Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26751 |
| ensemblid | ENSG00000035115.22 |
| hgncid | 29546 |
| symbol | SH3YL1 |
| name | SH3 and SYLF domain containing 1 |
| refseq_nuc | NM_015677.4 |
| refseq_prot | NP_056492.2 |
| ensembl_nuc | ENST00000356150.10 |
| ensembl_prot | ENSP00000348471.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 218144 |
| end | 264032 |
| strand | - |
| ver | v1.2 |
| region | chr2:218144-264032 |
| region5000 | chr2:213144-269032 |
| regionname0 | SH3YL1_chr2_218144_264032 |
| regionname5000 | SH3YL1_chr2_213144_269032 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1025 | 263 | 74 | 55 | 98 | 6 | 28 | SH3YL1_chr2_213144_269032 | SH3YL1 | TGAAT others(1020): Show |
chr2 | 213144 | 269032 | ||
| a0001c0002 | 0/0 | 1025 | 91 | 14 | 19 | 38 | 7 | 13 | SH3YL1_chr2_213144_269032 | SH3YL1 | TGAAT others(1020): Show |
chr2 | 213144 | 269032 | ||
| a0001c0003 | 0/0 | 1025 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | TGAAT others(1020): Show |
chr2 | 213144 | 269032 | ||
| a0001c0004 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | TGAAT others(1020): Show |
chr2 | 213144 | 269032 | ||
| a0001c0005 | 0/0 | 1025 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | TGAAT others(1020): Show |
chr2 | 213144 | 269032 | ||
| a0001c0006 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | TGAAT others(1020): Show |
chr2 | 213144 | 269032 | ||
| a0001c0007 | 0/0 | 1025 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | TGAAT others(1020): Show |
chr2 | 213144 | 269032 | ||
| a0001c0008 | 0/0 | 1025 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | TGAAT others(1020): Show |
chr2 | 213144 | 269032 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1743 | 246 | 63 | 51 | 98 | 6 | 27 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0001t0002 | 0/0 | 1743 | 4 | 4 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0001t0003 | 0/1 | 1743 | 4 | 0 | 2 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0001t0004 | 0/0 | 1743 | 3 | 1 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0001t0005 | 0/0 | 1743 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0001t0006 | 0/0 | 1743 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0001t0007 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0001t0008 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0002t0002 | 0/0 | 1743 | 91 | 14 | 19 | 38 | 7 | 13 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0003t0001 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0004t0001 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0005t0002 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0006t0002 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0007t0001 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| a0001c0008t0001 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | CTCTT others(1738): Show |
chr2 | 213144 | 269032 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 1 | 1 | 12 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 3 | 7 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0003g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0003 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0004 | 0/0 | 6 | 0 | 0 | 4 | 1 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0005 | 0/0 | 6 | 0 | 4 | 1 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0005t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0006t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| a0001c0008t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0258 | EUR | GBR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0225 | EUR | GBR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0255 | EUR | FIN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0004 | EUR | FIN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0219 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0123 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0242 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0209 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0226 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0262 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0250 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0253 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0038 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01516 | hp2 | a0001 | c0007 | t0001 | g0102 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0038 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01884 | hp2 | a0001 | c0008 | t0001 | g0203 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0233 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0264 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0236 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0042 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0238 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0211 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0246 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02976 | hp1 | a0001 | c0005 | t0002 | g0257 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0088 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0267 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0042 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0218 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0208 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0039 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0039 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0237 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0191 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0247 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0261 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18939 | hp2 | a0001 | c0006 | t0002 | g0229 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0260 | AFR | YRI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | ASW | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ASW | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0043 | EUR | TSI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0205 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | USA | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18955 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0249 | AFR | USA | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | USA | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0069 | REF | REF | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0058 | REF | REF | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218858 | G | A | 1 | a0001 | 1 | HG01516.hp2 | stop_gained | HIGH | c.982C>T | p.Arg328* | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 1030/1744 | 982/1029 | 328/342 | chr2 | 218858 | |||
| chr2:224885 | A | G | 1 | a0001 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.817T>C | p.Ser273Pro | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/10 | 865/1744 | 817/1029 | 273/342 | chr2 | 224885 | |||
| chr2:231153 | A | G | 1 | a0001 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.572T>C | p.Phe191Ser | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/10 | 620/1744 | 572/1029 | 191/342 | chr2 | 231153 | |||
| chr2:231171 | C | G | 1 | a0001 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.554G>C | p.Arg185Pro | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/10 | 602/1744 | 554/1029 | 185/342 | chr2 | 231171 | |||
| chr2:233172 | C | G | 1 | a0001 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.462G>C | p.Lys154Asn | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/10 | 510/1744 | 462/1029 | 154/342 | chr2 | 233172 | |||
| chr2:233195 | C | T | 1 | a0001 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.439G>A | p.Ala147Thr | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/10 | 487/1744 | 439/1029 | 147/342 | chr2 | 233195 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:224919 | A | G | 3 | a0001c0002 a0001c0005 a0001c0006 |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
splice_region_variant&synonymous_variant | LOW | c.783T>C | p.Ser261Ser | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/10 | 831/1744 | 783/1029 | 261/342 | chr2 | 224919 | |||
| chr2:249792 | G | A | 1 | a0001c0008 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.165C>T | p.Ala55Ala | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/10 | 213/1744 | 165/1029 | 55/342 | chr2 | 249792 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218165 | A | T | 1 | a0001c0001t0005 | 2 | HG02109.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*646T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 646 | chr2 | 218165 | ||||||
| chr2:218386 | G | A | 7 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(4): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*425C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 425 | chr2 | 218386 | ||||||
| chr2:218476 | C | G | 1 | a0001c0001t0003 | 3 | HG01106.hp1 HG01167.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*335G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 335 | chr2 | 218476 | ||||||
| chr2:218542 | G | A | 1 | a0001c0001t0008 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 269 | chr2 | 218542 | ||||||
| chr2:263995 | C | T | 1 | a0001c0001t0006 | 2 | HG02559.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-11G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/10 | 11 | chr2 | 263995 | ||||||
| chr2:264014 | C | A | 1 | a0001c0001t0007 | 1 | HG02559.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-30G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/10 | chr2 | 264014 | |||||||
| chr2:264019 | C | A | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(3): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/10 | 35 | chr2 | 264019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:219018 | G | A | 1 | a0001c0001t0001g0013 | 3 | HG02257.hp2 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839-17C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219018 | |||||||
| chr2:219051 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.839-50C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219051 | |||||||
| chr2:219082 | C | A | 2 | a0001c0001t0004g0122 a0001c0001t0004g0123 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.839-81G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219082 | |||||||
| chr2:219140 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0007g0204 |
3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.839-139A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219140 | |||||||
| chr2:219346 | G | T | 2 | a0001c0002t0002g0217 a0001c0002t0002g0218 |
2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.839-345C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219346 | |||||||
| chr2:219461 | C | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.839-460G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219461 | |||||||
| chr2:219482 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0066 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.839-481A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219482 | |||||||
| chr2:219622 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0007g0204 |
3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.839-621G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219622 | |||||||
| chr2:219641 | A | C | 2 | a0001c0001t0001g0032 a0001c0003t0001g0191 |
3 | HG03704.hp1 HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.839-640T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219641 | |||||||
| chr2:219932 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.839-931C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219932 | |||||||
| chr2:220084 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0066 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.839-1083A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220084 | |||||||
| chr2:220188 | C | CAAT | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(116): Show |
153 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.839-1190_839-1188d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220188 | |||||||
| chr2:220188 | C | CAATAAT | 30 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
39 | HG00642.hp1 HG01069.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.839-1193_839-1188d others(8): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220188 | |||||||
| chr2:220188 | C | CAATAATA others(2): Show |
10 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0099 others(7): Show |
14 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.839-1196_839-1188d others(11): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220188 | |||||||
| chr2:220542 | T | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.839-1541A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220542 | |||||||
| chr2:220548 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0062 others(7): Show |
13 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.839-1547C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220548 | |||||||
| chr2:220615 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.839-1614C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220615 | |||||||
| chr2:220638 | C | T | 1 | a0001c0002t0002g0240 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.839-1637G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220638 | |||||||
| chr2:220647 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.839-1646C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220647 | |||||||
| chr2:220889 | G | A | 64 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(61): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.839-1888C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220889 | |||||||
| chr2:221032 | T | TCAGGCAC others(4): Show |
168 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(165): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.839-2032_839-2031i others(13): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221032 | |||||||
| chr2:221069 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.839-2068C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221069 | |||||||
| chr2:221384 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.839-2383T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221384 | |||||||
| chr2:221391 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.839-2390A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221391 | |||||||
| chr2:221451 | C | T | 2 | a0001c0001t0006g0205 a0001c0001t0006g0206 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.839-2450G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221451 | |||||||
| chr2:221456 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.839-2455A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221456 | |||||||
| chr2:221492 | G | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.839-2491C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221492 | |||||||
| chr2:221560 | G | A | 65 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(62): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.839-2559C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221560 | |||||||
| chr2:221799 | AGAGT | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0026 others(15): Show |
26 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.839-2802_839-2799d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221799 | |||||||
| chr2:221943 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.838+2921A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221943 | |||||||
| chr2:221981 | C | T | 78 | a0001c0001t0001g0127 a0001c0001t0002g0210 a0001c0001t0002g0212 others(75): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.838+2883G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221981 | |||||||
| chr2:222050 | C | T | 2 | a0001c0001t0004g0122 a0001c0001t0004g0123 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.838+2814G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222050 | |||||||
| chr2:222145 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0027 |
6 | HG01069.hp2 HG01261.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+2719C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222145 | |||||||
| chr2:222164 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.838+2700A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222164 | |||||||
| chr2:222213 | T | C | 6 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+2651A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222213 | |||||||
| chr2:222307 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
8 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.838+2557G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222307 | |||||||
| chr2:222336 | T | C | 68 | a0001c0001t0008g0267 a0001c0002t0002g0003 a0001c0002t0002g0004 others(65): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+2528A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222336 | |||||||
| chr2:222483 | A | T | 2 | a0001c0001t0004g0122 a0001c0001t0004g0123 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.838+2381T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222483 | |||||||
| chr2:222501 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.838+2363A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222501 | |||||||
| chr2:222553 | G | T | 1 | a0001c0001t0004g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.838+2311C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222553 | |||||||
| chr2:222561 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.838+2303T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222561 | |||||||
| chr2:222690 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.838+2174C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222690 | |||||||
| chr2:222854 | T | C | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0201 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+2010A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222854 | |||||||
| chr2:222903 | G | A | 1 | a0001c0001t0004g0122 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.838+1961C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222903 | |||||||
| chr2:222958 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.838+1906G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222958 | |||||||
| chr2:223088 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | NA18984.hp1 NA19060.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+1776T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223088 | |||||||
| chr2:223135 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.838+1729G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223135 | |||||||
| chr2:223180 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.838+1684C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223180 | |||||||
| chr2:223375 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.838+1489C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223375 | |||||||
| chr2:223549 | T | C | 1 | a0001c0001t0008g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.838+1315A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223549 | |||||||
| chr2:223724 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.838+1140A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223724 | |||||||
| chr2:223783 | A | C | 2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.838+1081T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223783 | |||||||
| chr2:223818 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.838+1046G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223818 | |||||||
| chr2:223823 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.838+1041G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223823 | |||||||
| chr2:223897 | G | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.838+967C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223897 | |||||||
| chr2:224086 | T | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(166): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.838+778A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224086 | |||||||
| chr2:224123 | C | T | 4 | a0001c0001t0001g0151 a0001c0001t0001g0164 a0001c0001t0001g0171 others(1): Show |
4 | HG00408.hp2 HG00609.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+741G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224123 | |||||||
| chr2:224160 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.838+704A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224160 | |||||||
| chr2:224192 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(91): Show |
118 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.838+672T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224192 | |||||||
| chr2:224266 | G | A | 1 | a0001c0002t0002g0231 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.838+598C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224266 | |||||||
| chr2:224317 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.838+547G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224317 | |||||||
| chr2:224517 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0150 |
2 | HG00673.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.838+347T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224517 | |||||||
| chr2:224607 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.838+257C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224607 | |||||||
| chr2:224625 | T | C | 1 | a0001c0002t0002g0239 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.838+239A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224625 | |||||||
| chr2:224829 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.838+35A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224829 | |||||||
| chr2:224970 | C | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(164): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.782-50G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 224970 | |||||||
| chr2:225059 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.782-139G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225059 | |||||||
| chr2:225140 | A | G | 1 | a0001c0001t0004g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.782-220T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225140 | |||||||
| chr2:225258 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.782-338G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225258 | |||||||
| chr2:225437 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0062 others(10): Show |
16 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.782-517A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225437 | |||||||
| chr2:225515 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.782-595G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225515 | |||||||
| chr2:225578 | A | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0067 |
6 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-658T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225578 | |||||||
| chr2:225708 | A | G | 1 | a0001c0002t0002g0225 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.782-788T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225708 | |||||||
| chr2:225753 | T | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0172 |
2 | NA18980.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.782-833A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225753 | |||||||
| chr2:225886 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.782-966A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225886 | |||||||
| chr2:225951 | A | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(166): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.782-1031T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225951 | |||||||
| chr2:226231 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.782-1311C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226231 | |||||||
| chr2:226243 | T | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0166 |
3 | HG01168.hp2 HG01255.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.782-1323A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226243 | |||||||
| chr2:226330 | T | C | 1 | a0001c0002t0002g0262 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.782-1410A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226330 | |||||||
| chr2:226528 | C | T | 2 | a0001c0001t0006g0205 a0001c0001t0006g0206 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.782-1608G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226528 | |||||||
| chr2:226529 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0166 |
3 | HG01168.hp2 HG01255.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.782-1609C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226529 | |||||||
| chr2:226568 | C | T | 1 | a0001c0002t0002g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.782-1648G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226568 | |||||||
| chr2:226594 | C | T | 4 | a0001c0002t0002g0040 a0001c0002t0002g0225 a0001c0002t0002g0237 others(1): Show |
5 | HG00140.hp2 HG00738.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-1674G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226594 | |||||||
| chr2:226749 | TTGGGGAG others(11): Show |
T | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.782-1847_782-1830d others(20): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226749 | |||||||
| chr2:226753 | G | T | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.782-1833C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226753 | |||||||
| chr2:226781 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.782-1861A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226781 | |||||||
| chr2:226855 | C | T | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.782-1935G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226855 | |||||||
| chr2:226856 | G | A | 2 | a0001c0002t0002g0041 a0001c0002t0002g0235 |
3 | NA18962.hp1 NA19003.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.782-1936C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226856 | |||||||
| chr2:226867 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.782-1947G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226867 | |||||||
| chr2:226933 | A | G | 77 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0002g0210 others(74): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.782-2013T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226933 | |||||||
| chr2:226999 | A | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0062 others(10): Show |
16 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.782-2079T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226999 | |||||||
| chr2:227066 | G | A | 77 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0002g0210 others(74): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.782-2146C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227066 | |||||||
| chr2:227081 | T | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.782-2161A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227081 | |||||||
| chr2:227121 | A | G | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.782-2201T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227121 | |||||||
| chr2:227201 | C | T | 74 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(71): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.782-2281G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227201 | |||||||
| chr2:227505 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.781+2461G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227505 | |||||||
| chr2:227553 | A | C | 1 | a0001c0001t0004g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.781+2413T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227553 | |||||||
| chr2:227684 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.781+2282C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227684 | |||||||
| chr2:227722 | TAATTTAT others(7): Show |
T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.781+2230_781+2243d others(16): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227722 | |||||||
| chr2:227806 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781+2160C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227806 | |||||||
| chr2:227889 | A | ATG | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(85): Show |
112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.781+2075_781+2076d others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227889 | |||||||
| chr2:227889 | ATG | A | 74 | a0001c0001t0001g0093 a0001c0001t0001g0127 a0001c0001t0002g0210 others(71): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.781+2075_781+2076d others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227889 | |||||||
| chr2:227978 | A | C | 1 | a0001c0001t0001g0095 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.781+1988T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227978 | |||||||
| chr2:228088 | G | A | 69 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(66): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.781+1878C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228088 | |||||||
| chr2:228268 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.781+1698T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228268 | |||||||
| chr2:228450 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0007g0204 |
3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.781+1516G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228450 | |||||||
| chr2:228505 | C | T | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.781+1461G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228505 | |||||||
| chr2:228670 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.781+1296G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228670 | |||||||
| chr2:229000 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.781+966G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229000 | |||||||
| chr2:229112 | A | G | 1 | a0001c0001t0004g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.781+854T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229112 | |||||||
| chr2:229456 | A | G | 83 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0154 others(80): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.781+510T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229456 | |||||||
| chr2:229536 | C | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0062 others(10): Show |
16 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.781+430G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229536 | |||||||
| chr2:229590 | G | A | 2 | a0001c0001t0001g0125 a0001c0003t0001g0191 |
2 | HG02809.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.781+376C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229590 | |||||||
| chr2:229597 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.781+369G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229597 | |||||||
| chr2:229644 | G | A | 6 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0134 others(3): Show |
6 | HG00597.hp1 HG02074.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+322C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229644 | |||||||
| chr2:229646 | G | C | 2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.781+320C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229646 | |||||||
| chr2:229686 | G | A | 1 | a0001c0002t0002g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.781+280C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229686 | |||||||
| chr2:229716 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.781+250C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229716 | |||||||
| chr2:229723 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.781+243G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229723 | |||||||
| chr2:229728 | C | CA | 84 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(81): Show |
107 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.781+237dupT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229728 | |||||||
| chr2:229728 | CA | C | 75 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0053 others(72): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.781+237delT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229728 | |||||||
| chr2:229728 | CAA | C | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0002g0214 others(3): Show |
6 | HG01496.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+236_781+237del others(2): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229728 | |||||||
| chr2:230055 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.703-11G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230055 | |||||||
| chr2:230141 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-97A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230141 | |||||||
| chr2:230233 | T | A | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.703-189A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230233 | |||||||
| chr2:230440 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.703-396G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230440 | |||||||
| chr2:230442 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(139): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.703-398A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230442 | |||||||
| chr2:230658 | C | T | 1 | a0001c0002t0002g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702+365G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230658 | |||||||
| chr2:230716 | C | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.702+307G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230716 | |||||||
| chr2:230721 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.702+302G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230721 | |||||||
| chr2:230912 | A | C | 75 | a0001c0001t0001g0127 a0001c0001t0002g0210 a0001c0001t0002g0212 others(72): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.702+111T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230912 | |||||||
| chr2:231260 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.534-69C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231260 | |||||||
| chr2:231532 | A | G | 2 | a0001c0002t0002g0232 a0001c0002t0002g0259 |
2 | NA18969.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.534-341T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231532 | |||||||
| chr2:231571 | A | T | 1 | a0001c0002t0002g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.534-380T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231571 | |||||||
| chr2:231583 | C | G | 14 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0062 others(11): Show |
17 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.534-392G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231583 | |||||||
| chr2:231741 | C | T | 63 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(60): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.534-550G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231741 | |||||||
| chr2:231742 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.534-551C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231742 | |||||||
| chr2:231905 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.534-714G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231905 | |||||||
| chr2:231995 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.534-804G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231995 | |||||||
| chr2:232238 | CT | C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG00639.hp2 HG02723.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+862delA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232238 | |||||||
| chr2:232276 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.533+825A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232276 | |||||||
| chr2:232343 | G | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0032 others(64): Show |
87 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.533+758C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232343 | |||||||
| chr2:232445 | C | CT | 240 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(237): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.533+655dupA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232445 | |||||||
| chr2:232550 | G | A | 2 | a0001c0002t0002g0233 a0001c0002t0002g0246 |
2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.533+551C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232550 | |||||||
| chr2:232701 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.533+400A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232701 | |||||||
| chr2:233077 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.533+24T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 233077 | |||||||
| chr2:233355 | T | C | 1 | a0001c0008t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.405-126A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233355 | |||||||
| chr2:233382 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.405-153C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233382 | |||||||
| chr2:233416 | G | A | 53 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(50): Show |
75 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.405-187C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233416 | |||||||
| chr2:233570 | A | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0007g0204 |
3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.405-341T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233570 | |||||||
| chr2:233693 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.405-464G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233693 | |||||||
| chr2:233713 | A | C | 1 | a0001c0001t0001g0030 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.404+447T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233713 | |||||||
| chr2:233752 | G | T | 2 | a0001c0001t0004g0122 a0001c0001t0004g0123 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.404+408C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233752 | |||||||
| chr2:233848 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.404+312T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233848 | |||||||
| chr2:234130 | T | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.404+30A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 234130 | |||||||
| chr2:234454 | C | T | 1 | a0001c0001t0001g0033 | 2 | NA18943.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.292-182G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234454 | |||||||
| chr2:234668 | A | AAC | 82 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0201 others(79): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.292-398_292-397dup others(2): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234668 | |||||||
| chr2:234716 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292-444C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234716 | |||||||
| chr2:234737 | T | C | 6 | a0001c0002t0002g0014 a0001c0002t0002g0223 a0001c0002t0002g0242 others(3): Show |
8 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-465A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234737 | |||||||
| chr2:234801 | A | C | 2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-529T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234801 | |||||||
| chr2:235158 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.292-886C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235158 | |||||||
| chr2:235278 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.292-1006G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235278 | |||||||
| chr2:235332 | AGAGGCAG others(12): Show |
A | 1 | a0001c0002t0002g0245 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.292-1079_292-1061d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235332 | |||||||
| chr2:235346 | T | TCAGGGGA others(12): Show |
1 | a0001c0001t0001g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292-1093_292-1075d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235346 | |||||||
| chr2:235376 | A | AGCAGCAT others(12): Show |
73 | a0001c0001t0001g0127 a0001c0001t0001g0201 a0001c0001t0001g0202 others(70): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.292-1123_292-1105d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235376 | |||||||
| chr2:235376 | AGCAGCAT others(12): Show |
A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(85): Show |
112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.292-1123_292-1105d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235376 | |||||||
| chr2:235425 | T | C | 5 | a0001c0001t0006g0205 a0001c0001t0006g0206 a0001c0002t0002g0039 others(2): Show |
6 | HG02559.hp1 HG03209.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-1153A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235425 | |||||||
| chr2:235444 | C | T | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1172G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235444 | |||||||
| chr2:235478 | G | A | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1206C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235478 | |||||||
| chr2:235484 | C | CGGGCCAG others(12): Show |
6 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
8 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-1231_292-1213d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235484 | |||||||
| chr2:235484 | C | T | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1212G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235484 | |||||||
| chr2:235503 | T | C | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1231A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235503 | |||||||
| chr2:235507 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.292-1235G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235507 | |||||||
| chr2:235526 | T | C | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1254A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235526 | |||||||
| chr2:235545 | C | T | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1273G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235545 | |||||||
| chr2:235557 | A | G | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1285T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235557 | |||||||
| chr2:235585 | C | CGGGCCAG others(34): Show |
1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1314_292-1313i others(43): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235585 | |||||||
| chr2:235585 | C | T | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1313G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235585 | |||||||
| chr2:235586 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0066 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.292-1314C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235586 | |||||||
| chr2:235604 | T | C | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1332A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235604 | |||||||
| chr2:235608 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1336G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235608 | |||||||
| chr2:235627 | T | C | 2 | a0001c0001t0001g0127 a0001c0002t0002g0039 |
3 | HG02055.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1355A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235627 | |||||||
| chr2:235627 | T | TCAGGGGA others(15): Show |
50 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(47): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.292-1377_292-1356d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235627 | |||||||
| chr2:235627 | T | TCAGGGGA others(116): Show |
2 | a0001c0001t0006g0205 a0001c0001t0006g0206 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.292-1356_292-1355i others(125): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235627 | |||||||
| chr2:235635 | GGCA | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02258.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-1366_292-1364d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235635 | |||||||
| chr2:235638 | A | AGCAGCAT others(56): Show |
1 | a0001c0002t0002g0041 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1367_292-1366i others(65): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235638 | |||||||
| chr2:235639 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1367C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235639 | |||||||
| chr2:235639 | G | GCATGGGC others(12): Show |
5 | a0001c0001t0001g0126 a0001c0001t0004g0122 a0001c0001t0004g0123 others(2): Show |
5 | HG00642.hp1 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1368_292-1367i others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235639 | |||||||
| chr2:235645 | T | C | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1373A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235645 | |||||||
| chr2:235649 | C | T | 1 | a0001c0002t0002g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1377G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235649 | |||||||
| chr2:235660 | AGCAGCAC others(12): Show |
A | 1 | a0001c0002t0002g0246 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1407_292-1389d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235660 | |||||||
| chr2:235661 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02258.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-1389C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235661 | |||||||
| chr2:235667 | C | T | 26 | a0001c0001t0001g0125 a0001c0001t0001g0201 a0001c0001t0001g0202 others(23): Show |
33 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.292-1395G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235667 | |||||||
| chr2:235671 | C | T | 1 | a0001c0002t0002g0041 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1399G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235671 | |||||||
| chr2:235673 | A | G | 1 | a0001c0002t0002g0235 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.292-1401T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235673 | |||||||
| chr2:235679 | G | GGCA | 22 | a0001c0001t0001g0125 a0001c0001t0001g0201 a0001c0001t0001g0202 others(19): Show |
28 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.292-1410_292-1408d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235679 | |||||||
| chr2:235686 | T | C | 20 | a0001c0001t0001g0125 a0001c0001t0008g0267 a0001c0002t0002g0004 others(17): Show |
26 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.292-1414A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235686 | |||||||
| chr2:235698 | GGCA | G | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
9 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-1429_292-1427d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235698 | |||||||
| chr2:235701 | A | AGCATGGG others(31): Show |
19 | a0001c0001t0008g0267 a0001c0002t0002g0004 a0001c0002t0002g0040 others(16): Show |
25 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.292-1430_292-1429i others(40): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235701 | |||||||
| chr2:235702 | G | A | 1 | a0001c0002t0002g0041 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1430C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235702 | |||||||
| chr2:235708 | T | C | 54 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(51): Show |
73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.292-1436A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235708 | |||||||
| chr2:235712 | C | T | 58 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0002g0210 others(55): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.292-1440G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235712 | |||||||
| chr2:235720 | GGCAGCAT others(15): Show |
G | 1 | a0001c0001t0001g0052 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.292-1470_292-1449d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235720 | |||||||
| chr2:235721 | G | GCAA | 19 | a0001c0001t0008g0267 a0001c0002t0002g0004 a0001c0002t0002g0040 others(16): Show |
25 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.292-1450_292-1449i others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235721 | |||||||
| chr2:235727 | T | C | 1 | a0001c0002t0002g0041 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1455A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235727 | |||||||
| chr2:235731 | T | C | 80 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0002g0210 others(77): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.292-1459A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235731 | |||||||
| chr2:235742 | A | AGCAGCAC others(31): Show |
19 | a0001c0001t0008g0267 a0001c0002t0002g0004 a0001c0002t0002g0040 others(16): Show |
25 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.292-1471_292-1470i others(40): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235742 | |||||||
| chr2:235742 | A | AGCATGGG others(9): Show |
1 | a0001c0002t0002g0041 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1471_292-1470i others(18): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235742 | |||||||
| chr2:235743 | G | A | 58 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0002g0210 others(55): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.292-1471C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235743 | |||||||
| chr2:235749 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1477A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235749 | |||||||
| chr2:235753 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(144): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.292-1481A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235753 | |||||||
| chr2:235753 | TCAGGGGA others(53): Show |
T | 1 | a0001c0002t0002g0246 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1541_292-1482d others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235753 | |||||||
| chr2:235764 | AGCAGCAT others(31): Show |
A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(82): Show |
109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.292-1530_292-1493d others(40): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235764 | |||||||
| chr2:235771 | T | C | 61 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(58): Show |
79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.292-1499A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235771 | |||||||
| chr2:235775 | T | C | 83 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(80): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.292-1503A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235775 | |||||||
| chr2:235775 | TCAGGGGA others(12): Show |
T | 1 | a0001c0001t0001g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292-1522_292-1504d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235775 | |||||||
| chr2:235783 | G | GGCA | 21 | a0001c0001t0008g0267 a0001c0002t0002g0004 a0001c0002t0002g0039 others(18): Show |
29 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.292-1514_292-1512d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235783 | |||||||
| chr2:235790 | TGGGCCAG others(53): Show |
T | 1 | a0001c0001t0001g0175 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.292-1578_292-1519d others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235790 | |||||||
| chr2:235802 | G | GGCA | 21 | a0001c0001t0008g0267 a0001c0002t0002g0004 a0001c0002t0002g0039 others(18): Show |
29 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.292-1533_292-1531d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235802 | |||||||
| chr2:235805 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02074.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.292-1533T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235805 | |||||||
| chr2:235805 | AGCATGGG others(9): Show |
A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02258.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-1549_292-1534d others(18): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235805 | |||||||
| chr2:235809 | T | C | 21 | a0001c0001t0008g0267 a0001c0002t0002g0004 a0001c0002t0002g0039 others(18): Show |
29 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.292-1537A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235809 | |||||||
| chr2:235813 | C | T | 58 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0002g0210 others(55): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.292-1541G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235813 | |||||||
| chr2:235821 | G | GGCA | 55 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0002g0210 others(52): Show |
73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.292-1552_292-1550d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235821 | |||||||
| chr2:235840 | GGCA | G | 24 | a0001c0001t0001g0125 a0001c0001t0001g0201 a0001c0001t0001g0202 others(21): Show |
32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.292-1571_292-1569d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235840 | |||||||
| chr2:235844 | G | A | 4 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1572C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235844 | |||||||
| chr2:235850 | C | T | 80 | a0001c0001t0001g0125 a0001c0001t0001g0201 a0001c0001t0001g0202 others(77): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.292-1578G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235850 | |||||||
| chr2:235851 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0174 |
2 | HG00642.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.292-1579C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235851 | |||||||
| chr2:235854 | C | CCAGGGGA others(53): Show |
52 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(49): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.292-1583_292-1582i others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235854 | |||||||
| chr2:235854 | C | CCAGGGGA others(53): Show |
2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1583_292-1582i others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235854 | |||||||
| chr2:235854 | C | T | 24 | a0001c0001t0001g0125 a0001c0001t0001g0201 a0001c0001t0001g0202 others(21): Show |
32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.292-1582G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235854 | |||||||
| chr2:235872 | T | C | 5 | a0001c0001t0001g0175 a0001c0001t0004g0122 a0001c0001t0004g0123 others(2): Show |
5 | HG00642.hp1 HG01109.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1600A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235872 | |||||||
| chr2:235876 | T | C | 84 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(81): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.292-1604A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235876 | |||||||
| chr2:235887 | A | AGCATGGG others(9): Show |
3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1616_292-1615i others(18): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235887 | |||||||
| chr2:235898 | T | C | 80 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(77): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.292-1626A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235898 | |||||||
| chr2:235906 | G | GGCA | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1637_292-1635d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235906 | |||||||
| chr2:235913 | TGGGCCAG others(15): Show |
T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
77 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.292-1663_292-1642d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235913 | |||||||
| chr2:235917 | C | T | 2 | a0001c0001t0001g0127 a0001c0002t0002g0246 |
2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.292-1645G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235917 | |||||||
| chr2:235922 | G | C | 4 | a0001c0001t0001g0165 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | NA18984.hp1 NA19060.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1650C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235922 | |||||||
| chr2:235935 | C | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0121 a0001c0001t0001g0127 others(28): Show |
35 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.292-1663G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235935 | |||||||
| chr2:235939 | C | CCAGGGGA others(15): Show |
2 | a0001c0001t0001g0090 a0001c0001t0003g0088 |
2 | HG02109.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.292-1689_292-1668d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235939 | |||||||
| chr2:235939 | C | CCAGGGGA others(53): Show |
3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1668_292-1667i others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235939 | |||||||
| chr2:235961 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0029 others(59): Show |
82 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.292-1689A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235961 | |||||||
| chr2:235972 | AGCAGCAT others(31): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.292-1738_292-1701d others(40): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235972 | |||||||
| chr2:235979 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1707A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235979 | |||||||
| chr2:235983 | T | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0121 a0001c0001t0001g0127 others(30): Show |
37 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.292-1711A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235983 | |||||||
| chr2:235983 | TCAGGGGA others(12): Show |
T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0067 |
6 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-1730_292-1712d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235983 | |||||||
| chr2:235994 | AGCATGGG others(28): Show |
A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
76 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.292-1757_292-1723d others(37): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235994 | |||||||
| chr2:235998 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1726A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235998 | |||||||
| chr2:236010 | G | GGCA | 4 | a0001c0001t0001g0127 a0001c0001t0004g0122 a0001c0001t0004g0123 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-1741_292-1739d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236010 | |||||||
| chr2:236017 | T | C | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1745A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236017 | |||||||
| chr2:236021 | C | T | 2 | a0001c0001t0001g0127 a0001c0002t0002g0246 |
2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.292-1749G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236021 | |||||||
| chr2:236029 | G | GGCA | 5 | a0001c0001t0001g0127 a0001c0001t0004g0122 a0001c0001t0004g0123 others(2): Show |
5 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-1760_292-1758d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236029 | |||||||
| chr2:236029 | GGCAGCAT others(15): Show |
G | 1 | a0001c0001t0001g0175 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.292-1779_292-1758d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236029 | |||||||
| chr2:236029 | GGCAGCAT others(97): Show |
G | 1 | a0001c0001t0001g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.292-1861_292-1758d others(2): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236029 | |||||||
| chr2:236040 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
77 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.292-1768A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236040 | |||||||
| chr2:236048 | GGCA | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
77 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.292-1779_292-1777d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236048 | |||||||
| chr2:236058 | TGGGCCAG others(116): Show |
T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0121 a0001c0001t0001g0125 others(28): Show |
35 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.292-1909_292-1787d others(2): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236058 | |||||||
| chr2:236062 | C | T | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1790G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236062 | |||||||
| chr2:236070 | G | GGCAGCAG others(37): Show |
72 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(69): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.292-1799_292-1798i others(46): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236070 | |||||||
| chr2:236070 | G | GGCAGCAG others(37): Show |
1 | a0001c0001t0008g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292-1799_292-1798i others(46): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236070 | |||||||
| chr2:236096 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1824A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236096 | |||||||
| chr2:236100 | T | C | 3 | a0001c0001t0001g0126 a0001c0001t0007g0204 a0001c0002t0002g0246 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1828A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236100 | |||||||
| chr2:236104 | G | A | 1 | a0001c0002t0002g0256 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.292-1832C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236104 | |||||||
| chr2:236108 | GGCA | G | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1839_292-1837d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236108 | |||||||
| chr2:236122 | C | T | 1 | a0001c0002t0002g0246 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1850G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236122 | |||||||
| chr2:236130 | GGCA | G | 5 | a0001c0001t0001g0126 a0001c0001t0004g0122 a0001c0001t0004g0123 others(2): Show |
5 | HG00642.hp1 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1861_292-1859d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236130 | |||||||
| chr2:236140 | T | C | 1 | a0001c0002t0002g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.292-1868A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236140 | |||||||
| chr2:236144 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0007g0204 a0001c0002t0002g0246 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1872G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236144 | |||||||
| chr2:236152 | GGCAGCAT others(59): Show |
G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
77 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.292-1946_292-1881d others(68): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236152 | |||||||
| chr2:236159 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1887A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236159 | |||||||
| chr2:236163 | C | T | 4 | a0001c0001t0001g0176 a0001c0001t0004g0122 a0001c0001t0004g0123 others(1): Show |
4 | HG00408.hp2 HG00642.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1891G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236163 | |||||||
| chr2:236181 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0176 others(5): Show |
8 | HG00408.hp2 HG00642.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.292-1909G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236181 | |||||||
| chr2:236185 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1913G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236185 | |||||||
| chr2:236185 | CCAGGGGA others(15): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.292-1935_292-1914d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236185 | |||||||
| chr2:236193 | GGCAGCAG others(18): Show |
G | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1946_292-1922d others(27): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236193 | |||||||
| chr2:236196 | A | AGCAGCAT others(72): Show |
63 | a0001c0001t0008g0267 a0001c0002t0002g0003 a0001c0002t0002g0004 others(60): Show |
87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.292-1925_292-1924i others(81): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236196 | |||||||
| chr2:236196 | A | AGCAGCAT others(72): Show |
4 | a0001c0002t0002g0043 a0001c0002t0002g0226 a0001c0002t0002g0254 others(1): Show |
5 | HG01192.hp1 HG01346.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1925_292-1924i others(81): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236196 | |||||||
| chr2:236207 | T | C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0121 a0001c0001t0001g0125 others(32): Show |
39 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.292-1935A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236207 | |||||||
| chr2:236207 | T | TCAGGGGA others(15): Show |
1 | a0001c0001t0001g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292-1957_292-1936d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236207 | |||||||
| chr2:236207 | T | TCAGGGGA others(72): Show |
1 | a0001c0002t0002g0005 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.292-1936_292-1935i others(81): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236207 | |||||||
| chr2:236215 | GGCA | G | 35 | a0001c0001t0001g0006 a0001c0001t0001g0121 a0001c0001t0001g0125 others(32): Show |
39 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.292-1946_292-1944d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236215 | |||||||
| chr2:236218 | A | AGCAGCAT others(113): Show |
6 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-1947_292-1946i others(122): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236218 | |||||||
| chr2:236218 | A | AGCATGGG others(50): Show |
2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1947_292-1946i others(59): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236218 | |||||||
| chr2:236559 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-2287G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236559 | |||||||
| chr2:236838 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292-2566A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236838 | |||||||
| chr2:236950 | C | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.292-2678G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236950 | |||||||
| chr2:237137 | AT | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.292-2866delA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237137 | |||||||
| chr2:237140 | T | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.292-2868A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237140 | |||||||
| chr2:237142 | C | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.292-2870G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237142 | |||||||
| chr2:237208 | G | A | 1 | a0001c0002t0002g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.292-2936C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237208 | |||||||
| chr2:237346 | GGTGACAC others(5): Show |
G | 74 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(71): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.292-3086_292-3075d others(14): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237346 | |||||||
| chr2:237471 | G | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.292-3199C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237471 | |||||||
| chr2:237506 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-3234G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237506 | |||||||
| chr2:237826 | A | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0078 |
4 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-3554T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237826 | |||||||
| chr2:237867 | T | C | 1 | a0001c0001t0008g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292-3595A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237867 | |||||||
| chr2:238259 | T | TTG | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0045 others(13): Show |
18 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.292-3989_292-3988d others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | |||||||
| chr2:238259 | TTG | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(53): Show |
79 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.292-3989_292-3988d others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | |||||||
| chr2:238259 | TTGTG | T | 62 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(59): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.292-3991_292-3988d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | |||||||
| chr2:238259 | TTGTGTG | T | 7 | a0001c0001t0001g0094 a0001c0001t0006g0205 a0001c0002t0002g0228 others(4): Show |
7 | HG01192.hp2 HG01358.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-3993_292-3988d others(8): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | |||||||
| chr2:238259 | TTGTGTGT others(3): Show |
T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0129 a0001c0001t0001g0144 others(9): Show |
13 | HG00558.hp2 HG00597.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.292-3997_292-3988d others(12): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | |||||||
| chr2:238259 | TTGTGTGT others(5): Show |
T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(71): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.292-3999_292-3988d others(14): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | |||||||
| chr2:238308 | G | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.292-4036C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238308 | |||||||
| chr2:238328 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.292-4056G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238328 | |||||||
| chr2:238600 | G | C | 1 | a0001c0002t0002g0224 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.292-4328C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238600 | |||||||
| chr2:238975 | A | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.292-4703T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238975 | |||||||
| chr2:238989 | G | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0142 others(1): Show |
4 | HG03491.hp1 HG03710.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-4717C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238989 | |||||||
| chr2:239111 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.292-4839T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239111 | |||||||
| chr2:239144 | G | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0008t0001g0203 |
3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.292-4872C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239144 | |||||||
| chr2:239263 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-4991A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239263 | |||||||
| chr2:239416 | C | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.292-5144G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239416 | |||||||
| chr2:239515 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.292-5243T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239515 | |||||||
| chr2:239597 | C | G | 74 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(71): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.292-5325G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239597 | |||||||
| chr2:239612 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
4 | HG02647.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-5340G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239612 | |||||||
| chr2:239655 | TAAC | T | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
17 | HG00597.hp1 HG02074.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.292-5386_292-5384d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239655 | |||||||
| chr2:239736 | C | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0032 others(64): Show |
87 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.292-5464G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239736 | |||||||
| chr2:239898 | A | G | 1 | a0001c0001t0007g0204 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.292-5626T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239898 | |||||||
| chr2:239964 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.292-5692C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239964 | |||||||
| chr2:239969 | C | T | 82 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0201 others(79): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.292-5697G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239969 | |||||||
| chr2:240053 | C | T | 1 | a0001c0001t0004g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.292-5781G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240053 | |||||||
| chr2:240054 | A | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(166): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.292-5782T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240054 | |||||||
| chr2:240085 | C | G | 4 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-5813G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240085 | |||||||
| chr2:240210 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.292-5938C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240210 | |||||||
| chr2:240255 | A | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.292-5983T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240255 | |||||||
| chr2:240326 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.292-6054G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240326 | |||||||
| chr2:240342 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0060 others(1): Show |
5 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-6070C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240342 | |||||||
| chr2:240567 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-6295T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240567 | |||||||
| chr2:240575 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.292-6303G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240575 | |||||||
| chr2:240630 | T | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.292-6358A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240630 | |||||||
| chr2:240696 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0162 |
2 | HG00423.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.292-6424G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240696 | |||||||
| chr2:240785 | G | A | 71 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(68): Show |
96 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.292-6513C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240785 | |||||||
| chr2:240800 | C | T | 1 | a0001c0002t0002g0227 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.292-6528G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240800 | |||||||
| chr2:240824 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0181 |
3 | HG00438.hp1 HG02040.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.292-6552A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240824 | |||||||
| chr2:240923 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.291+6615T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240923 | |||||||
| chr2:240926 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0062 others(10): Show |
16 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.291+6612A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240926 | |||||||
| chr2:240976 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.291+6562T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240976 | |||||||
| chr2:241049 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.291+6489G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241049 | |||||||
| chr2:241167 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
4 | HG02698.hp1 HG02738.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+6371G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241167 | |||||||
| chr2:241263 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.291+6275A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241263 | |||||||
| chr2:241669 | A | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.291+5869T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241669 | |||||||
| chr2:241692 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.291+5846A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241692 | |||||||
| chr2:241719 | G | A | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.291+5819C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241719 | |||||||
| chr2:241842 | T | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG01361.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.291+5696A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241842 | |||||||
| chr2:241852 | A | G | 2 | a0001c0002t0002g0217 a0001c0002t0002g0218 |
2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.291+5686T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241852 | |||||||
| chr2:242132 | G | A | 74 | a0001c0001t0001g0127 a0001c0001t0002g0210 a0001c0001t0002g0212 others(71): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.291+5406C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242132 | |||||||
| chr2:242177 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0007g0204 |
3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.291+5361G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242177 | |||||||
| chr2:242202 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.291+5336C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242202 | |||||||
| chr2:242426 | A | G | 66 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(63): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.291+5112T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242426 | |||||||
| chr2:242458 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0008t0001g0203 |
3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291+5080T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242458 | |||||||
| chr2:242605 | C | A | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
90 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.291+4933G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242605 | |||||||
| chr2:242732 | T | TAAC | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(166): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.291+4803_291+4805d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242732 | |||||||
| chr2:242778 | C | T | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0004g0122 others(1): Show |
4 | HG00642.hp1 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+4760G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242778 | |||||||
| chr2:242793 | G | C | 57 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(54): Show |
81 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.291+4745C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242793 | |||||||
| chr2:242800 | T | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(86): Show |
114 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.291+4738A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242800 | |||||||
| chr2:242860 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.291+4678A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242860 | |||||||
| chr2:242879 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291+4659A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242879 | |||||||
| chr2:243056 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.291+4482A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243056 | |||||||
| chr2:243107 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.291+4431A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243107 | |||||||
| chr2:243504 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(83): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.291+4034G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243504 | |||||||
| chr2:243567 | T | TA | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(166): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.291+3970dupT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243567 | |||||||
| chr2:243806 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.291+3732C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243806 | |||||||
| chr2:243929 | G | A | 81 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0201 others(78): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.291+3609C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243929 | |||||||
| chr2:243987 | G | T | 1 | a0001c0002t0002g0224 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.291+3551C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243987 | |||||||
| chr2:244003 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.291+3535G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244003 | |||||||
| chr2:244133 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.291+3405A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244133 | |||||||
| chr2:244139 | C | T | 2 | a0001c0001t0001g0100 a0001c0002t0002g0209 |
2 | HG01175.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.291+3399G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244139 | |||||||
| chr2:244188 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG01993.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.291+3350A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244188 | |||||||
| chr2:244201 | T | TA | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(85): Show |
112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.291+3336dupT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244201 | |||||||
| chr2:244209 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.291+3329T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244209 | |||||||
| chr2:244239 | T | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.291+3299A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244239 | |||||||
| chr2:244262 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 |
3 | HG02622.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.291+3276G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244262 | |||||||
| chr2:244292 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.291+3246G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244292 | |||||||
| chr2:244474 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0200 |
2 | HG00621.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.291+3064G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244474 | |||||||
| chr2:244496 | A | AAAAG | 8 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0127 others(5): Show |
9 | HG01168.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.291+3038_291+3041d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244496 | |||||||
| chr2:244568 | A | AAAAG | 168 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(165): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.291+2966_291+2969d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244568 | |||||||
| chr2:244568 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.291+2970T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244568 | |||||||
| chr2:244568 | AAAAG | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
38 | HG00323.hp1 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.291+2966_291+2969d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244568 | |||||||
| chr2:244736 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.291+2802A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244736 | |||||||
| chr2:244805 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0156 |
3 | NA18964.hp1 NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.291+2733G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244805 | |||||||
| chr2:244847 | A | G | 2 | a0001c0001t0006g0205 a0001c0001t0006g0206 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.291+2691T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244847 | |||||||
| chr2:244877 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.291+2661A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244877 | |||||||
| chr2:244894 | G | A | 1 | a0001c0002t0002g0255 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.291+2644C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244894 | |||||||
| chr2:244994 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291+2544A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244994 | |||||||
| chr2:245184 | A | C | 19 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0201 others(16): Show |
19 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.291+2354T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245184 | |||||||
| chr2:245257 | A | G | 19 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0201 others(16): Show |
19 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.291+2281T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245257 | |||||||
| chr2:245286 | TTCTTA | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0140 |
3 | HG02647.hp1 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.291+2247_291+2251d others(7): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245286 | |||||||
| chr2:245311 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.291+2227A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245311 | |||||||
| chr2:245350 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.291+2188A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245350 | |||||||
| chr2:245507 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.291+2031T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245507 | |||||||
| chr2:245511 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.291+2027T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245511 | |||||||
| chr2:245613 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291+1925C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245613 | |||||||
| chr2:245661 | T | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0085 |
3 | HG00609.hp1 NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.291+1877A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245661 | |||||||
| chr2:245672 | T | A | 72 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(69): Show |
97 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.291+1866A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245672 | |||||||
| chr2:245689 | T | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0072 others(4): Show |
10 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.291+1849A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245689 | |||||||
| chr2:245778 | T | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0062 others(11): Show |
17 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.291+1760A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245778 | |||||||
| chr2:245806 | G | A | 1 | a0001c0002t0002g0256 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.291+1732C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245806 | |||||||
| chr2:246077 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(77): Show |
104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.291+1461G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246077 | |||||||
| chr2:246156 | T | C | 1 | a0001c0004t0001g0138 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.291+1382A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246156 | |||||||
| chr2:246211 | A | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 |
4 | HG01074.hp2 HG01099.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1327T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246211 | |||||||
| chr2:246301 | T | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.291+1237A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246301 | |||||||
| chr2:246435 | C | A | 2 | a0001c0001t0004g0122 a0001c0001t0004g0123 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.291+1103G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246435 | |||||||
| chr2:246592 | GGAAAGGG others(3): Show |
G | 1 | a0001c0001t0008g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.291+936_291+945del others(10): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246592 | |||||||
| chr2:246651 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.291+887T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246651 | |||||||
| chr2:246800 | GAATA | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
32 | HG00673.hp1 HG01346.hp1 HG01952.hp1 others(29): Show |
intron_variant | MODIFIER | c.291+734_291+737del others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246800 | |||||||
| chr2:246875 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.291+663G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246875 | |||||||
| chr2:246974 | G | A | 1 | a0001c0004t0001g0138 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.291+564C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246974 | |||||||
| chr2:247138 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.291+400T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 247138 | |||||||
| chr2:247303 | A | T | 2 | a0001c0001t0004g0122 a0001c0001t0004g0123 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.291+235T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 247303 | |||||||
| chr2:247319 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.291+219C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 247319 | |||||||
| chr2:247466 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.291+72T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 247466 | |||||||
| chr2:247620 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.227-18C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 247620 | |||||||
| chr2:247635 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.227-33T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 247635 | |||||||
| chr2:248037 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(143): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.227-435T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248037 | |||||||
| chr2:248340 | A | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0154 a0001c0003t0001g0191 |
4 | HG03704.hp1 HG03942.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-738T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248340 | |||||||
| chr2:248375 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.227-773A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248375 | |||||||
| chr2:248428 | G | A | 1 | a0001c0002t0002g0258 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.227-826C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248428 | |||||||
| chr2:248644 | T | G | 1 | a0001c0002t0002g0259 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.227-1042A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248644 | |||||||
| chr2:248754 | T | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | NA18984.hp1 NA19080.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.226+977A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248754 | |||||||
| chr2:248759 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.226+972G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248759 | |||||||
| chr2:248822 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.226+909T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248822 | |||||||
| chr2:248910 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.226+821G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248910 | |||||||
| chr2:249092 | A | C | 77 | a0001c0001t0001g0121 a0001c0001t0001g0152 a0001c0001t0001g0153 others(74): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.226+639T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249092 | |||||||
| chr2:249337 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.226+394A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249337 | |||||||
| chr2:249463 | C | T | 2 | a0001c0001t0006g0205 a0001c0001t0006g0206 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.226+268G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249463 | |||||||
| chr2:249586 | G | A | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.226+145C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249586 | |||||||
| chr2:249598 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02074.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.226+133C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249598 | |||||||
| chr2:249919 | G | C | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0004g0122 others(2): Show |
5 | HG00642.hp1 HG01109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-75C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 249919 | |||||||
| chr2:250008 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 |
3 | HG02622.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.113-164G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250008 | |||||||
| chr2:250195 | TA | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
6 | HG01891.hp1 HG02647.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-352delT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250195 | |||||||
| chr2:250219 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.113-375A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250219 | |||||||
| chr2:250332 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.113-488A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250332 | |||||||
| chr2:250412 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.113-568A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250412 | |||||||
| chr2:250541 | C | T | 1 | a0001c0002t0002g0223 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113-697G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250541 | |||||||
| chr2:250562 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.113-718G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250562 | |||||||
| chr2:250584 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.113-740T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250584 | |||||||
| chr2:250751 | C | A | 1 | a0001c0002t0002g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.113-907G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250751 | |||||||
| chr2:250806 | T | C | 1 | a0001c0002t0002g0261 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.113-962A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250806 | |||||||
| chr2:250902 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.113-1058A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250902 | |||||||
| chr2:250936 | T | C | 2 | a0001c0002t0002g0215 a0001c0002t0002g0216 |
2 | NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.113-1092A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250936 | |||||||
| chr2:250958 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
14 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-1114T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250958 | |||||||
| chr2:250982 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.113-1138G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250982 | |||||||
| chr2:251104 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.113-1260T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251104 | |||||||
| chr2:251369 | T | C | 1 | a0001c0002t0002g0261 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.113-1525A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251369 | |||||||
| chr2:251379 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.113-1535T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251379 | |||||||
| chr2:251388 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.113-1544G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251388 | |||||||
| chr2:251449 | G | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | NA18984.hp1 NA19080.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.112+1556C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251449 | |||||||
| chr2:251514 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.112+1491G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251514 | |||||||
| chr2:251534 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.112+1471G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251534 | |||||||
| chr2:251535 | G | A | 1 | a0001c0001t0008g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.112+1470C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251535 | |||||||
| chr2:251606 | G | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0008t0001g0203 |
3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.112+1399C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251606 | |||||||
| chr2:251673 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(169): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.112+1332C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251673 | |||||||
| chr2:251774 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.112+1231C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251774 | |||||||
| chr2:251839 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.112+1166T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251839 | |||||||
| chr2:251877 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.112+1128T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251877 | |||||||
| chr2:252197 | C | T | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.112+808G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252197 | |||||||
| chr2:252309 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.112+696T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252309 | |||||||
| chr2:252340 | C | A | 1 | a0001c0001t0005g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.112+665G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252340 | |||||||
| chr2:252418 | A | G | 1 | a0001c0001t0008g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.112+587T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252418 | |||||||
| chr2:252471 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.112+534T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252471 | |||||||
| chr2:252692 | C | T | 3 | a0001c0002t0002g0220 a0001c0002t0002g0221 a0001c0002t0002g0222 |
3 | HG02809.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.112+313G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252692 | |||||||
| chr2:253227 | G | A | 4 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2-112C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253227 | |||||||
| chr2:253291 | A | G | 69 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(66): Show |
93 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.2-176T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253291 | |||||||
| chr2:253348 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG03540.hp2 NA18964.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2-233G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253348 | |||||||
| chr2:253411 | A | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(168): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2-296T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253411 | |||||||
| chr2:253468 | C | T | 1 | a0001c0002t0002g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2-353G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253468 | |||||||
| chr2:253469 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2-354C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253469 | |||||||
| chr2:253533 | G | C | 1 | a0001c0002t0002g0264 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2-418C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253533 | |||||||
| chr2:253566 | C | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(168): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2-451G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253566 | |||||||
| chr2:253604 | A | G | 2 | a0001c0001t0006g0205 a0001c0001t0006g0206 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2-489T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253604 | |||||||
| chr2:253636 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2-521T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253636 | |||||||
| chr2:253760 | C | G | 2 | a0001c0001t0006g0205 a0001c0001t0006g0206 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2-645G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253760 | |||||||
| chr2:253833 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2-718T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253833 | |||||||
| chr2:253953 | C | T | 1 | a0001c0001t0008g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2-838G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253953 | |||||||
| chr2:254215 | G | A | 75 | a0001c0001t0001g0020 a0001c0001t0001g0072 a0001c0001t0001g0126 others(72): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.2-1100C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254215 | |||||||
| chr2:254393 | G | A | 1 | a0001c0002t0002g0262 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2-1278C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254393 | |||||||
| chr2:254488 | G | C | 1 | a0001c0001t0007g0204 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2-1373C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254488 | |||||||
| chr2:254510 | G | A | 2 | a0001c0002t0002g0263 a0001c0002t0002g0268 |
2 | NA18968.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2-1395C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254510 | |||||||
| chr2:254791 | T | C | 1 | a0001c0002t0002g0264 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2-1676A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254791 | |||||||
| chr2:254882 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2-1767T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254882 | |||||||
| chr2:254972 | G | C | 2 | a0001c0001t0004g0122 a0001c0001t0004g0123 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2-1857C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254972 | |||||||
| chr2:255062 | C | G | 1 | a0001c0001t0002g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2-1947G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255062 | |||||||
| chr2:255073 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2-1958G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255073 | |||||||
| chr2:255154 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG02647.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2-2039A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255154 | |||||||
| chr2:255262 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2-2147T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255262 | |||||||
| chr2:255446 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2-2331T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255446 | |||||||
| chr2:255497 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0007g0204 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2-2382C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255497 | |||||||
| chr2:255580 | G | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(82): Show |
109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2-2465C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255580 | |||||||
| chr2:255581 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2-2466C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255581 | |||||||
| chr2:255674 | G | A | 2 | a0001c0001t0006g0205 a0001c0001t0006g0206 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2-2559C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255674 | |||||||
| chr2:255729 | GA | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0099 others(9): Show |
16 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2-2615delT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255729 | |||||||
| chr2:256116 | G | T | 82 | a0001c0001t0001g0020 a0001c0001t0001g0072 a0001c0001t0001g0121 others(79): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.2-3001C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256116 | |||||||
| chr2:256278 | T | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0032 others(63): Show |
86 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2-3163A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256278 | |||||||
| chr2:256278 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2-3163A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256278 | |||||||
| chr2:256295 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2-3180T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256295 | |||||||
| chr2:256414 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2-3299C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256414 | |||||||
| chr2:256440 | C | G | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
16 | HG00597.hp1 HG02074.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2-3325G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256440 | |||||||
| chr2:256529 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2-3414A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256529 | |||||||
| chr2:256839 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(82): Show |
109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2-3724G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256839 | |||||||
| chr2:256841 | A | G | 1 | a0001c0001t0001g0015 | 2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.2-3726T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256841 | |||||||
| chr2:256897 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2-3782G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256897 | |||||||
| chr2:257206 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2-4091G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257206 | |||||||
| chr2:257341 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2-4226G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257341 | |||||||
| chr2:257432 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2-4317A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257432 | |||||||
| chr2:257434 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2-4319A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257434 | |||||||
| chr2:257635 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 |
3 | HG02622.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2-4520C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257635 | |||||||
| chr2:257725 | C | T | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2-4610G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257725 | |||||||
| chr2:257733 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0197 a0001c0007t0001g0102 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2-4618T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257733 | |||||||
| chr2:257763 | A | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 |
3 | HG02622.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2-4648T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257763 | |||||||
| chr2:257820 | G | GT | 5 | a0001c0001t0001g0072 a0001c0001t0001g0128 a0001c0001t0001g0192 others(2): Show |
5 | HG00544.hp1 HG00741.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2-4706dupA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257820 | |||||||
| chr2:257900 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2-4785A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257900 | |||||||
| chr2:257907 | T | C | 1 | a0001c0001t0004g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2-4792A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257907 | |||||||
| chr2:257991 | C | T | 2 | a0001c0002t0002g0215 a0001c0002t0002g0216 |
2 | NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2-4876G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257991 | |||||||
| chr2:257992 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0062 others(7): Show |
13 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2-4877C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257992 | |||||||
| chr2:258210 | T | C | 69 | a0001c0001t0001g0121 a0001c0001t0008g0267 a0001c0002t0002g0003 others(66): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.2-5095A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258210 | |||||||
| chr2:258463 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2-5348G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258463 | |||||||
| chr2:258546 | A | C | 1 | a0001c0001t0001g0044 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2-5431T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258546 | |||||||
| chr2:258763 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1+5221C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258763 | |||||||
| chr2:258767 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0100 |
4 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1+5217G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258767 | |||||||
| chr2:258790 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1+5194C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258790 | |||||||
| chr2:258938 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1+5046C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258938 | |||||||
| chr2:259015 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1+4969A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259015 | |||||||
| chr2:259221 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1+4763C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259221 | |||||||
| chr2:259296 | C | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(82): Show |
109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1+4688G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259296 | |||||||
| chr2:259588 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1+4396C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259588 | |||||||
| chr2:259772 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1+4212G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259772 | |||||||
| chr2:259774 | T | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(82): Show |
109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1+4210A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259774 | |||||||
| chr2:260049 | T | C | 1 | a0001c0001t0008g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1+3935A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260049 | |||||||
| chr2:260107 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1+3877T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260107 | |||||||
| chr2:260303 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0008t0001g0203 |
3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1+3681A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260303 | |||||||
| chr2:260378 | T | C | 2 | a0001c0001t0006g0205 a0001c0001t0006g0206 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1+3606A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260378 | |||||||
| chr2:260391 | T | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1+3593A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260391 | |||||||
| chr2:260402 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1+3582C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260402 | |||||||
| chr2:260661 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1+3323G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260661 | |||||||
| chr2:260677 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(82): Show |
109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1+3307C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260677 | |||||||
| chr2:261432 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1+2552G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261432 | |||||||
| chr2:261433 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1+2551G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261433 | |||||||
| chr2:261478 | A | G | 1 | a0001c0002t0002g0209 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1+2506T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261478 | |||||||
| chr2:261513 | AT | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1+2470delA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261513 | |||||||
| chr2:261524 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1+2460T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261524 | |||||||
| chr2:261800 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1+2184G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261800 | |||||||
| chr2:261839 | T | C | 1 | a0001c0003t0001g0191 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1+2145A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261839 | |||||||
| chr2:262119 | T | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(26): Show |
39 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1+1865A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262119 | |||||||
| chr2:262189 | G | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0008t0001g0203 |
3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1+1795C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262189 | |||||||
| chr2:262250 | C | T | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1+1734G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262250 | |||||||
| chr2:262297 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1+1687T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262297 | |||||||
| chr2:262335 | A | G | 75 | a0001c0001t0001g0121 a0001c0001t0002g0210 a0001c0001t0002g0212 others(72): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1+1649T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262335 | |||||||
| chr2:262408 | C | G | 1 | a0001c0002t0002g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1+1576G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262408 | |||||||
| chr2:262490 | G | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG00408.hp1 HG00438.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1+1494C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262490 | |||||||
| chr2:262553 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(169): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1+1431A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262553 | |||||||
| chr2:262886 | A | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0062 others(5): Show |
11 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1+1098T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262886 | |||||||
| chr2:263270 | T | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.1+714A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263270 | |||||||
| chr2:263392 | A | G | 1 | a0001c0002t0002g0207 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1+592T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263392 | |||||||
| chr2:263435 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1+549G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263435 | |||||||
| chr2:263540 | G | T | 1 | a0001c0002t0002g0268 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1+444C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263540 | |||||||
| chr2:263541 | T | C | 1 | a0001c0008t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1+443A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263541 | |||||||
| chr2:263542 | T | G | 1 | a0001c0002t0002g0268 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1+442A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263542 | |||||||
| chr2:263666 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
5 | HG00621.hp2 NA18968.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.1+318C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263666 | |||||||
| chr2:263709 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1+275C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263709 | |||||||
| chr2:263938 | T | C | 1 | a0001c0008t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1+46A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263938 | |||||||
| chr2:263972 | C | A | 1 | a0001c0002t0002g0268 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1+12G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263972 |