show |
5 | a0001c0004t0003g0110 a0001c0010t0012g0010 a0001c0010t0012g0012 others(2): Show |
5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347-281_1347-272d others(12): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | A | AAAAACAA others(8): Show |
1 | a0001c0004t0003g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1347-286_1347-272d others(17): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | A | AAAAACAA others(13): Show |
1 | a0001c0004t0003g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1347-291_1347-272d others(22): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | AAAAAC | A | 109 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0209 others(106): Show |
109 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1347-276_1347-272d others(7): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | AAAAACAA others(3): Show |
A | 15 | a0001c0001t0001g0205 a0001c0001t0001g0250 a0001c0001t0001g0254 others(12): Show |
15 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.1347-281_1347-272d others(12): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | AAAAACAA others(8): Show |
A | 77 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0224 others(74): Show |
80 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1347-286_1347-272d others(17): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | AAAAACAA others(13): Show |
A | 18 | a0001c0001t0063g0234 a0001c0005t0006g0051 a0001c0005t0011g0046 others(15): Show |
18 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.1347-291_1347-272d others(22): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | AAAAACAA others(18): Show |
A | 1 | a0001c0001t0002g0316 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1347-296_1347-272d others(27): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920275 | AAAAACAA others(28): Show |
A | 17 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1347-306_1347-272d others(37): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920275 | |||||||
| chr9:37920326 | AAAACAAA others(3): Show |
A | 1 | a0001c0001t0048g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1347-332_1347-323d others(12): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920326 | |||||||
| chr9:37920331 | A | T | 2 | a0001c0002t0041g0175 a0001c0004t0049g0077 |
2 | HG02717.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1347-327T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920331 | |||||||
| chr9:37920364 | T | C | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-360A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920364 | |||||||
| chr9:37920815 | T | C | 32 | a0001c0003t0030g0014 a0001c0004t0049g0077 a0001c0004t0068g0181 others(29): Show |
32 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1347-811A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920815 | |||||||
| chr9:37920970 | A | G | 41 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(38): Show |
41 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.1347-966T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37920970 | |||||||
| chr9:37921195 | A | G | 1 | a0001c0005t0069g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1347-1191T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921195 | |||||||
| chr9:37921309 | C | A | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1347-1305G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921309 | |||||||
| chr9:37921326 | G | A | 1 | a0001c0006t0067g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1347-1322C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921326 | |||||||
| chr9:37921422 | G | A | 1 | a0001c0002t0072g0324 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1347-1418C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921422 | |||||||
| chr9:37921493 | C | T | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1347-1489G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921493 | |||||||
| chr9:37921499 | A | G | 7 | a0001c0001t0001g0211 a0001c0003t0016g0016 a0001c0003t0016g0017 others(4): Show |
7 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347-1495T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921499 | |||||||
| chr9:37921699 | C | T | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347-1695G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921699 | |||||||
| chr9:37921715 | G | A | 23 | a0001c0004t0003g0058 a0001c0004t0003g0082 a0001c0004t0003g0105 others(20): Show |
23 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.1347-1711C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921715 | |||||||
| chr9:37921724 | G | C | 1 | a0001c0001t0002g0261 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1347-1720C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921724 | |||||||
| chr9:37921778 | C | A | 1 | a0001c0006t0032g0024 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1347-1774G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921778 | |||||||
| chr9:37921845 | G | A | 1 | a0001c0002t0040g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1347-1841C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921845 | |||||||
| chr9:37921883 | T | C | 1 | a0001c0001t0038g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1347-1879A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921883 | |||||||
| chr9:37921932 | C | T | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-1928G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921932 | |||||||
| chr9:37921935 | G | T | 91 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0001t0048g0235 others(88): Show |
93 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.1347-1931C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921935 | |||||||
| chr9:37921962 | G | C | 92 | a0001c0001t0001g0211 a0001c0001t0014g0217 a0001c0001t0023g0215 others(89): Show |
94 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1347-1958C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37921962 | |||||||
| chr9:37922049 | C | A | 1 | a0003c0019t0001g0320 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1347-2045G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37922049 | |||||||
| chr9:37922055 | C | T | 2 | a0001c0003t0001g0081 a0001c0003t0001g0116 |
2 | NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1347-2051G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37922055 | |||||||
| chr9:37922241 | A | G | 1 | a0001c0003t0001g0169 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1347-2237T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37922241 | |||||||
| chr9:37922434 | G | A | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1347-2430C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37922434 | |||||||
| chr9:37922763 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0310 |
2 | NA18968.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1347-2759G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37922763 | |||||||
| chr9:37922920 | G | A | 2 | a0005c0014t0013g0037 a0005c0014t0013g0038 |
2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1347-2916C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37922920 | |||||||
| chr9:37922975 | C | T | 1 | a0001c0001t0044g0276 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1347-2971G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37922975 | |||||||
| chr9:37923229 | C | T | 2 | a0001c0001t0048g0235 a0001c0001t0063g0234 |
2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1347-3225G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923229 | |||||||
| chr9:37923280 | C | T | 3 | a0001c0004t0049g0077 a0001c0015t0018g0192 a0001c0015t0018g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1347-3276G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923280 | |||||||
| chr9:37923375 | C | T | 14 | a0001c0005t0006g0051 a0001c0005t0011g0046 a0001c0005t0011g0054 others(11): Show |
14 | HG02630.hp2 HG03209.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.1347-3371G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923375 | |||||||
| chr9:37923551 | T | C | 1 | a0001c0007t0001g0227 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1347-3547A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923551 | |||||||
| chr9:37923582 | G | A | 2 | a0001c0002t0002g0059 a0001c0002t0002g0060 |
2 | HG00639.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1347-3578C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923582 | |||||||
| chr9:37923596 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1347-3592G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923596 | |||||||
| chr9:37923599 | T | C | 7 | a0001c0001t0001g0211 a0001c0003t0016g0016 a0001c0003t0016g0017 others(4): Show |
7 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347-3595A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923599 | |||||||
| chr9:37923692 | C | T | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-3688G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923692 | |||||||
| chr9:37923847 | C | T | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-3843G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923847 | |||||||
| chr9:37923909 | G | A | 1 | a0001c0001t0063g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1347-3905C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37923909 | |||||||
| chr9:37924038 | A | G | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-4034T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37924038 | |||||||
| chr9:37924090 | G | A | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347-4086C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37924090 | |||||||
| chr9:37924249 | C | T | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1347-4245G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37924249 | |||||||
| chr9:37924429 | G | A | 14 | a0001c0005t0006g0051 a0001c0005t0011g0046 a0001c0005t0011g0054 others(11): Show |
14 | HG02630.hp2 HG03209.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.1347-4425C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37924429 | |||||||
| chr9:37924502 | C | A | 3 | a0001c0004t0049g0077 a0001c0015t0018g0192 a0001c0015t0018g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1347-4498G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37924502 | |||||||
| chr9:37924823 | A | G | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-4819T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37924823 | |||||||
| chr9:37924842 | T | C | 1 | a0001c0001t0002g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1347-4838A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37924842 | |||||||
| chr9:37925022 | T | C | 2 | a0001c0001t0002g0295 a0001c0002t0002g0062 |
2 | HG00544.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1347-5018A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925022 | |||||||
| chr9:37925338 | A | G | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1347-5334T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925338 | |||||||
| chr9:37925406 | G | A | 5 | a0001c0002t0001g0080 a0001c0007t0001g0226 a0001c0007t0001g0245 others(2): Show |
6 | HG01928.hp2 HG01934.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1347-5402C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925406 | |||||||
| chr9:37925408 | G | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1347-5404C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925408 | |||||||
| chr9:37925610 | GGTAAT | G | 17 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1347-5611_1347-560 others(9): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925610 | |||||||
| chr9:37925661 | C | T | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-5657G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925661 | |||||||
| chr9:37925694 | C | G | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-5690G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925694 | |||||||
| chr9:37925750 | T | C | 4 | a0001c0001t0048g0235 a0001c0001t0063g0234 a0001c0016t0026g0322 others(1): Show |
4 | HG02451.hp2 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-5746A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925750 | |||||||
| chr9:37925829 | G | C | 23 | a0001c0004t0003g0058 a0001c0004t0003g0082 a0001c0004t0003g0105 others(20): Show |
23 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.1347-5825C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925829 | |||||||
| chr9:37925841 | G | A | 40 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0080 others(37): Show |
42 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1347-5837C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37925841 | |||||||
| chr9:37926059 | G | A | 1 | a0001c0003t0029g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1347-6055C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37926059 | |||||||
| chr9:37926263 | C | T | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347-6259G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37926263 | |||||||
| chr9:37926382 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1347-6378C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37926382 | |||||||
| chr9:37926451 | T | G | 31 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(28): Show |
31 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1347-6447A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37926451 | |||||||
| chr9:37926711 | C | G | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-6707G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37926711 | |||||||
| chr9:37926896 | GCCCAGGC others(4): Show |
G | 1 | a0001c0004t0003g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1347-6903_1347-689 others(15): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37926896 | |||||||
| chr9:37926927 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1347-6923C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37926927 | |||||||
| chr9:37926975 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1347-6971A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37926975 | |||||||
| chr9:37926980 | G | A | 14 | a0001c0005t0006g0051 a0001c0005t0011g0046 a0001c0005t0011g0054 others(11): Show |
14 | HG02630.hp2 HG03209.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.1347-6976C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37926980 | |||||||
| chr9:37927266 | T | C | 33 | a0001c0005t0005g0044 a0001c0005t0005g0047 a0001c0005t0005g0048 others(30): Show |
33 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1347-7262A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37927266 | |||||||
| chr9:37927356 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1347-7352C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37927356 | |||||||
| chr9:37927421 | G | A | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-7417C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37927421 | |||||||
| chr9:37927527 | T | C | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347-7523A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37927527 | |||||||
| chr9:37927531 | G | A | 2 | a0001c0002t0004g0132 a0001c0002t0004g0134 |
2 | HG00642.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1347-7527C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37927531 | |||||||
| chr9:37927931 | CCTCTCTT others(7): Show |
C | 1 | a0001c0003t0002g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1347-7941_1347-792 others(18): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37927931 | |||||||
| chr9:37927944 | TTCTC | T | 16 | a0001c0003t0030g0014 a0001c0005t0005g0044 a0001c0005t0005g0047 others(13): Show |
16 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1347-7944_1347-794 others(8): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37927944 | |||||||
| chr9:37927952 | T | C | 6 | a0001c0001t0001g0224 a0001c0001t0001g0265 a0001c0001t0002g0005 others(3): Show |
7 | HG00558.hp1 NA18954.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.1347-7948A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37927952 | |||||||
| chr9:37928001 | C | CTA | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-7998_1347-799 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928001 | |||||||
| chr9:37928183 | C | T | 1 | a0001c0003t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1347-8179G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928183 | |||||||
| chr9:37928186 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1347-8182T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928186 | |||||||
| chr9:37928295 | T | C | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-8291A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928295 | |||||||
| chr9:37928373 | C | A | 3 | a0001c0001t0063g0234 a0001c0016t0026g0322 a0001c0016t0026g0323 |
3 | HG02451.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1347-8369G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928373 | |||||||
| chr9:37928394 | C | T | 1 | a0001c0004t0035g0106 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1347-8390G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928394 | |||||||
| chr9:37928401 | A | G | 14 | a0001c0005t0006g0051 a0001c0005t0011g0046 a0001c0005t0011g0054 others(11): Show |
14 | HG02630.hp2 HG03209.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.1347-8397T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928401 | |||||||
| chr9:37928473 | C | T | 5 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0301 others(2): Show |
5 | NA18978.hp2 NA18979.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347-8469G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928473 | |||||||
| chr9:37928491 | A | G | 165 | a0001c0001t0001g0211 a0001c0001t0014g0217 a0001c0001t0023g0215 others(162): Show |
167 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1347-8487T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928491 | |||||||
| chr9:37928507 | TA | T | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-8504delT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928507 | |||||||
| chr9:37928509 | A | T | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-8505T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928509 | |||||||
| chr9:37928584 | C | T | 31 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(28): Show |
31 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1347-8580G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928584 | |||||||
| chr9:37928707 | T | G | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-8703A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928707 | |||||||
| chr9:37928721 | T | C | 2 | a0001c0006t0031g0021 a0001c0006t0032g0024 |
2 | NA18986.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1347-8717A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928721 | |||||||
| chr9:37928774 | G | T | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-8770C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928774 | |||||||
| chr9:37928869 | A | G | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347-8865T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928869 | |||||||
| chr9:37928884 | C | G | 1 | a0001c0003t0002g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1347-8880G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928884 | |||||||
| chr9:37928886 | A | G | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-8882T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37928886 | |||||||
| chr9:37929012 | G | A | 17 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1347-9008C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929012 | |||||||
| chr9:37929043 | G | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1347-9039C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929043 | |||||||
| chr9:37929061 | T | C | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-9057A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929061 | |||||||
| chr9:37929062 | G | A | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-9058C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929062 | |||||||
| chr9:37929075 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1347-9071C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929075 | |||||||
| chr9:37929141 | G | A | 1 | a0001c0002t0041g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1347-9137C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929141 | |||||||
| chr9:37929320 | T | C | 1 | a0001c0002t0001g0156 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1347-9316A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929320 | |||||||
| chr9:37929327 | A | G | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-9323T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929327 | |||||||
| chr9:37929425 | G | A | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-9421C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929425 | |||||||
| chr9:37929447 | G | A | 31 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(28): Show |
31 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1347-9443C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929447 | |||||||
| chr9:37929515 | G | A | 1 | a0001c0008t0022g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1347-9511C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929515 | |||||||
| chr9:37929621 | G | C | 1 | a0001c0002t0001g0152 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1347-9617C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929621 | |||||||
| chr9:37929686 | C | T | 31 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(28): Show |
31 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1347-9682G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929686 | |||||||
| chr9:37929812 | G | C | 74 | a0001c0001t0048g0235 a0001c0001t0063g0234 a0001c0003t0008g0065 others(71): Show |
74 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1347-9808C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929812 | |||||||
| chr9:37929841 | T | C | 163 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0001t0048g0235 others(160): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1347-9837A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929841 | |||||||
| chr9:37929959 | G | A | 14 | a0001c0005t0006g0051 a0001c0005t0011g0046 a0001c0005t0011g0054 others(11): Show |
14 | HG02630.hp2 HG03209.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.1347-9955C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37929959 | |||||||
| chr9:37930015 | T | C | 1 | a0001c0002t0001g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1347-10011A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930015 | |||||||
| chr9:37930121 | G | A | 2 | a0001c0002t0004g0100 a0001c0002t0004g0170 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1347-10117C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930121 | |||||||
| chr9:37930156 | G | A | 1 | a0001c0002t0040g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1347-10152C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930156 | |||||||
| chr9:37930189 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1347-10185A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930189 | |||||||
| chr9:37930296 | G | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1347-10292C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930296 | |||||||
| chr9:37930311 | C | T | 1 | a0001c0003t0001g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1347-10307G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930311 | |||||||
| chr9:37930339 | A | G | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1347-10335T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930339 | |||||||
| chr9:37930489 | T | G | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-10485A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930489 | |||||||
| chr9:37930512 | T | G | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-10508A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930512 | |||||||
| chr9:37930837 | G | A | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-10833C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930837 | |||||||
| chr9:37930846 | A | G | 4 | a0001c0005t0007g0040 a0001c0005t0007g0041 a0001c0005t0007g0042 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347-10842T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930846 | |||||||
| chr9:37930930 | A | G | 35 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(32): Show |
35 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1347-10926T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37930930 | |||||||
| chr9:37931356 | T | G | 1 | a0001c0005t0024g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1347-11352A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37931356 | |||||||
| chr9:37931536 | T | A | 1 | a0001c0002t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1347-11532A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37931536 | |||||||
| chr9:37931888 | C | T | 31 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(28): Show |
31 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1347-11884G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37931888 | |||||||
| chr9:37931920 | T | C | 1 | a0001c0003t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1347-11916A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37931920 | |||||||
| chr9:37931942 | C | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1347-11938G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37931942 | |||||||
| chr9:37931955 | AG | A | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-11952delC | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37931955 | |||||||
| chr9:37931985 | T | TA | 73 | a0001c0001t0063g0234 a0001c0003t0008g0065 a0001c0003t0008g0066 others(70): Show |
73 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1347-11982dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37931985 | |||||||
| chr9:37932019 | C | A | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-12015G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932019 | |||||||
| chr9:37932128 | A | G | 92 | a0001c0001t0001g0211 a0001c0001t0014g0217 a0001c0001t0023g0215 others(89): Show |
94 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1347-12124T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932128 | |||||||
| chr9:37932136 | G | C | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1347-12132C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932136 | |||||||
| chr9:37932230 | G | A | 1 | a0011c0027t0033g0195 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1347-12226C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932230 | |||||||
| chr9:37932273 | CA | C | 278 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(275): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1347-12270delT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932273 | |||||||
| chr9:37932273 | CAA | C | 13 | a0001c0001t0001g0228 a0001c0001t0002g0271 a0001c0001t0002g0277 others(10): Show |
13 | HG01099.hp1 HG01256.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1347-12271_1347-12 others(8): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932273 | |||||||
| chr9:37932317 | T | C | 244 | a0001c0001t0001g0211 a0001c0001t0001g0254 a0001c0001t0001g0265 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1347-12313A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932317 | |||||||
| chr9:37932330 | A | G | 7 | a0001c0002t0001g0087 a0001c0002t0001g0092 a0001c0002t0001g0097 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1347-12326T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932330 | |||||||
| chr9:37932403 | A | T | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347-12399T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932403 | |||||||
| chr9:37932562 | C | CA | 45 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0307 others(42): Show |
45 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1347-12559dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932562 | |||||||
| chr9:37932562 | C | CAA | 67 | a0001c0001t0001g0254 a0001c0001t0001g0291 a0001c0001t0001g0314 others(64): Show |
69 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1347-12560_1347-12 others(8): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932562 | |||||||
| chr9:37932562 | C | CAAA | 8 | a0001c0001t0001g0265 a0001c0001t0002g0005 a0001c0001t0002g0257 others(5): Show |
9 | HG00558.hp1 HG02683.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.1347-12561_1347-12 others(9): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932562 | |||||||
| chr9:37932562 | CAA | C | 13 | a0001c0005t0006g0051 a0001c0005t0011g0046 a0001c0005t0011g0054 others(10): Show |
13 | HG02630.hp2 HG03209.hp1 HG04184.hp2 others(10): Show |
intron_variant | MODIFIER | c.1347-12560_1347-12 others(8): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932562 | |||||||
| chr9:37932626 | G | A | 1 | a0001c0001t0063g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1347-12622C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932626 | |||||||
| chr9:37932645 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1347-12641A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932645 | |||||||
| chr9:37932787 | A | C | 2 | a0001c0002t0002g0079 a0001c0002t0002g0096 |
2 | HG01109.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1347-12783T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932787 | |||||||
| chr9:37932800 | T | G | 74 | a0001c0001t0048g0235 a0001c0001t0063g0234 a0001c0003t0008g0065 others(71): Show |
74 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1347-12796A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932800 | |||||||
| chr9:37932842 | C | T | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1347-12838G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932842 | |||||||
| chr9:37932879 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0230 |
2 | NA18994.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1347-12875G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932879 | |||||||
| chr9:37932884 | G | A | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1347-12880C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37932884 | |||||||
| chr9:37933021 | C | A | 1 | a0001c0005t0001g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1347-13017G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37933021 | |||||||
| chr9:37933054 | T | C | 14 | a0001c0005t0006g0051 a0001c0005t0011g0046 a0001c0005t0011g0054 others(11): Show |
14 | HG02630.hp2 HG03209.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.1347-13050A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37933054 | |||||||
| chr9:37933656 | A | G | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1347-13652T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37933656 | |||||||
| chr9:37933699 | C | T | 1 | a0001c0008t0022g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1347-13695G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37933699 | |||||||
| chr9:37933822 | A | G | 2 | a0001c0003t0030g0014 a0001c0004t0068g0181 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1347-13818T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37933822 | |||||||
| chr9:37933992 | G | A | 1 | a0001c0002t0004g0132 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1347-13988C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37933992 | |||||||
| chr9:37934143 | T | C | 131 | a0001c0001t0001g0211 a0001c0001t0001g0229 a0001c0001t0001g0291 others(128): Show |
132 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1347-14139A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934143 | |||||||
| chr9:37934185 | C | T | 1 | a0001c0003t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1347-14181G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934185 | |||||||
| chr9:37934492 | C | T | 2 | a0001c0002t0021g0086 a0001c0002t0022g0098 |
2 | HG01168.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1346+14143G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934492 | |||||||
| chr9:37934571 | G | T | 1 | a0001c0003t0001g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1346+14064C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934571 | |||||||
| chr9:37934576 | C | T | 1 | a0001c0011t0005g0197 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1346+14059G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934576 | |||||||
| chr9:37934586 | C | T | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1346+14049G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934586 | |||||||
| chr9:37934593 | G | A | 3 | a0001c0001t0002g0298 a0001c0001t0002g0303 a0001c0001t0002g0304 |
3 | NA18978.hp2 NA19060.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1346+14042C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934593 | |||||||
| chr9:37934667 | A | G | 17 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0005t0005g0044 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1346+13968T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934667 | |||||||
| chr9:37934673 | C | G | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+13962G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934673 | |||||||
| chr9:37934705 | T | A | 28 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(25): Show |
28 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.1346+13930A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934705 | |||||||
| chr9:37934783 | T | C | 48 | a0001c0001t0001g0211 a0001c0001t0014g0217 a0001c0001t0023g0215 others(45): Show |
48 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1346+13852A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934783 | |||||||
| chr9:37934901 | T | C | 80 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0291 others(77): Show |
83 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1346+13734A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934901 | |||||||
| chr9:37934927 | A | C | 5 | a0001c0008t0002g0026 a0001c0008t0002g0027 a0001c0008t0002g0029 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346+13708T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934927 | |||||||
| chr9:37934967 | T | C | 1 | a0001c0002t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1346+13668A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37934967 | |||||||
| chr9:37935322 | C | T | 65 | a0001c0001t0063g0234 a0001c0003t0030g0014 a0001c0004t0001g0115 others(62): Show |
65 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1346+13313G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935322 | |||||||
| chr9:37935386 | T | C | 1 | a0001c0001t0002g0269 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1346+13249A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935386 | |||||||
| chr9:37935536 | G | A | 4 | a0001c0002t0001g0064 a0001c0002t0001g0158 a0001c0002t0001g0164 others(1): Show |
4 | HG02602.hp2 NA18970.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+13099C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935536 | |||||||
| chr9:37935601 | G | C | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1346+13034C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935601 | |||||||
| chr9:37935649 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1346+12986C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935649 | |||||||
| chr9:37935721 | T | C | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+12914A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935721 | |||||||
| chr9:37935753 | G | A | 2 | a0001c0015t0018g0192 a0001c0015t0018g0193 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1346+12882C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935753 | |||||||
| chr9:37935770 | C | T | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1346+12865G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935770 | |||||||
| chr9:37935784 | T | C | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+12851A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935784 | |||||||
| chr9:37935817 | A | G | 3 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0064g0238 |
3 | HG02698.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1346+12818T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935817 | |||||||
| chr9:37935818 | T | A | 1 | a0001c0007t0001g0253 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1346+12817A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935818 | |||||||
| chr9:37935869 | C | T | 2 | a0001c0003t0002g0145 a0001c0003t0002g0167 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1346+12766G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935869 | |||||||
| chr9:37935877 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1346+12758G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935877 | |||||||
| chr9:37935925 | GA | G | 122 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0001t0048g0235 others(119): Show |
122 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1346+12709delT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935925 | |||||||
| chr9:37935951 | G | A | 79 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0291 others(76): Show |
82 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1346+12684C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37935951 | |||||||
| chr9:37936040 | T | TA | 24 | a0001c0001t0001g0209 a0001c0001t0002g0269 a0001c0001t0002g0301 others(21): Show |
24 | HG00099.hp2 HG00438.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1346+12594dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936040 | |||||||
| chr9:37936040 | T | TAA | 46 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0105 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1346+12593_1346+12 others(8): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936040 | |||||||
| chr9:37936041 | A | T | 1 | a0006c0025t0042g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1346+12594T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936041 | |||||||
| chr9:37936072 | C | T | 1 | a0001c0004t0003g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1346+12563G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936072 | |||||||
| chr9:37936164 | C | T | 1 | a0001c0001t0002g0302 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1346+12471G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936164 | |||||||
| chr9:37936184 | C | T | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+12451G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936184 | |||||||
| chr9:37936265 | G | A | 1 | a0001c0017t0025g0306 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1346+12370C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936265 | |||||||
| chr9:37936284 | C | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1346+12351G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936284 | |||||||
| chr9:37936467 | C | A | 241 | a0001c0001t0001g0211 a0001c0001t0001g0254 a0001c0001t0001g0265 others(238): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1346+12168G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936467 | |||||||
| chr9:37936479 | A | T | 1 | a0001c0001t0002g0302 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1346+12156T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936479 | |||||||
| chr9:37936480 | C | T | 5 | a0001c0001t0002g0302 a0001c0017t0025g0305 a0001c0017t0025g0306 others(2): Show |
5 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346+12155G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936480 | |||||||
| chr9:37936485 | C | T | 1 | a0001c0001t0002g0302 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1346+12150G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936485 | |||||||
| chr9:37936506 | C | T | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+12129G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936506 | |||||||
| chr9:37936703 | T | C | 2 | a0001c0010t0012g0010 a0001c0010t0012g0012 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1346+11932A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936703 | |||||||
| chr9:37936765 | A | G | 2 | a0001c0001t0048g0235 a0001c0001t0063g0234 |
2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1346+11870T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936765 | |||||||
| chr9:37936905 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1346+11730C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936905 | |||||||
| chr9:37936906 | G | T | 1 | a0001c0001t0013g0225 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1346+11729C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37936906 | |||||||
| chr9:37937083 | C | T | 2 | a0001c0003t0030g0014 a0001c0004t0068g0181 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1346+11552G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937083 | |||||||
| chr9:37937109 | A | C | 5 | a0001c0004t0049g0077 a0001c0017t0025g0305 a0001c0017t0025g0306 others(2): Show |
5 | HG02486.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346+11526T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937109 | |||||||
| chr9:37937129 | T | C | 1 | a0001c0002t0001g0156 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1346+11506A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937129 | |||||||
| chr9:37937268 | G | A | 1 | a0001c0001t0043g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1346+11367C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937268 | |||||||
| chr9:37937282 | C | T | 5 | a0001c0008t0002g0026 a0001c0008t0002g0027 a0001c0008t0002g0029 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346+11353G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937282 | |||||||
| chr9:37937283 | G | A | 2 | a0001c0001t0071g0243 a0001c0003t0029g0015 |
2 | HG03195.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1346+11352C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937283 | |||||||
| chr9:37937311 | GGCCATAA | G | 3 | a0001c0001t0063g0234 a0004c0018t0017g0248 a0004c0018t0017g0249 |
3 | HG02055.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1346+11317_1346+11 others(13): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937311 | |||||||
| chr9:37937466 | G | GA | 13 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(10): Show |
13 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1346+11168dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937466 | |||||||
| chr9:37937467 | A | G | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1346+11168T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937467 | |||||||
| chr9:37937619 | C | T | 41 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0080 others(38): Show |
43 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1346+11016G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937619 | |||||||
| chr9:37937642 | T | C | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+10993A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937642 | |||||||
| chr9:37937936 | T | C | 1 | a0001c0001t0060g0297 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1346+10699A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937936 | |||||||
| chr9:37937937 | C | T | 1 | a0001c0001t0060g0297 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1346+10698G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937937 | |||||||
| chr9:37937946 | C | A | 74 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0291 others(71): Show |
77 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1346+10689G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37937946 | |||||||
| chr9:37938091 | C | G | 1 | a0001c0002t0059g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1346+10544G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938091 | |||||||
| chr9:37938133 | C | G | 1 | a0001c0001t0063g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1346+10502G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938133 | |||||||
| chr9:37938151 | T | C | 1 | a0001c0001t0002g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1346+10484A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938151 | |||||||
| chr9:37938227 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1346+10408G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938227 | |||||||
| chr9:37938390 | C | G | 163 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0001t0048g0235 others(160): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1346+10245G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938390 | |||||||
| chr9:37938549 | G | A | 1 | a0001c0001t0053g0247 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1346+10086C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938549 | |||||||
| chr9:37938555 | C | T | 1 | a0001c0002t0061g0061 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1346+10080G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938555 | |||||||
| chr9:37938556 | G | A | 16 | a0001c0001t0063g0234 a0001c0003t0030g0014 a0001c0004t0068g0181 others(13): Show |
16 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1346+10079C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938556 | |||||||
| chr9:37938672 | C | G | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+9963G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938672 | |||||||
| chr9:37938849 | G | C | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+9786C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938849 | |||||||
| chr9:37938976 | T | A | 1 | a0001c0002t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1346+9659A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37938976 | |||||||
| chr9:37939563 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1346+9072C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37939563 | |||||||
| chr9:37939596 | C | A | 1 | a0001c0004t0003g0107 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1346+9039G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37939596 | |||||||
| chr9:37939659 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1346+8976A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37939659 | |||||||
| chr9:37939676 | G | T | 161 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0001t0048g0235 others(158): Show |
163 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1346+8959C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37939676 | |||||||
| chr9:37939754 | A | G | 1 | a0001c0001t0002g0299 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1346+8881T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37939754 | |||||||
| chr9:37939771 | A | G | 1 | a0001c0001t0043g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1346+8864T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37939771 | |||||||
| chr9:37939782 | C | A | 1 | a0001c0002t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1346+8853G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37939782 | |||||||
| chr9:37939955 | G | A | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1346+8680C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37939955 | |||||||
| chr9:37940053 | G | A | 1 | a0003c0019t0001g0321 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1346+8582C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940053 | |||||||
| chr9:37940108 | A | T | 1 | a0001c0002t0001g0156 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1346+8527T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940108 | |||||||
| chr9:37940148 | G | C | 1 | a0001c0001t0002g0302 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1346+8487C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940148 | |||||||
| chr9:37940239 | G | A | 1 | a0001c0002t0004g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1346+8396C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940239 | |||||||
| chr9:37940350 | T | C | 1 | a0001c0003t0002g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1346+8285A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940350 | |||||||
| chr9:37940384 | G | A | 1 | a0001c0005t0024g0045 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1346+8251C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940384 | |||||||
| chr9:37940442 | T | C | 252 | a0001c0001t0001g0211 a0001c0001t0001g0254 a0001c0001t0001g0265 others(249): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.1346+8193A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940442 | |||||||
| chr9:37940648 | CTT | C | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+7985_1346+798 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940648 | |||||||
| chr9:37940771 | A | G | 1 | a0001c0003t0001g0155 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1346+7864T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940771 | |||||||
| chr9:37940792 | C | T | 1 | a0001c0005t0069g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1346+7843G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37940792 | |||||||
| chr9:37941306 | A | G | 165 | a0001c0001t0001g0211 a0001c0001t0014g0217 a0001c0001t0023g0215 others(162): Show |
167 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1346+7329T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941306 | |||||||
| chr9:37941314 | C | T | 25 | a0001c0004t0028g0018 a0001c0004t0049g0077 a0001c0005t0005g0044 others(22): Show |
25 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(22): Show |
intron_variant | MODIFIER | c.1346+7321G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941314 | |||||||
| chr9:37941318 | G | T | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1346+7317C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941318 | |||||||
| chr9:37941487 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1346+7148G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941487 | |||||||
| chr9:37941567 | A | G | 1 | a0001c0003t0023g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1346+7068T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941567 | |||||||
| chr9:37941644 | G | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1346+6991C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941644 | |||||||
| chr9:37941696 | C | T | 1 | a0001c0006t0010g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1346+6939G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941696 | |||||||
| chr9:37941748 | C | T | 46 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0002t0001g0072 others(43): Show |
46 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1346+6887G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941748 | |||||||
| chr9:37941799 | T | C | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1346+6836A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941799 | |||||||
| chr9:37941855 | C | CA | 24 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1346+6779dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37941855 | |||||||
| chr9:37942001 | A | G | 2 | a0001c0003t0002g0179 a0001c0003t0002g0180 |
2 | HG02080.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1346+6634T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942001 | |||||||
| chr9:37942008 | A | G | 24 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1346+6627T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942008 | |||||||
| chr9:37942114 | C | T | 1 | a0001c0003t0001g0155 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1346+6521G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942114 | |||||||
| chr9:37942155 | C | A | 159 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0001t0048g0235 others(156): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1346+6480G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942155 | |||||||
| chr9:37942172 | G | A | 1 | a0001c0003t0001g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1346+6463C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942172 | |||||||
| chr9:37942234 | T | C | 1 | a0001c0001t0002g0300 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1346+6401A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942234 | |||||||
| chr9:37942513 | G | C | 1 | a0001c0003t0029g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346+6122C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942513 | |||||||
| chr9:37942677 | T | A | 1 | a0001c0002t0040g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1346+5958A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942677 | |||||||
| chr9:37942712 | G | C | 1 | a0001c0002t0001g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1346+5923C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942712 | |||||||
| chr9:37942903 | G | A | 20 | a0001c0005t0005g0044 a0001c0005t0005g0047 a0001c0005t0005g0048 others(17): Show |
20 | HG02630.hp2 HG03209.hp1 HG04184.hp2 others(17): Show |
intron_variant | MODIFIER | c.1346+5732C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942903 | |||||||
| chr9:37942976 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1346+5659G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37942976 | |||||||
| chr9:37943004 | C | T | 1 | a0001c0002t0058g0166 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1346+5631G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943004 | |||||||
| chr9:37943068 | C | A | 1 | a0001c0002t0019g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1346+5567G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943068 | |||||||
| chr9:37943095 | T | C | 70 | a0001c0001t0048g0235 a0001c0001t0063g0234 a0001c0003t0030g0014 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1346+5540A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943095 | |||||||
| chr9:37943167 | C | T | 70 | a0001c0001t0048g0235 a0001c0001t0063g0234 a0001c0003t0030g0014 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1346+5468G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943167 | |||||||
| chr9:37943408 | C | T | 5 | a0001c0010t0012g0013 a0001c0016t0026g0322 a0001c0016t0026g0323 others(2): Show |
5 | HG02055.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346+5227G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943408 | |||||||
| chr9:37943510 | T | C | 1 | a0001c0002t0001g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1346+5125A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943510 | |||||||
| chr9:37943537 | G | A | 3 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0064g0238 |
3 | HG02698.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1346+5098C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943537 | |||||||
| chr9:37943563 | C | T | 11 | a0001c0003t0030g0014 a0001c0004t0068g0181 a0001c0006t0010g0019 others(8): Show |
11 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1346+5072G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943563 | |||||||
| chr9:37943568 | G | A | 2 | a0001c0002t0001g0072 a0001c0002t0001g0075 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1346+5067C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943568 | |||||||
| chr9:37943574 | T | C | 66 | a0001c0001t0048g0235 a0001c0001t0063g0234 a0001c0003t0030g0014 others(63): Show |
66 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1346+5061A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943574 | |||||||
| chr9:37943637 | C | T | 1 | a0001c0005t0006g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1346+4998G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943637 | |||||||
| chr9:37943982 | T | C | 20 | a0001c0005t0005g0044 a0001c0005t0005g0047 a0001c0005t0005g0048 others(17): Show |
20 | HG02630.hp2 HG03209.hp1 HG04184.hp2 others(17): Show |
intron_variant | MODIFIER | c.1346+4653A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37943982 | |||||||
| chr9:37944161 | C | T | 1 | a0001c0013t0008g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1346+4474G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37944161 | |||||||
| chr9:37944336 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1346+4299C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37944336 | |||||||
| chr9:37944430 | G | A | 66 | a0001c0001t0002g0295 a0001c0001t0051g0240 a0001c0002t0001g0174 others(63): Show |
66 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1346+4205C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37944430 | |||||||
| chr9:37944492 | G | A | 84 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0023g0215 others(81): Show |
86 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.1346+4143C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37944492 | |||||||
| chr9:37944591 | A | G | 6 | a0001c0001t0014g0217 a0001c0004t0049g0077 a0001c0005t0070g0071 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346+4044T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37944591 | |||||||
| chr9:37944710 | C | T | 4 | a0001c0001t0001g0232 a0001c0003t0001g0125 a0003c0019t0001g0320 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+3925G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37944710 | |||||||
| chr9:37944717 | C | T | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1346+3918G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37944717 | |||||||
| chr9:37944908 | AC | A | 76 | a0001c0002t0040g0176 a0001c0004t0001g0115 a0001c0004t0003g0058 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1346+3726delG | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37944908 | |||||||
| chr9:37945040 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1346+3595A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37945040 | |||||||
| chr9:37945417 | G | A | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346+3218C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37945417 | |||||||
| chr9:37945509 | A | G | 71 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(68): Show |
71 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1346+3126T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37945509 | |||||||
| chr9:37945554 | C | T | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1346+3081G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37945554 | |||||||
| chr9:37945964 | G | A | 3 | a0001c0011t0056g0199 a0001c0016t0026g0322 a0001c0016t0026g0323 |
3 | HG02451.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1346+2671C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37945964 | |||||||
| chr9:37946105 | C | T | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+2530G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946105 | |||||||
| chr9:37946133 | C | A | 1 | a0001c0001t0002g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1346+2502G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946133 | |||||||
| chr9:37946176 | G | A | 28 | a0001c0004t0007g0039 a0001c0005t0001g0069 a0001c0005t0001g0076 others(25): Show |
28 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1346+2459C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946176 | |||||||
| chr9:37946562 | C | T | 1 | a0001c0011t0056g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1346+2073G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946562 | |||||||
| chr9:37946632 | A | G | 73 | a0001c0001t0048g0235 a0001c0001t0063g0234 a0001c0004t0001g0115 others(70): Show |
73 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1346+2003T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946632 | |||||||
| chr9:37946655 | C | G | 1 | a0001c0002t0019g0157 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1346+1980G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946655 | |||||||
| chr9:37946689 | C | T | 1 | a0001c0004t0003g0114 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1346+1946G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946689 | |||||||
| chr9:37946693 | T | C | 3 | a0001c0011t0056g0199 a0001c0016t0026g0322 a0001c0016t0026g0323 |
3 | HG02451.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1346+1942A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946693 | |||||||
| chr9:37946720 | C | A | 2 | a0001c0002t0001g0072 a0001c0002t0001g0075 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1346+1915G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946720 | |||||||
| chr9:37946906 | CACTTGAG others(6): Show |
C | 1 | a0001c0003t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1346+1716_1346+172 others(17): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946906 | |||||||
| chr9:37946920 | C | T | 1 | a0001c0007t0001g0227 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1346+1715G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946920 | |||||||
| chr9:37946964 | C | T | 1 | a0001c0001t0051g0240 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1346+1671G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37946964 | |||||||
| chr9:37947046 | G | A | 2 | a0001c0003t0002g0143 a0001c0003t0002g0144 |
2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1346+1589C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947046 | |||||||
| chr9:37947111 | G | A | 1 | a0002c0009t0006g0032 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1346+1524C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947111 | |||||||
| chr9:37947128 | C | T | 1 | a0001c0006t0010g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1346+1507G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947128 | |||||||
| chr9:37947390 | G | A | 1 | a0001c0001t0015g0255 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1346+1245C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947390 | |||||||
| chr9:37947423 | C | G | 70 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1346+1212G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947423 | |||||||
| chr9:37947604 | T | C | 233 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(230): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1346+1031A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947604 | |||||||
| chr9:37947649 | T | C | 2 | a0001c0002t0001g0161 a0001c0002t0001g0162 |
2 | HG01496.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1346+986A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947649 | |||||||
| chr9:37947700 | T | C | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346+935A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947700 | |||||||
| chr9:37947809 | G | C | 2 | a0001c0004t0003g0112 a0001c0011t0003g0198 |
2 | HG03704.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1346+826C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947809 | |||||||
| chr9:37947854 | G | A | 3 | a0001c0011t0056g0199 a0001c0016t0026g0322 a0001c0016t0026g0323 |
3 | HG02451.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1346+781C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947854 | |||||||
| chr9:37947855 | C | G | 3 | a0001c0011t0056g0199 a0001c0016t0026g0322 a0001c0016t0026g0323 |
3 | HG02451.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1346+780G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37947855 | |||||||
| chr9:37948006 | A | G | 3 | a0001c0011t0056g0199 a0001c0016t0026g0322 a0001c0016t0026g0323 |
3 | HG02451.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1346+629T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948006 | |||||||
| chr9:37948060 | A | G | 75 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(72): Show |
75 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1346+575T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948060 | |||||||
| chr9:37948066 | C | T | 24 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1346+569G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948066 | |||||||
| chr9:37948078 | T | C | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+557A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948078 | |||||||
| chr9:37948228 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1346+407C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948228 | |||||||
| chr9:37948234 | C | A | 1 | a0001c0001t0045g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1346+401G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948234 | |||||||
| chr9:37948241 | A | C | 70 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1346+394T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948241 | |||||||
| chr9:37948325 | A | C | 70 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1346+310T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948325 | |||||||
| chr9:37948390 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1346+245A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948390 | |||||||
| chr9:37948435 | G | A | 70 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1346+200C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948435 | |||||||
| chr9:37948439 | G | C | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346+196C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948439 | |||||||
| chr9:37948502 | C | T | 3 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0002g0281 |
3 | HG02257.hp1 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1346+133G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948502 | |||||||
| chr9:37948572 | G | A | 1 | a0001c0003t0002g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1346+63C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 5/5 | chr9 | 37948572 | |||||||
| chr9:37948868 | A | C | 4 | a0001c0004t0028g0018 a0001c0004t0049g0077 a0001c0015t0018g0192 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227-114T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37948868 | |||||||
| chr9:37949265 | C | T | 72 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0291 others(69): Show |
75 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1227-511G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949265 | |||||||
| chr9:37949325 | G | A | 1 | a0001c0017t0025g0306 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1227-571C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949325 | |||||||
| chr9:37949370 | A | G | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0231 others(2): Show |
5 | HG02015.hp2 HG02155.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227-616T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949370 | |||||||
| chr9:37949392 | C | CA | 19 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(16): Show |
19 | HG00544.hp1 HG00673.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1227-639dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949392 | |||||||
| chr9:37949392 | CA | C | 73 | a0001c0001t0001g0250 a0001c0002t0001g0084 a0001c0002t0001g0097 others(70): Show |
73 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1227-639delT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949392 | |||||||
| chr9:37949412 | A | C | 70 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1227-658T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949412 | |||||||
| chr9:37949457 | G | A | 1 | a0001c0002t0040g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1227-703C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949457 | |||||||
| chr9:37949470 | G | A | 27 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0005g0044 others(24): Show |
27 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1227-716C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949470 | |||||||
| chr9:37949545 | C | A | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227-791G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949545 | |||||||
| chr9:37949561 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1227-807C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949561 | |||||||
| chr9:37949625 | G | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1227-871C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949625 | |||||||
| chr9:37949641 | G | A | 70 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1227-887C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949641 | |||||||
| chr9:37949642 | C | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1227-888G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949642 | |||||||
| chr9:37949681 | T | C | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1227-927A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949681 | |||||||
| chr9:37949702 | G | A | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1227-948C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949702 | |||||||
| chr9:37949753 | T | C | 1 | a0001c0003t0029g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1227-999A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949753 | |||||||
| chr9:37949765 | C | T | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1227-1011G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949765 | |||||||
| chr9:37949815 | T | C | 1 | a0001c0001t0002g0288 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1227-1061A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949815 | |||||||
| chr9:37949934 | A | G | 1 | a0001c0015t0018g0192 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1227-1180T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949934 | |||||||
| chr9:37949962 | G | A | 27 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0005g0044 others(24): Show |
27 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1227-1208C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949962 | |||||||
| chr9:37949972 | C | T | 75 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(72): Show |
75 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1227-1218G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37949972 | |||||||
| chr9:37950000 | G | A | 1 | a0001c0002t0001g0148 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1227-1246C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37950000 | |||||||
| chr9:37950233 | A | G | 75 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(72): Show |
75 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1227-1479T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37950233 | |||||||
| chr9:37950263 | C | CT | 7 | a0001c0002t0001g0147 a0001c0002t0001g0152 a0001c0007t0001g0244 others(4): Show |
7 | HG01192.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227-1510dupA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37950263 | |||||||
| chr9:37950512 | T | C | 1 | a0001c0002t0001g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1227-1758A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37950512 | |||||||
| chr9:37950546 | C | A | 70 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1227-1792G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37950546 | |||||||
| chr9:37950607 | T | C | 75 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(72): Show |
75 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1227-1853A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37950607 | |||||||
| chr9:37950829 | G | C | 1 | a0001c0001t0002g0296 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1227-2075C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37950829 | |||||||
| chr9:37950939 | C | T | 54 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(51): Show |
54 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1227-2185G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37950939 | |||||||
| chr9:37951032 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1227-2278G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951032 | |||||||
| chr9:37951045 | T | C | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1227-2291A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951045 | |||||||
| chr9:37951147 | G | A | 1 | a0001c0004t0003g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1227-2393C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951147 | |||||||
| chr9:37951179 | T | C | 75 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(72): Show |
75 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1227-2425A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951179 | |||||||
| chr9:37951190 | T | C | 3 | a0001c0004t0049g0077 a0001c0015t0018g0192 a0001c0015t0018g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1227-2436A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951190 | |||||||
| chr9:37951357 | A | C | 28 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(25): Show |
28 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227-2603T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951357 | |||||||
| chr9:37951390 | G | A | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG01069.hp2 HG01928.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.1227-2636C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951390 | |||||||
| chr9:37951487 | T | A | 27 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0005g0044 others(24): Show |
27 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1227-2733A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951487 | |||||||
| chr9:37951582 | G | A | 1 | a0001c0007t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1227-2828C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951582 | |||||||
| chr9:37951862 | A | G | 27 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(24): Show |
27 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.1227-3108T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37951862 | |||||||
| chr9:37952051 | G | A | 16 | a0001c0004t0007g0039 a0001c0004t0068g0181 a0001c0006t0010g0019 others(13): Show |
16 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1227-3297C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952051 | |||||||
| chr9:37952147 | G | A | 24 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1227-3393C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952147 | |||||||
| chr9:37952152 | CAG | C | 16 | a0001c0004t0007g0039 a0001c0004t0068g0181 a0001c0006t0010g0019 others(13): Show |
16 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1227-3400_1227-339 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952152 | |||||||
| chr9:37952172 | T | C | 2 | a0001c0003t0001g0081 a0001c0003t0001g0116 |
2 | NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1227-3418A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952172 | |||||||
| chr9:37952195 | G | A | 27 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0005g0044 others(24): Show |
27 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1227-3441C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952195 | |||||||
| chr9:37952233 | C | T | 241 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(238): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1227-3479G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952233 | |||||||
| chr9:37952339 | ACATCTCT others(13): Show |
A | 1 | a0001c0001t0002g0292 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1226+3524_1226+354 others(24): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952339 | |||||||
| chr9:37952389 | G | A | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1226+3494C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952389 | |||||||
| chr9:37952424 | ATGACCCA others(7): Show |
A | 1 | a0001c0001t0002g0260 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1226+3445_1226+345 others(18): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952424 | |||||||
| chr9:37952551 | A | T | 27 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0005g0044 others(24): Show |
27 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1226+3332T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952551 | |||||||
| chr9:37952564 | T | C | 1 | a0001c0003t0001g0185 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1226+3319A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952564 | |||||||
| chr9:37952621 | G | A | 27 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0005g0044 others(24): Show |
27 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1226+3262C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952621 | |||||||
| chr9:37952634 | A | G | 241 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(238): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1226+3249T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952634 | |||||||
| chr9:37952731 | C | A | 2 | a0001c0001t0001g0218 a0001c0001t0045g0236 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1226+3152G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952731 | |||||||
| chr9:37952756 | GAACC | G | 27 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(24): Show |
27 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.1226+3123_1226+312 others(8): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952756 | |||||||
| chr9:37952781 | C | A | 1 | a0001c0002t0021g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1226+3102G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952781 | |||||||
| chr9:37952811 | G | A | 1 | a0001c0004t0003g0107 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1226+3072C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952811 | |||||||
| chr9:37952915 | G | A | 1 | a0001c0003t0002g0145 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1226+2968C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37952915 | |||||||
| chr9:37953133 | G | A | 5 | a0001c0001t0001g0232 a0001c0001t0063g0234 a0001c0003t0001g0125 others(2): Show |
5 | HG00140.hp1 HG01074.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1226+2750C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37953133 | |||||||
| chr9:37953174 | C | G | 6 | a0001c0005t0005g0044 a0001c0005t0005g0047 a0001c0005t0005g0048 others(3): Show |
6 | NA18946.hp2 NA18955.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1226+2709G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37953174 | |||||||
| chr9:37953240 | G | A | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1226+2643C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37953240 | |||||||
| chr9:37953314 | T | C | 1 | a0001c0001t0044g0276 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1226+2569A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37953314 | |||||||
| chr9:37953340 | G | A | 1 | a0001c0002t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1226+2543C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37953340 | |||||||
| chr9:37953394 | G | A | 27 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0005g0044 others(24): Show |
27 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1226+2489C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37953394 | |||||||
| chr9:37953927 | A | G | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1226+1956T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37953927 | |||||||
| chr9:37953941 | C | G | 1 | a0001c0005t0047g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1226+1942G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37953941 | |||||||
| chr9:37954291 | C | T | 2 | a0001c0015t0018g0192 a0001c0015t0018g0193 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1226+1592G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37954291 | |||||||
| chr9:37954376 | C | A | 1 | a0001c0002t0004g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1226+1507G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37954376 | |||||||
| chr9:37954427 | T | G | 27 | a0001c0004t0001g0115 a0001c0004t0003g0058 a0001c0004t0003g0082 others(24): Show |
27 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.1226+1456A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37954427 | |||||||
| chr9:37954525 | G | T | 1 | a0001c0003t0001g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1226+1358C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37954525 | |||||||
| chr9:37954685 | G | A | 1 | a0001c0005t0011g0046 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1226+1198C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37954685 | |||||||
| chr9:37954897 | G | C | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1226+986C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37954897 | |||||||
| chr9:37954916 | G | A | 204 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(201): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1226+967C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37954916 | |||||||
| chr9:37955268 | C | T | 23 | a0001c0003t0002g0140 a0001c0004t0003g0058 a0001c0004t0003g0082 others(20): Show |
23 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.1226+615G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37955268 | |||||||
| chr9:37955436 | G | A | 25 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1226+447C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37955436 | |||||||
| chr9:37955503 | G | C | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1226+380C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37955503 | |||||||
| chr9:37955509 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0284 |
2 | NA18957.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1226+374C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37955509 | |||||||
| chr9:37955652 | AT | A | 211 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(208): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1226+230delA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 4/5 | chr9 | 37955652 | |||||||
| chr9:37956129 | C | CG | 44 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0080 others(41): Show |
46 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1055-76dupC | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37956129 | |||||||
| chr9:37956274 | G | A | 212 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(209): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1055-220C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37956274 | |||||||
| chr9:37956354 | C | G | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-300G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37956354 | |||||||
| chr9:37956355 | G | T | 154 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(151): Show |
157 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1055-301C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37956355 | |||||||
| chr9:37956376 | A | G | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-322T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37956376 | |||||||
| chr9:37956727 | C | T | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-673G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37956727 | |||||||
| chr9:37956789 | T | C | 1 | a0001c0001t0071g0243 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1055-735A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37956789 | |||||||
| chr9:37956875 | C | T | 1 | a0001c0001t0064g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1055-821G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37956875 | |||||||
| chr9:37957232 | A | G | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-1178T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37957232 | |||||||
| chr9:37957350 | C | CG | 7 | a0001c0001t0001g0228 a0001c0001t0001g0237 a0001c0002t0001g0150 others(4): Show |
7 | HG01175.hp1 HG02109.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1055-1297dupC | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37957350 | |||||||
| chr9:37957467 | C | T | 6 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(3): Show |
6 | HG02257.hp2 HG03130.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1055-1413G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37957467 | |||||||
| chr9:37957601 | A | G | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-1547T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37957601 | |||||||
| chr9:37957931 | A | G | 10 | a0001c0001t0001g0291 a0001c0001t0002g0288 a0001c0001t0002g0290 others(7): Show |
10 | HG00673.hp2 HG02148.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.1055-1877T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37957931 | |||||||
| chr9:37958040 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1055-1986C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958040 | |||||||
| chr9:37958220 | A | AGGCAGTG others(10): Show |
9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1055-2183_1055-216 others(21): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958220 | |||||||
| chr9:37958311 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1055-2257C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958311 | |||||||
| chr9:37958337 | T | G | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1055-2283A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958337 | |||||||
| chr9:37958361 | C | T | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1055-2307G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958361 | |||||||
| chr9:37958425 | G | A | 1 | a0001c0004t0003g0171 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1055-2371C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958425 | |||||||
| chr9:37958474 | T | C | 1 | a0001c0002t0004g0132 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1055-2420A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958474 | |||||||
| chr9:37958732 | T | C | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-2678A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958732 | |||||||
| chr9:37958868 | GAGA | G | 3 | a0001c0001t0002g0259 a0001c0001t0002g0313 a0001c0001t0002g0316 |
3 | HG01516.hp2 HG01978.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1055-2817_1055-281 others(7): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958868 | |||||||
| chr9:37958937 | C | A | 1 | a0001c0008t0002g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1055-2883G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958937 | |||||||
| chr9:37958994 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1055-2940C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37958994 | |||||||
| chr9:37959132 | T | C | 1 | a0001c0001t0039g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1055-3078A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959132 | |||||||
| chr9:37959199 | G | A | 3 | a0001c0001t0001g0287 a0001c0003t0001g0120 a0001c0003t0001g0123 |
3 | HG01099.hp1 HG01168.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1055-3145C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959199 | |||||||
| chr9:37959384 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1055-3330G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959384 | |||||||
| chr9:37959400 | C | T | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-3346G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959400 | |||||||
| chr9:37959414 | G | A | 1 | a0002c0009t0006g0032 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1055-3360C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959414 | |||||||
| chr9:37959560 | T | C | 1 | a0001c0002t0004g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1055-3506A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959560 | |||||||
| chr9:37959669 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1055-3615C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959669 | |||||||
| chr9:37959685 | C | T | 1 | a0001c0002t0036g0135 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1055-3631G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959685 | |||||||
| chr9:37959696 | C | T | 42 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0080 others(39): Show |
44 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1055-3642G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959696 | |||||||
| chr9:37959698 | G | A | 1 | a0001c0003t0002g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1055-3644C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959698 | |||||||
| chr9:37959843 | AC | A | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-3790delG | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959843 | |||||||
| chr9:37959861 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1055-3807G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37959861 | |||||||
| chr9:37960160 | C | T | 1 | a0001c0007t0001g0253 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1055-4106G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960160 | |||||||
| chr9:37960184 | C | T | 3 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0047g0068 |
3 | HG02109.hp1 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1055-4130G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960184 | |||||||
| chr9:37960205 | C | T | 155 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(152): Show |
158 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1055-4151G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960205 | |||||||
| chr9:37960261 | T | C | 1 | a0001c0002t0002g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1055-4207A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960261 | |||||||
| chr9:37960396 | G | A | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-4342C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960396 | |||||||
| chr9:37960433 | C | A | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1055-4379G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960433 | |||||||
| chr9:37960620 | T | C | 4 | a0001c0001t0001g0232 a0001c0003t0001g0125 a0003c0019t0001g0320 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-4566A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960620 | |||||||
| chr9:37960696 | C | A | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-4642G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960696 | |||||||
| chr9:37960885 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1055-4831C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960885 | |||||||
| chr9:37960983 | G | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1055-4929C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37960983 | |||||||
| chr9:37961346 | C | T | 1 | a0001c0001t0002g0292 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1055-5292G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37961346 | |||||||
| chr9:37961783 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1055-5729G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37961783 | |||||||
| chr9:37961925 | C | T | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-5871G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37961925 | |||||||
| chr9:37962096 | G | C | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1055-6042C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37962096 | |||||||
| chr9:37962111 | A | C | 1 | a0001c0001t0039g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1055-6057T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37962111 | |||||||
| chr9:37962186 | G | A | 1 | a0001c0001t0064g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1055-6132C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37962186 | |||||||
| chr9:37962279 | A | T | 2 | a0001c0003t0002g0142 a0001c0003t0002g0146 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1055-6225T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37962279 | |||||||
| chr9:37962509 | C | CT | 148 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(145): Show |
151 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1055-6456dupA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37962509 | |||||||
| chr9:37962586 | C | A | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-6532G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37962586 | |||||||
| chr9:37962595 | C | T | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-6541G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37962595 | |||||||
| chr9:37962802 | T | C | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-6748A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37962802 | |||||||
| chr9:37962804 | T | C | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-6750A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37962804 | |||||||
| chr9:37963050 | C | T | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-6996G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37963050 | |||||||
| chr9:37963206 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1055-7152G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37963206 | |||||||
| chr9:37963318 | G | A | 8 | a0001c0002t0001g0064 a0001c0002t0001g0158 a0001c0002t0001g0160 others(5): Show |
8 | HG00621.hp2 HG02129.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1055-7264C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37963318 | |||||||
| chr9:37963368 | C | G | 24 | a0001c0005t0005g0044 a0001c0005t0005g0047 a0001c0005t0005g0048 others(21): Show |
24 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.1055-7314G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37963368 | |||||||
| chr9:37963471 | G | A | 1 | a0001c0002t0057g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1055-7417C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37963471 | |||||||
| chr9:37963531 | G | A | 1 | a0001c0001t0045g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1055-7477C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37963531 | |||||||
| chr9:37963878 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1055-7824G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37963878 | |||||||
| chr9:37964331 | A | C | 1 | a0001c0001t0045g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1055-8277T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37964331 | |||||||
| chr9:37964648 | G | C | 1 | a0001c0003t0002g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1055-8594C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37964648 | |||||||
| chr9:37964733 | T | C | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1055-8679A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37964733 | |||||||
| chr9:37964828 | A | G | 1 | a0001c0004t0007g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1055-8774T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37964828 | |||||||
| chr9:37964851 | A | G | 190 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(187): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1055-8797T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37964851 | |||||||
| chr9:37965572 | A | G | 2 | a0001c0002t0001g0089 a0001c0002t0001g0091 |
2 | HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1054+9050T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37965572 | |||||||
| chr9:37965576 | C | CT | 134 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(131): Show |
134 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1054+9045dupA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37965576 | |||||||
| chr9:37965576 | C | CTT | 75 | a0001c0001t0001g0216 a0001c0001t0001g0221 a0001c0001t0001g0241 others(72): Show |
78 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1054+9044_1054+904 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37965576 | |||||||
| chr9:37965644 | C | T | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1054+8978G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37965644 | |||||||
| chr9:37965662 | A | G | 5 | a0001c0004t0003g0058 a0001c0004t0003g0108 a0001c0004t0003g0110 others(2): Show |
5 | HG00741.hp2 HG01106.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+8960T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37965662 | |||||||
| chr9:37965819 | T | C | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1054+8803A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37965819 | |||||||
| chr9:37965903 | C | T | 1 | a0001c0003t0001g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1054+8719G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37965903 | |||||||
| chr9:37966134 | T | C | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1054+8488A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37966134 | |||||||
| chr9:37966152 | T | C | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054+8470A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37966152 | |||||||
| chr9:37966216 | G | A | 1 | a0001c0001t0002g0290 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1054+8406C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37966216 | |||||||
| chr9:37966218 | C | T | 22 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(19): Show |
22 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1054+8404G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37966218 | |||||||
| chr9:37966338 | T | TTTC | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1054+8281_1054+828 others(7): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37966338 | |||||||
| chr9:37966346 | A | T | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054+8276T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37966346 | |||||||
| chr9:37966526 | C | G | 7 | a0001c0002t0001g0087 a0001c0002t0001g0092 a0001c0002t0001g0097 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+8096G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37966526 | |||||||
| chr9:37966680 | T | C | 1 | a0001c0002t0041g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1054+7942A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37966680 | |||||||
| chr9:37966973 | G | A | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1054+7649C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37966973 | |||||||
| chr9:37967150 | C | A | 4 | a0001c0016t0026g0322 a0001c0016t0026g0323 a0001c0017t0025g0305 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+7472G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37967150 | |||||||
| chr9:37967320 | T | C | 1 | a0001c0002t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1054+7302A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37967320 | |||||||
| chr9:37967470 | C | T | 1 | a0001c0007t0001g0245 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1054+7152G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37967470 | |||||||
| chr9:37967527 | C | T | 4 | a0001c0001t0001g0310 a0001c0001t0002g0309 a0001c0001t0002g0311 others(1): Show |
4 | NA18994.hp2 NA19081.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054+7095G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37967527 | |||||||
| chr9:37967581 | T | C | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1054+7041A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37967581 | |||||||
| chr9:37967610 | T | C | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054+7012A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37967610 | |||||||
| chr9:37968004 | G | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1054+6618C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37968004 | |||||||
| chr9:37968207 | C | A | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1054+6415G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37968207 | |||||||
| chr9:37968261 | T | C | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1054+6361A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37968261 | |||||||
| chr9:37968270 | T | C | 17 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1054+6352A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37968270 | |||||||
| chr9:37968918 | C | T | 25 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1054+5704G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37968918 | |||||||
| chr9:37969038 | T | A | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1054+5584A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37969038 | |||||||
| chr9:37969662 | G | A | 76 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0291 others(73): Show |
79 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1054+4960C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37969662 | |||||||
| chr9:37969871 | G | T | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1054+4751C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37969871 | |||||||
| chr9:37969885 | C | T | 214 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(211): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1054+4737G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37969885 | |||||||
| chr9:37969949 | T | C | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1054+4673A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37969949 | |||||||
| chr9:37970031 | C | T | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1054+4591G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37970031 | |||||||
| chr9:37970112 | C | T | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054+4510G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37970112 | |||||||
| chr9:37970181 | T | C | 1 | a0001c0004t0009g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1054+4441A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37970181 | |||||||
| chr9:37970391 | G | T | 1 | a0001c0002t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1054+4231C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37970391 | |||||||
| chr9:37970451 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1054+4171C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37970451 | |||||||
| chr9:37970488 | G | A | 191 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(188): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1054+4134C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37970488 | |||||||
| chr9:37970647 | T | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1054+3975A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37970647 | |||||||
| chr9:37970835 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1054+3787G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37970835 | |||||||
| chr9:37970967 | G | A | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1054+3655C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37970967 | |||||||
| chr9:37971033 | A | G | 18 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(15): Show |
18 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1054+3589T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971033 | |||||||
| chr9:37971289 | C | T | 3 | a0001c0001t0001g0211 a0001c0003t0016g0016 a0001c0003t0016g0017 |
3 | HG02630.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1054+3333G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971289 | |||||||
| chr9:37971333 | C | T | 2 | a0001c0002t0002g0059 a0001c0002t0002g0060 |
2 | HG00639.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1054+3289G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971333 | |||||||
| chr9:37971349 | G | A | 72 | a0001c0001t0001g0214 a0001c0001t0001g0232 a0001c0001t0001g0254 others(69): Show |
75 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1054+3273C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971349 | |||||||
| chr9:37971392 | C | G | 30 | a0001c0001t0013g0225 a0001c0002t0001g0084 a0001c0003t0002g0140 others(27): Show |
30 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.1054+3230G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971392 | |||||||
| chr9:37971524 | G | A | 1 | a0001c0004t0007g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1054+3098C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971524 | |||||||
| chr9:37971706 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1054+2916C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971706 | |||||||
| chr9:37971759 | T | C | 2 | a0001c0002t0002g0079 a0001c0002t0002g0096 |
2 | HG01109.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1054+2863A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971759 | |||||||
| chr9:37971768 | C | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0231 |
3 | HG02015.hp2 HG02155.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1054+2854G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971768 | |||||||
| chr9:37971984 | G | A | 2 | a0001c0001t0002g0313 a0001c0001t0002g0316 |
2 | HG01978.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1054+2638C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971984 | |||||||
| chr9:37971988 | C | A | 1 | a0001c0002t0002g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1054+2634G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971988 | |||||||
| chr9:37971990 | G | A | 1 | a0001c0002t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1054+2632C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37971990 | |||||||
| chr9:37972146 | C | T | 3 | a0001c0004t0028g0018 a0001c0015t0018g0192 a0001c0015t0018g0193 |
3 | HG02622.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1054+2476G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972146 | |||||||
| chr9:37972168 | A | G | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1054+2454T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972168 | |||||||
| chr9:37972221 | C | T | 1 | a0001c0002t0004g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1054+2401G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972221 | |||||||
| chr9:37972378 | G | A | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1054+2244C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972378 | |||||||
| chr9:37972386 | G | A | 25 | a0001c0001t0001g0211 a0001c0003t0002g0142 a0001c0003t0002g0143 others(22): Show |
25 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1054+2236C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972386 | |||||||
| chr9:37972394 | T | G | 43 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0080 others(40): Show |
45 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1054+2228A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972394 | |||||||
| chr9:37972403 | A | G | 182 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(179): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1054+2219T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972403 | |||||||
| chr9:37972500 | C | T | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1054+2122G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972500 | |||||||
| chr9:37972515 | T | C | 209 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(206): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1054+2107A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972515 | |||||||
| chr9:37972610 | G | A | 4 | a0001c0002t0001g0147 a0001c0002t0001g0152 a0001c0002t0014g0151 others(1): Show |
4 | HG01192.hp1 HG02015.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+2012C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972610 | |||||||
| chr9:37972707 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1054+1915C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972707 | |||||||
| chr9:37972742 | C | T | 1 | a0001c0005t0011g0056 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1054+1880G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972742 | |||||||
| chr9:37972820 | G | C | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1054+1802C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37972820 | |||||||
| chr9:37973099 | C | T | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1054+1523G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37973099 | |||||||
| chr9:37973213 | G | A | 1 | a0001c0001t0038g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1054+1409C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37973213 | |||||||
| chr9:37973268 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1054+1354C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37973268 | |||||||
| chr9:37973292 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1054+1330G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37973292 | |||||||
| chr9:37973317 | A | G | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1054+1305T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37973317 | |||||||
| chr9:37973348 | T | C | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1054+1274A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37973348 | |||||||
| chr9:37973443 | G | A | 17 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1054+1179C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37973443 | |||||||
| chr9:37973611 | G | C | 1 | a0001c0005t0070g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1054+1011C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37973611 | |||||||
| chr9:37974114 | G | A | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1054+508C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37974114 | |||||||
| chr9:37974351 | C | A | 2 | a0001c0003t0001g0117 a0001c0003t0001g0118 |
2 | HG02129.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1054+271G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37974351 | |||||||
| chr9:37974484 | G | T | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1054+138C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37974484 | |||||||
| chr9:37974509 | C | T | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1054+113G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 3/5 | chr9 | 37974509 | |||||||
| chr9:37974917 | A | T | 6 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(3): Show |
6 | HG02257.hp2 HG03130.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-80T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37974917 | |||||||
| chr9:37974947 | C | T | 1 | a0001c0002t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.839-110G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37974947 | |||||||
| chr9:37974960 | G | A | 1 | a0001c0002t0040g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.839-123C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37974960 | |||||||
| chr9:37975005 | G | A | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-168C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975005 | |||||||
| chr9:37975056 | G | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.839-219C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975056 | |||||||
| chr9:37975107 | C | T | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-270G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975107 | |||||||
| chr9:37975117 | A | C | 29 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(26): Show |
29 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.839-280T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975117 | |||||||
| chr9:37975558 | C | T | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-721G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975558 | |||||||
| chr9:37975573 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.839-736C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975573 | |||||||
| chr9:37975617 | T | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0231 others(3): Show |
6 | HG02015.hp2 HG02148.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-780A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975617 | |||||||
| chr9:37975752 | T | C | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.839-915A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975752 | |||||||
| chr9:37975775 | C | T | 1 | a0001c0005t0070g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.839-938G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975775 | |||||||
| chr9:37975859 | G | A | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.839-1022C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975859 | |||||||
| chr9:37975915 | G | A | 1 | a0001c0003t0001g0125 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.839-1078C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975915 | |||||||
| chr9:37975924 | C | T | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-1087G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975924 | |||||||
| chr9:37975953 | C | T | 1 | a0001c0004t0003g0114 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.839-1116G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975953 | |||||||
| chr9:37975964 | G | C | 17 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.839-1127C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37975964 | |||||||
| chr9:37976082 | C | G | 2 | a0001c0001t0001g0241 a0001c0001t0051g0240 |
2 | NA18995.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.839-1245G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976082 | |||||||
| chr9:37976100 | A | G | 1 | a0001c0004t0003g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.839-1263T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976100 | |||||||
| chr9:37976104 | C | T | 1 | a0002c0012t0001g0034 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.839-1267G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976104 | |||||||
| chr9:37976129 | G | A | 2 | a0001c0001t0020g0283 a0001c0001t0073g0325 |
2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.839-1292C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976129 | |||||||
| chr9:37976176 | C | G | 1 | a0001c0002t0021g0086 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.839-1339G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976176 | |||||||
| chr9:37976449 | T | G | 1 | a0001c0001t0001g0229 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.839-1612A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976449 | |||||||
| chr9:37976485 | T | C | 1 | a0001c0001t0073g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.839-1648A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976485 | |||||||
| chr9:37976519 | C | A | 9 | a0001c0001t0001g0211 a0001c0003t0008g0065 a0001c0003t0008g0066 others(6): Show |
9 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.839-1682G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976519 | |||||||
| chr9:37976666 | C | T | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-1829G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976666 | |||||||
| chr9:37976670 | G | A | 184 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(181): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.839-1833C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976670 | |||||||
| chr9:37976695 | C | A | 72 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(69): Show |
72 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.839-1858G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37976695 | |||||||
| chr9:37977031 | C | T | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.839-2194G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37977031 | |||||||
| chr9:37977045 | G | A | 8 | a0001c0001t0001g0291 a0001c0001t0002g0290 a0001c0001t0002g0292 others(5): Show |
8 | HG02148.hp2 NA18612.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.839-2208C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37977045 | |||||||
| chr9:37977158 | A | T | 1 | a0001c0004t0003g0107 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.839-2321T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37977158 | |||||||
| chr9:37977562 | C | A | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-2725G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37977562 | |||||||
| chr9:37977787 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.839-2950G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37977787 | |||||||
| chr9:37977993 | C | T | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-3156G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37977993 | |||||||
| chr9:37978291 | C | T | 1 | a0001c0003t0001g0085 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.839-3454G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37978291 | |||||||
| chr9:37978446 | T | C | 1 | a0001c0002t0059g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.839-3609A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37978446 | |||||||
| chr9:37978554 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.839-3717T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37978554 | |||||||
| chr9:37978586 | C | T | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-3749G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37978586 | |||||||
| chr9:37978613 | AAT | A | 3 | a0001c0001t0001g0211 a0001c0003t0016g0016 a0001c0003t0016g0017 |
3 | HG02630.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.839-3778_839-3777d others(4): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37978613 | |||||||
| chr9:37978803 | G | A | 1 | a0001c0007t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.839-3966C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37978803 | |||||||
| chr9:37978951 | C | A | 17 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.839-4114G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37978951 | |||||||
| chr9:37979086 | G | A | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.839-4249C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979086 | |||||||
| chr9:37979223 | G | A | 149 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(146): Show |
152 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.839-4386C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979223 | |||||||
| chr9:37979282 | G | A | 1 | a0001c0002t0014g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.839-4445C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979282 | |||||||
| chr9:37979381 | A | T | 149 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(146): Show |
152 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.839-4544T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979381 | |||||||
| chr9:37979475 | G | A | 1 | a0001c0003t0001g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.839-4638C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979475 | |||||||
| chr9:37979620 | G | GA | 14 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0001g0230 others(11): Show |
14 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.839-4784dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979620 | |||||||
| chr9:37979633 | C | A | 8 | a0001c0001t0001g0310 a0001c0001t0002g0258 a0001c0001t0002g0271 others(5): Show |
8 | HG02083.hp1 HG02523.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.839-4796G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979633 | |||||||
| chr9:37979680 | G | A | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.839-4843C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979680 | |||||||
| chr9:37979794 | T | C | 9 | a0001c0001t0001g0211 a0001c0003t0008g0065 a0001c0003t0008g0066 others(6): Show |
9 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.839-4957A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979794 | |||||||
| chr9:37979860 | C | T | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-5023G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979860 | |||||||
| chr9:37979864 | A | C | 1 | a0001c0002t0040g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.839-5027T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979864 | |||||||
| chr9:37979967 | C | T | 1 | a0001c0006t0010g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.839-5130G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37979967 | |||||||
| chr9:37980013 | G | A | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.839-5176C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980013 | |||||||
| chr9:37980016 | T | C | 1 | a0001c0001t0043g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.839-5179A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980016 | |||||||
| chr9:37980063 | T | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.839-5226A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980063 | |||||||
| chr9:37980107 | C | A | 2 | a0001c0002t0001g0161 a0001c0002t0001g0162 |
2 | HG01496.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.839-5270G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980107 | |||||||
| chr9:37980159 | C | T | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.839-5322G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980159 | |||||||
| chr9:37980213 | C | T | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-5376G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980213 | |||||||
| chr9:37980438 | T | A | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-5601A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980438 | |||||||
| chr9:37980614 | A | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.839-5777T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980614 | |||||||
| chr9:37980788 | G | A | 1 | a0001c0011t0056g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.839-5951C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980788 | |||||||
| chr9:37980900 | T | TG | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-6064_839-6063i others(3): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980900 | |||||||
| chr9:37980901 | T | A | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-6064A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980901 | |||||||
| chr9:37980936 | G | A | 1 | a0001c0002t0004g0130 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.839-6099C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37980936 | |||||||
| chr9:37981008 | G | A | 2 | a0001c0003t0002g0179 a0001c0003t0002g0180 |
2 | HG02080.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.839-6171C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981008 | |||||||
| chr9:37981059 | C | A | 1 | a0001c0006t0067g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.839-6222G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981059 | |||||||
| chr9:37981247 | T | C | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.839-6410A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981247 | |||||||
| chr9:37981327 | T | C | 3 | a0001c0001t0001g0211 a0001c0003t0016g0016 a0001c0003t0016g0017 |
3 | HG02630.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.839-6490A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981327 | |||||||
| chr9:37981332 | A | G | 1 | a0001c0006t0067g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.839-6495T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981332 | |||||||
| chr9:37981509 | C | CAT | 200 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(197): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.839-6673_839-6672i others(4): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981509 | |||||||
| chr9:37981572 | T | TCAA | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-6738_839-6736d others(5): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981572 | |||||||
| chr9:37981631 | T | C | 210 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(207): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.839-6794A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981631 | |||||||
| chr9:37981714 | C | G | 1 | a0001c0004t0003g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.839-6877G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981714 | |||||||
| chr9:37981745 | G | A | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.839-6908C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981745 | |||||||
| chr9:37981768 | A | C | 1 | a0001c0001t0002g0273 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.839-6931T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981768 | |||||||
| chr9:37981796 | G | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.839-6959C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981796 | |||||||
| chr9:37981884 | G | A | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.839-7047C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981884 | |||||||
| chr9:37981921 | A | C | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.839-7084T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37981921 | |||||||
| chr9:37982085 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.839-7248A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982085 | |||||||
| chr9:37982094 | T | TA | 22 | a0001c0001t0001g0204 a0001c0001t0001g0287 a0001c0001t0015g0256 others(19): Show |
22 | HG00438.hp2 HG00735.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.839-7258dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982094 | |||||||
| chr9:37982246 | G | A | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.839-7409C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982246 | |||||||
| chr9:37982260 | A | AG | 7 | a0001c0002t0001g0160 a0001c0004t0001g0115 a0001c0004t0035g0106 others(4): Show |
7 | HG00597.hp1 HG00621.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.839-7424dupC | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982260 | |||||||
| chr9:37982330 | T | C | 2 | a0001c0002t0002g0059 a0001c0002t0002g0060 |
2 | HG00639.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.839-7493A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982330 | |||||||
| chr9:37982332 | A | G | 2 | a0001c0002t0002g0059 a0001c0002t0002g0060 |
2 | HG00639.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.839-7495T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982332 | |||||||
| chr9:37982505 | T | A | 14 | a0001c0001t0001g0291 a0001c0001t0002g0288 a0001c0001t0002g0289 others(11): Show |
14 | HG00544.hp1 HG00673.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.839-7668A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982505 | |||||||
| chr9:37982508 | G | C | 1 | a0001c0005t0006g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.839-7671C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982508 | |||||||
| chr9:37982596 | T | C | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.839-7759A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982596 | |||||||
| chr9:37982609 | G | A | 147 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(144): Show |
150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.839-7772C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982609 | |||||||
| chr9:37982639 | G | GA | 206 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.839-7803dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982639 | |||||||
| chr9:37982671 | C | T | 5 | a0001c0008t0002g0026 a0001c0008t0002g0027 a0001c0008t0002g0029 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-7834G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982671 | |||||||
| chr9:37982756 | G | A | 208 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(205): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.839-7919C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982756 | |||||||
| chr9:37982814 | G | A | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.839-7977C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982814 | |||||||
| chr9:37982919 | C | T | 208 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(205): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.839-8082G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982919 | |||||||
| chr9:37982973 | G | GCCC | 106 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0206 others(103): Show |
108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.839-8139_839-8137d others(5): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982973 | |||||||
| chr9:37982973 | G | GCCCC | 32 | a0001c0001t0001g0205 a0001c0001t0001g0216 a0001c0001t0001g0223 others(29): Show |
33 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.839-8140_839-8137d others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982973 | |||||||
| chr9:37982973 | G | GCCCCC | 22 | a0001c0001t0002g0259 a0001c0001t0002g0313 a0001c0001t0002g0315 others(19): Show |
22 | HG00735.hp1 HG00741.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.839-8141_839-8137d others(7): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982973 | |||||||
| chr9:37982973 | G | GCCCCCC | 21 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(18): Show |
21 | HG00597.hp1 HG00621.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.839-8142_839-8137d others(8): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982973 | |||||||
| chr9:37982976 | C | CA | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.839-8140_839-8139i others(3): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982976 | |||||||
| chr9:37982982 | T | C | 4 | a0001c0016t0026g0322 a0001c0016t0026g0323 a0004c0018t0017g0248 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.839-8145A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37982982 | |||||||
| chr9:37983270 | G | A | 1 | a0011c0027t0033g0195 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.839-8433C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37983270 | |||||||
| chr9:37983272 | C | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.839-8435G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37983272 | |||||||
| chr9:37983437 | T | C | 208 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(205): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.839-8600A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37983437 | |||||||
| chr9:37983445 | C | T | 208 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(205): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.839-8608G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37983445 | |||||||
| chr9:37983501 | G | A | 5 | a0002c0009t0006g0030 a0002c0009t0006g0031 a0002c0009t0006g0032 others(2): Show |
5 | NA18951.hp1 NA18968.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-8664C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37983501 | |||||||
| chr9:37983660 | C | T | 148 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(145): Show |
151 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.839-8823G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37983660 | |||||||
| chr9:37983731 | G | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.839-8894C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37983731 | |||||||
| chr9:37983773 | C | T | 198 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(195): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.839-8936G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37983773 | |||||||
| chr9:37983971 | G | C | 2 | a0001c0001t0001g0218 a0001c0001t0045g0236 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.839-9134C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37983971 | |||||||
| chr9:37984112 | G | A | 34 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(31): Show |
34 | HG00558.hp2 HG01069.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.839-9275C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984112 | |||||||
| chr9:37984218 | G | A | 1 | a0001c0011t0056g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.839-9381C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984218 | |||||||
| chr9:37984223 | C | A | 1 | a0001c0003t0052g0126 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.839-9386G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984223 | |||||||
| chr9:37984341 | C | T | 1 | a0001c0023t0066g0183 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.839-9504G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984341 | |||||||
| chr9:37984356 | C | T | 1 | a0001c0004t0003g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.839-9519G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984356 | |||||||
| chr9:37984363 | G | C | 1 | a0001c0002t0001g0156 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.839-9526C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984363 | |||||||
| chr9:37984475 | G | T | 1 | a0001c0003t0002g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.839-9638C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984475 | |||||||
| chr9:37984723 | A | C | 2 | a0001c0001t0023g0215 a0001c0003t0023g0168 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.839-9886T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984723 | |||||||
| chr9:37984734 | C | G | 208 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(205): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.839-9897G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984734 | |||||||
| chr9:37984779 | C | A | 2 | a0001c0015t0018g0192 a0001c0015t0018g0193 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.839-9942G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984779 | |||||||
| chr9:37984806 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.839-9969C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984806 | |||||||
| chr9:37984848 | C | T | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.839-10011G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984848 | |||||||
| chr9:37984975 | C | T | 1 | a0001c0003t0001g0085 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.839-10138G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37984975 | |||||||
| chr9:37985050 | A | C | 1 | a0001c0003t0001g0085 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.839-10213T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985050 | |||||||
| chr9:37985173 | A | G | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.839-10336T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985173 | |||||||
| chr9:37985309 | A | G | 309 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(306): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.839-10472T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985309 | |||||||
| chr9:37985373 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0045g0236 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.839-10536A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985373 | |||||||
| chr9:37985411 | C | T | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.839-10574G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985411 | |||||||
| chr9:37985535 | G | A | 1 | a0008c0028t0001g0319 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.839-10698C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985535 | |||||||
| chr9:37985556 | C | T | 1 | a0001c0003t0001g0122 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.839-10719G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985556 | |||||||
| chr9:37985649 | A | C | 1 | a0001c0005t0005g0047 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.839-10812T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985649 | |||||||
| chr9:37985698 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.839-10861G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985698 | |||||||
| chr9:37985851 | C | CAGTGACG | 207 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(204): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.839-11015_839-1101 others(11): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37985851 | |||||||
| chr9:37986112 | T | G | 207 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(204): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.839-11275A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37986112 | |||||||
| chr9:37986455 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.839-11618G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37986455 | |||||||
| chr9:37986636 | T | C | 1 | a0001c0002t0001g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.839-11799A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37986636 | |||||||
| chr9:37986805 | G | A | 154 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(151): Show |
157 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.839-11968C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37986805 | |||||||
| chr9:37986831 | A | G | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.839-11994T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37986831 | |||||||
| chr9:37986981 | G | A | 207 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(204): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.839-12144C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37986981 | |||||||
| chr9:37986993 | T | C | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.839-12156A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37986993 | |||||||
| chr9:37987023 | C | T | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.839-12186G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987023 | |||||||
| chr9:37987053 | C | T | 1 | a0001c0005t0024g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.839-12216G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987053 | |||||||
| chr9:37987075 | C | A | 1 | a0001c0002t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.839-12238G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987075 | |||||||
| chr9:37987083 | C | T | 1 | a0001c0002t0019g0157 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.839-12246G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987083 | |||||||
| chr9:37987117 | G | C | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.839-12280C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987117 | |||||||
| chr9:37987147 | C | A | 208 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(205): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.839-12310G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987147 | |||||||
| chr9:37987170 | A | G | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.839-12333T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987170 | |||||||
| chr9:37987230 | T | C | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.839-12393A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987230 | |||||||
| chr9:37987253 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.839-12416C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987253 | |||||||
| chr9:37987300 | G | A | 63 | a0001c0001t0001g0205 a0001c0001t0001g0254 a0001c0001t0001g0265 others(60): Show |
66 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.839-12463C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987300 | |||||||
| chr9:37987320 | C | T | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.839-12483G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987320 | |||||||
| chr9:37987389 | A | G | 319 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(316): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.839-12552T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987389 | |||||||
| chr9:37987411 | T | C | 9 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0161 others(6): Show |
11 | HG00639.hp1 HG01074.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.839-12574A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987411 | |||||||
| chr9:37987527 | G | A | 199 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(196): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.839-12690C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987527 | |||||||
| chr9:37987544 | C | T | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(6): Show |
9 | HG01069.hp2 HG01928.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.839-12707G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987544 | |||||||
| chr9:37987614 | T | C | 1 | a0001c0002t0019g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.839-12777A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37987614 | |||||||
| chr9:37988224 | C | T | 1 | a0001c0004t0003g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.839-13387G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37988224 | |||||||
| chr9:37988573 | C | T | 1 | a0001c0001t0038g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.839-13736G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37988573 | |||||||
| chr9:37988650 | T | C | 206 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.839-13813A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37988650 | |||||||
| chr9:37988832 | C | T | 206 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.839-13995G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37988832 | |||||||
| chr9:37988833 | G | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.839-13996C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37988833 | |||||||
| chr9:37989041 | AT | A | 204 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(201): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.839-14205delA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989041 | |||||||
| chr9:37989072 | C | A | 1 | a0001c0002t0001g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.839-14235G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989072 | |||||||
| chr9:37989076 | T | TAC | 47 | a0001c0003t0002g0140 a0001c0003t0002g0142 a0001c0003t0002g0143 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.839-14241_839-1424 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989076 | |||||||
| chr9:37989079 | A | G | 1 | a0001c0007t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.839-14242T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989079 | |||||||
| chr9:37989080 | C | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.839-14243G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989080 | |||||||
| chr9:37989089 | A | ACT | 144 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(141): Show |
147 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.839-14254_839-1425 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989089 | |||||||
| chr9:37989144 | A | G | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.839-14307T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989144 | |||||||
| chr9:37989178 | A | G | 1 | a0001c0004t0003g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.839-14341T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989178 | |||||||
| chr9:37989263 | A | T | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.839-14426T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989263 | |||||||
| chr9:37989317 | C | T | 23 | a0001c0005t0005g0044 a0001c0005t0005g0047 a0001c0005t0005g0048 others(20): Show |
23 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(20): Show |
intron_variant | MODIFIER | c.839-14480G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989317 | |||||||
| chr9:37989600 | T | A | 1 | a0010c0026t0001g0188 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.839-14763A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989600 | |||||||
| chr9:37989621 | G | C | 7 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(4): Show |
7 | HG01175.hp2 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.839-14784C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989621 | |||||||
| chr9:37989700 | G | A | 206 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.839-14863C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989700 | |||||||
| chr9:37989791 | C | A | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.839-14954G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989791 | |||||||
| chr9:37989896 | A | G | 206 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.839-15059T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37989896 | |||||||
| chr9:37990144 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.839-15307C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990144 | |||||||
| chr9:37990174 | C | T | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.839-15337G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990174 | |||||||
| chr9:37990202 | C | T | 185 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(182): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.839-15365G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990202 | |||||||
| chr9:37990211 | TGTTCA | T | 206 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.839-15379_839-1537 others(9): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990211 | |||||||
| chr9:37990269 | G | A | 1 | a0001c0002t0001g0090 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.839-15432C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990269 | |||||||
| chr9:37990400 | C | T | 185 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(182): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.839-15563G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990400 | |||||||
| chr9:37990536 | T | C | 1 | a0001c0001t0002g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.839-15699A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990536 | |||||||
| chr9:37990538 | TA | T | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-15702delT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990538 | |||||||
| chr9:37990543 | A | C | 5 | a0001c0002t0001g0064 a0001c0002t0002g0062 a0001c0002t0014g0063 others(2): Show |
5 | HG00544.hp2 HG00673.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-15706T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990543 | |||||||
| chr9:37990696 | C | T | 206 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.839-15859G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990696 | |||||||
| chr9:37990804 | G | A | 144 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(141): Show |
147 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.839-15967C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990804 | |||||||
| chr9:37990822 | C | T | 5 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0049g0077 others(2): Show |
5 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-15985G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990822 | |||||||
| chr9:37990913 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.839-16076A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990913 | |||||||
| chr9:37990960 | G | A | 18 | a0001c0005t0005g0044 a0001c0005t0005g0047 a0001c0005t0005g0048 others(15): Show |
18 | HG04184.hp2 NA18943.hp2 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.839-16123C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37990960 | |||||||
| chr9:37991173 | C | T | 181 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(178): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.839-16336G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991173 | |||||||
| chr9:37991284 | C | A | 1 | a0001c0006t0010g0019 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.839-16447G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991284 | |||||||
| chr9:37991313 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.839-16476G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991313 | |||||||
| chr9:37991386 | G | A | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.839-16549C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991386 | |||||||
| chr9:37991396 | C | T | 2 | a0001c0003t0016g0016 a0001c0003t0016g0017 |
2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.839-16559G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991396 | |||||||
| chr9:37991702 | G | A | 117 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(114): Show |
119 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.839-16865C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991702 | |||||||
| chr9:37991792 | T | C | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.839-16955A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991792 | |||||||
| chr9:37991806 | C | T | 6 | a0001c0005t0011g0046 a0002c0009t0006g0030 a0002c0009t0006g0031 others(3): Show |
6 | NA18944.hp1 NA18951.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.839-16969G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991806 | |||||||
| chr9:37991897 | G | A | 3 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0003t0023g0168 |
3 | HG02630.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.839-17060C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991897 | |||||||
| chr9:37991906 | G | A | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-17069C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991906 | |||||||
| chr9:37991916 | C | T | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.839-17079G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37991916 | |||||||
| chr9:37992122 | C | T | 119 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(116): Show |
121 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.839-17285G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37992122 | |||||||
| chr9:37992274 | G | A | 1 | a0001c0002t0001g0156 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.839-17437C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37992274 | |||||||
| chr9:37992333 | G | A | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.839-17496C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37992333 | |||||||
| chr9:37992369 | C | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.839-17532G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37992369 | |||||||
| chr9:37992469 | G | A | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-17632C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37992469 | |||||||
| chr9:37992524 | AAGAGGCT others(8): Show |
A | 4 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0001t0048g0235 others(1): Show |
4 | HG02630.hp1 HG03139.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.839-17702_839-1768 others(19): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37992524 | |||||||
| chr9:37992585 | C | T | 117 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(114): Show |
119 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.839-17748G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37992585 | |||||||
| chr9:37992880 | AACAC | A | 117 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(114): Show |
119 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.839-18047_839-1804 others(8): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37992880 | |||||||
| chr9:37992922 | G | A | 1 | a0001c0002t0004g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.839-18085C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37992922 | |||||||
| chr9:37993046 | G | A | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.839-18209C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37993046 | |||||||
| chr9:37993272 | G | A | 20 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(17): Show |
20 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.839-18435C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37993272 | |||||||
| chr9:37993306 | G | T | 25 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.839-18469C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37993306 | |||||||
| chr9:37993339 | C | T | 8 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0152 others(5): Show |
8 | HG01192.hp1 HG02015.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.839-18502G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37993339 | |||||||
| chr9:37993511 | G | A | 137 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(134): Show |
139 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.839-18674C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37993511 | |||||||
| chr9:37993518 | C | T | 1 | a0001c0003t0029g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.839-18681G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37993518 | |||||||
| chr9:37993699 | C | T | 70 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0291 others(67): Show |
73 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.839-18862G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37993699 | |||||||
| chr9:37994023 | G | C | 177 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(174): Show |
179 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.839-19186C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37994023 | |||||||
| chr9:37994145 | G | T | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.839-19308C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37994145 | |||||||
| chr9:37994337 | A | G | 117 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(114): Show |
119 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.839-19500T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37994337 | |||||||
| chr9:37994479 | C | T | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.839-19642G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37994479 | |||||||
| chr9:37994657 | C | T | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-19820G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37994657 | |||||||
| chr9:37994993 | A | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.839-20156T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37994993 | |||||||
| chr9:37995102 | G | A | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.839-20265C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37995102 | |||||||
| chr9:37995220 | G | A | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.839-20383C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37995220 | |||||||
| chr9:37995364 | C | T | 1 | a0001c0004t0003g0141 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.839-20527G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37995364 | |||||||
| chr9:37995422 | G | T | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.839-20585C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37995422 | |||||||
| chr9:37995461 | T | TCTGGCAG others(5): Show |
115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+20549_838+2055 others(16): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37995461 | |||||||
| chr9:37995848 | T | C | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+20163A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37995848 | |||||||
| chr9:37995955 | C | A | 1 | a0001c0011t0005g0196 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.838+20056G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37995955 | |||||||
| chr9:37996049 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.838+19962A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996049 | |||||||
| chr9:37996125 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.838+19886G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996125 | |||||||
| chr9:37996146 | G | A | 4 | a0001c0008t0002g0026 a0001c0008t0002g0027 a0001c0008t0002g0029 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+19865C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996146 | |||||||
| chr9:37996276 | C | T | 1 | a0005c0014t0013g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.838+19735G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996276 | |||||||
| chr9:37996382 | A | G | 1 | a0001c0002t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.838+19629T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996382 | |||||||
| chr9:37996443 | G | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.838+19568C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996443 | |||||||
| chr9:37996499 | G | A | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.838+19512C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996499 | |||||||
| chr9:37996506 | A | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.838+19505T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996506 | |||||||
| chr9:37996651 | T | C | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.838+19360A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996651 | |||||||
| chr9:37996727 | G | T | 67 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0272 others(64): Show |
70 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.838+19284C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996727 | |||||||
| chr9:37996790 | C | T | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.838+19221G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37996790 | |||||||
| chr9:37997082 | T | TA | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.838+18928dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997082 | |||||||
| chr9:37997102 | A | G | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.838+18909T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997102 | |||||||
| chr9:37997163 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.838+18848G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997163 | |||||||
| chr9:37997310 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.838+18701G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997310 | |||||||
| chr9:37997311 | G | A | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.838+18700C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997311 | |||||||
| chr9:37997456 | G | A | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.838+18555C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997456 | |||||||
| chr9:37997457 | C | T | 1 | a0001c0001t0002g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.838+18554G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997457 | |||||||
| chr9:37997531 | A | G | 1 | a0001c0007t0001g0227 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.838+18480T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997531 | |||||||
| chr9:37997564 | T | C | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+18447A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997564 | |||||||
| chr9:37997571 | T | A | 14 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(11): Show |
14 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.838+18440A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997571 | |||||||
| chr9:37997608 | T | C | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.838+18403A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997608 | |||||||
| chr9:37997684 | TGTG | T | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.838+18324_838+1832 others(7): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997684 | |||||||
| chr9:37997691 | G | C | 1 | a0001c0017t0025g0305 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.838+18320C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997691 | |||||||
| chr9:37997766 | C | T | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.838+18245G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997766 | |||||||
| chr9:37997790 | A | G | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+18221T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997790 | |||||||
| chr9:37997830 | C | T | 11 | a0001c0001t0002g0302 a0001c0004t0068g0181 a0001c0006t0010g0019 others(8): Show |
11 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.838+18181G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37997830 | |||||||
| chr9:37998197 | A | G | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.838+17814T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998197 | |||||||
| chr9:37998205 | T | TGGAGGGA | 40 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0133 others(37): Show |
42 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.838+17799_838+1780 others(11): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998205 | |||||||
| chr9:37998205 | T | TGGAGGGA others(7): Show |
75 | a0001c0002t0001g0064 a0001c0002t0001g0072 a0001c0002t0001g0073 others(72): Show |
75 | HG00544.hp2 HG00639.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.838+17792_838+1780 others(18): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998205 | |||||||
| chr9:37998492 | A | G | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+17519T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998492 | |||||||
| chr9:37998581 | T | C | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.838+17430A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998581 | |||||||
| chr9:37998609 | C | T | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.838+17402G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998609 | |||||||
| chr9:37998643 | G | A | 4 | a0001c0002t0001g0147 a0001c0002t0001g0152 a0001c0002t0014g0151 others(1): Show |
4 | HG01192.hp1 HG02015.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+17368C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998643 | |||||||
| chr9:37998757 | A | G | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+17254T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998757 | |||||||
| chr9:37998814 | T | A | 1 | a0001c0002t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.838+17197A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998814 | |||||||
| chr9:37998832 | T | G | 10 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.838+17179A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998832 | |||||||
| chr9:37998862 | A | G | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.838+17149T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998862 | |||||||
| chr9:37998974 | G | A | 1 | a0001c0003t0052g0126 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.838+17037C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37998974 | |||||||
| chr9:37999040 | A | G | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+16971T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37999040 | |||||||
| chr9:37999073 | A | G | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.838+16938T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37999073 | |||||||
| chr9:37999109 | C | T | 1 | a0001c0004t0003g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.838+16902G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37999109 | |||||||
| chr9:37999162 | C | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.838+16849G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37999162 | |||||||
| chr9:37999372 | G | A | 2 | a0001c0004t0003g0112 a0001c0011t0003g0198 |
2 | HG03704.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.838+16639C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37999372 | |||||||
| chr9:37999608 | C | T | 1 | a0001c0003t0001g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.838+16403G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37999608 | |||||||
| chr9:37999613 | TGGA | T | 14 | a0001c0004t0068g0181 a0001c0006t0010g0019 a0001c0006t0010g0020 others(11): Show |
14 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.838+16395_838+1639 others(7): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37999613 | |||||||
| chr9:37999786 | G | C | 1 | a0001c0002t0057g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.838+16225C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37999786 | |||||||
| chr9:37999876 | T | G | 1 | a0001c0003t0016g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.838+16135A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 37999876 | |||||||
| chr9:38000203 | A | G | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+15808T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000203 | |||||||
| chr9:38000419 | T | C | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838+15592A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000419 | |||||||
| chr9:38000443 | C | A | 19 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(16): Show |
19 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.838+15568G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000443 | |||||||
| chr9:38000474 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0053g0247 |
2 | NA18963.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.838+15537C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000474 | |||||||
| chr9:38000586 | C | T | 5 | a0002c0009t0006g0030 a0002c0009t0006g0031 a0002c0009t0006g0032 others(2): Show |
5 | NA18951.hp1 NA18968.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+15425G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000586 | |||||||
| chr9:38000587 | G | A | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.838+15424C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000587 | |||||||
| chr9:38000650 | C | T | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+15361G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000650 | |||||||
| chr9:38000656 | G | C | 1 | a0001c0003t0002g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.838+15355C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000656 | |||||||
| chr9:38000663 | C | T | 14 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(11): Show |
14 | HG01109.hp2 HG01175.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.838+15348G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000663 | |||||||
| chr9:38000727 | G | A | 2 | a0001c0003t0002g0142 a0001c0003t0002g0146 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.838+15284C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000727 | |||||||
| chr9:38000897 | G | A | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.838+15114C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38000897 | |||||||
| chr9:38001076 | T | C | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+14935A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001076 | |||||||
| chr9:38001146 | T | C | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.838+14865A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001146 | |||||||
| chr9:38001314 | G | A | 17 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.838+14697C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001314 | |||||||
| chr9:38001318 | C | T | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG01069.hp2 HG01928.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.838+14693G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001318 | |||||||
| chr9:38001336 | G | T | 1 | a0001c0002t0001g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.838+14675C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001336 | |||||||
| chr9:38001482 | G | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838+14529C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001482 | |||||||
| chr9:38001589 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.838+14422C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001589 | |||||||
| chr9:38001625 | G | A | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+14386C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001625 | |||||||
| chr9:38001669 | A | C | 1 | a0001c0002t0061g0061 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.838+14342T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001669 | |||||||
| chr9:38001714 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.838+14297C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001714 | |||||||
| chr9:38001720 | T | TAGGGTTA others(6): Show |
1 | a0001c0002t0001g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.838+14290_838+1429 others(17): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001720 | |||||||
| chr9:38001740 | G | T | 1 | a0001c0002t0001g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.838+14271C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001740 | |||||||
| chr9:38001741 | C | T | 1 | a0001c0002t0001g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.838+14270G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001741 | |||||||
| chr9:38001837 | G | C | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+14174C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001837 | |||||||
| chr9:38001905 | C | T | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+14106G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001905 | |||||||
| chr9:38001984 | GCA | G | 115 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+14025_838+1402 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38001984 | |||||||
| chr9:38002245 | T | C | 1 | a0001c0002t0004g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.838+13766A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002245 | |||||||
| chr9:38002259 | A | G | 168 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0072 others(165): Show |
170 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.838+13752T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002259 | |||||||
| chr9:38002412 | G | T | 2 | a0001c0015t0018g0192 a0001c0015t0018g0193 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.838+13599C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002412 | |||||||
| chr9:38002415 | A | T | 17 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(14): Show |
17 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.838+13596T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002415 | |||||||
| chr9:38002563 | C | T | 1 | a0001c0008t0022g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.838+13448G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002563 | |||||||
| chr9:38002601 | C | T | 6 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(3): Show |
6 | HG02257.hp2 HG03130.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+13410G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002601 | |||||||
| chr9:38002624 | C | G | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.838+13387G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002624 | |||||||
| chr9:38002663 | A | C | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.838+13348T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002663 | |||||||
| chr9:38002795 | T | G | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.838+13216A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002795 | |||||||
| chr9:38002825 | A | G | 1 | a0001c0002t0001g0154 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.838+13186T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002825 | |||||||
| chr9:38002866 | C | T | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838+13145G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002866 | |||||||
| chr9:38002920 | G | C | 1 | a0001c0003t0029g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.838+13091C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38002920 | |||||||
| chr9:38003127 | G | T | 24 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(21): Show |
24 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.838+12884C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003127 | |||||||
| chr9:38003164 | G | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838+12847C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003164 | |||||||
| chr9:38003363 | G | A | 6 | a0001c0001t0002g0267 a0001c0001t0002g0268 a0001c0008t0002g0026 others(3): Show |
6 | HG00099.hp1 HG01106.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+12648C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003363 | |||||||
| chr9:38003516 | G | A | 8 | a0001c0002t0001g0087 a0001c0002t0001g0092 a0001c0002t0001g0097 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.838+12495C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003516 | |||||||
| chr9:38003549 | C | G | 26 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0087 others(23): Show |
26 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.838+12462G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003549 | |||||||
| chr9:38003570 | C | T | 98 | a0001c0001t0020g0286 a0001c0002t0001g0002 a0001c0002t0001g0064 others(95): Show |
100 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.838+12441G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003570 | |||||||
| chr9:38003574 | T | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.838+12437A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003574 | |||||||
| chr9:38003660 | G | C | 120 | a0001c0001t0020g0286 a0001c0002t0001g0002 a0001c0002t0001g0064 others(117): Show |
122 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.838+12351C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003660 | |||||||
| chr9:38003665 | G | T | 120 | a0001c0001t0020g0286 a0001c0002t0001g0002 a0001c0002t0001g0064 others(117): Show |
122 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.838+12346C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003665 | |||||||
| chr9:38003758 | G | A | 42 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0133 others(39): Show |
44 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.838+12253C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003758 | |||||||
| chr9:38003775 | A | G | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.838+12236T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003775 | |||||||
| chr9:38003806 | C | T | 115 | a0001c0001t0020g0286 a0001c0002t0001g0002 a0001c0002t0001g0064 others(112): Show |
117 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.838+12205G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003806 | |||||||
| chr9:38003827 | C | T | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.838+12184G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003827 | |||||||
| chr9:38003859 | G | A | 79 | a0001c0002t0001g0002 a0001c0002t0001g0064 a0001c0002t0001g0080 others(76): Show |
81 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.838+12152C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003859 | |||||||
| chr9:38003981 | G | A | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.838+12030C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38003981 | |||||||
| chr9:38004142 | T | C | 254 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0265 others(251): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.838+11869A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004142 | |||||||
| chr9:38004148 | A | C | 143 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(140): Show |
145 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.838+11863T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004148 | |||||||
| chr9:38004240 | A | C | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.838+11771T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004240 | |||||||
| chr9:38004276 | T | G | 4 | a0001c0008t0002g0026 a0001c0008t0002g0027 a0001c0008t0002g0029 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+11735A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004276 | |||||||
| chr9:38004308 | AAGC | A | 3 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0064g0238 |
3 | HG02698.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.838+11700_838+1170 others(7): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004308 | |||||||
| chr9:38004354 | G | T | 3 | a0001c0001t0014g0217 a0001c0001t0048g0235 a0001c0001t0063g0234 |
3 | HG02818.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.838+11657C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004354 | |||||||
| chr9:38004401 | C | T | 3 | a0001c0004t0049g0077 a0001c0015t0018g0192 a0001c0015t0018g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.838+11610G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004401 | |||||||
| chr9:38004444 | G | A | 74 | a0001c0001t0001g0205 a0001c0001t0001g0209 a0001c0001t0001g0211 others(71): Show |
77 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.838+11567C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004444 | |||||||
| chr9:38004512 | C | T | 315 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(312): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.838+11499G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004512 | |||||||
| chr9:38004663 | G | A | 2 | a0001c0003t0002g0179 a0001c0003t0002g0180 |
2 | HG02080.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.838+11348C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004663 | |||||||
| chr9:38004712 | A | G | 1 | a0001c0001t0071g0243 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.838+11299T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004712 | |||||||
| chr9:38004758 | G | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.838+11253C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004758 | |||||||
| chr9:38004862 | T | C | 116 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(113): Show |
118 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.838+11149A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004862 | |||||||
| chr9:38004884 | G | A | 2 | a0001c0001t0002g0271 a0001c0001t0002g0274 |
2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.838+11127C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38004884 | |||||||
| chr9:38005438 | T | C | 156 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(153): Show |
158 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.838+10573A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38005438 | |||||||
| chr9:38005452 | C | T | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.838+10559G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38005452 | |||||||
| chr9:38005460 | T | C | 20 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0087 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.838+10551A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38005460 | |||||||
| chr9:38005463 | C | T | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+10548G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38005463 | |||||||
| chr9:38005622 | C | T | 1 | a0001c0002t0002g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.838+10389G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38005622 | |||||||
| chr9:38005623 | G | T | 1 | a0001c0003t0002g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.838+10388C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38005623 | |||||||
| chr9:38005628 | C | G | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.838+10383G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38005628 | |||||||
| chr9:38005719 | C | T | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.838+10292G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38005719 | |||||||
| chr9:38005800 | G | A | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.838+10211C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38005800 | |||||||
| chr9:38006262 | C | T | 1 | a0011c0027t0033g0195 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.838+9749G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38006262 | |||||||
| chr9:38006559 | G | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838+9452C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38006559 | |||||||
| chr9:38006619 | C | A | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.838+9392G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38006619 | |||||||
| chr9:38006670 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.838+9341C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38006670 | |||||||
| chr9:38006739 | T | A | 1 | a0001c0003t0002g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.838+9272A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38006739 | |||||||
| chr9:38006760 | C | T | 118 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(115): Show |
120 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.838+9251G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38006760 | |||||||
| chr9:38007030 | T | C | 1 | a0001c0004t0003g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.838+8981A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38007030 | |||||||
| chr9:38007112 | G | A | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.838+8899C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38007112 | |||||||
| chr9:38007364 | T | C | 2 | a0001c0001t0001g0223 a0001c0003t0001g0104 |
2 | NA18973.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.838+8647A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38007364 | |||||||
| chr9:38007490 | G | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.838+8521C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38007490 | |||||||
| chr9:38007525 | T | C | 1 | a0007c0022t0065g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.838+8486A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38007525 | |||||||
| chr9:38007750 | A | G | 149 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(146): Show |
151 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.838+8261T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38007750 | |||||||
| chr9:38007778 | G | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838+8233C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38007778 | |||||||
| chr9:38008138 | C | A | 1 | a0001c0002t0002g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.838+7873G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008138 | |||||||
| chr9:38008221 | G | T | 1 | a0001c0002t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.838+7790C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008221 | |||||||
| chr9:38008249 | G | A | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.838+7762C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008249 | |||||||
| chr9:38008370 | C | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838+7641G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008370 | |||||||
| chr9:38008380 | A | G | 2 | a0001c0001t0001g0252 a0001c0003t0001g0185 |
2 | NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.838+7631T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008380 | |||||||
| chr9:38008395 | T | C | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+7616A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008395 | |||||||
| chr9:38008495 | C | T | 1 | a0001c0006t0067g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.838+7516G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008495 | |||||||
| chr9:38008500 | T | G | 1 | a0001c0002t0002g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.838+7511A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008500 | |||||||
| chr9:38008534 | T | C | 1 | a0001c0013t0008g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.838+7477A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008534 | |||||||
| chr9:38008572 | G | A | 1 | a0001c0002t0021g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.838+7439C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008572 | |||||||
| chr9:38008614 | C | T | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.838+7397G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008614 | |||||||
| chr9:38008684 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+7327C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008684 | |||||||
| chr9:38008735 | G | A | 118 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(115): Show |
120 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.838+7276C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008735 | |||||||
| chr9:38008849 | G | A | 118 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(115): Show |
120 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.838+7162C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008849 | |||||||
| chr9:38008908 | C | G | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+7103G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008908 | |||||||
| chr9:38008955 | T | C | 1 | a0001c0001t0002g0277 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.838+7056A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38008955 | |||||||
| chr9:38009226 | T | C | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+6785A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009226 | |||||||
| chr9:38009258 | A | G | 60 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0083 others(57): Show |
60 | HG00544.hp2 HG00639.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.838+6753T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009258 | |||||||
| chr9:38009409 | C | T | 124 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(121): Show |
126 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.838+6602G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009409 | |||||||
| chr9:38009473 | G | C | 1 | a0001c0001t0045g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.838+6538C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009473 | |||||||
| chr9:38009480 | G | C | 1 | a0008c0028t0001g0319 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.838+6531C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009480 | |||||||
| chr9:38009630 | T | C | 1 | a0001c0001t0002g0295 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.838+6381A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009630 | |||||||
| chr9:38009648 | G | A | 2 | a0001c0003t0001g0121 a0001c0003t0001g0124 |
2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.838+6363C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009648 | |||||||
| chr9:38009666 | A | G | 149 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(146): Show |
151 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.838+6345T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009666 | |||||||
| chr9:38009711 | A | T | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+6300T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009711 | |||||||
| chr9:38009848 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.838+6163C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009848 | |||||||
| chr9:38009902 | T | C | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.838+6109A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38009902 | |||||||
| chr9:38010028 | C | T | 118 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(115): Show |
120 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.838+5983G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38010028 | |||||||
| chr9:38010088 | A | T | 149 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(146): Show |
151 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.838+5923T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38010088 | |||||||
| chr9:38010206 | T | C | 1 | a0001c0002t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.838+5805A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38010206 | |||||||
| chr9:38010219 | C | T | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838+5792G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38010219 | |||||||
| chr9:38010273 | A | T | 1 | a0001c0002t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.838+5738T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38010273 | |||||||
| chr9:38010276 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.838+5735C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38010276 | |||||||
| chr9:38010396 | G | T | 1 | a0001c0001t0002g0288 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.838+5615C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38010396 | |||||||
| chr9:38010438 | A | G | 25 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.838+5573T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38010438 | |||||||
| chr9:38010866 | C | T | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.838+5145G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38010866 | |||||||
| chr9:38011050 | T | C | 176 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(173): Show |
178 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.838+4961A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011050 | |||||||
| chr9:38011090 | G | C | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+4921C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011090 | |||||||
| chr9:38011093 | A | G | 25 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(22): Show |
25 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.838+4918T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011093 | |||||||
| chr9:38011178 | G | A | 1 | a0001c0005t0007g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.838+4833C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011178 | |||||||
| chr9:38011286 | A | C | 1 | a0001c0003t0001g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.838+4725T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011286 | |||||||
| chr9:38011392 | G | A | 3 | a0001c0005t0007g0041 a0001c0005t0007g0042 a0001c0005t0007g0043 |
3 | HG02451.hp1 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.838+4619C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011392 | |||||||
| chr9:38011443 | GC | G | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+4567delG | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011443 | |||||||
| chr9:38011564 | C | T | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+4447G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011564 | |||||||
| chr9:38011615 | C | T | 6 | a0001c0002t0001g0087 a0001c0002t0001g0092 a0001c0002t0001g0097 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+4396G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011615 | |||||||
| chr9:38011882 | C | T | 1 | a0001c0003t0016g0017 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.838+4129G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38011882 | |||||||
| chr9:38012101 | C | T | 1 | a0001c0002t0001g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.838+3910G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012101 | |||||||
| chr9:38012494 | CGTT | C | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.838+3514_838+3516d others(5): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012494 | |||||||
| chr9:38012495 | G | A | 117 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(114): Show |
119 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.838+3516C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012495 | |||||||
| chr9:38012526 | T | C | 4 | a0001c0023t0066g0183 a0004c0018t0017g0248 a0004c0018t0017g0249 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+3485A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012526 | |||||||
| chr9:38012658 | G | A | 1 | a0001c0005t0006g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.838+3353C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012658 | |||||||
| chr9:38012687 | T | C | 2 | a0005c0014t0013g0037 a0005c0014t0013g0038 |
2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.838+3324A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012687 | |||||||
| chr9:38012690 | C | A | 1 | a0001c0002t0002g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.838+3321G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012690 | |||||||
| chr9:38012732 | C | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.838+3279G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012732 | |||||||
| chr9:38012749 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.838+3262C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012749 | |||||||
| chr9:38012814 | C | T | 1 | a0001c0004t0003g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.838+3197G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012814 | |||||||
| chr9:38012829 | A | G | 1 | a0001c0001t0002g0261 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.838+3182T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012829 | |||||||
| chr9:38012837 | A | G | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01069.hp2 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+3174T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012837 | |||||||
| chr9:38012881 | T | C | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.838+3130A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012881 | |||||||
| chr9:38012942 | C | T | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+3069G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012942 | |||||||
| chr9:38012975 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+3036C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38012975 | |||||||
| chr9:38013096 | C | T | 3 | a0001c0001t0001g0211 a0001c0001t0023g0215 a0001c0003t0023g0168 |
3 | HG02630.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.838+2915G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38013096 | |||||||
| chr9:38013227 | G | C | 118 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(115): Show |
120 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.838+2784C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38013227 | |||||||
| chr9:38013437 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.838+2574T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38013437 | |||||||
| chr9:38013438 | CT | C | 22 | a0001c0005t0005g0044 a0001c0005t0005g0047 a0001c0005t0005g0048 others(19): Show |
22 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(19): Show |
intron_variant | MODIFIER | c.838+2572delA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38013438 | |||||||
| chr9:38013474 | C | T | 1 | a0001c0002t0021g0086 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.838+2537G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38013474 | |||||||
| chr9:38013590 | G | A | 4 | a0001c0008t0002g0026 a0001c0008t0002g0027 a0001c0008t0002g0029 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+2421C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38013590 | |||||||
| chr9:38013692 | C | T | 1 | a0001c0008t0022g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.838+2319G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38013692 | |||||||
| chr9:38014158 | C | A | 3 | a0001c0002t0001g0072 a0001c0002t0001g0075 a0001c0002t0001g0173 |
3 | HG02717.hp2 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.838+1853G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014158 | |||||||
| chr9:38014246 | A | G | 1 | a0001c0002t0001g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.838+1765T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014246 | |||||||
| chr9:38014277 | C | G | 25 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(22): Show |
25 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.838+1734G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014277 | |||||||
| chr9:38014325 | T | C | 124 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(121): Show |
126 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.838+1686A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014325 | |||||||
| chr9:38014334 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+1677C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014334 | |||||||
| chr9:38014368 | G | C | 3 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0047g0068 |
3 | HG02109.hp1 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.838+1643C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014368 | |||||||
| chr9:38014477 | G | T | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+1534C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014477 | |||||||
| chr9:38014639 | T | C | 124 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(121): Show |
126 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.838+1372A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014639 | |||||||
| chr9:38014678 | C | T | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.838+1333G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014678 | |||||||
| chr9:38014698 | G | A | 124 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(121): Show |
126 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.838+1313C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014698 | |||||||
| chr9:38014758 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.838+1253C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014758 | |||||||
| chr9:38014776 | A | G | 1 | a0001c0001t0002g0260 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.838+1235T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014776 | |||||||
| chr9:38014777 | ACAG | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+1231_838+1233d others(5): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014777 | |||||||
| chr9:38014787 | C | T | 1 | a0001c0001t0043g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.838+1224G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014787 | |||||||
| chr9:38014899 | C | T | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+1112G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014899 | |||||||
| chr9:38014907 | C | G | 1 | a0001c0003t0001g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.838+1104G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38014907 | |||||||
| chr9:38015040 | T | C | 118 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(115): Show |
120 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.838+971A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015040 | |||||||
| chr9:38015088 | A | C | 1 | a0001c0002t0001g0152 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.838+923T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015088 | |||||||
| chr9:38015240 | G | C | 1 | a0006c0025t0042g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.838+771C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015240 | |||||||
| chr9:38015330 | C | G | 124 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(121): Show |
126 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.838+681G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015330 | |||||||
| chr9:38015412 | C | T | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.838+599G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015412 | |||||||
| chr9:38015577 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.838+434A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015577 | |||||||
| chr9:38015649 | C | G | 317 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(314): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.838+362G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015649 | |||||||
| chr9:38015732 | T | G | 118 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(115): Show |
120 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.838+279A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015732 | |||||||
| chr9:38015814 | G | C | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.838+197C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015814 | |||||||
| chr9:38015882 | C | G | 2 | a0001c0002t0001g0147 a0001c0007t0001g0244 |
2 | NA18960.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.838+129G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 2/5 | chr9 | 38015882 | |||||||
| chr9:38016161 | C | T | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.718-30G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38016161 | |||||||
| chr9:38016250 | T | C | 149 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(146): Show |
151 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.718-119A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38016250 | |||||||
| chr9:38016403 | G | A | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.718-272C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38016403 | |||||||
| chr9:38016404 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.718-273C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38016404 | |||||||
| chr9:38016422 | A | C | 25 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.718-291T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38016422 | |||||||
| chr9:38016686 | T | C | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-555A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38016686 | |||||||
| chr9:38016925 | C | A | 1 | a0001c0001t0002g0301 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.718-794G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38016925 | |||||||
| chr9:38016927 | A | G | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.718-796T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38016927 | |||||||
| chr9:38017034 | G | A | 1 | a0001c0003t0002g0180 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.718-903C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38017034 | |||||||
| chr9:38017133 | C | G | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG01069.hp2 HG01928.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.718-1002G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38017133 | |||||||
| chr9:38017134 | G | A | 1 | a0001c0002t0004g0137 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.718-1003C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38017134 | |||||||
| chr9:38017333 | G | A | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-1202C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38017333 | |||||||
| chr9:38017684 | A | G | 149 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(146): Show |
151 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.718-1553T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38017684 | |||||||
| chr9:38017692 | C | T | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-1561G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38017692 | |||||||
| chr9:38017752 | C | T | 1 | a0001c0003t0001g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.718-1621G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38017752 | |||||||
| chr9:38018256 | T | C | 3 | a0001c0002t0001g0072 a0001c0002t0001g0075 a0001c0002t0001g0173 |
3 | HG02717.hp2 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.718-2125A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38018256 | |||||||
| chr9:38018263 | T | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-2132A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38018263 | |||||||
| chr9:38018372 | T | C | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.718-2241A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38018372 | |||||||
| chr9:38018380 | C | T | 23 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(20): Show |
23 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.718-2249G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38018380 | |||||||
| chr9:38018404 | G | A | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.718-2273C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38018404 | |||||||
| chr9:38018506 | G | GA | 147 | a0001c0001t0001g0252 a0001c0001t0053g0247 a0001c0002t0001g0002 others(144): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.718-2376dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38018506 | |||||||
| chr9:38018636 | G | C | 4 | a0001c0005t0007g0040 a0001c0005t0007g0041 a0001c0005t0007g0042 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-2505C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38018636 | |||||||
| chr9:38018693 | T | C | 118 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(115): Show |
120 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.718-2562A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38018693 | |||||||
| chr9:38019009 | T | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-2878A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019009 | |||||||
| chr9:38019084 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.718-2953G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019084 | |||||||
| chr9:38019108 | C | A | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.718-2977G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019108 | |||||||
| chr9:38019148 | T | C | 117 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(114): Show |
119 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.718-3017A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019148 | |||||||
| chr9:38019176 | A | G | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.718-3045T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019176 | |||||||
| chr9:38019195 | C | T | 1 | a0001c0005t0001g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.718-3064G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019195 | |||||||
| chr9:38019196 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-3065C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019196 | |||||||
| chr9:38019461 | A | G | 150 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(147): Show |
152 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.718-3330T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019461 | |||||||
| chr9:38019566 | C | A | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.718-3435G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019566 | |||||||
| chr9:38019612 | T | C | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.718-3481A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019612 | |||||||
| chr9:38019665 | C | T | 2 | a0001c0003t0002g0143 a0001c0003t0002g0144 |
2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.718-3534G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019665 | |||||||
| chr9:38019706 | C | T | 25 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.718-3575G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019706 | |||||||
| chr9:38019725 | A | G | 4 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-3594T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019725 | |||||||
| chr9:38019772 | G | GC | 181 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(178): Show |
183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.718-3642_718-3641i others(3): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019772 | |||||||
| chr9:38019804 | C | A | 77 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(74): Show |
77 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.718-3673G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019804 | |||||||
| chr9:38019809 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.718-3678C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019809 | |||||||
| chr9:38019869 | G | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.718-3738C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019869 | |||||||
| chr9:38019922 | T | C | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-3791A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019922 | |||||||
| chr9:38019923 | G | C | 2 | a0001c0003t0016g0016 a0001c0003t0016g0017 |
2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.718-3792C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38019923 | |||||||
| chr9:38020039 | A | G | 25 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.718-3908T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020039 | |||||||
| chr9:38020106 | G | A | 1 | a0001c0004t0068g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.718-3975C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020106 | |||||||
| chr9:38020355 | A | C | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.718-4224T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020355 | |||||||
| chr9:38020547 | T | G | 253 | a0001c0001t0001g0218 a0001c0001t0001g0252 a0001c0001t0001g0254 others(250): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.718-4416A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020547 | |||||||
| chr9:38020658 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.718-4527C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020658 | |||||||
| chr9:38020664 | G | A | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.718-4533C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020664 | |||||||
| chr9:38020811 | G | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.718-4680C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020811 | |||||||
| chr9:38020813 | G | T | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-4682C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020813 | |||||||
| chr9:38020827 | G | T | 25 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.718-4696C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020827 | |||||||
| chr9:38020889 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.718-4758T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020889 | |||||||
| chr9:38020947 | C | A | 59 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0133 others(56): Show |
61 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.718-4816G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38020947 | |||||||
| chr9:38021043 | AATG | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-4915_718-4913d others(5): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021043 | |||||||
| chr9:38021049 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-4918C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021049 | |||||||
| chr9:38021153 | C | T | 77 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(74): Show |
77 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.718-5022G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021153 | |||||||
| chr9:38021192 | T | A | 1 | a0001c0001t0002g0296 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.718-5061A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021192 | |||||||
| chr9:38021271 | T | C | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.718-5140A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021271 | |||||||
| chr9:38021383 | C | T | 77 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(74): Show |
77 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.718-5252G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021383 | |||||||
| chr9:38021413 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.718-5282A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021413 | |||||||
| chr9:38021596 | A | G | 1 | a0001c0006t0010g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.718-5465T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021596 | |||||||
| chr9:38021689 | T | C | 77 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(74): Show |
77 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.718-5558A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021689 | |||||||
| chr9:38021771 | G | A | 1 | a0001c0004t0003g0138 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.718-5640C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021771 | |||||||
| chr9:38021833 | T | C | 1 | a0001c0001t0015g0246 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.718-5702A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021833 | |||||||
| chr9:38021892 | C | T | 83 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(80): Show |
83 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.718-5761G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38021892 | |||||||
| chr9:38022064 | A | G | 1 | a0003c0019t0001g0320 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.718-5933T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022064 | |||||||
| chr9:38022102 | T | C | 1 | a0001c0001t0002g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.718-5971A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022102 | |||||||
| chr9:38022198 | A | G | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-6067T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022198 | |||||||
| chr9:38022429 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-6298C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022429 | |||||||
| chr9:38022492 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.718-6361A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022492 | |||||||
| chr9:38022507 | G | A | 2 | a0001c0004t0009g0006 a0001c0004t0009g0009 |
2 | HG01175.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.718-6376C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022507 | |||||||
| chr9:38022549 | C | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-6418G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022549 | |||||||
| chr9:38022621 | A | AC | 10 | a0001c0001t0001g0221 a0001c0001t0002g0303 a0001c0002t0001g0094 others(7): Show |
10 | HG01192.hp1 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.718-6491dupG | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022621 | |||||||
| chr9:38022645 | C | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-6514G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022645 | |||||||
| chr9:38022662 | G | A | 3 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0047g0068 |
3 | HG02109.hp1 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.718-6531C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022662 | |||||||
| chr9:38022806 | G | C | 1 | a0001c0002t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.718-6675C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022806 | |||||||
| chr9:38022907 | C | A | 1 | a0001c0002t0001g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.718-6776G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022907 | |||||||
| chr9:38022932 | G | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-6801C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022932 | |||||||
| chr9:38022956 | A | G | 175 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(172): Show |
177 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.718-6825T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38022956 | |||||||
| chr9:38023134 | G | GGCTGCAG others(7): Show |
1 | a0001c0001t0001g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.718-7017_718-7004d others(16): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023134 | |||||||
| chr9:38023200 | C | A | 249 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0265 others(246): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.718-7069G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023200 | |||||||
| chr9:38023375 | T | G | 4 | a0001c0002t0001g0147 a0001c0002t0001g0152 a0001c0002t0014g0151 others(1): Show |
4 | HG01192.hp1 HG02015.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-7244A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023375 | |||||||
| chr9:38023388 | T | C | 2 | a0001c0002t0001g0093 a0001c0002t0002g0096 |
2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.718-7257A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023388 | |||||||
| chr9:38023414 | G | A | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-7283C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023414 | |||||||
| chr9:38023453 | G | C | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.718-7322C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023453 | |||||||
| chr9:38023503 | G | A | 83 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(80): Show |
83 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.718-7372C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023503 | |||||||
| chr9:38023590 | G | C | 179 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(176): Show |
181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.718-7459C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023590 | |||||||
| chr9:38023597 | T | C | 1 | a0006c0025t0042g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.718-7466A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023597 | |||||||
| chr9:38023656 | C | T | 83 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(80): Show |
83 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.718-7525G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023656 | |||||||
| chr9:38023882 | G | A | 1 | a0001c0002t0001g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.718-7751C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023882 | |||||||
| chr9:38023909 | A | G | 6 | a0001c0001t0001g0314 a0001c0001t0002g0259 a0001c0001t0002g0313 others(3): Show |
6 | HG01070.hp1 HG01516.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-7778T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38023909 | |||||||
| chr9:38024044 | C | T | 1 | a0001c0002t0002g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.718-7913G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024044 | |||||||
| chr9:38024236 | A | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-8105T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024236 | |||||||
| chr9:38024267 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.718-8136A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024267 | |||||||
| chr9:38024377 | G | T | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.718-8246C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024377 | |||||||
| chr9:38024438 | T | C | 1 | a0001c0017t0025g0305 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.718-8307A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024438 | |||||||
| chr9:38024461 | G | A | 251 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0265 others(248): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.718-8330C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024461 | |||||||
| chr9:38024506 | C | A | 1 | a0001c0002t0002g0096 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.718-8375G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024506 | |||||||
| chr9:38024507 | C | G | 1 | a0001c0002t0002g0096 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.718-8376G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024507 | |||||||
| chr9:38024526 | A | G | 83 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(80): Show |
83 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.718-8395T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024526 | |||||||
| chr9:38024658 | C | A | 1 | a0001c0002t0001g0152 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.718-8527G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024658 | |||||||
| chr9:38024750 | A | C | 1 | a0001c0002t0001g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.718-8619T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024750 | |||||||
| chr9:38024815 | G | A | 83 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(80): Show |
83 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.718-8684C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024815 | |||||||
| chr9:38024909 | G | A | 1 | a0010c0026t0001g0188 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.718-8778C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024909 | |||||||
| chr9:38024913 | T | C | 1 | a0001c0004t0003g0114 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.718-8782A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38024913 | |||||||
| chr9:38025200 | T | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-9069A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025200 | |||||||
| chr9:38025228 | C | T | 64 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0133 others(61): Show |
66 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.718-9097G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025228 | |||||||
| chr9:38025230 | G | A | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718-9099C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025230 | |||||||
| chr9:38025756 | C | T | 2 | a0001c0002t0001g0099 a0001c0002t0004g0100 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.718-9625G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025756 | |||||||
| chr9:38025784 | T | G | 1 | a0001c0001t0060g0297 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.718-9653A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025784 | |||||||
| chr9:38025839 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.718-9708C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025839 | |||||||
| chr9:38025901 | G | C | 77 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(74): Show |
77 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.718-9770C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025901 | |||||||
| chr9:38025914 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.718-9783T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025914 | |||||||
| chr9:38025959 | A | G | 1 | a0001c0002t0001g0163 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.718-9828T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025959 | |||||||
| chr9:38025985 | G | C | 41 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0133 others(38): Show |
43 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.718-9854C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38025985 | |||||||
| chr9:38026066 | G | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-9935C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38026066 | |||||||
| chr9:38026228 | T | C | 83 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(80): Show |
83 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.718-10097A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38026228 | |||||||
| chr9:38026340 | G | A | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.718-10209C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38026340 | |||||||
| chr9:38026492 | T | A | 1 | a0001c0005t0005g0049 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.718-10361A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38026492 | |||||||
| chr9:38026657 | T | C | 1 | a0001c0023t0066g0183 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718-10526A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38026657 | |||||||
| chr9:38026762 | C | T | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.718-10631G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38026762 | |||||||
| chr9:38026964 | G | C | 1 | a0001c0002t0001g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.718-10833C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38026964 | |||||||
| chr9:38027056 | T | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-10925A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027056 | |||||||
| chr9:38027076 | G | A | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.718-10945C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027076 | |||||||
| chr9:38027089 | C | T | 8 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(5): Show |
8 | HG02257.hp2 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.718-10958G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027089 | |||||||
| chr9:38027165 | C | T | 55 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(52): Show |
55 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.718-11034G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027165 | |||||||
| chr9:38027263 | A | G | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.718-11132T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027263 | |||||||
| chr9:38027362 | C | T | 3 | a0001c0005t0011g0054 a0001c0005t0011g0055 a0001c0005t0011g0056 |
3 | NA18957.hp1 NA18960.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.718-11231G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027362 | |||||||
| chr9:38027383 | C | T | 1 | a0001c0016t0026g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.718-11252G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027383 | |||||||
| chr9:38027439 | C | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-11308G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027439 | |||||||
| chr9:38027492 | G | A | 12 | a0001c0005t0005g0044 a0001c0005t0005g0047 a0001c0005t0005g0048 others(9): Show |
12 | HG04184.hp2 NA18943.hp2 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.718-11361C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027492 | |||||||
| chr9:38027527 | G | T | 41 | a0001c0001t0001g0200 a0001c0001t0001g0228 a0001c0001t0001g0265 others(38): Show |
44 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.718-11396C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027527 | |||||||
| chr9:38027553 | G | A | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.718-11422C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027553 | |||||||
| chr9:38027647 | C | T | 240 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(237): Show |
245 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(242): Show |
intron_variant | MODIFIER | c.718-11516G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027647 | |||||||
| chr9:38027752 | G | A | 2 | a0001c0005t0007g0042 a0001c0005t0007g0043 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.718-11621C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027752 | |||||||
| chr9:38027908 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.718-11777C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027908 | |||||||
| chr9:38027946 | A | T | 70 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0272 others(67): Show |
73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.718-11815T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027946 | |||||||
| chr9:38027949 | C | CT | 70 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0272 others(67): Show |
73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.718-11819_718-1181 others(5): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38027949 | |||||||
| chr9:38028001 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-11870C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028001 | |||||||
| chr9:38028065 | G | C | 3 | a0001c0002t0001g0133 a0001c0002t0004g0132 a0001c0002t0004g0134 |
3 | HG00642.hp2 HG00741.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.718-11934C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028065 | |||||||
| chr9:38028193 | C | T | 1 | a0001c0002t0002g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.718-12062G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028193 | |||||||
| chr9:38028407 | C | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-12276G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028407 | |||||||
| chr9:38028429 | C | A | 112 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0083 others(109): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.718-12298G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028429 | |||||||
| chr9:38028578 | C | T | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.718-12447G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028578 | |||||||
| chr9:38028615 | T | C | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.718-12484A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028615 | |||||||
| chr9:38028889 | C | G | 1 | a0001c0007t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.718-12758G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028889 | |||||||
| chr9:38028933 | G | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-12802C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028933 | |||||||
| chr9:38028934 | C | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-12803G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38028934 | |||||||
| chr9:38029061 | C | A | 1 | a0001c0004t0054g0139 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.718-12930G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029061 | |||||||
| chr9:38029139 | T | G | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.718-13008A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029139 | |||||||
| chr9:38029162 | C | A | 67 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.718-13031G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029162 | |||||||
| chr9:38029301 | A | G | 67 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.718-13170T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029301 | |||||||
| chr9:38029458 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.718-13327G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029458 | |||||||
| chr9:38029552 | C | T | 2 | a0002c0009t0006g0030 a0002c0009t0006g0031 |
2 | NA18968.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.718-13421G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029552 | |||||||
| chr9:38029595 | ATTCTCT | A | 67 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.718-13470_718-1346 others(10): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029595 | |||||||
| chr9:38029616 | G | A | 2 | a0001c0002t0002g0059 a0001c0002t0002g0060 |
2 | HG00639.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.718-13485C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029616 | |||||||
| chr9:38029639 | C | A | 5 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(2): Show |
5 | HG02622.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-13508G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029639 | |||||||
| chr9:38029819 | T | G | 41 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0002g0059 others(38): Show |
41 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.718-13688A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029819 | |||||||
| chr9:38029968 | T | A | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-13837A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029968 | |||||||
| chr9:38029995 | A | G | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-13864T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38029995 | |||||||
| chr9:38030033 | G | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.718-13902C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030033 | |||||||
| chr9:38030170 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.718-14039G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030170 | |||||||
| chr9:38030298 | C | T | 67 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.718-14167G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030298 | |||||||
| chr9:38030345 | C | G | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-14214G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030345 | |||||||
| chr9:38030358 | T | C | 1 | a0001c0003t0002g0145 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.718-14227A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030358 | |||||||
| chr9:38030601 | G | A | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.718-14470C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030601 | |||||||
| chr9:38030717 | G | T | 67 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.718-14586C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030717 | |||||||
| chr9:38030788 | A | T | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.718-14657T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030788 | |||||||
| chr9:38030953 | C | CA | 62 | a0001c0001t0001g0252 a0001c0001t0002g0270 a0001c0002t0001g0064 others(59): Show |
62 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.718-14823dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030953 | |||||||
| chr9:38030963 | A | G | 1 | a0001c0001t0043g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.718-14832T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030963 | |||||||
| chr9:38030985 | C | A | 179 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(176): Show |
181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.718-14854G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38030985 | |||||||
| chr9:38031029 | A | C | 1 | a0004c0018t0017g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.718-14898T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031029 | |||||||
| chr9:38031033 | A | G | 112 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0083 others(109): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.718-14902T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031033 | |||||||
| chr9:38031225 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.718-15094C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031225 | |||||||
| chr9:38031269 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0231 |
3 | HG02015.hp2 HG02155.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.718-15138G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031269 | |||||||
| chr9:38031460 | C | T | 1 | a0001c0001t0063g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.718-15329G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031460 | |||||||
| chr9:38031541 | T | A | 1 | a0001c0008t0002g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.718-15410A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031541 | |||||||
| chr9:38031622 | A | G | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-15491T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031622 | |||||||
| chr9:38031637 | T | C | 67 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.718-15506A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031637 | |||||||
| chr9:38031679 | G | C | 1 | a0001c0003t0029g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-15548C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031679 | |||||||
| chr9:38031731 | C | T | 57 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(54): Show |
57 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.718-15600G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031731 | |||||||
| chr9:38031926 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.718-15795C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38031926 | |||||||
| chr9:38032013 | G | C | 2 | a0001c0001t0020g0283 a0001c0001t0073g0325 |
2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.718-15882C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032013 | |||||||
| chr9:38032218 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.718-16087C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032218 | |||||||
| chr9:38032338 | C | T | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-16207G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032338 | |||||||
| chr9:38032354 | C | G | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-16223G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032354 | |||||||
| chr9:38032377 | T | C | 182 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(179): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.718-16246A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032377 | |||||||
| chr9:38032446 | G | A | 1 | a0001c0013t0008g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718-16315C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032446 | |||||||
| chr9:38032587 | G | A | 1 | a0006c0025t0042g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.718-16456C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032587 | |||||||
| chr9:38032593 | C | T | 6 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0003t0030g0014 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-16462G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032593 | |||||||
| chr9:38032611 | C | T | 57 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(54): Show |
57 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.718-16480G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032611 | |||||||
| chr9:38032625 | G | C | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.718-16494C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032625 | |||||||
| chr9:38032701 | T | C | 14 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(11): Show |
14 | HG01109.hp2 HG01175.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-16570A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032701 | |||||||
| chr9:38032828 | C | T | 4 | a0001c0002t0001g0147 a0001c0002t0001g0152 a0001c0002t0014g0151 others(1): Show |
4 | HG01192.hp1 HG02015.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-16697G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032828 | |||||||
| chr9:38032871 | C | T | 24 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.718-16740G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38032871 | |||||||
| chr9:38033226 | C | T | 1 | a0001c0007t0001g0227 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.718-17095G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033226 | |||||||
| chr9:38033425 | C | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-17294G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033425 | |||||||
| chr9:38033457 | G | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-17326C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033457 | |||||||
| chr9:38033459 | A | G | 182 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(179): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.718-17328T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033459 | |||||||
| chr9:38033494 | G | A | 1 | a0001c0002t0021g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.718-17363C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033494 | |||||||
| chr9:38033571 | G | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.718-17440C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033571 | |||||||
| chr9:38033612 | C | T | 14 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(11): Show |
14 | HG01109.hp2 HG01175.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-17481G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033612 | |||||||
| chr9:38033678 | T | C | 4 | a0001c0005t0005g0047 a0001c0005t0005g0048 a0001c0005t0005g0049 others(1): Show |
4 | NA18955.hp2 NA18979.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-17547A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033678 | |||||||
| chr9:38033767 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.718-17636G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033767 | |||||||
| chr9:38033861 | C | CT | 67 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.718-17731_718-1773 others(5): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38033861 | |||||||
| chr9:38034024 | C | T | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-17893G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38034024 | |||||||
| chr9:38034134 | T | G | 1 | a0001c0002t0001g0158 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.718-18003A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38034134 | |||||||
| chr9:38034184 | T | A | 113 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0083 others(110): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.718-18053A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38034184 | |||||||
| chr9:38034234 | G | A | 63 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(60): Show |
63 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.718-18103C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38034234 | |||||||
| chr9:38034325 | A | T | 14 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(11): Show |
14 | HG01109.hp2 HG01175.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-18194T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38034325 | |||||||
| chr9:38034479 | C | T | 1 | a0001c0005t0024g0045 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.718-18348G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38034479 | |||||||
| chr9:38034681 | C | T | 182 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(179): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.718-18550G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38034681 | |||||||
| chr9:38035061 | G | A | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.718-18930C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035061 | |||||||
| chr9:38035098 | A | G | 67 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.718-18967T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035098 | |||||||
| chr9:38035134 | C | T | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.718-19003G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035134 | |||||||
| chr9:38035288 | T | TG | 11 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(8): Show |
11 | HG02040.hp2 HG02135.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.718-19158dupC | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035288 | |||||||
| chr9:38035310 | T | C | 182 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(179): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.718-19179A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035310 | |||||||
| chr9:38035317 | G | A | 1 | a0001c0002t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.718-19186C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035317 | |||||||
| chr9:38035337 | G | A | 1 | a0001c0007t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.718-19206C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035337 | |||||||
| chr9:38035349 | G | C | 57 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(54): Show |
57 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.718-19218C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035349 | |||||||
| chr9:38035519 | G | GA | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-19389dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035519 | |||||||
| chr9:38035668 | C | A | 251 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0265 others(248): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.718-19537G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035668 | |||||||
| chr9:38035761 | C | T | 30 | a0001c0003t0002g0140 a0001c0003t0008g0065 a0001c0003t0008g0066 others(27): Show |
30 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.718-19630G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38035761 | |||||||
| chr9:38036010 | C | T | 1 | a0002c0009t0006g0035 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.718-19879G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036010 | |||||||
| chr9:38036103 | C | G | 67 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.718-19972G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036103 | |||||||
| chr9:38036125 | C | A | 2 | a0001c0001t0002g0271 a0001c0001t0002g0274 |
2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.718-19994G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036125 | |||||||
| chr9:38036202 | C | G | 1 | a0001c0010t0027g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.718-20071G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036202 | |||||||
| chr9:38036247 | C | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-20116G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036247 | |||||||
| chr9:38036329 | AAC | A | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-20200_718-2019 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036329 | |||||||
| chr9:38036398 | A | G | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718-20267T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036398 | |||||||
| chr9:38036400 | C | T | 14 | a0001c0001t0001g0291 a0001c0001t0002g0288 a0001c0001t0002g0289 others(11): Show |
14 | HG00544.hp1 HG00673.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.718-20269G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036400 | |||||||
| chr9:38036436 | A | G | 3 | a0001c0001t0002g0301 a0001c0023t0066g0183 a0007c0022t0065g0182 |
3 | HG02818.hp1 NA18522.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.718-20305T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036436 | |||||||
| chr9:38036743 | C | T | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718-20612G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036743 | |||||||
| chr9:38036744 | T | C | 69 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(66): Show |
69 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.718-20613A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036744 | |||||||
| chr9:38036793 | A | G | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-20662T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036793 | |||||||
| chr9:38036881 | A | G | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718-20750T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036881 | |||||||
| chr9:38036918 | G | A | 1 | a0001c0007t0001g0226 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.718-20787C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38036918 | |||||||
| chr9:38037008 | C | T | 2 | a0001c0016t0026g0322 a0001c0016t0026g0323 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.718-20877G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037008 | |||||||
| chr9:38037089 | C | T | 182 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(179): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.718-20958G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037089 | |||||||
| chr9:38037094 | C | T | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-20963G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037094 | |||||||
| chr9:38037599 | T | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-21468A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037599 | |||||||
| chr9:38037615 | C | T | 1 | a0001c0002t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.718-21484G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037615 | |||||||
| chr9:38037855 | G | T | 141 | a0001c0001t0001g0252 a0001c0001t0002g0316 a0001c0002t0001g0002 others(138): Show |
143 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.718-21724C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037855 | |||||||
| chr9:38037951 | A | AT | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-21821dupA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037951 | |||||||
| chr9:38037959 | T | A | 30 | a0001c0003t0002g0140 a0001c0003t0008g0065 a0001c0003t0008g0066 others(27): Show |
30 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.718-21828A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037959 | |||||||
| chr9:38037960 | A | T | 2 | a0001c0003t0002g0142 a0001c0003t0002g0146 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.718-21829T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037960 | |||||||
| chr9:38037964 | T | C | 1 | a0001c0001t0013g0225 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.718-21833A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38037964 | |||||||
| chr9:38038078 | T | C | 1 | a0001c0002t0001g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.718-21947A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38038078 | |||||||
| chr9:38038242 | C | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-22111G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38038242 | |||||||
| chr9:38038338 | G | A | 31 | a0001c0002t0001g0093 a0001c0002t0002g0096 a0001c0003t0002g0140 others(28): Show |
31 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.718-22207C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38038338 | |||||||
| chr9:38038356 | G | A | 2 | a0001c0002t0001g0064 a0001c0002t0014g0063 |
2 | NA19086.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.718-22225C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38038356 | |||||||
| chr9:38038434 | G | C | 178 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(175): Show |
180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.718-22303C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38038434 | |||||||
| chr9:38038737 | G | A | 1 | a0001c0006t0067g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.718-22606C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38038737 | |||||||
| chr9:38038780 | C | G | 1 | a0001c0001t0002g0258 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.718-22649G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38038780 | |||||||
| chr9:38038783 | G | A | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0239 others(3): Show |
6 | HG02135.hp2 NA18973.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-22652C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38038783 | |||||||
| chr9:38038787 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0053g0247 |
2 | NA18963.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.718-22656C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38038787 | |||||||
| chr9:38039001 | A | G | 1 | a0001c0005t0024g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.718-22870T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039001 | |||||||
| chr9:38039054 | G | A | 8 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(5): Show |
8 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.718-22923C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039054 | |||||||
| chr9:38039116 | C | T | 1 | a0001c0004t0003g0107 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.718-22985G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039116 | |||||||
| chr9:38039692 | C | T | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-23561G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039692 | |||||||
| chr9:38039741 | A | G | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-23610T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039741 | |||||||
| chr9:38039789 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0002g0207 |
2 | NA18968.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.718-23658G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039789 | |||||||
| chr9:38039810 | T | C | 1 | a0001c0023t0066g0183 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718-23679A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039810 | |||||||
| chr9:38039849 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-23718C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039849 | |||||||
| chr9:38039851 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-23720C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039851 | |||||||
| chr9:38039875 | T | G | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-23744A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039875 | |||||||
| chr9:38039899 | G | A | 1 | a0001c0002t0001g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.718-23768C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039899 | |||||||
| chr9:38039911 | G | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.718-23780C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039911 | |||||||
| chr9:38039928 | A | G | 114 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0083 others(111): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.718-23797T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38039928 | |||||||
| chr9:38040002 | G | A | 1 | a0001c0001t0039g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.718-23871C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040002 | |||||||
| chr9:38040098 | C | T | 109 | a0001c0002t0001g0002 a0001c0002t0001g0080 a0001c0002t0001g0083 others(106): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.718-23967G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040098 | |||||||
| chr9:38040099 | G | C | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.718-23968C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040099 | |||||||
| chr9:38040117 | C | A | 63 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(60): Show |
63 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.718-23986G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040117 | |||||||
| chr9:38040244 | G | A | 4 | a0001c0016t0026g0322 a0001c0016t0026g0323 a0001c0023t0066g0183 others(1): Show |
4 | HG02451.hp2 HG02818.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-24113C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040244 | |||||||
| chr9:38040262 | C | T | 2 | a0001c0003t0002g0142 a0001c0003t0002g0146 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.718-24131G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040262 | |||||||
| chr9:38040348 | C | T | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-24217G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040348 | |||||||
| chr9:38040352 | A | C | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-24221T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040352 | |||||||
| chr9:38040476 | G | A | 14 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(11): Show |
14 | HG01109.hp2 HG01175.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-24345C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040476 | |||||||
| chr9:38040500 | T | C | 1 | a0001c0003t0002g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.718-24369A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040500 | |||||||
| chr9:38040592 | G | A | 1 | a0001c0007t0001g0226 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.718-24461C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040592 | |||||||
| chr9:38040628 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0230 |
2 | NA18994.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.718-24497G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040628 | |||||||
| chr9:38040653 | G | T | 1 | a0008c0028t0001g0319 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.718-24522C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040653 | |||||||
| chr9:38040675 | C | T | 174 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(171): Show |
176 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.718-24544G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040675 | |||||||
| chr9:38040831 | T | C | 174 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(171): Show |
176 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.718-24700A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040831 | |||||||
| chr9:38040979 | C | T | 1 | a0007c0022t0065g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.718-24848G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38040979 | |||||||
| chr9:38041057 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.718-24926C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041057 | |||||||
| chr9:38041105 | C | A | 1 | a0001c0001t0013g0225 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.718-24974G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041105 | |||||||
| chr9:38041145 | T | G | 179 | a0001c0001t0001g0252 a0001c0002t0001g0002 a0001c0002t0001g0064 others(176): Show |
181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.718-25014A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041145 | |||||||
| chr9:38041489 | T | A | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-25358A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041489 | |||||||
| chr9:38041498 | T | A | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.718-25367A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041498 | |||||||
| chr9:38041538 | G | A | 22 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0087 others(19): Show |
22 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.718-25407C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041538 | |||||||
| chr9:38041688 | A | AC | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-25558dupG | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041688 | |||||||
| chr9:38041817 | G | C | 5 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0013t0008g0189 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-25686C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041817 | |||||||
| chr9:38041855 | C | T | 1 | a0001c0002t0001g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.718-25724G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041855 | |||||||
| chr9:38041998 | C | T | 72 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0291 others(69): Show |
75 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.718-25867G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38041998 | |||||||
| chr9:38042059 | GCCGACGT others(11): Show |
G | 1 | a0001c0001t0002g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.717+25852_717+2586 others(22): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38042059 | |||||||
| chr9:38042061 | C | G | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.717+25868G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38042061 | |||||||
| chr9:38042173 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.717+25756G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38042173 | |||||||
| chr9:38042228 | A | G | 68 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(65): Show |
68 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.717+25701T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38042228 | |||||||
| chr9:38042459 | A | C | 64 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(61): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.717+25470T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38042459 | |||||||
| chr9:38042532 | A | G | 64 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(61): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.717+25397T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38042532 | |||||||
| chr9:38042650 | C | A | 1 | a0001c0002t0021g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.717+25279G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38042650 | |||||||
| chr9:38043091 | T | A | 3 | a0001c0003t0001g0117 a0001c0003t0001g0118 a0001c0003t0001g0178 |
3 | HG02129.hp2 NA18612.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.717+24838A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043091 | |||||||
| chr9:38043224 | T | C | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+24705A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043224 | |||||||
| chr9:38043260 | C | T | 1 | a0001c0004t0003g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.717+24669G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043260 | |||||||
| chr9:38043422 | T | C | 64 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(61): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.717+24507A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043422 | |||||||
| chr9:38043437 | A | G | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.717+24492T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043437 | |||||||
| chr9:38043582 | C | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.717+24347G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043582 | |||||||
| chr9:38043666 | G | A | 1 | a0001c0002t0036g0135 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.717+24263C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043666 | |||||||
| chr9:38043802 | T | C | 3 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0047g0068 |
3 | HG02109.hp1 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.717+24127A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043802 | |||||||
| chr9:38043820 | T | C | 64 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(61): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.717+24109A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043820 | |||||||
| chr9:38043889 | C | CA | 56 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(53): Show |
56 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.717+24039dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043889 | |||||||
| chr9:38043889 | C | CAA | 7 | a0001c0003t0001g0185 a0001c0003t0016g0016 a0001c0003t0016g0017 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+24038_717+2403 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043889 | |||||||
| chr9:38043889 | CA | C | 6 | a0001c0003t0001g0120 a0001c0003t0008g0066 a0001c0004t0068g0181 others(3): Show |
6 | HG01099.hp2 HG01168.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+24039delT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043889 | |||||||
| chr9:38043923 | C | T | 1 | a0001c0005t0070g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.717+24006G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043923 | |||||||
| chr9:38043970 | T | G | 64 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(61): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.717+23959A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38043970 | |||||||
| chr9:38044011 | T | C | 64 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0072 others(61): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.717+23918A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044011 | |||||||
| chr9:38044091 | G | T | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+23838C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044091 | |||||||
| chr9:38044195 | C | T | 1 | a0001c0001t0044g0276 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.717+23734G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044195 | |||||||
| chr9:38044521 | G | A | 1 | a0001c0001t0050g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.717+23408C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044521 | |||||||
| chr9:38044700 | G | A | 1 | a0001c0001t0002g0300 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.717+23229C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044700 | |||||||
| chr9:38044716 | T | A | 6 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(3): Show |
6 | HG01175.hp2 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+23213A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044716 | |||||||
| chr9:38044800 | C | T | 1 | a0001c0003t0001g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.717+23129G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044800 | |||||||
| chr9:38044938 | G | A | 1 | a0001c0005t0070g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.717+22991C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044938 | |||||||
| chr9:38044966 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.717+22963C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044966 | |||||||
| chr9:38044978 | G | A | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.717+22951C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38044978 | |||||||
| chr9:38045317 | A | G | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.717+22612T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045317 | |||||||
| chr9:38045425 | A | AC | 29 | a0001c0001t0001g0205 a0001c0001t0002g0257 a0001c0003t0001g0081 others(26): Show |
29 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.717+22503dupG | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045425 | |||||||
| chr9:38045447 | T | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.717+22482A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045447 | |||||||
| chr9:38045452 | A | C | 9 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(6): Show |
9 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.717+22477T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045452 | |||||||
| chr9:38045472 | T | C | 1 | a0001c0002t0001g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.717+22457A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045472 | |||||||
| chr9:38045479 | C | T | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.717+22450G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045479 | |||||||
| chr9:38045482 | G | A | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.717+22447C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045482 | |||||||
| chr9:38045656 | A | G | 3 | a0001c0001t0015g0246 a0001c0001t0015g0255 a0001c0001t0015g0256 |
3 | HG03942.hp2 HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.717+22273T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045656 | |||||||
| chr9:38045772 | G | A | 1 | a0001c0003t0016g0017 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+22157C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045772 | |||||||
| chr9:38045821 | G | T | 1 | a0001c0004t0009g0008 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.717+22108C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045821 | |||||||
| chr9:38045965 | G | A | 2 | a0001c0003t0001g0117 a0001c0003t0001g0118 |
2 | HG02129.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.717+21964C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38045965 | |||||||
| chr9:38046002 | G | A | 24 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(21): Show |
24 | HG01109.hp2 HG01175.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.717+21927C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046002 | |||||||
| chr9:38046030 | C | T | 1 | a0001c0001t0043g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.717+21899G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046030 | |||||||
| chr9:38046168 | A | G | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+21761T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046168 | |||||||
| chr9:38046256 | T | C | 2 | a0001c0004t0003g0105 a0001c0004t0003g0114 |
2 | HG00323.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.717+21673A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046256 | |||||||
| chr9:38046368 | T | A | 40 | a0001c0001t0001g0252 a0001c0001t0020g0286 a0001c0002t0001g0064 others(37): Show |
40 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.717+21561A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046368 | |||||||
| chr9:38046451 | C | G | 4 | a0001c0004t0028g0018 a0001c0004t0049g0077 a0001c0015t0018g0192 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+21478G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046451 | |||||||
| chr9:38046791 | G | A | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.717+21138C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046791 | |||||||
| chr9:38046822 | C | T | 1 | a0001c0010t0012g0010 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.717+21107G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046822 | |||||||
| chr9:38046880 | C | T | 2 | a0001c0003t0002g0167 a0001c0003t0023g0168 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.717+21049G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046880 | |||||||
| chr9:38046896 | G | T | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+21033C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38046896 | |||||||
| chr9:38047276 | A | T | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+20653T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38047276 | |||||||
| chr9:38047359 | C | CCTAGAA | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+20569_717+2057 others(10): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38047359 | |||||||
| chr9:38047360 | T | A | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+20569A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38047360 | |||||||
| chr9:38047363 | T | A | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+20566A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38047363 | |||||||
| chr9:38047377 | G | A | 5 | a0001c0001t0001g0228 a0001c0005t0007g0040 a0001c0005t0007g0041 others(2): Show |
5 | HG02451.hp1 HG02523.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+20552C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38047377 | |||||||
| chr9:38047493 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.717+20436G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38047493 | |||||||
| chr9:38047515 | G | A | 1 | a0005c0014t0013g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.717+20414C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38047515 | |||||||
| chr9:38047623 | C | G | 1 | a0001c0002t0001g0148 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.717+20306G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38047623 | |||||||
| chr9:38047713 | G | A | 24 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.717+20216C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38047713 | |||||||
| chr9:38048024 | C | T | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+19905G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38048024 | |||||||
| chr9:38048276 | A | G | 1 | a0001c0004t0035g0106 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.717+19653T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38048276 | |||||||
| chr9:38048444 | G | A | 28 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(25): Show |
28 | HG01109.hp2 HG01175.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.717+19485C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38048444 | |||||||
| chr9:38048525 | G | A | 1 | a0001c0002t0001g0160 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.717+19404C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38048525 | |||||||
| chr9:38048563 | G | A | 2 | a0001c0002t0001g0093 a0001c0002t0002g0096 |
2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.717+19366C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38048563 | |||||||
| chr9:38048765 | C | G | 1 | a0001c0003t0001g0057 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.717+19164G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38048765 | |||||||
| chr9:38048822 | T | C | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+19107A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38048822 | |||||||
| chr9:38048887 | A | G | 1 | a0001c0006t0067g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.717+19042T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38048887 | |||||||
| chr9:38048999 | C | G | 28 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(25): Show |
28 | HG01109.hp2 HG01175.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.717+18930G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38048999 | |||||||
| chr9:38049089 | C | T | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+18840G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049089 | |||||||
| chr9:38049090 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+18839C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049090 | |||||||
| chr9:38049223 | A | G | 1 | a0001c0003t0002g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.717+18706T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049223 | |||||||
| chr9:38049246 | C | A | 1 | a0001c0008t0022g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.717+18683G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049246 | |||||||
| chr9:38049331 | G | A | 1 | a0001c0005t0070g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.717+18598C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049331 | |||||||
| chr9:38049396 | G | A | 1 | a0001c0008t0022g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.717+18533C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049396 | |||||||
| chr9:38049458 | A | C | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+18471T>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049458 | |||||||
| chr9:38049481 | C | T | 3 | a0001c0007t0001g0318 a0005c0014t0013g0037 a0005c0014t0013g0038 |
3 | HG03540.hp2 HG03688.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.717+18448G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049481 | |||||||
| chr9:38049635 | C | CA | 24 | a0001c0001t0001g0229 a0001c0001t0001g0250 a0001c0001t0002g0273 others(21): Show |
24 | HG00735.hp2 HG01175.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.717+18293dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049635 | |||||||
| chr9:38049670 | G | C | 28 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(25): Show |
28 | HG01109.hp2 HG01175.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.717+18259C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049670 | |||||||
| chr9:38049706 | G | A | 1 | a0001c0002t0002g0096 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.717+18223C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049706 | |||||||
| chr9:38049747 | C | T | 24 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.717+18182G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049747 | |||||||
| chr9:38049773 | C | G | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.717+18156G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049773 | |||||||
| chr9:38049943 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+17986C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38049943 | |||||||
| chr9:38050220 | TCA | T | 7 | a0001c0003t0002g0142 a0001c0003t0002g0143 a0001c0003t0002g0144 others(4): Show |
7 | HG02257.hp2 HG03130.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+17707_717+1770 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38050220 | |||||||
| chr9:38050470 | T | C | 1 | a0001c0004t0028g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.717+17459A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38050470 | |||||||
| chr9:38050499 | T | C | 1 | a0001c0004t0001g0115 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.717+17430A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38050499 | |||||||
| chr9:38050527 | G | T | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+17402C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38050527 | |||||||
| chr9:38050858 | C | CA | 20 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(17): Show |
20 | HG01109.hp2 HG01175.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.717+17070dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38050858 | |||||||
| chr9:38051036 | A | T | 3 | a0001c0004t0068g0181 a0001c0016t0026g0322 a0001c0016t0026g0323 |
3 | HG02451.hp2 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.717+16893T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051036 | |||||||
| chr9:38051052 | T | G | 1 | a0001c0004t0003g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.717+16877A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051052 | |||||||
| chr9:38051128 | T | C | 1 | a0001c0002t0004g0137 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.717+16801A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051128 | |||||||
| chr9:38051234 | G | A | 1 | a0001c0004t0003g0141 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.717+16695C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051234 | |||||||
| chr9:38051237 | C | T | 1 | a0001c0005t0069g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.717+16692G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051237 | |||||||
| chr9:38051313 | C | G | 4 | a0001c0002t0001g0002 a0001c0002t0001g0161 a0001c0002t0001g0162 others(1): Show |
5 | HG00639.hp1 HG01074.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+16616G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051313 | |||||||
| chr9:38051314 | A | G | 4 | a0001c0002t0001g0002 a0001c0002t0001g0161 a0001c0002t0001g0162 others(1): Show |
5 | HG00639.hp1 HG01074.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+16615T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051314 | |||||||
| chr9:38051315 | T | C | 4 | a0001c0002t0001g0002 a0001c0002t0001g0161 a0001c0002t0001g0162 others(1): Show |
5 | HG00639.hp1 HG01074.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+16614A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051315 | |||||||
| chr9:38051440 | T | TA | 12 | a0001c0001t0001g0230 a0001c0001t0001g0241 a0001c0001t0001g0275 others(9): Show |
12 | HG02083.hp1 HG02083.hp2 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.717+16488dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051440 | |||||||
| chr9:38051440 | TA | T | 119 | a0001c0001t0001g0201 a0001c0001t0002g0290 a0001c0002t0001g0002 others(116): Show |
121 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.717+16488delT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051440 | |||||||
| chr9:38051440 | TAA | T | 16 | a0001c0002t0001g0072 a0001c0002t0001g0084 a0001c0002t0001g0147 others(13): Show |
16 | HG00735.hp2 HG01099.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.717+16487_717+1648 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051440 | |||||||
| chr9:38051750 | G | A | 1 | a0001c0005t0006g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.717+16179C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051750 | |||||||
| chr9:38051765 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0231 others(2): Show |
5 | HG02015.hp2 HG02155.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+16164C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38051765 | |||||||
| chr9:38052230 | C | G | 3 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0002g0281 |
3 | HG02257.hp1 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.717+15699G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38052230 | |||||||
| chr9:38052306 | A | G | 1 | a0001c0001t0064g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.717+15623T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38052306 | |||||||
| chr9:38052327 | C | G | 5 | a0001c0002t0004g0129 a0001c0002t0004g0130 a0001c0002t0057g0128 others(2): Show |
5 | HG00099.hp2 HG00738.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+15602G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38052327 | |||||||
| chr9:38052393 | G | A | 8 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(5): Show |
8 | HG02622.hp1 HG02717.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+15536C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38052393 | |||||||
| chr9:38052498 | G | A | 1 | a0001c0006t0032g0024 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.717+15431C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38052498 | |||||||
| chr9:38052502 | G | A | 3 | a0001c0005t0011g0054 a0001c0005t0011g0055 a0001c0005t0011g0056 |
3 | NA18957.hp1 NA18960.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.717+15427C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38052502 | |||||||
| chr9:38052858 | T | C | 4 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(1): Show |
4 | HG01175.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+15071A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38052858 | |||||||
| chr9:38053021 | C | T | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.717+14908G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38053021 | |||||||
| chr9:38053102 | C | CCT | 140 | a0001c0002t0001g0002 a0001c0002t0001g0072 a0001c0002t0001g0073 others(137): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.717+14826_717+1482 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38053102 | |||||||
| chr9:38053184 | G | A | 1 | a0001c0001t0002g0304 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.717+14745C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38053184 | |||||||
| chr9:38053240 | G | T | 3 | a0001c0005t0001g0069 a0001c0005t0001g0076 a0001c0005t0047g0068 |
3 | HG02109.hp1 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.717+14689C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38053240 | |||||||
| chr9:38053514 | G | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.717+14415C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38053514 | |||||||
| chr9:38053661 | C | T | 1 | a0001c0001t0064g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.717+14268G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38053661 | |||||||
| chr9:38053975 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.717+13954C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38053975 | |||||||
| chr9:38054025 | G | GA | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+13903dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38054025 | |||||||
| chr9:38054102 | A | G | 1 | a0001c0002t0002g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.717+13827T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38054102 | |||||||
| chr9:38054152 | G | A | 3 | a0001c0005t0011g0054 a0001c0005t0011g0055 a0001c0005t0011g0056 |
3 | NA18957.hp1 NA18960.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.717+13777C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38054152 | |||||||
| chr9:38054489 | G | A | 1 | a0001c0002t0001g0164 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.717+13440C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38054489 | |||||||
| chr9:38054620 | T | C | 3 | a0001c0003t0008g0065 a0001c0003t0008g0066 a0001c0005t0069g0078 |
3 | HG02895.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.717+13309A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38054620 | |||||||
| chr9:38054730 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.717+13199C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38054730 | |||||||
| chr9:38054837 | A | G | 4 | a0001c0004t0009g0006 a0001c0004t0009g0007 a0001c0004t0009g0008 others(1): Show |
4 | HG01123.hp1 HG01175.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+13092T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38054837 | |||||||
| chr9:38055104 | T | C | 3 | a0001c0004t0068g0181 a0001c0016t0026g0322 a0001c0016t0026g0323 |
3 | HG02451.hp2 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.717+12825A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38055104 | |||||||
| chr9:38055131 | A | G | 214 | a0001c0001t0001g0250 a0001c0001t0001g0254 a0001c0001t0001g0265 others(211): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.717+12798T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38055131 | |||||||
| chr9:38055381 | G | GA | 4 | a0001c0001t0048g0235 a0001c0001t0063g0234 a0001c0002t0001g0099 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+12547dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38055381 | |||||||
| chr9:38055434 | C | T | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.717+12495G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38055434 | |||||||
| chr9:38055441 | G | A | 1 | a0001c0002t0019g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.717+12488C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38055441 | |||||||
| chr9:38055509 | A | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02015.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.717+12420T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38055509 | |||||||
| chr9:38055601 | T | C | 3 | a0001c0004t0049g0077 a0001c0015t0018g0192 a0001c0015t0018g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.717+12328A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38055601 | |||||||
| chr9:38055792 | C | G | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+12137G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38055792 | |||||||
| chr9:38055922 | T | A | 63 | a0001c0002t0001g0002 a0001c0002t0001g0083 a0001c0002t0001g0084 others(60): Show |
65 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.717+12007A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38055922 | |||||||
| chr9:38056213 | T | C | 1 | a0001c0001t0044g0276 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.717+11716A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38056213 | |||||||
| chr9:38056262 | G | A | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.717+11667C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38056262 | |||||||
| chr9:38056293 | C | T | 24 | a0001c0003t0002g0140 a0001c0004t0001g0115 a0001c0004t0003g0058 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.717+11636G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38056293 | |||||||
| chr9:38056317 | T | C | 1 | a0001c0001t0002g0317 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.717+11612A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38056317 | |||||||
| chr9:38056577 | C | T | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+11352G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38056577 | |||||||
| chr9:38056630 | A | G | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.717+11299T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38056630 | |||||||
| chr9:38056869 | T | C | 1 | a0001c0001t0045g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.717+11060A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38056869 | |||||||
| chr9:38057022 | C | T | 4 | a0001c0005t0007g0040 a0001c0005t0007g0041 a0001c0005t0007g0042 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+10907G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057022 | |||||||
| chr9:38057140 | G | A | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+10789C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057140 | |||||||
| chr9:38057164 | A | T | 1 | a0001c0001t0002g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.717+10765T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057164 | |||||||
| chr9:38057165 | G | T | 1 | a0001c0001t0002g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.717+10764C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057165 | |||||||
| chr9:38057311 | C | CAT | 7 | a0001c0003t0001g0169 a0001c0003t0016g0016 a0001c0003t0016g0017 others(4): Show |
7 | HG02083.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+10616_717+1061 others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057311 | |||||||
| chr9:38057335 | T | C | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.717+10594A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057335 | |||||||
| chr9:38057339 | T | C | 2 | a0001c0001t0001g0237 a0001c0001t0001g0284 |
2 | NA18957.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.717+10590A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057339 | |||||||
| chr9:38057341 | G | C | 1 | a0006c0025t0042g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.717+10588C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057341 | |||||||
| chr9:38057369 | G | A | 39 | a0001c0001t0001g0252 a0001c0002t0001g0064 a0001c0002t0001g0080 others(36): Show |
39 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.717+10560C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057369 | |||||||
| chr9:38057452 | T | A | 2 | a0001c0023t0066g0183 a0007c0022t0065g0182 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.717+10477A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057452 | |||||||
| chr9:38057532 | G | A | 4 | a0001c0005t0007g0040 a0001c0005t0007g0041 a0001c0005t0007g0042 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+10397C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057532 | |||||||
| chr9:38057594 | G | A | 4 | a0001c0002t0001g0064 a0001c0002t0002g0062 a0001c0002t0014g0063 others(1): Show |
4 | HG00544.hp2 HG00673.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+10335C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057594 | |||||||
| chr9:38057606 | C | T | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+10323G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057606 | |||||||
| chr9:38057610 | C | T | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.717+10319G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057610 | |||||||
| chr9:38057731 | A | G | 1 | a0001c0001t0002g0288 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.717+10198T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057731 | |||||||
| chr9:38057748 | G | A | 1 | a0001c0003t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.717+10181C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057748 | |||||||
| chr9:38057764 | T | C | 1 | a0001c0002t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.717+10165A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057764 | |||||||
| chr9:38057857 | G | A | 1 | a0001c0003t0023g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.717+10072C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057857 | |||||||
| chr9:38057865 | C | G | 2 | a0004c0018t0017g0248 a0004c0018t0017g0249 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.717+10064G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057865 | |||||||
| chr9:38057973 | C | T | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+9956G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38057973 | |||||||
| chr9:38058000 | G | C | 3 | a0001c0002t0001g0136 a0001c0002t0004g0137 a0001c0002t0004g0170 |
3 | HG01070.hp2 HG01071.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.717+9929C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058000 | |||||||
| chr9:38058305 | A | G | 142 | a0001c0001t0001g0254 a0001c0002t0001g0002 a0001c0002t0001g0072 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.717+9624T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058305 | |||||||
| chr9:38058427 | C | T | 213 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0272 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.717+9502G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058427 | |||||||
| chr9:38058525 | T | C | 1 | a0001c0002t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.717+9404A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058525 | |||||||
| chr9:38058581 | G | A | 64 | a0001c0002t0001g0002 a0001c0002t0001g0083 a0001c0002t0001g0084 others(61): Show |
66 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.717+9348C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058581 | |||||||
| chr9:38058645 | C | T | 1 | a0001c0002t0057g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.717+9284G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058645 | |||||||
| chr9:38058668 | G | A | 68 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0272 others(65): Show |
71 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.717+9261C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058668 | |||||||
| chr9:38058700 | G | A | 2 | a0001c0003t0008g0065 a0001c0003t0008g0066 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.717+9229C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058700 | |||||||
| chr9:38058754 | T | C | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.717+9175A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058754 | |||||||
| chr9:38058758 | T | A | 1 | a0001c0007t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.717+9171A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058758 | |||||||
| chr9:38058890 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.717+9039G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38058890 | |||||||
| chr9:38059116 | C | CTGAA | 4 | a0001c0001t0002g0277 a0001c0003t0002g0180 a0001c0004t0049g0077 others(1): Show |
4 | HG02486.hp1 HG02717.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+8809_717+8812d others(6): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059116 | |||||||
| chr9:38059227 | T | C | 6 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0004t0028g0018 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+8702A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059227 | |||||||
| chr9:38059228 | T | C | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.717+8701A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059228 | |||||||
| chr9:38059254 | T | C | 9 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.717+8675A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059254 | |||||||
| chr9:38059264 | C | T | 12 | a0001c0002t0001g0133 a0001c0002t0001g0136 a0001c0002t0004g0129 others(9): Show |
12 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.717+8665G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059264 | |||||||
| chr9:38059349 | T | G | 1 | a0001c0005t0001g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.717+8580A>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059349 | |||||||
| chr9:38059458 | G | C | 1 | a0001c0001t0039g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.717+8471C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059458 | |||||||
| chr9:38059721 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.717+8208C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059721 | |||||||
| chr9:38059733 | T | C | 3 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0002g0281 |
3 | HG02257.hp1 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.717+8196A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059733 | |||||||
| chr9:38059810 | G | A | 3 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0064g0238 |
3 | HG02698.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.717+8119C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059810 | |||||||
| chr9:38059891 | A | G | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.717+8038T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059891 | |||||||
| chr9:38059898 | G | A | 20 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(17): Show |
20 | HG01109.hp2 HG01175.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.717+8031C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38059898 | |||||||
| chr9:38060056 | A | G | 4 | a0001c0017t0025g0305 a0001c0017t0025g0306 a0001c0023t0066g0183 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+7873T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060056 | |||||||
| chr9:38060186 | A | T | 1 | a0001c0002t0001g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.717+7743T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060186 | |||||||
| chr9:38060232 | T | A | 3 | a0001c0001t0001g0239 a0001c0001t0001g0241 a0001c0001t0051g0240 |
3 | HG02135.hp2 NA18995.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.717+7697A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060232 | |||||||
| chr9:38060364 | A | G | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.717+7565T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060364 | |||||||
| chr9:38060428 | C | T | 1 | a0001c0011t0056g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.717+7501G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060428 | |||||||
| chr9:38060489 | T | C | 1 | a0001c0001t0043g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.717+7440A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060489 | |||||||
| chr9:38060637 | T | A | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+7292A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060637 | |||||||
| chr9:38060814 | C | A | 1 | a0001c0001t0002g0317 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.717+7115G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060814 | |||||||
| chr9:38060881 | A | G | 1 | a0001c0004t0003g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.717+7048T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060881 | |||||||
| chr9:38060916 | C | G | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+7013G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060916 | |||||||
| chr9:38060950 | T | C | 1 | a0001c0001t0002g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.717+6979A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060950 | |||||||
| chr9:38060971 | T | C | 133 | a0001c0002t0001g0002 a0001c0002t0001g0072 a0001c0002t0001g0073 others(130): Show |
135 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.717+6958A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38060971 | |||||||
| chr9:38061103 | A | G | 141 | a0001c0002t0001g0002 a0001c0002t0001g0072 a0001c0002t0001g0073 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.717+6826T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38061103 | |||||||
| chr9:38061311 | C | CA | 8 | a0001c0001t0071g0243 a0001c0003t0016g0016 a0001c0003t0016g0017 others(5): Show |
8 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+6617dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38061311 | |||||||
| chr9:38061311 | CA | C | 6 | a0001c0001t0001g0201 a0001c0003t0001g0116 a0001c0003t0008g0066 others(3): Show |
6 | HG01069.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+6617delT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38061311 | |||||||
| chr9:38061436 | C | T | 1 | a0001c0004t0003g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.717+6493G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38061436 | |||||||
| chr9:38061588 | G | A | 1 | a0001c0008t0002g0026 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.717+6341C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38061588 | |||||||
| chr9:38061617 | T | C | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.717+6312A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38061617 | |||||||
| chr9:38061684 | G | A | 3 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0002g0281 |
3 | HG02257.hp1 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.717+6245C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38061684 | |||||||
| chr9:38061908 | A | T | 1 | a0001c0003t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.717+6021T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38061908 | |||||||
| chr9:38061955 | C | T | 1 | a0001c0011t0003g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.717+5974G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38061955 | |||||||
| chr9:38062308 | G | A | 1 | a0001c0013t0008g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.717+5621C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062308 | |||||||
| chr9:38062360 | G | T | 1 | a0001c0002t0004g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.717+5569C>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062360 | |||||||
| chr9:38062430 | T | C | 23 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(20): Show |
23 | HG01109.hp2 HG01175.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.717+5499A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062430 | |||||||
| chr9:38062468 | C | T | 7 | a0001c0003t0001g0081 a0001c0003t0001g0116 a0001c0003t0001g0117 others(4): Show |
7 | HG02083.hp2 HG02129.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+5461G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062468 | |||||||
| chr9:38062501 | C | T | 1 | a0001c0004t0009g0007 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.717+5428G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062501 | |||||||
| chr9:38062519 | GA | G | 4 | a0001c0005t0007g0040 a0001c0005t0007g0041 a0001c0005t0007g0042 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+5409delT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062519 | |||||||
| chr9:38062578 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.717+5351G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062578 | |||||||
| chr9:38062633 | G | A | 1 | a0001c0002t0058g0166 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.717+5296C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062633 | |||||||
| chr9:38062828 | T | C | 2 | a0001c0003t0002g0167 a0001c0003t0023g0168 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.717+5101A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062828 | |||||||
| chr9:38062964 | T | A | 1 | a0001c0013t0008g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.717+4965A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38062964 | |||||||
| chr9:38063100 | C | A | 3 | a0001c0008t0002g0027 a0001c0008t0002g0029 a0001c0008t0055g0028 |
3 | HG01891.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.717+4829G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063100 | |||||||
| chr9:38063236 | C | A | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+4693G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063236 | |||||||
| chr9:38063345 | A | G | 1 | a0001c0017t0025g0305 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.717+4584T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063345 | |||||||
| chr9:38063380 | A | G | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+4549T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063380 | |||||||
| chr9:38063533 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.717+4396G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063533 | |||||||
| chr9:38063605 | G | C | 213 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0272 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.717+4324C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063605 | |||||||
| chr9:38063658 | C | G | 1 | a0001c0003t0030g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+4271G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063658 | |||||||
| chr9:38063676 | C | T | 1 | a0001c0011t0056g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.717+4253G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063676 | |||||||
| chr9:38063719 | T | C | 2 | a0001c0003t0002g0179 a0001c0003t0002g0180 |
2 | HG02080.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.717+4210A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063719 | |||||||
| chr9:38063770 | G | C | 3 | a0001c0005t0011g0054 a0001c0005t0011g0055 a0001c0005t0011g0056 |
3 | NA18957.hp1 NA18960.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.717+4159C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063770 | |||||||
| chr9:38063795 | G | GT | 50 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.717+4133dupA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063795 | |||||||
| chr9:38063795 | GT | G | 99 | a0001c0001t0001g0250 a0001c0001t0001g0252 a0001c0001t0001g0254 others(96): Show |
102 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.717+4133delA | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063795 | |||||||
| chr9:38063795 | GTT | G | 9 | a0001c0001t0002g0282 a0001c0001t0002g0312 a0001c0003t0001g0057 others(6): Show |
9 | HG00323.hp1 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.717+4132_717+4133d others(4): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063795 | |||||||
| chr9:38063834 | T | C | 20 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(17): Show |
20 | HG01109.hp2 HG01175.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.717+4095A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063834 | |||||||
| chr9:38063872 | A | T | 22 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0087 others(19): Show |
22 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.717+4057T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38063872 | |||||||
| chr9:38064069 | A | G | 3 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 |
3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.717+3860T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38064069 | |||||||
| chr9:38064402 | A | G | 1 | a0001c0016t0026g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.717+3527T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38064402 | |||||||
| chr9:38064459 | G | A | 2 | a0001c0001t0020g0283 a0001c0001t0073g0325 |
2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.717+3470C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38064459 | |||||||
| chr9:38064474 | CAT | C | 4 | a0001c0004t0009g0006 a0001c0004t0009g0007 a0001c0004t0009g0008 others(1): Show |
4 | HG01123.hp1 HG01175.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+3453_717+3454d others(4): Show |
SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38064474 | |||||||
| chr9:38064524 | G | A | 1 | a0001c0004t0007g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.717+3405C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38064524 | |||||||
| chr9:38064669 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.717+3260C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38064669 | |||||||
| chr9:38064940 | C | G | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.717+2989G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38064940 | |||||||
| chr9:38065026 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.717+2903C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065026 | |||||||
| chr9:38065032 | T | C | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.717+2897A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065032 | |||||||
| chr9:38065234 | C | G | 1 | a0001c0001t0002g0288 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.717+2695G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065234 | |||||||
| chr9:38065466 | G | C | 1 | a0001c0003t0001g0057 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.717+2463C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065466 | |||||||
| chr9:38065498 | G | A | 1 | a0001c0002t0001g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.717+2431C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065498 | |||||||
| chr9:38065557 | C | T | 1 | a0001c0004t0003g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.717+2372G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065557 | |||||||
| chr9:38065575 | G | C | 1 | a0001c0001t0020g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.717+2354C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065575 | |||||||
| chr9:38065598 | G | C | 31 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(28): Show |
31 | HG01109.hp2 HG01175.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.717+2331C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065598 | |||||||
| chr9:38065705 | G | C | 1 | a0001c0006t0067g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.717+2224C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065705 | |||||||
| chr9:38065724 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.717+2205A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065724 | |||||||
| chr9:38065764 | G | A | 4 | a0001c0008t0002g0026 a0001c0008t0002g0027 a0001c0008t0002g0029 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+2165C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065764 | |||||||
| chr9:38065937 | T | C | 2 | a0001c0015t0018g0192 a0001c0015t0018g0193 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.717+1992A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065937 | |||||||
| chr9:38065957 | C | A | 1 | a0001c0002t0041g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.717+1972G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065957 | |||||||
| chr9:38065975 | C | A | 18 | a0001c0001t0001g0291 a0001c0001t0002g0288 a0001c0001t0002g0289 others(15): Show |
18 | HG00544.hp1 HG00673.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.717+1954G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38065975 | |||||||
| chr9:38066156 | T | C | 2 | a0001c0017t0025g0305 a0001c0017t0025g0306 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.717+1773A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066156 | |||||||
| chr9:38066184 | T | A | 1 | a0001c0004t0049g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.717+1745A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066184 | |||||||
| chr9:38066251 | A | T | 1 | a0001c0003t0001g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.717+1678T>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066251 | |||||||
| chr9:38066325 | C | A | 2 | a0001c0002t0040g0176 a0001c0024t0002g0186 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.717+1604G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066325 | |||||||
| chr9:38066426 | C | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG02698.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.717+1503G>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066426 | |||||||
| chr9:38066439 | T | C | 1 | a0001c0005t0001g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.717+1490A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066439 | |||||||
| chr9:38066556 | T | C | 8 | a0001c0002t0040g0176 a0001c0003t0016g0016 a0001c0003t0016g0017 others(5): Show |
8 | HG01496.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+1373A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066556 | |||||||
| chr9:38066575 | G | A | 1 | a0001c0004t0003g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.717+1354C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066575 | |||||||
| chr9:38066602 | C | G | 1 | a0001c0004t0009g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.717+1327G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066602 | |||||||
| chr9:38066623 | T | C | 1 | a0001c0003t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.717+1306A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066623 | |||||||
| chr9:38066722 | T | C | 5 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0003t0029g0015 others(2): Show |
5 | HG02717.hp1 HG02895.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+1207A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066722 | |||||||
| chr9:38066811 | C | T | 22 | a0001c0003t0001g0057 a0001c0003t0002g0053 a0001c0005t0005g0044 others(19): Show |
22 | HG00323.hp1 HG02451.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.717+1118G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38066811 | |||||||
| chr9:38067053 | G | C | 11 | a0001c0001t0001g0310 a0001c0001t0002g0309 a0001c0001t0002g0311 others(8): Show |
11 | HG02080.hp1 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.717+876C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067053 | |||||||
| chr9:38067070 | G | A | 1 | a0001c0005t0069g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.717+859C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067070 | |||||||
| chr9:38067114 | G | A | 11 | a0001c0006t0010g0020 a0001c0006t0010g0022 a0001c0006t0010g0023 others(8): Show |
11 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.717+815C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067114 | |||||||
| chr9:38067346 | G | C | 14 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(11): Show |
14 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.717+583C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067346 | |||||||
| chr9:38067391 | T | C | 5 | a0001c0001t0001g0314 a0001c0001t0002g0313 a0001c0001t0002g0315 others(2): Show |
5 | HG01070.hp1 HG01978.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+538A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067391 | |||||||
| chr9:38067468 | G | C | 2 | a0001c0002t0001g0080 a0001c0002t0002g0079 |
2 | HG01109.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.717+461C>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067468 | |||||||
| chr9:38067469 | T | A | 54 | a0001c0002t0001g0064 a0001c0002t0001g0072 a0001c0002t0001g0073 others(51): Show |
55 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.717+460A>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067469 | |||||||
| chr9:38067630 | T | C | 1 | a0001c0007t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.717+299A>G | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067630 | |||||||
| chr9:38067635 | C | T | 60 | a0001c0002t0001g0064 a0001c0002t0001g0072 a0001c0002t0001g0073 others(57): Show |
61 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.717+294G>A | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067635 | |||||||
| chr9:38067651 | A | G | 18 | a0001c0006t0010g0019 a0001c0006t0010g0020 a0001c0006t0010g0022 others(15): Show |
18 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.717+278T>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067651 | |||||||
| chr9:38067659 | G | A | 3 | a0001c0004t0068g0181 a0001c0023t0066g0183 a0007c0022t0065g0182 |
3 | HG02818.hp1 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.717+270C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067659 | |||||||
| chr9:38067703 | G | A | 5 | a0001c0013t0008g0189 a0001c0013t0008g0190 a0001c0013t0008g0191 others(2): Show |
5 | HG02622.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+226C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067703 | |||||||
| chr9:38067879 | G | A | 2 | a0001c0003t0001g0185 a0009c0021t0034g0184 |
2 | NA18971.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.717+50C>T | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067879 | |||||||
| chr9:38067901 | C | G | 4 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0003t0029g0015 others(1): Show |
4 | HG02895.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+28G>C | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067901 | |||||||
| chr9:38067914 | C | CA | 4 | a0001c0003t0016g0016 a0001c0003t0016g0017 a0001c0003t0029g0015 others(1): Show |
4 | HG02895.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+14dupT | SHB | ENSG00000107338.10 | transcript | ENST00000377707.4 | protein_coding | 1/5 | chr9 | 38067914 |