Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55668 |
| ensemblid | ENSG00000089916.18 |
| hgncid | 20210 |
| symbol | GPATCH2L |
| name | G-patch domain containing 2 like |
| refseq_nuc | NM_017926.4 |
| refseq_prot | NP_060396.2 |
| ensembl_nuc | ENST00000261530.12 |
| ensembl_prot | ENSP00000261530.7 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 76151922 |
| end | 76214343 |
| strand | + |
| ver | v1.2 |
| region | chr14:76151922-76214343 |
| region5000 | chr14:76146922-76219343 |
| regionname0 | GPATCH2L_chr14_76151922_76214343 |
| regionname5000 | GPATCH2L_chr14_76146922_76219343 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 482 | 399 | 74 | 68 | 202 | 12 | 41 | 158 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | MDELV others(477): Show |
chr14 | 76146922 | 76219343 |
| a0002 | 0/0 | 482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | MDELV others(477): Show |
chr14 | 76146922 | 76219343 |
| a0003 | 0/0 | 482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | MDELV others(477): Show |
chr14 | 76146922 | 76219343 |
| a0004 | 0/0 | 482 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | MDELV others(477): Show |
chr14 | 76146922 | 76219343 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1446 | 375 | 67 | 64 | 189 | 12 | 41 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | ATGGA others(1441): Show |
chr14 | 76146922 | 76219343 | ||
| a0001c0002 | 0/0 | 1446 | 12 | 0 | 0 | 12 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | ATGGA others(1441): Show |
chr14 | 76146922 | 76219343 | ||
| a0001c0003 | 0/0 | 1446 | 4 | 4 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | ATGGA others(1441): Show |
chr14 | 76146922 | 76219343 | ||
| a0001c0004 | 0/0 | 1446 | 4 | 0 | 3 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | ATGGA others(1441): Show |
chr14 | 76146922 | 76219343 | ||
| a0001c0005 | 0/0 | 1446 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | ATGGA others(1441): Show |
chr14 | 76146922 | 76219343 | ||
| a0001c0008 | 0/0 | 1446 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | ATGGA others(1441): Show |
chr14 | 76146922 | 76219343 | ||
| a0002c0007 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | ATGGA others(1441): Show |
chr14 | 76146922 | 76219343 | ||
| a0003c0006 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | ATGGA others(1441): Show |
chr14 | 76146922 | 76219343 | ||
| a0004c0009 | 0/0 | 1446 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | ATGGA others(1441): Show |
chr14 | 76146922 | 76219343 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 14023 | 76 | 2 | 16 | 40 | 2 | 15 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0002 | 0/0 | 14019 | 51 | 3 | 10 | 35 | 2 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0003 | 0/0 | 14019 | 34 | 0 | 0 | 29 | 0 | 5 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0004 | 0/0 | 14020 | 20 | 3 | 4 | 11 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0005 | 0/0 | 14032 | 15 | 0 | 4 | 11 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14027): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0006 | 0/0 | 14032 | 13 | 6 | 1 | 5 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14027): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0007 | 0/0 | 14020 | 10 | 0 | 0 | 10 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0008 | 0/0 | 14032 | 8 | 0 | 5 | 0 | 1 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14027): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0009 | 0/0 | 14019 | 8 | 0 | 0 | 8 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0010 | 0/0 | 14019 | 8 | 0 | 6 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0011 | 0/0 | 14010 | 7 | 7 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14005): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0012 | 0/0 | 14023 | 7 | 0 | 0 | 7 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0013 | 0/0 | 14030 | 6 | 4 | 1 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14025): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0014 | 0/0 | 14023 | 6 | 1 | 1 | 2 | 1 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0015 | 0/0 | 14034 | 4 | 3 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14029): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0017 | 0/0 | 14020 | 4 | 3 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0018 | 0/0 | 14023 | 4 | 0 | 0 | 4 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0020 | 0/0 | 14019 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0021 | 0/0 | 14019 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0022 | 0/0 | 14023 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0023 | 0/0 | 14021 | 3 | 0 | 1 | 0 | 2 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14016): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0024 | 0/0 | 14020 | 3 | 0 | 0 | 0 | 3 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0025 | 0/0 | 14020 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0026 | 0/0 | 14030 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14025): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0027 | 0/0 | 14028 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14023): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0028 | 0/0 | 14019 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0029 | 0/0 | 14020 | 2 | 1 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0030 | 0/0 | 14023 | 2 | 0 | 1 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0031 | 0/0 | 14023 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0032 | 0/0 | 14021 | 2 | 1 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14016): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0033 | 0/0 | 14021 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14016): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0034 | 0/0 | 14020 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0035 | 0/0 | 14019 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0036 | 0/0 | 14020 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0037 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0039 | 0/0 | 14036 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14031): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0040 | 0/0 | 14032 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14027): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0041 | 0/0 | 14032 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14027): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0042 | 0/0 | 14031 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14026): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0043 | 0/0 | 14032 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14027): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0044 | 0/0 | 14032 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14027): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0045 | 0/0 | 14032 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14027): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0046 | 0/0 | 14030 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14025): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0047 | 0/0 | 14030 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14025): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0048 | 0/0 | 14028 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14023): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0049 | 0/0 | 14021 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14016): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0050 | 0/0 | 14021 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14016): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0051 | 1/0 | 14021 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14016): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0052 | 0/0 | 14021 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14016): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0053 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0054 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0055 | 0/0 | 14019 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0056 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0057 | 0/0 | 14019 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0058 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0059 | 0/0 | 14010 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14005): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0060 | 0/0 | 14010 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14005): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0061 | 0/0 | 14010 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14005): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0062 | 0/0 | 14019 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0063 | 0/0 | 14011 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14006): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0064 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0065 | 0/0 | 14019 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0066 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0067 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0068 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0069 | 0/0 | 14023 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0070 | 0/0 | 14023 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0071 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0072 | 0/0 | 14023 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0073 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0074 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0075 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0076 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0077 | 0/0 | 14021 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14016): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0078 | 0/0 | 14021 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14016): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0079 | 0/0 | 14019 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0080 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0081 | 0/0 | 14020 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0082 | 0/0 | 14019 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0083 | 0/0 | 14020 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0084 | 0/0 | 14020 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0085 | 0/0 | 14020 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0086 | 0/0 | 14019 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0087 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0089 | 0/0 | 14020 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0090 | 0/0 | 14020 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0091 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0001t0092 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0002t0001 | 0/0 | 14023 | 12 | 0 | 0 | 12 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0001c0003t0006 | 0/0 | 14032 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14027): Show |
chr14 | 76146922 | 76219343 |
| a0001c0003t0019 | 0/0 | 14036 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14031): Show |
chr14 | 76146922 | 76219343 |
| a0001c0004t0004 | 0/0 | 14020 | 4 | 0 | 3 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14015): Show |
chr14 | 76146922 | 76219343 |
| a0001c0005t0016 | 0/0 | 14019 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0001c0008t0038 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| a0002c0007t0088 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0003c0006t0016 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14014): Show |
chr14 | 76146922 | 76219343 |
| a0004c0009t0001 | 0/0 | 14023 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | AGAGA others(14018): Show |
chr14 | 76146922 | 76219343 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 1 | 5 | 11 | 2 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0002 | 0/0 | 12 | 0 | 0 | 10 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0015g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0015g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0017g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0017g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0018g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0018g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0018g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0020g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0020g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0021g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0021g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0021g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0022g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0022g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0022g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0023g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0024g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0024g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0025g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0026g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0026g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0027g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0027g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0028g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0028g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0029g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0029g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0030g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0030g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0031g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0031g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0032g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0032g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0033g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0033g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0034g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0034g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0035g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0035g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0036g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0037g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0039g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0040g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0041g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0042g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0043g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0044g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0045g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0046g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0047g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0048g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0049g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0050g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0051g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0052g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0053g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0054g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0055g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0056g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0057g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0058g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0059g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0060g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0061g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0062g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0063g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0064g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0065g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0066g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0067g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0068g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0069g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0070g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0071g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0072g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0073g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0074g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0075g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0076g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0077g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0078g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0079g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0080g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0081g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0082g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0083g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0084g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0085g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0086g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0087g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0089g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0090g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0091g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0092g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0003t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0003t0019g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0003t0019g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0003t0019g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0004t0004g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0004t0004g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0005t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0005t0016g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0005t0016g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0008t0038g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0002c0007t0088g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0003c0006t0016g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0004c0009t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0200 | EUR | GBR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00140 | hp1 | a0001 | c0001 | t0014 | g0020 | EUR | GBR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00140 | hp2 | a0001 | c0001 | t0024 | g0038 | EUR | GBR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00323 | hp2 | a0001 | c0001 | t0008 | g0133 | EUR | FIN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00408 | hp2 | a0001 | c0001 | t0009 | g0198 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00423 | hp1 | a0001 | c0001 | t0027 | g0027 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0131 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00621 | hp2 | a0001 | c0001 | t0014 | g0066 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00642 | hp2 | a0001 | c0001 | t0074 | g0052 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00738 | hp2 | a0001 | c0008 | t0038 | g0255 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00741 | hp1 | a0001 | c0001 | t0023 | g0016 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01074 | hp1 | a0001 | c0001 | t0079 | g0229 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0222 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01081 | hp2 | a0001 | c0001 | t0015 | g0112 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01106 | hp1 | a0001 | c0001 | t0008 | g0160 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01106 | hp2 | a0001 | c0001 | t0055 | g0204 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01109 | hp1 | a0001 | c0001 | t0017 | g0225 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01167 | hp2 | a0001 | c0001 | t0010 | g0018 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0018 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0266 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0260 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01256 | hp2 | a0001 | c0001 | t0022 | g0077 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01258 | hp1 | a0001 | c0001 | t0010 | g0261 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01346 | hp1 | a0001 | c0001 | t0073 | g0061 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01346 | hp2 | a0001 | c0001 | t0030 | g0254 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01358 | hp1 | a0001 | c0001 | t0010 | g0018 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01358 | hp2 | a0001 | c0001 | t0084 | g0285 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0262 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01361 | hp2 | a0001 | c0001 | t0022 | g0075 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01433 | hp1 | a0001 | c0001 | t0014 | g0020 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0275 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01496 | hp1 | a0001 | c0001 | t0029 | g0180 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0136 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01515 | hp1 | a0001 | c0001 | t0024 | g0270 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01516 | hp1 | a0001 | c0001 | t0030 | g0256 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01516 | hp2 | a0001 | c0001 | t0023 | g0016 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01517 | hp1 | a0001 | c0001 | t0023 | g0016 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01517 | hp2 | a0001 | c0001 | t0024 | g0038 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01891 | hp1 | a0001 | c0001 | t0059 | g0171 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01891 | hp2 | a0001 | c0001 | t0053 | g0177 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01928 | hp1 | a0001 | c0004 | t0004 | g0037 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01934 | hp1 | a0001 | c0001 | t0022 | g0059 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01934 | hp2 | a0001 | c0001 | t0013 | g0123 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0128 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0139 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01975 | hp2 | a0001 | c0001 | t0075 | g0022 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0110 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0132 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01993 | hp2 | a0001 | c0004 | t0004 | g0037 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02004 | hp1 | a0001 | c0001 | t0008 | g0025 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02004 | hp2 | a0001 | c0001 | t0082 | g0264 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02015 | hp1 | a0001 | c0001 | t0033 | g0050 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02015 | hp2 | a0001 | c0001 | t0057 | g0215 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0146 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02027 | hp2 | a0001 | c0001 | t0009 | g0212 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02040 | hp1 | a0001 | c0001 | t0035 | g0245 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02040 | hp2 | a0001 | c0001 | t0009 | g0006 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02055 | hp1 | a0001 | c0001 | t0054 | g0034 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02074 | hp1 | a0001 | c0001 | t0028 | g0185 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02083 | hp1 | a0001 | c0001 | t0092 | g0007 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02132 | hp2 | a0001 | c0001 | t0077 | g0002 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02145 | hp1 | a0001 | c0001 | t0011 | g0170 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0015 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02148 | hp1 | a0001 | c0004 | t0004 | g0010 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02148 | hp2 | a0001 | c0001 | t0068 | g0051 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02155 | hp2 | a0001 | c0001 | t0028 | g0186 | EAS | CDX | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02165 | hp1 | a0001 | c0001 | t0033 | g0253 | EAS | CDX | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02165 | hp2 | a0001 | c0001 | t0009 | g0006 | EAS | CDX | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0175 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02293 | hp2 | a0001 | c0001 | t0008 | g0025 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0142 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02451 | hp1 | a0001 | c0001 | t0025 | g0017 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02451 | hp2 | a0001 | c0001 | t0032 | g0104 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02572 | hp1 | a0001 | c0001 | t0049 | g0163 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02615 | hp1 | a0001 | c0001 | t0080 | g0228 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0137 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02622 | hp1 | a0001 | c0003 | t0019 | g0111 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02622 | hp2 | a0001 | c0001 | t0058 | g0168 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0113 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02630 | hp2 | a0002 | c0007 | t0088 | g0227 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02647 | hp1 | a0001 | c0001 | t0052 | g0178 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02647 | hp2 | a0001 | c0001 | t0042 | g0134 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0138 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02723 | hp1 | a0001 | c0001 | t0047 | g0127 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02723 | hp2 | a0001 | c0001 | t0061 | g0009 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02809 | hp1 | a0001 | c0001 | t0048 | g0143 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02809 | hp2 | a0003 | c0006 | t0016 | g0107 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0169 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02886 | hp2 | a0001 | c0001 | t0021 | g0224 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02897 | hp1 | a0001 | c0001 | t0039 | g0152 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02897 | hp2 | a0001 | c0003 | t0006 | g0118 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02922 | hp1 | a0001 | c0001 | t0011 | g0173 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02922 | hp2 | a0001 | c0001 | t0020 | g0029 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02965 | hp1 | a0001 | c0003 | t0019 | g0116 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02965 | hp2 | a0001 | c0005 | t0016 | g0167 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02976 | hp1 | a0001 | c0001 | t0045 | g0157 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0030 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03098 | hp1 | a0001 | c0001 | t0091 | g0009 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0114 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0015 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0126 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0015 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03195 | hp1 | a0001 | c0003 | t0019 | g0117 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03195 | hp2 | a0001 | c0001 | t0025 | g0017 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03209 | hp1 | a0001 | c0001 | t0060 | g0286 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03239 | hp1 | a0001 | c0001 | t0014 | g0078 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03239 | hp2 | a0001 | c0001 | t0026 | g0162 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03453 | hp1 | a0001 | c0001 | t0029 | g0181 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03453 | hp2 | a0001 | c0001 | t0025 | g0017 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03490 | hp1 | a0001 | c0001 | t0070 | g0011 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0129 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0130 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03540 | hp1 | a0001 | c0001 | t0050 | g0165 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03579 | hp1 | a0001 | c0001 | t0083 | g0257 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0115 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03654 | hp1 | a0001 | c0001 | t0031 | g0093 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03654 | hp2 | a0001 | c0001 | t0010 | g0265 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03669 | hp1 | a0001 | c0001 | t0013 | g0226 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03669 | hp2 | a0001 | c0001 | t0069 | g0001 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03704 | hp1 | a0001 | c0001 | t0040 | g0026 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03831 | hp1 | a0001 | c0001 | t0034 | g0267 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03834 | hp2 | a0001 | c0001 | t0031 | g0094 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04199 | hp2 | a0001 | c0001 | t0026 | g0161 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04204 | hp2 | a0004 | c0009 | t0001 | g0092 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04228 | hp1 | a0001 | c0001 | t0065 | g0247 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04228 | hp2 | a0001 | c0001 | t0010 | g0269 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0135 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | CHB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18747 | hp2 | a0001 | c0001 | t0089 | g0272 | EAS | CHB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0174 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18939 | hp2 | a0001 | c0001 | t0012 | g0065 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18942 | hp1 | a0001 | c0001 | t0036 | g0039 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18949 | hp1 | a0001 | c0001 | t0009 | g0192 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18950 | hp1 | a0001 | c0001 | t0032 | g0064 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18952 | hp1 | a0001 | c0001 | t0027 | g0158 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0281 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18960 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18968 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18968 | hp2 | a0001 | c0004 | t0004 | g0010 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18969 | hp1 | a0001 | c0001 | t0014 | g0095 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18969 | hp2 | a0001 | c0001 | t0007 | g0282 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18970 | hp2 | a0001 | c0001 | t0076 | g0109 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18974 | hp1 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18974 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18975 | hp1 | a0001 | c0001 | t0007 | g0274 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18978 | hp2 | a0001 | c0001 | t0046 | g0147 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18982 | hp2 | a0001 | c0001 | t0066 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18987 | hp1 | a0001 | c0001 | t0071 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18990 | hp1 | a0001 | c0001 | t0086 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18991 | hp1 | a0001 | c0001 | t0018 | g0058 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18991 | hp2 | a0001 | c0001 | t0044 | g0141 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0273 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18999 | hp1 | a0001 | c0001 | t0012 | g0081 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18999 | hp2 | a0001 | c0001 | t0085 | g0283 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0213 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19003 | hp1 | a0001 | c0001 | t0009 | g0032 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19006 | hp1 | a0001 | c0001 | t0062 | g0189 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19007 | hp1 | a0001 | c0001 | t0035 | g0250 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0280 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19012 | hp2 | a0001 | c0001 | t0043 | g0125 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19030 | hp1 | a0001 | c0001 | t0020 | g0029 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19030 | hp2 | a0001 | c0005 | t0016 | g0179 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19043 | hp1 | a0001 | c0001 | t0087 | g0252 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19043 | hp2 | a0001 | c0001 | t0081 | g0258 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19055 | hp1 | a0001 | c0001 | t0090 | g0271 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19055 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19056 | hp1 | a0001 | c0001 | t0012 | g0011 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19057 | hp1 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19062 | hp2 | a0001 | c0001 | t0018 | g0080 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19077 | hp1 | a0001 | c0001 | t0067 | g0013 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0284 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19081 | hp2 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19082 | hp2 | a0001 | c0001 | t0009 | g0218 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19085 | hp1 | a0001 | c0001 | t0037 | g0013 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19088 | hp2 | a0001 | c0001 | t0012 | g0055 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19090 | hp1 | a0001 | c0001 | t0036 | g0039 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19240 | hp1 | a0001 | c0001 | t0021 | g0190 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19240 | hp2 | a0001 | c0001 | t0063 | g0164 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA20905 | hp1 | a0001 | c0001 | t0072 | g0082 | SAS | GIH | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA20905 | hp2 | a0001 | c0001 | t0034 | g0268 | SAS | GIH | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02109 | hp1 | a0001 | c0001 | t0041 | g0156 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02486 | hp2 | a0001 | c0001 | t0021 | g0034 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02559 | hp1 | a0001 | c0001 | t0064 | g0191 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0144 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0172 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0030 | AFR | USA | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG06807 | hp2 | a0001 | c0001 | t0056 | g0176 | AFR | USA | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA20300 | hp1 | a0001 | c0005 | t0016 | g0166 | AFR | USA | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA21309 | hp1 | a0001 | c0001 | t0078 | g0287 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0079 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0043 | REF | REF | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0051 | g0108 | REF | REF | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:76171870 | A | G | 1 | a0004 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.755A>G | p.Tyr252Cys | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/10 | 835/14021 | 755/1449 | 252/482 | chr14 | 76171870 | |||
| chr14:76177998 | G | A | 1 | a0002 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1063G>A | p.Ala355Thr | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/10 | 1143/14021 | 1063/1449 | 355/482 | chr14 | 76177998 | |||
| chr14:76201798 | A | G | 1 | a0003 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1396A>G | p.Thr466Ala | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1476/14021 | 1396/1449 | 466/482 | chr14 | 76201798 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:76154729 | T | G | 1 | a0001c0003 | 4 | HG02622.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.366T>G | p.Pro122Pro | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/10 | 446/14021 | 366/1449 | 122/482 | chr14 | 76154729 | |||
| chr14:76154753 | G | A | 2 | a0001c0005 a0003c0006 |
4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
synonymous_variant | LOW | c.390G>A | p.Arg130Arg | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/10 | 470/14021 | 390/1449 | 130/482 | chr14 | 76154753 | |||
| chr14:76171895 | C | T | 1 | a0001c0004 | 4 | HG01928.hp1 HG01993.hp2 HG02148.hp1 others(1): Show |
synonymous_variant | LOW | c.780C>T | p.Phe260Phe | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/10 | 860/14021 | 780/1449 | 260/482 | chr14 | 76171895 | |||
| chr14:76172015 | A | G | 1 | a0001c0002 | 12 | NA18947.hp1 NA18949.hp2 NA18975.hp2 others(9): Show |
synonymous_variant | LOW | c.900A>G | p.Gln300Gln | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/10 | 980/14021 | 900/1449 | 300/482 | chr14 | 76172015 | |||
| chr14:76180805 | C | T | 1 | a0001c0008 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1149C>T | p.Ala383Ala | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/10 | 1229/14021 | 1149/1449 | 383/482 | chr14 | 76180805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:76151931 | A | C | 1 | a0001c0001t0092 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-71A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/10 | 2433 | chr14 | 76151931 | ||||||
| chr14:76151940 | G | T | 1 | a0001c0001t0091 | 1 | HG03098.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-62G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/10 | chr14 | 76151940 | |||||||
| chr14:76201903 | T | G | 1 | a0001c0001t0037 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*52T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 52 | chr14 | 76201903 | ||||||
| chr14:76201940 | G | A | 1 | a0001c0008t0038 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 89 | chr14 | 76201940 | ||||||
| chr14:76202013 | A | G | 51 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(48): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 162 | chr14 | 76202013 | ||||||
| chr14:76202165 | G | A | 1 | a0001c0001t0065 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*314G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 314 | chr14 | 76202165 | ||||||
| chr14:76202424 | C | T | 1 | a0001c0001t0064 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 573 | chr14 | 76202424 | ||||||
| chr14:76202536 | T | TACACAC | 2 | a0001c0001t0027 a0001c0001t0048 |
3 | HG00423.hp1 HG02809.hp1 NA18952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*707_*712dupCACACA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | |||||
| chr14:76202536 | T | TACACACA others(1): Show |
4 | a0001c0001t0013 a0001c0001t0026 a0001c0001t0046 others(1): Show |
10 | HG01934.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*705_*712dupCACACA others(2): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | |||||
| chr14:76202536 | T | TACACACA others(3): Show |
10 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(7): Show |
43 | HG00323.hp2 HG00558.hp2 HG01106.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*703_*712dupCACACA others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | |||||
| chr14:76202536 | T | TACACACA others(5): Show |
1 | a0001c0001t0015 | 4 | HG01081.hp2 HG02630.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*701_*712dupCACACA others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | |||||
| chr14:76202536 | T | TACACACA others(7): Show |
2 | a0001c0001t0039 a0001c0003t0019 |
4 | HG02622.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*699_*712dupCACACA others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | |||||
| chr14:76202536 | TAC | T | 45 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(42): Show |
197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*711_*712delCA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 711 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | |||||
| chr14:76202536 | TACACACA others(3): Show |
T | 1 | a0001c0001t0063 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703_*712delCACACA others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 703 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | |||||
| chr14:76202562 | C | CAG | 23 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0014 others(20): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*713_*714dupGA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 715 | INFO_REALIGN_3_PRIME | chr14 | 76202562 | |||||
| chr14:76202562 | C | G | 27 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(24): Show |
108 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*711C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 711 | chr14 | 76202562 | ||||||
| chr14:76202929 | A | G | 3 | a0001c0001t0036 a0001c0001t0089 a0001c0001t0090 |
4 | NA18747.hp2 NA18942.hp1 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1078 | chr14 | 76202929 | ||||||
| chr14:76202966 | C | A | 42 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(39): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*1115C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1115 | chr14 | 76202966 | ||||||
| chr14:76203109 | T | C | 1 | a0001c0001t0079 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1258T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1258 | chr14 | 76203109 | ||||||
| chr14:76203116 | T | G | 1 | a0001c0001t0080 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1265T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1265 | chr14 | 76203116 | ||||||
| chr14:76203126 | C | G | 1 | a0001c0001t0026 | 2 | HG03239.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1275C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1275 | chr14 | 76203126 | ||||||
| chr14:76203131 | T | C | 1 | a0001c0001t0086 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1280 | chr14 | 76203131 | ||||||
| chr14:76203315 | A | G | 72 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(69): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*1464A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1464 | chr14 | 76203315 | ||||||
| chr14:76203439 | G | A | 1 | a0001c0001t0009 | 8 | HG00408.hp2 HG02027.hp2 HG02040.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1588G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1588 | chr14 | 76203439 | ||||||
| chr14:76203449 | G | C | 1 | a0001c0001t0053 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1598G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1598 | chr14 | 76203449 | ||||||
| chr14:76203509 | T | C | 1 | a0001c0001t0033 | 2 | HG02015.hp1 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1658T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1658 | chr14 | 76203509 | ||||||
| chr14:76203550 | G | A | 1 | a0001c0001t0087 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1699 | chr14 | 76203550 | ||||||
| chr14:76203693 | G | A | 7 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0065 others(4): Show |
41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1842G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1842 | chr14 | 76203693 | ||||||
| chr14:76203853 | G | A | 1 | a0001c0001t0066 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2002G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2002 | chr14 | 76203853 | ||||||
| chr14:76204150 | C | T | 1 | a0001c0001t0062 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2299C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2299 | chr14 | 76204150 | ||||||
| chr14:76204245 | G | T | 1 | a0001c0001t0022 | 3 | HG01256.hp2 HG01361.hp2 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2394G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2394 | chr14 | 76204245 | ||||||
| chr14:76204290 | A | G | 1 | a0001c0001t0018 | 4 | NA18960.hp1 NA18991.hp1 NA19062.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2439A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2439 | chr14 | 76204290 | ||||||
| chr14:76204310 | C | G | 1 | a0001c0001t0023 | 3 | HG00741.hp1 HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2459C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2459 | chr14 | 76204310 | ||||||
| chr14:76204438 | C | T | 22 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0014 others(19): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2587C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2587 | chr14 | 76204438 | ||||||
| chr14:76204554 | G | A | 5 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0065 others(2): Show |
39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2703G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2703 | chr14 | 76204554 | ||||||
| chr14:76204597 | T | G | 1 | a0001c0001t0054 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2746T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2746 | chr14 | 76204597 | ||||||
| chr14:76204661 | A | G | 1 | a0001c0001t0080 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2810A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2810 | chr14 | 76204661 | ||||||
| chr14:76204784 | A | G | 1 | a0001c0001t0052 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2933A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2933 | chr14 | 76204784 | ||||||
| chr14:76204956 | TTTGTTGT others(2): Show |
T | 4 | a0001c0001t0011 a0001c0001t0059 a0001c0001t0060 others(1): Show |
10 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3123_*3131delGTTG others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3123 | INFO_REALIGN_3_PRIME | chr14 | 76204956 | |||||
| chr14:76205015 | G | A | 3 | a0001c0001t0036 a0001c0001t0089 a0001c0001t0090 |
4 | NA18747.hp2 NA18942.hp1 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3164G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3164 | chr14 | 76205015 | ||||||
| chr14:76205364 | G | C | 1 | a0001c0001t0036 | 2 | NA18942.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3513G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3513 | chr14 | 76205364 | ||||||
| chr14:76205484 | G | A | 1 | a0001c0001t0029 | 2 | HG01496.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3633G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3633 | chr14 | 76205484 | ||||||
| chr14:76205608 | A | G | 23 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0014 others(20): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*3757A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3757 | chr14 | 76205608 | ||||||
| chr14:76205618 | G | T | 8 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0065 others(5): Show |
42 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3767G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3767 | chr14 | 76205618 | ||||||
| chr14:76205711 | A | C | 8 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0065 others(5): Show |
42 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3860A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3860 | chr14 | 76205711 | ||||||
| chr14:76205761 | A | C | 15 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(12): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3910A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3910 | chr14 | 76205761 | ||||||
| chr14:76205863 | T | C | 1 | a0001c0001t0055 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4012T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4012 | chr14 | 76205863 | ||||||
| chr14:76205921 | G | A | 1 | a0001c0001t0087 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4070G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4070 | chr14 | 76205921 | ||||||
| chr14:76206088 | T | C | 1 | a0001c0001t0059 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4237T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4237 | chr14 | 76206088 | ||||||
| chr14:76206203 | C | T | 1 | a0001c0001t0045 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4352C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4352 | chr14 | 76206203 | ||||||
| chr14:76206284 | T | C | 95 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(92): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
3_prime_UTR_variant | MODIFIER | c.*4433T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4433 | chr14 | 76206284 | ||||||
| chr14:76206328 | A | G | 1 | a0001c0001t0023 | 3 | HG00741.hp1 HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4477A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4477 | chr14 | 76206328 | ||||||
| chr14:76206431 | T | C | 1 | a0001c0001t0080 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4580T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4580 | chr14 | 76206431 | ||||||
| chr14:76206664 | G | A | 1 | a0001c0001t0081 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4813G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4813 | chr14 | 76206664 | ||||||
| chr14:76206770 | T | C | 1 | a0001c0001t0067 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4919T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4919 | chr14 | 76206770 | ||||||
| chr14:76206794 | G | A | 2 | a0001c0005t0016 a0003c0006t0016 |
4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4943G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4943 | chr14 | 76206794 | ||||||
| chr14:76206863 | G | C | 1 | a0001c0001t0079 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5012G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5012 | chr14 | 76206863 | ||||||
| chr14:76206921 | T | A | 1 | a0001c0001t0034 | 2 | HG03831.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5070T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5070 | chr14 | 76206921 | ||||||
| chr14:76206931 | T | C | 2 | a0001c0001t0010 a0001c0001t0082 |
9 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5080T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5080 | chr14 | 76206931 | ||||||
| chr14:76206931 | T | TC | 13 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0024 others(10): Show |
50 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*5080_*5081insC | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5081 | chr14 | 76206931 | ||||||
| chr14:76206932 | T | C | 15 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(12): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*5081T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5081 | chr14 | 76206932 | ||||||
| chr14:76206940 | A | G | 8 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0065 others(5): Show |
42 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*5089A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5089 | chr14 | 76206940 | ||||||
| chr14:76207007 | G | A | 1 | a0001c0001t0087 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5156G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5156 | chr14 | 76207007 | ||||||
| chr14:76207016 | T | C | 8 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0065 others(5): Show |
42 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*5165T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5165 | chr14 | 76207016 | ||||||
| chr14:76207057 | A | G | 91 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(88): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
3_prime_UTR_variant | MODIFIER | c.*5206A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5206 | chr14 | 76207057 | ||||||
| chr14:76207075 | G | A | 1 | a0001c0001t0008 | 8 | HG00323.hp2 HG01106.hp1 HG01978.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5224G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5224 | chr14 | 76207075 | ||||||
| chr14:76207153 | A | G | 6 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0027 others(3): Show |
28 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5302A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5302 | chr14 | 76207153 | ||||||
| chr14:76207242 | G | A | 2 | a0001c0001t0049 a0001c0001t0056 |
2 | HG02572.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5391G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5391 | chr14 | 76207242 | ||||||
| chr14:76207376 | A | G | 1 | a0001c0001t0079 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5525A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5525 | chr14 | 76207376 | ||||||
| chr14:76207399 | G | A | 1 | a0001c0001t0087 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5548G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5548 | chr14 | 76207399 | ||||||
| chr14:76207530 | G | GA | 20 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(17): Show |
69 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*5689dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5690 | INFO_REALIGN_3_PRIME | chr14 | 76207530 | |||||
| chr14:76207658 | G | T | 6 | a0001c0001t0007 a0001c0001t0036 a0001c0001t0081 others(3): Show |
16 | NA18747.hp2 NA18942.hp1 NA18953.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5807G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5807 | chr14 | 76207658 | ||||||
| chr14:76207678 | C | T | 1 | a0001c0001t0082 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5827C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5827 | chr14 | 76207678 | ||||||
| chr14:76207736 | G | A | 1 | a0001c0001t0083 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5885G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5885 | chr14 | 76207736 | ||||||
| chr14:76207777 | A | G | 1 | a0001c0001t0090 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5926A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5926 | chr14 | 76207777 | ||||||
| chr14:76208216 | A | T | 1 | a0001c0001t0087 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6365A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6365 | chr14 | 76208216 | ||||||
| chr14:76208274 | C | T | 22 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0014 others(19): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*6423C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6423 | chr14 | 76208274 | ||||||
| chr14:76208289 | A | G | 5 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(2): Show |
9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6438A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6438 | chr14 | 76208289 | ||||||
| chr14:76208338 | T | C | 12 | a0001c0001t0003 a0001c0001t0023 a0001c0001t0030 others(9): Show |
50 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*6487T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6487 | chr14 | 76208338 | ||||||
| chr14:76208430 | T | C | 22 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0014 others(19): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*6579T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6579 | chr14 | 76208430 | ||||||
| chr14:76208497 | A | C | 1 | a0001c0001t0035 | 2 | HG02040.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6646A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6646 | chr14 | 76208497 | ||||||
| chr14:76208581 | G | A | 1 | a0001c0001t0068 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6730G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6730 | chr14 | 76208581 | ||||||
| chr14:76208581 | G | C | 5 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(2): Show |
9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6730G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6730 | chr14 | 76208581 | ||||||
| chr14:76208615 | C | G | 1 | a0001c0001t0075 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6764C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6764 | chr14 | 76208615 | ||||||
| chr14:76208876 | A | G | 21 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(18): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*7025A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7025 | chr14 | 76208876 | ||||||
| chr14:76208947 | G | A | 3 | a0001c0001t0036 a0001c0001t0089 a0001c0001t0090 |
4 | NA18747.hp2 NA18942.hp1 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7096G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7096 | chr14 | 76208947 | ||||||
| chr14:76208972 | G | T | 2 | a0001c0001t0068 a0001c0001t0074 |
2 | HG00642.hp2 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7121G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7121 | chr14 | 76208972 | ||||||
| chr14:76209031 | G | C | 10 | a0001c0001t0003 a0001c0001t0023 a0001c0001t0030 others(7): Show |
48 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*7180G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7180 | chr14 | 76209031 | ||||||
| chr14:76209066 | A | G | 5 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(2): Show |
9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7215A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7215 | chr14 | 76209066 | ||||||
| chr14:76209109 | A | G | 23 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0014 others(20): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*7258A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7258 | chr14 | 76209109 | ||||||
| chr14:76209197 | G | C | 72 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(69): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*7346G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7346 | chr14 | 76209197 | ||||||
| chr14:76209201 | A | G | 1 | a0001c0001t0031 | 2 | HG03654.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7350A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7350 | chr14 | 76209201 | ||||||
| chr14:76209253 | C | A | 1 | a0001c0001t0024 | 3 | HG00140.hp2 HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7402C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7402 | chr14 | 76209253 | ||||||
| chr14:76209258 | G | A | 1 | a0002c0007t0088 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7407G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7407 | chr14 | 76209258 | ||||||
| chr14:76209531 | T | C | 2 | a0001c0001t0025 a0001c0001t0083 |
4 | HG02451.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7680T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7680 | chr14 | 76209531 | ||||||
| chr14:76209655 | T | A | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7804T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7804 | chr14 | 76209655 | ||||||
| chr14:76209711 | G | T | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7860G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7860 | chr14 | 76209711 | ||||||
| chr14:76210012 | A | G | 11 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0021 others(8): Show |
71 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*8161A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8161 | chr14 | 76210012 | ||||||
| chr14:76210092 | C | G | 1 | a0001c0001t0065 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8241C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8241 | chr14 | 76210092 | ||||||
| chr14:76210097 | C | A | 2 | a0001c0001t0021 a0001c0001t0064 |
4 | HG02486.hp2 HG02559.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8246C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8246 | chr14 | 76210097 | ||||||
| chr14:76210098 | T | C | 5 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(2): Show |
9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8247T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8247 | chr14 | 76210098 | ||||||
| chr14:76210170 | T | C | 1 | a0001c0001t0052 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8319T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8319 | chr14 | 76210170 | ||||||
| chr14:76210237 | A | T | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8386A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8386 | chr14 | 76210237 | ||||||
| chr14:76210357 | C | T | 1 | a0002c0007t0088 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8506C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8506 | chr14 | 76210357 | ||||||
| chr14:76210360 | T | C | 5 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(2): Show |
9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8509T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8509 | chr14 | 76210360 | ||||||
| chr14:76210408 | G | C | 1 | a0001c0001t0079 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8557G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8557 | chr14 | 76210408 | ||||||
| chr14:76210464 | C | T | 1 | a0001c0001t0039 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8613C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8613 | chr14 | 76210464 | ||||||
| chr14:76210484 | T | C | 22 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0014 others(19): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*8633T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8633 | chr14 | 76210484 | ||||||
| chr14:76210557 | A | G | 18 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(15): Show |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*8706A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8706 | chr14 | 76210557 | ||||||
| chr14:76210651 | T | G | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8800T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8800 | chr14 | 76210651 | ||||||
| chr14:76210653 | C | G | 1 | a0001c0001t0080 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8802C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8802 | chr14 | 76210653 | ||||||
| chr14:76210662 | G | A | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8811G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8811 | chr14 | 76210662 | ||||||
| chr14:76210714 | T | C | 78 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(75): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*8863T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8863 | chr14 | 76210714 | ||||||
| chr14:76210715 | G | A | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8864G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8864 | chr14 | 76210715 | ||||||
| chr14:76210762 | T | C | 1 | a0001c0001t0069 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8911T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8911 | chr14 | 76210762 | ||||||
| chr14:76210852 | T | A | 1 | a0001c0001t0070 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9001T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9001 | chr14 | 76210852 | ||||||
| chr14:76211305 | G | A | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*9454G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9454 | chr14 | 76211305 | ||||||
| chr14:76211380 | G | A | 1 | a0001c0001t0040 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9529G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9529 | chr14 | 76211380 | ||||||
| chr14:76211582 | G | A | 1 | a0001c0001t0087 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9731G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9731 | chr14 | 76211582 | ||||||
| chr14:76211725 | T | C | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*9874T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9874 | chr14 | 76211725 | ||||||
| chr14:76211817 | G | A | 1 | a0001c0001t0044 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9966G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9966 | chr14 | 76211817 | ||||||
| chr14:76212155 | A | G | 1 | a0001c0001t0087 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10304A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10304 | chr14 | 76212155 | ||||||
| chr14:76212250 | T | C | 1 | a0001c0001t0057 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10399T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10399 | chr14 | 76212250 | ||||||
| chr14:76212351 | G | A | 1 | a0001c0001t0049 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10500G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10500 | chr14 | 76212351 | ||||||
| chr14:76212377 | G | A | 1 | a0001c0001t0046 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10526G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10526 | chr14 | 76212377 | ||||||
| chr14:76212412 | A | C | 1 | a0001c0001t0047 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10561A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10561 | chr14 | 76212412 | ||||||
| chr14:76212413 | C | A | 6 | a0001c0001t0014 a0001c0001t0023 a0001c0001t0030 others(3): Show |
15 | HG00140.hp1 HG00621.hp2 HG00738.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*10562C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10562 | chr14 | 76212413 | ||||||
| chr14:76212453 | C | T | 4 | a0001c0001t0011 a0001c0001t0059 a0001c0001t0060 others(1): Show |
10 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*10602C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10602 | chr14 | 76212453 | ||||||
| chr14:76212465 | T | C | 1 | a0001c0001t0084 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10614T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10614 | chr14 | 76212465 | ||||||
| chr14:76212551 | T | C | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10700T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10700 | chr14 | 76212551 | ||||||
| chr14:76212716 | T | G | 27 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(24): Show |
131 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*10865T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10865 | chr14 | 76212716 | ||||||
| chr14:76212759 | G | A | 94 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(91): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
3_prime_UTR_variant | MODIFIER | c.*10908G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10908 | chr14 | 76212759 | ||||||
| chr14:76212800 | A | C | 1 | a0001c0001t0073 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10949A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10949 | chr14 | 76212800 | ||||||
| chr14:76212823 | G | A | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10972G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10972 | chr14 | 76212823 | ||||||
| chr14:76212844 | A | G | 2 | a0001c0001t0078 a0002c0007t0088 |
2 | HG02630.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10993A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10993 | chr14 | 76212844 | ||||||
| chr14:76212946 | C | A | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11095C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11095 | chr14 | 76212946 | ||||||
| chr14:76213055 | A | G | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11204A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11204 | chr14 | 76213055 | ||||||
| chr14:76213225 | A | G | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11374A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11374 | chr14 | 76213225 | ||||||
| chr14:76213268 | G | A | 1 | a0001c0001t0050 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11417G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11417 | chr14 | 76213268 | ||||||
| chr14:76213532 | G | A | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11681G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11681 | chr14 | 76213532 | ||||||
| chr14:76213610 | G | A | 1 | a0001c0001t0072 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11759G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11759 | chr14 | 76213610 | ||||||
| chr14:76213696 | A | T | 1 | a0001c0001t0007 | 2 | NA18953.hp1 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11845A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11845 | chr14 | 76213696 | ||||||
| chr14:76213804 | G | A | 1 | a0001c0001t0017 | 4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11953G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11953 | chr14 | 76213804 | ||||||
| chr14:76213833 | C | G | 1 | a0001c0001t0041 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11982C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11982 | chr14 | 76213833 | ||||||
| chr14:76213860 | G | A | 4 | a0001c0001t0023 a0001c0001t0030 a0001c0001t0033 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12009G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12009 | chr14 | 76213860 | ||||||
| chr14:76213891 | G | C | 19 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(16): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*12040G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12040 | chr14 | 76213891 | ||||||
| chr14:76213900 | T | C | 1 | a0001c0001t0085 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12049T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12049 | chr14 | 76213900 | ||||||
| chr14:76213923 | T | G | 1 | a0001c0001t0028 | 2 | HG02074.hp1 HG02155.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12072T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12072 | chr14 | 76213923 | ||||||
| chr14:76214035 | T | G | 1 | a0001c0001t0012 | 7 | NA18939.hp2 NA18968.hp1 NA18974.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12184T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12184 | chr14 | 76214035 | ||||||
| chr14:76214216 | T | A | 1 | a0001c0001t0060 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12365T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12365 | chr14 | 76214216 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:76151998 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
splice_region_variant&intron_variant | LOW | c.-11+7G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76151998 | |||||||
| chr14:76152002 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11+11G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152002 | |||||||
| chr14:76152097 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-11+106C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152097 | |||||||
| chr14:76152112 | G | T | 1 | a0001c0001t0003g0288 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-11+121G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152112 | |||||||
| chr14:76152158 | C | T | 1 | a0001c0001t0078g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+167C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152158 | |||||||
| chr14:76152221 | C | T | 1 | a0001c0001t0060g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+230C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152221 | |||||||
| chr14:76152250 | C | A | 1 | a0003c0006t0016g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-11+259C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152250 | |||||||
| chr14:76152259 | CCGAGCCA others(22): Show |
C | 1 | a0001c0001t0084g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-11+271_-11+299del others(29): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 76152259 | ||||||
| chr14:76152263 | G | A | 1 | a0001c0001t0055g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-11+272G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152263 | |||||||
| chr14:76152416 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-11+425A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152416 | |||||||
| chr14:76152484 | G | T | 101 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(98): Show |
121 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-11+493G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152484 | |||||||
| chr14:76152495 | C | G | 3 | a0001c0001t0030g0254 a0001c0001t0030g0256 a0001c0008t0038g0255 |
3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-11+504C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152495 | |||||||
| chr14:76152506 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(82): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-11+515C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152506 | |||||||
| chr14:76152506 | C | T | 161 | a0001c0001t0001g0044 a0001c0001t0002g0004 a0001c0001t0002g0006 others(158): Show |
212 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.-11+515C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152506 | |||||||
| chr14:76152685 | G | T | 1 | a0001c0001t0033g0253 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-11+694G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152685 | |||||||
| chr14:76152767 | G | T | 1 | a0001c0001t0087g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-11+776G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152767 | |||||||
| chr14:76152824 | A | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(119): Show |
175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-11+833A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152824 | |||||||
| chr14:76152846 | G | T | 2 | a0001c0001t0007g0284 a0001c0001t0085g0283 |
2 | NA18999.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-11+855G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152846 | |||||||
| chr14:76152939 | C | CT | 63 | a0001c0001t0001g0106 a0001c0001t0005g0024 a0001c0001t0005g0026 others(60): Show |
66 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-11+958dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 76152939 | ||||||
| chr14:76152949 | T | C | 1 | a0001c0001t0049g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11+958T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152949 | |||||||
| chr14:76153106 | G | T | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-11+1115G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153106 | |||||||
| chr14:76153267 | A | C | 3 | a0001c0001t0030g0254 a0001c0001t0030g0256 a0001c0008t0038g0255 |
3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-10-1087A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153267 | |||||||
| chr14:76153292 | A | G | 2 | a0001c0001t0017g0015 a0001c0001t0017g0225 |
4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-1062A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153292 | |||||||
| chr14:76153403 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(181): Show |
240 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.-10-951T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153403 | |||||||
| chr14:76153406 | C | T | 1 | a0001c0001t0021g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-10-948C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153406 | |||||||
| chr14:76153618 | A | G | 57 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0009 others(54): Show |
73 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10-736A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153618 | |||||||
| chr14:76154144 | A | C | 2 | a0001c0001t0007g0284 a0001c0001t0085g0283 |
2 | NA18999.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-10-210A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76154144 | |||||||
| chr14:76154350 | G | A | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | NA18989.hp2 NA19080.hp2 |
splice_region_variant&intron_variant | LOW | c.-10-4G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76154350 | |||||||
| chr14:76155224 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.662+199G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155224 | |||||||
| chr14:76155328 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(181): Show |
240 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.662+303C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155328 | |||||||
| chr14:76155334 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(181): Show |
240 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.662+309A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155334 | |||||||
| chr14:76155458 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.662+433T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155458 | |||||||
| chr14:76155693 | T | C | 57 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0009 others(54): Show |
73 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.662+668T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155693 | |||||||
| chr14:76155877 | T | G | 1 | a0001c0001t0049g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.662+852T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155877 | |||||||
| chr14:76155898 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.662+873G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155898 | |||||||
| chr14:76155999 | A | G | 4 | a0001c0001t0017g0015 a0001c0001t0017g0225 a0001c0001t0029g0180 others(1): Show |
6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.662+974A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155999 | |||||||
| chr14:76156036 | C | G | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.662+1011C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156036 | |||||||
| chr14:76156264 | A | G | 27 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(24): Show |
39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.662+1239A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156264 | |||||||
| chr14:76156637 | T | G | 1 | a0001c0001t0008g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.662+1612T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156637 | |||||||
| chr14:76156762 | G | T | 1 | a0001c0001t0002g0219 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.662+1737G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156762 | |||||||
| chr14:76156785 | G | A | 8 | a0001c0001t0015g0112 a0001c0001t0015g0113 a0001c0001t0015g0114 others(5): Show |
8 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.662+1760G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156785 | |||||||
| chr14:76156860 | T | A | 1 | a0001c0001t0083g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.662+1835T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156860 | |||||||
| chr14:76156875 | C | T | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.662+1850C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156875 | |||||||
| chr14:76157344 | AG | A | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(1): Show |
4 | NA18982.hp1 NA19005.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.662+2321delG | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76157344 | ||||||
| chr14:76157363 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(181): Show |
240 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.662+2338G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157363 | |||||||
| chr14:76157377 | G | A | 29 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(26): Show |
41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.662+2352G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157377 | |||||||
| chr14:76157480 | A | G | 2 | a0001c0002t0001g0023 a0001c0002t0001g0105 |
3 | NA18981.hp1 NA19068.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.662+2455A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157480 | |||||||
| chr14:76157673 | G | GT | 73 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 others(70): Show |
82 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.662+2658dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76157673 | ||||||
| chr14:76157683 | TC | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
161 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.662+2659delC | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157683 | |||||||
| chr14:76157684 | C | T | 74 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(71): Show |
79 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.662+2659C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157684 | |||||||
| chr14:76157783 | A | T | 1 | a0001c0001t0050g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.662+2758A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157783 | |||||||
| chr14:76158139 | T | C | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.662+3114T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158139 | |||||||
| chr14:76158198 | A | C | 1 | a0001c0001t0057g0215 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.662+3173A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158198 | |||||||
| chr14:76158199 | T | C | 2 | a0001c0001t0068g0051 a0001c0001t0074g0052 |
2 | HG00642.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.662+3174T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158199 | |||||||
| chr14:76158204 | T | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(113): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.662+3179T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158204 | |||||||
| chr14:76158357 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.662+3332A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158357 | |||||||
| chr14:76158541 | A | G | 55 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0009 others(52): Show |
71 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.662+3516A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158541 | |||||||
| chr14:76158544 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.662+3519A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158544 | |||||||
| chr14:76158682 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.662+3657G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158682 | |||||||
| chr14:76158811 | C | A | 2 | a0001c0001t0017g0015 a0001c0001t0017g0225 |
4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+3786C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158811 | |||||||
| chr14:76158933 | G | T | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.662+3908G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158933 | |||||||
| chr14:76159099 | G | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.662+4074G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159099 | |||||||
| chr14:76159129 | C | G | 1 | a0001c0001t0052g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.662+4104C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159129 | |||||||
| chr14:76159150 | G | A | 27 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(24): Show |
39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.662+4125G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159150 | |||||||
| chr14:76159189 | A | T | 2 | a0001c0001t0026g0161 a0001c0001t0026g0162 |
2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.662+4164A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159189 | |||||||
| chr14:76159316 | T | G | 4 | a0001c0001t0013g0123 a0001c0001t0013g0226 a0001c0001t0026g0161 others(1): Show |
4 | HG01934.hp2 HG03239.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.662+4291T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159316 | |||||||
| chr14:76159339 | G | T | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.662+4314G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159339 | |||||||
| chr14:76159375 | G | A | 3 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0233 |
3 | HG00673.hp1 HG02083.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.662+4350G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159375 | |||||||
| chr14:76159474 | A | G | 1 | a0001c0001t0005g0122 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.662+4449A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159474 | |||||||
| chr14:76159475 | C | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.662+4450C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159475 | |||||||
| chr14:76159524 | T | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0216 |
2 | NA18951.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.662+4499T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159524 | |||||||
| chr14:76159567 | A | G | 29 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(26): Show |
41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.662+4542A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159567 | |||||||
| chr14:76159738 | C | T | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.662+4713C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159738 | |||||||
| chr14:76159860 | T | G | 1 | a0001c0001t0003g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.662+4835T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159860 | |||||||
| chr14:76159934 | C | T | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.662+4909C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159934 | |||||||
| chr14:76159965 | T | C | 1 | a0001c0001t0006g0124 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.662+4940T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159965 | |||||||
| chr14:76159989 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.662+4964C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159989 | |||||||
| chr14:76160040 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.662+5015G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160040 | |||||||
| chr14:76160057 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.662+5032C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160057 | |||||||
| chr14:76160082 | C | T | 1 | a0001c0001t0087g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.662+5057C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160082 | |||||||
| chr14:76160126 | A | G | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.662+5101A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160126 | |||||||
| chr14:76160129 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.662+5104G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160129 | |||||||
| chr14:76160155 | A | G | 1 | a0001c0001t0032g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.662+5130A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160155 | |||||||
| chr14:76160173 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.662+5148G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160173 | |||||||
| chr14:76160247 | C | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.662+5222C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160247 | |||||||
| chr14:76160333 | C | T | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.662+5308C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160333 | |||||||
| chr14:76160360 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(221): Show |
297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.662+5335T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160360 | |||||||
| chr14:76160430 | A | G | 1 | a0001c0001t0002g0184 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.662+5405A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160430 | |||||||
| chr14:76160771 | A | G | 3 | a0001c0001t0030g0254 a0001c0001t0030g0256 a0001c0008t0038g0255 |
3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.662+5746A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160771 | |||||||
| chr14:76160787 | C | T | 1 | a0001c0001t0003g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.662+5762C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160787 | |||||||
| chr14:76160958 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.663-5705A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160958 | |||||||
| chr14:76161322 | C | CTTTAT | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.663-5337_663-5336i others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76161322 | ||||||
| chr14:76161576 | T | C | 42 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(39): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.663-5087T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161576 | |||||||
| chr14:76161592 | C | T | 1 | a0001c0001t0008g0160 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.663-5071C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161592 | |||||||
| chr14:76161625 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0100 others(4): Show |
8 | HG01257.hp1 HG01928.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.663-5038A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161625 | |||||||
| chr14:76161660 | T | G | 1 | a0001c0001t0003g0235 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.663-5003T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161660 | |||||||
| chr14:76161836 | G | T | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.663-4827G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161836 | |||||||
| chr14:76161896 | C | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-4767C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161896 | |||||||
| chr14:76162014 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.663-4649T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162014 | |||||||
| chr14:76162062 | T | C | 2 | a0001c0001t0078g0287 a0002c0007t0088g0227 |
2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.663-4601T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162062 | |||||||
| chr14:76162129 | C | CAG | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.663-4533_663-4532d others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76162129 | ||||||
| chr14:76162169 | C | T | 1 | a0001c0001t0005g0159 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.663-4494C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162169 | |||||||
| chr14:76162188 | C | T | 1 | a0001c0001t0027g0158 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.663-4475C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162188 | |||||||
| chr14:76162281 | C | T | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.663-4382C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162281 | |||||||
| chr14:76162315 | G | C | 3 | a0001c0005t0016g0166 a0001c0005t0016g0167 a0001c0005t0016g0179 |
3 | HG02965.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.663-4348G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162315 | |||||||
| chr14:76162345 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.663-4318G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162345 | |||||||
| chr14:76162471 | C | T | 42 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(39): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.663-4192C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162471 | |||||||
| chr14:76162520 | A | G | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.663-4143A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162520 | |||||||
| chr14:76162650 | T | C | 27 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(24): Show |
39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.663-4013T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162650 | |||||||
| chr14:76162703 | T | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.663-3960T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162703 | |||||||
| chr14:76162925 | T | G | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-3738T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162925 | |||||||
| chr14:76163045 | C | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-3618C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163045 | |||||||
| chr14:76163138 | C | T | 42 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(39): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.663-3525C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163138 | |||||||
| chr14:76163174 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.663-3489T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163174 | |||||||
| chr14:76163330 | A | G | 1 | a0001c0001t0049g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.663-3333A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163330 | |||||||
| chr14:76163338 | G | A | 2 | a0001c0001t0004g0222 a0001c0001t0004g0223 |
2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.663-3325G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163338 | |||||||
| chr14:76163526 | A | G | 1 | a0003c0006t0016g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.663-3137A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163526 | |||||||
| chr14:76163579 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-3084G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163579 | |||||||
| chr14:76163761 | A | G | 1 | a0001c0001t0053g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.663-2902A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163761 | |||||||
| chr14:76163790 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(222): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.663-2873G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163790 | |||||||
| chr14:76164154 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.663-2509T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76164154 | |||||||
| chr14:76164725 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(303): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.663-1938A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76164725 | |||||||
| chr14:76164793 | G | A | 1 | a0001c0001t0076g0109 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.663-1870G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76164793 | |||||||
| chr14:76165092 | G | A | 2 | a0001c0001t0020g0029 a0001c0001t0020g0169 |
3 | HG02886.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.663-1571G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165092 | |||||||
| chr14:76165363 | G | A | 2 | a0001c0001t0028g0185 a0001c0001t0028g0186 |
2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.663-1300G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165363 | |||||||
| chr14:76165365 | G | A | 1 | a0001c0001t0043g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.663-1298G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165365 | |||||||
| chr14:76165490 | CA | C | 10 | a0001c0001t0001g0099 a0001c0001t0002g0214 a0001c0001t0004g0223 others(7): Show |
12 | HG01099.hp1 HG01169.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.663-1158delA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76165490 | ||||||
| chr14:76165546 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(298): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.663-1117G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165546 | |||||||
| chr14:76165592 | A | G | 12 | a0001c0001t0007g0040 a0001c0001t0007g0041 a0001c0001t0007g0273 others(9): Show |
15 | NA18747.hp2 NA18942.hp1 NA18953.hp1 others(12): Show |
intron_variant | MODIFIER | c.663-1071A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165592 | |||||||
| chr14:76165689 | T | C | 1 | a0001c0001t0056g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.663-974T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165689 | |||||||
| chr14:76165718 | T | C | 7 | a0001c0001t0002g0004 a0001c0001t0002g0184 a0001c0001t0002g0187 others(4): Show |
14 | HG00438.hp2 HG02056.hp2 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.663-945T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165718 | |||||||
| chr14:76165750 | A | G | 1 | a0001c0001t0004g0042 | 2 | NA18960.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.663-913A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165750 | |||||||
| chr14:76165892 | C | G | 2 | a0001c0001t0020g0029 a0001c0001t0020g0169 |
3 | HG02886.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.663-771C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165892 | |||||||
| chr14:76165921 | A | G | 2 | a0001c0001t0033g0050 a0001c0001t0033g0253 |
2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.663-742A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165921 | |||||||
| chr14:76165992 | G | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.663-671G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165992 | |||||||
| chr14:76166113 | A | G | 2 | a0001c0001t0078g0287 a0002c0007t0088g0227 |
2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.663-550A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166113 | |||||||
| chr14:76166120 | T | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.663-543T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166120 | |||||||
| chr14:76166154 | C | T | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.663-509C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166154 | |||||||
| chr14:76166218 | G | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-445G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166218 | |||||||
| chr14:76166438 | T | G | 42 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(39): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.663-225T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166438 | |||||||
| chr14:76166637 | T | A | 3 | a0001c0005t0016g0166 a0001c0005t0016g0167 a0001c0005t0016g0179 |
3 | HG02965.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.663-26T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166637 | |||||||
| chr14:76166735 | C | T | 1 | a0001c0001t0009g0213 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.727+8C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76166735 | |||||||
| chr14:76166899 | T | C | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727+172T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76166899 | |||||||
| chr14:76167053 | A | C | 1 | a0001c0001t0052g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.727+326A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167053 | |||||||
| chr14:76167303 | T | C | 2 | a0001c0001t0004g0222 a0001c0001t0004g0223 |
2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.727+576T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167303 | |||||||
| chr14:76167343 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+616G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167343 | |||||||
| chr14:76167344 | T | TG | 3 | a0001c0001t0062g0189 a0001c0002t0001g0023 a0001c0002t0001g0105 |
4 | NA18981.hp1 NA19006.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+621dupG | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76167344 | ||||||
| chr14:76167396 | C | T | 1 | a0001c0001t0062g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.727+669C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167396 | |||||||
| chr14:76167397 | T | C | 1 | a0001c0001t0062g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.727+670T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167397 | |||||||
| chr14:76167399 | A | T | 1 | a0001c0001t0062g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.727+672A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167399 | |||||||
| chr14:76167421 | A | G | 1 | a0001c0001t0009g0212 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.727+694A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167421 | |||||||
| chr14:76167467 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.727+740C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167467 | |||||||
| chr14:76167580 | A | AT | 4 | a0001c0005t0016g0166 a0001c0005t0016g0167 a0001c0005t0016g0179 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+858dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76167580 | ||||||
| chr14:76167613 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.727+886G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167613 | |||||||
| chr14:76167614 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.727+887T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167614 | |||||||
| chr14:76167624 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.727+897G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167624 | |||||||
| chr14:76167652 | C | T | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727+925C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167652 | |||||||
| chr14:76167668 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+941G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167668 | |||||||
| chr14:76167920 | A | G | 1 | a0001c0001t0035g0250 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.727+1193A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167920 | |||||||
| chr14:76168121 | A | C | 29 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(26): Show |
41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.727+1394A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168121 | |||||||
| chr14:76168299 | G | C | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+1572G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168299 | |||||||
| chr14:76168310 | C | T | 3 | a0001c0001t0030g0254 a0001c0001t0030g0256 a0001c0008t0038g0255 |
3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.727+1583C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168310 | |||||||
| chr14:76168333 | A | T | 12 | a0001c0001t0011g0030 a0001c0001t0011g0170 a0001c0001t0011g0172 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+1606A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168333 | |||||||
| chr14:76168453 | A | G | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+1726A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168453 | |||||||
| chr14:76168793 | G | A | 1 | a0001c0001t0083g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.727+2066G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168793 | |||||||
| chr14:76168962 | A | G | 2 | a0001c0001t0028g0185 a0001c0001t0028g0186 |
2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.727+2235A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168962 | |||||||
| chr14:76169034 | T | C | 64 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(61): Show |
67 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.727+2307T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169034 | |||||||
| chr14:76169242 | C | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+2515C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169242 | |||||||
| chr14:76169332 | G | C | 42 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(39): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.728-2511G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169332 | |||||||
| chr14:76169491 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.728-2352A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169491 | |||||||
| chr14:76169561 | A | G | 1 | a0001c0008t0038g0255 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.728-2282A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169561 | |||||||
| chr14:76169616 | C | T | 27 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(24): Show |
39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.728-2227C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169616 | |||||||
| chr14:76169712 | C | T | 8 | a0001c0001t0004g0010 a0001c0001t0004g0222 a0001c0001t0004g0223 others(5): Show |
12 | HG00140.hp2 HG01074.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.728-2131C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169712 | |||||||
| chr14:76169715 | C | G | 1 | a0001c0001t0045g0157 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.728-2128C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169715 | |||||||
| chr14:76169784 | G | T | 1 | a0001c0008t0038g0255 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.728-2059G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169784 | |||||||
| chr14:76169853 | A | T | 1 | a0001c0001t0062g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1990A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169853 | |||||||
| chr14:76169854 | T | A | 1 | a0001c0001t0062g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1989T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169854 | |||||||
| chr14:76169855 | C | T | 1 | a0001c0001t0062g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1988C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169855 | |||||||
| chr14:76169856 | T | G | 1 | a0001c0001t0062g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1987T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169856 | |||||||
| chr14:76169937 | G | GAAATACA others(7): Show |
1 | a0001c0001t0062g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1905_728-1892d others(16): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76169937 | ||||||
| chr14:76169943 | C | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.728-1900C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169943 | |||||||
| chr14:76169998 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(298): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.728-1845A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169998 | |||||||
| chr14:76170019 | T | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.728-1824T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170019 | |||||||
| chr14:76170128 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.728-1715A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170128 | |||||||
| chr14:76170355 | G | A | 1 | a0001c0001t0012g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.728-1488G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170355 | |||||||
| chr14:76170393 | T | G | 2 | a0001c0001t0021g0190 a0001c0001t0064g0191 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.728-1450T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170393 | |||||||
| chr14:76170444 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.728-1399A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170444 | |||||||
| chr14:76170530 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.728-1313G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170530 | |||||||
| chr14:76170594 | G | T | 12 | a0001c0001t0007g0040 a0001c0001t0007g0041 a0001c0001t0007g0273 others(9): Show |
15 | NA18747.hp2 NA18942.hp1 NA18953.hp1 others(12): Show |
intron_variant | MODIFIER | c.728-1249G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170594 | |||||||
| chr14:76170670 | A | G | 1 | a0001c0001t0056g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.728-1173A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170670 | |||||||
| chr14:76170733 | T | C | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.728-1110T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170733 | |||||||
| chr14:76170858 | G | T | 1 | a0001c0001t0074g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.728-985G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170858 | |||||||
| chr14:76171050 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0061g0009 a0001c0001t0091g0009 |
4 | HG02723.hp2 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-793G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171050 | |||||||
| chr14:76171197 | G | A | 1 | a0001c0001t0007g0273 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.728-646G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171197 | |||||||
| chr14:76171277 | T | TA | 50 | a0001c0001t0001g0057 a0001c0001t0004g0005 a0001c0001t0004g0010 others(47): Show |
69 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.728-551dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76171277 | ||||||
| chr14:76171294 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.728-549A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171294 | |||||||
| chr14:76171346 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.728-497G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171346 | |||||||
| chr14:76171366 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(84): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.728-477G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171366 | |||||||
| chr14:76171445 | C | T | 2 | a0001c0001t0033g0050 a0001c0001t0033g0253 |
2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.728-398C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171445 | |||||||
| chr14:76171449 | C | A | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.728-394C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171449 | |||||||
| chr14:76171511 | A | G | 8 | a0001c0001t0011g0030 a0001c0001t0011g0170 a0001c0001t0011g0172 others(5): Show |
9 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.728-332A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171511 | |||||||
| chr14:76171583 | CAA | C | 59 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(56): Show |
62 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.728-254_728-253del others(2): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76171583 | ||||||
| chr14:76171718 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.728-125G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171718 | |||||||
| chr14:76171729 | GA | G | 15 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0006g0153 others(12): Show |
17 | HG00673.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.728-100delA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76171729 | ||||||
| chr14:76171815 | A | G | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.728-28A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171815 | |||||||
| chr14:76172123 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(167): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.904+104A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172123 | |||||||
| chr14:76172243 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(303): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.904+224T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172243 | |||||||
| chr14:76172271 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.904+252C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172271 | |||||||
| chr14:76172651 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.904+632T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172651 | |||||||
| chr14:76172683 | T | C | 33 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(30): Show |
47 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.904+664T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172683 | |||||||
| chr14:76172976 | A | G | 42 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(39): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.905-570A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172976 | |||||||
| chr14:76173079 | T | C | 1 | a0001c0001t0005g0128 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.905-467T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173079 | |||||||
| chr14:76173129 | G | A | 1 | a0001c0001t0022g0059 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.905-417G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173129 | |||||||
| chr14:76173221 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(82): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.905-325T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173221 | |||||||
| chr14:76173226 | G | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.905-320G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173226 | |||||||
| chr14:76173271 | T | C | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.905-275T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173271 | |||||||
| chr14:76173782 | A | C | 55 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0009 others(52): Show |
71 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.984+157A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76173782 | |||||||
| chr14:76173837 | CA | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(215): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.984+224delA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 76173837 | ||||||
| chr14:76173850 | C | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.984+225C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76173850 | |||||||
| chr14:76173877 | T | G | 3 | a0001c0001t0013g0226 a0001c0001t0026g0161 a0001c0001t0026g0162 |
3 | HG03239.hp2 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.984+252T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76173877 | |||||||
| chr14:76174035 | T | TA | 62 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(59): Show |
65 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.984+422dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 76174035 | ||||||
| chr14:76174167 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.984+542A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174167 | |||||||
| chr14:76174218 | A | G | 1 | a0001c0001t0043g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.984+593A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174218 | |||||||
| chr14:76174225 | T | C | 1 | a0001c0001t0045g0157 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.984+600T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174225 | |||||||
| chr14:76174277 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.984+652C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174277 | |||||||
| chr14:76174475 | C | T | 27 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(24): Show |
39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.984+850C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174475 | |||||||
| chr14:76174556 | C | T | 2 | a0001c0001t0034g0267 a0001c0001t0034g0268 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.984+931C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174556 | |||||||
| chr14:76174928 | C | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.984+1303C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174928 | |||||||
| chr14:76175246 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.985-1377G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175246 | |||||||
| chr14:76175256 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.985-1367G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175256 | |||||||
| chr14:76175361 | G | A | 41 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(38): Show |
58 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.985-1262G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175361 | |||||||
| chr14:76175391 | C | G | 1 | a0001c0001t0014g0095 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.985-1232C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175391 | |||||||
| chr14:76175796 | G | GT | 4 | a0001c0001t0002g0014 a0001c0001t0002g0209 a0001c0001t0002g0210 others(1): Show |
6 | NA18979.hp1 NA18981.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.985-824dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 76175796 | ||||||
| chr14:76175959 | A | G | 1 | a0001c0001t0053g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.985-664A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175959 | |||||||
| chr14:76176173 | A | G | 2 | a0001c0001t0049g0163 a0001c0001t0056g0176 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.985-450A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176173 | |||||||
| chr14:76176367 | A | G | 3 | a0001c0005t0016g0166 a0001c0005t0016g0167 a0001c0005t0016g0179 |
3 | HG02965.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.985-256A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176367 | |||||||
| chr14:76176414 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.985-209G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176414 | |||||||
| chr14:76176426 | A | G | 1 | a0001c0001t0002g0035 | 2 | HG01261.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.985-197A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176426 | |||||||
| chr14:76176427 | TGTAGG | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.985-192_985-188del others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 76176427 | ||||||
| chr14:76176454 | A | G | 5 | a0001c0001t0006g0028 a0001c0001t0006g0124 a0001c0001t0006g0146 others(2): Show |
6 | HG02027.hp1 NA18972.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-169A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176454 | |||||||
| chr14:76176556 | T | C | 1 | a0001c0001t0003g0236 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.985-67T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176556 | |||||||
| chr14:76176814 | G | A | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1052+124G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76176814 | |||||||
| chr14:76176855 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1052+165G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76176855 | |||||||
| chr14:76176901 | T | A | 1 | a0001c0001t0053g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1052+211T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76176901 | |||||||
| chr14:76176972 | A | AT | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1052+293dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 76176972 | ||||||
| chr14:76177000 | C | A | 1 | a0001c0001t0008g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1052+310C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177000 | |||||||
| chr14:76177019 | T | C | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1052+329T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177019 | |||||||
| chr14:76177084 | C | T | 6 | a0001c0001t0001g0045 a0001c0001t0001g0097 a0001c0001t0031g0093 others(3): Show |
6 | HG02135.hp1 HG03654.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.1052+394C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177084 | |||||||
| chr14:76177152 | C | A | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1052+462C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177152 | |||||||
| chr14:76177191 | G | T | 1 | a0001c0001t0003g0233 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1052+501G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177191 | |||||||
| chr14:76177304 | C | T | 1 | a0001c0001t0084g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1052+614C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177304 | |||||||
| chr14:76177333 | G | A | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1052+643G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177333 | |||||||
| chr14:76177384 | C | T | 1 | a0001c0005t0016g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1053-604C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177384 | |||||||
| chr14:76177662 | T | C | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1053-326T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177662 | |||||||
| chr14:76177697 | G | GT | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0103 others(4): Show |
7 | HG00738.hp1 HG00738.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1053-282dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 76177697 | ||||||
| chr14:76177697 | G | GTTT | 42 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0119 others(39): Show |
45 | HG00323.hp2 HG00558.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.1053-284_1053-282d others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 76177697 | ||||||
| chr14:76177697 | G | GTTTT | 17 | a0001c0001t0005g0027 a0001c0001t0005g0145 a0001c0001t0006g0148 others(14): Show |
17 | HG00423.hp1 HG01106.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1053-285_1053-282d others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 76177697 | ||||||
| chr14:76177706 | TG | T | 68 | a0001c0001t0001g0091 a0001c0001t0003g0002 a0001c0001t0003g0036 others(65): Show |
97 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1053-281delG | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177706 | |||||||
| chr14:76177707 | G | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(229): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1053-281G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177707 | |||||||
| chr14:76177709 | T | G | 28 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(25): Show |
40 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1053-279T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177709 | |||||||
| chr14:76177713 | G | T | 62 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(59): Show |
65 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1053-275G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177713 | |||||||
| chr14:76177760 | A | G | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1053-228A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177760 | |||||||
| chr14:76177923 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1053-65C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177923 | |||||||
| chr14:76178280 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1107+238G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178280 | |||||||
| chr14:76178504 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1107+462G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178504 | |||||||
| chr14:76178550 | A | G | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1107+508A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178550 | |||||||
| chr14:76178740 | C | T | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1107+698C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178740 | |||||||
| chr14:76178752 | C | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1107+710C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178752 | |||||||
| chr14:76178795 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0037g0013 a0001c0001t0067g0013 |
3 | NA18971.hp1 NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1107+753C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178795 | |||||||
| chr14:76178813 | C | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1107+771C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178813 | |||||||
| chr14:76178963 | A | AT | 2 | a0001c0001t0001g0008 a0001c0001t0001g0089 |
5 | NA18941.hp1 NA18972.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1107+928dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76178963 | ||||||
| chr14:76178979 | G | A | 3 | a0001c0001t0013g0226 a0001c0001t0026g0161 a0001c0001t0026g0162 |
3 | HG03239.hp2 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1107+937G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178979 | |||||||
| chr14:76179063 | G | GT | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(218): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1107+1033dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76179063 | ||||||
| chr14:76179171 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1107+1129G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179171 | |||||||
| chr14:76179180 | A | G | 2 | a0001c0001t0024g0038 a0001c0001t0024g0270 |
3 | HG00140.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1107+1138A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179180 | |||||||
| chr14:76179311 | A | G | 3 | a0001c0005t0016g0166 a0001c0005t0016g0167 a0001c0005t0016g0179 |
3 | HG02965.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1107+1269A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179311 | |||||||
| chr14:76179420 | A | T | 1 | a0001c0001t0087g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1108-1344A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179420 | |||||||
| chr14:76179706 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1108-1058A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179706 | |||||||
| chr14:76179738 | A | G | 1 | a0001c0001t0006g0130 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1108-1026A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179738 | |||||||
| chr14:76179927 | G | A | 1 | a0001c0001t0021g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1108-837G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179927 | |||||||
| chr14:76180005 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(163): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1108-759C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180005 | |||||||
| chr14:76180030 | C | CA | 7 | a0001c0001t0002g0009 a0001c0001t0009g0218 a0001c0001t0011g0170 others(4): Show |
8 | HG02145.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108-718dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76180030 | ||||||
| chr14:76180030 | C | CAAA | 45 | a0001c0001t0003g0249 a0001c0001t0004g0005 a0001c0001t0004g0010 others(42): Show |
64 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1108-720_1108-718d others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76180030 | ||||||
| chr14:76180030 | C | CAAAA | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(165): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1108-721_1108-718d others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76180030 | ||||||
| chr14:76180030 | C | CAAAAA | 11 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(8): Show |
11 | HG00558.hp2 HG00621.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1108-722_1108-718d others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76180030 | ||||||
| chr14:76180069 | G | A | 1 | a0001c0001t0087g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1108-695G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180069 | |||||||
| chr14:76180283 | G | A | 1 | a0001c0001t0007g0274 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1108-481G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180283 | |||||||
| chr14:76180289 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1108-475A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180289 | |||||||
| chr14:76180355 | G | A | 41 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0014 others(38): Show |
56 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1108-409G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180355 | |||||||
| chr14:76180490 | T | A | 1 | a0003c0006t0016g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1108-274T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180490 | |||||||
| chr14:76180535 | A | T | 29 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(26): Show |
41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1108-229A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180535 | |||||||
| chr14:76180567 | T | C | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1108-197T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180567 | |||||||
| chr14:76180569 | C | T | 6 | a0001c0001t0001g0063 a0001c0001t0023g0016 a0001c0001t0030g0254 others(3): Show |
8 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108-195C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180569 | |||||||
| chr14:76180693 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1108-71T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180693 | |||||||
| chr14:76180711 | A | T | 2 | a0001c0001t0021g0190 a0001c0001t0064g0191 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1108-53A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180711 | |||||||
| chr14:76180719 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1108-45C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180719 | |||||||
| chr14:76180745 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1108-19G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180745 | |||||||
| chr14:76180854 | T | C | 1 | a0001c0001t0087g0252 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.1193+5T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76180854 | |||||||
| chr14:76181000 | T | C | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1193+151T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181000 | |||||||
| chr14:76181229 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(224): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1193+380A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181229 | |||||||
| chr14:76181239 | A | G | 8 | a0001c0001t0015g0112 a0001c0001t0015g0113 a0001c0001t0015g0114 others(5): Show |
8 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1193+390A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181239 | |||||||
| chr14:76181254 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(224): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1193+405T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181254 | |||||||
| chr14:76181267 | T | C | 1 | a0001c0005t0016g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1193+418T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181267 | |||||||
| chr14:76181302 | A | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(224): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1193+453A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181302 | |||||||
| chr14:76181323 | A | G | 1 | a0001c0001t0033g0253 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1193+474A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181323 | |||||||
| chr14:76181521 | T | A | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1193+672T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181521 | |||||||
| chr14:76181547 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1193+698C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181547 | |||||||
| chr14:76181693 | T | C | 1 | a0001c0001t0063g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1193+844T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181693 | |||||||
| chr14:76181754 | T | C | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1193+905T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181754 | |||||||
| chr14:76181764 | A | G | 2 | a0001c0001t0017g0015 a0001c0001t0017g0225 |
4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193+915A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181764 | |||||||
| chr14:76181858 | A | G | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1193+1009A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181858 | |||||||
| chr14:76181905 | A | G | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+1056A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181905 | |||||||
| chr14:76181937 | A | C | 2 | a0001c0001t0013g0126 a0001c0001t0047g0127 |
2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1193+1088A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181937 | |||||||
| chr14:76182174 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+1325G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182174 | |||||||
| chr14:76182281 | C | T | 1 | a0001c0001t0052g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1193+1432C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182281 | |||||||
| chr14:76182321 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(226): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1193+1472C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182321 | |||||||
| chr14:76182343 | C | T | 1 | a0001c0001t0011g0175 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1193+1494C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182343 | |||||||
| chr14:76182348 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1193+1499C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182348 | |||||||
| chr14:76182351 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1193+1502C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182351 | |||||||
| chr14:76182363 | G | GA | 58 | a0001c0001t0001g0103 a0001c0001t0002g0004 a0001c0001t0002g0006 others(55): Show |
75 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1193+1535dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182363 | ||||||
| chr14:76182363 | G | GAA | 188 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(185): Show |
249 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1193+1534_1193+153 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182363 | ||||||
| chr14:76182363 | G | GAAA | 36 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(33): Show |
46 | HG00423.hp2 HG01074.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.1193+1533_1193+153 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182363 | ||||||
| chr14:76182363 | G | GAAAA | 7 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(4): Show |
9 | HG00741.hp1 HG01346.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1193+1532_1193+153 others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182363 | ||||||
| chr14:76182421 | A | AT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(163): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1193+1584dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182421 | ||||||
| chr14:76182422 | T | A | 1 | a0001c0001t0048g0143 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1193+1573T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182422 | |||||||
| chr14:76182441 | T | C | 1 | a0003c0006t0016g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1193+1592T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182441 | |||||||
| chr14:76182443 | G | A | 1 | a0001c0001t0013g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1193+1594G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182443 | |||||||
| chr14:76182585 | C | CA | 8 | a0001c0001t0002g0209 a0001c0001t0009g0192 a0001c0001t0009g0218 others(5): Show |
8 | HG02965.hp2 HG03540.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.1193+1757dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182585 | ||||||
| chr14:76182585 | CA | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(117): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1193+1757delA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182585 | ||||||
| chr14:76182585 | CAA | C | 75 | a0001c0001t0001g0076 a0001c0001t0001g0086 a0001c0001t0001g0089 others(72): Show |
80 | HG00423.hp1 HG00558.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1193+1756_1193+175 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182585 | ||||||
| chr14:76182585 | CAAAAA | C | 27 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(24): Show |
39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1193+1753_1193+175 others(9): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182585 | ||||||
| chr14:76182636 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1193+1787A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182636 | |||||||
| chr14:76182702 | C | T | 1 | a0001c0001t0022g0075 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1193+1853C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182702 | |||||||
| chr14:76182718 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1193+1869A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182718 | |||||||
| chr14:76182782 | G | A | 1 | a0001c0001t0033g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1193+1933G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182782 | |||||||
| chr14:76182822 | A | G | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1193+1973A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182822 | |||||||
| chr14:76182946 | A | C | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.1193+2097A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182946 | |||||||
| chr14:76182968 | G | T | 2 | a0001c0001t0004g0005 a0001c0001t0004g0276 |
7 | NA18939.hp1 NA18943.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1193+2119G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182968 | |||||||
| chr14:76183099 | T | C | 2 | a0001c0001t0033g0050 a0001c0001t0033g0253 |
2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1193+2250T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183099 | |||||||
| chr14:76183373 | G | A | 1 | a0001c0001t0049g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1193+2524G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183373 | |||||||
| chr14:76183485 | A | AT | 5 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0205 others(2): Show |
5 | HG01081.hp1 HG02602.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193+2644dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76183485 | ||||||
| chr14:76183485 | A | T | 2 | a0001c0001t0078g0287 a0002c0007t0088g0227 |
2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1193+2636A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183485 | |||||||
| chr14:76183558 | A | G | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+2709A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183558 | |||||||
| chr14:76183583 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1193+2734C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183583 | |||||||
| chr14:76183596 | C | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+2747C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183596 | |||||||
| chr14:76183723 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1193+2874G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183723 | |||||||
| chr14:76183758 | C | T | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+2909C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183758 | |||||||
| chr14:76183759 | G | A | 2 | a0001c0001t0014g0066 a0001c0001t0014g0095 |
2 | HG00621.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1193+2910G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183759 | |||||||
| chr14:76183789 | T | C | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+2940T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183789 | |||||||
| chr14:76184022 | T | TGG | 38 | a0001c0001t0003g0002 a0001c0001t0003g0230 a0001c0001t0003g0231 others(35): Show |
47 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1193+3174_1193+317 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184022 | ||||||
| chr14:76184023 | G | GGGGT | 7 | a0001c0001t0001g0102 a0001c0001t0003g0002 a0001c0001t0003g0036 others(4): Show |
8 | HG01346.hp2 HG01516.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1193+3175_1193+317 others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184023 | ||||||
| chr14:76184023 | GGT | G | 22 | a0001c0001t0002g0035 a0001c0001t0002g0196 a0001c0001t0003g0234 others(19): Show |
24 | HG00323.hp2 HG01106.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.1193+3216_1193+321 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184023 | ||||||
| chr14:76184023 | GGTGT | G | 76 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0053 others(73): Show |
95 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1193+3214_1193+321 others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184023 | ||||||
| chr14:76184023 | GGTGTGT | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(114): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1193+3212_1193+321 others(10): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184023 | ||||||
| chr14:76184024 | GTGT | G | 3 | a0001c0001t0001g0097 a0001c0001t0002g0202 a0001c0001t0002g0216 |
3 | HG02071.hp1 HG02135.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1193+3176_1193+317 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184024 | |||||||
| chr14:76184025 | T | G | 53 | a0001c0001t0002g0195 a0001c0001t0003g0242 a0001c0001t0005g0024 others(50): Show |
58 | HG00423.hp1 HG00558.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1193+3176T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184025 | |||||||
| chr14:76184027 | T | G | 49 | a0001c0001t0002g0035 a0001c0001t0002g0196 a0001c0001t0003g0234 others(46): Show |
52 | HG00323.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.1193+3178T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184027 | |||||||
| chr14:76184029 | T | G | 87 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0053 others(84): Show |
107 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1193+3180T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184029 | |||||||
| chr14:76184031 | T | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(122): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1193+3182T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184031 | |||||||
| chr14:76184033 | T | G | 3 | a0001c0001t0001g0063 a0001c0001t0013g0226 a0001c0001t0087g0252 |
3 | HG00738.hp1 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1193+3184T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184033 | |||||||
| chr14:76184087 | G | A | 1 | a0001c0001t0028g0186 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1193+3238G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184087 | |||||||
| chr14:76184421 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.1193+3572T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184421 | |||||||
| chr14:76184501 | G | A | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1193+3652G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184501 | |||||||
| chr14:76184609 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1193+3760G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184609 | |||||||
| chr14:76184678 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0074 |
2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1193+3829A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184678 | |||||||
| chr14:76184721 | A | G | 1 | a0001c0001t0004g0042 | 2 | NA18960.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1193+3872A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184721 | |||||||
| chr14:76184788 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1193+3939T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184788 | |||||||
| chr14:76184793 | G | A | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1193+3944G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184793 | |||||||
| chr14:76185307 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1193+4458A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185307 | |||||||
| chr14:76185321 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+4472G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185321 | |||||||
| chr14:76185739 | G | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(301): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1193+4890G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185739 | |||||||
| chr14:76185927 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1193+5078G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185927 | |||||||
| chr14:76185972 | C | T | 1 | a0001c0001t0078g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1193+5123C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185972 | |||||||
| chr14:76186096 | G | C | 1 | a0001c0001t0003g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1193+5247G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76186096 | |||||||
| chr14:76186127 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1193+5278G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76186127 | |||||||
| chr14:76186341 | A | G | 1 | a0001c0001t0002g0199 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1193+5492A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76186341 | |||||||
| chr14:76186921 | C | T | 1 | a0004c0009t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1193+6072C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76186921 | |||||||
| chr14:76187025 | G | GT | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1193+6188dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76187025 | ||||||
| chr14:76187025 | GT | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1193+6188delT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76187025 | ||||||
| chr14:76187143 | T | C | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1193+6294T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187143 | |||||||
| chr14:76187188 | A | G | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+6339A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187188 | |||||||
| chr14:76187240 | T | G | 1 | a0001c0001t0015g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1193+6391T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187240 | |||||||
| chr14:76187241 | T | C | 1 | a0001c0001t0015g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1193+6392T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187241 | |||||||
| chr14:76187283 | T | C | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1193+6434T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187283 | |||||||
| chr14:76187408 | A | C | 1 | a0002c0007t0088g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1193+6559A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187408 | |||||||
| chr14:76187744 | T | C | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1193+6895T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187744 | |||||||
| chr14:76187851 | C | T | 57 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(54): Show |
60 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1193+7002C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187851 | |||||||
| chr14:76188138 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1193+7289T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188138 | |||||||
| chr14:76188235 | A | G | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1193+7386A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188235 | |||||||
| chr14:76188285 | G | A | 1 | a0001c0001t0055g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1193+7436G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188285 | |||||||
| chr14:76188344 | C | T | 1 | a0001c0001t0002g0188 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1193+7495C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188344 | |||||||
| chr14:76188360 | A | C | 1 | a0001c0001t0089g0272 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1193+7511A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188360 | |||||||
| chr14:76188479 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1194-7399T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188479 | |||||||
| chr14:76188535 | C | CTTTTGCC others(2): Show |
231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1194-7339_1194-733 others(13): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76188535 | ||||||
| chr14:76188547 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0089 |
5 | NA18941.hp1 NA18972.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194-7331G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188547 | |||||||
| chr14:76188798 | T | C | 12 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0071 others(9): Show |
13 | HG00140.hp1 HG01256.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1194-7080T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188798 | |||||||
| chr14:76188826 | T | C | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1194-7052T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188826 | |||||||
| chr14:76188831 | G | C | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1194-7047G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188831 | |||||||
| chr14:76188834 | T | C | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1194-7044T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188834 | |||||||
| chr14:76189147 | AGTTTT | A | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1194-6727_1194-672 others(9): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76189147 | ||||||
| chr14:76189170 | T | C | 3 | a0001c0001t0030g0254 a0001c0001t0030g0256 a0001c0008t0038g0255 |
3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1194-6708T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189170 | |||||||
| chr14:76189181 | G | C | 2 | a0001c0001t0011g0030 a0001c0001t0059g0171 |
3 | HG01891.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1194-6697G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189181 | |||||||
| chr14:76189268 | G | A | 1 | a0001c0001t0042g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1194-6610G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189268 | |||||||
| chr14:76189330 | C | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1194-6548C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189330 | |||||||
| chr14:76189364 | GTCT | G | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1194-6508_1194-650 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76189364 | ||||||
| chr14:76189473 | G | C | 1 | a0001c0001t0022g0059 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1194-6405G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189473 | |||||||
| chr14:76189643 | A | G | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1194-6235A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189643 | |||||||
| chr14:76189785 | A | G | 2 | a0001c0001t0078g0287 a0002c0007t0088g0227 |
2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1194-6093A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189785 | |||||||
| chr14:76189857 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1194-6021T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189857 | |||||||
| chr14:76189969 | C | A | 1 | a0001c0001t0013g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1194-5909C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189969 | |||||||
| chr14:76189989 | C | T | 1 | a0004c0009t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1194-5889C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189989 | |||||||
| chr14:76190072 | G | A | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1194-5806G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190072 | |||||||
| chr14:76190114 | A | AT | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1194-5755dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76190114 | ||||||
| chr14:76190160 | T | G | 42 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(39): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.1194-5718T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190160 | |||||||
| chr14:76190166 | C | T | 1 | a0001c0001t0047g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1194-5712C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190166 | |||||||
| chr14:76190208 | C | T | 1 | a0001c0001t0087g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1194-5670C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190208 | |||||||
| chr14:76190299 | C | G | 1 | a0001c0001t0050g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1194-5579C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190299 | |||||||
| chr14:76190323 | C | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1194-5555C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190323 | |||||||
| chr14:76190434 | A | C | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1194-5444A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190434 | |||||||
| chr14:76190436 | A | G | 1 | a0001c0001t0087g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1194-5442A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190436 | |||||||
| chr14:76190488 | A | G | 1 | a0001c0001t0015g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1194-5390A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190488 | |||||||
| chr14:76190860 | A | G | 7 | a0001c0001t0010g0018 a0001c0001t0010g0260 a0001c0001t0010g0261 others(4): Show |
9 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1194-5018A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190860 | |||||||
| chr14:76190929 | G | T | 1 | a0001c0001t0081g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1194-4949G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190929 | |||||||
| chr14:76190941 | T | C | 1 | a0001c0001t0087g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1194-4937T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190941 | |||||||
| chr14:76191070 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1194-4808A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191070 | |||||||
| chr14:76191127 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(227): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1194-4751C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191127 | |||||||
| chr14:76191132 | CTTG | C | 7 | a0001c0001t0011g0030 a0001c0001t0011g0170 a0001c0001t0011g0172 others(4): Show |
8 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1194-4740_1194-473 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76191132 | ||||||
| chr14:76191413 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(163): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1194-4465G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191413 | |||||||
| chr14:76191610 | C | A | 4 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(1): Show |
6 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194-4268C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191610 | |||||||
| chr14:76191732 | A | T | 1 | a0001c0001t0046g0147 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1194-4146A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191732 | |||||||
| chr14:76191783 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1194-4095T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191783 | |||||||
| chr14:76191829 | T | C | 1 | a0001c0001t0052g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194-4049T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191829 | |||||||
| chr14:76191931 | T | TC | 4 | a0001c0001t0017g0015 a0001c0001t0017g0225 a0001c0001t0029g0180 others(1): Show |
6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194-3944dupC | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76191931 | ||||||
| chr14:76191968 | G | T | 1 | a0001c0001t0008g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1194-3910G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191968 | |||||||
| chr14:76192119 | C | CT | 63 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0005g0024 others(60): Show |
68 | HG00423.hp1 HG00558.hp2 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1194-3741dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76192119 | ||||||
| chr14:76192119 | CT | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0096 others(10): Show |
13 | HG00099.hp1 HG01099.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1194-3741delT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76192119 | ||||||
| chr14:76192174 | G | C | 2 | a0001c0001t0017g0015 a0001c0001t0017g0225 |
4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1194-3704G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192174 | |||||||
| chr14:76192318 | T | A | 1 | a0001c0001t0018g0080 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1194-3560T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192318 | |||||||
| chr14:76192480 | T | C | 1 | a0001c0001t0002g0197 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1194-3398T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192480 | |||||||
| chr14:76192522 | G | A | 1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1194-3356G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192522 | |||||||
| chr14:76192547 | C | T | 1 | a0001c0001t0052g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194-3331C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192547 | |||||||
| chr14:76192597 | C | T | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(1): Show |
4 | NA18982.hp1 NA19005.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194-3281C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192597 | |||||||
| chr14:76192861 | T | G | 1 | a0001c0001t0083g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1194-3017T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192861 | |||||||
| chr14:76193024 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1194-2854G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193024 | |||||||
| chr14:76193226 | A | T | 1 | a0001c0001t0055g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1194-2652A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193226 | |||||||
| chr14:76193380 | G | A | 3 | a0001c0001t0013g0226 a0001c0001t0026g0161 a0001c0001t0026g0162 |
3 | HG03239.hp2 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1194-2498G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193380 | |||||||
| chr14:76193499 | T | A | 1 | a0001c0001t0001g0106 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1194-2379T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193499 | |||||||
| chr14:76193555 | A | C | 1 | a0001c0001t0002g0206 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1194-2323A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193555 | |||||||
| chr14:76193709 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1194-2169T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193709 | |||||||
| chr14:76193878 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(163): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1194-2000A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193878 | |||||||
| chr14:76194081 | C | T | 1 | a0001c0001t0005g0139 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1194-1797C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194081 | |||||||
| chr14:76194097 | C | CTG | 4 | a0001c0001t0002g0014 a0001c0001t0002g0209 a0001c0001t0002g0210 others(1): Show |
6 | NA18979.hp1 NA18981.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1194-1779_1194-177 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194097 | ||||||
| chr14:76194177 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1194-1701C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194177 | |||||||
| chr14:76194484 | A | AGT | 91 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0009 others(88): Show |
118 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1194-1374_1194-137 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGT | 13 | a0001c0001t0001g0054 a0001c0001t0002g0014 a0001c0001t0002g0187 others(10): Show |
15 | HG00642.hp2 HG00733.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1194-1376_1194-137 others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGTGT | 5 | a0001c0001t0030g0254 a0001c0001t0030g0256 a0001c0001t0076g0109 others(2): Show |
5 | HG01074.hp1 HG01346.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194-1378_1194-137 others(10): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGTGTG others(1): Show |
82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1194-1380_1194-137 others(12): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGTGTG others(3): Show |
6 | a0001c0001t0005g0119 a0001c0001t0005g0121 a0001c0001t0005g0159 others(3): Show |
8 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1194-1382_1194-137 others(14): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGTGTG others(5): Show |
32 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(29): Show |
35 | HG00323.hp2 HG00423.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1194-1384_1194-137 others(16): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGTGTG others(7): Show |
4 | a0001c0001t0005g0131 a0001c0001t0006g0136 a0001c0001t0029g0181 others(1): Show |
4 | HG00558.hp2 HG01496.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194-1386_1194-137 others(18): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGTGTG others(9): Show |
14 | a0001c0001t0006g0150 a0001c0001t0006g0151 a0001c0001t0013g0123 others(11): Show |
14 | HG01081.hp2 HG01934.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1194-1388_1194-137 others(20): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGTGTG others(11): Show |
5 | a0001c0001t0013g0135 a0001c0001t0013g0144 a0001c0001t0026g0161 others(2): Show |
5 | HG02559.hp2 HG02897.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194-1390_1194-137 others(22): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGTGTG others(13): Show |
5 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0001t0006g0155 others(2): Show |
5 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194-1392_1194-137 others(24): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194484 | A | AGTGTGTG others(15): Show |
1 | a0001c0001t0006g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1194-1373_1194-137 others(26): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | ||||||
| chr14:76194502 | T | TGTGTGTG others(5): Show |
1 | a0001c0001t0080g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1194-1373_1194-137 others(16): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194502 | ||||||
| chr14:76194513 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1194-1365A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194513 | |||||||
| chr14:76194521 | G | A | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1194-1357G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194521 | |||||||
| chr14:76194544 | T | C | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1194-1334T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194544 | |||||||
| chr14:76194670 | G | T | 1 | a0001c0001t0015g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1194-1208G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194670 | |||||||
| chr14:76194721 | TTA | T | 4 | a0001c0001t0017g0015 a0001c0001t0017g0225 a0001c0001t0029g0180 others(1): Show |
6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194-1153_1194-115 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194721 | ||||||
| chr14:76194746 | T | G | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1194-1132T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194746 | |||||||
| chr14:76194756 | TGTG | T | 4 | a0001c0001t0017g0015 a0001c0001t0017g0225 a0001c0001t0029g0180 others(1): Show |
6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194-1119_1194-111 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194756 | ||||||
| chr14:76194851 | C | T | 2 | a0001c0001t0033g0050 a0001c0001t0033g0253 |
2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1194-1027C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194851 | |||||||
| chr14:76195024 | C | T | 1 | a0001c0001t0013g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1194-854C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76195024 | |||||||
| chr14:76195175 | A | G | 1 | a0002c0007t0088g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1194-703A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76195175 | |||||||
| chr14:76195265 | T | C | 1 | a0001c0001t0004g0262 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1194-613T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76195265 | |||||||
| chr14:76195518 | C | G | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1194-360C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76195518 | |||||||
| chr14:76196010 | G | A | 4 | a0001c0001t0017g0015 a0001c0001t0017g0225 a0001c0001t0029g0180 others(1): Show |
6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+38G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196010 | |||||||
| chr14:76196027 | T | C | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1288+55T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196027 | |||||||
| chr14:76196033 | G | GT | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1288+65dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196033 | ||||||
| chr14:76196103 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(163): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1288+131C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196103 | |||||||
| chr14:76196421 | A | G | 1 | a0001c0001t0014g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1288+449A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196421 | |||||||
| chr14:76196437 | G | GT | 43 | a0001c0001t0002g0184 a0001c0001t0002g0195 a0001c0001t0004g0010 others(40): Show |
54 | HG00140.hp2 HG00408.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1288+485dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196437 | ||||||
| chr14:76196437 | G | GTT | 53 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0009 others(50): Show |
68 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1288+484_1288+485d others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196437 | ||||||
| chr14:76196437 | G | GTTT | 9 | a0001c0001t0002g0033 a0001c0001t0002g0200 a0001c0001t0015g0112 others(6): Show |
10 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1288+483_1288+485d others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196437 | ||||||
| chr14:76196438 | T | TTTTG | 10 | a0001c0001t0005g0159 a0001c0001t0006g0153 a0001c0001t0006g0154 others(7): Show |
10 | HG01934.hp2 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1288+469_1288+470i others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196438 | ||||||
| chr14:76196439 | T | TTTG | 44 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(41): Show |
47 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1288+469_1288+470i others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196439 | ||||||
| chr14:76196440 | T | TTG | 4 | a0001c0001t0017g0015 a0001c0001t0017g0225 a0001c0001t0029g0180 others(1): Show |
6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+469_1288+470i others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196440 | ||||||
| chr14:76196559 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1288+587A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196559 | |||||||
| chr14:76196676 | A | G | 2 | a0001c0001t0078g0287 a0002c0007t0088g0227 |
2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1288+704A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196676 | |||||||
| chr14:76197008 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(163): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1288+1036C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197008 | |||||||
| chr14:76197095 | C | G | 1 | a0001c0001t0009g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1288+1123C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197095 | |||||||
| chr14:76197208 | A | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1288+1236A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197208 | |||||||
| chr14:76197234 | T | C | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1288+1262T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197234 | |||||||
| chr14:76197495 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1288+1523T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197495 | |||||||
| chr14:76197525 | C | T | 2 | a0001c0001t0014g0066 a0001c0001t0014g0095 |
2 | HG00621.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1288+1553C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197525 | |||||||
| chr14:76197566 | A | G | 2 | a0001c0001t0029g0180 a0001c0001t0029g0181 |
2 | HG01496.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1288+1594A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197566 | |||||||
| chr14:76197592 | C | T | 4 | a0001c0001t0017g0015 a0001c0001t0017g0225 a0001c0001t0029g0180 others(1): Show |
6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+1620C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197592 | |||||||
| chr14:76197595 | A | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1288+1623A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197595 | |||||||
| chr14:76197863 | G | C | 1 | a0001c0001t0033g0253 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1288+1891G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197863 | |||||||
| chr14:76197937 | T | A | 2 | a0001c0001t0035g0245 a0001c0001t0035g0250 |
2 | HG02040.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1288+1965T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197937 | |||||||
| chr14:76197959 | G | C | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0201 |
3 | NA19060.hp1 NA19063.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1288+1987G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197959 | |||||||
| chr14:76198051 | C | A | 6 | a0001c0001t0023g0016 a0001c0001t0030g0254 a0001c0001t0030g0256 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1288+2079C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198051 | |||||||
| chr14:76198096 | A | C | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1288+2124A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198096 | |||||||
| chr14:76198105 | A | AG | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(296): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1288+2135dupG | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76198105 | ||||||
| chr14:76198120 | C | A | 1 | a0001c0001t0079g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1288+2148C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198120 | |||||||
| chr14:76198184 | C | T | 1 | a0001c0001t0087g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1288+2212C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198184 | |||||||
| chr14:76198276 | G | A | 1 | a0001c0001t0043g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1288+2304G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198276 | |||||||
| chr14:76198533 | G | A | 1 | a0001c0001t0006g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1288+2561G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198533 | |||||||
| chr14:76198730 | A | G | 2 | a0001c0001t0049g0163 a0001c0001t0056g0176 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1288+2758A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198730 | |||||||
| chr14:76198732 | CGA | C | 8 | a0001c0001t0015g0112 a0001c0001t0015g0113 a0001c0001t0015g0114 others(5): Show |
8 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1288+2771_1288+277 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76198732 | ||||||
| chr14:76198762 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1288+2790A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198762 | |||||||
| chr14:76198793 | C | CT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(163): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1288+2823dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76198793 | ||||||
| chr14:76198808 | C | T | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | NA18989.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1288+2836C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198808 | |||||||
| chr14:76198825 | C | T | 4 | a0001c0005t0016g0166 a0001c0005t0016g0167 a0001c0005t0016g0179 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+2853C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198825 | |||||||
| chr14:76199134 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(227): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1289-2557C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199134 | |||||||
| chr14:76199189 | A | T | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1289-2502A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199189 | |||||||
| chr14:76199397 | C | T | 42 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0042 others(39): Show |
59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.1289-2294C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199397 | |||||||
| chr14:76199486 | T | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0010g0018 others(8): Show |
13 | HG00673.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1289-2205T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199486 | |||||||
| chr14:76199553 | T | C | 2 | a0001c0001t0049g0163 a0001c0001t0056g0176 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1289-2138T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199553 | |||||||
| chr14:76199629 | T | C | 1 | a0001c0001t0006g0153 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1289-2062T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199629 | |||||||
| chr14:76199664 | GTGTTGGT others(5): Show |
G | 2 | a0001c0001t0028g0185 a0001c0001t0028g0186 |
2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1289-2023_1289-201 others(16): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76199664 | ||||||
| chr14:76199701 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1289-1990T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199701 | |||||||
| chr14:76199891 | A | G | 2 | a0001c0001t0017g0015 a0001c0001t0017g0225 |
4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1289-1800A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199891 | |||||||
| chr14:76199913 | A | C | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1289-1778A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199913 | |||||||
| chr14:76199929 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(163): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1289-1762T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199929 | |||||||
| chr14:76199930 | G | A | 8 | a0001c0001t0004g0010 a0001c0001t0004g0222 a0001c0001t0004g0223 others(5): Show |
12 | HG00140.hp2 HG01074.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1289-1761G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199930 | |||||||
| chr14:76199956 | G | T | 1 | a0001c0001t0032g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1289-1735G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199956 | |||||||
| chr14:76200019 | A | G | 3 | a0001c0001t0012g0012 a0001c0001t0012g0055 a0001c0001t0012g0065 |
5 | NA18939.hp2 NA18968.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289-1672A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200019 | |||||||
| chr14:76200302 | T | C | 1 | a0001c0001t0001g0019 | 2 | HG00423.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1289-1389T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200302 | |||||||
| chr14:76200453 | G | GTA | 65 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(62): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1289-1234_1289-123 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76200453 | ||||||
| chr14:76200547 | C | T | 1 | a0001c0001t0014g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1289-1144C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200547 | |||||||
| chr14:76200575 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1289-1116C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200575 | |||||||
| chr14:76200831 | C | T | 8 | a0001c0001t0015g0112 a0001c0001t0015g0113 a0001c0001t0015g0114 others(5): Show |
8 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1289-860C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200831 | |||||||
| chr14:76200925 | A | G | 1 | a0001c0001t0007g0282 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1289-766A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200925 | |||||||
| chr14:76201012 | A | T | 1 | a0001c0001t0003g0036 | 2 | NA18988.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1289-679A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201012 | |||||||
| chr14:76201014 | C | T | 1 | a0001c0001t0010g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1289-677C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201014 | |||||||
| chr14:76201175 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1289-516G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201175 | |||||||
| chr14:76201363 | C | T | 1 | a0001c0004t0004g0037 | 2 | HG01928.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1289-328C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201363 | |||||||
| chr14:76201409 | A | G | 1 | a0001c0001t0056g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1289-282A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201409 | |||||||
| chr14:76201417 | A | G | 1 | a0001c0001t0056g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1289-274A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201417 | |||||||
| chr14:76201469 | G | A | 61 | a0001c0001t0005g0024 a0001c0001t0005g0026 a0001c0001t0005g0027 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1289-222G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201469 | |||||||
| chr14:76201599 | A | C | 27 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0003g0230 others(24): Show |
39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1289-92A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201599 | |||||||
| chr14:76201680 | A | T | 1 | a0001c0001t0006g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1289-11A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201680 |