Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1183 |
| ensemblid | ENSG00000073464.13 |
| hgncid | 2022 |
| symbol | CLCN4 |
| name | chloride voltage-gated channel 4 |
| refseq_nuc | NM_001830.4 |
| refseq_prot | NP_001821.2 |
| ensembl_nuc | ENST00000380833.9 |
| ensembl_prot | ENSP00000370213.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 10156975 |
| end | 10237660 |
| strand | + |
| ver | v1.2 |
| region | chrX:10156975-10237660 |
| region5000 | chrX:10151975-10242660 |
| regionname0 | CLCN4_chrX_10156975_10237660 |
| regionname5000 | CLCN4_chrX_10151975_10242660 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2280 | 229 | 43 | 45 | 99 | 13 | 27 | CLCN4_chrX_10151975_10242660 | CLCN4 | ATGGT others(2275): Show |
chrX | 10151975 | 10242660 | ||
| a0001c0002 | 0/0 | 2280 | 30 | 24 | 5 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | ATGGT others(2275): Show |
chrX | 10151975 | 10242660 | ||
| a0001c0003 | 0/0 | 2280 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | ATGGT others(2275): Show |
chrX | 10151975 | 10242660 | ||
| a0001c0004 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | ATGGT others(2275): Show |
chrX | 10151975 | 10242660 | ||
| a0001c0005 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | ATGGT others(2275): Show |
chrX | 10151975 | 10242660 | ||
| a0001c0006 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | ATGGT others(2275): Show |
chrX | 10151975 | 10242660 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6760 | 70 | 1 | 18 | 40 | 3 | 7 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6755): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0002 | 0/0 | 6759 | 39 | 13 | 3 | 20 | 1 | 2 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0003 | 0/0 | 6759 | 45 | 0 | 5 | 25 | 2 | 13 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0004 | 1/0 | 6759 | 27 | 8 | 9 | 0 | 7 | 2 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0005 | 0/0 | 6760 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6755): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0006 | 0/0 | 6759 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0007 | 0/0 | 6759 | 4 | 0 | 4 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0008 | 0/0 | 6759 | 4 | 3 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0009 | 0/0 | 6759 | 3 | 2 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0010 | 0/0 | 6759 | 3 | 0 | 2 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0011 | 0/0 | 6759 | 3 | 0 | 0 | 3 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0012 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0013 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0014 | 0/0 | 6760 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6755): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0015 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0017 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0019 | 0/0 | 6759 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0020 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0021 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0022 | 0/0 | 6759 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0023 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0024 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0026 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6755): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0027 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0028 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6755): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0029 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6755): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0030 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0031 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6755): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0032 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0033 | 0/0 | 6759 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0001t0037 | 0/0 | 6759 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0002 | 0/0 | 6759 | 8 | 5 | 3 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0004 | 0/0 | 6759 | 14 | 12 | 2 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0009 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0013 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0015 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0018 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0025 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0034 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0035 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0002t0036 | 0/0 | 6759 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0003t0016 | 0/0 | 6760 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6755): Show |
chrX | 10151975 | 10242660 |
| a0001c0004t0002 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0005t0012 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| a0001c0006t0002 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | GAAAT others(6754): Show |
chrX | 10151975 | 10242660 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0008g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0009g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0010g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0011g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0011g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0013g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0014g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0015g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0017g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0019g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0020g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0021g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0022g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0023g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0024g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0026g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0027g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0028g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0029g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0030g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0031g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0032g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0033g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0001t0037g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0015g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0018g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0025g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0034g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0035g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0002t0036g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0003t0016g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0003t0016g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0004t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0005t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| a0001c0006t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0080 | EUR | GBR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0112 | EUR | GBR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0189 | EUR | FIN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | FIN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0187 | EUR | FIN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00597 | hp2 | a0001 | c0001 | t0026 | g0092 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00609 | hp1 | a0001 | c0001 | t0021 | g0244 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01074 | hp1 | a0001 | c0002 | t0004 | g0050 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01106 | hp1 | a0001 | c0002 | t0004 | g0042 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0148 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0141 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0142 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01192 | hp1 | a0001 | c0001 | t0019 | g0261 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0078 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0168 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01261 | hp1 | a0001 | c0001 | t0010 | g0167 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01346 | hp2 | a0001 | c0001 | t0037 | g0156 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0081 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0028 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0088 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0089 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01884 | hp1 | a0001 | c0002 | t0034 | g0033 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0145 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02015 | hp1 | a0001 | c0001 | t0011 | g0243 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0077 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02129 | hp1 | a0001 | c0001 | t0024 | g0118 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | CDX | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CDX | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02258 | hp1 | a0001 | c0004 | t0002 | g0100 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02293 | hp1 | a0001 | c0001 | t0007 | g0107 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02293 | hp2 | a0001 | c0001 | t0008 | g0056 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02451 | hp1 | a0001 | c0002 | t0035 | g0034 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0040 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02572 | hp1 | a0001 | c0002 | t0004 | g0037 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02602 | hp1 | a0001 | c0002 | t0036 | g0155 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0135 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02622 | hp2 | a0001 | c0002 | t0004 | g0031 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02630 | hp1 | a0001 | c0006 | t0002 | g0099 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0046 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02683 | hp1 | a0001 | c0001 | t0022 | g0123 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0132 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02818 | hp1 | a0001 | c0002 | t0004 | g0106 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02886 | hp2 | a0001 | c0001 | t0027 | g0098 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0057 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0047 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02970 | hp2 | a0001 | c0005 | t0012 | g0101 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02976 | hp1 | a0001 | c0001 | t0030 | g0066 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0049 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0068 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03195 | hp1 | a0001 | c0002 | t0009 | g0075 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0084 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0137 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03486 | hp1 | a0001 | c0002 | t0013 | g0032 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0048 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03516 | hp2 | a0001 | c0003 | t0016 | g0086 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03669 | hp2 | a0001 | c0001 | t0033 | g0016 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0226 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0184 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG04184 | hp2 | a0001 | c0001 | t0010 | g0059 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18522 | hp1 | a0001 | c0002 | t0018 | g0041 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | CHB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | CHB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18906 | hp1 | a0001 | c0001 | t0032 | g0073 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0045 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18942 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18961 | hp1 | a0001 | c0001 | t0014 | g0005 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18970 | hp1 | a0001 | c0001 | t0028 | g0258 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18983 | hp1 | a0001 | c0001 | t0031 | g0214 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19006 | hp1 | a0001 | c0001 | t0020 | g0172 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19010 | hp1 | a0001 | c0001 | t0011 | g0248 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19060 | hp2 | a0001 | c0001 | t0011 | g0180 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19080 | hp1 | a0001 | c0001 | t0023 | g0207 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19086 | hp1 | a0001 | c0001 | t0015 | g0199 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19088 | hp1 | a0001 | c0001 | t0029 | g0241 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19240 | hp1 | a0001 | c0003 | t0016 | g0087 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ASW | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0147 | AFR | ASW | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0116 | EUR | TSI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0262 | EUR | TSI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0246 | SAS | GIH | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0122 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02109 | hp2 | a0001 | c0002 | t0025 | g0035 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | USA | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0053 | AFR | USA | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0074 | AFR | USA | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA20300 | hp2 | a0001 | c0002 | t0015 | g0029 | AFR | USA | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0085 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0091 | REF | REF | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0114 | REF | REF | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:10208176 | G | A | 1 | a0001c0003 | 2 | HG03516.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.975G>A | p.Thr325Thr | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/13 | 1375/6759 | 975/2283 | 325/760 | chrX | 10208176 | |||
| chrX:10212514 | G | A | 2 | a0001c0002 a0001c0004 |
31 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(28): Show |
synonymous_variant | LOW | c.1437G>A | p.Ala479Ala | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/13 | 1837/6759 | 1437/2283 | 479/760 | chrX | 10212514 | |||
| chrX:10220716 | G | A | 1 | a0001c0005 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2031G>A | p.Thr677Thr | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/13 | 2431/6759 | 2031/2283 | 677/760 | chrX | 10220716 | |||
| chrX:10220869 | G | A | 2 | a0001c0004 a0001c0006 |
2 | HG02258.hp1 HG02630.hp1 |
synonymous_variant | LOW | c.2184G>A | p.Thr728Thr | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/13 | 2584/6759 | 2184/2283 | 728/760 | chrX | 10220869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:10158391 | C | T | 2 | a0001c0001t0037 a0001c0002t0036 |
2 | HG01346.hp2 HG02602.hp1 |
5_prime_UTR_variant | MODIFIER | c.-172C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26642 | chrX | 10158391 | ||||||
| chrX:10158392 | C | A | 1 | a0001c0001t0017 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-171C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26641 | chrX | 10158392 | ||||||
| chrX:10158394 | C | G | 1 | a0001c0003t0016 | 2 | HG03516.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-169C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26639 | chrX | 10158394 | ||||||
| chrX:10158419 | C | T | 2 | a0001c0002t0034 a0001c0002t0035 |
2 | HG01884.hp1 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-144C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26614 | chrX | 10158419 | ||||||
| chrX:10158424 | G | C | 2 | a0001c0002t0034 a0001c0002t0035 |
2 | HG01884.hp1 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-139G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26609 | chrX | 10158424 | ||||||
| chrX:10158425 | G | T | 2 | a0001c0002t0034 a0001c0002t0035 |
2 | HG01884.hp1 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-138G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26608 | chrX | 10158425 | ||||||
| chrX:10233677 | T | C | 2 | a0001c0001t0010 a0001c0002t0036 |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*93T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 93 | chrX | 10233677 | ||||||
| chrX:10233740 | A | G | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(25): Show |
159 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*156A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 156 | chrX | 10233740 | ||||||
| chrX:10233783 | C | T | 1 | a0001c0001t0033 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*199C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 199 | chrX | 10233783 | ||||||
| chrX:10234303 | C | T | 26 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(23): Show |
157 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*719C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 719 | chrX | 10234303 | ||||||
| chrX:10234708 | G | T | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0012 others(7): Show |
58 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1124G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1124 | chrX | 10234708 | ||||||
| chrX:10234796 | C | G | 1 | a0001c0001t0032 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1212 | chrX | 10234796 | ||||||
| chrX:10234814 | C | T | 1 | a0001c0001t0031 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1230C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1230 | chrX | 10234814 | ||||||
| chrX:10234891 | C | T | 1 | a0001c0002t0035 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1307 | chrX | 10234891 | ||||||
| chrX:10235148 | G | A | 13 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(10): Show |
66 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1564G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1564 | chrX | 10235148 | ||||||
| chrX:10235302 | G | A | 1 | a0001c0001t0007 | 4 | HG01168.hp2 HG01169.hp2 HG01981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1718G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1718 | chrX | 10235302 | ||||||
| chrX:10235308 | C | T | 2 | a0001c0001t0006 a0001c0001t0030 |
6 | HG02615.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1724C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1724 | chrX | 10235308 | ||||||
| chrX:10235355 | A | C | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(14): Show |
100 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1771A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1771 | chrX | 10235355 | ||||||
| chrX:10235487 | T | C | 2 | a0001c0001t0010 a0001c0002t0036 |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1903T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1903 | chrX | 10235487 | ||||||
| chrX:10235681 | G | A | 1 | a0001c0001t0024 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2097 | chrX | 10235681 | ||||||
| chrX:10235691 | C | T | 1 | a0001c0001t0029 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2107 | chrX | 10235691 | ||||||
| chrX:10235896 | T | C | 2 | a0001c0001t0005 a0001c0003t0016 |
7 | HG02809.hp2 HG03139.hp1 HG03516.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2312T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2312 | chrX | 10235896 | ||||||
| chrX:10236210 | G | A | 1 | a0001c0001t0011 | 3 | HG02015.hp1 NA19010.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2626G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2626 | chrX | 10236210 | ||||||
| chrX:10236227 | T | A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(28): Show |
164 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*2643T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2643 | chrX | 10236227 | ||||||
| chrX:10236232 | C | A | 1 | a0001c0001t0020 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2648C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2648 | chrX | 10236232 | ||||||
| chrX:10236591 | T | A | 1 | a0001c0001t0021 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3007T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3007 | chrX | 10236591 | ||||||
| chrX:10236669 | A | G | 1 | a0001c0001t0019 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3085A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3085 | chrX | 10236669 | ||||||
| chrX:10236772 | A | G | 15 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(12): Show |
96 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*3188A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3188 | chrX | 10236772 | ||||||
| chrX:10236835 | G | C | 1 | a0001c0001t0014 | 2 | NA18942.hp1 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3251G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3251 | chrX | 10236835 | ||||||
| chrX:10236983 | A | G | 2 | a0001c0001t0010 a0001c0002t0036 |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3399A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3399 | chrX | 10236983 | ||||||
| chrX:10237436 | G | A | 1 | a0001c0001t0028 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3852G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3852 | chrX | 10237436 | ||||||
| chrX:10237541 | C | A | 11 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0020 others(8): Show |
59 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3957C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3957 | chrX | 10237541 | ||||||
| chrX:10237548 | G | GT | 8 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(5): Show |
82 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3973dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3974 | INFO_REALIGN_3_PRIME | chrX | 10237548 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:10157125 | A | G | 4 | a0001c0001t0002g0260 a0001c0001t0004g0262 a0001c0001t0004g0263 others(1): Show |
4 | HG01081.hp2 HG01192.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-275+25A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157125 | |||||||
| chrX:10157233 | C | T | 105 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(102): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-275+133C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157233 | |||||||
| chrX:10157362 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-275+262G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157362 | |||||||
| chrX:10157394 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(48): Show |
52 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.-275+294C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157394 | |||||||
| chrX:10157520 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0003g0153 |
2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-275+420A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157520 | |||||||
| chrX:10157530 | T | C | 6 | a0001c0001t0004g0054 a0001c0001t0008g0055 a0001c0001t0008g0056 others(3): Show |
6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-275+430T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157530 | |||||||
| chrX:10157939 | G | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(50): Show |
54 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.-274-350G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157939 | |||||||
| chrX:10158030 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(48): Show |
52 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.-274-259C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10158030 | |||||||
| chrX:10158063 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(48): Show |
52 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.-274-226G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10158063 | |||||||
| chrX:10158088 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(2): Show |
5 | HG01081.hp1 HG02273.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-274-201G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10158088 | |||||||
| chrX:10158217 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-274-72T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10158217 | |||||||
| chrX:10158588 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-12+37G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10158588 | |||||||
| chrX:10158673 | T | C | 1 | a0001c0001t0003g0157 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-12+122T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10158673 | |||||||
| chrX:10159086 | T | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(26): Show |
30 | HG01070.hp1 HG01081.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12+535T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159086 | |||||||
| chrX:10159132 | AT | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(45): Show |
49 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-12+591delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10159132 | ||||||
| chrX:10159155 | T | A | 2 | a0001c0001t0005g0060 a0001c0001t0006g0062 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-12+604T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159155 | |||||||
| chrX:10159217 | T | G | 2 | a0001c0002t0002g0030 a0001c0002t0015g0029 |
2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-12+666T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159217 | |||||||
| chrX:10159426 | G | C | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+875G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159426 | |||||||
| chrX:10159597 | T | C | 1 | a0001c0002t0004g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-12+1046T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159597 | |||||||
| chrX:10159810 | G | C | 1 | a0001c0001t0006g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-12+1259G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159810 | |||||||
| chrX:10159845 | G | A | 1 | a0001c0001t0004g0069 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-12+1294G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159845 | |||||||
| chrX:10160159 | G | C | 2 | a0001c0001t0003g0071 a0001c0001t0004g0070 |
2 | HG00639.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-12+1608G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160159 | |||||||
| chrX:10160539 | A | G | 5 | a0001c0001t0004g0051 a0001c0002t0004g0046 a0001c0002t0004g0048 others(2): Show |
5 | HG01074.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1988A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160539 | |||||||
| chrX:10160665 | G | A | 2 | a0001c0001t0037g0156 a0001c0002t0036g0155 |
2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-12+2114G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160665 | |||||||
| chrX:10160727 | C | T | 6 | a0001c0001t0002g0152 a0001c0001t0004g0148 a0001c0001t0004g0151 others(3): Show |
6 | HG01109.hp1 HG02559.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+2176C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160727 | |||||||
| chrX:10160748 | A | G | 109 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(106): Show |
109 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-12+2197A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160748 | |||||||
| chrX:10160873 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-12+2322T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160873 | |||||||
| chrX:10160911 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(43): Show |
47 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.-12+2360C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160911 | |||||||
| chrX:10160937 | C | A | 2 | a0001c0001t0037g0156 a0001c0002t0036g0155 |
2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-12+2386C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160937 | |||||||
| chrX:10160939 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-12+2388G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160939 | |||||||
| chrX:10161029 | G | A | 1 | a0001c0001t0003g0159 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-12+2478G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161029 | |||||||
| chrX:10161124 | G | GCT | 27 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0250 others(24): Show |
27 | HG00597.hp2 HG01346.hp1 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.-12+2610_-12+2611d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | G | GCTCT | 22 | a0001c0001t0001g0237 a0001c0001t0001g0240 a0001c0001t0001g0242 others(19): Show |
22 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-12+2608_-12+2611d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | G | GCTCTCT | 10 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(7): Show |
10 | HG01346.hp2 HG02027.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+2606_-12+2611d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | G | GCTCTCTC others(1): Show |
50 | a0001c0001t0001g0193 a0001c0001t0001g0196 a0001c0001t0001g0197 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-12+2604_-12+2611d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | G | GCTCTCTC others(3): Show |
22 | a0001c0001t0001g0171 a0001c0001t0001g0174 a0001c0001t0001g0178 others(19): Show |
22 | HG00438.hp2 HG00597.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-12+2602_-12+2611d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | G | GCTCTCTC others(5): Show |
12 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0161 others(9): Show |
12 | HG00323.hp1 HG00438.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12+2600_-12+2611d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | G | GCTCTCTC others(7): Show |
3 | a0001c0001t0003g0160 a0001c0001t0004g0054 a0001c0002t0004g0049 |
3 | HG02976.hp2 NA18948.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-12+2598_-12+2611d others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | G | GCTCTCTC others(9): Show |
2 | a0001c0002t0004g0046 a0001c0002t0004g0048 |
2 | HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-12+2596_-12+2611d others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | G | GCTCTCTC others(11): Show |
1 | a0001c0002t0002g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-12+2594_-12+2611d others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | G | GCTCTCTC others(13): Show |
1 | a0001c0002t0002g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-12+2592_-12+2611d others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | GCT | G | 9 | a0001c0001t0002g0065 a0001c0001t0002g0260 a0001c0001t0005g0143 others(6): Show |
9 | HG01168.hp2 HG01169.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+2610_-12+2611d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | GCTCT | G | 11 | a0001c0001t0001g0144 a0001c0001t0002g0152 a0001c0001t0004g0148 others(8): Show |
11 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+2608_-12+2611d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | GCTCTCT | G | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0146 others(1): Show |
4 | HG02723.hp1 NA18970.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+2606_-12+2611d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161124 | GCTCTCTC others(3): Show |
G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(44): Show |
48 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-12+2602_-12+2611d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | ||||||
| chrX:10161334 | C | T | 11 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0008g0036 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+2783C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161334 | |||||||
| chrX:10161440 | G | T | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-12+2889G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161440 | |||||||
| chrX:10161532 | C | T | 6 | a0001c0001t0002g0152 a0001c0001t0004g0148 a0001c0001t0004g0151 others(3): Show |
6 | HG01109.hp1 HG02559.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+2981C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161532 | |||||||
| chrX:10161533 | G | A | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+2982G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161533 | |||||||
| chrX:10161657 | G | A | 102 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(99): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-12+3106G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161657 | |||||||
| chrX:10161794 | T | C | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-12+3243T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161794 | |||||||
| chrX:10161796 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-12+3245C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161796 | |||||||
| chrX:10161827 | G | A | 1 | a0001c0001t0006g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-12+3276G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161827 | |||||||
| chrX:10162013 | C | CT | 9 | a0001c0001t0002g0260 a0001c0001t0003g0071 a0001c0001t0003g0104 others(6): Show |
9 | HG00639.hp1 HG01256.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+3484dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10162013 | ||||||
| chrX:10162013 | CT | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(55): Show |
59 | HG00735.hp1 HG01070.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.-12+3484delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10162013 | ||||||
| chrX:10162013 | CTT | C | 89 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(86): Show |
89 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.-12+3483_-12+3484d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10162013 | ||||||
| chrX:10162064 | C | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(45): Show |
49 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-12+3513C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162064 | |||||||
| chrX:10162078 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-12+3527T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162078 | |||||||
| chrX:10162111 | T | G | 2 | a0001c0003t0016g0086 a0001c0003t0016g0087 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-12+3560T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162111 | |||||||
| chrX:10162121 | C | T | 6 | a0001c0001t0004g0054 a0001c0001t0008g0055 a0001c0001t0008g0056 others(3): Show |
6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+3570C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162121 | |||||||
| chrX:10162168 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-12+3617G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162168 | |||||||
| chrX:10162310 | C | T | 2 | a0001c0002t0002g0052 a0001c0002t0002g0053 |
2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-12+3759C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162310 | |||||||
| chrX:10162319 | G | A | 3 | a0001c0001t0004g0187 a0001c0001t0010g0167 a0001c0001t0010g0168 |
3 | HG00323.hp2 HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-12+3768G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162319 | |||||||
| chrX:10162913 | C | T | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+4362C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162913 | |||||||
| chrX:10162979 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
170 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.-12+4428G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162979 | |||||||
| chrX:10163118 | T | C | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+4567T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163118 | |||||||
| chrX:10163363 | A | AT | 8 | a0001c0001t0001g0249 a0001c0001t0004g0051 a0001c0001t0037g0156 others(5): Show |
8 | HG01074.hp1 HG01346.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+4825dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163363 | ||||||
| chrX:10163363 | A | ATT | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(43): Show |
47 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.-12+4824_-12+4825d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163363 | ||||||
| chrX:10163410 | TTTTC | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(43): Show |
47 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.-12+4863_-12+4866d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163410 | ||||||
| chrX:10163455 | C | T | 1 | a0001c0001t0003g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-12+4904C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163455 | |||||||
| chrX:10163563 | C | T | 17 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(14): Show |
17 | HG02135.hp1 HG03710.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.-12+5012C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163563 | |||||||
| chrX:10163628 | A | G | 2 | a0001c0001t0037g0156 a0001c0002t0036g0155 |
2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-12+5077A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163628 | |||||||
| chrX:10163657 | C | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0249 others(5): Show |
8 | NA18970.hp1 NA18981.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+5106C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163657 | |||||||
| chrX:10163702 | G | A | 1 | a0001c0002t0004g0106 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-12+5151G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163702 | |||||||
| chrX:10163981 | T | G | 1 | a0001c0002t0013g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12+5430T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163981 | |||||||
| chrX:10164101 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-12+5550G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164101 | |||||||
| chrX:10164127 | C | T | 1 | a0001c0001t0028g0258 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-12+5576C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164127 | |||||||
| chrX:10164210 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(45): Show |
49 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-12+5659T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164210 | |||||||
| chrX:10164784 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(26): Show |
30 | HG01070.hp1 HG01081.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12+6233G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164784 | |||||||
| chrX:10164942 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-12+6391C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164942 | |||||||
| chrX:10165010 | C | T | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+6459C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165010 | |||||||
| chrX:10165085 | C | T | 4 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0004t0002g0100 others(1): Show |
4 | HG02258.hp1 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+6534C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165085 | |||||||
| chrX:10165104 | A | G | 102 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(99): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-12+6553A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165104 | |||||||
| chrX:10165189 | G | A | 2 | a0001c0001t0003g0159 a0001c0001t0003g0169 |
2 | NA18747.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-12+6638G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165189 | |||||||
| chrX:10165213 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(2): Show |
5 | HG01081.hp1 HG02273.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+6662A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165213 | |||||||
| chrX:10165309 | C | T | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-12+6758C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165309 | |||||||
| chrX:10165377 | C | T | 1 | a0001c0002t0004g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-12+6826C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165377 | |||||||
| chrX:10165448 | C | T | 1 | a0001c0002t0004g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-12+6897C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165448 | |||||||
| chrX:10165717 | C | G | 2 | a0001c0001t0001g0245 a0001c0001t0004g0246 |
2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+7166C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165717 | |||||||
| chrX:10166361 | C | T | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-12+7810C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166361 | |||||||
| chrX:10166493 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(44): Show |
48 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-12+7942A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166493 | |||||||
| chrX:10166872 | G | A | 2 | a0001c0002t0034g0033 a0001c0002t0035g0034 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-12+8321G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166872 | |||||||
| chrX:10166899 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
171 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-12+8348A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166899 | |||||||
| chrX:10166909 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-12+8358C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166909 | |||||||
| chrX:10167042 | G | C | 2 | a0001c0001t0001g0245 a0001c0001t0004g0246 |
2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+8491G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167042 | |||||||
| chrX:10167121 | G | A | 6 | a0001c0001t0004g0054 a0001c0001t0008g0055 a0001c0001t0008g0056 others(3): Show |
6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+8570G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167121 | |||||||
| chrX:10167148 | T | G | 1 | a0001c0001t0003g0010 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-12+8597T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167148 | |||||||
| chrX:10167237 | G | T | 1 | a0001c0001t0004g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-12+8686G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167237 | |||||||
| chrX:10167325 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-12+8774C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167325 | |||||||
| chrX:10167409 | A | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG00597.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-12+8858A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167409 | |||||||
| chrX:10167702 | C | T | 6 | a0001c0001t0004g0054 a0001c0001t0008g0055 a0001c0001t0008g0056 others(3): Show |
6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+9151C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167702 | |||||||
| chrX:10167818 | G | C | 1 | a0001c0001t0007g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-12+9267G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167818 | |||||||
| chrX:10168084 | T | C | 10 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+9533T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168084 | |||||||
| chrX:10168277 | A | T | 3 | a0001c0001t0009g0078 a0001c0001t0032g0073 a0001c0002t0004g0045 |
3 | HG01243.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-12+9726A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168277 | |||||||
| chrX:10168284 | A | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG00597.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-12+9733A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168284 | |||||||
| chrX:10168588 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(57): Show |
61 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-12+10037C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168588 | |||||||
| chrX:10168621 | T | C | 1 | a0001c0001t0004g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-12+10070T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168621 | |||||||
| chrX:10168662 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(184): Show |
188 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.-12+10111A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168662 | |||||||
| chrX:10168800 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-12+10249C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168800 | |||||||
| chrX:10168805 | C | T | 3 | a0001c0001t0002g0131 a0001c0001t0006g0062 a0001c0002t0009g0075 |
3 | HG03195.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12+10254C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168805 | |||||||
| chrX:10169123 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+10572A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169123 | |||||||
| chrX:10169321 | A | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+10770A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169321 | |||||||
| chrX:10169345 | C | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(57): Show |
61 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-12+10794C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169345 | |||||||
| chrX:10169364 | G | T | 7 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0136 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+10813G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169364 | |||||||
| chrX:10169483 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+10932A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169483 | |||||||
| chrX:10169500 | AAAAC | A | 5 | a0001c0001t0002g0146 a0001c0002t0004g0046 a0001c0002t0004g0048 others(2): Show |
5 | HG01074.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+10969_-12+1097 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169500 | ||||||
| chrX:10169516 | C | A | 14 | a0001c0001t0002g0065 a0001c0001t0004g0054 a0001c0001t0006g0063 others(11): Show |
14 | HG01346.hp2 HG01884.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+10965C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169516 | |||||||
| chrX:10169520 | C | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+10969C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169520 | |||||||
| chrX:10169667 | G | A | 4 | a0001c0002t0002g0038 a0001c0002t0002g0039 a0001c0002t0002g0040 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+11116G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169667 | |||||||
| chrX:10169775 | CTTTTTCT others(11): Show |
C | 1 | a0001c0001t0006g0067 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-12+11230_-12+1124 others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169775 | ||||||
| chrX:10169776 | TTTTTCTT others(3): Show |
T | 4 | a0001c0001t0003g0010 a0001c0002t0004g0046 a0001c0002t0004g0049 others(1): Show |
4 | HG01074.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+11235_-12+1124 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169776 | ||||||
| chrX:10169779 | TTCTTTTC others(5): Show |
T | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-12+11230_-12+1124 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169779 | ||||||
| chrX:10169780 | TCTTTTCT others(4): Show |
T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(50): Show |
54 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+11230_-12+1124 others(15): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169780 | |||||||
| chrX:10169790 | T | C | 7 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0017g0057 others(4): Show |
7 | HG01346.hp2 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+11239T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169790 | |||||||
| chrX:10169791 | C | CT | 16 | a0001c0001t0001g0093 a0001c0001t0002g0131 a0001c0001t0002g0146 others(13): Show |
16 | HG01516.hp2 HG01517.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-12+11255dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169791 | ||||||
| chrX:10169791 | C | T | 13 | a0001c0001t0003g0010 a0001c0001t0004g0054 a0001c0001t0008g0055 others(10): Show |
13 | HG01074.hp1 HG01346.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+11240C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169791 | |||||||
| chrX:10169810 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-12+11259A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169810 | |||||||
| chrX:10169898 | C | G | 3 | a0001c0001t0003g0208 a0001c0001t0003g0209 a0001c0001t0003g0210 |
3 | NA18967.hp1 NA18984.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-12+11347C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169898 | |||||||
| chrX:10169934 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+11383A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169934 | |||||||
| chrX:10170330 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
171 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-12+11779A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170330 | |||||||
| chrX:10170357 | C | T | 6 | a0001c0001t0004g0054 a0001c0001t0008g0055 a0001c0001t0008g0056 others(3): Show |
6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+11806C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170357 | |||||||
| chrX:10170505 | G | C | 3 | a0001c0001t0004g0080 a0001c0001t0004g0109 a0001c0002t0002g0081 |
3 | HG00099.hp1 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-12+11954G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170505 | |||||||
| chrX:10170537 | G | T | 1 | a0001c0001t0002g0130 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-12+11986G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170537 | |||||||
| chrX:10170704 | C | T | 1 | a0001c0001t0017g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+12153C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170704 | |||||||
| chrX:10170733 | C | T | 1 | a0001c0001t0003g0177 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-12+12182C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170733 | |||||||
| chrX:10170758 | C | A | 5 | a0001c0001t0002g0065 a0001c0001t0006g0064 a0001c0001t0006g0067 others(2): Show |
5 | HG02622.hp1 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+12207C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170758 | |||||||
| chrX:10170758 | C | T | 2 | a0001c0001t0037g0156 a0001c0002t0036g0155 |
2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-12+12207C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170758 | |||||||
| chrX:10171517 | C | T | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+12966C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10171517 | |||||||
| chrX:10171609 | A | G | 5 | a0001c0001t0001g0128 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | NA18944.hp1 NA18981.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+13058A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10171609 | |||||||
| chrX:10171992 | A | G | 3 | a0001c0001t0009g0078 a0001c0001t0032g0073 a0001c0002t0004g0045 |
3 | HG01243.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11-13030A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10171992 | |||||||
| chrX:10172296 | C | T | 1 | a0001c0001t0007g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-11-12726C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10172296 | |||||||
| chrX:10172639 | G | T | 1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11-12383G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10172639 | |||||||
| chrX:10172684 | C | CGT | 110 | a0001c0001t0001g0124 a0001c0001t0001g0163 a0001c0001t0001g0164 others(107): Show |
110 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-11-12322_-11-1232 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10172684 | ||||||
| chrX:10172684 | C | CGTGT | 7 | a0001c0001t0003g0166 a0001c0001t0004g0054 a0001c0001t0008g0055 others(4): Show |
7 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-12324_-11-1232 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10172684 | ||||||
| chrX:10172691 | G | GTC | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(57): Show |
61 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-11-12330_-11-1232 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10172691 | ||||||
| chrX:10172734 | A | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.-11-12288A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10172734 | |||||||
| chrX:10173244 | C | T | 4 | a0001c0002t0004g0046 a0001c0002t0004g0048 a0001c0002t0004g0049 others(1): Show |
4 | HG01074.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11778C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173244 | |||||||
| chrX:10173263 | G | A | 7 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0136 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-11759G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173263 | |||||||
| chrX:10173317 | C | G | 1 | a0001c0001t0023g0207 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-11-11705C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173317 | |||||||
| chrX:10173328 | C | G | 2 | a0001c0001t0037g0156 a0001c0002t0036g0155 |
2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-11-11694C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173328 | |||||||
| chrX:10173333 | C | T | 1 | a0001c0001t0022g0123 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-11-11689C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173333 | |||||||
| chrX:10173375 | G | A | 1 | a0001c0002t0013g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11-11647G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173375 | |||||||
| chrX:10173383 | G | A | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-11639G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173383 | |||||||
| chrX:10173400 | G | A | 3 | a0001c0001t0002g0131 a0001c0001t0006g0062 a0001c0002t0009g0075 |
3 | HG03195.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-11622G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173400 | |||||||
| chrX:10173460 | G | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(54): Show |
58 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11-11562G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173460 | |||||||
| chrX:10173735 | C | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(54): Show |
58 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11-11287C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173735 | |||||||
| chrX:10173847 | C | G | 102 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(99): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-11-11175C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173847 | |||||||
| chrX:10174105 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-11-10917C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174105 | |||||||
| chrX:10174211 | C | T | 110 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(107): Show |
110 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-11-10811C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174211 | |||||||
| chrX:10174212 | C | T | 7 | a0001c0001t0002g0152 a0001c0001t0004g0148 a0001c0001t0004g0151 others(4): Show |
7 | HG01109.hp1 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-10810C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174212 | |||||||
| chrX:10174376 | T | G | 111 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(108): Show |
111 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.-11-10646T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174376 | |||||||
| chrX:10174420 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-11-10602C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174420 | |||||||
| chrX:10174532 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-10490G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174532 | |||||||
| chrX:10174601 | G | C | 2 | a0001c0001t0010g0167 a0001c0001t0010g0168 |
2 | HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-11-10421G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174601 | |||||||
| chrX:10174728 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(47): Show |
51 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.-11-10294C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174728 | |||||||
| chrX:10174841 | C | A | 1 | a0001c0001t0004g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11-10181C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174841 | |||||||
| chrX:10174965 | A | G | 103 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(100): Show |
103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-11-10057A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174965 | |||||||
| chrX:10175060 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0010g0059 |
3 | HG01515.hp1 HG01517.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-11-9962G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175060 | |||||||
| chrX:10175175 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(56): Show |
60 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.-11-9847G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175175 | |||||||
| chrX:10175357 | T | TTGGACCA others(8): Show |
4 | a0001c0001t0002g0076 a0001c0001t0002g0082 a0001c0001t0002g0083 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-9662_-11-9648d others(17): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175357 | ||||||
| chrX:10175404 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-11-9618G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175404 | |||||||
| chrX:10175444 | GCAGCCAG others(5): Show |
G | 1 | a0001c0001t0003g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-9577_-11-9566d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175444 | |||||||
| chrX:10175490 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
184 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-11-9532A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175490 | |||||||
| chrX:10175681 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
184 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-11-9341A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175681 | |||||||
| chrX:10175744 | C | T | 1 | a0001c0001t0004g0263 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-11-9278C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175744 | |||||||
| chrX:10175855 | C | CCT | 7 | a0001c0001t0005g0060 a0001c0001t0005g0143 a0001c0001t0009g0061 others(4): Show |
7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-9151_-11-9150d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175855 | ||||||
| chrX:10175857 | T | C | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-11-9165T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175857 | |||||||
| chrX:10175917 | T | TCTCTCTC others(15): Show |
6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-9099_-11-9078d others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175917 | ||||||
| chrX:10175941 | T | TCTCTCTC others(9): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0004g0176 |
3 | HG01168.hp1 HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-11-9078_-11-9077i others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175941 | ||||||
| chrX:10175945 | C | CCT | 7 | a0001c0001t0005g0060 a0001c0001t0005g0143 a0001c0001t0009g0061 others(4): Show |
7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-9052_-11-9051d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175945 | ||||||
| chrX:10175945 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
165 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-11-9077C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175945 | |||||||
| chrX:10175947 | T | TCTCCCCC others(7): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(43): Show |
47 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.-11-9072_-11-9071i others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175947 | ||||||
| chrX:10175947 | T | TCTCCCCC others(29): Show |
2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | HG03834.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-11-9072_-11-9071i others(38): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175947 | ||||||
| chrX:10175949 | T | TCCCCCCT others(12): Show |
1 | a0001c0001t0003g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-9072_-11-9071i others(21): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175949 | ||||||
| chrX:10175949 | T | TCCCCCTC others(11): Show |
115 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(112): Show |
115 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-11-9072_-11-9071i others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175949 | ||||||
| chrX:10175951 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0004g0176 |
3 | HG01168.hp1 HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-11-9071T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175951 | |||||||
| chrX:10175953 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(45): Show |
49 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11-9069T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175953 | |||||||
| chrX:10175972 | G | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-11-9050G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175972 | |||||||
| chrX:10175974 | G | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-11-9048G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175974 | |||||||
| chrX:10175976 | G | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(169): Show |
173 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-11-9046G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175976 | |||||||
| chrX:10176617 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-11-8405C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10176617 | |||||||
| chrX:10176866 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(61): Show |
65 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-11-8156G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10176866 | |||||||
| chrX:10177234 | C | T | 7 | a0001c0001t0004g0054 a0001c0001t0004g0148 a0001c0001t0008g0055 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7788C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177234 | |||||||
| chrX:10177271 | C | T | 7 | a0001c0001t0004g0054 a0001c0001t0004g0148 a0001c0001t0008g0055 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7751C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177271 | |||||||
| chrX:10177455 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(77): Show |
81 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.-11-7567T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177455 | |||||||
| chrX:10177661 | C | T | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-11-7361C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177661 | |||||||
| chrX:10177742 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-11-7280T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177742 | |||||||
| chrX:10178038 | ATACTGCA others(10): Show |
A | 2 | a0001c0001t0001g0024 a0001c0001t0003g0020 |
2 | HG01928.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-11-6964_-11-6948d others(19): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10178038 | ||||||
| chrX:10178287 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-11-6735G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10178287 | |||||||
| chrX:10178342 | T | C | 7 | a0001c0001t0004g0054 a0001c0001t0004g0148 a0001c0001t0008g0055 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-6680T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10178342 | |||||||
| chrX:10178512 | G | A | 7 | a0001c0001t0004g0054 a0001c0001t0004g0148 a0001c0001t0008g0055 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-6510G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10178512 | |||||||
| chrX:10179063 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(77): Show |
81 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.-11-5959T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179063 | |||||||
| chrX:10179236 | G | T | 103 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(100): Show |
103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-11-5786G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179236 | |||||||
| chrX:10179247 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(68): Show |
72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-5775C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179247 | |||||||
| chrX:10179259 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(68): Show |
72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-5763A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179259 | |||||||
| chrX:10179721 | A | G | 1 | a0001c0001t0023g0207 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-11-5301A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179721 | |||||||
| chrX:10179754 | C | T | 1 | a0001c0001t0004g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-11-5268C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179754 | |||||||
| chrX:10180041 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(68): Show |
72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-4981T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180041 | |||||||
| chrX:10180086 | A | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(68): Show |
72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-4936A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180086 | |||||||
| chrX:10180091 | G | A | 7 | a0001c0001t0005g0060 a0001c0001t0005g0143 a0001c0001t0009g0061 others(4): Show |
7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-4931G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180091 | |||||||
| chrX:10180201 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-4821G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180201 | |||||||
| chrX:10180455 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-11-4567C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180455 | |||||||
| chrX:10180640 | G | A | 102 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(99): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-11-4382G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180640 | |||||||
| chrX:10180707 | C | T | 11 | a0001c0001t0002g0065 a0001c0001t0004g0054 a0001c0001t0004g0148 others(8): Show |
11 | HG01109.hp1 HG02293.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-4315C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180707 | |||||||
| chrX:10180767 | C | CA | 85 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0174 others(82): Show |
85 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-11-4228dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | ||||||
| chrX:10180767 | C | CAA | 28 | a0001c0001t0001g0171 a0001c0001t0001g0222 a0001c0001t0001g0230 others(25): Show |
28 | HG00280.hp1 HG00738.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-4229_-11-4228d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | ||||||
| chrX:10180767 | CA | C | 11 | a0001c0001t0001g0093 a0001c0001t0004g0054 a0001c0001t0004g0148 others(8): Show |
11 | HG01109.hp1 HG01168.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-4228delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | ||||||
| chrX:10180767 | CAAAAA | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(29): Show |
33 | HG01070.hp1 HG01074.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-11-4232_-11-4228d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | ||||||
| chrX:10180767 | CAAAAAA | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(13): Show |
16 | HG00609.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11-4233_-11-4228d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | ||||||
| chrX:10180785 | AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0004g0133 a0001c0001t0004g0134 a0001c0002t0004g0147 |
3 | HG03195.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-11-4233_-11-4224d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180785 | ||||||
| chrX:10180841 | G | C | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-4181G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180841 | |||||||
| chrX:10180846 | G | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-11-4176G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180846 | |||||||
| chrX:10180877 | A | C | 1 | a0001c0001t0004g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-11-4145A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180877 | |||||||
| chrX:10181039 | A | G | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(6): Show |
9 | HG00639.hp2 HG01099.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11-3983A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181039 | |||||||
| chrX:10181114 | T | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(67): Show |
71 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-3908T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181114 | |||||||
| chrX:10181176 | A | T | 1 | a0001c0001t0011g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-11-3846A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181176 | |||||||
| chrX:10181196 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0025 |
2 | HG01070.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-11-3826G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181196 | |||||||
| chrX:10181330 | C | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(66): Show |
70 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11-3692C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181330 | |||||||
| chrX:10181331 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(66): Show |
70 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11-3691T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181331 | |||||||
| chrX:10181339 | A | G | 3 | a0001c0002t0004g0046 a0001c0002t0004g0048 a0001c0002t0004g0049 |
3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-11-3683A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181339 | |||||||
| chrX:10181361 | AAAAG | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(66): Show |
70 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11-3653_-11-3650d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10181361 | ||||||
| chrX:10181365 | GAAAGAAA others(8): Show |
G | 5 | a0001c0001t0004g0069 a0001c0001t0008g0036 a0001c0002t0002g0052 others(2): Show |
5 | HG01884.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-3634_-11-3620d others(17): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10181365 | ||||||
| chrX:10181718 | C | A | 1 | a0001c0002t0004g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-3304C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181718 | |||||||
| chrX:10181858 | G | A | 3 | a0001c0002t0004g0046 a0001c0002t0004g0048 a0001c0002t0004g0049 |
3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-11-3164G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181858 | |||||||
| chrX:10181868 | A | T | 2 | a0001c0001t0005g0060 a0001c0001t0005g0143 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-11-3154A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181868 | |||||||
| chrX:10182448 | T | C | 1 | a0001c0001t0007g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-11-2574T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182448 | |||||||
| chrX:10182457 | G | A | 4 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0169 others(1): Show |
4 | HG00323.hp1 NA18747.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-2565G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182457 | |||||||
| chrX:10182465 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-11-2557G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182465 | |||||||
| chrX:10182467 | G | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-2555G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182467 | |||||||
| chrX:10182743 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-2279T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182743 | |||||||
| chrX:10182748 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-2274A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182748 | |||||||
| chrX:10182937 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-2085T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182937 | |||||||
| chrX:10182991 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(67): Show |
71 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-2031C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182991 | |||||||
| chrX:10183157 | C | T | 2 | a0001c0001t0002g0131 a0001c0002t0009g0075 |
2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-1865C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183157 | |||||||
| chrX:10183232 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-1790A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183232 | |||||||
| chrX:10183325 | T | G | 1 | a0001c0001t0003g0191 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-11-1697T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183325 | |||||||
| chrX:10183387 | G | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-11-1635G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183387 | |||||||
| chrX:10183592 | C | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
176 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.-11-1430C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183592 | |||||||
| chrX:10183772 | A | G | 106 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(103): Show |
106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-11-1250A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183772 | |||||||
| chrX:10183832 | A | C | 9 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11-1190A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183832 | |||||||
| chrX:10184135 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(56): Show |
60 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.-11-887C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184135 | |||||||
| chrX:10184323 | GC | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(67): Show |
71 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-693delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10184323 | ||||||
| chrX:10184428 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-11-594G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184428 | |||||||
| chrX:10184585 | T | C | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-437T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184585 | |||||||
| chrX:10184599 | G | A | 1 | a0001c0001t0013g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11-423G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184599 | |||||||
| chrX:10184847 | T | C | 1 | a0001c0002t0004g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11-175T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184847 | |||||||
| chrX:10185334 | A | G | 104 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(101): Show |
104 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.144+158A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185334 | |||||||
| chrX:10185413 | C | G | 1 | a0001c0001t0004g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.144+237C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185413 | |||||||
| chrX:10185431 | C | G | 1 | a0001c0001t0002g0130 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.144+255C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185431 | |||||||
| chrX:10185433 | T | C | 2 | a0001c0002t0002g0052 a0001c0002t0002g0053 |
2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.144+257T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185433 | |||||||
| chrX:10185584 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.144+408G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185584 | |||||||
| chrX:10185623 | G | T | 1 | a0001c0001t0013g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.144+447G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185623 | |||||||
| chrX:10185710 | C | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(2): Show |
5 | HG01081.hp1 HG02273.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+534C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185710 | |||||||
| chrX:10185808 | G | C | 1 | a0001c0002t0009g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.144+632G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185808 | |||||||
| chrX:10185841 | G | A | 7 | a0001c0001t0005g0060 a0001c0001t0005g0143 a0001c0001t0009g0061 others(4): Show |
7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.144+665G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185841 | |||||||
| chrX:10185849 | C | T | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.144+673C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185849 | |||||||
| chrX:10186146 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.144+970C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186146 | |||||||
| chrX:10186176 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.144+1000C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186176 | |||||||
| chrX:10186229 | G | A | 1 | a0001c0001t0002g0129 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.144+1053G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186229 | |||||||
| chrX:10186255 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(56): Show |
60 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.144+1079G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186255 | |||||||
| chrX:10186560 | G | A | 102 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(99): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.145-955G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186560 | |||||||
| chrX:10186608 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.145-907G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186608 | |||||||
| chrX:10186629 | G | T | 105 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(102): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.145-886G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186629 | |||||||
| chrX:10186874 | C | T | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-641C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186874 | |||||||
| chrX:10186940 | C | A | 1 | a0001c0001t0003g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.145-575C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186940 | |||||||
| chrX:10187343 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(56): Show |
60 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.145-172G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10187343 | |||||||
| chrX:10187473 | G | A | 2 | a0001c0001t0009g0078 a0001c0002t0004g0045 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.145-42G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10187473 | |||||||
| chrX:10187618 | C | G | 5 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.244+4C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10187618 | |||||||
| chrX:10187681 | C | T | 4 | a0001c0001t0002g0152 a0001c0001t0004g0151 a0001c0001t0005g0149 others(1): Show |
4 | HG02559.hp2 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+67C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10187681 | |||||||
| chrX:10187721 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.244+107T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10187721 | |||||||
| chrX:10188143 | T | C | 3 | a0001c0002t0004g0050 a0001c0002t0004g0106 a0001c0002t0025g0035 |
3 | HG01074.hp1 HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.244+529T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188143 | |||||||
| chrX:10188198 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.244+584A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188198 | |||||||
| chrX:10188244 | G | T | 6 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.244+630G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188244 | |||||||
| chrX:10188509 | A | G | 1 | a0001c0001t0008g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.244+895A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188509 | |||||||
| chrX:10188969 | G | A | 103 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(100): Show |
103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.244+1355G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188969 | |||||||
| chrX:10189096 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(87): Show |
91 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.244+1482A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189096 | |||||||
| chrX:10189377 | G | T | 23 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(20): Show |
23 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.244+1763G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189377 | |||||||
| chrX:10189489 | G | A | 1 | a0001c0002t0004g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244+1875G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189489 | |||||||
| chrX:10189770 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
94 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(91): Show |
intron_variant | MODIFIER | c.244+2156T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189770 | |||||||
| chrX:10189837 | G | A | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.244+2223G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189837 | |||||||
| chrX:10190072 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.244+2458G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10190072 | |||||||
| chrX:10190113 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.244+2499C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10190113 | |||||||
| chrX:10190306 | C | T | 1 | a0001c0002t0002g0040 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244+2692C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10190306 | |||||||
| chrX:10190720 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.244+3106C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10190720 | |||||||
| chrX:10191387 | A | C | 1 | a0001c0001t0003g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.245-3524A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10191387 | |||||||
| chrX:10191542 | G | A | 4 | a0001c0001t0002g0131 a0001c0001t0006g0062 a0001c0001t0032g0073 others(1): Show |
4 | HG03195.hp1 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-3369G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10191542 | |||||||
| chrX:10191618 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
93 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.245-3293T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10191618 | |||||||
| chrX:10191692 | A | AT | 93 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0124 others(90): Show |
93 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.245-3191dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | A | ATT | 29 | a0001c0001t0001g0072 a0001c0001t0001g0182 a0001c0001t0001g0183 others(26): Show |
29 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.245-3192_245-3191d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | A | ATTT | 8 | a0001c0001t0001g0249 a0001c0001t0001g0255 a0001c0001t0002g0120 others(5): Show |
8 | HG00438.hp2 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.245-3193_245-3191d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | A | ATTTTTTT others(9): Show |
1 | a0001c0002t0002g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.245-3206_245-3191d others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | A | ATTTTTTT others(10): Show |
3 | a0001c0001t0002g0094 a0001c0001t0006g0067 a0001c0001t0030g0066 |
3 | HG02622.hp1 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.245-3207_245-3191d others(19): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | A | ATTTTTTT others(11): Show |
5 | a0001c0001t0002g0096 a0001c0001t0006g0063 a0001c0001t0006g0064 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-3208_245-3191d others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | A | ATTTTTTT others(13): Show |
1 | a0001c0006t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.245-3210_245-3191d others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0002g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.245-3211_245-3191d others(23): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0002g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-3212_245-3191d others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | A | ATTTTTTT others(19): Show |
1 | a0001c0001t0027g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.245-3216_245-3191d others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | AT | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0002g0018 others(9): Show |
12 | HG01168.hp2 HG01169.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.245-3191delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | ATT | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(33): Show |
37 | HG00609.hp1 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.245-3192_245-3191d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191692 | ATTT | A | 14 | a0001c0001t0001g0012 a0001c0001t0002g0043 a0001c0001t0004g0089 others(11): Show |
14 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.245-3193_245-3191d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | ||||||
| chrX:10191966 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(31): Show |
35 | HG00609.hp1 HG01070.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.245-2945C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10191966 | |||||||
| chrX:10192175 | A | AC | 9 | a0001c0001t0002g0131 a0001c0001t0004g0054 a0001c0001t0004g0148 others(6): Show |
9 | HG01109.hp1 HG02293.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.245-2730dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192175 | ||||||
| chrX:10192244 | T | TAC | 13 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0144 others(10): Show |
13 | HG02083.hp1 HG02132.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.245-2640_245-2639d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | ||||||
| chrX:10192244 | T | TACAC | 19 | a0001c0001t0001g0115 a0001c0001t0002g0131 a0001c0001t0002g0146 others(16): Show |
19 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.245-2642_245-2639d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | ||||||
| chrX:10192244 | T | TACACACA others(3): Show |
10 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-2648_245-2639d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | ||||||
| chrX:10192244 | T | TACACACA others(5): Show |
3 | a0001c0002t0004g0046 a0001c0002t0004g0048 a0001c0002t0004g0049 |
3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.245-2650_245-2639d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | ||||||
| chrX:10192244 | T | TACACACA others(7): Show |
1 | a0001c0001t0002g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-2652_245-2639d others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | ||||||
| chrX:10192286 | AAGAG | A | 11 | a0001c0001t0002g0065 a0001c0001t0002g0094 a0001c0001t0002g0096 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.245-2622_245-2619d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192286 | ||||||
| chrX:10192342 | C | A | 1 | a0001c0001t0032g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.245-2569C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192342 | |||||||
| chrX:10192438 | A | G | 1 | a0001c0001t0003g0177 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.245-2473A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192438 | |||||||
| chrX:10192598 | G | C | 23 | a0001c0001t0002g0131 a0001c0001t0002g0146 a0001c0001t0004g0054 others(20): Show |
23 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.245-2313G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192598 | |||||||
| chrX:10192803 | T | C | 1 | a0001c0002t0004g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.245-2108T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192803 | |||||||
| chrX:10192874 | T | G | 1 | a0001c0002t0004g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.245-2037T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192874 | |||||||
| chrX:10193030 | G | C | 1 | a0001c0001t0001g0227 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.245-1881G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193030 | |||||||
| chrX:10193060 | A | G | 1 | a0001c0001t0003g0219 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.245-1851A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193060 | |||||||
| chrX:10193254 | G | A | 5 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-1657G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193254 | |||||||
| chrX:10193259 | G | A | 2 | a0001c0002t0004g0050 a0001c0002t0004g0106 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.245-1652G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193259 | |||||||
| chrX:10193561 | G | A | 205 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0110 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.245-1350G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193561 | |||||||
| chrX:10193613 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.245-1298G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193613 | |||||||
| chrX:10193859 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.245-1052C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193859 | |||||||
| chrX:10193861 | T | G | 110 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(107): Show |
110 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.245-1050T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193861 | |||||||
| chrX:10193961 | G | GT | 108 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(105): Show |
108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.245-938dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10193961 | ||||||
| chrX:10193961 | GT | G | 69 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0110 others(66): Show |
69 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(66): Show |
intron_variant | MODIFIER | c.245-938delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10193961 | ||||||
| chrX:10193961 | GTT | G | 5 | a0001c0001t0002g0146 a0001c0001t0005g0079 a0001c0002t0004g0046 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-939_245-938del others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10193961 | ||||||
| chrX:10194154 | T | C | 18 | a0001c0001t0002g0065 a0001c0001t0002g0094 a0001c0001t0002g0096 others(15): Show |
18 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.245-757T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194154 | |||||||
| chrX:10194184 | G | A | 59 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0110 others(56): Show |
59 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(56): Show |
intron_variant | MODIFIER | c.245-727G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194184 | |||||||
| chrX:10194222 | G | T | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-689G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194222 | |||||||
| chrX:10194622 | A | G | 2 | a0001c0002t0034g0033 a0001c0002t0035g0034 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.245-289A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194622 | |||||||
| chrX:10194840 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0011g0248 |
2 | NA18997.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.245-71C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194840 | |||||||
| chrX:10195127 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.432+29G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195127 | |||||||
| chrX:10195138 | G | A | 5 | a0001c0001t0002g0146 a0001c0001t0005g0079 a0001c0002t0004g0046 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.432+40G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195138 | |||||||
| chrX:10195217 | C | T | 16 | a0001c0001t0002g0065 a0001c0001t0002g0094 a0001c0001t0002g0096 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.432+119C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195217 | |||||||
| chrX:10195314 | CAT | C | 11 | a0001c0001t0002g0065 a0001c0001t0002g0094 a0001c0001t0002g0096 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.432+232_432+233del others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195314 | ||||||
| chrX:10195574 | C | T | 6 | a0001c0001t0001g0197 a0001c0001t0002g0146 a0001c0001t0005g0079 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+476C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195574 | |||||||
| chrX:10195840 | G | A | 25 | a0001c0001t0002g0131 a0001c0001t0002g0146 a0001c0001t0004g0054 others(22): Show |
25 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.432+742G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195840 | |||||||
| chrX:10195866 | C | A | 1 | a0001c0001t0003g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+768C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195866 | |||||||
| chrX:10196059 | C | T | 1 | a0001c0001t0003g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+961C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196059 | |||||||
| chrX:10196066 | A | G | 228 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0110 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.432+968A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196066 | |||||||
| chrX:10196138 | T | C | 11 | a0001c0001t0002g0065 a0001c0001t0002g0094 a0001c0001t0002g0096 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.432+1040T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196138 | |||||||
| chrX:10196282 | G | T | 24 | a0001c0001t0002g0131 a0001c0001t0002g0146 a0001c0001t0004g0054 others(21): Show |
24 | HG01109.hp1 HG01243.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.432+1184G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196282 | |||||||
| chrX:10196495 | T | G | 205 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0110 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.432+1397T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196495 | |||||||
| chrX:10196538 | C | CTTTT | 12 | a0001c0001t0002g0065 a0001c0001t0002g0094 a0001c0001t0002g0096 others(9): Show |
12 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.433-1387_433-1384d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | ||||||
| chrX:10196538 | C | CTTTTT | 15 | a0001c0001t0002g0131 a0001c0001t0004g0054 a0001c0001t0005g0060 others(12): Show |
15 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.433-1388_433-1384d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | ||||||
| chrX:10196538 | C | CTTTTTT | 11 | a0001c0001t0004g0088 a0001c0001t0004g0148 a0001c0001t0005g0079 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-1389_433-1384d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | ||||||
| chrX:10196538 | C | CTTTTTTT | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(47): Show |
51 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.433-1390_433-1384d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | ||||||
| chrX:10196538 | CT | C | 60 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0110 others(57): Show |
60 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(57): Show |
intron_variant | MODIFIER | c.433-1384delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | ||||||
| chrX:10196651 | A | G | 1 | a0001c0001t0004g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.433-1288A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196651 | |||||||
| chrX:10196687 | T | C | 38 | a0001c0001t0002g0065 a0001c0001t0002g0094 a0001c0001t0002g0096 others(35): Show |
38 | HG01109.hp1 HG01243.hp1 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.433-1252T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196687 | |||||||
| chrX:10196768 | G | A | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-1171G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196768 | |||||||
| chrX:10196969 | G | T | 57 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0110 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(54): Show |
intron_variant | MODIFIER | c.433-970G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196969 | |||||||
| chrX:10197363 | T | A | 169 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0110 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.433-576T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197363 | |||||||
| chrX:10197507 | G | A | 3 | a0001c0002t0004g0046 a0001c0002t0004g0048 a0001c0002t0004g0049 |
3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.433-432G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197507 | |||||||
| chrX:10197519 | G | T | 4 | a0001c0001t0002g0146 a0001c0002t0004g0046 a0001c0002t0004g0048 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-420G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197519 | |||||||
| chrX:10197560 | A | G | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-379A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197560 | |||||||
| chrX:10197755 | C | T | 1 | a0001c0001t0004g0134 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.433-184C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197755 | |||||||
| chrX:10198158 | A | C | 72 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0110 others(69): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.555+97A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198158 | |||||||
| chrX:10198437 | C | T | 5 | a0001c0001t0009g0078 a0001c0002t0004g0045 a0001c0002t0004g0046 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.555+376C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198437 | |||||||
| chrX:10198615 | G | A | 2 | a0001c0001t0037g0156 a0001c0002t0036g0155 |
2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.555+554G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198615 | |||||||
| chrX:10198842 | C | G | 11 | a0001c0001t0002g0065 a0001c0001t0002g0146 a0001c0001t0006g0063 others(8): Show |
11 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.555+781C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198842 | |||||||
| chrX:10198884 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(68): Show |
72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.555+823C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198884 | |||||||
| chrX:10198984 | C | T | 1 | a0001c0001t0009g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.555+923C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198984 | |||||||
| chrX:10199082 | A | G | 1 | a0001c0001t0006g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.555+1021A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10199082 | |||||||
| chrX:10199515 | ACAG | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
132 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.555+1458_555+1460d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10199515 | ||||||
| chrX:10199849 | C | T | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.555+1788C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10199849 | |||||||
| chrX:10199906 | G | GT | 9 | a0001c0001t0005g0060 a0001c0001t0005g0143 a0001c0001t0009g0061 others(6): Show |
9 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+1846dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10199906 | ||||||
| chrX:10200031 | G | A | 1 | a0001c0005t0012g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.555+1970G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200031 | |||||||
| chrX:10200066 | T | A | 1 | a0001c0002t0013g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.555+2005T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200066 | |||||||
| chrX:10200257 | A | C | 7 | a0001c0001t0002g0065 a0001c0001t0002g0146 a0001c0001t0006g0063 others(4): Show |
7 | HG02615.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+2196A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200257 | |||||||
| chrX:10200582 | C | G | 61 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0182 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.555+2521C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200582 | |||||||
| chrX:10200661 | G | T | 61 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0182 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.555+2600G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200661 | |||||||
| chrX:10200729 | C | T | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.555+2668C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200729 | |||||||
| chrX:10201051 | AT | A | 4 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0136 others(1): Show |
4 | HG02258.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+2991delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201051 | |||||||
| chrX:10201091 | G | A | 61 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0182 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.555+3030G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201091 | |||||||
| chrX:10201202 | G | C | 10 | a0001c0001t0002g0131 a0001c0001t0005g0060 a0001c0001t0005g0143 others(7): Show |
10 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.555+3141G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201202 | |||||||
| chrX:10201272 | G | A | 1 | a0001c0002t0004g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.555+3211G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201272 | |||||||
| chrX:10201417 | A | G | 2 | a0001c0001t0004g0069 a0001c0002t0004g0135 |
2 | HG02615.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.555+3356A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201417 | |||||||
| chrX:10201648 | G | A | 11 | a0001c0001t0004g0051 a0001c0001t0004g0148 a0001c0001t0008g0055 others(8): Show |
11 | HG01109.hp1 HG01346.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.555+3587G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201648 | |||||||
| chrX:10201664 | C | T | 10 | a0001c0001t0002g0131 a0001c0001t0005g0060 a0001c0001t0005g0143 others(7): Show |
10 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.555+3603C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201664 | |||||||
| chrX:10201706 | C | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
214 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.555+3645C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201706 | |||||||
| chrX:10201835 | C | T | 3 | a0001c0001t0002g0162 a0001c0001t0003g0159 a0001c0001t0003g0169 |
3 | HG00323.hp1 NA18747.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.555+3774C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201835 | |||||||
| chrX:10201941 | C | G | 2 | a0001c0001t0007g0141 a0001c0001t0007g0142 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.555+3880C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201941 | |||||||
| chrX:10201999 | A | C | 51 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0182 others(48): Show |
51 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.555+3938A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201999 | |||||||
| chrX:10202115 | T | C | 3 | a0001c0001t0002g0131 a0001c0001t0006g0062 a0001c0002t0009g0075 |
3 | HG03195.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.555+4054T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202115 | |||||||
| chrX:10202231 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(123): Show |
127 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.556-4127T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202231 | |||||||
| chrX:10202245 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0014g0003 others(1): Show |
4 | HG02273.hp1 NA18942.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-4113G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202245 | |||||||
| chrX:10202324 | A | G | 51 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0182 others(48): Show |
51 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.556-4034A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202324 | |||||||
| chrX:10202414 | A | G | 1 | a0001c0002t0002g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.556-3944A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202414 | |||||||
| chrX:10202638 | C | CA | 6 | a0001c0001t0001g0245 a0001c0001t0002g0120 a0001c0001t0003g0140 others(3): Show |
6 | HG01192.hp1 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-3688dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CA | C | 36 | a0001c0001t0001g0128 a0001c0001t0001g0154 a0001c0001t0001g0182 others(33): Show |
36 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.556-3688delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CAA | C | 13 | a0001c0001t0003g0157 a0001c0001t0003g0184 a0001c0001t0003g0208 others(10): Show |
13 | HG01109.hp1 HG02293.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.556-3689_556-3688d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CAAA | C | 7 | a0001c0001t0002g0065 a0001c0001t0006g0063 a0001c0001t0006g0064 others(4): Show |
7 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.556-3690_556-3688d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CAAAA | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0183 others(15): Show |
18 | HG01081.hp1 HG01123.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.556-3691_556-3688d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CAAAAA | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(93): Show |
97 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.556-3692_556-3688d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CAAAAAA | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0197 a0001c0001t0001g0212 others(7): Show |
10 | HG01884.hp2 HG02735.hp1 HG06807.hp2 others(7): Show |
intron_variant | MODIFIER | c.556-3693_556-3688d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CAAAAAAA | C | 6 | a0001c0001t0001g0144 a0001c0001t0002g0094 a0001c0001t0002g0096 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-3694_556-3688d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0002g0131 a0001c0001t0005g0060 a0001c0001t0005g0143 others(6): Show |
9 | HG02630.hp1 HG02809.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.556-3695_556-3688d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0012g0137 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.556-3700_556-3688d others(15): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202638 | CAAAAAAA others(8): Show |
C | 8 | a0001c0001t0002g0076 a0001c0001t0002g0082 a0001c0001t0002g0083 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.556-3702_556-3688d others(17): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | ||||||
| chrX:10202697 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
133 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.556-3661G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202697 | |||||||
| chrX:10202697 | G | T | 10 | a0001c0001t0002g0131 a0001c0001t0005g0060 a0001c0001t0005g0143 others(7): Show |
10 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.556-3661G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202697 | |||||||
| chrX:10202922 | C | T | 7 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-3436C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202922 | |||||||
| chrX:10202952 | C | T | 3 | a0001c0001t0003g0173 a0001c0001t0003g0188 a0001c0001t0003g0192 |
3 | NA18612.hp1 NA18974.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.556-3406C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202952 | |||||||
| chrX:10203025 | A | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.556-3333A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10203025 | |||||||
| chrX:10203386 | G | C | 1 | a0001c0001t0004g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.556-2972G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10203386 | |||||||
| chrX:10204025 | C | T | 3 | a0001c0001t0002g0131 a0001c0001t0006g0062 a0001c0002t0009g0075 |
3 | HG03195.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.556-2333C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10204025 | |||||||
| chrX:10204135 | A | G | 1 | a0001c0002t0013g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.556-2223A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10204135 | |||||||
| chrX:10204613 | C | CT | 32 | a0001c0001t0001g0072 a0001c0001t0001g0110 a0001c0001t0001g0124 others(29): Show |
32 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.556-1709dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | C | CTT | 52 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0027 others(49): Show |
52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.556-1710_556-1709d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | C | CTTT | 30 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(27): Show |
31 | HG01255.hp1 HG01257.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.556-1711_556-1709d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | C | CTTTT | 47 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0171 others(44): Show |
47 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.556-1712_556-1709d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | C | CTTTTT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0164 a0001c0001t0001g0185 others(13): Show |
16 | HG00438.hp1 HG01258.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.556-1713_556-1709d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | C | CTTTTTT | 8 | a0001c0001t0001g0213 a0001c0001t0001g0231 a0001c0001t0001g0232 others(5): Show |
8 | HG02027.hp1 HG02074.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.556-1714_556-1709d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0030g0066 a0001c0001t0037g0156 a0001c0002t0036g0155 |
3 | HG01346.hp2 HG02602.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.556-1720_556-1709d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0006g0064 a0001c0001t0032g0073 |
2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.556-1721_556-1709d others(15): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | C | CTTTTTTT others(7): Show |
5 | a0001c0001t0002g0065 a0001c0001t0002g0146 a0001c0001t0006g0063 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.556-1722_556-1709d others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0002g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.556-1718_556-1709d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0240 a0001c0001t0003g0157 a0001c0001t0005g0060 others(3): Show |
6 | HG02040.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-1719_556-1709d others(13): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0001g0254 a0001c0001t0002g0131 a0001c0001t0006g0062 others(3): Show |
6 | HG02965.hp1 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-1720_556-1709d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0193 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.556-1721_556-1709d others(15): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0004g0069 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.556-1723_556-1709d others(17): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | CTTTTTTT others(9): Show |
C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(2): Show |
5 | HG01123.hp2 HG02273.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.556-1724_556-1709d others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204613 | CTTTTTTT others(13): Show |
C | 16 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(13): Show |
16 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.556-1728_556-1709d others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | ||||||
| chrX:10204992 | C | T | 1 | a0001c0005t0012g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.556-1366C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10204992 | |||||||
| chrX:10205240 | A | G | 6 | a0001c0001t0001g0128 a0001c0001t0002g0105 a0001c0001t0002g0125 others(3): Show |
6 | NA18944.hp1 NA18968.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-1118A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205240 | |||||||
| chrX:10205256 | A | G | 6 | a0001c0001t0001g0128 a0001c0001t0002g0105 a0001c0001t0002g0125 others(3): Show |
6 | NA18944.hp1 NA18968.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-1102A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205256 | |||||||
| chrX:10205259 | A | G | 6 | a0001c0001t0001g0128 a0001c0001t0002g0105 a0001c0001t0002g0125 others(3): Show |
6 | NA18944.hp1 NA18968.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-1099A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205259 | |||||||
| chrX:10205269 | G | C | 21 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(18): Show |
21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.556-1089G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205269 | |||||||
| chrX:10205273 | T | A | 21 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(18): Show |
21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.556-1085T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205273 | |||||||
| chrX:10205428 | G | T | 19 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(16): Show |
19 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.556-930G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205428 | |||||||
| chrX:10205447 | T | A | 1 | a0001c0001t0002g0019 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.556-911T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205447 | |||||||
| chrX:10205472 | C | CA | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(122): Show |
126 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.556-868dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205472 | ||||||
| chrX:10205472 | C | CAA | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0235 others(10): Show |
13 | HG02074.hp1 HG02622.hp2 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.556-869_556-868dup others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205472 | ||||||
| chrX:10205484 | AAAAAAAG | A | 5 | a0001c0001t0004g0148 a0001c0001t0006g0062 a0001c0001t0008g0055 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-868_556-862del others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205484 | ||||||
| chrX:10205485 | AAAAAAG | A | 7 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0017g0057 others(4): Show |
7 | HG02717.hp1 HG02886.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-863_556-858del others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205485 | ||||||
| chrX:10205607 | C | CT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0213 others(4): Show |
7 | HG01346.hp2 HG02135.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-733dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205607 | ||||||
| chrX:10205607 | CT | C | 30 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(27): Show |
30 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.556-733delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205607 | ||||||
| chrX:10205751 | G | T | 2 | a0001c0001t0037g0156 a0001c0002t0036g0155 |
2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.556-607G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205751 | |||||||
| chrX:10205758 | T | C | 21 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(18): Show |
21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.556-600T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205758 | |||||||
| chrX:10205784 | CT | C | 6 | a0001c0001t0005g0079 a0001c0001t0005g0149 a0001c0001t0005g0150 others(3): Show |
6 | HG02647.hp1 HG02976.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-563delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205784 | ||||||
| chrX:10206049 | T | C | 21 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(18): Show |
21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.556-309T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10206049 | |||||||
| chrX:10206099 | G | A | 7 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-259G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10206099 | |||||||
| chrX:10206346 | C | T | 52 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0182 others(49): Show |
52 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.556-12C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10206346 | |||||||
| chrX:10206900 | T | TTTTTGTT others(3): Show |
19 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(16): Show |
19 | HG01109.hp1 HG02293.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.843+128_843+129ins others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206900 | ||||||
| chrX:10206905 | T | TTGTTTTG | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0003g0160 others(3): Show |
6 | HG01257.hp2 HG01258.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.843+129_843+130ins others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10206905 | |||||||
| chrX:10206905 | T | TTGTTTTG others(6): Show |
41 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0182 others(38): Show |
41 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.843+129_843+130ins others(13): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10206905 | |||||||
| chrX:10206906 | G | GT | 21 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(18): Show |
21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.843+134dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206906 | ||||||
| chrX:10206906 | G | GTTTTGT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): Show |
124 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.843+153_843+158dup others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206906 | ||||||
| chrX:10206906 | G | GTTTTGTT others(5): Show |
17 | a0001c0001t0002g0065 a0001c0001t0002g0094 a0001c0001t0002g0096 others(14): Show |
17 | HG01243.hp1 HG01346.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.843+147_843+158dup others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206906 | ||||||
| chrX:10206906 | G | T | 47 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0182 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.843+130G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10206906 | |||||||
| chrX:10207128 | T | G | 1 | a0001c0001t0009g0078 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.843+352T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207128 | |||||||
| chrX:10207196 | C | T | 1 | a0001c0002t0004g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.843+420C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207196 | |||||||
| chrX:10207225 | G | C | 12 | a0001c0001t0002g0131 a0001c0001t0005g0060 a0001c0001t0005g0143 others(9): Show |
12 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+449G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207225 | |||||||
| chrX:10207348 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.843+572C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207348 | |||||||
| chrX:10207421 | G | A | 21 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(18): Show |
21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-624G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207421 | |||||||
| chrX:10207440 | C | T | 21 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(18): Show |
21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-605C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207440 | |||||||
| chrX:10207512 | T | C | 21 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(18): Show |
21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-533T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207512 | |||||||
| chrX:10207551 | GTTTT | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0014g0003 others(1): Show |
4 | HG02273.hp1 NA18942.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-493_844-490del others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207551 | |||||||
| chrX:10207682 | C | A | 3 | a0001c0001t0005g0079 a0001c0001t0005g0149 a0001c0001t0005g0150 |
3 | NA19030.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.844-363C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207682 | |||||||
| chrX:10207702 | A | G | 22 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(19): Show |
22 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(19): Show |
intron_variant | MODIFIER | c.844-343A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207702 | |||||||
| chrX:10207882 | C | T | 7 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.844-163C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207882 | |||||||
| chrX:10208670 | G | A | 7 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+80G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10208670 | |||||||
| chrX:10208741 | A | G | 52 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0182 others(49): Show |
52 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1389+151A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10208741 | |||||||
| chrX:10208934 | G | A | 2 | a0001c0001t0002g0223 a0001c0001t0003g0195 |
2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1389+344G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10208934 | |||||||
| chrX:10208991 | T | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
211 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1389+401T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10208991 | |||||||
| chrX:10209089 | C | A | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1389+499C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209089 | |||||||
| chrX:10209255 | G | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(184): Show |
188 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1389+665G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209255 | |||||||
| chrX:10209267 | T | TCCTC | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
121 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.1389+701_1389+704d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | ||||||
| chrX:10209267 | T | TCCTCCCT others(1): Show |
60 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0193 others(57): Show |
60 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1389+697_1389+704d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | ||||||
| chrX:10209267 | T | TCCTCCCT others(5): Show |
2 | a0001c0001t0001g0182 a0001c0001t0001g0247 |
2 | NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1389+693_1389+704d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | ||||||
| chrX:10209267 | T | TCCTCCCT others(13): Show |
1 | a0001c0001t0001g0255 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1389+685_1389+704d others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | ||||||
| chrX:10209267 | TCCTCCCT others(1): Show |
T | 7 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+697_1389+704d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | ||||||
| chrX:10209289 | C | CTCCCTCC others(18): Show |
4 | a0001c0002t0002g0074 a0001c0003t0016g0086 a0001c0003t0016g0087 others(1): Show |
4 | HG02630.hp1 HG03516.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+704_1389+705i others(27): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209289 | ||||||
| chrX:10209289 | C | CTCCCTCC others(14): Show |
3 | a0001c0001t0009g0061 a0001c0002t0004g0085 a0001c0002t0013g0032 |
3 | HG02965.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1389+704_1389+705i others(23): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209289 | ||||||
| chrX:10209289 | C | CTCCCTCC others(10): Show |
2 | a0001c0001t0005g0060 a0001c0001t0005g0143 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1389+704_1389+705i others(19): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209289 | ||||||
| chrX:10209376 | C | CCCCTT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(209): Show |
213 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1389+794_1389+798d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209376 | ||||||
| chrX:10209393 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1389+803G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209393 | |||||||
| chrX:10209433 | T | A | 1 | a0001c0001t0003g0204 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1389+843T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209433 | |||||||
| chrX:10209545 | A | G | 4 | a0001c0001t0005g0079 a0001c0002t0004g0046 a0001c0002t0004g0048 others(1): Show |
4 | HG02647.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+955A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209545 | |||||||
| chrX:10209778 | G | A | 1 | a0001c0001t0003g0020 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1389+1188G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209778 | |||||||
| chrX:10209829 | C | CT | 10 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1389+1254dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209829 | ||||||
| chrX:10209829 | CT | C | 9 | a0001c0001t0001g0072 a0001c0001t0002g0260 a0001c0001t0003g0220 others(6): Show |
9 | HG01081.hp2 HG01168.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1389+1254delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209829 | ||||||
| chrX:10209973 | C | T | 4 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0136 others(1): Show |
4 | HG02258.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+1383C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209973 | |||||||
| chrX:10210238 | T | C | 1 | a0001c0001t0003g0251 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1389+1648T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210238 | |||||||
| chrX:10210485 | T | A | 1 | a0001c0001t0001g0250 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1389+1895T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210485 | |||||||
| chrX:10210569 | T | C | 1 | a0001c0001t0002g0021 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1390-1898T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210569 | |||||||
| chrX:10210650 | C | CT | 58 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0154 others(55): Show |
58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1390-1795dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210650 | ||||||
| chrX:10210650 | C | CTT | 8 | a0001c0001t0001g0203 a0001c0001t0003g0140 a0001c0001t0003g0209 others(5): Show |
8 | HG00323.hp2 HG01257.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1796_1390-179 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210650 | ||||||
| chrX:10210650 | CT | C | 7 | a0001c0001t0001g0231 a0001c0001t0003g0251 a0001c0001t0004g0070 others(4): Show |
7 | HG01256.hp1 HG02602.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-1795delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210650 | ||||||
| chrX:10210927 | C | T | 9 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0097 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1390-1540C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210927 | |||||||
| chrX:10210932 | G | C | 8 | a0001c0001t0002g0065 a0001c0001t0002g0146 a0001c0001t0006g0063 others(5): Show |
8 | HG02615.hp1 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1535G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210932 | |||||||
| chrX:10210956 | C | CT | 26 | a0001c0001t0001g0213 a0001c0001t0002g0119 a0001c0001t0002g0130 others(23): Show |
26 | HG01071.hp1 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1390-1493dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210956 | ||||||
| chrX:10210956 | CT | C | 8 | a0001c0001t0001g0247 a0001c0001t0002g0082 a0001c0001t0002g0162 others(5): Show |
8 | HG00323.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1493delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210956 | ||||||
| chrX:10210990 | G | A | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1390-1477G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210990 | |||||||
| chrX:10211077 | C | G | 12 | a0001c0001t0004g0051 a0001c0001t0004g0069 a0001c0001t0004g0148 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1390-1390C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211077 | |||||||
| chrX:10211107 | A | T | 8 | a0001c0001t0002g0065 a0001c0001t0002g0146 a0001c0001t0006g0063 others(5): Show |
8 | HG02615.hp1 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1360A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211107 | |||||||
| chrX:10211136 | C | T | 1 | a0001c0002t0004g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1390-1331C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211136 | |||||||
| chrX:10211237 | G | C | 1 | a0001c0001t0002g0126 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1230G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211237 | |||||||
| chrX:10211238 | C | A | 1 | a0001c0001t0002g0126 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1229C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211238 | |||||||
| chrX:10211265 | C | CA | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1390-1179dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211265 | ||||||
| chrX:10211265 | C | CAA | 79 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0024 others(76): Show |
79 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1390-1180_1390-117 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211265 | ||||||
| chrX:10211265 | C | CAAA | 8 | a0001c0001t0001g0015 a0001c0001t0003g0153 a0001c0001t0003g0173 others(5): Show |
8 | HG01243.hp1 HG03098.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1181_1390-117 others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211265 | ||||||
| chrX:10211280 | A | G | 16 | a0001c0001t0002g0131 a0001c0001t0004g0051 a0001c0001t0004g0148 others(13): Show |
16 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1390-1187A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211280 | |||||||
| chrX:10211505 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1390-962G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211505 | |||||||
| chrX:10211676 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1390-791G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211676 | |||||||
| chrX:10211744 | T | A | 3 | a0001c0001t0002g0076 a0001c0001t0002g0082 a0001c0001t0002g0083 |
3 | HG01167.hp1 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1390-723T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211744 | |||||||
| chrX:10211791 | G | A | 1 | a0001c0001t0028g0258 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1390-676G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211791 | |||||||
| chrX:10211884 | A | G | 4 | a0001c0002t0002g0040 a0001c0002t0002g0052 a0001c0002t0002g0053 others(1): Show |
4 | HG01884.hp2 HG02451.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-583A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211884 | |||||||
| chrX:10211943 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
179 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(176): Show |
intron_variant | MODIFIER | c.1390-524T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211943 | |||||||
| chrX:10212015 | C | T | 4 | a0001c0001t0001g0163 a0001c0001t0001g0171 a0001c0001t0001g0197 others(1): Show |
4 | HG00738.hp1 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-452C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10212015 | |||||||
| chrX:10212259 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0193 others(58): Show |
62 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1390-208C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10212259 | |||||||
| chrX:10212409 | C | T | 44 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0113 others(41): Show |
44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1390-58C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10212409 | |||||||
| chrX:10212463 | C | T | 1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | splice_region_variant&intron_variant | LOW | c.1390-4C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10212463 | |||||||
| chrX:10212778 | A | G | 1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1576+125A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212778 | |||||||
| chrX:10212809 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0023 others(80): Show |
83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1576+156C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212809 | |||||||
| chrX:10212837 | G | GCA | 124 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1576+185_1576+186d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212837 | G | GCACACAC others(1): Show |
4 | a0001c0001t0006g0062 a0001c0001t0008g0036 a0001c0001t0008g0055 others(1): Show |
4 | HG02293.hp2 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212837 | G | GCACACAC others(3): Show |
1 | a0001c0001t0009g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1576+186_1576+187i others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212837 | G | GCACACAC others(9): Show |
3 | a0001c0001t0003g0221 a0001c0001t0005g0079 a0001c0001t0009g0078 |
3 | HG01243.hp1 NA18973.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1576+186_1576+187i others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212837 | G | GCACACAC others(11): Show |
8 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0002g0146 others(5): Show |
8 | HG01257.hp2 HG01258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212837 | G | GCACACAC others(13): Show |
46 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0023 others(43): Show |
46 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212837 | G | GCACACAC others(15): Show |
7 | a0001c0001t0002g0065 a0001c0001t0003g0140 a0001c0001t0003g0189 others(4): Show |
7 | HG00280.hp1 HG02809.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212837 | G | GCACACAC others(17): Show |
9 | a0001c0001t0002g0190 a0001c0001t0005g0060 a0001c0001t0005g0143 others(6): Show |
9 | HG01255.hp1 HG01261.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212837 | G | GCACACAC others(21): Show |
1 | a0001c0002t0015g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1576+186_1576+187i others(30): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212837 | G | GCACACAC others(25): Show |
1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1576+186_1576+187i others(34): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | ||||||
| chrX:10212840 | G | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(206): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1576+187G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212840 | |||||||
| chrX:10212852 | C | G | 1 | a0001c0002t0004g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1576+199C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212852 | |||||||
| chrX:10212859 | A | ACACACAC others(16): Show |
1 | a0001c0001t0003g0010 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1576+206_1576+207i others(25): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212859 | |||||||
| chrX:10212955 | C | T | 5 | a0001c0001t0002g0065 a0001c0001t0005g0060 a0001c0001t0005g0143 others(2): Show |
5 | HG02809.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576+302C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212955 | |||||||
| chrX:10213051 | AT | A | 55 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0111 others(52): Show |
55 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1576+402delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10213051 | ||||||
| chrX:10213077 | T | C | 1 | a0001c0001t0032g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1576+424T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213077 | |||||||
| chrX:10213174 | G | A | 1 | a0001c0002t0013g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1577-507G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213174 | |||||||
| chrX:10213239 | G | C | 1 | a0001c0001t0003g0208 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1577-442G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213239 | |||||||
| chrX:10213295 | C | A | 57 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0111 others(54): Show |
57 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1577-386C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213295 | |||||||
| chrX:10213295 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1577-386C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213295 | |||||||
| chrX:10213477 | T | G | 3 | a0001c0001t0010g0167 a0001c0001t0010g0168 a0001c0002t0036g0155 |
3 | HG01255.hp1 HG01261.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1577-204T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213477 | |||||||
| chrX:10213641 | G | A | 1 | a0001c0001t0004g0187 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1577-40G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213641 | |||||||
| chrX:10213675 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG02735.hp1 | splice_region_variant&intron_variant | LOW | c.1577-6T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213675 | |||||||
| chrX:10214209 | G | T | 1 | a0001c0001t0004g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1975+130G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214209 | |||||||
| chrX:10214304 | G | A | 4 | a0001c0001t0009g0078 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01243.hp1 HG01255.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+225G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214304 | |||||||
| chrX:10214362 | G | C | 3 | a0001c0002t0002g0052 a0001c0002t0002g0053 a0001c0002t0002g0074 |
3 | HG01884.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1975+283G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214362 | |||||||
| chrX:10214373 | T | C | 10 | a0001c0001t0004g0051 a0001c0002t0002g0038 a0001c0002t0002g0039 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1975+294T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214373 | |||||||
| chrX:10214520 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(143): Show |
147 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.1975+441A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214520 | |||||||
| chrX:10214531 | G | A | 1 | a0001c0002t0009g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1975+452G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214531 | |||||||
| chrX:10214581 | T | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): Show |
106 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.1975+502T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214581 | |||||||
| chrX:10214711 | A | G | 1 | a0001c0002t0015g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1975+632A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214711 | |||||||
| chrX:10214772 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
160 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1975+693T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214772 | |||||||
| chrX:10214778 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1975+699C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214778 | |||||||
| chrX:10215062 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1975+983C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215062 | |||||||
| chrX:10215150 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1975+1071C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215150 | |||||||
| chrX:10215399 | C | T | 4 | a0001c0001t0005g0149 a0001c0001t0005g0150 a0001c0001t0033g0016 others(1): Show |
4 | HG03669.hp2 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+1320C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215399 | |||||||
| chrX:10215485 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1975+1406T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215485 | |||||||
| chrX:10215486 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1975+1407G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215486 | |||||||
| chrX:10215520 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1975+1441A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215520 | |||||||
| chrX:10215625 | C | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1975+1546C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215625 | |||||||
| chrX:10216086 | A | G | 2 | a0001c0001t0009g0061 a0001c0002t0013g0032 |
2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1975+2007A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216086 | |||||||
| chrX:10216186 | G | A | 1 | a0001c0002t0013g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1975+2107G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216186 | |||||||
| chrX:10216449 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1975+2370C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216449 | |||||||
| chrX:10216455 | T | G | 4 | a0001c0001t0010g0167 a0001c0001t0010g0168 a0001c0001t0032g0073 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2376T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216455 | |||||||
| chrX:10216744 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1975+2665A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216744 | |||||||
| chrX:10216767 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(81): Show |
85 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1975+2688T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216767 | |||||||
| chrX:10216879 | A | ATGTG | 12 | a0001c0001t0001g0224 a0001c0001t0001g0233 a0001c0001t0001g0250 others(9): Show |
12 | HG02129.hp1 HG03490.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.1975+2816_1975+281 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216879 | ||||||
| chrX:10216879 | A | ATGTGTG | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0179 |
3 | HG00597.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1975+2814_1975+281 others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216879 | ||||||
| chrX:10216879 | A | ATGTGTGT others(1): Show |
10 | a0001c0001t0002g0136 a0001c0001t0007g0107 a0001c0001t0008g0095 others(7): Show |
10 | HG01255.hp1 HG01261.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1975+2812_1975+281 others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216879 | ||||||
| chrX:10216879 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1975+2810_1975+281 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216879 | ||||||
| chrX:10216879 | A | G | 6 | a0001c0001t0002g0065 a0001c0001t0005g0060 a0001c0001t0005g0079 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1975+2800A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216879 | |||||||
| chrX:10216895 | G | GTATATAT others(7): Show |
1 | a0001c0002t0004g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1975+2817_1975+281 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | ||||||
| chrX:10216895 | G | GTATATAT others(9): Show |
2 | a0001c0002t0004g0048 a0001c0002t0004g0049 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1975+2817_1975+281 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | ||||||
| chrX:10216895 | G | GTATATAT others(25): Show |
1 | a0001c0001t0004g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1975+2817_1975+281 others(36): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | ||||||
| chrX:10216895 | G | GTATATAT others(27): Show |
1 | a0001c0002t0004g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1975+2817_1975+281 others(38): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | ||||||
| chrX:10216895 | G | GTATATAT others(35): Show |
1 | a0001c0001t0004g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1975+2817_1975+281 others(46): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | ||||||
| chrX:10216897 | G | A | 11 | a0001c0001t0004g0133 a0001c0001t0004g0134 a0001c0001t0004g0148 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1975+2818G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216897 | |||||||
| chrX:10216897 | G | GTATATAT others(3): Show |
1 | a0001c0001t0004g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1975+2831_1975+284 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(7): Show |
1 | a0001c0001t0004g0263 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1975+2827_1975+284 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(9): Show |
1 | a0001c0001t0004g0112 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1975+2825_1975+284 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(13): Show |
1 | a0001c0001t0004g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1975+2821_1975+284 others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(15): Show |
6 | a0001c0001t0004g0028 a0001c0001t0004g0088 a0001c0001t0004g0089 others(3): Show |
6 | HG01516.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1975+2819_1975+284 others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(17): Show |
6 | a0001c0001t0004g0054 a0001c0001t0004g0069 a0001c0001t0004g0070 others(3): Show |
6 | HG01123.hp1 HG01256.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(19): Show |
4 | a0001c0001t0004g0187 a0001c0001t0019g0261 a0001c0002t0002g0074 others(1): Show |
4 | HG00323.hp2 HG01192.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(30): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(21): Show |
4 | a0001c0001t0004g0158 a0001c0002t0002g0038 a0001c0002t0002g0039 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(32): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(23): Show |
5 | a0001c0001t0004g0139 a0001c0001t0004g0246 a0001c0002t0002g0052 others(2): Show |
5 | HG01358.hp1 HG01884.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(34): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(27): Show |
2 | a0001c0002t0004g0050 a0001c0002t0034g0033 |
2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(38): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(33): Show |
1 | a0001c0001t0004g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(44): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTATATAT others(37): Show |
1 | a0001c0002t0004g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(48): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTATAT others(19): Show |
1 | a0001c0002t0004g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(30): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTATAT others(45): Show |
1 | a0001c0002t0018g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(56): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTAT others(3): Show |
13 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0024 others(10): Show |
13 | HG01257.hp2 HG01258.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTAT others(5): Show |
63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(60): Show |
64 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTAT others(7): Show |
38 | a0001c0001t0001g0113 a0001c0001t0001g0206 a0001c0001t0001g0232 others(35): Show |
38 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTAT others(9): Show |
1 | a0001c0001t0001g0193 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0008g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(7): Show |
4 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0008g0055 others(1): Show |
4 | HG02083.hp1 HG02293.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(9): Show |
3 | a0001c0001t0002g0065 a0001c0001t0005g0060 a0001c0001t0005g0143 |
3 | HG02809.hp1 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(3): Show |
3 | a0001c0001t0006g0062 a0001c0001t0032g0073 a0001c0006t0002g0099 |
3 | HG02630.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(5): Show |
9 | a0001c0001t0002g0076 a0001c0001t0002g0082 a0001c0001t0002g0083 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(7): Show |
17 | a0001c0001t0001g0230 a0001c0001t0002g0019 a0001c0001t0002g0021 others(14): Show |
17 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(9): Show |
3 | a0001c0001t0002g0018 a0001c0001t0002g0022 a0001c0001t0002g0120 |
3 | NA18997.hp2 NA19079.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(11): Show |
7 | a0001c0001t0001g0093 a0001c0001t0003g0071 a0001c0001t0003g0104 others(4): Show |
7 | HG00639.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(5): Show |
2 | a0001c0001t0002g0097 a0001c0001t0027g0098 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(7): Show |
3 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0152 |
3 | HG01891.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(9): Show |
1 | a0001c0001t0026g0092 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216897 | G | GTGTGTGT others(15): Show |
3 | a0001c0001t0007g0141 a0001c0001t0007g0142 a0001c0001t0007g0145 |
3 | HG01168.hp2 HG01169.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | ||||||
| chrX:10216899 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0003g0020 a0001c0001t0006g0063 others(8): Show |
11 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1975+2820A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216899 | |||||||
| chrX:10216901 | A | G | 4 | a0001c0001t0001g0174 a0001c0001t0003g0020 a0001c0002t0013g0032 others(1): Show |
4 | HG03486.hp1 NA18942.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2822A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216901 | |||||||
| chrX:10216916 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0012g0137 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975+2838_1975+283 others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216916 | ||||||
| chrX:10216916 | T | TACACACA others(3): Show |
2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1975+2838_1975+283 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216916 | ||||||
| chrX:10216918 | T | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0002g0043 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1975+2839T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216918 | |||||||
| chrX:10216918 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0093 a0001c0001t0001g0193 a0001c0001t0002g0018 others(1): Show |
4 | HG00621.hp1 NA19079.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975+2845_1975+285 others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TACACACA others(3): Show |
165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.1975+2843_1975+285 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TACACACA others(5): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0027 others(9): Show |
13 | HG00280.hp1 HG01346.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.1975+2841_1975+285 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TACACACA others(7): Show |
1 | a0001c0001t0008g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1975+2852_1975+285 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATACACA others(5): Show |
1 | a0001c0001t0001g0174 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATACACA others(7): Show |
1 | a0001c0002t0013g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(15): Show |
1 | a0001c0001t0033g0016 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(9): Show |
2 | a0001c0001t0009g0061 a0001c0001t0009g0078 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(15): Show |
6 | a0001c0001t0001g0224 a0001c0001t0001g0233 a0001c0001t0003g0194 others(3): Show |
6 | HG02293.hp1 HG03490.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(17): Show |
4 | a0001c0001t0005g0149 a0001c0001t0005g0150 a0001c0003t0016g0086 others(1): Show |
4 | HG03516.hp2 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(17): Show |
3 | a0001c0001t0002g0165 a0001c0001t0003g0160 a0001c0001t0020g0172 |
3 | NA18948.hp1 NA18960.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0250 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(19): Show |
1 | a0001c0001t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(30): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(21): Show |
1 | a0001c0001t0024g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(32): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(25): Show |
2 | a0001c0001t0006g0063 a0001c0001t0030g0066 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(36): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(27): Show |
1 | a0001c0001t0006g0067 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(38): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(29): Show |
1 | a0001c0001t0006g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(40): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(25): Show |
1 | a0001c0001t0004g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(36): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(33): Show |
1 | a0001c0001t0006g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(44): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(29): Show |
2 | a0001c0001t0004g0133 a0001c0001t0017g0057 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(40): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(33): Show |
1 | a0001c0001t0004g0134 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(44): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(35): Show |
1 | a0001c0001t0004g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(46): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216918 | T | TATATATA others(37): Show |
1 | a0001c0002t0004g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(48): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | ||||||
| chrX:10216989 | T | C | 1 | a0001c0001t0013g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1975+2910T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216989 | |||||||
| chrX:10217026 | C | G | 1 | a0001c0001t0032g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1975+2947C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217026 | |||||||
| chrX:10217112 | A | T | 1 | a0001c0001t0008g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1975+3033A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217112 | |||||||
| chrX:10217267 | A | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1975+3188A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217267 | |||||||
| chrX:10217271 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1975+3192T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217271 | |||||||
| chrX:10217382 | G | A | 1 | a0001c0001t0004g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1976-3279G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217382 | |||||||
| chrX:10217508 | G | A | 1 | a0001c0001t0026g0092 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1976-3153G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217508 | |||||||
| chrX:10217650 | T | A | 1 | a0001c0002t0009g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1976-3011T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217650 | |||||||
| chrX:10217746 | CA | C | 4 | a0001c0001t0008g0036 a0001c0001t0008g0055 a0001c0001t0008g0056 others(1): Show |
4 | HG02109.hp1 HG02293.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1976-2914delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217746 | |||||||
| chrX:10217747 | A | AT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(164): Show |
168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1976-2899dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10217747 | ||||||
| chrX:10217812 | G | T | 4 | a0001c0001t0009g0061 a0001c0001t0009g0078 a0001c0001t0013g0077 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976-2849G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217812 | |||||||
| chrX:10217813 | G | A | 2 | a0001c0001t0004g0070 a0001c0001t0004g0112 |
2 | HG00099.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1976-2848G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217813 | |||||||
| chrX:10217963 | G | A | 4 | a0001c0001t0010g0059 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976-2698G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217963 | |||||||
| chrX:10217986 | G | A | 1 | a0001c0001t0033g0016 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1976-2675G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217986 | |||||||
| chrX:10217989 | C | T | 1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1976-2672C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217989 | |||||||
| chrX:10218070 | G | C | 4 | a0001c0001t0008g0036 a0001c0001t0008g0055 a0001c0001t0008g0056 others(1): Show |
4 | HG02109.hp1 HG02293.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1976-2591G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10218070 | |||||||
| chrX:10218120 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0235 |
2 | HG02027.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1976-2541A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10218120 | |||||||
| chrX:10218321 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(222): Show |
226 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1976-2340T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10218321 | |||||||
| chrX:10218588 | T | A | 2 | a0001c0001t0033g0016 a0001c0002t0015g0029 |
2 | HG03669.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1976-2073T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10218588 | |||||||
| chrX:10219080 | T | G | 9 | a0001c0001t0004g0028 a0001c0001t0004g0070 a0001c0001t0004g0090 others(6): Show |
9 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1976-1581T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219080 | |||||||
| chrX:10219327 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(217): Show |
221 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1976-1334G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219327 | |||||||
| chrX:10219445 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(154): Show |
158 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1976-1216G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219445 | |||||||
| chrX:10219463 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0212 |
2 | NA19002.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1976-1198G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219463 | |||||||
| chrX:10219916 | A | G | 1 | a0001c0001t0006g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1976-745A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219916 | |||||||
| chrX:10220044 | G | T | 8 | a0001c0001t0005g0060 a0001c0001t0005g0079 a0001c0001t0005g0143 others(5): Show |
8 | HG02809.hp2 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1976-617G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10220044 | |||||||
| chrX:10220335 | A | T | 1 | a0001c0001t0003g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1976-326A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10220335 | |||||||
| chrX:10220352 | G | A | 2 | a0001c0001t0004g0088 a0001c0001t0004g0089 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1976-309G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10220352 | |||||||
| chrX:10220527 | T | C | 2 | a0001c0001t0004g0054 a0001c0001t0004g0069 |
2 | HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1976-134T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10220527 | |||||||
| chrX:10221210 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2192+333A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221210 | |||||||
| chrX:10221212 | A | G | 7 | a0001c0001t0008g0036 a0001c0001t0008g0055 a0001c0001t0008g0056 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.2192+335A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221212 | |||||||
| chrX:10221547 | G | T | 1 | a0001c0002t0025g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2192+670G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221547 | |||||||
| chrX:10221781 | G | A | 1 | a0001c0002t0015g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2192+904G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221781 | |||||||
| chrX:10221798 | G | A | 2 | a0001c0002t0004g0048 a0001c0002t0004g0049 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2192+921G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221798 | |||||||
| chrX:10222101 | G | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
153 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.2192+1224G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10222101 | |||||||
| chrX:10222128 | C | T | 3 | a0001c0001t0007g0141 a0001c0001t0007g0142 a0001c0001t0007g0145 |
3 | HG01168.hp2 HG01169.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2192+1251C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10222128 | |||||||
| chrX:10222628 | G | A | 71 | a0001c0001t0001g0093 a0001c0001t0002g0018 a0001c0001t0002g0019 others(68): Show |
71 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2192+1751G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10222628 | |||||||
| chrX:10223280 | C | A | 1 | a0001c0002t0015g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2192+2403C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223280 | |||||||
| chrX:10223284 | A | T | 69 | a0001c0001t0001g0093 a0001c0001t0002g0018 a0001c0001t0002g0019 others(66): Show |
69 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.2192+2407A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223284 | |||||||
| chrX:10223295 | G | A | 2 | a0001c0002t0004g0048 a0001c0002t0004g0049 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2192+2418G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223295 | |||||||
| chrX:10223341 | C | T | 1 | a0001c0001t0027g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2192+2464C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223341 | |||||||
| chrX:10223606 | G | A | 1 | a0001c0001t0003g0205 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2192+2729G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223606 | |||||||
| chrX:10223706 | C | T | 2 | a0001c0001t0003g0173 a0001c0001t0003g0192 |
2 | NA18974.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2192+2829C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223706 | |||||||
| chrX:10223815 | A | G | 1 | a0001c0001t0009g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2192+2938A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223815 | |||||||
| chrX:10223874 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0002g0018 a0001c0001t0002g0022 |
3 | NA19079.hp1 NA19080.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2192+2997T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223874 | |||||||
| chrX:10224191 | T | TAA | 8 | a0001c0001t0003g0160 a0001c0001t0003g0173 a0001c0001t0003g0192 others(5): Show |
8 | HG01934.hp1 NA18948.hp1 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2192+3317_2192+331 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224191 | ||||||
| chrX:10224248 | A | G | 1 | a0001c0001t0003g0238 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2192+3371A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224248 | |||||||
| chrX:10224275 | A | G | 4 | a0001c0001t0010g0059 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3398A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224275 | |||||||
| chrX:10224293 | C | CGT | 34 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0026 others(31): Show |
34 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.2192+3455_2192+345 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | C | CGTGT | 7 | a0001c0001t0001g0231 a0001c0001t0001g0249 a0001c0001t0002g0130 others(4): Show |
7 | HG01346.hp2 HG02615.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.2192+3453_2192+345 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | C | CGTGTGT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(55): Show |
58 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.2192+3451_2192+345 others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | C | CGTGTGTG others(1): Show |
25 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0024 others(22): Show |
26 | HG00597.hp1 HG00735.hp1 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.2192+3449_2192+345 others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | C | CGTGTGTG others(3): Show |
7 | a0001c0001t0001g0216 a0001c0001t0002g0076 a0001c0001t0002g0082 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.2192+3447_2192+345 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | C | CGTGTGTG others(5): Show |
5 | a0001c0001t0002g0096 a0001c0001t0002g0136 a0001c0001t0002g0152 others(2): Show |
5 | HG01891.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2192+3445_2192+345 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | C | CGTGTGTG others(7): Show |
3 | a0001c0001t0002g0094 a0001c0001t0002g0102 a0001c0004t0002g0100 |
3 | HG02258.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2192+3443_2192+345 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | C | CGTGTGTG others(9): Show |
2 | a0001c0001t0002g0097 a0001c0005t0012g0101 |
2 | HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2192+3441_2192+345 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | CGT | C | 58 | a0001c0001t0001g0015 a0001c0001t0001g0093 a0001c0001t0001g0193 others(55): Show |
58 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.2192+3455_2192+345 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | CGTGT | C | 7 | a0001c0001t0003g0160 a0001c0001t0003g0219 a0001c0001t0005g0060 others(4): Show |
7 | HG01074.hp1 HG02809.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2192+3453_2192+345 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | CGTGTGT | C | 4 | a0001c0001t0009g0061 a0001c0001t0013g0077 a0001c0001t0030g0066 others(1): Show |
4 | HG02055.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3451_2192+345 others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224293 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0015g0199 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2192+3447_2192+345 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | ||||||
| chrX:10224318 | G | A | 1 | a0001c0006t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2192+3441G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224318 | |||||||
| chrX:10224319 | TGTGTGTG others(13): Show |
T | 1 | a0001c0006t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2192+3455_2192+347 others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224319 | ||||||
| chrX:10224320 | G | A | 4 | a0001c0001t0010g0059 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3443G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224320 | |||||||
| chrX:10224325 | T | A | 4 | a0001c0001t0010g0059 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3448T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224325 | |||||||
| chrX:10224327 | TGTGTGTA others(5): Show |
T | 4 | a0001c0001t0010g0059 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3457_2192+346 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224327 | ||||||
| chrX:10224406 | A | G | 69 | a0001c0001t0001g0093 a0001c0001t0002g0018 a0001c0001t0002g0019 others(66): Show |
69 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.2192+3529A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224406 | |||||||
| chrX:10224474 | TA | T | 51 | a0001c0001t0001g0015 a0001c0001t0001g0193 a0001c0001t0001g0212 others(48): Show |
51 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2192+3609delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224474 | ||||||
| chrX:10224656 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2192+3779G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224656 | |||||||
| chrX:10225047 | G | A | 1 | a0001c0002t0025g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2192+4170G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225047 | |||||||
| chrX:10225319 | G | C | 1 | a0001c0001t0011g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2192+4442G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225319 | |||||||
| chrX:10225390 | T | C | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2192+4513T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225390 | |||||||
| chrX:10225580 | G | T | 1 | a0001c0001t0002g0018 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2192+4703G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225580 | |||||||
| chrX:10225581 | A | T | 1 | a0001c0001t0002g0018 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2192+4704A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225581 | |||||||
| chrX:10225840 | T | C | 67 | a0001c0001t0001g0093 a0001c0001t0002g0018 a0001c0001t0002g0019 others(64): Show |
67 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.2192+4963T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225840 | |||||||
| chrX:10225879 | T | A | 1 | a0001c0001t0027g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2192+5002T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225879 | |||||||
| chrX:10226003 | G | A | 59 | a0001c0001t0001g0093 a0001c0001t0002g0018 a0001c0001t0002g0019 others(56): Show |
59 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2192+5126G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10226003 | |||||||
| chrX:10226008 | A | G | 4 | a0001c0001t0010g0059 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+5131A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10226008 | |||||||
| chrX:10226245 | AACC | A | 58 | a0001c0001t0001g0093 a0001c0001t0002g0018 a0001c0001t0002g0019 others(55): Show |
58 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.2192+5374_2192+537 others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10226245 | ||||||
| chrX:10226360 | C | T | 1 | a0001c0001t0004g0080 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2192+5483C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10226360 | |||||||
| chrX:10227035 | G | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
153 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.2192+6158G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227035 | |||||||
| chrX:10227235 | A | G | 1 | a0001c0002t0015g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2193-6259A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227235 | |||||||
| chrX:10227247 | C | T | 1 | a0001c0001t0003g0219 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2193-6247C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227247 | |||||||
| chrX:10227253 | C | G | 1 | a0001c0002t0025g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2193-6241C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227253 | |||||||
| chrX:10227548 | T | A | 1 | a0001c0002t0013g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2193-5946T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227548 | |||||||
| chrX:10227751 | A | G | 1 | a0001c0002t0009g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2193-5743A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227751 | |||||||
| chrX:10227921 | GT | G | 6 | a0001c0001t0004g0133 a0001c0001t0004g0134 a0001c0001t0004g0148 others(3): Show |
6 | HG01106.hp1 HG01109.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2193-5570delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10227921 | ||||||
| chrX:10228158 | A | AT | 4 | a0001c0001t0010g0059 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2193-5335dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10228158 | ||||||
| chrX:10228486 | G | T | 2 | a0001c0001t0005g0060 a0001c0001t0005g0143 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2193-5008G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228486 | |||||||
| chrX:10228498 | A | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
145 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.2193-4996A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228498 | |||||||
| chrX:10228546 | G | T | 1 | a0001c0001t0033g0016 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2193-4948G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228546 | |||||||
| chrX:10228572 | A | C | 1 | a0001c0001t0001g0257 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2193-4922A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228572 | |||||||
| chrX:10228607 | C | G | 72 | a0001c0001t0001g0093 a0001c0001t0002g0018 a0001c0001t0002g0019 others(69): Show |
72 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2193-4887C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228607 | |||||||
| chrX:10229021 | T | G | 4 | a0001c0001t0010g0059 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2193-4473T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229021 | |||||||
| chrX:10229386 | AAT | A | 16 | a0001c0001t0005g0060 a0001c0001t0005g0079 a0001c0001t0005g0143 others(13): Show |
16 | HG02615.hp1 HG02622.hp1 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.2193-4091_2193-409 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10229386 | ||||||
| chrX:10229390 | T | A | 8 | a0001c0001t0006g0062 a0001c0001t0006g0063 a0001c0001t0006g0064 others(5): Show |
8 | HG02615.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2193-4104T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229390 | |||||||
| chrX:10229392 | T | C | 2 | a0001c0001t0027g0098 a0001c0001t0032g0073 |
2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2193-4102T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229392 | |||||||
| chrX:10229442 | C | T | 60 | a0001c0001t0001g0093 a0001c0001t0002g0018 a0001c0001t0002g0019 others(57): Show |
60 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2193-4052C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229442 | |||||||
| chrX:10229545 | T | TC | 12 | a0001c0001t0001g0182 a0001c0001t0001g0193 a0001c0001t0002g0127 others(9): Show |
12 | HG00621.hp1 HG01256.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.2193-3943dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10229545 | ||||||
| chrX:10229569 | G | A | 8 | a0001c0001t0005g0060 a0001c0001t0005g0079 a0001c0001t0005g0143 others(5): Show |
8 | HG02809.hp2 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2193-3925G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229569 | |||||||
| chrX:10229937 | A | G | 1 | a0001c0002t0015g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2193-3557A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229937 | |||||||
| chrX:10230096 | G | T | 2 | a0001c0001t0004g0109 a0001c0001t0004g0187 |
2 | HG00323.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2193-3398G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10230096 | |||||||
| chrX:10230110 | A | AT | 12 | a0001c0001t0008g0036 a0001c0001t0008g0055 a0001c0001t0008g0056 others(9): Show |
12 | HG01243.hp1 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2193-3379dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10230110 | ||||||
| chrX:10230348 | A | G | 1 | a0001c0001t0032g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2193-3146A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10230348 | |||||||
| chrX:10230647 | C | T | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0048 others(1): Show |
4 | HG02647.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2193-2847C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10230647 | |||||||
| chrX:10231166 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0233 |
2 | NA18952.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2193-2328C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10231166 | |||||||
| chrX:10231358 | A | G | 12 | a0001c0001t0008g0036 a0001c0001t0008g0055 a0001c0001t0008g0056 others(9): Show |
12 | HG01243.hp1 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2193-2136A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10231358 | |||||||
| chrX:10231516 | A | C | 1 | a0001c0001t0002g0152 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2193-1978A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10231516 | |||||||
| chrX:10231544 | T | G | 12 | a0001c0001t0008g0036 a0001c0001t0008g0055 a0001c0001t0008g0056 others(9): Show |
12 | HG01243.hp1 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2193-1950T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10231544 | |||||||
| chrX:10232388 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(209): Show |
213 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.2193-1106G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232388 | |||||||
| chrX:10232389 | T | C | 2 | a0001c0001t0013g0077 a0001c0002t0013g0032 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2193-1105T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232389 | |||||||
| chrX:10232503 | C | A | 1 | a0001c0002t0013g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2193-991C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232503 | |||||||
| chrX:10232586 | A | C | 4 | a0001c0001t0010g0059 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2193-908A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232586 | |||||||
| chrX:10232709 | A | C | 1 | a0001c0002t0004g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2193-785A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232709 | |||||||
| chrX:10232873 | G | A | 58 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0021 others(55): Show |
58 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.2193-621G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232873 | |||||||
| chrX:10233127 | G | A | 59 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0021 others(56): Show |
59 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2193-367G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10233127 | |||||||
| chrX:10233274 | A | T | 1 | a0001c0002t0025g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2193-220A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10233274 |