Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6450 |
| ensemblid | ENSG00000185437.16 |
| hgncid | 10822 |
| symbol | SH3BGR |
| name | SH3 domain binding glutamate rich protein |
| refseq_nuc | NM_007341.3 |
| refseq_prot | NP_031367.2 |
| ensembl_nuc | ENST00000333634.10 |
| ensembl_prot | ENSP00000332513.5 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 39451970 |
| end | 39515504 |
| strand | + |
| ver | v1.2 |
| region | chr21:39451970-39515504 |
| region5000 | chr21:39446970-39520504 |
| regionname0 | SH3BGR_chr21_39451970_39515504 |
| regionname5000 | SH3BGR_chr21_39446970_39520504 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 177 | 159 | 46 | 29 | 55 | 9 | 20 | 39 | SH3BGR_chr21_39446970_39520504 | SH3BGR | MVIKV others(172): Show |
chr21 | 39446970 | 39520504 |
| a0002 | 1/1 | 176 | 135 | 30 | 27 | 51 | 6 | 19 | 39 | SH3BGR_chr21_39446970_39520504 | SH3BGR | MVIKV others(171): Show |
chr21 | 39446970 | 39520504 |
| a0003 | 0/0 | 177 | 6 | 3 | 2 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | MVIKV others(172): Show |
chr21 | 39446970 | 39520504 |
| a0004 | 0/0 | 176 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | MVIKV others(171): Show |
chr21 | 39446970 | 39520504 |
| a0005 | 0/0 | 177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | MVIKV others(172): Show |
chr21 | 39446970 | 39520504 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 531 | 159 | 46 | 29 | 55 | 9 | 20 | SH3BGR_chr21_39446970_39520504 | SH3BGR | ATGGT others(526): Show |
chr21 | 39446970 | 39520504 | ||
| a0002c0002 | 1/1 | 528 | 135 | 30 | 27 | 51 | 6 | 19 | SH3BGR_chr21_39446970_39520504 | SH3BGR | ATGGT others(523): Show |
chr21 | 39446970 | 39520504 | ||
| a0003c0003 | 0/0 | 531 | 6 | 3 | 2 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | ATGGT others(526): Show |
chr21 | 39446970 | 39520504 | ||
| a0004c0004 | 0/0 | 528 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | ATGGT others(523): Show |
chr21 | 39446970 | 39520504 | ||
| a0005c0005 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | ATGGT others(526): Show |
chr21 | 39446970 | 39520504 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1112 | 128 | 20 | 25 | 54 | 9 | 20 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1107): Show |
chr21 | 39446970 | 39520504 |
| a0001c0001t0002 | 0/0 | 1112 | 3 | 2 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1107): Show |
chr21 | 39446970 | 39520504 |
| a0001c0001t0003 | 0/0 | 1111 | 10 | 10 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1106): Show |
chr21 | 39446970 | 39520504 |
| a0001c0001t0004 | 0/0 | 1111 | 3 | 2 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1106): Show |
chr21 | 39446970 | 39520504 |
| a0001c0001t0005 | 0/0 | 1112 | 7 | 7 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1107): Show |
chr21 | 39446970 | 39520504 |
| a0001c0001t0006 | 0/0 | 1112 | 5 | 5 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1107): Show |
chr21 | 39446970 | 39520504 |
| a0001c0001t0009 | 0/0 | 1112 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1107): Show |
chr21 | 39446970 | 39520504 |
| a0001c0001t0010 | 0/0 | 1112 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1107): Show |
chr21 | 39446970 | 39520504 |
| a0001c0001t0011 | 0/0 | 1112 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1107): Show |
chr21 | 39446970 | 39520504 |
| a0002c0002t0001 | 0/0 | 1109 | 97 | 20 | 14 | 45 | 3 | 15 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1104): Show |
chr21 | 39446970 | 39520504 |
| a0002c0002t0002 | 0/1 | 1109 | 34 | 10 | 11 | 5 | 3 | 4 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1104): Show |
chr21 | 39446970 | 39520504 |
| a0002c0002t0007 | 1/0 | 1109 | 3 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1104): Show |
chr21 | 39446970 | 39520504 |
| a0002c0002t0008 | 0/0 | 1109 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1104): Show |
chr21 | 39446970 | 39520504 |
| a0003c0003t0003 | 0/0 | 1111 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1106): Show |
chr21 | 39446970 | 39520504 |
| a0003c0003t0004 | 0/0 | 1111 | 5 | 2 | 2 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1106): Show |
chr21 | 39446970 | 39520504 |
| a0004c0004t0001 | 0/0 | 1109 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1104): Show |
chr21 | 39446970 | 39520504 |
| a0005c0005t0001 | 0/0 | 1112 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | AGTGG others(1107): Show |
chr21 | 39446970 | 39520504 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0006g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0009g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0011g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0253 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0007g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0007g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0004c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0005c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | GBR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00140 | hp1 | a0004 | c0004 | t0001 | g0206 | EUR | GBR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0248 | EUR | FIN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0205 | EUR | FIN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0089 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00642 | hp1 | a0003 | c0003 | t0004 | g0239 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0268 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0271 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00735 | hp2 | a0003 | c0003 | t0004 | g0277 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0078 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0249 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0242 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0276 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0262 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01358 | hp2 | a0002 | c0002 | t0007 | g0147 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0250 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0251 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01433 | hp2 | a0002 | c0002 | t0007 | g0148 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0275 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0274 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0269 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02074 | hp2 | a0002 | c0002 | t0008 | g0011 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | CDX | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0265 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0233 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02630 | hp1 | a0003 | c0003 | t0004 | g0278 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02717 | hp2 | a0003 | c0003 | t0004 | g0241 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0192 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0270 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0254 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0145 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0232 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0272 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0231 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0186 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0109 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0243 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0259 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0220 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03209 | hp1 | a0005 | c0005 | t0001 | g0224 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0236 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0260 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0203 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0164 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03688 | hp2 | a0003 | c0003 | t0004 | g0240 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0211 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0247 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0021 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0193 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | YRI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | YRI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | CHB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19010 | hp2 | a0001 | c0001 | t0010 | g0140 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0264 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | YRI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ASW | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | TSI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0204 | SAS | GIH | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0163 | SAS | GIH | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0237 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | USA | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0229 | AFR | USA | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0253 | REF | REF | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0007 | g0151 | REF | REF | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:39499884 | T | C | 2 | a0001 a0004 |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
missense_variant | MODERATE | c.374T>C | p.Val125Ala | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/7 | 501/1109 | 374/531 | 125/176 | chr21 | 39499884 | |||
| chr21:39511719 | G | A | 1 | a0005 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.475G>A | p.Glu159Lys | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/7 | 602/1109 | 475/531 | 159/176 | chr21 | 39511719 | |||
| chr21:39511744 | G | GAGA | 3 | a0001 a0003 a0005 |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
disruptive_inframe_insertion | MODERATE | c.504_506dupAGA | p.Glu169dup | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/7 | 634/1109 | 507/531 | 169/176 | INFO_REALIGN_3_PRIME | chr21 | 39511744 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:39451976 | C | G | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(2): Show |
51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-121C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/7 | 121 | chr21 | 39451976 | ||||||
| chr21:39451977 | C | T | 1 | a0001c0001t0011 | 1 | HG01074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-120C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/7 | 120 | chr21 | 39451977 | ||||||
| chr21:39452055 | G | A | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(13): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
5_prime_UTR_variant | MODIFIER | c.-42G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/7 | 42 | chr21 | 39452055 | ||||||
| chr21:39452064 | G | A | 1 | a0002c0002t0008 | 1 | HG02074.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/7 | chr21 | 39452064 | |||||||
| chr21:39511785 | T | C | 4 | a0001c0001t0003 a0001c0001t0004 a0003c0003t0003 others(1): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*10T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/7 | 10 | chr21 | 39511785 | ||||||
| chr21:39515258 | C | A | 4 | a0001c0001t0003 a0001c0001t0004 a0003c0003t0003 others(1): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3483 | chr21 | 39515258 | ||||||
| chr21:39515296 | T | C | 1 | a0001c0001t0009 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*243T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3521 | chr21 | 39515296 | ||||||
| chr21:39515303 | AT | A | 4 | a0001c0001t0003 a0001c0001t0004 a0003c0003t0003 others(1): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*259delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3537 | INFO_REALIGN_3_PRIME | chr21 | 39515303 | |||||
| chr21:39515423 | T | C | 2 | a0001c0001t0005 a0001c0001t0006 |
12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*370T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3648 | chr21 | 39515423 | ||||||
| chr21:39515434 | A | T | 1 | a0001c0001t0010 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*381A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3659 | chr21 | 39515434 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:39452210 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.45+69A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452210 | |||||||
| chr21:39452235 | C | T | 44 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(41): Show |
46 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+94C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452235 | |||||||
| chr21:39452557 | G | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+416G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452557 | |||||||
| chr21:39452567 | T | G | 1 | a0002c0002t0002g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.45+426T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452567 | |||||||
| chr21:39452705 | A | G | 5 | a0001c0001t0006g0019 a0001c0001t0006g0231 a0001c0001t0006g0232 others(2): Show |
6 | HG02280.hp2 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+564A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452705 | |||||||
| chr21:39452716 | C | T | 1 | a0001c0001t0003g0230 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.45+575C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452716 | |||||||
| chr21:39452806 | C | A | 1 | a0002c0002t0002g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45+665C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452806 | |||||||
| chr21:39453017 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45+876G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453017 | |||||||
| chr21:39453084 | T | A | 1 | a0002c0002t0001g0023 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.45+943T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453084 | |||||||
| chr21:39453326 | C | T | 1 | a0003c0003t0004g0278 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.45+1185C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453326 | |||||||
| chr21:39453402 | TA | T | 44 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(41): Show |
46 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+1268delA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39453402 | ||||||
| chr21:39453409 | A | T | 4 | a0001c0001t0002g0235 a0001c0001t0004g0022 a0001c0001t0004g0229 others(1): Show |
5 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+1268A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453409 | |||||||
| chr21:39453525 | A | G | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.45+1384A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453525 | |||||||
| chr21:39453620 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.45+1479T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453620 | |||||||
| chr21:39453629 | T | C | 44 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(41): Show |
46 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+1488T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453629 | |||||||
| chr21:39453824 | G | T | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.45+1683G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453824 | |||||||
| chr21:39453882 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.45+1741A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453882 | |||||||
| chr21:39453957 | A | G | 1 | a0002c0002t0001g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.45+1816A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453957 | |||||||
| chr21:39454038 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.45+1897A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454038 | |||||||
| chr21:39454089 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.45+1948A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454089 | |||||||
| chr21:39454137 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(243): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.45+1996A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454137 | |||||||
| chr21:39454198 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.45+2057A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454198 | |||||||
| chr21:39454379 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.45+2238G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454379 | |||||||
| chr21:39454574 | C | A | 3 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 |
4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+2433C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454574 | |||||||
| chr21:39454600 | G | A | 1 | a0001c0001t0005g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.45+2459G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454600 | |||||||
| chr21:39454680 | C | G | 1 | a0003c0003t0004g0277 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.45+2539C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454680 | |||||||
| chr21:39454689 | T | C | 44 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(41): Show |
46 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+2548T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454689 | |||||||
| chr21:39454849 | G | A | 1 | a0002c0002t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+2708G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454849 | |||||||
| chr21:39454981 | A | C | 5 | a0001c0001t0001g0168 a0002c0002t0001g0012 a0002c0002t0001g0167 others(2): Show |
6 | HG01255.hp1 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+2840A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454981 | |||||||
| chr21:39455022 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45+2881G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455022 | |||||||
| chr21:39455416 | G | A | 3 | a0001c0001t0004g0022 a0001c0001t0004g0229 a0002c0002t0002g0018 |
4 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+3275G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455416 | |||||||
| chr21:39455430 | G | A | 42 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(39): Show |
48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.45+3289G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455430 | |||||||
| chr21:39455656 | G | A | 49 | a0001c0001t0002g0235 a0001c0001t0002g0246 a0001c0001t0002g0273 others(46): Show |
52 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+3515G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455656 | |||||||
| chr21:39455804 | G | A | 6 | a0001c0001t0004g0242 a0003c0003t0004g0239 a0003c0003t0004g0240 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+3663G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455804 | |||||||
| chr21:39455811 | A | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG00438.hp1 NA18983.hp2 NA19010.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+3670A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455811 | |||||||
| chr21:39456011 | C | T | 48 | a0001c0001t0002g0235 a0001c0001t0002g0246 a0001c0001t0002g0273 others(45): Show |
51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+3870C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456011 | |||||||
| chr21:39456219 | C | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.45+4078C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456219 | |||||||
| chr21:39456330 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+4189C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456330 | |||||||
| chr21:39456456 | T | C | 44 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(41): Show |
46 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+4315T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456456 | |||||||
| chr21:39456526 | A | G | 48 | a0001c0001t0002g0235 a0001c0001t0002g0246 a0001c0001t0002g0273 others(45): Show |
51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+4385A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456526 | |||||||
| chr21:39456557 | G | C | 44 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(41): Show |
46 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+4416G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456557 | |||||||
| chr21:39456572 | T | C | 48 | a0001c0001t0002g0235 a0001c0001t0002g0246 a0001c0001t0002g0273 others(45): Show |
51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+4431T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456572 | |||||||
| chr21:39456574 | G | A | 8 | a0002c0002t0001g0004 a0002c0002t0001g0027 a0002c0002t0001g0028 others(5): Show |
9 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+4433G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456574 | |||||||
| chr21:39456625 | A | AT | 48 | a0001c0001t0002g0235 a0001c0001t0002g0246 a0001c0001t0002g0273 others(45): Show |
51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+4484_45+4485ins others(1): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456625 | |||||||
| chr21:39456940 | GTTAA | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.45+4804_45+4807del others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39456940 | ||||||
| chr21:39457142 | A | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.45+5001A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457142 | |||||||
| chr21:39457231 | TAA | T | 3 | a0001c0001t0004g0022 a0001c0001t0004g0229 a0002c0002t0002g0018 |
4 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+5092_45+5093del others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457231 | ||||||
| chr21:39457244 | C | CTTA | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.45+5108_45+5110dup others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457244 | ||||||
| chr21:39457244 | C | CTTATATG others(1): Show |
47 | a0001c0001t0002g0235 a0001c0001t0002g0246 a0001c0001t0002g0273 others(44): Show |
50 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.45+5107_45+5108ins others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457244 | ||||||
| chr21:39457249 | T | A | 1 | a0003c0003t0004g0278 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.45+5108T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457249 | |||||||
| chr21:39457250 | A | T | 1 | a0003c0003t0004g0278 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.45+5109A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457250 | |||||||
| chr21:39457289 | TTATAA | T | 45 | a0001c0001t0002g0235 a0001c0001t0002g0246 a0001c0001t0002g0273 others(42): Show |
47 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.46-5081_46-5077del others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457289 | ||||||
| chr21:39457317 | A | G | 42 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(39): Show |
48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.46-5058A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457317 | |||||||
| chr21:39457372 | AGATTATT others(121): Show |
A | 4 | a0001c0001t0006g0019 a0001c0001t0006g0231 a0001c0001t0006g0232 others(1): Show |
5 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-4932_46-4805del | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457372 | ||||||
| chr21:39457449 | T | G | 1 | a0001c0001t0001g0222 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.46-4926T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457449 | |||||||
| chr21:39457460 | AT | A | 43 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.46-4913delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457460 | ||||||
| chr21:39457478 | ATATATAT others(36): Show |
A | 2 | a0002c0002t0002g0252 a0002c0002t0002g0256 |
2 | NA18950.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.46-4875_46-4833del others(43): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457478 | ||||||
| chr21:39457500 | T | A | 1 | a0002c0002t0001g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.46-4875T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457500 | |||||||
| chr21:39457856 | T | C | 2 | a0001c0001t0003g0172 a0002c0002t0002g0018 |
3 | HG01257.hp2 HG01258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.46-4519T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457856 | |||||||
| chr21:39457880 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.46-4495G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457880 | |||||||
| chr21:39457901 | G | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46-4474G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457901 | |||||||
| chr21:39457938 | A | C | 1 | a0001c0001t0005g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-4437A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457938 | |||||||
| chr21:39457960 | A | G | 3 | a0002c0002t0002g0274 a0002c0002t0002g0275 a0002c0002t0002g0276 |
3 | HG01169.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.46-4415A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457960 | |||||||
| chr21:39458015 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46-4360G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458015 | |||||||
| chr21:39458096 | G | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.46-4279G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458096 | |||||||
| chr21:39458135 | A | G | 44 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(41): Show |
46 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.46-4240A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458135 | |||||||
| chr21:39458206 | GCT | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.46-4166_46-4165del others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39458206 | ||||||
| chr21:39458350 | A | T | 47 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0022 others(44): Show |
50 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.46-4025A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458350 | |||||||
| chr21:39458351 | A | T | 3 | a0001c0001t0004g0022 a0001c0001t0004g0229 a0002c0002t0002g0018 |
4 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-4024A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458351 | |||||||
| chr21:39458412 | C | T | 3 | a0001c0001t0004g0022 a0001c0001t0004g0229 a0002c0002t0002g0018 |
4 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-3963C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458412 | |||||||
| chr21:39458431 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46-3944C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458431 | |||||||
| chr21:39458499 | A | G | 1 | a0002c0002t0001g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46-3876A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458499 | |||||||
| chr21:39458532 | T | C | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46-3843T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458532 | |||||||
| chr21:39458544 | G | A | 44 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(41): Show |
46 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.46-3831G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458544 | |||||||
| chr21:39458603 | G | C | 2 | a0002c0002t0002g0274 a0002c0002t0002g0275 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.46-3772G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458603 | |||||||
| chr21:39458647 | C | CT | 8 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG02698.hp2 HG03130.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-3711dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39458647 | ||||||
| chr21:39458647 | C | CTT | 42 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(39): Show |
44 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.46-3712_46-3711dup others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39458647 | ||||||
| chr21:39458772 | A | G | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-3603A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458772 | |||||||
| chr21:39458795 | C | T | 3 | a0002c0002t0001g0023 a0002c0002t0001g0144 a0002c0002t0001g0145 |
3 | HG02647.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.46-3580C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458795 | |||||||
| chr21:39458835 | C | T | 1 | a0002c0002t0001g0221 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-3540C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458835 | |||||||
| chr21:39458839 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-3536G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458839 | |||||||
| chr21:39459009 | A | G | 3 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 |
4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-3366A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459009 | |||||||
| chr21:39459624 | C | T | 1 | a0001c0001t0004g0242 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.46-2751C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459624 | |||||||
| chr21:39459690 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.46-2685C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459690 | |||||||
| chr21:39459720 | T | C | 1 | a0002c0002t0001g0146 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.46-2655T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459720 | |||||||
| chr21:39459775 | G | T | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-2600G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459775 | |||||||
| chr21:39459996 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.46-2379A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459996 | |||||||
| chr21:39460062 | G | A | 8 | a0002c0002t0001g0004 a0002c0002t0001g0027 a0002c0002t0001g0028 others(5): Show |
9 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-2313G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460062 | |||||||
| chr21:39460095 | A | G | 6 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-2280A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460095 | |||||||
| chr21:39460306 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(214): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.46-2069G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460306 | |||||||
| chr21:39460439 | T | C | 48 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(45): Show |
51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.46-1936T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460439 | |||||||
| chr21:39460520 | C | T | 39 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(36): Show |
46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.46-1855C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460520 | |||||||
| chr21:39460630 | C | T | 95 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.46-1745C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460630 | |||||||
| chr21:39460650 | A | G | 1 | a0002c0002t0001g0170 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.46-1725A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460650 | |||||||
| chr21:39461082 | A | G | 3 | a0002c0002t0001g0123 a0002c0002t0001g0124 a0002c0002t0001g0215 |
3 | HG02080.hp2 NA19009.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.46-1293A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461082 | |||||||
| chr21:39461113 | T | C | 42 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(39): Show |
49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.46-1262T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461113 | |||||||
| chr21:39461135 | A | AT | 26 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(23): Show |
26 | HG01109.hp1 HG01243.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.46-1220dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39461135 | ||||||
| chr21:39461135 | AT | A | 53 | a0001c0001t0001g0034 a0001c0001t0001g0125 a0001c0001t0001g0136 others(50): Show |
56 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.46-1220delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39461135 | ||||||
| chr21:39461231 | G | C | 1 | a0002c0002t0001g0187 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.46-1144G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461231 | |||||||
| chr21:39461261 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-1114C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461261 | |||||||
| chr21:39461438 | T | C | 2 | a0001c0001t0006g0231 a0001c0001t0006g0232 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.46-937T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461438 | |||||||
| chr21:39461760 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-615G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461760 | |||||||
| chr21:39461836 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.46-539A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461836 | |||||||
| chr21:39461994 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.46-381G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461994 | |||||||
| chr21:39462057 | C | A | 1 | a0002c0002t0001g0212 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.46-318C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462057 | |||||||
| chr21:39462138 | C | T | 2 | a0002c0002t0001g0211 a0002c0002t0001g0226 |
2 | HG03139.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.46-237C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462138 | |||||||
| chr21:39462139 | G | A | 1 | a0001c0001t0003g0230 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.46-236G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462139 | |||||||
| chr21:39462202 | G | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | NA18954.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.46-173G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462202 | |||||||
| chr21:39462216 | C | G | 4 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0108 others(1): Show |
4 | HG01884.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-159C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462216 | |||||||
| chr21:39462268 | C | G | 1 | a0001c0001t0005g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-107C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462268 | |||||||
| chr21:39462710 | A | G | 48 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(45): Show |
51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.231+150A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39462710 | |||||||
| chr21:39462923 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.231+363A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39462923 | |||||||
| chr21:39462978 | A | G | 96 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.231+418A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39462978 | |||||||
| chr21:39463173 | G | A | 1 | a0002c0002t0007g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.231+613G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463173 | |||||||
| chr21:39463382 | T | C | 1 | a0002c0002t0001g0188 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.231+822T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463382 | |||||||
| chr21:39463632 | T | G | 3 | a0002c0002t0001g0217 a0002c0002t0001g0218 a0002c0002t0001g0219 |
3 | HG01243.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.231+1072T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463632 | |||||||
| chr21:39463897 | A | G | 96 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.231+1337A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463897 | |||||||
| chr21:39463940 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.231+1380C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463940 | |||||||
| chr21:39464442 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.231+1882C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464442 | |||||||
| chr21:39464515 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.231+1955G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464515 | |||||||
| chr21:39464544 | G | A | 19 | a0001c0001t0002g0246 a0002c0002t0002g0020 a0002c0002t0002g0021 others(16): Show |
21 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.231+1984G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464544 | |||||||
| chr21:39464570 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.231+2010A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464570 | |||||||
| chr21:39464830 | A | G | 1 | a0002c0002t0001g0215 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.231+2270A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464830 | |||||||
| chr21:39464856 | A | G | 1 | a0002c0002t0001g0188 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.231+2296A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464856 | |||||||
| chr21:39464948 | G | T | 42 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(39): Show |
49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.231+2388G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464948 | |||||||
| chr21:39464950 | A | C | 96 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.231+2390A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464950 | |||||||
| chr21:39465342 | T | C | 96 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.231+2782T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465342 | |||||||
| chr21:39465344 | G | A | 1 | a0002c0002t0007g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.231+2784G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465344 | |||||||
| chr21:39465418 | G | T | 3 | a0002c0002t0001g0023 a0002c0002t0001g0144 a0002c0002t0001g0145 |
3 | HG02647.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.231+2858G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465418 | |||||||
| chr21:39465475 | C | A | 48 | a0001c0001t0002g0246 a0001c0001t0002g0273 a0001c0001t0004g0242 others(45): Show |
51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.231+2915C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465475 | |||||||
| chr21:39465781 | A | G | 42 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(39): Show |
49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.231+3221A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465781 | |||||||
| chr21:39465892 | C | T | 39 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(36): Show |
46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+3332C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465892 | |||||||
| chr21:39465925 | G | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231+3365G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465925 | |||||||
| chr21:39465944 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231+3384C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465944 | |||||||
| chr21:39466241 | C | G | 95 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.231+3681C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39466241 | |||||||
| chr21:39466516 | A | G | 95 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.231+3956A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39466516 | |||||||
| chr21:39466900 | A | AT | 7 | a0001c0001t0001g0037 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
8 | HG00558.hp2 HG00673.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.231+4350dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39466900 | ||||||
| chr21:39466900 | A | ATT | 39 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(36): Show |
45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.231+4349_231+4350d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39466900 | ||||||
| chr21:39467041 | T | C | 1 | a0003c0003t0004g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.231+4481T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467041 | |||||||
| chr21:39467136 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.231+4576C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467136 | |||||||
| chr21:39467258 | A | AT | 53 | a0001c0001t0001g0216 a0001c0001t0002g0235 a0001c0001t0002g0246 others(50): Show |
56 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.231+4707dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39467258 | ||||||
| chr21:39467296 | G | T | 39 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(36): Show |
46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+4736G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467296 | |||||||
| chr21:39467704 | T | G | 39 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 others(36): Show |
46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+5144T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467704 | |||||||
| chr21:39467743 | G | A | 1 | a0002c0002t0001g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.231+5183G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467743 | |||||||
| chr21:39467747 | A | G | 2 | a0002c0002t0002g0257 a0002c0002t0002g0258 |
2 | NA18985.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.231+5187A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467747 | |||||||
| chr21:39467822 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231+5262C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467822 | |||||||
| chr21:39467853 | A | G | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.231+5293A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467853 | |||||||
| chr21:39467896 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.231+5336C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467896 | |||||||
| chr21:39468282 | T | C | 11 | a0001c0001t0005g0238 a0002c0002t0001g0004 a0002c0002t0001g0027 others(8): Show |
12 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.231+5722T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468282 | |||||||
| chr21:39468596 | A | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0176 a0001c0001t0001g0177 others(8): Show |
12 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.231+6036A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468596 | |||||||
| chr21:39468678 | A | G | 112 | a0001c0001t0001g0013 a0001c0001t0001g0101 a0001c0001t0001g0112 others(109): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.231+6118A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468678 | |||||||
| chr21:39468701 | C | T | 29 | a0001c0001t0001g0100 a0001c0001t0001g0168 a0001c0001t0001g0210 others(26): Show |
32 | HG00408.hp1 HG01255.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.231+6141C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468701 | |||||||
| chr21:39468889 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.232-6246T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468889 | |||||||
| chr21:39468928 | C | T | 8 | a0002c0002t0001g0186 a0002c0002t0002g0247 a0002c0002t0002g0255 others(5): Show |
8 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.232-6207C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468928 | |||||||
| chr21:39468952 | T | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.232-6183T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468952 | |||||||
| chr21:39469011 | G | GT | 38 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(35): Show |
39 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.232-6108dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39469011 | ||||||
| chr21:39469011 | GT | G | 12 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0125 others(9): Show |
12 | HG00438.hp1 HG01169.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.232-6108delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39469011 | ||||||
| chr21:39469027 | TG | T | 4 | a0001c0001t0004g0022 a0002c0002t0002g0244 a0002c0002t0002g0269 others(1): Show |
4 | HG02055.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-6107delG | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469027 | |||||||
| chr21:39469174 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.232-5961C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469174 | |||||||
| chr21:39469220 | C | T | 12 | a0001c0001t0001g0112 a0001c0001t0003g0003 a0001c0001t0003g0025 others(9): Show |
13 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.232-5915C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469220 | |||||||
| chr21:39469277 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.232-5858T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469277 | |||||||
| chr21:39469353 | G | A | 93 | a0001c0001t0004g0242 a0001c0001t0005g0238 a0001c0001t0005g0261 others(90): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.232-5782G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469353 | |||||||
| chr21:39469387 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.232-5748C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469387 | |||||||
| chr21:39469587 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.232-5548A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469587 | |||||||
| chr21:39469629 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232-5506T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469629 | |||||||
| chr21:39469638 | TA | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.232-5494delA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39469638 | ||||||
| chr21:39469639 | A | T | 109 | a0001c0001t0001g0112 a0001c0001t0001g0223 a0001c0001t0002g0235 others(106): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.232-5496A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469639 | |||||||
| chr21:39469803 | C | T | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.232-5332C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469803 | |||||||
| chr21:39469811 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.232-5324C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469811 | |||||||
| chr21:39469858 | G | A | 17 | a0002c0002t0001g0043 a0002c0002t0002g0020 a0002c0002t0002g0236 others(14): Show |
18 | HG00280.hp2 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.232-5277G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469858 | |||||||
| chr21:39469943 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-5192G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469943 | |||||||
| chr21:39469947 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.232-5188T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469947 | |||||||
| chr21:39470019 | A | C | 1 | a0002c0002t0007g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.232-5116A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470019 | |||||||
| chr21:39470022 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.232-5113T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470022 | |||||||
| chr21:39470104 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.232-5031C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470104 | |||||||
| chr21:39470337 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232-4798C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470337 | |||||||
| chr21:39470371 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG01175.hp2 HG01261.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-4764G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470371 | |||||||
| chr21:39470534 | T | C | 93 | a0001c0001t0005g0238 a0001c0001t0005g0261 a0001c0001t0005g0263 others(90): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.232-4601T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470534 | |||||||
| chr21:39470591 | A | G | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-4544A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470591 | |||||||
| chr21:39470742 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232-4393T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470742 | |||||||
| chr21:39471170 | TTAA | T | 40 | a0002c0002t0001g0002 a0002c0002t0001g0014 a0002c0002t0001g0015 others(37): Show |
46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.232-3959_232-3957d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39471170 | ||||||
| chr21:39471224 | C | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.232-3911C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471224 | |||||||
| chr21:39471308 | G | A | 128 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(125): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.232-3827G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471308 | |||||||
| chr21:39471310 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0183 |
3 | HG02922.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.232-3825G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471310 | |||||||
| chr21:39471319 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.232-3816C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471319 | |||||||
| chr21:39471379 | G | A | 128 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(125): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.232-3756G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471379 | |||||||
| chr21:39471599 | GTTGT | G | 105 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(102): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.232-3517_232-3514d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39471599 | ||||||
| chr21:39471622 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.232-3513A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471622 | |||||||
| chr21:39471638 | T | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.232-3497T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471638 | |||||||
| chr21:39471639 | A | T | 1 | a0002c0002t0002g0254 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.232-3496A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471639 | |||||||
| chr21:39471777 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.232-3358A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471777 | |||||||
| chr21:39471811 | G | A | 6 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-3324G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471811 | |||||||
| chr21:39472033 | C | T | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.232-3102C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472033 | |||||||
| chr21:39472166 | CAG | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.232-2967_232-2966d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39472166 | ||||||
| chr21:39472170 | A | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.232-2965A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472170 | |||||||
| chr21:39472354 | A | G | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-2781A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472354 | |||||||
| chr21:39472374 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.232-2761T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472374 | |||||||
| chr21:39472819 | T | C | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-2316T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472819 | |||||||
| chr21:39472889 | CAT | C | 6 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-2245_232-2244d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472889 | |||||||
| chr21:39472917 | A | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.232-2218A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472917 | |||||||
| chr21:39473326 | T | G | 2 | a0001c0001t0001g0095 a0001c0001t0002g0246 |
2 | HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.232-1809T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39473326 | |||||||
| chr21:39473700 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.232-1435C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39473700 | |||||||
| chr21:39473884 | C | CA | 135 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(132): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.232-1240dupA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39473884 | ||||||
| chr21:39473884 | C | CAA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.232-1241_232-1240d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39473884 | ||||||
| chr21:39473994 | G | T | 1 | a0002c0002t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.232-1141G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39473994 | |||||||
| chr21:39474032 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232-1103A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474032 | |||||||
| chr21:39474258 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.232-877G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474258 | |||||||
| chr21:39474281 | G | C | 1 | a0002c0002t0001g0201 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.232-854G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474281 | |||||||
| chr21:39474685 | C | T | 1 | a0002c0002t0001g0165 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.232-450C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474685 | |||||||
| chr21:39474735 | A | G | 1 | a0001c0001t0003g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.232-400A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474735 | |||||||
| chr21:39474745 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.232-390C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474745 | |||||||
| chr21:39474881 | A | G | 6 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-254A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474881 | |||||||
| chr21:39474890 | G | GGT | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.232-229_232-228dup others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39474890 | ||||||
| chr21:39475085 | T | C | 94 | a0001c0001t0005g0238 a0001c0001t0005g0261 a0001c0001t0005g0263 others(91): Show |
104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.232-50T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39475085 | |||||||
| chr21:39475270 | A | G | 38 | a0001c0001t0005g0261 a0001c0001t0005g0263 a0001c0001t0005g0264 others(35): Show |
41 | HG00280.hp2 HG00642.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.312+55A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475270 | |||||||
| chr21:39475280 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.312+65G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475280 | |||||||
| chr21:39475293 | T | C | 1 | a0002c0002t0001g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.312+78T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475293 | |||||||
| chr21:39475323 | T | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.312+108T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475323 | |||||||
| chr21:39475439 | C | A | 1 | a0002c0002t0002g0248 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.312+224C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475439 | |||||||
| chr21:39475465 | G | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 |
4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+250G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475465 | |||||||
| chr21:39475509 | A | G | 3 | a0002c0002t0001g0217 a0002c0002t0001g0218 a0002c0002t0001g0219 |
3 | HG01243.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.312+294A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475509 | |||||||
| chr21:39475610 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.312+395C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475610 | |||||||
| chr21:39475688 | C | T | 40 | a0002c0002t0001g0002 a0002c0002t0001g0014 a0002c0002t0001g0015 others(37): Show |
46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.312+473C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475688 | |||||||
| chr21:39476153 | G | A | 2 | a0001c0001t0006g0231 a0001c0001t0006g0232 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.312+938G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476153 | |||||||
| chr21:39476248 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.312+1033T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476248 | |||||||
| chr21:39476579 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.312+1364G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476579 | |||||||
| chr21:39476673 | G | A | 1 | a0002c0002t0002g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.312+1458G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476673 | |||||||
| chr21:39476694 | C | T | 1 | a0002c0002t0002g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.312+1479C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476694 | |||||||
| chr21:39476741 | T | C | 129 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(126): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.312+1526T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476741 | |||||||
| chr21:39476935 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+1720A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476935 | |||||||
| chr21:39477501 | A | G | 12 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(9): Show |
13 | HG01168.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.312+2286A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477501 | |||||||
| chr21:39477515 | T | C | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+2300T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477515 | |||||||
| chr21:39477595 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+2380G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477595 | |||||||
| chr21:39477625 | C | T | 6 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.312+2410C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477625 | |||||||
| chr21:39477779 | A | G | 12 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(9): Show |
13 | HG01168.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.312+2564A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477779 | |||||||
| chr21:39477963 | C | A | 9 | a0002c0002t0001g0017 a0002c0002t0001g0126 a0002c0002t0001g0127 others(6): Show |
10 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+2748C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477963 | |||||||
| chr21:39478167 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.312+2952C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478167 | |||||||
| chr21:39478373 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
5 | HG02083.hp1 NA18950.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.312+3158C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478373 | |||||||
| chr21:39478463 | A | G | 1 | a0002c0002t0001g0212 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.312+3248A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478463 | |||||||
| chr21:39478481 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA18982.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.312+3266T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478481 | |||||||
| chr21:39478498 | G | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.312+3283G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478498 | |||||||
| chr21:39478520 | G | A | 1 | a0002c0002t0001g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.312+3305G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478520 | |||||||
| chr21:39478561 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.312+3346G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478561 | |||||||
| chr21:39478602 | G | A | 17 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0042 others(14): Show |
19 | HG00558.hp2 HG00673.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.312+3387G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478602 | |||||||
| chr21:39479101 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.312+3886G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479101 | |||||||
| chr21:39479224 | GGGT | G | 4 | a0001c0001t0001g0149 a0001c0001t0001g0279 a0001c0001t0002g0273 others(1): Show |
4 | HG02895.hp2 HG03225.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+4041_312+4043d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479224 | ||||||
| chr21:39479224 | GGGTGGTG others(5): Show |
G | 1 | a0002c0002t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.312+4032_312+4043d others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479224 | ||||||
| chr21:39479226 | G | GTGGTGAT others(5): Show |
4 | a0001c0001t0001g0112 a0002c0002t0001g0035 a0003c0003t0004g0240 others(1): Show |
4 | HG01884.hp2 HG02630.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+4016_312+4017i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479226 | ||||||
| chr21:39479226 | G | GTGGTGGT others(5): Show |
2 | a0001c0001t0005g0238 a0002c0002t0001g0028 |
2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.312+4022_312+4023i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479226 | ||||||
| chr21:39479229 | G | A | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.312+4014G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479229 | |||||||
| chr21:39479229 | G | GTGGTGGT others(8): Show |
10 | a0001c0001t0001g0119 a0001c0001t0003g0025 a0001c0001t0003g0122 others(7): Show |
10 | HG01168.hp2 HG01361.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.312+4028_312+4029i others(17): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479229 | ||||||
| chr21:39479232 | G | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0095 others(9): Show |
12 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.312+4017G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479232 | |||||||
| chr21:39479238 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(82): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.312+4023G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479238 | |||||||
| chr21:39479241 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
5 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+4026G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479241 | |||||||
| chr21:39479244 | G | C | 6 | a0001c0001t0005g0238 a0002c0002t0001g0028 a0002c0002t0001g0035 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.312+4029G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479244 | |||||||
| chr21:39479244 | G | GTGGTGGT others(5): Show |
1 | a0001c0001t0004g0229 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.312+4040_312+4041i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479244 | ||||||
| chr21:39479304 | ATGGTGGT others(58): Show |
A | 7 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.312+4111_312+4175d others(67): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479304 | ||||||
| chr21:39479369 | G | GTGGTGGT others(53): Show |
2 | a0001c0001t0003g0122 a0001c0001t0003g0230 |
2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.312+4207_312+4208i others(62): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479369 | ||||||
| chr21:39479490 | T | C | 1 | a0002c0002t0001g0042 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.312+4275T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479490 | |||||||
| chr21:39479630 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.312+4415T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479630 | |||||||
| chr21:39479724 | G | A | 1 | a0003c0003t0003g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.312+4509G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479724 | |||||||
| chr21:39479858 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.312+4643C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479858 | |||||||
| chr21:39479864 | C | G | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+4649C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479864 | |||||||
| chr21:39479865 | AT | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.312+4660delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479865 | ||||||
| chr21:39479932 | T | A | 9 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.312+4717T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479932 | |||||||
| chr21:39479979 | A | C | 2 | a0002c0002t0002g0257 a0002c0002t0002g0258 |
2 | NA18985.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.312+4764A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479979 | |||||||
| chr21:39480150 | A | G | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.312+4935A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480150 | |||||||
| chr21:39480323 | A | G | 1 | a0002c0002t0001g0035 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.312+5108A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480323 | |||||||
| chr21:39480407 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.312+5192C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480407 | |||||||
| chr21:39480411 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+5196A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480411 | |||||||
| chr21:39480534 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.312+5319G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480534 | |||||||
| chr21:39480570 | G | A | 1 | a0001c0001t0003g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.312+5355G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480570 | |||||||
| chr21:39480574 | G | A | 1 | a0002c0002t0002g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.312+5359G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480574 | |||||||
| chr21:39480589 | A | G | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+5374A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480589 | |||||||
| chr21:39480650 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0132 |
2 | NA18954.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.312+5435G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480650 | |||||||
| chr21:39481163 | C | T | 2 | a0002c0002t0002g0274 a0002c0002t0002g0275 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.312+5948C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481163 | |||||||
| chr21:39481206 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.312+5991T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481206 | |||||||
| chr21:39481588 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.312+6373C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481588 | |||||||
| chr21:39481669 | A | AAATTAAT others(31): Show |
1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+6465_312+6466i others(40): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39481669 | ||||||
| chr21:39481780 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.312+6565C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481780 | |||||||
| chr21:39481886 | G | A | 4 | a0002c0002t0001g0154 a0002c0002t0001g0155 a0002c0002t0001g0156 others(1): Show |
4 | HG02040.hp2 NA18952.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+6671G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481886 | |||||||
| chr21:39481947 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.312+6732A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481947 | |||||||
| chr21:39482021 | G | GT | 14 | a0001c0001t0001g0112 a0001c0001t0002g0273 a0001c0001t0003g0102 others(11): Show |
15 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.312+6807dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39482021 | ||||||
| chr21:39482245 | C | T | 1 | a0002c0002t0001g0188 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.312+7030C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482245 | |||||||
| chr21:39482313 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.312+7098A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482313 | |||||||
| chr21:39482384 | T | C | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+7169T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482384 | |||||||
| chr21:39482574 | G | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+7359G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482574 | |||||||
| chr21:39482576 | T | C | 16 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.312+7361T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482576 | |||||||
| chr21:39482826 | C | T | 14 | a0001c0001t0001g0112 a0001c0001t0002g0273 a0001c0001t0003g0102 others(11): Show |
15 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.312+7611C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482826 | |||||||
| chr21:39482951 | G | A | 1 | a0002c0002t0001g0009 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.312+7736G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482951 | |||||||
| chr21:39483028 | T | C | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+7813T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39483028 | |||||||
| chr21:39483331 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+8116A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39483331 | |||||||
| chr21:39483371 | C | T | 1 | a0001c0001t0003g0102 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.312+8156C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39483371 | |||||||
| chr21:39484031 | G | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+8816G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484031 | |||||||
| chr21:39484361 | C | T | 9 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.312+9146C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484361 | |||||||
| chr21:39484399 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.312+9184T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484399 | |||||||
| chr21:39484433 | A | T | 1 | a0001c0001t0003g0228 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.312+9218A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484433 | |||||||
| chr21:39484471 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+9256G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484471 | |||||||
| chr21:39484537 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.312+9322C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484537 | |||||||
| chr21:39484538 | G | A | 1 | a0002c0002t0002g0257 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.312+9323G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484538 | |||||||
| chr21:39485111 | G | C | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+9896G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485111 | |||||||
| chr21:39485113 | T | C | 1 | a0002c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.312+9898T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485113 | |||||||
| chr21:39485427 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+10212T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485427 | |||||||
| chr21:39485437 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.312+10222G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485437 | |||||||
| chr21:39485515 | C | T | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+10300C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485515 | |||||||
| chr21:39485597 | G | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+10382G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485597 | |||||||
| chr21:39485598 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.312+10383G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485598 | |||||||
| chr21:39485605 | C | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+10390C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485605 | |||||||
| chr21:39485686 | CT | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.312+10490delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39485686 | ||||||
| chr21:39485711 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+10496G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485711 | |||||||
| chr21:39485719 | G | A | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+10504G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485719 | |||||||
| chr21:39485832 | C | T | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+10617C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485832 | |||||||
| chr21:39485844 | C | T | 2 | a0002c0002t0001g0193 a0002c0002t0001g0211 |
2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.312+10629C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485844 | |||||||
| chr21:39485889 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.312+10674T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485889 | |||||||
| chr21:39485906 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.312+10691T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485906 | |||||||
| chr21:39485930 | C | T | 3 | a0002c0002t0002g0244 a0002c0002t0002g0269 a0002c0002t0002g0270 |
3 | HG02055.hp2 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.312+10715C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485930 | |||||||
| chr21:39485978 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.312+10763A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485978 | |||||||
| chr21:39485984 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.312+10769G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485984 | |||||||
| chr21:39486120 | A | G | 1 | a0001c0001t0009g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.312+10905A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39486120 | |||||||
| chr21:39486830 | G | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.312+11615G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39486830 | |||||||
| chr21:39486938 | G | T | 2 | a0001c0001t0005g0266 a0001c0001t0005g0267 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.312+11723G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39486938 | |||||||
| chr21:39487168 | G | T | 1 | a0001c0001t0001g0045 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.312+11953G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487168 | |||||||
| chr21:39487405 | A | G | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+12190A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487405 | |||||||
| chr21:39487591 | A | G | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-12232A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487591 | |||||||
| chr21:39487704 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.313-12119A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487704 | |||||||
| chr21:39487782 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-12041G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487782 | |||||||
| chr21:39487787 | C | T | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.313-12036C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487787 | |||||||
| chr21:39488085 | T | C | 1 | a0002c0002t0001g0204 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.313-11738T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488085 | |||||||
| chr21:39488351 | C | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA18960.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.313-11472C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488351 | |||||||
| chr21:39488487 | C | T | 8 | a0001c0001t0005g0261 a0001c0001t0005g0263 a0001c0001t0005g0264 others(5): Show |
9 | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.313-11336C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488487 | |||||||
| chr21:39488577 | G | A | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-11246G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488577 | |||||||
| chr21:39488579 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG01243.hp1 HG01978.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-11244C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488579 | |||||||
| chr21:39488584 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.313-11239T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488584 | |||||||
| chr21:39488585 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.313-11238T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488585 | |||||||
| chr21:39488658 | C | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-11165C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488658 | |||||||
| chr21:39488758 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313-11065T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488758 | |||||||
| chr21:39488890 | C | T | 14 | a0001c0001t0001g0112 a0001c0001t0002g0273 a0001c0001t0003g0102 others(11): Show |
15 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.313-10933C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488890 | |||||||
| chr21:39489055 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.313-10768G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489055 | |||||||
| chr21:39489173 | A | G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.313-10650A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489173 | |||||||
| chr21:39489483 | C | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-10340C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489483 | |||||||
| chr21:39489601 | G | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-10222G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489601 | |||||||
| chr21:39489750 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-10073A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489750 | |||||||
| chr21:39489784 | C | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(15): Show |
19 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.313-10039C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489784 | |||||||
| chr21:39489795 | C | G | 9 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-10028C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489795 | |||||||
| chr21:39489797 | C | T | 1 | a0002c0002t0001g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.313-10026C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489797 | |||||||
| chr21:39489800 | A | G | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-10023A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489800 | |||||||
| chr21:39490023 | A | T | 1 | a0002c0002t0002g0018 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.313-9800A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490023 | |||||||
| chr21:39490203 | C | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-9620C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490203 | |||||||
| chr21:39490318 | T | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-9505T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490318 | |||||||
| chr21:39490386 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-9437G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490386 | |||||||
| chr21:39490391 | G | C | 1 | a0001c0001t0005g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.313-9432G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490391 | |||||||
| chr21:39490407 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(108): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.313-9416A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490407 | |||||||
| chr21:39490411 | G | A | 1 | a0003c0003t0004g0277 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.313-9412G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490411 | |||||||
| chr21:39490603 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-9220A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490603 | |||||||
| chr21:39490653 | G | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-9170G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490653 | |||||||
| chr21:39490663 | C | T | 1 | a0002c0002t0002g0256 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.313-9160C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490663 | |||||||
| chr21:39490739 | AT | A | 12 | a0002c0002t0001g0004 a0002c0002t0001g0023 a0002c0002t0001g0027 others(9): Show |
14 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-9067delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39490739 | ||||||
| chr21:39490739 | ATTTT | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.313-9070_313-9067d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39490739 | ||||||
| chr21:39490783 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-9040C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490783 | |||||||
| chr21:39490796 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.313-9027A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490796 | |||||||
| chr21:39490834 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8989A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490834 | |||||||
| chr21:39490870 | C | G | 1 | a0002c0002t0001g0208 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.313-8953C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490870 | |||||||
| chr21:39491075 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8748A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491075 | |||||||
| chr21:39491158 | T | TTTTA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.313-8645_313-8642d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39491158 | ||||||
| chr21:39491187 | T | A | 1 | a0002c0002t0001g0212 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.313-8636T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491187 | |||||||
| chr21:39491218 | C | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-8605C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491218 | |||||||
| chr21:39491235 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.313-8588C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491235 | |||||||
| chr21:39491297 | G | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8526G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491297 | |||||||
| chr21:39491511 | A | G | 3 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 |
4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-8312A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491511 | |||||||
| chr21:39491594 | G | A | 18 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(15): Show |
19 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.313-8229G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491594 | |||||||
| chr21:39491694 | A | G | 3 | a0002c0002t0002g0018 a0002c0002t0002g0262 a0002c0002t0002g0272 |
4 | HG01175.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-8129A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491694 | |||||||
| chr21:39491722 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.313-8101C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491722 | |||||||
| chr21:39491788 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8035C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491788 | |||||||
| chr21:39491809 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8014C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491809 | |||||||
| chr21:39491819 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313-8004G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491819 | |||||||
| chr21:39491828 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.313-7995G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491828 | |||||||
| chr21:39492288 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.313-7535G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492288 | |||||||
| chr21:39492440 | C | G | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-7383C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492440 | |||||||
| chr21:39492443 | G | GGT | 3 | a0002c0002t0001g0109 a0002c0002t0001g0123 a0002c0002t0001g0124 |
3 | HG02080.hp2 HG03098.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.313-7357_313-7356d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | ||||||
| chr21:39492443 | G | GGTGGGTG others(3): Show |
1 | a0001c0001t0003g0102 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.313-7377_313-7376i others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | ||||||
| chr21:39492443 | G | GGTGGGTG others(5): Show |
1 | a0001c0001t0002g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.313-7377_313-7376i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | ||||||
| chr21:39492443 | G | GGTGTGTG others(1): Show |
9 | a0001c0001t0005g0261 a0001c0001t0005g0263 a0001c0001t0005g0264 others(6): Show |
10 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-7363_313-7356d others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | ||||||
| chr21:39492443 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-7369_313-7356d others(16): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | ||||||
| chr21:39492445 | T | G | 1 | a0001c0001t0003g0228 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313-7378T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492445 | |||||||
| chr21:39492447 | T | G | 5 | a0001c0001t0004g0229 a0002c0002t0002g0236 a0002c0002t0002g0247 others(2): Show |
5 | HG00280.hp2 HG02738.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.313-7376T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492447 | |||||||
| chr21:39492466 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0137 |
2 | HG00438.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.313-7357G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492466 | |||||||
| chr21:39492466 | G | GTGTATA | 16 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.313-7356_313-7355i others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | ||||||
| chr21:39492466 | G | GTGTGTAT others(1): Show |
3 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0004g0022 |
3 | HG02615.hp2 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.313-7356_313-7355i others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | ||||||
| chr21:39492466 | G | GTGTGTAT others(3): Show |
5 | a0001c0001t0003g0122 a0001c0001t0003g0227 a0001c0001t0003g0228 others(2): Show |
5 | HG01168.hp2 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-7356_313-7355i others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | ||||||
| chr21:39492466 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0003g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.313-7356_313-7355i others(16): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | ||||||
| chr21:39492466 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-7356_313-7355i others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | ||||||
| chr21:39492466 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0004g0229 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.313-7356_313-7355i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | ||||||
| chr21:39492466 | GTA | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0104 others(3): Show |
6 | HG01243.hp1 HG01496.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-7342_313-7341d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | ||||||
| chr21:39492468 | A | G | 17 | a0001c0001t0001g0059 a0001c0001t0001g0112 a0001c0001t0002g0235 others(14): Show |
18 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-7355A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492468 | |||||||
| chr21:39492470 | A | G | 3 | a0001c0001t0002g0235 a0001c0001t0006g0231 a0001c0001t0006g0232 |
3 | HG02895.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.313-7353A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492470 | |||||||
| chr21:39492475 | TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0137 |
2 | HG00438.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.313-7346_313-7337d others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492475 | ||||||
| chr21:39492477 | TATATACA others(1): Show |
T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.313-7344_313-7337d others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492477 | ||||||
| chr21:39492481 | T | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0104 others(4): Show |
7 | HG01243.hp1 HG01496.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.313-7342T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492481 | |||||||
| chr21:39492481 | T | TAC | 9 | a0002c0002t0001g0012 a0002c0002t0001g0187 a0002c0002t0002g0244 others(6): Show |
9 | HG00642.hp1 HG00735.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-7325_313-7324d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492481 | ||||||
| chr21:39492483 | C | T | 43 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(40): Show |
46 | HG01168.hp2 HG01346.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.313-7340C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492483 | |||||||
| chr21:39492485 | C | T | 26 | a0001c0001t0001g0112 a0001c0001t0001g0223 a0001c0001t0002g0235 others(23): Show |
28 | HG01168.hp2 HG02055.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.313-7338C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492485 | |||||||
| chr21:39492487 | CACACACA others(11): Show |
C | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-7335_313-7318d others(20): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492487 | |||||||
| chr21:39492493 | C | G | 2 | a0001c0001t0004g0022 a0002c0002t0001g0226 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-7330C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492493 | |||||||
| chr21:39492569 | T | C | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-7254T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492569 | |||||||
| chr21:39492636 | C | G | 2 | a0001c0001t0004g0022 a0002c0002t0001g0226 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-7187C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492636 | |||||||
| chr21:39492703 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.313-7120T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492703 | |||||||
| chr21:39492794 | G | T | 11 | a0001c0001t0001g0112 a0001c0001t0005g0261 a0001c0001t0005g0263 others(8): Show |
12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-7029G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492794 | |||||||
| chr21:39493077 | C | T | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-6746C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493077 | |||||||
| chr21:39493145 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-6678G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493145 | |||||||
| chr21:39493298 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.313-6525G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493298 | |||||||
| chr21:39493306 | A | T | 1 | a0001c0001t0003g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.313-6517A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493306 | |||||||
| chr21:39493446 | G | C | 2 | a0001c0001t0004g0022 a0002c0002t0001g0226 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-6377G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493446 | |||||||
| chr21:39493523 | T | C | 1 | a0001c0001t0005g0263 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.313-6300T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493523 | |||||||
| chr21:39493781 | A | G | 2 | a0001c0001t0004g0022 a0002c0002t0001g0226 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-6042A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493781 | |||||||
| chr21:39494112 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.313-5711A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494112 | |||||||
| chr21:39494160 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.313-5663C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494160 | |||||||
| chr21:39494225 | T | G | 2 | a0002c0002t0002g0262 a0002c0002t0002g0272 |
2 | HG01175.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.313-5598T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494225 | |||||||
| chr21:39494228 | TTCC | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.313-5592_313-5590d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39494228 | ||||||
| chr21:39494231 | C | CTCT | 96 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0014 others(93): Show |
104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.313-5572_313-5570d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39494231 | ||||||
| chr21:39494231 | C | T | 53 | a0001c0001t0001g0013 a0001c0001t0001g0068 a0001c0001t0001g0069 others(50): Show |
56 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(53): Show |
intron_variant | MODIFIER | c.313-5592C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494231 | |||||||
| chr21:39494238 | T | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-5585T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494238 | |||||||
| chr21:39494247 | TCTTC | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG01109.hp1 HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.313-5575_313-5572d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494247 | |||||||
| chr21:39494251 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.313-5572C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494251 | |||||||
| chr21:39494342 | T | C | 2 | a0001c0001t0004g0022 a0002c0002t0001g0226 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-5481T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494342 | |||||||
| chr21:39494443 | G | A | 2 | a0001c0001t0004g0022 a0002c0002t0001g0226 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-5380G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494443 | |||||||
| chr21:39494481 | G | A | 4 | a0002c0002t0001g0108 a0002c0002t0001g0217 a0002c0002t0001g0218 others(1): Show |
4 | HG01243.hp2 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-5342G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494481 | |||||||
| chr21:39494697 | T | A | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-5126T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494697 | |||||||
| chr21:39494851 | T | G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-4972T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494851 | |||||||
| chr21:39495090 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-4733G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495090 | |||||||
| chr21:39495229 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-4594A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495229 | |||||||
| chr21:39495482 | C | CT | 36 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(33): Show |
38 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.313-4326dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39495482 | ||||||
| chr21:39495487 | T | TG | 11 | a0001c0001t0005g0238 a0001c0001t0005g0261 a0001c0001t0005g0263 others(8): Show |
12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-4336_313-4335i others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495487 | |||||||
| chr21:39495633 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-4190C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495633 | |||||||
| chr21:39495653 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.313-4170A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495653 | |||||||
| chr21:39495654 | A | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-4169A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495654 | |||||||
| chr21:39495707 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.313-4116C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495707 | |||||||
| chr21:39495806 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0104 others(3): Show |
6 | HG01243.hp1 HG01496.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-4017C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495806 | |||||||
| chr21:39495807 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-4016G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495807 | |||||||
| chr21:39495972 | A | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0038 others(15): Show |
19 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.313-3851A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495972 | |||||||
| chr21:39496137 | CG | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.313-3685delG | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496137 | |||||||
| chr21:39496226 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-3597C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496226 | |||||||
| chr21:39496229 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-3594G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496229 | |||||||
| chr21:39496236 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3587C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496236 | |||||||
| chr21:39496296 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3527C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496296 | |||||||
| chr21:39496317 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.313-3506G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496317 | |||||||
| chr21:39496327 | C | T | 9 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-3496C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496327 | |||||||
| chr21:39496356 | C | T | 1 | a0003c0003t0004g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.313-3467C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496356 | |||||||
| chr21:39496357 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.313-3466G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496357 | |||||||
| chr21:39496360 | T | C | 2 | a0001c0001t0004g0022 a0002c0002t0001g0226 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-3463T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496360 | |||||||
| chr21:39496362 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3461C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496362 | |||||||
| chr21:39496364 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.313-3459G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496364 | |||||||
| chr21:39496368 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-3455C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496368 | |||||||
| chr21:39496392 | C | G | 1 | a0002c0002t0001g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.313-3431C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496392 | |||||||
| chr21:39496392 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.313-3431C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496392 | |||||||
| chr21:39496425 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3398A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496425 | |||||||
| chr21:39496439 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.313-3384G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496439 | |||||||
| chr21:39496456 | C | T | 9 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-3367C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496456 | |||||||
| chr21:39496486 | G | A | 3 | a0001c0001t0002g0273 a0001c0001t0003g0102 a0001c0001t0004g0229 |
3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.313-3337G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496486 | |||||||
| chr21:39496489 | A | G | 2 | a0001c0001t0006g0231 a0001c0001t0006g0232 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.313-3334A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496489 | |||||||
| chr21:39496495 | A | G | 1 | a0002c0002t0001g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.313-3328A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496495 | |||||||
| chr21:39496501 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-3322C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496501 | |||||||
| chr21:39496506 | C | CA | 10 | a0001c0001t0003g0227 a0002c0002t0001g0042 a0002c0002t0001g0127 others(7): Show |
10 | HG01168.hp1 HG01358.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-3294dupA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | ||||||
| chr21:39496506 | CA | C | 56 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(53): Show |
60 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.313-3294delA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | ||||||
| chr21:39496506 | CAA | C | 21 | a0001c0001t0001g0050 a0001c0001t0001g0067 a0001c0001t0001g0080 others(18): Show |
22 | HG00558.hp1 HG01978.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.313-3295_313-3294d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | ||||||
| chr21:39496506 | CAAA | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.313-3296_313-3294d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | ||||||
| chr21:39496506 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3303_313-3294d others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | ||||||
| chr21:39496519 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-3304A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496519 | |||||||
| chr21:39496527 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3296A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496527 | |||||||
| chr21:39496556 | T | C | 2 | a0001c0001t0004g0022 a0002c0002t0001g0226 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-3267T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496556 | |||||||
| chr21:39496557 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3266G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496557 | |||||||
| chr21:39496796 | T | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-3027T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496796 | |||||||
| chr21:39497024 | T | C | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-2799T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497024 | |||||||
| chr21:39497215 | G | C | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-2608G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497215 | |||||||
| chr21:39497320 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-2503G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497320 | |||||||
| chr21:39497343 | C | T | 2 | a0002c0002t0001g0162 a0002c0002t0001g0163 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.313-2480C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497343 | |||||||
| chr21:39497344 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.313-2479G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497344 | |||||||
| chr21:39497425 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-2398C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497425 | |||||||
| chr21:39497746 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-2077A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497746 | |||||||
| chr21:39497822 | A | G | 1 | a0002c0002t0001g0161 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.313-2001A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497822 | |||||||
| chr21:39498037 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-1786A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498037 | |||||||
| chr21:39498200 | T | C | 2 | a0001c0001t0004g0022 a0002c0002t0001g0226 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-1623T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498200 | |||||||
| chr21:39498234 | A | ACCGT | 17 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-1588_313-1585d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39498234 | ||||||
| chr21:39498237 | G | C | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-1586G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498237 | |||||||
| chr21:39498345 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.313-1478C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498345 | |||||||
| chr21:39498387 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-1436A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498387 | |||||||
| chr21:39498449 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313-1374T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498449 | |||||||
| chr21:39498506 | G | T | 1 | a0002c0002t0001g0199 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.313-1317G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498506 | |||||||
| chr21:39498508 | T | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-1315T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498508 | |||||||
| chr21:39498532 | T | G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-1291T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498532 | |||||||
| chr21:39498709 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.313-1114T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498709 | |||||||
| chr21:39498718 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-1105C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498718 | |||||||
| chr21:39498775 | T | C | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-1048T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498775 | |||||||
| chr21:39498837 | C | G | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-986C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498837 | |||||||
| chr21:39498857 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-966A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498857 | |||||||
| chr21:39499009 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.313-814C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499009 | |||||||
| chr21:39499062 | T | A | 3 | a0002c0002t0002g0018 a0002c0002t0002g0262 a0002c0002t0002g0272 |
4 | HG01175.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-761T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499062 | |||||||
| chr21:39499106 | G | A | 1 | a0001c0001t0003g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.313-717G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499106 | |||||||
| chr21:39499113 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-710A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499113 | |||||||
| chr21:39499137 | C | G | 3 | a0001c0001t0002g0273 a0001c0001t0003g0102 a0001c0001t0004g0229 |
3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.313-686C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499137 | |||||||
| chr21:39499210 | A | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-613A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499210 | |||||||
| chr21:39499240 | C | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-583C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499240 | |||||||
| chr21:39499255 | C | CATCT | 9 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-567_313-564dup others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499255 | C | CATCTATC others(1): Show |
3 | a0001c0001t0002g0273 a0001c0001t0003g0102 a0001c0001t0004g0229 |
3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.313-564_313-563ins others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499255 | C | CATCTATC others(5): Show |
34 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(31): Show |
36 | HG00642.hp1 HG00735.hp2 HG01346.hp2 others(33): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499255 | C | CATCTATC others(9): Show |
2 | a0001c0001t0001g0049 a0001c0001t0002g0235 |
2 | HG02735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.313-564_313-563ins others(16): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499255 | C | CATCTATC others(13): Show |
7 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0071 others(4): Show |
7 | HG01123.hp2 HG01243.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(20): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499255 | C | CATCTATC others(17): Show |
51 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0034 others(48): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(24): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499255 | C | CATCTATC others(21): Show |
30 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(27): Show |
33 | HG01070.hp1 HG01109.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(28): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499255 | C | CATCTATC others(25): Show |
12 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0059 others(9): Show |
13 | HG00408.hp2 HG01261.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(32): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499255 | C | CATCTATC others(29): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02074.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.313-564_313-563ins others(36): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499255 | C | CATCTATC others(33): Show |
1 | a0001c0001t0001g0066 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.313-564_313-563ins others(40): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | ||||||
| chr21:39499258 | C | CTATCTAT others(17): Show |
1 | a0001c0001t0001g0062 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.313-564_313-563ins others(24): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499258 | ||||||
| chr21:39499260 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.313-563G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499260 | |||||||
| chr21:39499260 | GTCTA | G | 2 | a0002c0002t0001g0012 a0002c0002t0001g0169 |
3 | HG01255.hp1 HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.313-559_313-556del others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499260 | ||||||
| chr21:39499268 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0001g0149 others(1): Show |
4 | HG02809.hp2 HG03239.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-555G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499268 | |||||||
| chr21:39499272 | A | ATCTATCT others(17): Show |
1 | a0001c0001t0001g0149 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.313-542_313-541ins others(24): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499272 | ||||||
| chr21:39499276 | A | G | 1 | a0002c0002t0002g0254 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313-547A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499276 | |||||||
| chr21:39499280 | A | G | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-543A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499280 | |||||||
| chr21:39499326 | CTCCG | C | 11 | a0001c0001t0005g0238 a0001c0001t0005g0261 a0001c0001t0005g0263 others(8): Show |
12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-494_313-491del others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499326 | ||||||
| chr21:39499329 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0002g0273 a0001c0001t0003g0102 others(1): Show |
4 | HG02109.hp2 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-494C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499329 | |||||||
| chr21:39499463 | ATCT | A | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-355_313-353del others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499463 | ||||||
| chr21:39499591 | A | G | 1 | a0002c0002t0001g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.313-232A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499591 | |||||||
| chr21:39499641 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.313-182C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499641 | |||||||
| chr21:39499687 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-136C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499687 | |||||||
| chr21:39499785 | G | C | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-38G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499785 | |||||||
| chr21:39499800 | T | C | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-23T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499800 | |||||||
| chr21:39500159 | G | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.405+244G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500159 | |||||||
| chr21:39500202 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.405+287T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500202 | |||||||
| chr21:39500257 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.405+342C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500257 | |||||||
| chr21:39500274 | A | C | 1 | a0002c0002t0001g0198 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.405+359A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500274 | |||||||
| chr21:39500335 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.405+420G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500335 | |||||||
| chr21:39500462 | T | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(274): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.405+547T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500462 | |||||||
| chr21:39500509 | G | A | 4 | a0002c0002t0002g0020 a0002c0002t0002g0249 a0002c0002t0002g0250 others(1): Show |
5 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+594G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500509 | |||||||
| chr21:39500519 | A | G | 4 | a0001c0001t0003g0122 a0001c0001t0003g0227 a0001c0001t0003g0228 others(1): Show |
4 | HG02145.hp2 HG02922.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.405+604A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500519 | |||||||
| chr21:39500546 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.405+631C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500546 | |||||||
| chr21:39500589 | G | A | 1 | a0002c0002t0002g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.405+674G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500589 | |||||||
| chr21:39500751 | G | A | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.405+836G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500751 | |||||||
| chr21:39500779 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0178 a0001c0001t0001g0179 others(6): Show |
10 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.405+864C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500779 | |||||||
| chr21:39501157 | C | T | 1 | a0002c0002t0001g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.405+1242C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501157 | |||||||
| chr21:39501211 | A | G | 1 | a0002c0002t0001g0160 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.405+1296A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501211 | |||||||
| chr21:39501385 | C | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.405+1470C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501385 | |||||||
| chr21:39501497 | T | C | 1 | a0002c0002t0002g0254 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.405+1582T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501497 | |||||||
| chr21:39501561 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.405+1646A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501561 | |||||||
| chr21:39501600 | A | G | 1 | a0002c0002t0007g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.405+1685A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501600 | |||||||
| chr21:39501639 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.405+1724A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501639 | |||||||
| chr21:39501744 | T | G | 2 | a0001c0001t0003g0102 a0001c0001t0004g0229 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.405+1829T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501744 | |||||||
| chr21:39501837 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.405+1922A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501837 | |||||||
| chr21:39501900 | G | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.405+1985G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501900 | |||||||
| chr21:39501973 | G | C | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+2058G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501973 | |||||||
| chr21:39501976 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.405+2061C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501976 | |||||||
| chr21:39502046 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0002g0246 |
2 | HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.405+2131G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502046 | |||||||
| chr21:39502067 | G | C | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.405+2152G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502067 | |||||||
| chr21:39502112 | G | T | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+2197G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502112 | |||||||
| chr21:39502113 | C | T | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+2198C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502113 | |||||||
| chr21:39502166 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.405+2251A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502166 | |||||||
| chr21:39502199 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.405+2284T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502199 | |||||||
| chr21:39502259 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.405+2344C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502259 | |||||||
| chr21:39502498 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.405+2583A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502498 | |||||||
| chr21:39502596 | C | G | 3 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0001g0205 |
3 | HG00323.hp1 HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.405+2681C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502596 | |||||||
| chr21:39502690 | C | T | 1 | a0002c0002t0002g0254 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.405+2775C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502690 | |||||||
| chr21:39502715 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.405+2800G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502715 | |||||||
| chr21:39502719 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.405+2804G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502719 | |||||||
| chr21:39502733 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.405+2818G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502733 | |||||||
| chr21:39502806 | C | T | 28 | a0002c0002t0001g0043 a0002c0002t0001g0185 a0002c0002t0001g0234 others(25): Show |
30 | HG00280.hp2 HG00642.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.405+2891C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502806 | |||||||
| chr21:39502826 | G | A | 3 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 |
4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+2911G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502826 | |||||||
| chr21:39502985 | C | CT | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.405+3083dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 39502985 | ||||||
| chr21:39503090 | C | T | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.405+3175C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503090 | |||||||
| chr21:39503248 | A | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.405+3333A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503248 | |||||||
| chr21:39503359 | T | C | 6 | a0001c0001t0004g0022 a0003c0003t0004g0239 a0003c0003t0004g0240 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.405+3444T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503359 | |||||||
| chr21:39503385 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.405+3470A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503385 | |||||||
| chr21:39503417 | T | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.405+3502T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503417 | |||||||
| chr21:39503418 | T | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.405+3503T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503418 | |||||||
| chr21:39503418 | T | TA | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+3510dupA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 39503418 | ||||||
| chr21:39503482 | C | T | 15 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(12): Show |
16 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.405+3567C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503482 | |||||||
| chr21:39503487 | A | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(12): Show |
16 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.405+3572A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503487 | |||||||
| chr21:39503561 | C | T | 3 | a0002c0002t0001g0023 a0002c0002t0001g0144 a0002c0002t0001g0145 |
3 | HG02647.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.405+3646C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503561 | |||||||
| chr21:39503718 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.405+3803T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503718 | |||||||
| chr21:39503788 | C | T | 15 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(12): Show |
16 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.405+3873C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503788 | |||||||
| chr21:39503915 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0132 |
2 | NA18954.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.405+4000C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503915 | |||||||
| chr21:39504098 | G | T | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.405+4183G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504098 | |||||||
| chr21:39504323 | G | A | 9 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.405+4408G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504323 | |||||||
| chr21:39504416 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.405+4501A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504416 | |||||||
| chr21:39504459 | C | G | 17 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(14): Show |
18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-4539C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504459 | |||||||
| chr21:39504557 | A | G | 1 | a0001c0001t0002g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.406-4441A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504557 | |||||||
| chr21:39504708 | C | T | 17 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(14): Show |
18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-4290C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504708 | |||||||
| chr21:39504709 | C | T | 17 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(14): Show |
18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-4289C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504709 | |||||||
| chr21:39504726 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.406-4272C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504726 | |||||||
| chr21:39505070 | C | A | 12 | a0001c0001t0001g0112 a0001c0001t0005g0238 a0001c0001t0005g0261 others(9): Show |
13 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.406-3928C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505070 | |||||||
| chr21:39505104 | C | T | 39 | a0002c0002t0001g0002 a0002c0002t0001g0014 a0002c0002t0001g0015 others(36): Show |
45 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.406-3894C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505104 | |||||||
| chr21:39505264 | C | G | 17 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(14): Show |
18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-3734C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505264 | |||||||
| chr21:39505276 | C | T | 1 | a0002c0002t0001g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.406-3722C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505276 | |||||||
| chr21:39505286 | G | T | 12 | a0001c0001t0001g0112 a0001c0001t0005g0238 a0001c0001t0005g0261 others(9): Show |
13 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.406-3712G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505286 | |||||||
| chr21:39505398 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.406-3600C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505398 | |||||||
| chr21:39505451 | T | C | 1 | a0002c0002t0002g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.406-3547T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505451 | |||||||
| chr21:39505540 | A | G | 17 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(14): Show |
18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-3458A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505540 | |||||||
| chr21:39505571 | G | A | 12 | a0001c0001t0001g0112 a0001c0001t0002g0273 a0001c0001t0005g0261 others(9): Show |
13 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.406-3427G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505571 | |||||||
| chr21:39505665 | T | G | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.406-3333T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505665 | |||||||
| chr21:39505722 | G | A | 1 | a0002c0002t0002g0018 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.406-3276G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505722 | |||||||
| chr21:39505760 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.406-3238C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505760 | |||||||
| chr21:39505879 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.406-3119G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505879 | |||||||
| chr21:39505879 | G | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.406-3119G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505879 | |||||||
| chr21:39506089 | C | A | 17 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(14): Show |
18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-2909C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506089 | |||||||
| chr21:39506524 | G | A | 10 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(7): Show |
11 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.406-2474G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506524 | |||||||
| chr21:39506554 | G | T | 1 | a0002c0002t0001g0234 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.406-2444G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506554 | |||||||
| chr21:39506665 | T | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(13): Show |
17 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.406-2333T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506665 | |||||||
| chr21:39506682 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.406-2316C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506682 | |||||||
| chr21:39506695 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.406-2303A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506695 | |||||||
| chr21:39506834 | T | A | 17 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(14): Show |
18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-2164T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506834 | |||||||
| chr21:39506887 | T | C | 11 | a0001c0001t0005g0238 a0001c0001t0005g0261 a0001c0001t0005g0263 others(8): Show |
12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.406-2111T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506887 | |||||||
| chr21:39507026 | A | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1972A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507026 | |||||||
| chr21:39507124 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.406-1874G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507124 | |||||||
| chr21:39507132 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.406-1866C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507132 | |||||||
| chr21:39507274 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1724A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507274 | |||||||
| chr21:39507315 | A | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0100 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.406-1683A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507315 | |||||||
| chr21:39507394 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.406-1604C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507394 | |||||||
| chr21:39507407 | C | T | 2 | a0001c0001t0003g0102 a0001c0001t0004g0229 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.406-1591C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507407 | |||||||
| chr21:39507410 | C | T | 2 | a0001c0001t0001g0175 a0002c0002t0002g0252 |
2 | HG03195.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.406-1588C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507410 | |||||||
| chr21:39507451 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.406-1547A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507451 | |||||||
| chr21:39507459 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1539A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507459 | |||||||
| chr21:39507480 | T | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1518T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507480 | |||||||
| chr21:39507508 | T | G | 1 | a0005c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.406-1490T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507508 | |||||||
| chr21:39507521 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.406-1477C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507521 | |||||||
| chr21:39507569 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.406-1429G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507569 | |||||||
| chr21:39507659 | C | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1339C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507659 | |||||||
| chr21:39507728 | C | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1270C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507728 | |||||||
| chr21:39507813 | G | A | 2 | a0002c0002t0002g0268 a0003c0003t0004g0277 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.406-1185G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507813 | |||||||
| chr21:39507894 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.406-1104T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507894 | |||||||
| chr21:39508003 | T | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.406-995T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508003 | |||||||
| chr21:39508145 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-853A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508145 | |||||||
| chr21:39508158 | C | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-840C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508158 | |||||||
| chr21:39508212 | G | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-786G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508212 | |||||||
| chr21:39508223 | C | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-775C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508223 | |||||||
| chr21:39508248 | G | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.406-750G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508248 | |||||||
| chr21:39508290 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0002g0246 |
2 | HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.406-708C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508290 | |||||||
| chr21:39508464 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-534A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508464 | |||||||
| chr21:39508554 | C | G | 1 | a0002c0002t0001g0213 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.406-444C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508554 | |||||||
| chr21:39508784 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.406-214T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508784 | |||||||
| chr21:39508951 | G | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-47G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508951 | |||||||
| chr21:39508954 | CTTGAA | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.406-41_406-37delGA others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 39508954 | ||||||
| chr21:39509169 | A | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.435+142A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509169 | |||||||
| chr21:39509271 | G | T | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+244G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509271 | |||||||
| chr21:39509280 | G | A | 1 | a0002c0002t0002g0254 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.435+253G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509280 | |||||||
| chr21:39509301 | G | A | 1 | a0002c0002t0002g0252 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.435+274G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509301 | |||||||
| chr21:39509339 | C | T | 2 | a0001c0001t0003g0122 a0001c0001t0003g0230 |
2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.435+312C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509339 | |||||||
| chr21:39509471 | G | GT | 23 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(20): Show |
25 | HG00408.hp1 HG01070.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.435+465dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39509471 | ||||||
| chr21:39509471 | GT | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
15 | HG02080.hp1 HG02155.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.435+465delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39509471 | ||||||
| chr21:39509471 | GTT | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
103 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.435+464_435+465del others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39509471 | ||||||
| chr21:39509552 | G | A | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.435+525G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509552 | |||||||
| chr21:39509594 | C | T | 1 | a0002c0002t0002g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.435+567C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509594 | |||||||
| chr21:39509726 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.435+699C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509726 | |||||||
| chr21:39509854 | C | T | 2 | a0002c0002t0001g0042 a0002c0002t0001g0135 |
2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.435+827C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509854 | |||||||
| chr21:39509913 | C | T | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+886C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509913 | |||||||
| chr21:39509937 | TTTTGTTA others(297): Show |
T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.435+924_435+1227de others(1): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39509937 | ||||||
| chr21:39510034 | C | T | 1 | a0002c0002t0001g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.435+1007C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510034 | |||||||
| chr21:39510133 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.435+1106G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510133 | |||||||
| chr21:39510154 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1127A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510154 | |||||||
| chr21:39510156 | AT | A | 3 | a0002c0002t0001g0004 a0002c0002t0001g0027 a0002c0002t0002g0271 |
4 | HG00639.hp1 HG00735.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1130delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510156 | |||||||
| chr21:39510164 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1137G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510164 | |||||||
| chr21:39510177 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1150T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510177 | |||||||
| chr21:39510217 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1190C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510217 | |||||||
| chr21:39510222 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1195G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510222 | |||||||
| chr21:39510261 | A | G | 6 | a0002c0002t0001g0023 a0002c0002t0001g0035 a0002c0002t0001g0036 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.435+1234A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510261 | |||||||
| chr21:39510365 | T | TAC | 112 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.436-1290_436-1289d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | ||||||
| chr21:39510365 | T | TACAC | 4 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0005g0266 others(1): Show |
5 | HG00099.hp1 HG00323.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.436-1292_436-1289d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | ||||||
| chr21:39510365 | T | TACACAC | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0112 others(4): Show |
7 | HG00438.hp1 HG02080.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-1294_436-1289d others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | ||||||
| chr21:39510365 | T | TACGCGCA others(1): Show |
6 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(3): Show |
7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-1313_436-1312i others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | ||||||
| chr21:39510365 | T | TACGCGCA others(3): Show |
2 | a0001c0001t0003g0122 a0001c0001t0004g0242 |
2 | HG01168.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.436-1313_436-1312i others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | ||||||
| chr21:39510365 | T | TACGCGCG others(1): Show |
4 | a0003c0003t0004g0239 a0003c0003t0004g0241 a0003c0003t0004g0277 others(1): Show |
4 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-1313_436-1312i others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | ||||||
| chr21:39510365 | TAC | T | 7 | a0001c0001t0010g0140 a0002c0002t0001g0023 a0002c0002t0001g0035 others(4): Show |
7 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-1290_436-1289d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | ||||||
| chr21:39510366 | A | ACGCGCG | 3 | a0001c0001t0003g0102 a0001c0001t0004g0022 a0001c0001t0004g0229 |
3 | HG02109.hp2 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.436-1313_436-1312i others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510366 | ||||||
| chr21:39510368 | A | G | 3 | a0001c0001t0003g0172 a0003c0003t0003g0220 a0003c0003t0004g0240 |
3 | HG03195.hp1 HG03540.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.436-1312A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510368 | |||||||
| chr21:39510369 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.436-1311C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510369 | |||||||
| chr21:39510370 | A | G | 3 | a0001c0001t0003g0172 a0003c0003t0003g0220 a0003c0003t0004g0240 |
3 | HG03195.hp1 HG03540.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.436-1310A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510370 | |||||||
| chr21:39510372 | A | G | 1 | a0003c0003t0004g0240 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.436-1308A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510372 | |||||||
| chr21:39510373 | CACACACA others(49): Show |
C | 1 | a0003c0003t0004g0240 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.436-1288_436-1233d others(58): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510373 | ||||||
| chr21:39510375 | CACACACA others(16): Show |
C | 1 | a0001c0001t0003g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.436-1288_436-1266d others(25): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510375 | ||||||
| chr21:39510377 | CACACACA others(14): Show |
C | 1 | a0003c0003t0003g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.436-1288_436-1268d others(23): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510377 | ||||||
| chr21:39510398 | T | TAC | 11 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(8): Show |
11 | HG00597.hp1 HG02015.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.436-1259_436-1258d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510398 | ||||||
| chr21:39510398 | TAC | T | 86 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0104 others(83): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.436-1259_436-1258d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510398 | ||||||
| chr21:39510398 | TACACAC | T | 3 | a0001c0001t0003g0102 a0001c0001t0004g0022 a0001c0001t0004g0229 |
3 | HG02109.hp2 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.436-1263_436-1258d others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510398 | ||||||
| chr21:39510398 | TACACACA others(28): Show |
T | 1 | a0002c0002t0001g0187 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.436-1259_436-1225d others(37): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510398 | ||||||
| chr21:39510408 | CACACACA others(47): Show |
C | 4 | a0003c0003t0004g0239 a0003c0003t0004g0241 a0003c0003t0004g0277 others(1): Show |
4 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-1257_436-1204d others(56): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510408 | ||||||
| chr21:39510429 | T | TAC | 3 | a0002c0002t0001g0157 a0002c0002t0001g0171 a0003c0003t0003g0220 |
3 | HG01981.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.436-1226_436-1225d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510429 | ||||||
| chr21:39510429 | TAC | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.436-1226_436-1225d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510429 | ||||||
| chr21:39510429 | TACAC | T | 7 | a0001c0001t0001g0070 a0001c0001t0002g0235 a0002c0002t0001g0012 others(4): Show |
7 | HG01346.hp1 HG02559.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-1228_436-1225d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510429 | ||||||
| chr21:39510429 | TACACACA others(1): Show |
T | 13 | a0001c0001t0001g0112 a0001c0001t0002g0273 a0001c0001t0005g0238 others(10): Show |
14 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.436-1232_436-1225d others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510429 | ||||||
| chr21:39510435 | CACACACA others(20): Show |
C | 8 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(5): Show |
9 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.436-1226_436-1200d others(29): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510435 | ||||||
| chr21:39510437 | C | CACACACA others(18): Show |
6 | a0002c0002t0001g0023 a0002c0002t0001g0035 a0002c0002t0001g0036 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-1224_436-1200d others(27): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510437 | ||||||
| chr21:39510437 | CACACACA others(18): Show |
C | 2 | a0001c0001t0003g0102 a0001c0001t0004g0229 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.436-1224_436-1200d others(27): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510437 | ||||||
| chr21:39510454 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.436-1226A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510454 | |||||||
| chr21:39510454 | ACTGTAGC others(20): Show |
A | 1 | a0001c0001t0004g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.436-1224_436-1198d others(29): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510454 | ||||||
| chr21:39510462 | T | TAC | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.436-1201_436-1200d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510462 | ||||||
| chr21:39510462 | T | TACAC | 3 | a0001c0001t0001g0048 a0001c0001t0001g0063 a0003c0003t0004g0240 |
3 | HG03492.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.436-1203_436-1200d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510462 | ||||||
| chr21:39510481 | C | A | 2 | a0001c0001t0003g0102 a0001c0001t0004g0229 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.436-1199C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510481 | |||||||
| chr21:39510513 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.436-1167T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510513 | |||||||
| chr21:39510514 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.436-1166C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510514 | |||||||
| chr21:39510516 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.436-1164T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510516 | |||||||
| chr21:39510569 | T | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-1111T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510569 | |||||||
| chr21:39510664 | A | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0113 a0001c0001t0001g0168 |
3 | HG01943.hp2 HG02074.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.436-1016A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510664 | |||||||
| chr21:39510908 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.436-772_436-771ins others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510908 | |||||||
| chr21:39510909 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.436-771C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510909 | |||||||
| chr21:39510909 | C | CTA | 30 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0073 others(27): Show |
33 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.436-734_436-733dup others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | C | CTATA | 70 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0039 others(67): Show |
77 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.436-736_436-733dup others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | C | CTATATA | 65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(62): Show |
70 | HG00558.hp1 HG00597.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.436-738_436-733dup others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | C | CTATATAT others(1): Show |
20 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0065 others(17): Show |
21 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.436-740_436-733dup others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | C | CTATATAT others(3): Show |
4 | a0001c0001t0001g0279 a0002c0002t0001g0199 a0002c0002t0001g0208 others(1): Show |
4 | HG02809.hp1 NA18981.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-742_436-733dup others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | C | CTATATAT others(5): Show |
5 | a0001c0001t0001g0120 a0002c0002t0001g0124 a0002c0002t0001g0153 others(2): Show |
5 | HG00408.hp1 NA18981.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.436-744_436-733dup others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | C | CTATATAT others(7): Show |
3 | a0001c0001t0001g0046 a0001c0001t0001g0077 a0001c0001t0001g0136 |
3 | HG04204.hp1 NA19011.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.436-746_436-733dup others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | C | CTATATAT others(9): Show |
1 | a0001c0001t0001g0047 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.436-748_436-733dup others(16): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | C | CTATATAT others(13): Show |
1 | a0001c0001t0001g0210 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.436-752_436-733dup others(20): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | C | CTATATAT others(23): Show |
1 | a0001c0001t0001g0092 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.436-762_436-733dup others(30): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | CTA | C | 18 | a0001c0001t0001g0133 a0001c0001t0001g0174 a0001c0001t0001g0175 others(15): Show |
18 | HG00735.hp2 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.436-734_436-733del others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | CTATA | C | 11 | a0001c0001t0001g0106 a0001c0001t0001g0223 a0002c0002t0001g0234 others(8): Show |
13 | HG01070.hp2 HG01081.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.436-736_436-733del others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | CTATATA | C | 14 | a0001c0001t0001g0060 a0002c0002t0001g0043 a0002c0002t0001g0158 others(11): Show |
14 | HG00280.hp2 HG00642.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.436-738_436-733del others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | CTATATAT others(1): Show |
C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0173 a0001c0001t0003g0003 others(4): Show |
8 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.436-740_436-733del others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | CTATATAT others(3): Show |
C | 2 | a0001c0001t0001g0058 a0002c0002t0001g0194 |
2 | HG00099.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.436-742_436-733del others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | CTATATAT others(7): Show |
C | 1 | a0002c0002t0001g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.436-746_436-733del others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510909 | CTATATAT others(15): Show |
C | 2 | a0001c0001t0001g0112 a0002c0002t0001g0123 |
2 | HG02080.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.436-754_436-733del others(22): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | ||||||
| chr21:39510980 | A | C | 2 | a0002c0002t0001g0031 a0002c0002t0001g0032 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.436-700A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510980 | |||||||
| chr21:39510984 | T | G | 1 | a0002c0002t0002g0260 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436-696T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510984 | |||||||
| chr21:39511097 | AT | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.436-575delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39511097 | ||||||
| chr21:39511110 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.436-570G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511110 | |||||||
| chr21:39511215 | G | A | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-465G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511215 | |||||||
| chr21:39511309 | TGTG | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0100 a0005c0005t0001g0224 |
3 | HG03209.hp1 HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.436-367_436-365del others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39511309 | ||||||
| chr21:39511325 | T | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-355T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511325 | |||||||
| chr21:39511335 | T | A | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-345T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511335 | |||||||
| chr21:39511425 | G | T | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-255G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511425 | |||||||
| chr21:39511444 | A | T | 2 | a0002c0002t0001g0196 a0002c0002t0001g0213 |
2 | NA18970.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.436-236A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511444 | |||||||
| chr21:39511587 | T | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-93T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511587 | |||||||
| chr21:39511610 | A | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-70A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511610 | |||||||
| chr21:39511638 | C | A | 11 | a0001c0001t0005g0238 a0001c0001t0005g0261 a0001c0001t0005g0263 others(8): Show |
12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-42C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511638 | |||||||
| chr21:39511867 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*34+58C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39511867 | |||||||
| chr21:39511873 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+64A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39511873 | |||||||
| chr21:39511983 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*34+174C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39511983 | |||||||
| chr21:39512055 | T | G | 2 | a0001c0001t0001g0095 a0001c0001t0002g0246 |
2 | HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.*34+246T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512055 | |||||||
| chr21:39512101 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.*34+292T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512101 | |||||||
| chr21:39512102 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.*34+293T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512102 | |||||||
| chr21:39512131 | T | G | 1 | a0002c0002t0001g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.*34+322T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512131 | |||||||
| chr21:39512344 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG01346.hp2 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.*34+535C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512344 | |||||||
| chr21:39512345 | C | T | 1 | a0001c0001t0011g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.*34+536C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512345 | |||||||
| chr21:39512384 | G | T | 2 | a0001c0001t0003g0102 a0001c0001t0004g0229 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*34+575G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512384 | |||||||
| chr21:39512436 | T | C | 1 | a0002c0002t0002g0260 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.*34+627T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512436 | |||||||
| chr21:39512895 | A | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0128 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.*34+1086A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512895 | |||||||
| chr21:39512944 | A | G | 32 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0069 others(29): Show |
34 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.*34+1135A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512944 | |||||||
| chr21:39512997 | C | T | 4 | a0001c0001t0003g0122 a0001c0001t0003g0227 a0001c0001t0003g0228 others(1): Show |
4 | HG02145.hp2 HG02922.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.*34+1188C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512997 | |||||||
| chr21:39513017 | A | G | 5 | a0003c0003t0004g0239 a0003c0003t0004g0240 a0003c0003t0004g0241 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.*34+1208A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513017 | |||||||
| chr21:39513176 | C | T | 8 | a0001c0001t0003g0102 a0001c0001t0004g0022 a0001c0001t0004g0229 others(5): Show |
8 | HG00642.hp1 HG00735.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.*34+1367C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513176 | |||||||
| chr21:39513181 | G | A | 32 | a0001c0001t0001g0112 a0001c0001t0002g0273 a0001c0001t0003g0003 others(29): Show |
34 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.*34+1372G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513181 | |||||||
| chr21:39513232 | A | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1423A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513232 | |||||||
| chr21:39513255 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1446A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513255 | |||||||
| chr21:39513257 | G | C | 1 | a0002c0002t0001g0204 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.*34+1448G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513257 | |||||||
| chr21:39513265 | C | A | 1 | a0002c0002t0001g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.*34+1456C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513265 | |||||||
| chr21:39513272 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1463A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513272 | |||||||
| chr21:39513280 | T | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1471T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513280 | |||||||
| chr21:39513354 | T | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1545T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513354 | |||||||
| chr21:39513364 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.*34+1555A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513364 | |||||||
| chr21:39513391 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.*34+1582C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513391 | |||||||
| chr21:39513525 | G | GT | 11 | a0002c0002t0001g0004 a0002c0002t0001g0027 a0002c0002t0001g0028 others(8): Show |
12 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.*35-1559dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 39513525 | ||||||
| chr21:39513621 | C | G | 1 | a0002c0002t0001g0189 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.*35-1467C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513621 | |||||||
| chr21:39513795 | A | G | 3 | a0002c0002t0001g0023 a0002c0002t0001g0144 a0002c0002t0001g0145 |
3 | HG02647.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.*35-1293A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513795 | |||||||
| chr21:39514099 | A | G | 4 | a0002c0002t0002g0020 a0002c0002t0002g0249 a0002c0002t0002g0250 others(1): Show |
5 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.*35-989A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514099 | |||||||
| chr21:39514142 | C | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*35-946C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514142 | |||||||
| chr21:39514237 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.*35-851C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514237 | |||||||
| chr21:39514393 | G | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0128 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.*35-695G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514393 | |||||||
| chr21:39514398 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.*35-690A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514398 | |||||||
| chr21:39514610 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.*35-478C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514610 | |||||||
| chr21:39514642 | A | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0026 others(15): Show |
19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*35-446A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514642 | |||||||
| chr21:39514889 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.*35-199T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514889 | |||||||
| chr21:39514989 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*35-99G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514989 |