Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1186 |
| ensemblid | ENSG00000103249.19 |
| hgncid | 2025 |
| symbol | CLCN7 |
| name | chloride voltage-gated channel 7 |
| refseq_nuc | NM_001287.6 |
| refseq_prot | NP_001278.1 |
| ensembl_nuc | ENST00000382745.9 |
| ensembl_prot | ENSP00000372193.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 1444935 |
| end | 1475028 |
| strand | - |
| ver | v1.2 |
| region | chr16:1444935-1475028 |
| region5000 | chr16:1439935-1480028 |
| regionname0 | CLCN7_chr16_1444935_1475028 |
| regionname5000 | CLCN7_chr16_1439935_1480028 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 805 | 363 | 74 | 62 | 162 | 15 | 48 | 118 | CLCN7_chr16_1439935_1480028 | CLCN7 | MANVS others(800): Show |
chr16 | 1439935 | 1480028 |
| a0002 | 0/0 | 805 | 30 | 18 | 10 | 0 | 1 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | MANVS others(800): Show |
chr16 | 1439935 | 1480028 |
| a0003 | 0/0 | 802 | 5 | 2 | 2 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | MANVS others(797): Show |
chr16 | 1439935 | 1480028 |
| a0004 | 0/0 | 254 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | MANVS others(249): Show |
chr16 | 1439935 | 1480028 |
| a0005 | 0/0 | 805 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | MANVS others(800): Show |
chr16 | 1439935 | 1480028 |
| a0006 | 0/0 | 805 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | MANVS others(800): Show |
chr16 | 1439935 | 1480028 |
| a0007 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | MANVS others(800): Show |
chr16 | 1439935 | 1480028 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2415 | 125 | 17 | 8 | 84 | 1 | 14 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0002 | 0/0 | 2415 | 78 | 24 | 11 | 31 | 5 | 7 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0003 | 1/0 | 2415 | 62 | 0 | 23 | 18 | 6 | 14 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0004 | 0/0 | 2415 | 55 | 9 | 13 | 24 | 2 | 7 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0005 | 0/0 | 2415 | 28 | 11 | 6 | 4 | 1 | 6 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0007 | 0/0 | 2415 | 7 | 7 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0010 | 0/0 | 2415 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0015 | 0/0 | 2415 | 2 | 1 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0017 | 0/0 | 2415 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0019 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0001c0022 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0002c0006 | 0/0 | 2415 | 13 | 3 | 9 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0002c0008 | 0/0 | 2415 | 5 | 4 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0002c0009 | 0/0 | 2415 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0002c0011 | 0/0 | 2415 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0002c0012 | 0/0 | 2415 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0002c0026 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0003c0013 | 0/0 | 2406 | 2 | 0 | 1 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2401): Show |
chr16 | 1439935 | 1480028 | ||
| a0003c0016 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2401): Show |
chr16 | 1439935 | 1480028 | ||
| a0003c0021 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2401): Show |
chr16 | 1439935 | 1480028 | ||
| a0003c0023 | 0/0 | 2406 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2401): Show |
chr16 | 1439935 | 1480028 | ||
| a0004c0014 | 0/0 | 2615 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2610): Show |
chr16 | 1439935 | 1480028 | ||
| a0005c0018 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0005c0024 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0006c0025 | 0/0 | 2415 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 | ||
| a0007c0020 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | ATGGC others(2410): Show |
chr16 | 1439935 | 1480028 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4168 | 93 | 10 | 8 | 62 | 1 | 11 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0002 | 0/0 | 4168 | 3 | 1 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0004 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0005 | 0/0 | 4168 | 3 | 0 | 0 | 2 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0007 | 0/0 | 4168 | 5 | 0 | 0 | 5 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0008 | 0/0 | 4168 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0009 | 0/0 | 4168 | 7 | 0 | 0 | 7 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0012 | 0/0 | 4168 | 3 | 0 | 0 | 3 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0021 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0031 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0032 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0033 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0035 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0039 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0045 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0001t0049 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0001 | 0/0 | 4168 | 21 | 0 | 2 | 18 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0002 | 0/0 | 4168 | 31 | 8 | 5 | 8 | 4 | 6 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0003 | 0/0 | 4168 | 8 | 5 | 0 | 3 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0007 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0008 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0011 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0013 | 0/0 | 4168 | 3 | 2 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0015 | 0/0 | 4169 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0020 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0023 | 0/0 | 4168 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0034 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0036 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0042 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0043 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0044 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0002t0054 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0001 | 0/0 | 4168 | 10 | 0 | 2 | 6 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0002 | 0/0 | 4168 | 23 | 0 | 13 | 2 | 4 | 4 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0003 | 0/0 | 4168 | 15 | 0 | 2 | 8 | 0 | 5 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0005 | 0/0 | 4168 | 3 | 0 | 2 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0008 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0011 | 0/0 | 4168 | 2 | 0 | 0 | 0 | 2 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0019 | 1/0 | 4168 | 2 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0020 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0022 | 0/0 | 4168 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0037 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0038 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0003t0047 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0004t0001 | 0/0 | 4168 | 40 | 2 | 11 | 23 | 1 | 3 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0004t0002 | 0/0 | 4168 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0004t0004 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0004t0005 | 0/0 | 4168 | 2 | 0 | 1 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0004t0006 | 0/0 | 4168 | 7 | 6 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0004t0007 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0004t0012 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0004t0030 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0005t0001 | 0/0 | 4168 | 3 | 0 | 1 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0005t0004 | 0/0 | 4169 | 20 | 9 | 5 | 4 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0005t0005 | 0/0 | 4168 | 3 | 2 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0005t0011 | 0/0 | 4168 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0007t0002 | 0/0 | 4168 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0007t0003 | 0/0 | 4168 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0007t0004 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0007t0040 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0010t0008 | 0/0 | 4168 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0015t0028 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0015t0046 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0001c0017t0041 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0019t0002 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0001c0022t0048 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0002c0006t0010 | 0/0 | 4168 | 6 | 1 | 4 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0002c0006t0024 | 0/0 | 4169 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0002c0006t0025 | 0/0 | 4170 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4165): Show |
chr16 | 1439935 | 1480028 |
| a0002c0006t0026 | 0/0 | 4170 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4165): Show |
chr16 | 1439935 | 1480028 |
| a0002c0006t0051 | 0/0 | 4169 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0002c0006t0052 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0002c0008t0017 | 0/0 | 4166 | 3 | 2 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4161): Show |
chr16 | 1439935 | 1480028 |
| a0002c0008t0027 | 0/0 | 4168 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0002c0009t0005 | 0/0 | 4168 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0002c0009t0016 | 0/0 | 4169 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0002c0011t0018 | 0/0 | 4168 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0002c0012t0014 | 0/0 | 4168 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0002c0026t0024 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4164): Show |
chr16 | 1439935 | 1480028 |
| a0003c0013t0001 | 0/0 | 4159 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4154): Show |
chr16 | 1439935 | 1480028 |
| a0003c0013t0021 | 0/0 | 4159 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4154): Show |
chr16 | 1439935 | 1480028 |
| a0003c0016t0050 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4154): Show |
chr16 | 1439935 | 1480028 |
| a0003c0021t0013 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4154): Show |
chr16 | 1439935 | 1480028 |
| a0003c0023t0002 | 0/0 | 4159 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4154): Show |
chr16 | 1439935 | 1480028 |
| a0004c0014t0001 | 0/0 | 4368 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4363): Show |
chr16 | 1439935 | 1480028 |
| a0005c0018t0053 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4160): Show |
chr16 | 1439935 | 1480028 |
| a0005c0024t0029 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4160): Show |
chr16 | 1439935 | 1480028 |
| a0006c0025t0002 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| a0007c0020t0001 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | AACAA others(4163): Show |
chr16 | 1439935 | 1480028 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0007g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0009g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0012g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0012g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0021g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0031g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0032g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0033g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0035g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0039g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0045g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0001t0049g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0011g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0015g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0015g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0020g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0023g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0023g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0034g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0036g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0042g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0043g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0044g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0002t0054g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0002g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0003g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0005g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0005g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0005g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0008g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0011g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0011g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0019g0339 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0019g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0020g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0022g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0022g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0037g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0038g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0003t0047g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0005g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0005g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0007g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0012g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0004t0030g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0005t0011g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0007t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0007t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0007t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0007t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0007t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0007t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0007t0040g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0010t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0010t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0010t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0015t0028g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0015t0046g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0017t0041g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0019t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0001c0022t0048g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0010g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0010g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0010g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0010g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0010g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0024g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0025g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0025g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0026g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0026g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0051g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0006t0052g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0008t0017g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0008t0017g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0008t0027g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0008t0027g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0009t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0009t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0009t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0009t0016g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0009t0016g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0011t0018g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0011t0018g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0011t0018g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0012t0014g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0012t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0012t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0002c0026t0024g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0003c0013t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0003c0013t0021g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0003c0016t0050g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0003c0021t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0003c0023t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0004c0014t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0004c0014t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0005c0018t0053g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0005c0024t0029g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0006c0025t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| a0007c0020t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0317 | EUR | GBR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0380 | EUR | GBR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0313 | EUR | GBR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | GBR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00280 | hp1 | a0001 | c0005 | t0005 | g0103 | EUR | FIN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00280 | hp2 | a0001 | c0004 | t0005 | g0354 | EUR | FIN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0217 | EUR | FIN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0312 | EUR | FIN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00423 | hp2 | a0001 | c0004 | t0001 | g0306 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0325 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00609 | hp1 | a0001 | c0001 | t0031 | g0242 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0387 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0344 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00621 | hp2 | a0001 | c0002 | t0003 | g0126 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00639 | hp1 | a0002 | c0006 | t0010 | g0257 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00639 | hp2 | a0001 | c0002 | t0013 | g0030 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00642 | hp2 | a0002 | c0006 | t0010 | g0011 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00673 | hp1 | a0001 | c0004 | t0001 | g0334 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00733 | hp1 | a0001 | c0003 | t0019 | g0340 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0247 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00735 | hp1 | a0002 | c0006 | t0025 | g0265 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00738 | hp1 | a0001 | c0004 | t0005 | g0358 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0328 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00741 | hp1 | a0001 | c0003 | t0005 | g0377 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0287 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01070 | hp2 | a0001 | c0003 | t0008 | g0382 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01071 | hp1 | a0001 | c0005 | t0004 | g0180 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0349 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01074 | hp1 | a0002 | c0006 | t0025 | g0259 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01074 | hp2 | a0004 | c0014 | t0001 | g0115 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01081 | hp1 | a0001 | c0005 | t0004 | g0164 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01081 | hp2 | a0001 | c0003 | t0047 | g0318 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01099 | hp1 | a0002 | c0006 | t0010 | g0011 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01099 | hp2 | a0001 | c0017 | t0041 | g0162 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01106 | hp1 | a0001 | c0003 | t0022 | g0319 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01106 | hp2 | a0001 | c0005 | t0004 | g0184 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01109 | hp2 | a0001 | c0004 | t0006 | g0027 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0320 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01168 | hp1 | a0001 | c0005 | t0004 | g0192 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0323 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01192 | hp1 | a0002 | c0006 | t0024 | g0262 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01192 | hp2 | a0002 | c0006 | t0052 | g0263 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0330 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01243 | hp2 | a0002 | c0008 | t0017 | g0010 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01255 | hp2 | a0001 | c0002 | t0023 | g0077 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0332 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01256 | hp2 | a0001 | c0003 | t0002 | g0311 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0015 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0333 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0015 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01261 | hp1 | a0001 | c0003 | t0002 | g0368 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01261 | hp2 | a0001 | c0002 | t0023 | g0052 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01346 | hp2 | a0001 | c0004 | t0001 | g0297 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0079 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0295 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01433 | hp2 | a0001 | c0004 | t0001 | g0336 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01496 | hp1 | a0001 | c0005 | t0001 | g0181 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0304 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0150 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0212 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01516 | hp1 | a0002 | c0006 | t0010 | g0256 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01516 | hp2 | a0001 | c0003 | t0011 | g0321 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01517 | hp1 | a0001 | c0003 | t0011 | g0324 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0151 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01884 | hp1 | a0001 | c0004 | t0006 | g0023 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01884 | hp2 | a0001 | c0005 | t0005 | g0187 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01891 | hp1 | a0005 | c0024 | t0029 | g0025 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01891 | hp2 | a0001 | c0022 | t0048 | g0171 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0329 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0075 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01952 | hp2 | a0001 | c0003 | t0002 | g0291 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0292 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0076 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01978 | hp1 | a0002 | c0006 | t0051 | g0258 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01978 | hp2 | a0003 | c0013 | t0001 | g0108 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0293 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01981 | hp2 | a0002 | c0006 | t0010 | g0254 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01993 | hp1 | a0003 | c0023 | t0002 | g0322 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0352 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02004 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02004 | hp2 | a0001 | c0003 | t0005 | g0316 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0343 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02055 | hp1 | a0002 | c0009 | t0005 | g0283 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02055 | hp2 | a0001 | c0005 | t0004 | g0152 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02056 | hp2 | a0001 | c0004 | t0001 | g0342 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02080 | hp1 | a0001 | c0002 | t0020 | g0203 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0371 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02129 | hp1 | a0001 | c0004 | t0001 | g0350 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0346 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02145 | hp1 | a0001 | c0010 | t0008 | g0240 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0225 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02148 | hp1 | a0001 | c0004 | t0001 | g0355 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02148 | hp2 | a0001 | c0002 | t0008 | g0050 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0338 | EAS | CDX | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0309 | EAS | CDX | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02257 | hp2 | a0001 | c0004 | t0006 | g0026 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02258 | hp1 | a0002 | c0009 | t0016 | g0080 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02258 | hp2 | a0001 | c0004 | t0006 | g0020 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02273 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02273 | hp2 | a0006 | c0025 | t0002 | g0351 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0078 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02280 | hp2 | a0002 | c0008 | t0017 | g0159 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0327 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02451 | hp1 | a0001 | c0005 | t0004 | g0272 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02451 | hp2 | a0001 | c0007 | t0003 | g0190 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02572 | hp1 | a0001 | c0002 | t0036 | g0206 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02572 | hp2 | a0001 | c0007 | t0002 | g0169 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02602 | hp1 | a0001 | c0002 | t0011 | g0221 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02602 | hp2 | a0001 | c0004 | t0001 | g0353 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0043 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02615 | hp2 | a0001 | c0004 | t0006 | g0019 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02622 | hp1 | a0003 | c0021 | t0013 | g0188 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02622 | hp2 | a0003 | c0016 | t0050 | g0153 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02630 | hp1 | a0001 | c0002 | t0015 | g0274 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02647 | hp1 | a0001 | c0002 | t0054 | g0031 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0199 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0363 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02698 | hp1 | a0001 | c0001 | t0032 | g0118 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02698 | hp2 | a0002 | c0026 | t0024 | g0308 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02717 | hp1 | a0002 | c0008 | t0027 | g0252 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02717 | hp2 | a0001 | c0002 | t0015 | g0051 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02723 | hp1 | a0002 | c0009 | t0005 | g0032 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0228 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0231 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0178 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02738 | hp1 | a0001 | c0004 | t0002 | g0347 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02738 | hp2 | a0001 | c0005 | t0004 | g0167 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0348 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02809 | hp2 | a0001 | c0015 | t0028 | g0022 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0200 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02886 | hp2 | a0001 | c0001 | t0039 | g0173 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02896 | hp1 | a0001 | c0005 | t0004 | g0279 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02896 | hp2 | a0001 | c0007 | t0002 | g0170 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02897 | hp1 | a0001 | c0002 | t0013 | g0033 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02897 | hp2 | a0001 | c0005 | t0004 | g0266 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0281 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02965 | hp1 | a0001 | c0002 | t0013 | g0029 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0299 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02976 | hp1 | a0001 | c0005 | t0004 | g0264 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02976 | hp2 | a0001 | c0007 | t0002 | g0168 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03017 | hp1 | a0001 | c0001 | t0045 | g0229 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0385 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0174 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03041 | hp2 | a0001 | c0005 | t0005 | g0186 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03098 | hp1 | a0001 | c0010 | t0008 | g0239 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03098 | hp2 | a0002 | c0011 | t0018 | g0269 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03130 | hp2 | a0001 | c0005 | t0004 | g0185 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03139 | hp1 | a0002 | c0008 | t0017 | g0010 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03195 | hp1 | a0005 | c0018 | t0053 | g0275 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03195 | hp2 | a0002 | c0006 | t0026 | g0261 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03209 | hp1 | a0002 | c0012 | t0014 | g0016 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03209 | hp2 | a0001 | c0002 | t0044 | g0072 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03225 | hp1 | a0001 | c0005 | t0004 | g0273 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03225 | hp2 | a0001 | c0002 | t0042 | g0268 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03239 | hp1 | a0004 | c0014 | t0001 | g0116 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03239 | hp2 | a0001 | c0004 | t0012 | g0335 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03453 | hp1 | a0001 | c0005 | t0004 | g0271 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03486 | hp1 | a0001 | c0004 | t0030 | g0369 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03486 | hp2 | a0001 | c0004 | t0006 | g0021 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0224 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03490 | hp2 | a0001 | c0005 | t0011 | g0009 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0013 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03492 | hp1 | a0001 | c0003 | t0003 | g0013 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03492 | hp2 | a0001 | c0005 | t0011 | g0009 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0201 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03516 | hp2 | a0001 | c0010 | t0008 | g0238 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03540 | hp1 | a0001 | c0007 | t0004 | g0176 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03579 | hp1 | a0002 | c0012 | t0014 | g0017 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03579 | hp2 | a0002 | c0008 | t0027 | g0251 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0198 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0345 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0218 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0134 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0288 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0196 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03831 | hp2 | a0001 | c0005 | t0001 | g0189 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0289 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03834 | hp2 | a0001 | c0003 | t0003 | g0375 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03927 | hp1 | a0001 | c0004 | t0002 | g0360 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03927 | hp2 | a0001 | c0003 | t0037 | g0357 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03942 | hp1 | a0001 | c0004 | t0001 | g0361 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03942 | hp2 | a0001 | c0004 | t0007 | g0296 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0294 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0367 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04199 | hp1 | a0001 | c0003 | t0005 | g0298 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04204 | hp2 | a0001 | c0003 | t0003 | g0378 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG04228 | hp2 | a0001 | c0003 | t0022 | g0290 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18522 | hp1 | a0002 | c0006 | t0026 | g0260 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0278 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | CHB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18612 | hp2 | a0001 | c0001 | t0021 | g0064 | EAS | CHB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | CHB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0280 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18906 | hp2 | a0001 | c0005 | t0004 | g0179 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18939 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18943 | hp2 | a0001 | c0004 | t0001 | g0356 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18945 | hp1 | a0007 | c0020 | t0001 | g0146 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18950 | hp1 | a0001 | c0004 | t0001 | g0386 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18953 | hp1 | a0001 | c0001 | t0009 | g0055 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18953 | hp2 | a0001 | c0003 | t0003 | g0303 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18954 | hp1 | a0001 | c0005 | t0004 | g0166 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0365 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18962 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18964 | hp2 | a0001 | c0004 | t0004 | g0286 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18966 | hp1 | a0001 | c0004 | t0001 | g0284 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18970 | hp1 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18974 | hp2 | a0001 | c0003 | t0002 | g0315 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18979 | hp1 | a0001 | c0001 | t0012 | g0067 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18979 | hp2 | a0001 | c0001 | t0009 | g0096 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18982 | hp2 | a0001 | c0001 | t0007 | g0157 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0307 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18986 | hp2 | a0001 | c0001 | t0009 | g0101 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18987 | hp2 | a0001 | c0003 | t0003 | g0302 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18991 | hp2 | a0001 | c0005 | t0004 | g0163 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18993 | hp2 | a0001 | c0004 | t0001 | g0364 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18995 | hp1 | a0001 | c0004 | t0001 | g0310 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18995 | hp2 | a0001 | c0004 | t0001 | g0362 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18997 | hp2 | a0001 | c0003 | t0003 | g0384 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0301 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19004 | hp1 | a0001 | c0001 | t0009 | g0100 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19005 | hp1 | a0001 | c0004 | t0001 | g0331 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0300 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0366 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0376 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19043 | hp1 | a0001 | c0004 | t0006 | g0024 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19043 | hp2 | a0001 | c0001 | t0049 | g0237 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19054 | hp1 | a0001 | c0015 | t0046 | g0383 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19054 | hp2 | a0001 | c0004 | t0001 | g0370 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19056 | hp1 | a0001 | c0005 | t0004 | g0165 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0379 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19058 | hp2 | a0001 | c0003 | t0003 | g0373 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19063 | hp2 | a0001 | c0003 | t0003 | g0374 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19067 | hp1 | a0001 | c0003 | t0038 | g0314 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19067 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19070 | hp2 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19074 | hp1 | a0001 | c0004 | t0001 | g0285 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19079 | hp1 | a0003 | c0013 | t0021 | g0056 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19081 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19081 | hp2 | a0001 | c0003 | t0020 | g0372 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19082 | hp1 | a0001 | c0002 | t0007 | g0131 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19082 | hp2 | a0001 | c0003 | t0003 | g0381 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19084 | hp2 | a0001 | c0001 | t0009 | g0054 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0205 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19087 | hp1 | a0001 | c0004 | t0001 | g0337 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19087 | hp2 | a0001 | c0001 | t0033 | g0065 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0305 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA19240 | hp2 | a0002 | c0009 | t0016 | g0082 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA20129 | hp2 | a0001 | c0002 | t0015 | g0267 | AFR | ASW | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0326 | EUR | TSI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0219 | EUR | TSI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0341 | SAS | GIH | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA20905 | hp2 | a0001 | c0005 | t0004 | g0183 | SAS | GIH | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0359 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG01123 | hp2 | a0001 | c0005 | t0004 | g0182 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0211 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02486 | hp1 | a0001 | c0019 | t0002 | g0172 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02486 | hp2 | a0001 | c0007 | t0003 | g0191 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0195 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG02559 | hp2 | a0001 | c0001 | t0035 | g0035 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03471 | hp1 | a0001 | c0007 | t0040 | g0175 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG03471 | hp2 | a0002 | c0011 | t0018 | g0253 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG06807 | hp1 | a0001 | c0002 | t0043 | g0037 | AFR | USA | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| HG06807 | hp2 | a0001 | c0002 | t0034 | g0276 | AFR | USA | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18955 | hp1 | a0001 | c0005 | t0004 | g0038 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA20300 | hp1 | a0002 | c0006 | t0010 | g0255 | AFR | USA | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA20300 | hp2 | a0002 | c0011 | t0018 | g0270 | AFR | USA | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA21309 | hp1 | a0002 | c0009 | t0016 | g0081 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| NA21309 | hp2 | a0002 | c0012 | t0014 | g0018 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0095 | REF | REF | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0019 | g0339 | REF | REF | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1448407 | G | A | 1 | a0005 | 2 | HG01891.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.1961C>T | p.Thr654Met | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/25 | 2015/4168 | 1961/2418 | 654/805 | chr16 | 1448407 | |||
| chr16:1450651 | A | T | 1 | a0007 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.1463T>A | p.Leu488Gln | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/25 | 1517/4168 | 1463/2418 | 488/805 | chr16 | 1450651 | |||
| chr16:1452856 | C | T | 2 | a0002 a0005 |
32 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(29): Show |
missense_variant | MODERATE | c.1252G>A | p.Val418Met | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/25 | 1306/4168 | 1252/2418 | 418/805 | chr16 | 1452856 | |||
| chr16:1453892 | C | T | 1 | a0006 | 1 | HG02273.hp2 | missense_variant&splice_region_variant | MODERATE | c.1156G>A | p.Gly386Ser | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/25 | 1210/4168 | 1156/2418 | 386/805 | chr16 | 1453892 | |||
| chr16:1457328 | T | TCGGCCCT others(193): Show |
1 | a0004 | 2 | HG01074.hp2 HG03239.hp1 |
frameshift_variant&stop_gained | HIGH | c.747_748insCGTCACGC others(192): Show |
p.Met250fs | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 747/2418 | 249/805 | chr16 | 1457328 | |||
| chr16:1457328 | TCGGCCCT others(93): Show |
T | 1 | a0003 | 1 | HG01993.hp1 | splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.739-91_747delCGTCA others(95): Show |
p.Glu247_Met250del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 739/2418 | 247/805 | chr16 | 1457328 | |||
| chr16:1457328 | TCGGCCCT others(143): Show |
T | 1 | a0003 | 2 | HG02622.hp1 HG02622.hp2 |
splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.739-141_747del | p.Glu247_Met250del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 739/2418 | 247/805 | chr16 | 1457328 | |||
| chr16:1457328 | TCGGCCCT others(193): Show |
T | 1 | a0003 | 1 | NA19079.hp1 | splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.738+166_747del | p.Glu247_Met250del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 739/2418 | 247/805 | chr16 | 1457328 | |||
| chr16:1457328 | TCGGCCCT others(243): Show |
T | 1 | a0003 | 1 | HG01978.hp2 | splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.738+116_747del | p.Glu247_Met250del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 739/2418 | 247/805 | chr16 | 1457328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1448707 | C | T | 1 | a0001c0010 | 3 | HG02145.hp1 HG03098.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1857G>A | p.Pro619Pro | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/25 | 1911/4168 | 1857/2418 | 619/805 | chr16 | 1448707 | |||
| chr16:1449092 | G | A | 2 | a0002c0011 a0002c0012 |
6 | HG03098.hp2 HG03209.hp1 HG03471.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.1671C>T | p.Gly557Gly | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/25 | 1725/4168 | 1671/2418 | 557/805 | chr16 | 1449092 | |||
| chr16:1449319 | C | A | 1 | a0001c0022 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1626G>T | p.Ala542Ala | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 18/25 | 1680/4168 | 1626/2418 | 542/805 | chr16 | 1449319 | |||
| chr16:1450500 | C | T | 2 | a0002c0006 a0002c0026 |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
synonymous_variant | LOW | c.1614G>A | p.Ala538Ala | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/25 | 1668/4168 | 1614/2418 | 538/805 | chr16 | 1450500 | |||
| chr16:1450662 | G | C | 1 | a0001c0019 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1452C>G | p.Ser484Ser | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/25 | 1506/4168 | 1452/2418 | 484/805 | chr16 | 1450662 | |||
| chr16:1452863 | A | G | 7 | a0002c0006 a0002c0008 a0002c0011 others(4): Show |
27 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
synonymous_variant | LOW | c.1245T>C | p.Ile415Ile | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/25 | 1299/4168 | 1245/2418 | 415/805 | chr16 | 1452863 | |||
| chr16:1453878 | T | A | 14 | a0001c0001 a0001c0004 a0001c0005 others(11): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
synonymous_variant | LOW | c.1170A>T | p.Ala390Ala | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/25 | 1224/4168 | 1170/2418 | 390/805 | chr16 | 1453878 | |||
| chr16:1454436 | C | T | 2 | a0002c0006 a0002c0026 |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
synonymous_variant | LOW | c.1128G>A | p.Pro376Pro | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/25 | 1182/4168 | 1128/2418 | 376/805 | chr16 | 1454436 | |||
| chr16:1455791 | C | T | 3 | a0002c0008 a0005c0018 a0005c0024 |
7 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(4): Show |
synonymous_variant | LOW | c.921G>A | p.Gly307Gly | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/25 | 975/4168 | 921/2418 | 307/805 | chr16 | 1455791 | |||
| chr16:1456129 | C | T | 1 | a0004c0014 | 2 | HG01074.hp2 HG03239.hp1 |
synonymous_variant | LOW | c.900G>A | p.Ala300Ala | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/25 | 954/4168 | 900/2418 | 300/805 | chr16 | 1456129 | |||
| chr16:1457275 | C | T | 1 | a0001c0017 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.801G>A | p.Thr267Thr | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 855/4168 | 801/2418 | 267/805 | chr16 | 1457275 | |||
| chr16:1459122 | G | A | 7 | a0001c0005 a0001c0007 a0001c0015 others(4): Show |
53 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(50): Show |
synonymous_variant | LOW | c.660C>T | p.His220His | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/25 | 714/4168 | 660/2418 | 220/805 | chr16 | 1459122 | |||
| chr16:1474849 | A | G | 18 | a0001c0001 a0001c0002 a0001c0005 others(15): Show |
277 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(274): Show |
synonymous_variant | LOW | c.126T>C | p.Pro42Pro | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/25 | 180/4168 | 126/2418 | 42/805 | chr16 | 1474849 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1444986 | C | G | 2 | a0001c0002t0015 a0001c0002t0042 |
4 | HG02630.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1645G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1645 | chr16 | 1444986 | ||||||
| chr16:1445005 | C | G | 61 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(58): Show |
288 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*1626G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1626 | chr16 | 1445005 | ||||||
| chr16:1445006 | AACC | A | 3 | a0002c0008t0017 a0005c0018t0053 a0005c0024t0029 |
5 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1622_*1624delGGT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1622 | chr16 | 1445006 | ||||||
| chr16:1445033 | G | A | 2 | a0001c0001t0049 a0001c0002t0044 |
2 | HG03209.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1598C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1598 | chr16 | 1445033 | ||||||
| chr16:1445035 | T | C | 2 | a0001c0001t0049 a0001c0002t0044 |
2 | HG03209.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1596A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1596 | chr16 | 1445035 | ||||||
| chr16:1445105 | C | T | 1 | a0001c0002t0043 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1526G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1526 | chr16 | 1445105 | ||||||
| chr16:1445133 | G | GC | 3 | a0002c0006t0025 a0002c0006t0026 a0002c0006t0051 |
5 | HG00735.hp1 HG01074.hp1 HG01978.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1497dupG | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1497 | chr16 | 1445133 | ||||||
| chr16:1445152 | A | G | 3 | a0001c0002t0054 a0002c0011t0018 a0002c0012t0014 |
7 | HG02647.hp1 HG03098.hp2 HG03209.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1479T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1479 | chr16 | 1445152 | ||||||
| chr16:1445242 | T | G | 83 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(80): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
3_prime_UTR_variant | MODIFIER | c.*1389A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1389 | chr16 | 1445242 | ||||||
| chr16:1445264 | G | A | 1 | a0001c0003t0038 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1367C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1367 | chr16 | 1445264 | ||||||
| chr16:1445299 | G | A | 26 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(23): Show |
207 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*1332C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1332 | chr16 | 1445299 | ||||||
| chr16:1445451 | C | G | 2 | a0001c0001t0021 a0003c0013t0021 |
2 | NA18612.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1180G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1180 | chr16 | 1445451 | ||||||
| chr16:1445455 | G | A | 1 | a0002c0006t0010 | 6 | HG00639.hp1 HG00642.hp2 HG01099.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1176C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1176 | chr16 | 1445455 | ||||||
| chr16:1445474 | G | A | 14 | a0001c0001t0049 a0001c0002t0013 a0001c0002t0034 others(11): Show |
21 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1157C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1157 | chr16 | 1445474 | ||||||
| chr16:1445486 | G | GC | 17 | a0001c0001t0004 a0001c0001t0039 a0001c0001t0045 others(14): Show |
44 | HG00735.hp1 HG01071.hp1 HG01074.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1144dupG | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1144 | chr16 | 1445486 | ||||||
| chr16:1445567 | C | T | 1 | a0001c0002t0036 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1064G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1064 | chr16 | 1445567 | ||||||
| chr16:1445579 | C | T | 1 | a0001c0007t0040 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1052G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1052 | chr16 | 1445579 | ||||||
| chr16:1445641 | G | A | 7 | a0001c0002t0013 a0001c0002t0054 a0002c0008t0027 others(4): Show |
10 | HG00639.hp2 HG01891.hp1 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*990C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 990 | chr16 | 1445641 | ||||||
| chr16:1445744 | G | A | 73 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(70): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
3_prime_UTR_variant | MODIFIER | c.*887C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 887 | chr16 | 1445744 | ||||||
| chr16:1445745 | G | A | 73 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(70): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
3_prime_UTR_variant | MODIFIER | c.*886C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 886 | chr16 | 1445745 | ||||||
| chr16:1445896 | G | A | 46 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(43): Show |
257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*735C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 735 | chr16 | 1445896 | ||||||
| chr16:1446004 | T | C | 18 | a0001c0002t0013 a0001c0002t0054 a0001c0003t0047 others(15): Show |
34 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*627A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 627 | chr16 | 1446004 | ||||||
| chr16:1446101 | C | T | 1 | a0001c0002t0034 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 530 | chr16 | 1446101 | ||||||
| chr16:1446135 | A | G | 2 | a0001c0001t0035 a0001c0002t0034 |
2 | HG02559.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*496T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 496 | chr16 | 1446135 | ||||||
| chr16:1446206 | G | C | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*425C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 425 | chr16 | 1446206 | ||||||
| chr16:1446207 | G | C | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*424C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 424 | chr16 | 1446207 | ||||||
| chr16:1446208 | A | T | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*423T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 423 | chr16 | 1446208 | ||||||
| chr16:1446209 | G | T | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*422C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 422 | chr16 | 1446209 | ||||||
| chr16:1446210 | G | C | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*421C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 421 | chr16 | 1446210 | ||||||
| chr16:1446235 | C | T | 1 | a0001c0001t0033 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*396G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 396 | chr16 | 1446235 | ||||||
| chr16:1446250 | C | T | 1 | a0001c0001t0032 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*381G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 381 | chr16 | 1446250 | ||||||
| chr16:1446337 | C | G | 1 | a0001c0001t0031 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 294 | chr16 | 1446337 | ||||||
| chr16:1446338 | G | A | 1 | a0001c0001t0049 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 293 | chr16 | 1446338 | ||||||
| chr16:1446403 | G | A | 1 | a0001c0001t0009 | 7 | NA18953.hp1 NA18962.hp2 NA18979.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*228C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 228 | chr16 | 1446403 | ||||||
| chr16:1446568 | C | T | 1 | a0001c0004t0030 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*63G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 63 | chr16 | 1446568 | ||||||
| chr16:1446612 | T | C | 17 | a0001c0002t0013 a0001c0002t0054 a0002c0006t0010 others(14): Show |
33 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*19A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 19 | chr16 | 1446612 | ||||||
| chr16:1474994 | C | G | 4 | a0001c0004t0006 a0001c0015t0028 a0002c0012t0014 others(1): Show |
12 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-20G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/25 | chr16 | 1474994 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1446737 | C | T | 1 | a0001c0022t0048g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2332-20G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446737 | |||||||
| chr16:1446747 | C | T | 1 | a0002c0011t0018g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2332-30G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446747 | |||||||
| chr16:1446754 | C | T | 2 | a0001c0005t0004g0163 a0001c0015t0046g0383 |
2 | NA18991.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2332-37G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446754 | |||||||
| chr16:1446825 | G | C | 10 | a0001c0002t0002g0012 a0001c0002t0002g0280 a0001c0002t0002g0281 others(7): Show |
11 | HG00639.hp2 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2332-108C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446825 | |||||||
| chr16:1446914 | C | T | 1 | a0001c0001t0035g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2331+92G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446914 | |||||||
| chr16:1446927 | G | A | 9 | a0001c0005t0004g0152 a0001c0005t0004g0179 a0001c0005t0004g0180 others(6): Show |
9 | HG01071.hp1 HG01106.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2331+79C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446927 | |||||||
| chr16:1446964 | A | C | 1 | a0001c0007t0003g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2331+42T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446964 | |||||||
| chr16:1447124 | A | G | 36 | a0001c0001t0035g0035 a0001c0001t0049g0237 a0001c0002t0013g0029 others(33): Show |
38 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2251-38T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447124 | |||||||
| chr16:1447130 | G | A | 1 | a0001c0004t0001g0356 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2251-44C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447130 | |||||||
| chr16:1447136 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(197): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2251-50G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447136 | |||||||
| chr16:1447208 | C | T | 1 | a0001c0004t0001g0364 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2251-122G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447208 | |||||||
| chr16:1447271 | G | A | 2 | a0001c0001t0049g0237 a0001c0002t0044g0072 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2250+121C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447271 | |||||||
| chr16:1447319 | C | A | 1 | a0001c0002t0002g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2250+73G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447319 | |||||||
| chr16:1447344 | T | C | 1 | a0001c0002t0002g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2250+48A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447344 | |||||||
| chr16:1447372 | T | C | 5 | a0001c0002t0013g0029 a0001c0002t0013g0030 a0001c0002t0013g0033 others(2): Show |
5 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2250+20A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447372 | |||||||
| chr16:1447594 | G | C | 1 | a0002c0011t0018g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2074-26C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 22/24 | chr16 | 1447594 | |||||||
| chr16:1447622 | C | T | 5 | a0002c0009t0005g0032 a0002c0009t0005g0283 a0002c0009t0016g0080 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2073+33G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 22/24 | chr16 | 1447622 | |||||||
| chr16:1447639 | G | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.2073+16C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 22/24 | chr16 | 1447639 | |||||||
| chr16:1447731 | C | A | 1 | a0001c0005t0004g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2014-17G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1447731 | |||||||
| chr16:1447827 | T | C | 6 | a0001c0001t0001g0063 a0001c0001t0001g0194 a0001c0001t0001g0243 others(3): Show |
6 | HG02523.hp1 NA18945.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2014-113A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1447827 | |||||||
| chr16:1447900 | C | T | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2014-186G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1447900 | |||||||
| chr16:1447922 | C | T | 1 | a0001c0003t0002g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2014-208G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1447922 | |||||||
| chr16:1448196 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.2013+159T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1448196 | |||||||
| chr16:1448269 | A | G | 36 | a0001c0001t0035g0035 a0001c0002t0013g0029 a0001c0002t0013g0030 others(33): Show |
38 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2013+86T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1448269 | |||||||
| chr16:1448303 | G | A | 1 | a0001c0002t0001g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2013+52C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1448303 | |||||||
| chr16:1448500 | G | A | 1 | a0001c0003t0005g0377 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1884-16C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448500 | |||||||
| chr16:1448509 | T | C | 34 | a0001c0002t0013g0029 a0001c0002t0013g0030 a0001c0002t0013g0033 others(31): Show |
36 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1884-25A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448509 | |||||||
| chr16:1448519 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(237): Show |
252 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1884-35T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448519 | |||||||
| chr16:1448571 | T | C | 37 | a0001c0001t0035g0035 a0001c0001t0049g0237 a0001c0002t0013g0029 others(34): Show |
39 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1884-87A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448571 | |||||||
| chr16:1448578 | G | A | 9 | a0001c0002t0013g0029 a0001c0002t0013g0030 a0001c0002t0013g0033 others(6): Show |
9 | HG00639.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1884-94C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448578 | |||||||
| chr16:1448596 | G | A | 9 | a0001c0002t0013g0029 a0001c0002t0013g0030 a0001c0002t0013g0033 others(6): Show |
9 | HG00639.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1883+85C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448596 | |||||||
| chr16:1448602 | G | A | 2 | a0001c0005t0004g0152 a0001c0005t0004g0180 |
2 | HG01071.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1883+79C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448602 | |||||||
| chr16:1448609 | G | A | 1 | a0001c0002t0002g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1883+72C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448609 | |||||||
| chr16:1448774 | C | T | 27 | a0001c0004t0001g0299 a0001c0004t0030g0369 a0002c0006t0010g0011 others(24): Show |
29 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.1798-8G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448774 | |||||||
| chr16:1448776 | G | A | 8 | a0002c0006t0024g0262 a0002c0006t0025g0259 a0002c0006t0025g0265 others(5): Show |
8 | HG00735.hp1 HG01074.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1798-10C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448776 | |||||||
| chr16:1448821 | C | A | 1 | a0001c0003t0003g0378 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1798-55G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448821 | |||||||
| chr16:1448823 | C | T | 1 | a0001c0002t0001g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1798-57G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448823 | |||||||
| chr16:1448824 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1798-58C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448824 | |||||||
| chr16:1448851 | G | A | 1 | a0001c0002t0001g0036 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1798-85C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448851 | |||||||
| chr16:1448873 | C | A | 1 | a0001c0004t0005g0354 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1797+93G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448873 | |||||||
| chr16:1448874 | C | G | 7 | a0001c0001t0035g0035 a0001c0002t0034g0276 a0002c0009t0005g0032 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1797+92G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448874 | |||||||
| chr16:1448885 | G | A | 3 | a0002c0012t0014g0016 a0002c0012t0014g0017 a0002c0012t0014g0018 |
3 | HG03209.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1797+81C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448885 | |||||||
| chr16:1448950 | C | T | 25 | a0001c0007t0002g0169 a0001c0007t0002g0170 a0002c0006t0010g0011 others(22): Show |
27 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1797+16G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448950 | |||||||
| chr16:1449178 | C | A | 1 | a0001c0002t0002g0084 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1670-85G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 18/24 | chr16 | 1449178 | |||||||
| chr16:1449376 | C | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(188): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1618-49G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449376 | |||||||
| chr16:1449396 | G | A | 1 | a0001c0002t0002g0226 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1618-69C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449396 | |||||||
| chr16:1449407 | G | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1618-80C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449407 | |||||||
| chr16:1449411 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1618-84T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449411 | |||||||
| chr16:1449426 | A | G | 3 | a0001c0001t0035g0035 a0003c0016t0050g0153 a0003c0021t0013g0188 |
3 | HG02559.hp2 HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1618-99T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449426 | |||||||
| chr16:1449434 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1618-107C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449434 | |||||||
| chr16:1449452 | C | T | 1 | a0001c0003t0002g0328 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1618-125G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449452 | |||||||
| chr16:1449494 | C | T | 2 | a0001c0007t0004g0176 a0001c0022t0048g0171 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1618-167G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449494 | |||||||
| chr16:1449585 | C | T | 2 | a0001c0004t0001g0299 a0001c0004t0030g0369 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1618-258G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449585 | |||||||
| chr16:1449616 | T | C | 29 | a0001c0001t0001g0277 a0001c0002t0015g0267 a0001c0002t0015g0274 others(26): Show |
31 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1618-289A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449616 | |||||||
| chr16:1449663 | G | A | 2 | a0001c0001t0049g0237 a0001c0002t0044g0072 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1618-336C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449663 | |||||||
| chr16:1449667 | A | C | 3 | a0001c0002t0001g0127 a0001c0003t0001g0309 a0001c0003t0001g0338 |
3 | HG00558.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1618-340T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449667 | |||||||
| chr16:1449703 | T | C | 33 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0034g0276 others(30): Show |
35 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1618-376A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449703 | |||||||
| chr16:1449706 | A | AGATGCTG others(80): Show |
29 | a0001c0007t0003g0190 a0001c0007t0003g0191 a0002c0006t0010g0011 others(26): Show |
31 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1618-380_1618-379i others(89): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449706 | |||||||
| chr16:1449738 | G | A | 1 | a0001c0001t0007g0141 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1618-411C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449738 | |||||||
| chr16:1449767 | T | C | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1618-440A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449767 | |||||||
| chr16:1449796 | C | T | 1 | a0001c0005t0004g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1618-469G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449796 | |||||||
| chr16:1449836 | C | T | 2 | a0001c0001t0049g0237 a0001c0002t0044g0072 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1618-509G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449836 | |||||||
| chr16:1449869 | A | G | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1618-542T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449869 | |||||||
| chr16:1449891 | C | G | 2 | a0003c0016t0050g0153 a0003c0021t0013g0188 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1618-564G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449891 | |||||||
| chr16:1449907 | T | C | 40 | a0001c0001t0035g0035 a0001c0001t0049g0237 a0001c0002t0002g0278 others(37): Show |
42 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1618-580A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449907 | |||||||
| chr16:1449919 | A | C | 1 | a0001c0003t0022g0319 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1617+578T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449919 | |||||||
| chr16:1450050 | G | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1617+447C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450050 | |||||||
| chr16:1450160 | C | T | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1617+337G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450160 | |||||||
| chr16:1450174 | C | T | 1 | a0001c0004t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617+323G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450174 | |||||||
| chr16:1450240 | A | G | 13 | a0001c0019t0002g0172 a0002c0008t0017g0010 a0002c0008t0017g0159 others(10): Show |
14 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1617+257T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450240 | |||||||
| chr16:1450299 | C | T | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1617+198G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450299 | |||||||
| chr16:1450317 | T | C | 2 | a0002c0009t0005g0032 a0002c0009t0005g0283 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1617+180A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450317 | |||||||
| chr16:1450328 | C | CAGGACAA others(24): Show |
19 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(16): Show |
20 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617+138_1617+168d others(33): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450328 | |||||||
| chr16:1450367 | C | T | 4 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(1): Show |
4 | HG02622.hp2 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1617+130G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450367 | |||||||
| chr16:1450388 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1617+109C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450388 | |||||||
| chr16:1450484 | C | T | 3 | a0001c0002t0002g0012 a0001c0002t0002g0280 a0001c0002t0002g0281 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617+13G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450484 | |||||||
| chr16:1450687 | ACGGGGCC others(231): Show |
A | 26 | a0001c0003t0001g0363 a0002c0006t0010g0011 a0002c0006t0010g0254 others(23): Show |
28 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1448-259_1448-22de others(1): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450687 | |||||||
| chr16:1450688 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1448-22G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450688 | |||||||
| chr16:1450707 | G | GC | 121 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0053 others(118): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1448-42dupG | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450707 | |||||||
| chr16:1450743 | C | T | 1 | a0001c0004t0001g0310 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1448-77G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450743 | |||||||
| chr16:1450917 | C | T | 12 | a0001c0001t0001g0034 a0001c0001t0001g0087 a0001c0001t0001g0093 others(9): Show |
13 | HG00438.hp1 NA18951.hp1 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.1448-251G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450917 | |||||||
| chr16:1450939 | C | A | 8 | a0002c0011t0018g0253 a0002c0011t0018g0269 a0002c0011t0018g0270 others(5): Show |
8 | HG01891.hp1 HG03098.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1448-273G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450939 | |||||||
| chr16:1451011 | A | G | 7 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0098 others(4): Show |
7 | HG00735.hp2 HG01167.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1448-345T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451011 | |||||||
| chr16:1451047 | G | T | 2 | a0001c0001t0049g0237 a0001c0002t0044g0072 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1448-381C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451047 | |||||||
| chr16:1451135 | G | T | 8 | a0001c0004t0004g0286 a0001c0005t0004g0038 a0001c0005t0004g0163 others(5): Show |
8 | HG00280.hp1 HG01081.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.1448-469C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451135 | |||||||
| chr16:1451179 | G | A | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1447+444C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451179 | |||||||
| chr16:1451214 | C | A | 2 | a0003c0016t0050g0153 a0003c0021t0013g0188 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1447+409G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451214 | |||||||
| chr16:1451240 | C | T | 2 | a0001c0002t0002g0150 a0001c0002t0002g0151 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1447+383G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451240 | |||||||
| chr16:1451320 | G | A | 5 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(2): Show |
5 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447+303C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451320 | |||||||
| chr16:1451374 | G | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(218): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.1447+249C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451374 | |||||||
| chr16:1451464 | C | A | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1447+159G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451464 | |||||||
| chr16:1451575 | C | T | 1 | a0001c0002t0043g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1447+48G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451575 | |||||||
| chr16:1451605 | G | A | 1 | a0001c0002t0036g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1447+18C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451605 | |||||||
| chr16:1451788 | C | T | 12 | a0002c0008t0017g0010 a0002c0008t0017g0159 a0002c0008t0027g0251 others(9): Show |
13 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-72G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1451788 | |||||||
| chr16:1451957 | C | T | 26 | a0001c0001t0004g0145 a0001c0001t0045g0229 a0001c0004t0004g0286 others(23): Show |
26 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1354-241G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1451957 | |||||||
| chr16:1451970 | G | C | 1 | a0004c0014t0001g0116 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1354-254C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1451970 | |||||||
| chr16:1452021 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0235 |
2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1354-305G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452021 | |||||||
| chr16:1452049 | G | C | 1 | a0001c0001t0032g0118 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1354-333C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452049 | |||||||
| chr16:1452320 | C | T | 1 | a0001c0005t0004g0271 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1353+435G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452320 | |||||||
| chr16:1452324 | TGGTTCCT others(23): Show |
T | 1 | a0001c0003t0001g0379 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1353+401_1353+430d others(32): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452324 | |||||||
| chr16:1452337 | C | T | 25 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(22): Show |
27 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1353+418G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452337 | |||||||
| chr16:1452338 | G | A | 5 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(2): Show |
5 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+417C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452338 | |||||||
| chr16:1452378 | C | T | 8 | a0002c0006t0024g0262 a0002c0006t0025g0259 a0002c0006t0025g0265 others(5): Show |
8 | HG00735.hp1 HG01074.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1353+377G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452378 | |||||||
| chr16:1452382 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1353+373G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452382 | |||||||
| chr16:1452386 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1353+369G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452386 | |||||||
| chr16:1452429 | G | A | 1 | a0001c0004t0001g0352 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1353+326C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452429 | |||||||
| chr16:1452611 | T | C | 1 | a0001c0002t0002g0231 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1353+144A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452611 | |||||||
| chr16:1452640 | C | T | 1 | a0002c0006t0025g0259 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1353+115G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452640 | |||||||
| chr16:1452641 | G | A | 1 | a0001c0002t0001g0236 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1353+114C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452641 | |||||||
| chr16:1452672 | C | T | 1 | a0001c0003t0002g0326 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1353+83G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452672 | |||||||
| chr16:1452677 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1353+78G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452677 | |||||||
| chr16:1452683 | C | T | 2 | a0001c0001t0049g0237 a0001c0002t0044g0072 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1353+72G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452683 | |||||||
| chr16:1452705 | G | T | 5 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(2): Show |
5 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+50C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452705 | |||||||
| chr16:1452734 | C | T | 12 | a0002c0008t0017g0010 a0002c0008t0017g0159 a0002c0008t0027g0251 others(9): Show |
13 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1353+21G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452734 | |||||||
| chr16:1452930 | G | A | 1 | a0001c0004t0001g0362 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1215-37C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1452930 | |||||||
| chr16:1452941 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1215-48G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1452941 | |||||||
| chr16:1452946 | C | T | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1215-53G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1452946 | |||||||
| chr16:1453019 | G | T | 1 | a0001c0004t0012g0335 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1215-126C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453019 | |||||||
| chr16:1453032 | A | C | 5 | a0002c0009t0005g0032 a0002c0009t0005g0283 a0002c0009t0016g0080 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215-139T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453032 | |||||||
| chr16:1453114 | T | C | 3 | a0001c0002t0002g0012 a0001c0002t0002g0280 a0001c0002t0002g0281 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215-221A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453114 | |||||||
| chr16:1453153 | G | A | 6 | a0001c0002t0001g0216 a0001c0004t0001g0342 a0001c0004t0001g0350 others(3): Show |
6 | HG01109.hp1 HG02056.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215-260C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453153 | |||||||
| chr16:1453197 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1215-304C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453197 | |||||||
| chr16:1453203 | G | A | 1 | a0001c0002t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1215-310C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453203 | |||||||
| chr16:1453257 | C | A | 1 | a0001c0002t0036g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1215-364G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453257 | |||||||
| chr16:1453259 | C | T | 2 | a0001c0001t0049g0237 a0001c0002t0044g0072 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1215-366G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453259 | |||||||
| chr16:1453260 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1215-367C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453260 | |||||||
| chr16:1453265 | G | A | 2 | a0001c0004t0006g0023 a0001c0004t0006g0024 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1215-372C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453265 | |||||||
| chr16:1453288 | T | C | 33 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(30): Show |
35 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1215-395A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453288 | |||||||
| chr16:1453309 | G | A | 19 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(16): Show |
21 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1215-416C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453309 | |||||||
| chr16:1453428 | T | C | 34 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(31): Show |
36 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1214+406A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453428 | |||||||
| chr16:1453429 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1214+405C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453429 | |||||||
| chr16:1453433 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1214+401G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453433 | |||||||
| chr16:1453443 | C | T | 3 | a0002c0009t0016g0080 a0002c0009t0016g0081 a0002c0009t0016g0082 |
3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1214+391G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453443 | |||||||
| chr16:1453650 | C | T | 1 | a0002c0011t0018g0253 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1214+184G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453650 | |||||||
| chr16:1453662 | G | A | 1 | a0001c0003t0003g0375 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1214+172C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453662 | |||||||
| chr16:1453786 | T | C | 1 | a0001c0003t0002g0294 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1214+48A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453786 | |||||||
| chr16:1453948 | C | T | 1 | a0001c0001t0039g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1154-54G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1453948 | |||||||
| chr16:1453952 | C | T | 1 | a0001c0002t0002g0040 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1154-58G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1453952 | |||||||
| chr16:1454016 | A | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(260): Show |
273 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1154-122T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454016 | |||||||
| chr16:1454019 | G | A | 2 | a0001c0003t0002g0317 a0001c0003t0005g0316 |
2 | HG00099.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1154-125C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454019 | |||||||
| chr16:1454148 | T | C | 115 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0088 others(112): Show |
115 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1154-254A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454148 | |||||||
| chr16:1454214 | G | A | 23 | a0001c0001t0039g0173 a0001c0002t0002g0278 a0001c0002t0015g0267 others(20): Show |
24 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1153+197C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454214 | |||||||
| chr16:1454229 | C | T | 22 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0142 others(19): Show |
22 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1153+182G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454229 | |||||||
| chr16:1454277 | C | G | 1 | a0001c0019t0002g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+134G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454277 | |||||||
| chr16:1454285 | C | A | 1 | a0001c0005t0004g0038 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1153+126G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454285 | |||||||
| chr16:1454300 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1153+111C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454300 | |||||||
| chr16:1454496 | G | A | 3 | a0002c0009t0016g0080 a0002c0009t0016g0081 a0002c0009t0016g0082 |
3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1099-31C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454496 | |||||||
| chr16:1454621 | C | T | 1 | a0001c0004t0001g0300 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099-156G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454621 | |||||||
| chr16:1454629 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1099-164C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454629 | |||||||
| chr16:1454632 | C | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(289): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1099-167G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454632 | |||||||
| chr16:1454659 | G | A | 1 | a0001c0002t0001g0230 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1099-194C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454659 | |||||||
| chr16:1454701 | C | T | 118 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0002g0129 others(115): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1099-236G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454701 | |||||||
| chr16:1454709 | G | A | 3 | a0001c0001t0032g0118 a0001c0003t0002g0315 a0001c0003t0038g0314 |
3 | HG02698.hp1 NA18974.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1099-244C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454709 | |||||||
| chr16:1454733 | CAT | C | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1099-270_1099-269d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454733 | |||||||
| chr16:1454741 | G | A | 2 | a0001c0004t0006g0023 a0001c0004t0006g0024 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1099-276C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454741 | |||||||
| chr16:1454770 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(182): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1099-305G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454770 | |||||||
| chr16:1454850 | G | A | 1 | a0001c0004t0001g0362 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1098+284C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454850 | |||||||
| chr16:1454856 | G | A | 1 | a0001c0001t0005g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1098+278C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454856 | |||||||
| chr16:1454866 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0117 |
2 | NA18945.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1098+268G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454866 | |||||||
| chr16:1454880 | G | A | 30 | a0001c0001t0004g0145 a0001c0004t0004g0286 a0001c0005t0001g0189 others(27): Show |
31 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.1098+254C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454880 | |||||||
| chr16:1454904 | A | G | 1 | a0003c0013t0001g0108 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1098+230T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454904 | |||||||
| chr16:1454933 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(222): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1098+201A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454933 | |||||||
| chr16:1454935 | A | T | 1 | a0001c0004t0001g0353 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1098+199T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454935 | |||||||
| chr16:1455003 | C | T | 2 | a0002c0008t0017g0010 a0002c0008t0017g0159 |
3 | HG01243.hp2 HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+131G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1455003 | |||||||
| chr16:1455275 | C | T | 1 | a0001c0003t0003g0015 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.982-25G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455275 | |||||||
| chr16:1455276 | G | A | 3 | a0001c0001t0049g0237 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG03209.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.982-26C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455276 | |||||||
| chr16:1455277 | C | G | 2 | a0002c0012t0014g0016 a0002c0012t0014g0017 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.982-27G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455277 | |||||||
| chr16:1455307 | CACGGACC others(4): Show |
C | 1 | a0001c0001t0001g0034 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.982-68_982-58delTG others(9): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455307 | |||||||
| chr16:1455369 | G | A | 25 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(22): Show |
27 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.982-119C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455369 | |||||||
| chr16:1455418 | G | A | 2 | a0003c0016t0050g0153 a0003c0021t0013g0188 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.982-168C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455418 | |||||||
| chr16:1455428 | C | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(257): Show |
273 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.982-178G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455428 | |||||||
| chr16:1455493 | C | G | 1 | a0001c0005t0005g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.981+238G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455493 | |||||||
| chr16:1455494 | C | T | 3 | a0002c0009t0016g0080 a0002c0009t0016g0081 a0002c0009t0016g0082 |
3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.981+237G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455494 | |||||||
| chr16:1455557 | G | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.981+174C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455557 | |||||||
| chr16:1455587 | T | C | 37 | a0001c0001t0004g0145 a0001c0004t0004g0286 a0001c0005t0001g0178 others(34): Show |
38 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.981+144A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455587 | |||||||
| chr16:1455598 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(232): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.981+133G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455598 | |||||||
| chr16:1455825 | A | G | 2 | a0003c0016t0050g0153 a0003c0021t0013g0188 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.917-30T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455825 | |||||||
| chr16:1455866 | C | G | 11 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0107 others(8): Show |
11 | HG00423.hp1 HG01934.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.917-71G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455866 | |||||||
| chr16:1455891 | G | A | 16 | a0001c0002t0002g0199 a0001c0002t0013g0029 a0001c0002t0013g0030 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.917-96C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455891 | |||||||
| chr16:1455910 | G | A | 1 | a0001c0001t0012g0067 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.917-115C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455910 | |||||||
| chr16:1455931 | G | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.917-136C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455931 | |||||||
| chr16:1455977 | G | A | 8 | a0002c0008t0027g0251 a0002c0008t0027g0252 a0002c0011t0018g0253 others(5): Show |
8 | HG02717.hp1 HG03098.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.916+136C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455977 | |||||||
| chr16:1455979 | C | T | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+134G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455979 | |||||||
| chr16:1456010 | G | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+103C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1456010 | |||||||
| chr16:1456033 | C | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+80G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1456033 | |||||||
| chr16:1456072 | G | A | 5 | a0001c0001t0002g0227 a0001c0002t0003g0200 a0001c0002t0003g0201 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+41C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1456072 | |||||||
| chr16:1456252 | C | T | 5 | a0001c0001t0002g0227 a0001c0002t0003g0200 a0001c0002t0003g0201 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-46G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456252 | |||||||
| chr16:1456317 | A | G | 15 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(12): Show |
16 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-111T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456317 | |||||||
| chr16:1456389 | C | T | 2 | a0003c0016t0050g0153 a0003c0021t0013g0188 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.823-183G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456389 | |||||||
| chr16:1456396 | C | T | 1 | a0002c0026t0024g0308 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.823-190G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456396 | |||||||
| chr16:1456406 | G | C | 37 | a0001c0001t0004g0145 a0001c0004t0004g0286 a0001c0005t0001g0178 others(34): Show |
38 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.823-200C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456406 | |||||||
| chr16:1456462 | A | G | 15 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(12): Show |
16 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-256T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456462 | |||||||
| chr16:1456488 | C | A | 2 | a0001c0004t0006g0023 a0001c0004t0006g0024 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.823-282G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456488 | |||||||
| chr16:1456489 | G | A | 127 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0002g0129 others(124): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.823-283C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456489 | |||||||
| chr16:1456541 | C | T | 1 | a0001c0007t0004g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.823-335G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456541 | |||||||
| chr16:1456542 | C | T | 224 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(221): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.823-336G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456542 | |||||||
| chr16:1456607 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.823-401C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456607 | |||||||
| chr16:1456621 | C | T | 6 | a0002c0008t0017g0010 a0002c0008t0017g0159 a0002c0008t0027g0251 others(3): Show |
7 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-415G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456621 | |||||||
| chr16:1456648 | G | A | 2 | a0003c0016t0050g0153 a0003c0021t0013g0188 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.823-442C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456648 | |||||||
| chr16:1456701 | C | T | 1 | a0001c0004t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.823-495G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456701 | |||||||
| chr16:1456709 | C | T | 1 | a0001c0002t0001g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.823-503G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456709 | |||||||
| chr16:1456733 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.822+521G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456733 | |||||||
| chr16:1456773 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(177): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.822+481C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456773 | |||||||
| chr16:1456795 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.822+459A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456795 | |||||||
| chr16:1456812 | G | A | 2 | a0001c0003t0002g0289 a0001c0003t0003g0288 |
2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.822+442C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456812 | |||||||
| chr16:1456813 | C | G | 1 | a0001c0004t0001g0344 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.822+441G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456813 | |||||||
| chr16:1456815 | T | C | 2 | a0001c0002t0002g0075 a0001c0002t0002g0079 |
2 | HG01361.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.822+439A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456815 | |||||||
| chr16:1456838 | C | CAA | 14 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0256 others(11): Show |
15 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.822+414_822+415dup others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456838 | |||||||
| chr16:1456838 | CA | C | 8 | a0001c0001t0001g0092 a0001c0001t0001g0244 a0001c0001t0001g0246 others(5): Show |
8 | HG01167.hp1 HG03225.hp1 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+415delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456838 | |||||||
| chr16:1456919 | T | C | 1 | a0002c0011t0018g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.822+335A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456919 | |||||||
| chr16:1456920 | G | A | 1 | a0001c0004t0001g0014 | 2 | NA18939.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.822+334C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456920 | |||||||
| chr16:1456999 | T | C | 16 | a0001c0005t0004g0152 a0002c0006t0010g0011 a0002c0006t0010g0254 others(13): Show |
17 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.822+255A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456999 | |||||||
| chr16:1457126 | G | T | 5 | a0002c0009t0005g0032 a0002c0009t0005g0283 a0002c0009t0016g0080 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+128C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457126 | |||||||
| chr16:1457148 | C | A | 2 | a0002c0008t0027g0251 a0002c0008t0027g0252 |
2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.822+106G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457148 | |||||||
| chr16:1457182 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.822+72G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457182 | |||||||
| chr16:1457208 | C | T | 3 | a0001c0002t0002g0089 a0001c0003t0001g0345 a0001c0004t0001g0380 |
3 | HG00099.hp2 HG03704.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.822+46G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457208 | |||||||
| chr16:1457217 | G | A | 1 | a0001c0002t0044g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.822+37C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457217 | |||||||
| chr16:1457236 | C | T | 1 | a0001c0002t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.822+18G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457236 | |||||||
| chr16:1457237 | A | G | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.822+17T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457237 | |||||||
| chr16:1457357 | G | GTGCTCAG others(43): Show |
3 | a0001c0002t0002g0198 a0001c0004t0005g0354 a0001c0004t0005g0358 |
3 | HG00280.hp2 HG00738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.739-70_739-21dupTC others(48): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457357 | |||||||
| chr16:1457357 | GTGCTCAG others(43): Show |
G | 17 | a0001c0001t0001g0105 a0001c0002t0001g0060 a0001c0002t0001g0069 others(14): Show |
17 | HG00558.hp2 HG02155.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.739-70_739-21delTC others(48): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457357 | |||||||
| chr16:1457357 | GTGCTCAG others(93): Show |
G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0035g0035 others(1): Show |
4 | HG02559.hp2 NA19030.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-120_739-21delT others(99): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457357 | |||||||
| chr16:1457407 | A | G | 2 | a0001c0001t0001g0139 a0001c0005t0004g0152 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.739-70T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457407 | |||||||
| chr16:1457407 | ATGCTCAG others(93): Show |
A | 34 | a0001c0002t0001g0008 a0001c0002t0001g0149 a0001c0002t0002g0150 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.739-170_739-71delC others(99): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457407 | |||||||
| chr16:1457430 | G | T | 1 | a0001c0002t0044g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.739-93C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457430 | |||||||
| chr16:1457455 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | NA18957.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.739-118G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457455 | |||||||
| chr16:1457457 | A | ATGCTCAG others(43): Show |
5 | a0001c0001t0001g0125 a0001c0005t0004g0266 a0001c0005t0004g0273 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.739-170_739-121dup others(50): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | |||||||
| chr16:1457457 | A | ATGCTCAG others(93): Show |
1 | a0001c0001t0032g0118 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.738+137_739-121dup others(100): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | |||||||
| chr16:1457457 | A | ATGCTCAG others(143): Show |
2 | a0002c0009t0005g0032 a0002c0009t0005g0283 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.738+87_739-121dupC others(149): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | |||||||
| chr16:1457457 | A | ATGCTCAG others(293): Show |
1 | a0001c0004t0001g0362 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.739-121_739-120ins others(300): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | |||||||
| chr16:1457457 | A | ATGCTCAG others(143): Show |
3 | a0002c0009t0016g0080 a0002c0009t0016g0081 a0002c0009t0016g0082 |
3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.739-121_739-120ins others(150): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | |||||||
| chr16:1457457 | A | G | 20 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0001g0139 others(17): Show |
21 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.739-120T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | |||||||
| chr16:1457457 | ATGCTCAG others(43): Show |
A | 16 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0008g0078 others(13): Show |
17 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.739-170_739-121del others(50): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | |||||||
| chr16:1457457 | ATGCTCAG others(93): Show |
A | 8 | a0001c0001t0001g0246 a0001c0003t0003g0015 a0002c0006t0010g0011 others(5): Show |
10 | HG00642.hp2 HG01099.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.738+137_739-121del others(100): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | |||||||
| chr16:1457505 | C | T | 1 | a0001c0003t0020g0372 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.739-168G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457505 | |||||||
| chr16:1457507 | G | A | 2 | a0002c0009t0016g0081 a0002c0009t0016g0082 |
2 | NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.739-170C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457507 | |||||||
| chr16:1457516 | G | A | 3 | a0001c0002t0002g0210 a0001c0002t0002g0217 a0001c0002t0011g0221 |
3 | HG00323.hp1 HG01255.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.738+178C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457516 | |||||||
| chr16:1457521 | G | A | 2 | a0002c0008t0017g0010 a0002c0008t0017g0159 |
3 | HG01243.hp2 HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.738+173C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457521 | |||||||
| chr16:1457527 | C | T | 1 | a0002c0006t0025g0259 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.738+167G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457527 | |||||||
| chr16:1457579 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0085 |
3 | HG03654.hp2 HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.738+115G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457579 | |||||||
| chr16:1457605 | C | T | 8 | a0001c0005t0004g0038 a0001c0005t0004g0163 a0001c0005t0004g0164 others(5): Show |
8 | HG00280.hp1 HG01081.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.738+89G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457605 | |||||||
| chr16:1457628 | C | T | 1 | a0001c0017t0041g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.738+66G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457628 | |||||||
| chr16:1457777 | T | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(211): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.676-21A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457777 | |||||||
| chr16:1457813 | C | G | 1 | a0001c0002t0002g0075 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.676-57G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457813 | |||||||
| chr16:1457819 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0202 |
3 | HG02015.hp1 HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.676-63G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457819 | |||||||
| chr16:1457841 | C | T | 93 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0110 others(90): Show |
99 | HG00642.hp1 HG00673.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.676-85G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457841 | |||||||
| chr16:1457842 | G | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0110 others(79): Show |
88 | HG00642.hp1 HG00673.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.676-86C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457842 | |||||||
| chr16:1457934 | A | T | 1 | a0001c0004t0001g0306 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.676-178T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457934 | |||||||
| chr16:1457979 | C | T | 1 | a0001c0002t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.676-223G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457979 | |||||||
| chr16:1457987 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(240): Show |
255 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.676-231G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457987 | |||||||
| chr16:1458062 | C | CA | 214 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0034 others(211): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.676-307dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458062 | |||||||
| chr16:1458239 | T | C | 7 | a0001c0002t0002g0247 a0001c0003t0002g0291 a0001c0003t0002g0292 others(4): Show |
7 | HG00140.hp1 HG00733.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-483A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458239 | |||||||
| chr16:1458262 | T | C | 1 | a0001c0003t0002g0325 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.676-506A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458262 | |||||||
| chr16:1458330 | T | C | 11 | a0001c0001t0001g0160 a0001c0007t0002g0168 a0001c0007t0002g0169 others(8): Show |
11 | HG01891.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.676-574A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458330 | |||||||
| chr16:1458346 | C | T | 7 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0004g0182 others(4): Show |
8 | HG01106.hp2 HG01123.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-590G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458346 | |||||||
| chr16:1458414 | C | T | 3 | a0001c0002t0002g0012 a0001c0002t0002g0280 a0001c0002t0002g0281 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-658G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458414 | |||||||
| chr16:1458520 | C | T | 39 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0068 others(36): Show |
40 | HG00438.hp1 HG00735.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.675+587G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458520 | |||||||
| chr16:1458543 | A | C | 2 | a0001c0002t0002g0039 a0001c0002t0002g0040 |
2 | NA18942.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.675+564T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458543 | |||||||
| chr16:1458545 | G | A | 8 | a0002c0006t0010g0011 a0002c0006t0025g0259 a0002c0006t0025g0265 others(5): Show |
9 | HG00642.hp2 HG00735.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.675+562C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458545 | |||||||
| chr16:1458559 | G | A | 13 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0087 others(10): Show |
14 | HG00438.hp1 NA18951.hp1 NA18953.hp1 others(11): Show |
intron_variant | MODIFIER | c.675+548C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458559 | |||||||
| chr16:1458613 | G | A | 1 | a0001c0003t0001g0363 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.675+494C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458613 | |||||||
| chr16:1458643 | G | A | 4 | a0001c0002t0002g0089 a0001c0002t0020g0203 a0001c0003t0020g0372 others(1): Show |
4 | HG02080.hp1 HG03195.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+464C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458643 | |||||||
| chr16:1458668 | A | G | 207 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0058 others(204): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.675+439T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458668 | |||||||
| chr16:1458673 | G | A | 2 | a0001c0001t0045g0229 a0001c0002t0002g0196 |
2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.675+434C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458673 | |||||||
| chr16:1458681 | G | A | 2 | a0001c0001t0002g0223 a0001c0002t0002g0222 |
2 | HG02135.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.675+426C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458681 | |||||||
| chr16:1458735 | T | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.675+372A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458735 | |||||||
| chr16:1458899 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0139 |
3 | HG02970.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.675+208G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458899 | |||||||
| chr16:1458974 | C | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.675+133G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458974 | |||||||
| chr16:1458987 | T | C | 45 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(42): Show |
47 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.675+120A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458987 | |||||||
| chr16:1458995 | G | A | 3 | a0001c0001t0007g0007 a0001c0001t0007g0140 a0001c0001t0007g0141 |
4 | NA18948.hp2 NA18959.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+112C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458995 | |||||||
| chr16:1459097 | G | A | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.675+10C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1459097 | |||||||
| chr16:1459215 | G | A | 1 | a0001c0002t0002g0278 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.595-28C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459215 | |||||||
| chr16:1459220 | C | T | 1 | a0001c0005t0001g0181 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.595-33G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459220 | |||||||
| chr16:1459245 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.595-58G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459245 | |||||||
| chr16:1459270 | T | C | 1 | a0001c0001t0049g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.595-83A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459270 | |||||||
| chr16:1459277 | A | G | 5 | a0001c0007t0002g0168 a0001c0007t0002g0169 a0001c0007t0002g0170 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-90T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459277 | |||||||
| chr16:1459312 | C | A | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-125G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459312 | |||||||
| chr16:1459313 | T | G | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-126A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459313 | |||||||
| chr16:1459319 | C | G | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-132G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459319 | |||||||
| chr16:1459321 | CAA | C | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-136_595-135del others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459321 | |||||||
| chr16:1459335 | C | T | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-148G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459335 | |||||||
| chr16:1459346 | A | G | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-159T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459346 | |||||||
| chr16:1459349 | A | C | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-162T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459349 | |||||||
| chr16:1459350 | G | T | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-163C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459350 | |||||||
| chr16:1459354 | C | A | 1 | a0001c0001t0009g0100 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.595-167G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459354 | |||||||
| chr16:1459358 | C | CAA | 120 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-172_595-171ins others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459358 | |||||||
| chr16:1459360 | C | T | 40 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0002g0223 others(37): Show |
41 | HG00323.hp1 HG00544.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.595-173G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459360 | |||||||
| chr16:1459364 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(198): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.595-177T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459364 | |||||||
| chr16:1459368 | C | G | 1 | a0001c0003t0003g0384 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.595-181G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459368 | |||||||
| chr16:1459381 | G | A | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-194C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459381 | |||||||
| chr16:1459390 | G | A | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-203C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459390 | |||||||
| chr16:1459395 | C | T | 3 | a0001c0001t0035g0035 a0002c0008t0017g0010 a0002c0008t0017g0159 |
4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-208G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459395 | |||||||
| chr16:1459419 | C | A | 120 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-232G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459419 | |||||||
| chr16:1459420 | T | G | 120 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-233A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459420 | |||||||
| chr16:1459438 | C | G | 1 | a0001c0002t0015g0274 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.595-251G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459438 | |||||||
| chr16:1459439 | A | C | 139 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(136): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.595-252T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459439 | |||||||
| chr16:1459440 | T | C | 120 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-253A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459440 | |||||||
| chr16:1459454 | A | C | 120 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-267T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459454 | |||||||
| chr16:1459455 | G | T | 120 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-268C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459455 | |||||||
| chr16:1459464 | G | A | 196 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(193): Show |
203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.595-277C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459464 | |||||||
| chr16:1459465 | C | G | 19 | a0001c0001t0035g0035 a0001c0001t0049g0237 a0002c0008t0017g0010 others(16): Show |
20 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.595-278G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459465 | |||||||
| chr16:1459474 | C | A | 118 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-287G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459474 | |||||||
| chr16:1459490 | GCAGCACA others(203): Show |
G | 19 | a0001c0001t0035g0035 a0001c0001t0049g0237 a0002c0008t0017g0010 others(16): Show |
20 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.595-513_595-304del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459490 | |||||||
| chr16:1459500 | T | C | 116 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(113): Show |
120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.595-313A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459500 | |||||||
| chr16:1459500 | T | G | 51 | a0001c0001t0008g0078 a0001c0001t0045g0229 a0001c0002t0002g0196 others(48): Show |
53 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.595-313A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459500 | |||||||
| chr16:1459509 | C | A | 1 | a0001c0003t0001g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.595-322G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459509 | |||||||
| chr16:1459510 | TCAGGGAA others(28): Show |
T | 46 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(43): Show |
48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.595-358_595-324del others(35): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459510 | |||||||
| chr16:1459524 | C | A | 122 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-337G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459524 | |||||||
| chr16:1459525 | T | G | 122 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-338A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459525 | |||||||
| chr16:1459535 | C | G | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-348G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459535 | |||||||
| chr16:1459536 | T | G | 122 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-349A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459536 | |||||||
| chr16:1459540 | G | A | 5 | a0001c0001t0008g0078 a0001c0001t0045g0229 a0001c0002t0002g0196 others(2): Show |
5 | HG01515.hp2 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-353C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459540 | |||||||
| chr16:1459545 | C | T | 122 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-358G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459545 | |||||||
| chr16:1459560 | GCAGCACA others(133): Show |
G | 12 | a0001c0001t0001g0277 a0001c0001t0005g0041 a0001c0002t0001g0004 others(9): Show |
12 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-513_595-374del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459560 | |||||||
| chr16:1459570 | T | G | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-383A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459570 | |||||||
| chr16:1459574 | G | A | 48 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0246 others(45): Show |
52 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.595-387C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459574 | |||||||
| chr16:1459575 | G | A | 116 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(113): Show |
120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.595-388C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459575 | |||||||
| chr16:1459585 | G | A | 1 | a0001c0002t0002g0278 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.595-398C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459585 | |||||||
| chr16:1459592 | AGCTCAGC others(26): Show |
A | 3 | a0001c0001t0045g0229 a0001c0002t0002g0196 a0001c0002t0002g0212 |
3 | HG01515.hp2 HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.595-438_595-406del others(33): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459592 | |||||||
| chr16:1459594 | C | A | 118 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-407G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459594 | |||||||
| chr16:1459595 | T | G | 118 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-408A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459595 | |||||||
| chr16:1459605 | C | G | 118 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-418G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459605 | |||||||
| chr16:1459606 | T | G | 118 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-419A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459606 | |||||||
| chr16:1459615 | C | T | 118 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-428G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459615 | |||||||
| chr16:1459628 | GCT | G | 3 | a0001c0001t0045g0229 a0001c0002t0002g0196 a0001c0002t0002g0212 |
3 | HG01515.hp2 HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.595-443_595-442del others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459628 | |||||||
| chr16:1459629 | C | A | 119 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(116): Show |
123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.595-442G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459629 | |||||||
| chr16:1459630 | T | G | 119 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(116): Show |
123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.595-443A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459630 | |||||||
| chr16:1459640 | C | T | 1 | a0001c0002t0044g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.595-453G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459640 | |||||||
| chr16:1459641 | T | G | 122 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-454A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459641 | |||||||
| chr16:1459650 | C | T | 122 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-463G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459650 | |||||||
| chr16:1459663 | G | T | 2 | a0001c0005t0004g0184 a0001c0005t0004g0192 |
2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.595-476C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459663 | |||||||
| chr16:1459667 | G | A | 122 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-480C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459667 | |||||||
| chr16:1459675 | C | G | 121 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(118): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-488G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459675 | |||||||
| chr16:1459685 | T | TCAGGGAA others(63): Show |
1 | a0001c0002t0044g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.595-499_595-498ins others(70): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459685 | |||||||
| chr16:1459685 | TCAGGGAA others(273): Show |
T | 46 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(43): Show |
48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.594+453_595-499del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459685 | |||||||
| chr16:1459699 | C | A | 122 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-512G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459699 | |||||||
| chr16:1459700 | T | G | 122 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-513A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459700 | |||||||
| chr16:1459704 | C | A | 1 | a0001c0001t0049g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.595-517G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459704 | |||||||
| chr16:1459928 | C | A | 1 | a0001c0004t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.594+490G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459928 | |||||||
| chr16:1459941 | GAGAGCAG others(63): Show |
G | 3 | a0002c0008t0027g0251 a0002c0008t0027g0252 a0005c0018t0053g0275 |
3 | HG02717.hp1 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.594+407_594+476del others(70): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459941 | |||||||
| chr16:1459994 | G | A | 1 | a0001c0002t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.594+424C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459994 | |||||||
| chr16:1459997 | G | A | 120 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.594+421C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459997 | |||||||
| chr16:1460131 | G | A | 120 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.594+287C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460131 | |||||||
| chr16:1460202 | A | G | 46 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(43): Show |
48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.594+216T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460202 | |||||||
| chr16:1460283 | A | G | 197 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(194): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.594+135T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460283 | |||||||
| chr16:1460302 | C | T | 1 | a0002c0009t0016g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.594+116G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460302 | |||||||
| chr16:1460303 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0158 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.594+115C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460303 | |||||||
| chr16:1460305 | G | C | 8 | a0001c0002t0002g0075 a0001c0002t0002g0076 a0001c0002t0002g0079 others(5): Show |
8 | HG01255.hp2 HG01261.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.594+113C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460305 | |||||||
| chr16:1460401 | G | A | 2 | a0002c0008t0027g0251 a0002c0008t0027g0252 |
2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.594+17C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460401 | |||||||
| chr16:1460537 | A | G | 46 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(43): Show |
48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.485-10T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460537 | |||||||
| chr16:1460561 | C | T | 1 | a0001c0002t0043g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.485-34G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460561 | |||||||
| chr16:1460562 | G | A | 2 | a0001c0002t0015g0274 a0001c0002t0042g0268 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.485-35C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460562 | |||||||
| chr16:1460566 | T | G | 246 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0066 others(243): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.485-39A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460566 | |||||||
| chr16:1460609 | T | C | 1 | a0001c0001t0049g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485-82A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460609 | |||||||
| chr16:1460633 | G | A | 46 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(43): Show |
48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.485-106C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460633 | |||||||
| chr16:1460665 | G | A | 1 | a0001c0001t0049g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485-138C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460665 | |||||||
| chr16:1460706 | C | G | 46 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(43): Show |
48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.484+110G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460706 | |||||||
| chr16:1460780 | C | G | 3 | a0002c0009t0005g0032 a0002c0009t0005g0283 a0002c0011t0018g0253 |
3 | HG02055.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.484+36G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460780 | |||||||
| chr16:1460784 | C | T | 1 | a0001c0002t0044g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.484+32G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460784 | |||||||
| chr16:1460799 | C | T | 1 | a0001c0017t0041g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.484+17G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460799 | |||||||
| chr16:1461032 | A | T | 1 | a0001c0001t0001g0109 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.352-84T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461032 | |||||||
| chr16:1461099 | C | T | 1 | a0001c0002t0003g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.352-151G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461099 | |||||||
| chr16:1461109 | G | A | 5 | a0001c0007t0002g0168 a0001c0007t0002g0169 a0001c0007t0002g0170 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-161C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461109 | |||||||
| chr16:1461111 | C | T | 2 | a0001c0001t0008g0078 a0001c0002t0015g0051 |
2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.352-163G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461111 | |||||||
| chr16:1461118 | G | A | 1 | a0001c0002t0044g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.352-170C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461118 | |||||||
| chr16:1461138 | G | C | 1 | a0001c0004t0001g0366 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.352-190C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461138 | |||||||
| chr16:1461195 | A | G | 1 | a0001c0005t0011g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.351+210T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461195 | |||||||
| chr16:1461197 | C | T | 1 | a0002c0011t0018g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.351+208G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461197 | |||||||
| chr16:1461228 | C | T | 2 | a0002c0008t0017g0010 a0002c0008t0017g0159 |
3 | HG01243.hp2 HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.351+177G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461228 | |||||||
| chr16:1461236 | G | A | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.351+169C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461236 | |||||||
| chr16:1461371 | C | T | 44 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(41): Show |
46 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.351+34G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461371 | |||||||
| chr16:1461538 | C | T | 1 | a0003c0013t0001g0108 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.285+65G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 3/24 | chr16 | 1461538 | |||||||
| chr16:1461551 | G | T | 196 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(193): Show |
203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.285+52C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 3/24 | chr16 | 1461551 | |||||||
| chr16:1461567 | C | T | 1 | a0006c0025t0002g0351 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.285+36G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 3/24 | chr16 | 1461567 | |||||||
| chr16:1461568 | G | A | 1 | a0001c0001t0002g0223 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.285+35C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 3/24 | chr16 | 1461568 | |||||||
| chr16:1461757 | A | G | 69 | a0001c0001t0035g0035 a0001c0001t0049g0237 a0001c0002t0002g0278 others(66): Show |
72 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.214-83T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461757 | |||||||
| chr16:1461810 | C | T | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.214-136G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461810 | |||||||
| chr16:1461812 | C | T | 1 | a0001c0001t0049g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.214-138G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461812 | |||||||
| chr16:1461936 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.214-262A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461936 | |||||||
| chr16:1461999 | C | A | 1 | a0001c0003t0003g0381 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.214-325G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461999 | |||||||
| chr16:1462088 | GA | G | 182 | a0001c0001t0001g0092 a0001c0001t0001g0105 a0001c0001t0001g0197 others(179): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.214-415delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462088 | |||||||
| chr16:1462101 | A | G | 135 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(132): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.214-427T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462101 | |||||||
| chr16:1462251 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.214-577C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462251 | |||||||
| chr16:1462256 | C | G | 46 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(43): Show |
48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.214-582G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462256 | |||||||
| chr16:1462365 | C | CT | 50 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0049 others(47): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.214-692dupA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | |||||||
| chr16:1462365 | CT | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(16): Show |
20 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.214-692delA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | |||||||
| chr16:1462365 | CTTTTT | C | 6 | a0001c0002t0003g0126 a0001c0003t0002g0287 a0001c0003t0002g0294 others(3): Show |
7 | HG00621.hp2 HG00741.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-696_214-692del others(5): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | |||||||
| chr16:1462365 | CTTTTTT | C | 103 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(100): Show |
105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.214-697_214-692del others(6): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | |||||||
| chr16:1462365 | CTTTTTTT | C | 27 | a0001c0001t0035g0035 a0001c0001t0049g0237 a0001c0002t0001g0127 others(24): Show |
29 | HG00558.hp2 HG01070.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.214-698_214-692del others(7): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | |||||||
| chr16:1462365 | CTTTTTTT others(1): Show |
C | 44 | a0001c0003t0003g0302 a0001c0005t0001g0178 a0001c0005t0001g0181 others(41): Show |
46 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.214-699_214-692del others(8): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | |||||||
| chr16:1462462 | G | A | 15 | a0001c0001t0035g0035 a0001c0001t0049g0237 a0001c0002t0002g0278 others(12): Show |
16 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.214-788C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462462 | |||||||
| chr16:1462624 | G | A | 1 | a0003c0016t0050g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.214-950C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462624 | |||||||
| chr16:1462665 | C | CA | 28 | a0001c0001t0001g0044 a0001c0001t0001g0102 a0001c0001t0001g0132 others(25): Show |
28 | HG00597.hp1 HG00621.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.214-992dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462665 | |||||||
| chr16:1462665 | C | CAA | 8 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0003t0001g0346 others(5): Show |
8 | HG02055.hp1 HG02109.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-993_214-992dup others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462665 | |||||||
| chr16:1462665 | C | CAAAAAAA | 6 | a0001c0022t0048g0171 a0002c0008t0027g0251 a0002c0008t0027g0252 others(3): Show |
6 | HG01891.hp2 HG02717.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-998_214-992dup others(7): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462665 | |||||||
| chr16:1462665 | C | CAAAAAAA others(3): Show |
1 | a0003c0016t0050g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.214-1001_214-992du others(11): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462665 | |||||||
| chr16:1462666 | A | AAAAAC | 120 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.214-993_214-992ins others(5): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462666 | |||||||
| chr16:1462671 | A | C | 123 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(120): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.214-997T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462671 | |||||||
| chr16:1462672 | A | C | 1 | a0001c0003t0003g0302 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.214-998T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462672 | |||||||
| chr16:1462675 | A | C | 1 | a0001c0003t0005g0377 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.214-1001T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462675 | |||||||
| chr16:1462676 | A | C | 113 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0220 others(110): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.214-1002T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462676 | |||||||
| chr16:1462677 | A | AAC | 45 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(42): Show |
47 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.214-1004_214-1003i others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462677 | |||||||
| chr16:1462677 | A | C | 1 | a0001c0003t0003g0302 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.214-1003T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462677 | |||||||
| chr16:1462723 | G | A | 1 | a0002c0011t0018g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-1049C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462723 | |||||||
| chr16:1462730 | A | G | 46 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(43): Show |
48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.214-1056T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462730 | |||||||
| chr16:1462770 | C | T | 7 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0002c0009t0005g0032 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-1096G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462770 | |||||||
| chr16:1462884 | G | T | 1 | a0001c0001t0049g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.214-1210C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462884 | |||||||
| chr16:1462978 | T | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.214-1304A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462978 | |||||||
| chr16:1462984 | G | T | 1 | a0002c0011t0018g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-1310C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462984 | |||||||
| chr16:1463167 | C | T | 2 | a0001c0001t0001g0277 a0001c0002t0034g0276 |
2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214-1493G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463167 | |||||||
| chr16:1463356 | C | T | 5 | a0002c0009t0005g0032 a0002c0009t0005g0283 a0002c0009t0016g0080 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-1682G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463356 | |||||||
| chr16:1463393 | A | G | 154 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0277 others(151): Show |
159 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.214-1719T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463393 | |||||||
| chr16:1463422 | C | T | 138 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0002g0223 others(135): Show |
143 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.214-1748G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463422 | |||||||
| chr16:1463440 | C | T | 4 | a0001c0005t0004g0152 a0001c0005t0004g0179 a0001c0005t0004g0180 others(1): Show |
4 | HG01071.hp1 HG02055.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-1766G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463440 | |||||||
| chr16:1463505 | C | T | 33 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(30): Show |
34 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.213+1762G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463505 | |||||||
| chr16:1463515 | G | A | 2 | a0001c0001t0008g0078 a0001c0002t0015g0051 |
2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.213+1752C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463515 | |||||||
| chr16:1463573 | G | A | 124 | a0001c0001t0001g0197 a0001c0001t0001g0207 a0001c0001t0001g0220 others(121): Show |
128 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.213+1694C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463573 | |||||||
| chr16:1463646 | G | A | 1 | a0001c0002t0001g0086 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.213+1621C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463646 | |||||||
| chr16:1463684 | G | A | 155 | a0001c0001t0001g0197 a0001c0001t0001g0207 a0001c0001t0001g0220 others(152): Show |
160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.213+1583C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463684 | |||||||
| chr16:1463690 | T | C | 155 | a0001c0001t0001g0197 a0001c0001t0001g0207 a0001c0001t0001g0220 others(152): Show |
160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.213+1577A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463690 | |||||||
| chr16:1463704 | C | G | 155 | a0001c0001t0001g0197 a0001c0001t0001g0207 a0001c0001t0001g0220 others(152): Show |
160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.213+1563G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463704 | |||||||
| chr16:1463719 | A | G | 3 | a0001c0001t0035g0035 a0002c0008t0017g0010 a0002c0008t0017g0159 |
4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+1548T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463719 | |||||||
| chr16:1463774 | G | GA | 14 | a0001c0004t0002g0347 a0002c0006t0010g0011 a0002c0006t0010g0254 others(11): Show |
15 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.213+1492dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463774 | |||||||
| chr16:1463774 | G | GAA | 32 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(29): Show |
33 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.213+1491_213+1492d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463774 | |||||||
| chr16:1463774 | GA | G | 150 | a0001c0001t0001g0109 a0001c0001t0001g0197 a0001c0001t0001g0207 others(147): Show |
155 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.213+1492delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463774 | |||||||
| chr16:1463774 | GAA | G | 6 | a0001c0002t0044g0072 a0001c0007t0002g0168 a0001c0007t0002g0169 others(3): Show |
6 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+1491_213+1492d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463774 | |||||||
| chr16:1463827 | T | C | 5 | a0001c0007t0002g0168 a0001c0007t0002g0169 a0001c0007t0002g0170 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+1440A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463827 | |||||||
| chr16:1463949 | A | G | 5 | a0002c0009t0005g0032 a0002c0009t0005g0283 a0002c0009t0016g0080 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+1318T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463949 | |||||||
| chr16:1464105 | G | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0004t0006g0026 others(1): Show |
4 | HG01109.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+1162C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464105 | |||||||
| chr16:1464170 | G | A | 3 | a0001c0002t0002g0012 a0001c0002t0002g0280 a0001c0002t0002g0281 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+1097C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464170 | |||||||
| chr16:1464189 | A | G | 1 | a0001c0002t0002g0278 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.213+1078T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464189 | |||||||
| chr16:1464260 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.213+1007C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464260 | |||||||
| chr16:1464324 | C | T | 58 | a0001c0001t0001g0277 a0001c0001t0035g0035 a0001c0001t0049g0237 others(55): Show |
60 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.213+943G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464324 | |||||||
| chr16:1464343 | C | G | 25 | a0001c0001t0001g0277 a0001c0001t0035g0035 a0001c0001t0049g0237 others(22): Show |
26 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.213+924G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464343 | |||||||
| chr16:1464444 | C | T | 1 | a0001c0003t0002g0313 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.213+823G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464444 | |||||||
| chr16:1464445 | G | A | 1 | a0001c0017t0041g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.213+822C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464445 | |||||||
| chr16:1464463 | G | C | 6 | a0001c0002t0044g0072 a0001c0007t0002g0168 a0001c0007t0002g0169 others(3): Show |
6 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+804C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464463 | |||||||
| chr16:1464590 | G | T | 2 | a0001c0001t0001g0277 a0001c0002t0034g0276 |
2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.213+677C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464590 | |||||||
| chr16:1464651 | A | G | 203 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0207 others(200): Show |
210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.213+616T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464651 | |||||||
| chr16:1464673 | G | A | 6 | a0002c0011t0018g0253 a0002c0011t0018g0269 a0002c0011t0018g0270 others(3): Show |
6 | HG03098.hp2 HG03209.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+594C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464673 | |||||||
| chr16:1464691 | T | C | 8 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 others(5): Show |
8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+576A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464691 | |||||||
| chr16:1464721 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.213+546G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464721 | |||||||
| chr16:1464724 | G | A | 1 | a0001c0001t0049g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.213+543C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464724 | |||||||
| chr16:1464746 | G | A | 35 | a0001c0001t0001g0034 a0001c0001t0001g0068 a0001c0001t0001g0087 others(32): Show |
36 | HG00438.hp1 HG00735.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.213+521C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464746 | |||||||
| chr16:1464798 | G | C | 1 | a0001c0004t0001g0380 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.213+469C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464798 | |||||||
| chr16:1464824 | T | A | 1 | a0001c0002t0043g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.213+443A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464824 | |||||||
| chr16:1464851 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.213+416G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464851 | |||||||
| chr16:1464966 | G | GC | 117 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0207 others(114): Show |
120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.213+300dupG | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464966 | |||||||
| chr16:1465004 | C | T | 2 | a0001c0001t0001g0107 a0003c0013t0001g0108 |
2 | HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.213+263G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465004 | |||||||
| chr16:1465049 | C | T | 1 | a0001c0001t0045g0229 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.213+218G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465049 | |||||||
| chr16:1465068 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.213+199G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465068 | |||||||
| chr16:1465134 | C | G | 7 | a0001c0005t0004g0038 a0001c0005t0004g0163 a0001c0005t0004g0164 others(4): Show |
7 | HG00280.hp1 HG01081.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+133G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465134 | |||||||
| chr16:1465158 | G | A | 1 | a0001c0003t0002g0293 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.213+109C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465158 | |||||||
| chr16:1465161 | C | T | 129 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0001g0207 others(126): Show |
133 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.213+106G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465161 | |||||||
| chr16:1465195 | G | A | 5 | a0002c0009t0005g0032 a0002c0009t0005g0283 a0002c0009t0016g0080 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+72C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465195 | |||||||
| chr16:1465246 | C | T | 3 | a0001c0002t0002g0012 a0001c0002t0002g0280 a0001c0002t0002g0281 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+21G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465246 | |||||||
| chr16:1465247 | G | T | 6 | a0001c0002t0002g0075 a0001c0002t0002g0076 a0001c0002t0002g0079 others(3): Show |
6 | HG01255.hp2 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+20C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465247 | |||||||
| chr16:1465381 | C | T | 1 | a0001c0003t0008g0382 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.142-43G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465381 | |||||||
| chr16:1465391 | C | T | 1 | a0001c0002t0003g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.142-53G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465391 | |||||||
| chr16:1465413 | C | T | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-75G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465413 | |||||||
| chr16:1465414 | G | T | 50 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(47): Show |
52 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-76C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465414 | |||||||
| chr16:1465427 | G | A | 3 | a0001c0001t0001g0061 a0001c0004t0001g0284 a0001c0004t0001g0285 |
3 | HG00423.hp1 NA18966.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.142-89C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465427 | |||||||
| chr16:1465433 | C | A | 3 | a0001c0002t0003g0200 a0001c0002t0003g0201 a0001c0002t0003g0211 |
3 | HG02109.hp2 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.142-95G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465433 | |||||||
| chr16:1465502 | G | A | 195 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0277 others(192): Show |
202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.142-164C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465502 | |||||||
| chr16:1465514 | G | A | 50 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(47): Show |
52 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-176C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465514 | |||||||
| chr16:1465534 | C | G | 3 | a0001c0001t0035g0035 a0002c0008t0017g0010 a0002c0008t0017g0159 |
4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-196G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465534 | |||||||
| chr16:1465563 | G | A | 1 | a0001c0004t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142-225C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465563 | |||||||
| chr16:1465580 | G | A | 3 | a0001c0005t0005g0186 a0001c0005t0005g0187 a0003c0021t0013g0188 |
3 | HG01884.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.142-242C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465580 | |||||||
| chr16:1465643 | G | A | 5 | a0001c0007t0002g0168 a0001c0007t0002g0169 a0001c0007t0002g0170 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-305C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465643 | |||||||
| chr16:1465754 | C | T | 1 | a0001c0005t0004g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.142-416G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465754 | |||||||
| chr16:1465763 | C | G | 1 | a0001c0002t0015g0274 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142-425G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465763 | |||||||
| chr16:1465801 | C | G | 1 | a0001c0001t0001g0207 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.142-463G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465801 | |||||||
| chr16:1465869 | T | C | 1 | a0001c0001t0049g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142-531A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465869 | |||||||
| chr16:1465925 | T | C | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-587A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465925 | |||||||
| chr16:1465941 | G | A | 1 | a0002c0006t0024g0262 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142-603C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465941 | |||||||
| chr16:1466147 | G | A | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-809C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466147 | |||||||
| chr16:1466150 | C | T | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-812G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466150 | |||||||
| chr16:1466166 | G | A | 3 | a0001c0001t0035g0035 a0002c0008t0017g0010 a0002c0008t0017g0159 |
4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-828C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466166 | |||||||
| chr16:1466175 | C | T | 2 | a0001c0001t0001g0277 a0001c0002t0034g0276 |
2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.142-837G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466175 | |||||||
| chr16:1466176 | G | A | 117 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0002g0223 others(114): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.142-838C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466176 | |||||||
| chr16:1466197 | G | A | 1 | a0001c0003t0001g0363 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.142-859C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466197 | |||||||
| chr16:1466275 | G | A | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-937C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466275 | |||||||
| chr16:1466341 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0235 a0001c0002t0001g0004 |
4 | NA18948.hp1 NA18970.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1003G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466341 | |||||||
| chr16:1466392 | G | C | 1 | a0001c0003t0003g0378 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.142-1054C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466392 | |||||||
| chr16:1466662 | G | A | 1 | a0001c0003t0005g0298 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.142-1324C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466662 | |||||||
| chr16:1466685 | G | A | 49 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(46): Show |
51 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.142-1347C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466685 | |||||||
| chr16:1466712 | A | G | 196 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0248 others(193): Show |
203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.142-1374T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466712 | |||||||
| chr16:1466723 | C | T | 10 | a0001c0002t0002g0278 a0002c0008t0027g0251 a0002c0008t0027g0252 others(7): Show |
10 | HG02717.hp1 HG03098.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-1385G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466723 | |||||||
| chr16:1466810 | G | A | 2 | a0002c0008t0027g0251 a0002c0008t0027g0252 |
2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.142-1472C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466810 | |||||||
| chr16:1466851 | G | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-1513C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466851 | |||||||
| chr16:1466923 | C | CA | 48 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0044 others(45): Show |
52 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-1586dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | |||||||
| chr16:1466923 | C | CAA | 13 | a0001c0001t0001g0133 a0001c0001t0001g0245 a0001c0001t0005g0134 others(10): Show |
13 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-1587_142-1586d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | |||||||
| chr16:1466923 | CA | C | 65 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0068 others(62): Show |
68 | HG00438.hp1 HG00544.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.142-1586delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | |||||||
| chr16:1466923 | CAA | C | 102 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0197 others(99): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.142-1587_142-1586d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | |||||||
| chr16:1466923 | CAAA | C | 21 | a0001c0001t0001g0091 a0001c0001t0049g0237 a0001c0002t0002g0196 others(18): Show |
21 | HG00735.hp1 HG01074.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.142-1588_142-1586d others(5): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | |||||||
| chr16:1466923 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-1597_142-1586d others(14): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | |||||||
| chr16:1466923 | CAAAAAAA others(7): Show |
C | 30 | a0001c0005t0001g0181 a0001c0005t0001g0189 a0001c0005t0004g0152 others(27): Show |
31 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.142-1599_142-1586d others(16): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | |||||||
| chr16:1466923 | CAAAAAAA others(8): Show |
C | 2 | a0001c0005t0001g0178 a0001c0005t0004g0038 |
2 | HG02735.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.142-1600_142-1586d others(17): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | |||||||
| chr16:1466923 | CAAAAAAA others(9): Show |
C | 3 | a0002c0009t0016g0080 a0002c0009t0016g0081 a0002c0009t0016g0082 |
3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.142-1601_142-1586d others(18): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | |||||||
| chr16:1467024 | G | A | 29 | a0001c0001t0001g0277 a0001c0001t0035g0035 a0001c0001t0049g0237 others(26): Show |
30 | HG01081.hp1 HG01243.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-1686C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467024 | |||||||
| chr16:1467049 | G | A | 3 | a0001c0001t0035g0035 a0001c0001t0049g0237 a0002c0008t0017g0010 |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1711C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467049 | |||||||
| chr16:1467076 | A | C | 189 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0277 others(186): Show |
196 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.142-1738T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467076 | |||||||
| chr16:1467089 | T | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-1751A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467089 | |||||||
| chr16:1467103 | T | TG | 15 | a0001c0002t0002g0278 a0001c0007t0002g0168 a0001c0007t0002g0169 others(12): Show |
15 | HG01891.hp2 HG02572.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-1766dupC | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467103 | |||||||
| chr16:1467113 | C | T | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-1775G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467113 | |||||||
| chr16:1467225 | C | T | 49 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(46): Show |
51 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.142-1887G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467225 | |||||||
| chr16:1467297 | C | G | 13 | a0001c0002t0002g0012 a0001c0002t0002g0278 a0001c0002t0002g0280 others(10): Show |
14 | HG02257.hp1 HG02717.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-1959G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467297 | |||||||
| chr16:1467311 | C | T | 3 | a0001c0004t0001g0364 a0001c0004t0001g0365 a0001c0004t0001g0370 |
3 | NA18960.hp1 NA18993.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.142-1973G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467311 | |||||||
| chr16:1467373 | C | T | 5 | a0002c0009t0005g0032 a0002c0009t0005g0283 a0002c0009t0016g0080 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-2035G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467373 | |||||||
| chr16:1467409 | C | T | 32 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(29): Show |
33 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.142-2071G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467409 | |||||||
| chr16:1467412 | G | A | 1 | a0001c0002t0001g0086 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.142-2074C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467412 | |||||||
| chr16:1467454 | G | A | 3 | a0001c0001t0035g0035 a0002c0008t0017g0010 a0002c0008t0017g0159 |
4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-2116C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467454 | |||||||
| chr16:1467466 | C | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-2128G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467466 | |||||||
| chr16:1467556 | G | A | 1 | a0002c0006t0010g0011 | 2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.142-2218C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467556 | |||||||
| chr16:1467678 | T | C | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-2340A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467678 | |||||||
| chr16:1467727 | A | G | 191 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0248 others(188): Show |
198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.142-2389T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467727 | |||||||
| chr16:1467760 | G | A | 1 | a0002c0011t0018g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.142-2422C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467760 | |||||||
| chr16:1467851 | C | G | 53 | a0001c0001t0001g0277 a0001c0002t0015g0267 a0001c0002t0015g0274 others(50): Show |
55 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.142-2513G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467851 | |||||||
| chr16:1467864 | C | T | 1 | a0001c0004t0001g0386 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.142-2526G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467864 | |||||||
| chr16:1467999 | C | T | 5 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(2): Show |
6 | HG00639.hp1 HG00642.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2661G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467999 | |||||||
| chr16:1468008 | G | A | 15 | a0001c0001t0001g0068 a0001c0001t0001g0135 a0001c0001t0001g0136 others(12): Show |
15 | HG01109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-2670C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468008 | |||||||
| chr16:1468047 | C | T | 4 | a0001c0001t0035g0035 a0001c0004t0001g0334 a0002c0008t0017g0010 others(1): Show |
5 | HG00673.hp1 HG01243.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-2709G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468047 | |||||||
| chr16:1468067 | G | C | 2 | a0001c0004t0001g0361 a0001c0004t0002g0360 |
2 | HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.142-2729C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468067 | |||||||
| chr16:1468155 | G | A | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-2817C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468155 | |||||||
| chr16:1468285 | G | A | 1 | a0001c0004t0001g0362 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.142-2947C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468285 | |||||||
| chr16:1468300 | C | G | 32 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(29): Show |
33 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.142-2962G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468300 | |||||||
| chr16:1468389 | C | G | 1 | a0001c0001t0001g0088 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.142-3051G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468389 | |||||||
| chr16:1468456 | C | G | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-3118G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468456 | |||||||
| chr16:1468578 | C | T | 1 | a0001c0003t0002g0312 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.142-3240G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468578 | |||||||
| chr16:1468668 | G | C | 3 | a0002c0012t0014g0016 a0002c0012t0014g0017 a0002c0012t0014g0018 |
3 | HG03209.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.142-3330C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468668 | |||||||
| chr16:1468673 | G | A | 1 | a0003c0016t0050g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-3335C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468673 | |||||||
| chr16:1468683 | G | A | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0004t0001g0307 |
3 | NA18957.hp2 NA18983.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.142-3345C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468683 | |||||||
| chr16:1468699 | G | A | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-3361C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468699 | |||||||
| chr16:1468751 | G | A | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-3413C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468751 | |||||||
| chr16:1468771 | C | G | 114 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0248 others(111): Show |
118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.142-3433G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468771 | |||||||
| chr16:1468773 | G | A | 1 | a0001c0017t0041g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.142-3435C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468773 | |||||||
| chr16:1468795 | T | C | 56 | a0001c0001t0001g0277 a0001c0001t0007g0007 a0001c0001t0007g0140 others(53): Show |
59 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.142-3457A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468795 | |||||||
| chr16:1468806 | G | A | 47 | a0001c0005t0001g0178 a0001c0005t0001g0181 a0001c0005t0001g0189 others(44): Show |
49 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-3468C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468806 | |||||||
| chr16:1468826 | G | A | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0044g0072 |
3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-3488C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468826 | |||||||
| chr16:1468869 | T | A | 190 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0248 others(187): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.142-3531A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468869 | |||||||
| chr16:1468915 | G | A | 50 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(47): Show |
52 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.142-3577C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468915 | |||||||
| chr16:1468944 | G | A | 53 | a0001c0001t0001g0277 a0001c0002t0015g0267 a0001c0002t0015g0274 others(50): Show |
55 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.142-3606C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468944 | |||||||
| chr16:1468964 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.142-3626C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468964 | |||||||
| chr16:1469019 | C | T | 1 | a0003c0016t0050g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-3681G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469019 | |||||||
| chr16:1469039 | G | GA | 16 | a0001c0001t0001g0049 a0001c0001t0001g0142 a0001c0001t0001g0143 others(13): Show |
16 | HG00438.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-3702dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469039 | |||||||
| chr16:1469039 | GA | G | 52 | a0001c0001t0001g0070 a0001c0001t0002g0227 a0001c0001t0049g0237 others(49): Show |
54 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.142-3702delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469039 | |||||||
| chr16:1469099 | G | A | 1 | a0001c0001t0049g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142-3761C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469099 | |||||||
| chr16:1469099 | G | C | 2 | a0001c0003t0002g0332 a0001c0003t0002g0333 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.142-3761C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469099 | |||||||
| chr16:1469125 | G | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-3787C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469125 | |||||||
| chr16:1469456 | C | T | 189 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0248 others(186): Show |
196 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.142-4118G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469456 | |||||||
| chr16:1469501 | T | C | 1 | a0001c0022t0048g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142-4163A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469501 | |||||||
| chr16:1469624 | C | T | 112 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0248 others(109): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.142-4286G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469624 | |||||||
| chr16:1469673 | G | A | 50 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(47): Show |
52 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.142-4335C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469673 | |||||||
| chr16:1469706 | A | C | 1 | a0002c0026t0024g0308 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.142-4368T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469706 | |||||||
| chr16:1469743 | C | G | 1 | a0003c0016t0050g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-4405G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469743 | |||||||
| chr16:1469743 | C | T | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-4405G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469743 | |||||||
| chr16:1469764 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.142-4426G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469764 | |||||||
| chr16:1469805 | G | A | 49 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(46): Show |
51 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.142-4467C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469805 | |||||||
| chr16:1469859 | C | T | 2 | a0001c0001t0001g0053 a0001c0002t0002g0084 |
2 | NA18939.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.142-4521G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469859 | |||||||
| chr16:1469888 | A | T | 4 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0001c0002t0036g0206 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-4550T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469888 | |||||||
| chr16:1469897 | C | T | 1 | a0001c0004t0001g0310 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.142-4559G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469897 | |||||||
| chr16:1469914 | C | T | 1 | a0001c0004t0001g0334 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.142-4576G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469914 | |||||||
| chr16:1469926 | G | C | 1 | a0003c0016t0050g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-4588C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469926 | |||||||
| chr16:1469940 | G | A | 58 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 others(55): Show |
60 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.142-4602C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469940 | |||||||
| chr16:1469984 | C | T | 1 | a0001c0002t0036g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.142-4646G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469984 | |||||||
| chr16:1470037 | G | A | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-4699C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470037 | |||||||
| chr16:1470063 | G | A | 1 | a0001c0003t0003g0376 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.142-4725C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470063 | |||||||
| chr16:1470134 | A | T | 146 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0160 others(143): Show |
151 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.141+4700T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470134 | |||||||
| chr16:1470235 | A | G | 201 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0083 others(198): Show |
207 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.141+4599T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470235 | |||||||
| chr16:1470250 | G | A | 1 | a0001c0001t0039g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.141+4584C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470250 | |||||||
| chr16:1470268 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4566T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470268 | |||||||
| chr16:1470270 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4564C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470270 | |||||||
| chr16:1470272 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4562C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470272 | |||||||
| chr16:1470275 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4559C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470275 | |||||||
| chr16:1470276 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4558G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470276 | |||||||
| chr16:1470277 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4557C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470277 | |||||||
| chr16:1470278 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4556A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470278 | |||||||
| chr16:1470281 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4553T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470281 | |||||||
| chr16:1470282 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4552G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470282 | |||||||
| chr16:1470283 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4551G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470283 | |||||||
| chr16:1470285 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4549G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470285 | |||||||
| chr16:1470286 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4548G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470286 | |||||||
| chr16:1470289 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4545C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470289 | |||||||
| chr16:1470290 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4544G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470290 | |||||||
| chr16:1470291 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4543G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470291 | |||||||
| chr16:1470292 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4542A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470292 | |||||||
| chr16:1470295 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4539G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470295 | |||||||
| chr16:1470297 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4537G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470297 | |||||||
| chr16:1470301 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4533T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470301 | |||||||
| chr16:1470303 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4531C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470303 | |||||||
| chr16:1470304 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4530C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470304 | |||||||
| chr16:1470307 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4527T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470307 | |||||||
| chr16:1470313 | T | C | 35 | a0001c0001t0001g0177 a0001c0001t0001g0277 a0001c0002t0034g0276 others(32): Show |
36 | HG01071.hp1 HG01081.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.141+4521A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470313 | |||||||
| chr16:1470316 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4518A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470316 | |||||||
| chr16:1470319 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4515C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470319 | |||||||
| chr16:1470321 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4513C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470321 | |||||||
| chr16:1470322 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4512A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470322 | |||||||
| chr16:1470324 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4510G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470324 | |||||||
| chr16:1470325 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4509A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470325 | |||||||
| chr16:1470326 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4508A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470326 | |||||||
| chr16:1470329 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4505G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470329 | |||||||
| chr16:1470330 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4504G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470330 | |||||||
| chr16:1470331 | A | AAGGGGAT others(4): Show |
1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4502_141+4503i others(13): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470331 | |||||||
| chr16:1470335 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4499A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470335 | |||||||
| chr16:1470336 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4498A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470336 | |||||||
| chr16:1470337 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4497A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470337 | |||||||
| chr16:1470339 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4495A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470339 | |||||||
| chr16:1470340 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4494A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470340 | |||||||
| chr16:1470341 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4493A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470341 | |||||||
| chr16:1470346 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4488T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470346 | |||||||
| chr16:1470351 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4483T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470351 | |||||||
| chr16:1470357 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4477C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470357 | |||||||
| chr16:1470360 | TAAAGACC others(14): Show |
T | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4453_141+4473d others(23): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470360 | |||||||
| chr16:1470436 | C | T | 3 | a0001c0004t0006g0026 a0001c0004t0006g0027 a0005c0024t0029g0025 |
3 | HG01109.hp2 HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.141+4398G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470436 | |||||||
| chr16:1470467 | G | A | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.141+4367C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470467 | |||||||
| chr16:1470485 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.141+4349G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470485 | |||||||
| chr16:1470554 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.141+4280A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470554 | |||||||
| chr16:1470592 | A | C | 5 | a0001c0001t0001g0148 a0001c0002t0002g0039 a0001c0002t0002g0040 others(2): Show |
5 | HG00558.hp1 HG02080.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4242T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470592 | |||||||
| chr16:1470738 | C | T | 1 | a0001c0002t0020g0203 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.141+4096G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470738 | |||||||
| chr16:1470769 | C | T | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.141+4065G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470769 | |||||||
| chr16:1470794 | G | A | 1 | a0001c0003t0001g0363 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.141+4040C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470794 | |||||||
| chr16:1470893 | A | G | 1 | a0001c0003t0001g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.141+3941T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470893 | |||||||
| chr16:1470999 | C | T | 1 | a0005c0018t0053g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.141+3835G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470999 | |||||||
| chr16:1471451 | C | A | 137 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0034 others(134): Show |
142 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.141+3383G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471451 | |||||||
| chr16:1471513 | A | G | 1 | a0001c0003t0003g0015 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.141+3321T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471513 | |||||||
| chr16:1471555 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(247): Show |
261 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(258): Show |
intron_variant | MODIFIER | c.141+3279T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471555 | |||||||
| chr16:1471576 | C | T | 6 | a0001c0002t0013g0029 a0001c0002t0013g0030 a0001c0002t0013g0033 others(3): Show |
6 | HG00639.hp2 HG02055.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+3258G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471576 | |||||||
| chr16:1471577 | G | A | 2 | a0002c0008t0027g0251 a0002c0008t0027g0252 |
2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.141+3257C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471577 | |||||||
| chr16:1471581 | C | A | 1 | a0002c0006t0052g0263 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.141+3253G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471581 | |||||||
| chr16:1471612 | G | A | 1 | a0001c0001t0045g0229 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.141+3222C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471612 | |||||||
| chr16:1471665 | G | A | 5 | a0001c0001t0001g0243 a0001c0004t0006g0026 a0001c0004t0006g0027 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+3169C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471665 | |||||||
| chr16:1471744 | G | A | 182 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0034 others(179): Show |
189 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.141+3090C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471744 | |||||||
| chr16:1471761 | C | T | 1 | a0001c0002t0003g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.141+3073G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471761 | |||||||
| chr16:1471805 | C | T | 2 | a0001c0001t0001g0277 a0001c0002t0034g0276 |
2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+3029G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471805 | |||||||
| chr16:1471815 | G | C | 1 | a0001c0002t0020g0203 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.141+3019C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471815 | |||||||
| chr16:1471980 | CG | C | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.141+2853delC | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471980 | |||||||
| chr16:1472013 | G | A | 1 | a0001c0005t0001g0189 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.141+2821C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472013 | |||||||
| chr16:1472051 | C | A | 1 | a0001c0003t0003g0302 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.141+2783G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472051 | |||||||
| chr16:1472175 | A | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(55): Show |
62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2659T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472175 | |||||||
| chr16:1472223 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(55): Show |
62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2611A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472223 | |||||||
| chr16:1472244 | A | AT | 3 | a0001c0002t0015g0267 a0001c0002t0015g0274 a0001c0002t0042g0268 |
3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.141+2589dupA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472244 | |||||||
| chr16:1472250 | A | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(55): Show |
62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2584T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472250 | |||||||
| chr16:1472291 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(39): Show |
45 | HG00438.hp2 HG00741.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.141+2543G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472291 | |||||||
| chr16:1472333 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.141+2501G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472333 | |||||||
| chr16:1472354 | C | T | 1 | a0001c0002t0044g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.141+2480G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472354 | |||||||
| chr16:1472369 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(55): Show |
62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2465A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472369 | |||||||
| chr16:1472385 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(55): Show |
62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2449A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472385 | |||||||
| chr16:1472387 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(247): Show |
261 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(258): Show |
intron_variant | MODIFIER | c.141+2447A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472387 | |||||||
| chr16:1472403 | C | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(55): Show |
62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2431G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472403 | |||||||
| chr16:1472530 | C | A | 15 | a0001c0001t0049g0237 a0001c0002t0015g0267 a0001c0002t0015g0274 others(12): Show |
15 | HG02258.hp2 HG02615.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+2304G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472530 | |||||||
| chr16:1472539 | T | C | 3 | a0001c0002t0002g0012 a0001c0002t0002g0280 a0001c0002t0002g0281 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+2295A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472539 | |||||||
| chr16:1472572 | C | T | 5 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(2): Show |
6 | HG00639.hp1 HG00642.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+2262G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472572 | |||||||
| chr16:1472573 | A | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(49): Show |
56 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.141+2261T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472573 | |||||||
| chr16:1472669 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(191): Show |
204 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.141+2165T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472669 | |||||||
| chr16:1472711 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.141+2123G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472711 | |||||||
| chr16:1472744 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.141+2090T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472744 | |||||||
| chr16:1472745 | T | A | 2 | a0001c0005t0004g0266 a0001c0005t0004g0279 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.141+2089A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472745 | |||||||
| chr16:1472813 | G | GA | 14 | a0001c0001t0001g0070 a0001c0001t0001g0144 a0001c0002t0001g0069 others(11): Show |
14 | HG01261.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+2020dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472813 | |||||||
| chr16:1472813 | GA | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0047 others(25): Show |
31 | HG01081.hp1 HG01099.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.141+2020delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472813 | |||||||
| chr16:1472865 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0047 others(28): Show |
34 | HG00438.hp2 HG00741.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.141+1969G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472865 | |||||||
| chr16:1472871 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(187): Show |
200 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.141+1963G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472871 | |||||||
| chr16:1472938 | G | GT | 15 | a0001c0003t0001g0305 a0001c0003t0003g0371 a0001c0003t0003g0384 others(12): Show |
16 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.141+1895dupA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472938 | |||||||
| chr16:1473009 | C | CCTCCCCT others(1): Show |
12 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(9): Show |
13 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+1817_141+1824d others(10): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473009 | |||||||
| chr16:1473023 | G | C | 1 | a0001c0003t0003g0378 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.141+1811C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473023 | |||||||
| chr16:1473068 | C | CCTTA | 104 | a0001c0001t0001g0028 a0001c0001t0001g0160 a0001c0001t0001g0161 others(101): Show |
109 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.141+1765_141+1766i others(6): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473068 | |||||||
| chr16:1473086 | A | AAC | 4 | a0001c0001t0001g0046 a0001c0003t0002g0289 a0001c0003t0003g0288 others(1): Show |
4 | HG02055.hp1 HG03710.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+1746_141+1747d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473086 | |||||||
| chr16:1473086 | A | AACAC | 3 | a0001c0003t0002g0287 a0001c0003t0002g0304 a0001c0003t0002g0385 |
3 | HG00741.hp2 HG01496.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.141+1744_141+1747d others(6): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473086 | |||||||
| chr16:1473086 | AAC | A | 64 | a0001c0001t0001g0028 a0001c0001t0001g0160 a0001c0001t0001g0161 others(61): Show |
67 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.141+1746_141+1747d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473086 | |||||||
| chr16:1473118 | T | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1716A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473118 | |||||||
| chr16:1473212 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.141+1622G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473212 | |||||||
| chr16:1473299 | G | A | 14 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0002c0006t0010g0011 others(11): Show |
15 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+1535C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473299 | |||||||
| chr16:1473370 | C | CT | 74 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0158 others(71): Show |
75 | HG00639.hp1 HG00741.hp2 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.141+1463dupA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | |||||||
| chr16:1473370 | C | CTT | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0034 others(143): Show |
154 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.141+1462_141+1463d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | |||||||
| chr16:1473370 | C | CTTT | 40 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(37): Show |
40 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.141+1461_141+1463d others(5): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | |||||||
| chr16:1473370 | C | CTTTT | 8 | a0001c0002t0015g0267 a0001c0002t0042g0268 a0001c0005t0004g0264 others(5): Show |
8 | HG02451.hp1 HG02976.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+1460_141+1463d others(6): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | |||||||
| chr16:1473370 | CT | C | 13 | a0001c0001t0001g0045 a0001c0001t0049g0237 a0001c0002t0002g0012 others(10): Show |
15 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+1463delA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | |||||||
| chr16:1473401 | G | A | 1 | a0001c0003t0008g0382 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.141+1433C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473401 | |||||||
| chr16:1473411 | C | A | 222 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(219): Show |
231 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.141+1423G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473411 | |||||||
| chr16:1473414 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.141+1420G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473414 | |||||||
| chr16:1473452 | T | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1382A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473452 | |||||||
| chr16:1473463 | T | G | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1371A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473463 | |||||||
| chr16:1473474 | A | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1360T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473474 | |||||||
| chr16:1473475 | T | G | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1359A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473475 | |||||||
| chr16:1473476 | T | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1358A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473476 | |||||||
| chr16:1473477 | G | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1357C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473477 | |||||||
| chr16:1473485 | T | A | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1349A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473485 | |||||||
| chr16:1473522 | C | A | 2 | a0001c0001t0001g0194 a0001c0002t0001g0193 |
2 | HG02523.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.141+1312G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473522 | |||||||
| chr16:1473534 | T | C | 13 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(10): Show |
14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1300A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473534 | |||||||
| chr16:1473619 | C | T | 1 | a0001c0001t0005g0041 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.141+1215G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473619 | |||||||
| chr16:1473672 | C | T | 1 | a0001c0002t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.141+1162G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473672 | |||||||
| chr16:1473808 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.141+1026C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473808 | |||||||
| chr16:1473865 | A | G | 12 | a0002c0006t0010g0011 a0002c0006t0010g0254 a0002c0006t0010g0255 others(9): Show |
13 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+969T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473865 | |||||||
| chr16:1473883 | G | A | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0005c0018t0053g0275 |
3 | HG02109.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+951C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473883 | |||||||
| chr16:1473886 | G | A | 3 | a0001c0001t0001g0277 a0001c0002t0034g0276 a0005c0018t0053g0275 |
3 | HG02109.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+948C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473886 | |||||||
| chr16:1473891 | C | T | 7 | a0001c0004t0006g0019 a0001c0004t0006g0020 a0001c0004t0006g0021 others(4): Show |
7 | HG02258.hp2 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+943G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473891 | |||||||
| chr16:1474045 | T | C | 45 | a0001c0001t0001g0197 a0001c0001t0001g0202 a0001c0001t0001g0207 others(42): Show |
45 | HG00323.hp1 HG00597.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.141+789A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474045 | |||||||
| chr16:1474084 | C | CA | 238 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(235): Show |
248 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.141+749dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474084 | |||||||
| chr16:1474084 | C | CAA | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0002t0002g0012 others(2): Show |
6 | HG00673.hp2 HG02257.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+748_141+749dup others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474084 | |||||||
| chr16:1474237 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.141+597T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474237 | |||||||
| chr16:1474260 | G | T | 261 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(258): Show |
272 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.141+574C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474260 | |||||||
| chr16:1474293 | C | G | 5 | a0001c0002t0013g0029 a0001c0002t0013g0030 a0001c0002t0013g0033 others(2): Show |
5 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+541G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474293 | |||||||
| chr16:1474477 | C | G | 2 | a0002c0008t0027g0251 a0002c0008t0027g0252 |
2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.141+357G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474477 | |||||||
| chr16:1474483 | G | C | 5 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
5 | HG00609.hp1 NA18957.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+351C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474483 | |||||||
| chr16:1474521 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.141+313C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474521 | |||||||
| chr16:1474580 | G | A | 1 | a0001c0003t0002g0385 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.141+254C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474580 | |||||||
| chr16:1474603 | C | T | 274 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(271): Show |
285 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(282): Show |
intron_variant | MODIFIER | c.141+231G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474603 | |||||||
| chr16:1474695 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.141+139G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474695 | |||||||
| chr16:1474763 | G | A | 2 | a0001c0004t0001g0386 a0001c0004t0001g0387 |
2 | HG00609.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.141+71C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474763 | |||||||
| chr16:1474773 | G | GGCGC | 34 | a0001c0001t0001g0277 a0001c0002t0002g0012 a0001c0002t0002g0278 others(31): Show |
36 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.141+57_141+60dupGC others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474773 | |||||||
| chr16:1474815 | G | C | 1 | a0001c0002t0001g0282 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.141+19C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474815 | |||||||
| chr16:1474826 | G | C | 1 | a0002c0009t0005g0283 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.141+8C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474826 |