Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6549 |
| ensemblid | ENSG00000115616.3 |
| hgncid | 11072 |
| symbol | SLC9A2 |
| name | solute carrier family 9 member A2 |
| refseq_nuc | NM_003048.6 |
| refseq_prot | NP_003039.2 |
| ensembl_nuc | ENST00000233969.3 |
| ensembl_prot | ENSP00000233969.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 102619553 |
| end | 102711355 |
| strand | + |
| ver | v1.2 |
| region | chr2:102619553-102711355 |
| region5000 | chr2:102614553-102716355 |
| regionname0 | SLC9A2_chr2_102619553_102711355 |
| regionname5000 | SLC9A2_chr2_102614553_102716355 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 812 | 340 | 87 | 63 | 136 | 10 | 42 | 104 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | MEPLG others(807): Show |
chr2 | 102614553 | 102716355 |
| a0002 | 0/0 | 812 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | MEPLG others(807): Show |
chr2 | 102614553 | 102716355 |
| a0003 | 0/0 | 812 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | MEPLG others(807): Show |
chr2 | 102614553 | 102716355 |
| a0004 | 0/0 | 812 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | MEPLG others(807): Show |
chr2 | 102614553 | 102716355 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2436 | 335 | 87 | 62 | 133 | 9 | 42 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | ATGGA others(2431): Show |
chr2 | 102614553 | 102716355 | ||
| a0001c0002 | 0/0 | 2436 | 3 | 0 | 0 | 3 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | ATGGA others(2431): Show |
chr2 | 102614553 | 102716355 | ||
| a0001c0003 | 0/0 | 2436 | 2 | 0 | 1 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | ATGGA others(2431): Show |
chr2 | 102614553 | 102716355 | ||
| a0002c0004 | 0/0 | 2436 | 2 | 0 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | ATGGA others(2431): Show |
chr2 | 102614553 | 102716355 | ||
| a0003c0005 | 0/0 | 2436 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | ATGGA others(2431): Show |
chr2 | 102614553 | 102716355 | ||
| a0004c0006 | 0/0 | 2436 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | ATGGA others(2431): Show |
chr2 | 102614553 | 102716355 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5601 | 175 | 21 | 27 | 100 | 3 | 24 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0002 | 1/0 | 5601 | 70 | 16 | 11 | 27 | 4 | 11 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0003 | 0/1 | 5599 | 30 | 9 | 15 | 0 | 1 | 4 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5594): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0004 | 0/0 | 5597 | 4 | 3 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5592): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0005 | 0/0 | 5601 | 5 | 5 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0006 | 0/0 | 5601 | 5 | 3 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0007 | 0/0 | 5601 | 4 | 4 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0008 | 0/0 | 5601 | 3 | 3 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0009 | 0/0 | 5601 | 3 | 0 | 0 | 2 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0010 | 0/0 | 5601 | 3 | 0 | 3 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0011 | 0/0 | 5601 | 3 | 3 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0012 | 0/0 | 5601 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0013 | 0/0 | 5601 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0014 | 0/0 | 5601 | 2 | 0 | 0 | 2 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0015 | 0/0 | 5597 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5592): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0016 | 0/0 | 5599 | 2 | 1 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5594): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0017 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0018 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0019 | 0/0 | 5601 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0020 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5592): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0021 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0022 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0023 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5594): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0024 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5594): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0025 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0026 | 0/0 | 5601 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0027 | 0/0 | 5601 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0028 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0029 | 0/0 | 5601 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0030 | 0/0 | 5601 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0031 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5592): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0032 | 0/0 | 5601 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0033 | 0/0 | 5601 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0034 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0035 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0001t0036 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5594): Show |
chr2 | 102614553 | 102716355 |
| a0001c0002t0002 | 0/0 | 5601 | 3 | 0 | 0 | 3 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0001c0003t0003 | 0/0 | 5599 | 2 | 0 | 1 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5594): Show |
chr2 | 102614553 | 102716355 |
| a0002c0004t0001 | 0/0 | 5601 | 2 | 0 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0003c0005t0001 | 0/0 | 5601 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5596): Show |
chr2 | 102614553 | 102716355 |
| a0004c0006t0004 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | GGAGA others(5592): Show |
chr2 | 102614553 | 102716355 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0009g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0010g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0010g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0011g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0012g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0012g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0013g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0013g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0014g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0014g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0015g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0015g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0016g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0016g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0017g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0018g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0019g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0020g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0022g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0023g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0024g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0025g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0026g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0027g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0028g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0029g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0030g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0031g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0032g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0033g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0034g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0035g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0036g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0003t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0003t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0002c0004t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0002c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0003c0005t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0004c0006t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | GBR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | GBR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0035 | EUR | GBR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00280 | hp1 | a0001 | c0001 | t0033 | g0204 | EUR | FIN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | FIN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00408 | hp2 | a0001 | c0001 | t0014 | g0224 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00621 | hp2 | a0001 | c0001 | t0009 | g0218 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0295 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0083 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0316 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01169 | hp1 | a0001 | c0001 | t0010 | g0082 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01192 | hp1 | a0001 | c0001 | t0016 | g0293 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0294 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01358 | hp1 | a0003 | c0005 | t0001 | g0130 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01358 | hp2 | a0001 | c0003 | t0003 | g0232 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01433 | hp2 | a0001 | c0001 | t0026 | g0252 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01496 | hp1 | a0001 | c0001 | t0010 | g0077 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0246 | EUR | IBS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0342 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01943 | hp1 | a0001 | c0001 | t0027 | g0075 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01943 | hp2 | a0002 | c0004 | t0001 | g0134 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01993 | hp1 | a0002 | c0004 | t0001 | g0136 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0094 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02055 | hp2 | a0001 | c0001 | t0018 | g0265 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02280 | hp1 | a0001 | c0001 | t0035 | g0331 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0332 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0297 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02622 | hp2 | a0001 | c0001 | t0020 | g0003 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0273 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0329 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0282 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02735 | hp1 | a0001 | c0001 | t0019 | g0054 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0255 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0339 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0290 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0335 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0317 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02896 | hp2 | a0001 | c0001 | t0025 | g0340 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0333 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0278 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0328 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0299 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0269 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03098 | hp1 | a0001 | c0001 | t0028 | g0178 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0064 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0271 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0270 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0315 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03225 | hp1 | a0001 | c0001 | t0034 | g0289 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0337 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0288 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03486 | hp1 | a0001 | c0001 | t0022 | g0007 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03486 | hp2 | a0001 | c0001 | t0036 | g0296 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03540 | hp2 | a0001 | c0001 | t0031 | g0117 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03579 | hp1 | a0001 | c0001 | t0023 | g0008 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG04115 | hp1 | a0001 | c0001 | t0030 | g0010 | SAS | STU | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | STU | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0264 | SAS | STU | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | STU | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18522 | hp1 | a0004 | c0006 | t0004 | g0334 | AFR | YRI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0006 | AFR | YRI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | YRI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18974 | hp1 | a0001 | c0001 | t0009 | g0108 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18987 | hp2 | a0001 | c0001 | t0014 | g0133 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19000 | hp2 | a0001 | c0001 | t0032 | g0229 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19030 | hp2 | a0001 | c0001 | t0024 | g0341 | AFR | LWK | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0272 | AFR | LWK | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19056 | hp2 | a0001 | c0001 | t0029 | g0122 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | YRI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ASW | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA20805 | hp1 | a0001 | c0003 | t0003 | g0012 | EUR | TSI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0162 | EUR | TSI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | GIH | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02486 | hp1 | a0001 | c0001 | t0016 | g0291 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0105 | AFR | USA | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | USA | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | USA | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | USA | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | LWK | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | LWK | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0250 | REF | REF | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0254 | REF | REF | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102619895 | C | T | 1 | a0004 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.47C>T | p.Pro16Leu | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/12 | 343/5601 | 47/2439 | 16/812 | chr2 | 102619895 | |||
| chr2:102619964 | C | G | 1 | a0002 | 2 | HG01943.hp2 HG01993.hp1 |
missense_variant | MODERATE | c.116C>G | p.Ala39Gly | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/12 | 412/5601 | 116/2439 | 39/812 | chr2 | 102619964 | |||
| chr2:102708361 | G | A | 1 | a0003 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.2311G>A | p.Asp771Asn | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 2607/5601 | 2311/2439 | 771/812 | chr2 | 102708361 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102701217 | A | G | 1 | a0001c0003 | 2 | HG01358.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.1734A>G | p.Thr578Thr | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/12 | 2030/5601 | 1734/2439 | 578/812 | chr2 | 102701217 | |||
| chr2:102704576 | C | T | 1 | a0001c0002 | 3 | NA18968.hp2 NA18970.hp2 NA19006.hp1 |
synonymous_variant | LOW | c.1878C>T | p.Ala626Ala | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 10/12 | 2174/5601 | 1878/2439 | 626/812 | chr2 | 102704576 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102619563 | G | C | 2 | a0001c0001t0017 a0001c0001t0018 |
2 | HG02055.hp1 HG02055.hp2 |
5_prime_UTR_variant | MODIFIER | c.-286G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/12 | 286 | chr2 | 102619563 | ||||||
| chr2:102619579 | G | A | 1 | a0001c0001t0019 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-270G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/12 | 270 | chr2 | 102619579 | ||||||
| chr2:102619621 | C | G | 7 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0015 others(4): Show |
15 | HG00639.hp1 HG01192.hp1 HG01255.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-228C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/12 | 228 | chr2 | 102619621 | ||||||
| chr2:102619700 | C | T | 1 | a0001c0001t0033 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-149C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/12 | 149 | chr2 | 102619700 | ||||||
| chr2:102619770 | G | A | 5 | a0001c0001t0008 a0001c0001t0020 a0001c0001t0021 others(2): Show |
7 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-79G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/12 | 79 | chr2 | 102619770 | ||||||
| chr2:102619841 | C | A | 2 | a0001c0001t0024 a0001c0001t0025 |
2 | HG02896.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-8C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/12 | 8 | chr2 | 102619841 | ||||||
| chr2:102708539 | T | C | 1 | a0001c0001t0026 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*50T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 50 | chr2 | 102708539 | ||||||
| chr2:102708683 | A | G | 1 | a0001c0001t0010 | 3 | HG01167.hp1 HG01169.hp1 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*194A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 194 | chr2 | 102708683 | ||||||
| chr2:102708719 | T | C | 2 | a0001c0001t0007 a0001c0001t0017 |
5 | HG02055.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*230T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 230 | chr2 | 102708719 | ||||||
| chr2:102708975 | C | T | 1 | a0001c0001t0014 | 2 | HG00408.hp2 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*486C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 486 | chr2 | 102708975 | ||||||
| chr2:102709029 | A | G | 1 | a0001c0001t0032 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*540A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 540 | chr2 | 102709029 | ||||||
| chr2:102709286 | G | A | 4 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0020 others(1): Show |
8 | HG01167.hp2 HG01891.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*797G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 797 | chr2 | 102709286 | ||||||
| chr2:102709328 | A | T | 2 | a0001c0001t0013 a0001c0001t0025 |
3 | HG02896.hp2 HG02965.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*839A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 839 | chr2 | 102709328 | ||||||
| chr2:102709331 | A | G | 4 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0020 others(1): Show |
8 | HG01167.hp2 HG01891.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*842A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 842 | chr2 | 102709331 | ||||||
| chr2:102709365 | G | C | 1 | a0001c0001t0027 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*876G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 876 | chr2 | 102709365 | ||||||
| chr2:102709482 | G | A | 5 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0021 others(2): Show |
10 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*993G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 993 | chr2 | 102709482 | ||||||
| chr2:102709488 | G | A | 1 | a0001c0001t0028 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 999 | chr2 | 102709488 | ||||||
| chr2:102709501 | C | T | 2 | a0001c0001t0007 a0001c0001t0017 |
5 | HG02055.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1012C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 1012 | chr2 | 102709501 | ||||||
| chr2:102709809 | T | C | 1 | a0001c0001t0009 | 3 | HG00621.hp2 HG04228.hp1 NA18974.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1320T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 1320 | chr2 | 102709809 | ||||||
| chr2:102710315 | T | C | 1 | a0001c0001t0029 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1826T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 1826 | chr2 | 102710315 | ||||||
| chr2:102710449 | TAA | T | 6 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0023 others(3): Show |
36 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1962_*1963delAA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 1962 | INFO_REALIGN_3_PRIME | chr2 | 102710449 | |||||
| chr2:102710532 | G | A | 1 | a0001c0001t0030 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2043G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 2043 | chr2 | 102710532 | ||||||
| chr2:102710629 | ATGAC | A | 5 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0020 others(2): Show |
9 | HG01167.hp2 HG01891.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2141_*2144delTGAC | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 2141 | chr2 | 102710629 | ||||||
| chr2:102710782 | G | C | 3 | a0001c0001t0003 a0001c0001t0016 a0001c0003t0003 |
33 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2293G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 2293 | chr2 | 102710782 | ||||||
| chr2:102710937 | T | C | 2 | a0001c0001t0012 a0001c0001t0035 |
3 | HG02280.hp1 HG02647.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2448T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 2448 | chr2 | 102710937 | ||||||
| chr2:102711017 | A | G | 33 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(30): Show |
259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*2528A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 2528 | chr2 | 102711017 | ||||||
| chr2:102711183 | G | T | 1 | a0001c0001t0028 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2694G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 12/12 | 2694 | chr2 | 102711183 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102620330 | G | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(71): Show |
75 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.289+193G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102620330 | |||||||
| chr2:102620398 | C | G | 1 | a0001c0001t0003g0342 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.289+261C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102620398 | |||||||
| chr2:102620491 | C | T | 2 | a0001c0001t0024g0341 a0001c0001t0025g0340 |
2 | HG02896.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.289+354C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102620491 | |||||||
| chr2:102620492 | G | T | 1 | a0001c0001t0007g0269 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.289+355G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102620492 | |||||||
| chr2:102620904 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(66): Show |
70 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.289+767T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102620904 | |||||||
| chr2:102621049 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.289+912C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621049 | |||||||
| chr2:102621059 | AG | A | 7 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+925delG | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102621059 | ||||||
| chr2:102621172 | T | C | 80 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.289+1035T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621172 | |||||||
| chr2:102621183 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(9): Show |
12 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.289+1046T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621183 | |||||||
| chr2:102621219 | C | T | 5 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0002g0339 others(2): Show |
5 | HG01361.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+1082C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621219 | |||||||
| chr2:102621352 | G | GA | 20 | a0001c0001t0001g0095 a0001c0001t0001g0098 a0001c0001t0001g0100 others(17): Show |
20 | HG00438.hp1 HG01978.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.289+1236dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102621352 | ||||||
| chr2:102621352 | G | GAAA | 71 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.289+1234_289+1236d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102621352 | ||||||
| chr2:102621352 | G | GAAAA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
11 | HG00423.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+1233_289+1236d others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102621352 | ||||||
| chr2:102621352 | GA | G | 6 | a0001c0001t0001g0266 a0001c0001t0002g0267 a0001c0001t0005g0332 others(3): Show |
6 | HG01069.hp2 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+1236delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102621352 | ||||||
| chr2:102621389 | C | T | 1 | a0001c0001t0009g0264 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.289+1252C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621389 | |||||||
| chr2:102621453 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(64): Show |
68 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.289+1316C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621453 | |||||||
| chr2:102621561 | G | A | 1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.289+1424G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621561 | |||||||
| chr2:102621571 | T | C | 88 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.289+1434T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621571 | |||||||
| chr2:102621590 | G | A | 3 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0012g0337 |
3 | HG01361.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.289+1453G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621590 | |||||||
| chr2:102621673 | C | G | 3 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0012g0337 |
3 | HG01361.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.289+1536C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621673 | |||||||
| chr2:102621708 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.289+1571C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621708 | |||||||
| chr2:102621709 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(169): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.289+1572G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621709 | |||||||
| chr2:102621775 | T | G | 1 | a0001c0001t0011g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.289+1638T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102621775 | |||||||
| chr2:102622302 | G | A | 2 | a0001c0001t0017g0094 a0001c0001t0018g0265 |
2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.289+2165G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622302 | |||||||
| chr2:102622315 | ACCTGTTC | A | 10 | a0001c0001t0001g0095 a0001c0001t0001g0109 a0001c0001t0001g0110 others(7): Show |
10 | HG00642.hp2 HG01257.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.289+2184_289+2190d others(9): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102622315 | ||||||
| chr2:102622358 | T | C | 2 | a0001c0001t0002g0339 a0001c0001t0007g0335 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.289+2221T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622358 | |||||||
| chr2:102622411 | A | G | 7 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+2274A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622411 | |||||||
| chr2:102622420 | A | G | 3 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0012g0337 |
3 | HG01361.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.289+2283A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622420 | |||||||
| chr2:102622544 | T | C | 1 | a0001c0001t0003g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.289+2407T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622544 | |||||||
| chr2:102622580 | A | T | 1 | a0001c0001t0001g0262 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.289+2443A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622580 | |||||||
| chr2:102622595 | T | G | 22 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0286 others(19): Show |
22 | HG00639.hp1 HG01192.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.289+2458T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622595 | |||||||
| chr2:102622897 | C | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG00099.hp2 HG00140.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+2760C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622897 | |||||||
| chr2:102622903 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0002g0259 |
3 | HG00621.hp1 HG02071.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.289+2766A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622903 | |||||||
| chr2:102622998 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.289+2861G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102622998 | |||||||
| chr2:102623076 | A | G | 2 | a0001c0001t0011g0278 a0001c0001t0035g0331 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.289+2939A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623076 | |||||||
| chr2:102623087 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.289+2950T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623087 | |||||||
| chr2:102623188 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.289+3051T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623188 | |||||||
| chr2:102623405 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(64): Show |
68 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.289+3268G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623405 | |||||||
| chr2:102623508 | C | T | 1 | a0001c0001t0008g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.289+3371C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623508 | |||||||
| chr2:102623529 | G | A | 85 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.289+3392G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623529 | |||||||
| chr2:102623539 | G | A | 1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.289+3402G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623539 | |||||||
| chr2:102623674 | T | C | 2 | a0001c0001t0017g0094 a0001c0001t0018g0265 |
2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.289+3537T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623674 | |||||||
| chr2:102623755 | T | C | 7 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+3618T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623755 | |||||||
| chr2:102623819 | T | G | 2 | a0001c0001t0024g0341 a0001c0001t0025g0340 |
2 | HG02896.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.289+3682T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102623819 | |||||||
| chr2:102624235 | G | T | 14 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(11): Show |
15 | HG00280.hp2 HG01069.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.289+4098G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102624235 | |||||||
| chr2:102624251 | C | T | 1 | a0001c0001t0011g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.289+4114C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102624251 | |||||||
| chr2:102624330 | G | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(55): Show |
59 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.289+4193G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102624330 | |||||||
| chr2:102624399 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.289+4262C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102624399 | |||||||
| chr2:102624668 | C | G | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.289+4531C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102624668 | |||||||
| chr2:102624955 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.289+4818C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102624955 | |||||||
| chr2:102624998 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.289+4861A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102624998 | |||||||
| chr2:102625098 | AT | A | 5 | a0001c0001t0001g0119 a0001c0001t0002g0104 a0001c0001t0002g0118 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+4963delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102625098 | ||||||
| chr2:102625108 | C | T | 9 | a0001c0001t0002g0188 a0001c0001t0006g0270 a0001c0001t0006g0271 others(6): Show |
9 | HG02486.hp1 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+4971C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625108 | |||||||
| chr2:102625109 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0336 a0001c0001t0002g0104 others(3): Show |
6 | HG01361.hp1 HG02109.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+4972G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625109 | |||||||
| chr2:102625326 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.289+5189T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625326 | |||||||
| chr2:102625373 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.289+5236A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625373 | |||||||
| chr2:102625442 | G | A | 2 | a0001c0001t0002g0086 a0001c0001t0033g0204 |
2 | HG00280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.289+5305G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625442 | |||||||
| chr2:102625481 | G | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0091 others(241): Show |
246 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.289+5344G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625481 | |||||||
| chr2:102625791 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.289+5654G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625791 | |||||||
| chr2:102625891 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.289+5754G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625891 | |||||||
| chr2:102625912 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.289+5775G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625912 | |||||||
| chr2:102625939 | A | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(1): Show |
4 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+5802A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102625939 | |||||||
| chr2:102626204 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.289+6067G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102626204 | |||||||
| chr2:102626326 | A | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0319 a0001c0001t0001g0321 others(7): Show |
11 | NA18944.hp2 NA18957.hp2 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+6189A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102626326 | |||||||
| chr2:102626371 | T | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0095 others(232): Show |
237 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.289+6234T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102626371 | |||||||
| chr2:102626381 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | NA18942.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.289+6244A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102626381 | |||||||
| chr2:102626429 | GATTAAAG others(6): Show |
G | 1 | a0001c0001t0003g0268 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.289+6295_289+6307d others(15): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102626429 | ||||||
| chr2:102626488 | A | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(1): Show |
4 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+6351A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102626488 | |||||||
| chr2:102626710 | TCAAA | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(1): Show |
4 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+6578_289+6581d others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102626710 | ||||||
| chr2:102626736 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG00642.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.289+6599T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102626736 | |||||||
| chr2:102626881 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.289+6744G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102626881 | |||||||
| chr2:102626957 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.289+6820T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102626957 | |||||||
| chr2:102626962 | A | G | 4 | a0001c0001t0001g0119 a0001c0001t0002g0118 a0001c0001t0003g0096 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+6825A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102626962 | |||||||
| chr2:102627128 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(1): Show |
4 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+6991G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627128 | |||||||
| chr2:102627130 | T | TAAC | 15 | a0001c0001t0001g0119 a0001c0001t0002g0118 a0001c0001t0002g0339 others(12): Show |
15 | HG01192.hp1 HG02109.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.289+7014_289+7016d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102627130 | ||||||
| chr2:102627130 | T | TAACAAC | 10 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0001g0336 others(7): Show |
10 | HG01361.hp1 HG02055.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+7011_289+7016d others(8): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102627130 | ||||||
| chr2:102627132 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0002g0084 |
2 | NA18747.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.289+6995A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627132 | |||||||
| chr2:102627148 | CAACAAT | C | 153 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(150): Show |
154 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.289+7017_289+7022d others(8): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102627148 | ||||||
| chr2:102627151 | CAAT | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(26): Show |
30 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.289+7017_289+7019d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102627151 | ||||||
| chr2:102627154 | T | C | 62 | a0001c0001t0001g0091 a0001c0001t0001g0100 a0001c0001t0001g0107 others(59): Show |
62 | HG00609.hp1 HG01167.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.289+7017T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627154 | |||||||
| chr2:102627231 | T | G | 2 | a0001c0001t0001g0107 a0001c0001t0018g0265 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.289+7094T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627231 | |||||||
| chr2:102627259 | T | C | 1 | a0001c0002t0002g0121 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.289+7122T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627259 | |||||||
| chr2:102627331 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0181 others(61): Show |
65 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.289+7194A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627331 | |||||||
| chr2:102627531 | T | G | 1 | a0001c0001t0009g0108 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.289+7394T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627531 | |||||||
| chr2:102627637 | G | A | 1 | a0001c0001t0011g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.289+7500G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627637 | |||||||
| chr2:102627734 | T | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0186 others(1): Show |
4 | NA18960.hp1 NA18972.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+7597T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627734 | |||||||
| chr2:102627839 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0007g0105 |
2 | HG02258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.289+7702G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627839 | |||||||
| chr2:102627856 | A | G | 7 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0002g0339 others(4): Show |
7 | HG01361.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+7719A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627856 | |||||||
| chr2:102627980 | T | C | 6 | a0001c0001t0001g0109 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG00639.hp2 HG00642.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+7843T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102627980 | |||||||
| chr2:102628459 | T | C | 7 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0002g0339 others(4): Show |
7 | HG01361.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+8322T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102628459 | |||||||
| chr2:102628512 | G | C | 1 | a0001c0001t0002g0191 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.289+8375G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102628512 | |||||||
| chr2:102628566 | A | G | 327 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(324): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.289+8429A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102628566 | |||||||
| chr2:102628591 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.289+8454G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102628591 | |||||||
| chr2:102628625 | T | A | 1 | a0001c0001t0001g0030 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.289+8488T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102628625 | |||||||
| chr2:102628629 | C | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(1): Show |
4 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+8492C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102628629 | |||||||
| chr2:102628736 | A | T | 1 | a0001c0001t0003g0125 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.289+8599A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102628736 | |||||||
| chr2:102628943 | A | G | 1 | a0001c0001t0003g0177 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.289+8806A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102628943 | |||||||
| chr2:102629502 | G | A | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.289+9365G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102629502 | |||||||
| chr2:102629607 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.289+9470C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102629607 | |||||||
| chr2:102629666 | C | A | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.289+9529C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102629666 | |||||||
| chr2:102629705 | T | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0091 others(241): Show |
246 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.289+9568T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102629705 | |||||||
| chr2:102629718 | T | A | 1 | a0001c0001t0029g0122 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.289+9581T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102629718 | |||||||
| chr2:102629853 | G | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(55): Show |
59 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.289+9716G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102629853 | |||||||
| chr2:102629859 | C | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(55): Show |
59 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.289+9722C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102629859 | |||||||
| chr2:102629965 | G | T | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.289+9828G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102629965 | |||||||
| chr2:102630061 | C | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG00642.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.289+9924C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102630061 | |||||||
| chr2:102630061 | C | T | 15 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(12): Show |
15 | HG01891.hp2 HG02486.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.289+9924C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102630061 | |||||||
| chr2:102630220 | G | A | 1 | a0001c0001t0008g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.289+10083G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102630220 | |||||||
| chr2:102630520 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.289+10383G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102630520 | |||||||
| chr2:102630591 | T | C | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.289+10454T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102630591 | |||||||
| chr2:102630853 | A | T | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.289+10716A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102630853 | |||||||
| chr2:102631244 | G | A | 3 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0012g0329 |
3 | HG02647.hp1 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.289+11107G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631244 | |||||||
| chr2:102631294 | C | CT | 6 | a0001c0001t0001g0090 a0001c0001t0002g0089 a0001c0001t0002g0092 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+11167dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631294 | ||||||
| chr2:102631299 | T | C | 4 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0003g0022 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+11162T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631299 | |||||||
| chr2:102631311 | G | GTATT | 17 | a0001c0001t0001g0091 a0001c0001t0001g0107 a0001c0001t0001g0119 others(14): Show |
17 | HG01361.hp1 HG02109.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.289+11185_289+1118 others(8): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631311 | ||||||
| chr2:102631329 | C | A | 1 | a0001c0001t0001g0319 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.289+11192C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631329 | |||||||
| chr2:102631339 | G | A | 9 | a0001c0001t0001g0091 a0001c0001t0001g0119 a0001c0001t0001g0330 others(6): Show |
9 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+11202G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631339 | |||||||
| chr2:102631441 | G | A | 2 | a0001c0001t0001g0336 a0001c0001t0012g0337 |
2 | HG01361.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.289+11304G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631441 | |||||||
| chr2:102631445 | C | T | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.289+11308C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631445 | |||||||
| chr2:102631452 | G | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0091 others(241): Show |
246 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.289+11315G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631452 | |||||||
| chr2:102631478 | T | A | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11341T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631478 | |||||||
| chr2:102631575 | T | A | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.289+11438T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631575 | |||||||
| chr2:102631777 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0266 |
2 | NA18951.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.289+11640C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631777 | |||||||
| chr2:102631802 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG00408.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.289+11665G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631802 | |||||||
| chr2:102631927 | T | A | 2 | a0001c0001t0001g0015 a0001c0001t0002g0014 |
2 | HG00140.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.289+11790T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631927 | |||||||
| chr2:102631994 | G | GGA | 5 | a0001c0001t0001g0314 a0001c0001t0002g0104 a0001c0001t0007g0328 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+11858_289+1185 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631994 | ||||||
| chr2:102631995 | G | GAT | 11 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0080 others(8): Show |
11 | HG00280.hp1 HG01070.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.289+11900_289+1190 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GAT | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0034 others(18): Show |
21 | HG00639.hp1 HG00673.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.289+11900_289+1190 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATAT | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(15): Show |
18 | HG01884.hp1 HG01981.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.289+11898_289+1190 others(8): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATAT | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(20): Show |
24 | HG01167.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.289+11896_289+1190 others(10): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATATA others(1): Show |
G | 25 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0301 others(22): Show |
25 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.289+11894_289+1190 others(12): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATATA others(3): Show |
G | 2 | a0001c0001t0001g0258 a0001c0001t0005g0332 |
2 | HG00438.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.289+11892_289+1190 others(14): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATATA others(5): Show |
G | 11 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0281 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.289+11890_289+1190 others(16): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATATA others(7): Show |
G | 15 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(12): Show |
15 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.289+11888_289+1190 others(18): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATATA others(9): Show |
G | 140 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(137): Show |
141 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.289+11886_289+1190 others(20): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATATA others(11): Show |
G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0132 |
3 | HG03942.hp1 NA19006.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.289+11884_289+1190 others(22): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATATA others(13): Show |
G | 1 | a0001c0001t0001g0131 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.289+11882_289+1190 others(24): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATATA others(19): Show |
G | 1 | a0001c0001t0003g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.289+11876_289+1190 others(30): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631995 | GATATATA others(21): Show |
G | 1 | a0001c0001t0003g0038 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.289+11874_289+1190 others(32): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102631995 | ||||||
| chr2:102631997 | T | G | 30 | a0001c0001t0001g0091 a0001c0001t0001g0119 a0001c0001t0001g0286 others(27): Show |
30 | HG01361.hp1 HG01891.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.289+11860T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102631997 | |||||||
| chr2:102632001 | T | G | 3 | a0001c0001t0001g0283 a0001c0001t0001g0319 a0001c0001t0001g0326 |
3 | NA18906.hp1 NA18957.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.289+11864T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632001 | |||||||
| chr2:102632003 | T | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0313 a0001c0001t0001g0321 others(7): Show |
11 | HG02055.hp2 HG02717.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+11866T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632003 | |||||||
| chr2:102632005 | T | G | 15 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0301 others(12): Show |
15 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.289+11868T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632005 | |||||||
| chr2:102632009 | T | G | 7 | a0001c0001t0001g0281 a0001c0001t0001g0292 a0001c0001t0002g0274 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.289+11872T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632009 | |||||||
| chr2:102632011 | T | G | 15 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(12): Show |
15 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.289+11874T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632011 | |||||||
| chr2:102632013 | T | G | 140 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(137): Show |
141 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.289+11876T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632013 | |||||||
| chr2:102632015 | T | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0132 others(1): Show |
4 | HG01358.hp1 HG02683.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+11878T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632015 | |||||||
| chr2:102632017 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.289+11880T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632017 | |||||||
| chr2:102632021 | T | C | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11884T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632021 | |||||||
| chr2:102632023 | T | C | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11886T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632023 | |||||||
| chr2:102632023 | TATATATA others(9): Show |
T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(1): Show |
4 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+11890_289+1190 others(20): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632023 | ||||||
| chr2:102632027 | T | C | 10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0008g0004 others(7): Show |
10 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.289+11890T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632027 | |||||||
| chr2:102632029 | T | C | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11892T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632029 | |||||||
| chr2:102632031 | T | C | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11894T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632031 | |||||||
| chr2:102632033 | T | C | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11896T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632033 | |||||||
| chr2:102632033 | TATATAC | T | 5 | a0001c0001t0001g0119 a0001c0001t0002g0118 a0001c0001t0003g0096 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+11900_289+1190 others(10): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632033 | ||||||
| chr2:102632035 | T | C | 9 | a0001c0001t0001g0192 a0001c0001t0008g0004 a0001c0001t0008g0005 others(6): Show |
9 | HG00280.hp2 HG02622.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+11898T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632035 | |||||||
| chr2:102632037 | T | C | 175 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0095 others(172): Show |
176 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.289+11900T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632037 | |||||||
| chr2:102632039 | C | T | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11902C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632039 | |||||||
| chr2:102632041 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0275 others(55): Show |
59 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.289+11904T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632041 | |||||||
| chr2:102632041 | TAC | T | 7 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0327 others(4): Show |
7 | HG01891.hp2 HG02818.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.289+11914_289+1191 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632041 | ||||||
| chr2:102632043 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(56): Show |
60 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.289+11906C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632043 | |||||||
| chr2:102632045 | C | T | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11908C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632045 | |||||||
| chr2:102632051 | C | T | 4 | a0001c0001t0001g0119 a0001c0001t0002g0118 a0001c0001t0003g0096 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+11914C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632051 | |||||||
| chr2:102632053 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.289+11916T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632053 | |||||||
| chr2:102632061 | C | CACACATA others(3): Show |
8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11929_289+1193 others(14): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632061 | ||||||
| chr2:102632061 | C | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0091 others(230): Show |
235 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.289+11924C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632061 | |||||||
| chr2:102632075 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.289+11938T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632075 | |||||||
| chr2:102632081 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.289+11944C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632081 | |||||||
| chr2:102632086 | A | C | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.289+11949A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632086 | |||||||
| chr2:102632089 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.289+11952T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632089 | |||||||
| chr2:102632091 | CACATATA others(41): Show |
C | 8 | a0001c0001t0001g0091 a0001c0001t0001g0119 a0001c0001t0001g0330 others(5): Show |
8 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.289+11956_289+1200 others(52): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632091 | ||||||
| chr2:102632093 | CATATATA others(11): Show |
C | 1 | a0001c0001t0003g0298 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.289+11957_289+1197 others(22): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632093 | |||||||
| chr2:102632094 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0003g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.289+11974_289+1199 others(22): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632094 | ||||||
| chr2:102632095 | T | TATATATA others(19): Show |
15 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.289+11994_289+1201 others(30): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632095 | ||||||
| chr2:102632095 | TATATATA others(19): Show |
T | 1 | a0001c0001t0033g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.289+11994_289+1201 others(30): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632095 | ||||||
| chr2:102632095 | TATATATA others(45): Show |
T | 1 | a0001c0001t0001g0068 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.289+11968_289+1201 others(56): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632095 | ||||||
| chr2:102632110 | A | G | 2 | a0001c0001t0001g0336 a0001c0001t0012g0337 |
2 | HG01361.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.289+11973A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632110 | |||||||
| chr2:102632119 | TACATATA others(29): Show |
T | 8 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0002g0104 others(5): Show |
8 | HG01361.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+11994_289+1202 others(40): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632119 | ||||||
| chr2:102632121 | CATATATA others(11): Show |
C | 3 | a0001c0001t0002g0025 a0001c0001t0018g0265 a0001c0001t0024g0341 |
3 | HG00423.hp2 HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.289+12000_289+1201 others(22): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632121 | ||||||
| chr2:102632127 | T | C | 157 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(154): Show |
158 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.289+11990T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632127 | |||||||
| chr2:102632130 | A | G | 1 | a0001c0001t0003g0298 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.289+11993A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632130 | |||||||
| chr2:102632131 | T | C | 157 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(154): Show |
158 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.289+11994T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632131 | |||||||
| chr2:102632137 | T | TATACAC | 157 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(154): Show |
158 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.289+12000_289+1200 others(10): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632137 | |||||||
| chr2:102632138 | G | A | 159 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(156): Show |
160 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.289+12001G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632138 | |||||||
| chr2:102632139 | T | C | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.289+12002T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632139 | |||||||
| chr2:102632145 | TACATATA others(3): Show |
T | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.289+12028_289+1203 others(14): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632145 | ||||||
| chr2:102632147 | C | T | 10 | a0001c0001t0001g0091 a0001c0001t0001g0119 a0001c0001t0001g0330 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.289+12010C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632147 | |||||||
| chr2:102632148 | A | ATATATAT others(1): Show |
113 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0100 others(110): Show |
114 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.289+12017_289+1201 others(12): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632148 | ||||||
| chr2:102632148 | A | G | 10 | a0001c0001t0001g0091 a0001c0001t0001g0119 a0001c0001t0001g0330 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.289+12011A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632148 | |||||||
| chr2:102632150 | A | G | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.289+12013A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632150 | |||||||
| chr2:102632152 | A | ATATGTAT others(1): Show |
44 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0123 others(41): Show |
44 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.289+12017_289+1201 others(12): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632152 | ||||||
| chr2:102632155 | C | T | 167 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(164): Show |
168 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.289+12018C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632155 | |||||||
| chr2:102632239 | C | CAT | 21 | a0001c0001t0001g0011 a0001c0001t0001g0091 a0001c0001t0001g0119 others(18): Show |
21 | HG01346.hp1 HG01361.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.289+12117_289+1211 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632239 | ||||||
| chr2:102632239 | C | CATATATA others(28): Show |
1 | a0001c0001t0025g0340 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.289+12119_289+1212 others(39): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632239 | ||||||
| chr2:102632239 | C | CATATATA others(27): Show |
6 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(3): Show |
6 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+12116_289+1211 others(38): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632239 | ||||||
| chr2:102632239 | C | CATATATA others(25): Show |
1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.289+12114_289+1211 others(36): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102632239 | ||||||
| chr2:102632243 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.289+12106T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632243 | |||||||
| chr2:102632280 | A | G | 4 | a0001c0001t0001g0119 a0001c0001t0002g0118 a0001c0001t0003g0096 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+12143A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632280 | |||||||
| chr2:102632384 | C | T | 319 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0027 others(316): Show |
321 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.289+12247C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632384 | |||||||
| chr2:102632592 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.289+12455C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632592 | |||||||
| chr2:102632679 | C | A | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.289+12542C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632679 | |||||||
| chr2:102632682 | A | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(55): Show |
59 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.289+12545A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632682 | |||||||
| chr2:102633095 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.289+12958T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633095 | |||||||
| chr2:102633144 | G | A | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+13007G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633144 | |||||||
| chr2:102633199 | A | G | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.289+13062A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633199 | |||||||
| chr2:102633312 | A | G | 1 | a0001c0001t0011g0297 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.289+13175A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633312 | |||||||
| chr2:102633332 | C | T | 1 | a0001c0001t0033g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.289+13195C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633332 | |||||||
| chr2:102633370 | T | C | 17 | a0001c0001t0001g0091 a0001c0001t0001g0107 a0001c0001t0001g0119 others(14): Show |
17 | HG01361.hp1 HG02109.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.289+13233T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633370 | |||||||
| chr2:102633409 | C | G | 5 | a0001c0001t0001g0119 a0001c0001t0002g0104 a0001c0001t0002g0118 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+13272C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633409 | |||||||
| chr2:102633544 | C | T | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.289+13407C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633544 | |||||||
| chr2:102633547 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.289+13410A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633547 | |||||||
| chr2:102633593 | T | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(55): Show |
59 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.289+13456T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633593 | |||||||
| chr2:102633737 | T | C | 7 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0002g0339 others(4): Show |
7 | HG01361.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+13600T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633737 | |||||||
| chr2:102633753 | T | C | 6 | a0001c0001t0001g0090 a0001c0001t0002g0089 a0001c0001t0002g0092 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+13616T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633753 | |||||||
| chr2:102633873 | A | G | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.289+13736A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633873 | |||||||
| chr2:102633938 | C | T | 4 | a0001c0001t0001g0119 a0001c0001t0002g0118 a0001c0001t0003g0096 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+13801C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633938 | |||||||
| chr2:102633973 | C | A | 1 | a0001c0001t0002g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.289+13836C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633973 | |||||||
| chr2:102633991 | A | G | 1 | a0001c0001t0011g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.289+13854A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102633991 | |||||||
| chr2:102634043 | A | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(1): Show |
4 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+13906A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634043 | |||||||
| chr2:102634258 | T | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0014g0133 others(2): Show |
5 | HG01943.hp2 HG01993.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+14121T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634258 | |||||||
| chr2:102634392 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.289+14255C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634392 | |||||||
| chr2:102634457 | T | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0263 |
3 | NA18999.hp2 NA19003.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.289+14320T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634457 | |||||||
| chr2:102634694 | G | A | 1 | a0001c0001t0003g0298 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.289+14557G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634694 | |||||||
| chr2:102634717 | T | A | 8 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+14580T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634717 | |||||||
| chr2:102634721 | T | G | 1 | a0001c0001t0031g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.289+14584T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634721 | |||||||
| chr2:102634790 | G | C | 159 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(156): Show |
160 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.289+14653G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634790 | |||||||
| chr2:102634825 | T | C | 3 | a0001c0001t0002g0089 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02723.hp2 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.289+14688T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634825 | |||||||
| chr2:102634852 | G | A | 7 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0002g0339 others(4): Show |
7 | HG01361.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+14715G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634852 | |||||||
| chr2:102634916 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.289+14779C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102634916 | |||||||
| chr2:102635056 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.289+14919G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635056 | |||||||
| chr2:102635088 | C | T | 3 | a0001c0001t0005g0317 a0001c0001t0005g0333 a0001c0001t0035g0331 |
3 | HG02280.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.289+14951C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635088 | |||||||
| chr2:102635095 | T | C | 319 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0027 others(316): Show |
321 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.289+14958T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635095 | |||||||
| chr2:102635136 | C | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0292 |
2 | HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.289+14999C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635136 | |||||||
| chr2:102635148 | T | C | 3 | a0001c0001t0001g0107 a0001c0001t0018g0265 a0001c0001t0024g0341 |
3 | HG02055.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.289+15011T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635148 | |||||||
| chr2:102635232 | T | C | 184 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(181): Show |
185 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.289+15095T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635232 | |||||||
| chr2:102635321 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.289+15184C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635321 | |||||||
| chr2:102635321 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.289+15184C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635321 | |||||||
| chr2:102635368 | G | A | 1 | a0001c0001t0007g0105 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.289+15231G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635368 | |||||||
| chr2:102635447 | C | T | 1 | a0001c0001t0003g0079 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.289+15310C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635447 | |||||||
| chr2:102635468 | G | A | 64 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(61): Show |
64 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.289+15331G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635468 | |||||||
| chr2:102635486 | C | A | 1 | a0001c0001t0013g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.289+15349C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635486 | |||||||
| chr2:102635524 | A | G | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.289+15387A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635524 | |||||||
| chr2:102635649 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.289+15512A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635649 | |||||||
| chr2:102635650 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.289+15513C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635650 | |||||||
| chr2:102635878 | A | G | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.289+15741A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102635878 | |||||||
| chr2:102635888 | C | CT | 11 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0281 others(8): Show |
11 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.289+15764dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102635888 | ||||||
| chr2:102635888 | CT | C | 178 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(175): Show |
179 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.289+15764delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102635888 | ||||||
| chr2:102636008 | C | T | 157 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(154): Show |
158 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.289+15871C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636008 | |||||||
| chr2:102636015 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.289+15878C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636015 | |||||||
| chr2:102636104 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.289+15967G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636104 | |||||||
| chr2:102636143 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.289+16006C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636143 | |||||||
| chr2:102636299 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.289+16162T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636299 | |||||||
| chr2:102636553 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.289+16416G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636553 | |||||||
| chr2:102636570 | A | G | 9 | a0001c0001t0001g0120 a0001c0001t0001g0160 a0001c0001t0001g0187 others(6): Show |
9 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.289+16433A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636570 | |||||||
| chr2:102636645 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.289+16508T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636645 | |||||||
| chr2:102636669 | C | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG00099.hp2 HG00140.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+16532C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636669 | |||||||
| chr2:102636670 | G | A | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.289+16533G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102636670 | |||||||
| chr2:102637178 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0091 others(53): Show |
57 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.289+17041C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102637178 | |||||||
| chr2:102637405 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.289+17268T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102637405 | |||||||
| chr2:102637410 | C | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0003g0024 others(2): Show |
5 | HG01175.hp1 HG01884.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+17273C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102637410 | |||||||
| chr2:102637484 | G | T | 14 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(11): Show |
15 | HG00280.hp2 HG01069.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.289+17347G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102637484 | |||||||
| chr2:102637739 | C | T | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.289+17602C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102637739 | |||||||
| chr2:102637746 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0002g0182 |
2 | HG00609.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.289+17609A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102637746 | |||||||
| chr2:102637790 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.289+17653C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102637790 | |||||||
| chr2:102637917 | G | C | 3 | a0001c0001t0001g0336 a0001c0001t0012g0337 a0001c0001t0028g0178 |
3 | HG01361.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.289+17780G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102637917 | |||||||
| chr2:102638060 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.289+17923A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638060 | |||||||
| chr2:102638141 | G | A | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.289+18004G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638141 | |||||||
| chr2:102638192 | C | CT | 327 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(324): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.289+18059dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102638192 | ||||||
| chr2:102638223 | T | C | 172 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(169): Show |
173 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.289+18086T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638223 | |||||||
| chr2:102638244 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.289+18107A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638244 | |||||||
| chr2:102638349 | T | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0090 others(247): Show |
252 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.289+18212T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638349 | |||||||
| chr2:102638427 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.289+18290T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638427 | |||||||
| chr2:102638594 | A | C | 5 | a0001c0001t0002g0089 a0001c0001t0002g0092 a0001c0001t0002g0093 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+18457A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638594 | |||||||
| chr2:102638720 | C | A | 2 | a0001c0001t0001g0313 a0001c0001t0002g0318 |
2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.289+18583C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638720 | |||||||
| chr2:102638720 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.289+18583C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638720 | |||||||
| chr2:102638852 | C | A | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.290-18712C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638852 | |||||||
| chr2:102638875 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.290-18689T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102638875 | |||||||
| chr2:102639060 | T | C | 172 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(169): Show |
173 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.290-18504T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639060 | |||||||
| chr2:102639370 | T | C | 32 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0107 others(29): Show |
32 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.290-18194T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639370 | |||||||
| chr2:102639400 | G | A | 1 | a0001c0001t0003g0212 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.290-18164G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639400 | |||||||
| chr2:102639413 | A | G | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.290-18151A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639413 | |||||||
| chr2:102639419 | C | G | 7 | a0001c0001t0001g0281 a0001c0001t0001g0292 a0001c0001t0002g0274 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.290-18145C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639419 | |||||||
| chr2:102639532 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.290-18032C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639532 | |||||||
| chr2:102639823 | C | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.290-17741C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639823 | |||||||
| chr2:102639860 | T | TA | 15 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(12): Show |
15 | HG01891.hp2 HG02486.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.290-17703dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102639860 | ||||||
| chr2:102639894 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.290-17670T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639894 | |||||||
| chr2:102639898 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0078 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.290-17666C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639898 | |||||||
| chr2:102639899 | G | T | 1 | a0001c0001t0003g0079 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.290-17665G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102639899 | |||||||
| chr2:102640088 | T | C | 204 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(201): Show |
205 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.290-17476T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102640088 | |||||||
| chr2:102640291 | A | T | 15 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(12): Show |
15 | HG01891.hp2 HG02486.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.290-17273A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102640291 | |||||||
| chr2:102640304 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.290-17260C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102640304 | |||||||
| chr2:102640463 | T | TG | 43 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(40): Show |
44 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.290-17098dupG | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102640463 | ||||||
| chr2:102640659 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290-16905C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102640659 | |||||||
| chr2:102640690 | T | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0090 others(246): Show |
251 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.290-16874T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102640690 | |||||||
| chr2:102640710 | C | A | 3 | a0001c0001t0002g0300 a0001c0001t0003g0342 a0001c0001t0013g0299 |
3 | HG01884.hp2 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.290-16854C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102640710 | |||||||
| chr2:102640947 | C | T | 1 | a0001c0001t0002g0207 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.290-16617C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102640947 | |||||||
| chr2:102640994 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0194 |
3 | HG01069.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.290-16570G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102640994 | |||||||
| chr2:102641017 | C | T | 11 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0001g0119 others(8): Show |
11 | HG02109.hp2 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-16547C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641017 | |||||||
| chr2:102641056 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.290-16508T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641056 | |||||||
| chr2:102641101 | C | T | 200 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(197): Show |
201 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.290-16463C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641101 | |||||||
| chr2:102641370 | A | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(37): Show |
41 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.290-16194A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641370 | |||||||
| chr2:102641473 | G | A | 14 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(11): Show |
15 | HG00280.hp2 HG01069.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.290-16091G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641473 | |||||||
| chr2:102641527 | G | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(40): Show |
44 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.290-16037G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641527 | |||||||
| chr2:102641606 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0107 others(52): Show |
56 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.290-15958T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641606 | |||||||
| chr2:102641637 | G | A | 22 | a0001c0001t0001g0091 a0001c0001t0001g0283 a0001c0001t0001g0286 others(19): Show |
22 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.290-15927G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641637 | |||||||
| chr2:102641669 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290-15895G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641669 | |||||||
| chr2:102641896 | C | CG | 9 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-15662dupG | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102641896 | ||||||
| chr2:102641897 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.290-15667G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641897 | |||||||
| chr2:102641904 | G | C | 2 | a0001c0001t0001g0260 a0001c0001t0002g0259 |
2 | HG00621.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.290-15660G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641904 | |||||||
| chr2:102641931 | C | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0090 others(241): Show |
246 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.290-15633C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641931 | |||||||
| chr2:102641977 | A | G | 2 | a0001c0001t0022g0007 a0001c0001t0023g0008 |
2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.290-15587A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102641977 | |||||||
| chr2:102642023 | AG | A | 151 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(148): Show |
152 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.290-15540delG | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102642023 | |||||||
| chr2:102642042 | T | TATA | 80 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(77): Show |
80 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.290-15499_290-1549 others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102642042 | ||||||
| chr2:102642042 | T | TATAATA | 6 | a0001c0001t0001g0081 a0001c0001t0006g0290 a0001c0001t0010g0082 others(3): Show |
6 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-15502_290-1549 others(10): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102642042 | ||||||
| chr2:102642042 | TATA | T | 151 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(148): Show |
152 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.290-15499_290-1549 others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102642042 | ||||||
| chr2:102642108 | A | G | 6 | a0001c0001t0001g0090 a0001c0001t0002g0089 a0001c0001t0002g0092 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-15456A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102642108 | |||||||
| chr2:102642434 | GT | G | 185 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0095 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.290-15120delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102642434 | ||||||
| chr2:102642462 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(25): Show |
29 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.290-15102G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102642462 | |||||||
| chr2:102642764 | G | T | 151 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(148): Show |
152 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.290-14800G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102642764 | |||||||
| chr2:102642913 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.290-14651C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102642913 | |||||||
| chr2:102642937 | GT | G | 9 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-14625delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102642937 | ||||||
| chr2:102643161 | T | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0090 others(224): Show |
229 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.290-14403T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643161 | |||||||
| chr2:102643179 | C | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0123 a0001c0001t0003g0125 others(1): Show |
4 | HG00639.hp2 HG00642.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-14385C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643179 | |||||||
| chr2:102643194 | G | A | 2 | a0001c0001t0002g0104 a0001c0001t0024g0341 |
2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.290-14370G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643194 | |||||||
| chr2:102643197 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.290-14367G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643197 | |||||||
| chr2:102643306 | G | T | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.290-14258G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643306 | |||||||
| chr2:102643444 | A | C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0194 |
3 | HG01069.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.290-14120A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643444 | |||||||
| chr2:102643692 | A | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0095 others(213): Show |
218 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.290-13872A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643692 | |||||||
| chr2:102643699 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.290-13865A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643699 | |||||||
| chr2:102643717 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.290-13847C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643717 | |||||||
| chr2:102643826 | A | T | 1 | a0001c0001t0002g0207 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.290-13738A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643826 | |||||||
| chr2:102643910 | C | CT | 23 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0073 others(20): Show |
23 | HG00741.hp1 HG01070.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.290-13642dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102643910 | ||||||
| chr2:102643910 | CT | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0095 others(191): Show |
196 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.290-13642delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102643910 | ||||||
| chr2:102643929 | A | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0078 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.290-13635A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643929 | |||||||
| chr2:102643940 | G | A | 4 | a0001c0001t0001g0119 a0001c0001t0002g0118 a0001c0001t0003g0096 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-13624G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643940 | |||||||
| chr2:102643963 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.290-13601C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643963 | |||||||
| chr2:102643973 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.290-13591C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643973 | |||||||
| chr2:102643986 | T | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0090 others(224): Show |
229 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.290-13578T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643986 | |||||||
| chr2:102644085 | T | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0090 others(224): Show |
229 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.290-13479T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644085 | |||||||
| chr2:102644281 | G | C | 1 | a0001c0001t0002g0032 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.290-13283G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644281 | |||||||
| chr2:102644321 | C | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0090 others(224): Show |
229 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.290-13243C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644321 | |||||||
| chr2:102644429 | C | A | 1 | a0001c0001t0026g0252 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.290-13135C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644429 | |||||||
| chr2:102644429 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.290-13135C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644429 | |||||||
| chr2:102644465 | A | G | 1 | a0001c0001t0002g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.290-13099A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644465 | |||||||
| chr2:102644476 | C | T | 1 | a0001c0001t0013g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.290-13088C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644476 | |||||||
| chr2:102644511 | G | T | 7 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0002g0185 others(4): Show |
7 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.290-13053G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644511 | |||||||
| chr2:102644748 | G | A | 3 | a0001c0001t0006g0294 a0001c0001t0006g0295 a0001c0001t0016g0293 |
3 | HG00639.hp1 HG01192.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.290-12816G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644748 | |||||||
| chr2:102644798 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(40): Show |
44 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.290-12766G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644798 | |||||||
| chr2:102644806 | C | T | 152 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(149): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.290-12758C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644806 | |||||||
| chr2:102644813 | A | G | 14 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(11): Show |
15 | HG00280.hp2 HG01069.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.290-12751A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644813 | |||||||
| chr2:102644846 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.290-12718G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644846 | |||||||
| chr2:102644848 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290-12716G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644848 | |||||||
| chr2:102644864 | A | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0027 others(315): Show |
320 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.290-12700A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644864 | |||||||
| chr2:102644904 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(40): Show |
44 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.290-12660C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644904 | |||||||
| chr2:102644972 | G | A | 12 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(9): Show |
12 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-12592G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644972 | |||||||
| chr2:102644984 | C | G | 1 | a0001c0001t0005g0332 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.290-12580C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102644984 | |||||||
| chr2:102645096 | G | A | 12 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(9): Show |
12 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-12468G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645096 | |||||||
| chr2:102645250 | G | A | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.290-12314G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645250 | |||||||
| chr2:102645338 | C | T | 41 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0107 others(38): Show |
41 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(38): Show |
intron_variant | MODIFIER | c.290-12226C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645338 | |||||||
| chr2:102645403 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.290-12161G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645403 | |||||||
| chr2:102645436 | T | C | 11 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0001g0119 others(8): Show |
11 | HG02109.hp2 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-12128T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645436 | |||||||
| chr2:102645496 | A | G | 11 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0001g0119 others(8): Show |
11 | HG02109.hp2 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-12068A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645496 | |||||||
| chr2:102645531 | A | T | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.290-12033A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645531 | |||||||
| chr2:102645572 | T | A | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.290-11992T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645572 | |||||||
| chr2:102645594 | AAAG | A | 8 | a0001c0001t0001g0160 a0001c0001t0001g0187 a0001c0001t0002g0158 others(5): Show |
8 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-11964_290-1196 others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102645594 | ||||||
| chr2:102645615 | G | C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0194 |
3 | HG01069.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.290-11949G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645615 | |||||||
| chr2:102645673 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(40): Show |
44 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.290-11891C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645673 | |||||||
| chr2:102645685 | G | A | 29 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0107 others(26): Show |
29 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.290-11879G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645685 | |||||||
| chr2:102645697 | A | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG02129.hp2 NA18957.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-11867A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645697 | |||||||
| chr2:102645772 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.290-11792G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645772 | |||||||
| chr2:102645776 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.290-11788A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645776 | |||||||
| chr2:102645809 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | NA18942.hp2 NA18949.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.290-11755G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645809 | |||||||
| chr2:102645914 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0003g0072 |
2 | HG02258.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.290-11650C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645914 | |||||||
| chr2:102645956 | A | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0090 others(242): Show |
247 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.290-11608A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102645956 | |||||||
| chr2:102646036 | T | C | 3 | a0001c0001t0001g0249 a0001c0001t0001g0251 a0001c0001t0002g0102 |
3 | HG02738.hp1 HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.290-11528T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646036 | |||||||
| chr2:102646143 | G | C | 41 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0123 others(38): Show |
41 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.290-11421G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646143 | |||||||
| chr2:102646231 | C | A | 18 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0001g0336 others(15): Show |
18 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.290-11333C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646231 | |||||||
| chr2:102646315 | A | G | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.290-11249A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646315 | |||||||
| chr2:102646637 | C | A | 1 | a0001c0001t0002g0179 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.290-10927C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646637 | |||||||
| chr2:102646688 | C | G | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.290-10876C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646688 | |||||||
| chr2:102646696 | A | T | 2 | a0001c0001t0005g0317 a0001c0001t0005g0333 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.290-10868A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646696 | |||||||
| chr2:102646764 | C | CATATATA others(15): Show |
1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.290-10800_290-1079 others(26): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646764 | |||||||
| chr2:102646765 | C | A | 2 | a0001c0001t0002g0104 a0001c0001t0024g0341 |
2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.290-10799C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646765 | |||||||
| chr2:102646765 | C | CTATATAT others(17): Show |
1 | a0001c0001t0002g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.290-10797_290-1079 others(28): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646765 | ||||||
| chr2:102646768 | A | AAT | 37 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(34): Show |
38 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.290-10775_290-1077 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATAT | 20 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(17): Show |
20 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.290-10777_290-1077 others(8): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(1): Show |
66 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0101 others(63): Show |
66 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.290-10781_290-1077 others(12): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(3): Show |
46 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0112 others(43): Show |
47 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.290-10783_290-1077 others(14): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(5): Show |
20 | a0001c0001t0001g0091 a0001c0001t0001g0100 a0001c0001t0001g0106 others(17): Show |
20 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-10785_290-1077 others(16): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(7): Show |
4 | a0001c0001t0001g0131 a0001c0001t0001g0210 a0001c0001t0001g0251 others(1): Show |
4 | HG01258.hp2 HG02129.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-10787_290-1077 others(18): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(9): Show |
4 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0002g0097 others(1): Show |
4 | HG01891.hp1 HG02071.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-10789_290-1077 others(20): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(11): Show |
11 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0171 others(8): Show |
11 | HG02109.hp1 HG02602.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.290-10791_290-1077 others(22): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(13): Show |
4 | a0001c0001t0001g0164 a0001c0001t0001g0170 a0001c0001t0001g0181 others(1): Show |
4 | HG01891.hp2 HG03453.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-10793_290-1077 others(24): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(17): Show |
2 | a0001c0001t0001g0249 a0001c0001t0003g0096 |
2 | HG02109.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.290-10774_290-1077 others(28): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(19): Show |
5 | a0001c0001t0001g0119 a0001c0001t0001g0168 a0001c0001t0002g0188 others(2): Show |
5 | HG02055.hp1 HG02615.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-10774_290-1077 others(30): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(21): Show |
3 | a0001c0001t0001g0090 a0001c0001t0002g0093 a0001c0001t0011g0297 |
3 | HG02572.hp2 HG02723.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.290-10774_290-1077 others(32): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(23): Show |
1 | a0001c0001t0004g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.290-10774_290-1077 others(34): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(25): Show |
2 | a0001c0001t0007g0328 a0001c0001t0031g0117 |
2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.290-10774_290-1077 others(36): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(27): Show |
5 | a0001c0001t0001g0107 a0001c0001t0002g0092 a0001c0001t0002g0118 others(2): Show |
5 | HG02615.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-10774_290-1077 others(38): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(31): Show |
1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.290-10774_290-1077 others(42): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | AATATATA others(33): Show |
1 | a0001c0001t0002g0089 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.290-10774_290-1077 others(44): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646768 | A | ATATATAT others(26): Show |
2 | a0001c0001t0001g0330 a0001c0001t0036g0296 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.290-10796_290-1079 others(37): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646768 | |||||||
| chr2:102646768 | A | T | 3 | a0001c0001t0002g0104 a0001c0001t0002g0280 a0001c0001t0024g0341 |
3 | HG02818.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.290-10796A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646768 | |||||||
| chr2:102646768 | AATATAT | A | 5 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0011g0278 others(2): Show |
5 | HG01361.hp1 HG02922.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-10779_290-1077 others(10): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646768 | ||||||
| chr2:102646785 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0339 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.290-10774_290-1077 others(30): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102646785 | ||||||
| chr2:102646869 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.290-10695A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102646869 | |||||||
| chr2:102647125 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | NA18951.hp1 NA18966.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-10439C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102647125 | |||||||
| chr2:102647242 | G | A | 3 | a0001c0001t0003g0279 a0001c0001t0004g0316 a0001c0001t0013g0315 |
3 | HG01167.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.290-10322G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102647242 | |||||||
| chr2:102647301 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.290-10263G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102647301 | |||||||
| chr2:102647551 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.290-10013T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102647551 | |||||||
| chr2:102647624 | G | T | 1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.290-9940G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102647624 | |||||||
| chr2:102647641 | TA | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(40): Show |
44 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.290-9915delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102647641 | ||||||
| chr2:102647649 | AT | A | 4 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(1): Show |
4 | HG02717.hp2 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-9914delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102647649 | |||||||
| chr2:102647650 | T | A | 8 | a0001c0001t0006g0270 a0001c0001t0006g0271 a0001c0001t0006g0290 others(5): Show |
8 | HG02486.hp1 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.290-9914T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102647650 | |||||||
| chr2:102647775 | T | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0292 |
2 | HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.290-9789T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102647775 | |||||||
| chr2:102647862 | C | CA | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0128 others(6): Show |
9 | HG01175.hp1 HG01358.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-9694dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102647862 | ||||||
| chr2:102647862 | CA | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(201): Show |
206 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.290-9694delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102647862 | ||||||
| chr2:102647975 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0095 others(200): Show |
205 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.290-9589T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102647975 | |||||||
| chr2:102648153 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.290-9411T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102648153 | |||||||
| chr2:102648333 | G | C | 12 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(9): Show |
12 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-9231G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102648333 | |||||||
| chr2:102648341 | T | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0214 a0001c0001t0002g0141 |
3 | NA18998.hp2 NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.290-9223T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102648341 | |||||||
| chr2:102648384 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.290-9180T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102648384 | |||||||
| chr2:102648445 | G | A | 12 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(9): Show |
12 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-9119G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102648445 | |||||||
| chr2:102648471 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.290-9093A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102648471 | |||||||
| chr2:102648518 | A | G | 1 | a0001c0001t0034g0289 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.290-9046A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102648518 | |||||||
| chr2:102648803 | A | G | 30 | a0001c0001t0001g0091 a0001c0001t0001g0283 a0001c0001t0001g0286 others(27): Show |
30 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.290-8761A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102648803 | |||||||
| chr2:102648809 | G | A | 30 | a0001c0001t0001g0091 a0001c0001t0001g0283 a0001c0001t0001g0286 others(27): Show |
30 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.290-8755G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102648809 | |||||||
| chr2:102649091 | G | A | 30 | a0001c0001t0001g0091 a0001c0001t0001g0283 a0001c0001t0001g0286 others(27): Show |
30 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.290-8473G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649091 | |||||||
| chr2:102649099 | C | T | 12 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0287 others(9): Show |
12 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-8465C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649099 | |||||||
| chr2:102649245 | C | T | 18 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0001g0336 others(15): Show |
18 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.290-8319C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649245 | |||||||
| chr2:102649246 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.290-8318G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649246 | |||||||
| chr2:102649331 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.290-8233G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649331 | |||||||
| chr2:102649383 | C | T | 4 | a0001c0001t0005g0317 a0001c0001t0005g0333 a0001c0001t0018g0265 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-8181C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649383 | |||||||
| chr2:102649420 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0090 others(233): Show |
238 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.290-8144C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649420 | |||||||
| chr2:102649434 | A | G | 30 | a0001c0001t0001g0091 a0001c0001t0001g0283 a0001c0001t0001g0286 others(27): Show |
30 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.290-8130A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649434 | |||||||
| chr2:102649443 | G | A | 151 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(148): Show |
152 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.290-8121G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649443 | |||||||
| chr2:102649504 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.290-8060C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649504 | |||||||
| chr2:102649539 | A | G | 3 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0012g0329 |
3 | HG02647.hp1 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.290-8025A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649539 | |||||||
| chr2:102649629 | AAAAC | A | 19 | a0001c0001t0001g0091 a0001c0001t0001g0330 a0001c0001t0001g0336 others(16): Show |
19 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.290-7928_290-7925d others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102649629 | ||||||
| chr2:102649675 | G | A | 3 | a0001c0001t0001g0336 a0001c0001t0012g0337 a0001c0001t0028g0178 |
3 | HG01361.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.290-7889G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649675 | |||||||
| chr2:102649974 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.290-7590C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102649974 | |||||||
| chr2:102650038 | G | A | 152 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0098 others(149): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.290-7526G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650038 | |||||||
| chr2:102650112 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.290-7452A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650112 | |||||||
| chr2:102650154 | T | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0276 others(40): Show |
44 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.290-7410T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650154 | |||||||
| chr2:102650185 | C | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0080 others(196): Show |
201 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.290-7379C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650185 | |||||||
| chr2:102650322 | G | A | 2 | a0001c0001t0002g0104 a0001c0001t0024g0341 |
2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.290-7242G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650322 | |||||||
| chr2:102650405 | T | C | 8 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0002g0339 others(5): Show |
8 | HG01361.hp1 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-7159T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650405 | |||||||
| chr2:102650429 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.290-7135C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650429 | |||||||
| chr2:102650431 | T | C | 2 | a0001c0001t0006g0290 a0001c0001t0011g0273 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-7133T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650431 | |||||||
| chr2:102650453 | G | A | 1 | a0001c0001t0030g0010 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.290-7111G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650453 | |||||||
| chr2:102650666 | T | C | 1 | a0004c0006t0004g0334 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.290-6898T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650666 | |||||||
| chr2:102650676 | G | A | 7 | a0001c0001t0008g0004 a0001c0001t0008g0005 a0001c0001t0008g0009 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-6888G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650676 | |||||||
| chr2:102650834 | T | C | 18 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0107 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.290-6730T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650834 | |||||||
| chr2:102650943 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0002g0189 |
2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.290-6621G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102650943 | |||||||
| chr2:102651000 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.290-6564C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102651000 | |||||||
| chr2:102651074 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.290-6490C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102651074 | |||||||
| chr2:102651142 | C | T | 59 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0107 others(56): Show |
59 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.290-6422C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102651142 | |||||||
| chr2:102651185 | C | T | 1 | a0001c0001t0009g0108 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.290-6379C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102651185 | |||||||
| chr2:102651417 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.290-6147A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102651417 | |||||||
| chr2:102651461 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0107 others(17): Show |
20 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-6103C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102651461 | |||||||
| chr2:102651492 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.290-6072C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102651492 | |||||||
| chr2:102651934 | TTTG | T | 221 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(218): Show |
222 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.290-5609_290-5607d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102651934 | ||||||
| chr2:102651934 | TTTGTTG | T | 17 | a0001c0001t0001g0041 a0001c0001t0001g0164 a0001c0001t0001g0165 others(14): Show |
17 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.290-5612_290-5607d others(8): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102651934 | ||||||
| chr2:102651983 | T | C | 113 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(110): Show |
114 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.290-5581T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102651983 | |||||||
| chr2:102652052 | A | G | 306 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(303): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.290-5512A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102652052 | |||||||
| chr2:102652422 | T | A | 1 | a0001c0001t0002g0035 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.290-5142T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102652422 | |||||||
| chr2:102652693 | T | G | 2 | a0001c0001t0002g0148 a0001c0001t0002g0149 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.290-4871T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102652693 | |||||||
| chr2:102652695 | G | C | 1 | a0001c0001t0028g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.290-4869G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102652695 | |||||||
| chr2:102652846 | C | T | 1 | a0001c0001t0002g0339 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.290-4718C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102652846 | |||||||
| chr2:102652996 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.290-4568A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102652996 | |||||||
| chr2:102653006 | C | A | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.290-4558C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102653006 | |||||||
| chr2:102653115 | T | C | 10 | a0001c0001t0002g0300 a0001c0001t0004g0316 a0001c0001t0005g0317 others(7): Show |
10 | HG01167.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.290-4449T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102653115 | |||||||
| chr2:102653317 | C | T | 7 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0002g0089 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-4247C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102653317 | |||||||
| chr2:102653414 | C | T | 253 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(250): Show |
254 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.290-4150C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102653414 | |||||||
| chr2:102653483 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.290-4081G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102653483 | |||||||
| chr2:102653835 | T | G | 1 | a0001c0001t0002g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.290-3729T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102653835 | |||||||
| chr2:102653905 | G | A | 10 | a0001c0001t0002g0300 a0001c0001t0004g0316 a0001c0001t0005g0317 others(7): Show |
10 | HG01167.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.290-3659G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102653905 | |||||||
| chr2:102653946 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.290-3618G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102653946 | |||||||
| chr2:102653974 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0003g0212 |
2 | HG00140.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.290-3590T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102653974 | |||||||
| chr2:102654161 | A | G | 2 | a0001c0001t0002g0051 a0001c0001t0002g0167 |
2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.290-3403A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102654161 | |||||||
| chr2:102654195 | C | CT | 138 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0041 others(135): Show |
139 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.290-3346dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102654195 | ||||||
| chr2:102654195 | C | CTT | 22 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0100 others(19): Show |
22 | HG00621.hp2 HG00738.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.290-3347_290-3346d others(4): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102654195 | ||||||
| chr2:102654195 | C | CTTT | 7 | a0001c0001t0001g0119 a0001c0001t0001g0154 a0001c0001t0001g0249 others(4): Show |
7 | HG01884.hp2 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-3348_290-3346d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102654195 | ||||||
| chr2:102654195 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.290-3361_290-3346d others(18): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102654195 | ||||||
| chr2:102654363 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.290-3201G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102654363 | |||||||
| chr2:102654498 | A | T | 20 | a0001c0001t0001g0119 a0001c0001t0001g0154 a0001c0001t0001g0314 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.290-3066A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102654498 | |||||||
| chr2:102654697 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.290-2867C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102654697 | |||||||
| chr2:102654773 | C | T | 1 | a0001c0001t0003g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.290-2791C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102654773 | |||||||
| chr2:102654879 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.290-2685G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102654879 | |||||||
| chr2:102655054 | A | T | 1 | a0001c0001t0009g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.290-2510A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655054 | |||||||
| chr2:102655122 | G | GT | 5 | a0001c0001t0001g0027 a0001c0001t0001g0100 a0001c0001t0001g0238 others(2): Show |
5 | HG00738.hp2 NA18972.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-2435dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102655122 | ||||||
| chr2:102655122 | G | T | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-2442G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655122 | |||||||
| chr2:102655140 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.290-2424T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655140 | |||||||
| chr2:102655210 | C | CT | 32 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(29): Show |
32 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.290-2338dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102655210 | ||||||
| chr2:102655210 | C | CTT | 131 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
131 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.290-2339_290-2338d others(4): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102655210 | ||||||
| chr2:102655210 | C | CTTT | 6 | a0001c0001t0001g0090 a0001c0001t0002g0089 a0001c0001t0002g0092 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-2340_290-2338d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102655210 | ||||||
| chr2:102655501 | T | C | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-2063T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655501 | |||||||
| chr2:102655649 | A | G | 86 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0034 others(83): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.290-1915A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655649 | |||||||
| chr2:102655681 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.290-1883A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655681 | |||||||
| chr2:102655738 | A | G | 8 | a0001c0001t0002g0300 a0001c0001t0004g0316 a0001c0001t0005g0317 others(5): Show |
8 | HG01167.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.290-1826A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655738 | |||||||
| chr2:102655766 | T | G | 19 | a0001c0001t0001g0119 a0001c0001t0001g0154 a0001c0001t0001g0330 others(16): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.290-1798T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655766 | |||||||
| chr2:102655932 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.290-1632C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655932 | |||||||
| chr2:102655933 | C | T | 89 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0034 others(86): Show |
89 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.290-1631C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655933 | |||||||
| chr2:102655945 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.290-1619G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102655945 | |||||||
| chr2:102656026 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.290-1538C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656026 | |||||||
| chr2:102656027 | G | T | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.290-1537G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656027 | |||||||
| chr2:102656156 | C | A | 1 | a0001c0001t0002g0180 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.290-1408C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656156 | |||||||
| chr2:102656210 | A | G | 9 | a0001c0001t0001g0028 a0001c0001t0001g0078 a0001c0001t0001g0163 others(6): Show |
9 | HG01192.hp1 HG02083.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-1354A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656210 | |||||||
| chr2:102656254 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0002g0104 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.290-1310C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656254 | |||||||
| chr2:102656315 | A | G | 10 | a0001c0001t0001g0154 a0001c0001t0001g0330 a0001c0001t0002g0104 others(7): Show |
10 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.290-1249A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656315 | |||||||
| chr2:102656375 | A | G | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-1189A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656375 | |||||||
| chr2:102656376 | T | C | 1 | a0001c0001t0003g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.290-1188T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656376 | |||||||
| chr2:102656498 | G | A | 109 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(106): Show |
110 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.290-1066G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656498 | |||||||
| chr2:102656644 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.290-920T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656644 | |||||||
| chr2:102656696 | A | G | 3 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0012g0329 |
3 | HG02647.hp1 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.290-868A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656696 | |||||||
| chr2:102656780 | T | C | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-784T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656780 | |||||||
| chr2:102656795 | C | T | 2 | a0001c0001t0007g0335 a0004c0006t0004g0334 |
2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.290-769C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656795 | |||||||
| chr2:102656796 | G | A | 4 | a0001c0001t0002g0300 a0001c0001t0004g0316 a0001c0001t0013g0315 others(1): Show |
4 | HG01167.hp2 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-768G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656796 | |||||||
| chr2:102656926 | C | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0176 a0001c0001t0003g0024 others(3): Show |
6 | HG01175.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-638C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656926 | |||||||
| chr2:102656996 | G | T | 3 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0012g0329 |
3 | HG02647.hp1 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.290-568G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102656996 | |||||||
| chr2:102657002 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.290-562C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102657002 | |||||||
| chr2:102657189 | G | C | 1 | a0001c0001t0002g0267 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.290-375G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102657189 | |||||||
| chr2:102657205 | C | CA | 7 | a0001c0001t0001g0119 a0001c0001t0002g0274 a0001c0001t0003g0298 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.290-348dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102657205 | ||||||
| chr2:102657205 | CA | C | 27 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0107 others(24): Show |
27 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.290-348delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 102657205 | ||||||
| chr2:102657214 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0131 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-350A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102657214 | |||||||
| chr2:102657216 | AT | A | 5 | a0001c0001t0001g0081 a0001c0001t0001g0124 a0001c0001t0001g0266 others(2): Show |
5 | HG01070.hp1 HG02735.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-347delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102657216 | |||||||
| chr2:102657217 | T | A | 112 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0034 others(109): Show |
112 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.290-347T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102657217 | |||||||
| chr2:102657220 | T | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0186 a0001c0001t0007g0269 |
3 | HG02970.hp2 NA18941.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.290-344T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102657220 | |||||||
| chr2:102657240 | T | C | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-324T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102657240 | |||||||
| chr2:102657471 | C | T | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-93C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102657471 | |||||||
| chr2:102657493 | A | G | 1 | a0001c0001t0003g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.290-71A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102657493 | |||||||
| chr2:102658036 | C | A | 1 | a0001c0001t0003g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.753+9C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102658036 | |||||||
| chr2:102658065 | G | T | 1 | a0004c0006t0004g0334 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.753+38G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102658065 | |||||||
| chr2:102658257 | T | C | 3 | a0001c0001t0004g0282 a0001c0001t0018g0265 a0001c0001t0028g0178 |
3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+230T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102658257 | |||||||
| chr2:102658629 | T | C | 1 | a0001c0001t0002g0020 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.753+602T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102658629 | |||||||
| chr2:102658687 | A | G | 5 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0004g0284 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+660A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102658687 | |||||||
| chr2:102658736 | C | T | 4 | a0001c0001t0001g0154 a0001c0001t0002g0104 a0001c0001t0002g0118 others(1): Show |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+709C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102658736 | |||||||
| chr2:102658875 | G | A | 7 | a0001c0001t0001g0119 a0001c0001t0002g0274 a0001c0001t0003g0298 others(4): Show |
7 | HG01884.hp2 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+848G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102658875 | |||||||
| chr2:102658911 | C | T | 10 | a0001c0001t0002g0300 a0001c0001t0004g0316 a0001c0001t0005g0317 others(7): Show |
10 | HG01167.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.753+884C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102658911 | |||||||
| chr2:102659047 | T | G | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.753+1020T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659047 | |||||||
| chr2:102659140 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.753+1113C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659140 | |||||||
| chr2:102659141 | G | A | 1 | a0001c0001t0015g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.753+1114G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659141 | |||||||
| chr2:102659148 | G | A | 5 | a0001c0001t0001g0154 a0001c0001t0001g0314 a0001c0001t0002g0104 others(2): Show |
5 | HG02615.hp2 HG03209.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+1121G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659148 | |||||||
| chr2:102659207 | C | A | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.753+1180C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659207 | |||||||
| chr2:102659223 | G | A | 1 | a0001c0001t0014g0133 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.753+1196G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659223 | |||||||
| chr2:102659243 | A | G | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.753+1216A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659243 | |||||||
| chr2:102659255 | C | G | 1 | a0001c0001t0002g0158 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.753+1228C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659255 | |||||||
| chr2:102659273 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.753+1246A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659273 | |||||||
| chr2:102659274 | CA | C | 223 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(220): Show |
224 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.753+1264delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102659274 | ||||||
| chr2:102659274 | CAA | C | 13 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0076 others(10): Show |
13 | HG00639.hp2 HG00642.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+1263_753+1264d others(4): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102659274 | ||||||
| chr2:102659314 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0023g0008 |
2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.753+1287G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659314 | |||||||
| chr2:102659323 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.753+1296C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659323 | |||||||
| chr2:102659356 | G | A | 9 | a0001c0001t0001g0119 a0001c0001t0001g0338 a0001c0001t0002g0274 others(6): Show |
9 | HG01884.hp2 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+1329G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659356 | |||||||
| chr2:102659373 | G | A | 113 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(110): Show |
114 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.753+1346G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659373 | |||||||
| chr2:102659460 | A | C | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.753+1433A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659460 | |||||||
| chr2:102659482 | C | G | 1 | a0001c0001t0015g0288 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.753+1455C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659482 | |||||||
| chr2:102659482 | C | T | 1 | a0001c0001t0003g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.753+1455C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659482 | |||||||
| chr2:102659525 | C | T | 1 | a0004c0006t0004g0334 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.753+1498C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659525 | |||||||
| chr2:102659732 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.753+1705G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659732 | |||||||
| chr2:102659821 | C | T | 1 | a0001c0001t0016g0293 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.753+1794C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659821 | |||||||
| chr2:102659826 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.753+1799C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659826 | |||||||
| chr2:102659890 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.753+1863T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659890 | |||||||
| chr2:102659924 | G | T | 117 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(114): Show |
118 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.753+1897G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659924 | |||||||
| chr2:102659925 | C | T | 117 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(114): Show |
118 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.753+1898C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659925 | |||||||
| chr2:102659927 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.753+1900C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659927 | |||||||
| chr2:102660006 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.753+1979C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660006 | |||||||
| chr2:102660037 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.753+2010T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660037 | |||||||
| chr2:102660250 | C | G | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.753+2223C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660250 | |||||||
| chr2:102660462 | A | C | 10 | a0001c0001t0001g0040 a0001c0001t0001g0193 a0001c0001t0001g0198 others(7): Show |
10 | NA18946.hp1 NA18948.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.753+2435A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660462 | |||||||
| chr2:102660813 | A | G | 88 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0034 others(85): Show |
88 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.753+2786A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660813 | |||||||
| chr2:102660834 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.753+2807A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660834 | |||||||
| chr2:102660847 | T | A | 87 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0034 others(84): Show |
87 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.753+2820T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660847 | |||||||
| chr2:102660867 | T | C | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.753+2840T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660867 | |||||||
| chr2:102660872 | C | T | 24 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0107 others(21): Show |
24 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.753+2845C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660872 | |||||||
| chr2:102660990 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.753+2963G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102660990 | |||||||
| chr2:102661113 | G | A | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.753+3086G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661113 | |||||||
| chr2:102661160 | T | G | 43 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0107 others(40): Show |
43 | HG01167.hp2 HG01175.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.753+3133T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661160 | |||||||
| chr2:102661188 | T | C | 119 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(116): Show |
120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.753+3161T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661188 | |||||||
| chr2:102661258 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.753+3231C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661258 | |||||||
| chr2:102661401 | A | G | 1 | a0001c0001t0030g0010 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.753+3374A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661401 | |||||||
| chr2:102661403 | G | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0078 a0001c0001t0001g0160 others(12): Show |
15 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.753+3376G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661403 | |||||||
| chr2:102661736 | C | G | 87 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0034 others(84): Show |
87 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.754-3364C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661736 | |||||||
| chr2:102661814 | C | T | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-3286C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661814 | |||||||
| chr2:102661815 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.754-3285G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661815 | |||||||
| chr2:102661891 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.754-3209A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102661891 | |||||||
| chr2:102662076 | G | A | 7 | a0001c0001t0001g0090 a0001c0001t0002g0089 a0001c0001t0002g0092 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.754-3024G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102662076 | |||||||
| chr2:102662457 | G | A | 7 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(4): Show |
7 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-2643G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102662457 | |||||||
| chr2:102662519 | G | C | 27 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0091 others(24): Show |
27 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.754-2581G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102662519 | |||||||
| chr2:102662739 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0023g0008 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.754-2361G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102662739 | |||||||
| chr2:102662764 | T | TA | 104 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0033 others(101): Show |
104 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.754-2325dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102662764 | ||||||
| chr2:102663106 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0023g0008 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.754-1994G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102663106 | |||||||
| chr2:102663466 | A | T | 2 | a0001c0001t0002g0071 a0001c0001t0010g0077 |
2 | HG01496.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.754-1634A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102663466 | |||||||
| chr2:102663491 | T | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0338 a0001c0001t0002g0274 others(3): Show |
6 | HG02486.hp1 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-1609T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102663491 | |||||||
| chr2:102663528 | C | T | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.754-1572C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102663528 | |||||||
| chr2:102663534 | C | T | 88 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(85): Show |
88 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.754-1566C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102663534 | |||||||
| chr2:102663713 | C | A | 2 | a0001c0001t0001g0085 a0001c0001t0002g0084 |
2 | NA18747.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.754-1387C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102663713 | |||||||
| chr2:102663975 | T | C | 1 | a0001c0001t0003g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.754-1125T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102663975 | |||||||
| chr2:102664001 | C | T | 1 | a0001c0001t0003g0298 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754-1099C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664001 | |||||||
| chr2:102664041 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.754-1059C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664041 | |||||||
| chr2:102664047 | G | T | 1 | a0001c0001t0002g0188 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.754-1053G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664047 | |||||||
| chr2:102664082 | C | G | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-1018C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664082 | |||||||
| chr2:102664273 | C | CA | 14 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0330 others(11): Show |
14 | HG00099.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.754-812dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102664273 | ||||||
| chr2:102664314 | C | A | 1 | a0001c0001t0011g0297 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.754-786C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664314 | |||||||
| chr2:102664353 | C | T | 1 | a0001c0001t0002g0318 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.754-747C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664353 | |||||||
| chr2:102664445 | G | GCA | 98 | a0001c0001t0001g0033 a0001c0001t0001g0042 a0001c0001t0001g0043 others(95): Show |
98 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.754-624_754-623dup others(2): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102664445 | ||||||
| chr2:102664445 | G | GCACA | 104 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0069 others(101): Show |
105 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.754-626_754-623dup others(4): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102664445 | ||||||
| chr2:102664445 | G | GCACACA | 9 | a0001c0001t0001g0028 a0001c0001t0001g0112 a0001c0001t0001g0116 others(6): Show |
9 | HG02080.hp1 HG02723.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.754-628_754-623dup others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102664445 | ||||||
| chr2:102664445 | GCA | G | 38 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0023 others(35): Show |
38 | HG00280.hp1 HG00738.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.754-624_754-623del others(2): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102664445 | ||||||
| chr2:102664445 | GCACA | G | 20 | a0001c0001t0001g0040 a0001c0001t0001g0138 a0001c0001t0001g0190 others(17): Show |
20 | HG01167.hp2 HG02572.hp1 HG02895.hp2 others(17): Show |
intron_variant | MODIFIER | c.754-626_754-623del others(4): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102664445 | ||||||
| chr2:102664445 | GCACACA | G | 4 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0003g0279 others(1): Show |
4 | HG02970.hp2 HG03139.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-628_754-623del others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102664445 | ||||||
| chr2:102664537 | C | T | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-563C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664537 | |||||||
| chr2:102664616 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0033g0204 others(1): Show |
4 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-484A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664616 | |||||||
| chr2:102664638 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0314 a0001c0001t0002g0104 |
3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.754-462C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664638 | |||||||
| chr2:102664724 | C | A | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.754-376C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664724 | |||||||
| chr2:102664838 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.754-262A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664838 | |||||||
| chr2:102664875 | G | C | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-225G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664875 | |||||||
| chr2:102664958 | A | C | 102 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(99): Show |
103 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.754-142A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102664958 | |||||||
| chr2:102665019 | C | T | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-81C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102665019 | |||||||
| chr2:102665081 | G | GT | 70 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(67): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
splice_region_variant&intron_variant | LOW | c.754-8dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 102665081 | ||||||
| chr2:102665493 | G | A | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1004+143G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102665493 | |||||||
| chr2:102665517 | G | A | 1 | a0001c0003t0003g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1004+167G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102665517 | |||||||
| chr2:102665607 | T | C | 2 | a0001c0001t0006g0270 a0001c0001t0006g0271 |
2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1004+257T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102665607 | |||||||
| chr2:102665761 | A | G | 246 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(243): Show |
247 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1004+411A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102665761 | |||||||
| chr2:102665773 | T | TA | 37 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
37 | HG00099.hp2 HG00280.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1004+451dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | T | TAA | 45 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0018 others(42): Show |
46 | HG00140.hp2 HG00609.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.1004+450_1004+451d others(4): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | T | TAAA | 43 | a0001c0001t0001g0040 a0001c0001t0001g0112 a0001c0001t0001g0113 others(40): Show |
44 | HG00408.hp2 HG00609.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1004+449_1004+451d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | T | TAAAA | 53 | a0001c0001t0001g0030 a0001c0001t0001g0069 a0001c0001t0001g0095 others(50): Show |
53 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1004+448_1004+451d others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | T | TAAAAA | 41 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0066 others(38): Show |
41 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1004+447_1004+451d others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | T | TAAAAAA | 55 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0034 others(52): Show |
55 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1004+446_1004+451d others(8): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | T | TAAAAAAA | 15 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0076 others(12): Show |
15 | HG00741.hp2 HG01081.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1004+445_1004+451d others(9): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1004+439_1004+451d others(15): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | TAAAAA | T | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004+447_1004+451d others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | TAAAAAA | T | 6 | a0001c0001t0001g0087 a0001c0001t0002g0089 a0001c0001t0002g0092 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1004+446_1004+451d others(8): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665773 | TAAAAAAA | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0061 others(17): Show |
20 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.1004+445_1004+451d others(9): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102665773 | ||||||
| chr2:102665987 | G | C | 4 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(1): Show |
4 | NA18944.hp2 NA18977.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+637G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102665987 | |||||||
| chr2:102666008 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0314 a0001c0001t0002g0104 |
3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1004+658A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666008 | |||||||
| chr2:102666014 | T | C | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1004+664T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666014 | |||||||
| chr2:102666094 | A | T | 93 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(90): Show |
93 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1004+744A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666094 | |||||||
| chr2:102666137 | T | TA | 100 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(97): Show |
101 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1004+788dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102666137 | ||||||
| chr2:102666194 | C | CT | 63 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(60): Show |
64 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1004+863dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102666194 | ||||||
| chr2:102666194 | C | CTT | 84 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0001g0042 others(81): Show |
84 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1004+862_1004+863d others(4): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102666194 | ||||||
| chr2:102666194 | C | CTTT | 6 | a0001c0001t0001g0062 a0001c0001t0001g0076 a0001c0001t0001g0098 others(3): Show |
6 | HG00438.hp1 HG00642.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.1004+861_1004+863d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102666194 | ||||||
| chr2:102666194 | CT | C | 18 | a0001c0001t0001g0028 a0001c0001t0001g0078 a0001c0001t0001g0090 others(15): Show |
18 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1004+863delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102666194 | ||||||
| chr2:102666194 | CTTT | C | 6 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004+861_1004+863d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102666194 | ||||||
| chr2:102666219 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1004+869G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666219 | |||||||
| chr2:102666226 | C | T | 91 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(88): Show |
91 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1004+876C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666226 | |||||||
| chr2:102666238 | T | C | 1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1004+888T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666238 | |||||||
| chr2:102666258 | T | C | 130 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0023 others(127): Show |
130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1004+908T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666258 | |||||||
| chr2:102666289 | G | A | 3 | a0001c0001t0004g0282 a0001c0001t0018g0265 a0001c0001t0028g0178 |
3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1004+939G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666289 | |||||||
| chr2:102666336 | C | T | 24 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(21): Show |
24 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1004+986C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666336 | |||||||
| chr2:102666338 | G | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0314 a0001c0001t0002g0104 |
3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1004+988G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666338 | |||||||
| chr2:102666340 | C | G | 21 | a0001c0001t0001g0043 a0001c0001t0001g0073 a0001c0001t0001g0081 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1004+990C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666340 | |||||||
| chr2:102666355 | C | A | 3 | a0001c0001t0001g0091 a0001c0001t0016g0291 a0001c0001t0023g0008 |
3 | HG02486.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1004+1005C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666355 | |||||||
| chr2:102666363 | T | A | 1 | a0001c0001t0001g0042 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1004+1013T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666363 | |||||||
| chr2:102666437 | T | C | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004+1087T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666437 | |||||||
| chr2:102666682 | T | C | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004+1332T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666682 | |||||||
| chr2:102666820 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1004+1470A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666820 | |||||||
| chr2:102666830 | A | T | 100 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(97): Show |
101 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1004+1480A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666830 | |||||||
| chr2:102666867 | C | G | 3 | a0001c0001t0001g0091 a0001c0001t0016g0291 a0001c0001t0023g0008 |
3 | HG02486.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1004+1517C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666867 | |||||||
| chr2:102666941 | C | T | 7 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0002g0089 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1004+1591C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666941 | |||||||
| chr2:102666950 | T | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0164 others(12): Show |
15 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1004+1600T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102666950 | |||||||
| chr2:102667048 | C | A | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1004+1698C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102667048 | |||||||
| chr2:102667145 | C | G | 1 | a0001c0001t0025g0340 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1004+1795C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102667145 | |||||||
| chr2:102667459 | T | C | 1 | a0001c0001t0015g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1004+2109T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102667459 | |||||||
| chr2:102667698 | G | A | 88 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(85): Show |
88 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1004+2348G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102667698 | |||||||
| chr2:102667823 | A | G | 2 | a0001c0001t0018g0265 a0001c0001t0028g0178 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1004+2473A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102667823 | |||||||
| chr2:102667839 | A | G | 245 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(242): Show |
246 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.1004+2489A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102667839 | |||||||
| chr2:102667920 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1004+2570C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102667920 | |||||||
| chr2:102668110 | A | C | 1 | a0001c0001t0003g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1004+2760A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668110 | |||||||
| chr2:102668128 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1004+2778A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668128 | |||||||
| chr2:102668157 | T | C | 93 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(90): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1004+2807T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668157 | |||||||
| chr2:102668158 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1004+2808T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668158 | |||||||
| chr2:102668178 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1004+2828T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668178 | |||||||
| chr2:102668220 | A | G | 3 | a0001c0001t0004g0282 a0001c0001t0018g0265 a0001c0001t0028g0178 |
3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1004+2870A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668220 | |||||||
| chr2:102668272 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0314 a0001c0001t0002g0104 |
3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1004+2922C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668272 | |||||||
| chr2:102668469 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1004+3119C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668469 | |||||||
| chr2:102668471 | C | T | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1004+3121C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668471 | |||||||
| chr2:102668567 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1004+3217T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668567 | |||||||
| chr2:102668610 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1004+3260C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668610 | |||||||
| chr2:102668906 | A | G | 15 | a0001c0001t0001g0154 a0001c0001t0001g0314 a0001c0001t0002g0104 others(12): Show |
15 | HG01167.hp2 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1004+3556A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668906 | |||||||
| chr2:102668921 | A | C | 27 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(24): Show |
27 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1004+3571A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102668921 | |||||||
| chr2:102669012 | G | A | 2 | a0001c0001t0018g0265 a0001c0001t0028g0178 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1004+3662G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102669012 | |||||||
| chr2:102669015 | C | T | 90 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(87): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1004+3665C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102669015 | |||||||
| chr2:102669334 | G | A | 87 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(84): Show |
87 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1004+3984G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102669334 | |||||||
| chr2:102669366 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1004+4016G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102669366 | |||||||
| chr2:102669495 | C | A | 1 | a0001c0001t0002g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1004+4145C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102669495 | |||||||
| chr2:102669648 | T | C | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1004+4298T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102669648 | |||||||
| chr2:102669904 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1004+4554T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102669904 | |||||||
| chr2:102670011 | A | AT | 51 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0100 others(48): Show |
51 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1004+4669dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670011 | ||||||
| chr2:102670041 | A | AT | 221 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(218): Show |
222 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1004+4699dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670041 | ||||||
| chr2:102670041 | A | ATT | 108 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(105): Show |
109 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1004+4698_1004+469 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670041 | ||||||
| chr2:102670095 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0027 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1004+4745G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670095 | |||||||
| chr2:102670131 | C | T | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1004+4781C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670131 | |||||||
| chr2:102670132 | G | A | 3 | a0001c0001t0002g0280 a0001c0001t0004g0284 a0001c0001t0004g0285 |
3 | HG01891.hp2 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1004+4782G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670132 | |||||||
| chr2:102670178 | A | AT | 229 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0030 others(226): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1004+4839dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670178 | ||||||
| chr2:102670178 | A | ATT | 17 | a0001c0001t0001g0027 a0001c0001t0001g0090 a0001c0001t0001g0150 others(14): Show |
17 | HG00673.hp2 HG02055.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1004+4838_1004+483 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670178 | ||||||
| chr2:102670187 | T | TG | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004+4837_1004+483 others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670187 | |||||||
| chr2:102670258 | C | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(19): Show |
22 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1004+4908C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670258 | |||||||
| chr2:102670259 | G | A | 3 | a0001c0001t0004g0282 a0001c0001t0018g0265 a0001c0001t0028g0178 |
3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1004+4909G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670259 | |||||||
| chr2:102670449 | T | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0314 a0001c0001t0002g0104 |
3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1004+5099T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670449 | |||||||
| chr2:102670543 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1004+5193C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670543 | |||||||
| chr2:102670592 | C | T | 6 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004+5242C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670592 | |||||||
| chr2:102670596 | C | A | 3 | a0001c0001t0001g0119 a0001c0001t0006g0270 a0001c0001t0006g0271 |
3 | HG03130.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1004+5246C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670596 | |||||||
| chr2:102670599 | C | CA | 23 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0062 others(20): Show |
23 | HG00438.hp1 HG00738.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.1004+5272dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670599 | ||||||
| chr2:102670599 | CA | C | 29 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0090 others(26): Show |
29 | HG01070.hp1 HG01167.hp2 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.1004+5272delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670599 | ||||||
| chr2:102670599 | CAA | C | 50 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0030 others(47): Show |
50 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1004+5271_1004+527 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670599 | ||||||
| chr2:102670599 | CAAA | C | 77 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0069 others(74): Show |
78 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1004+5270_1004+527 others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670599 | ||||||
| chr2:102670620 | A | C | 2 | a0001c0001t0001g0151 a0001c0001t0002g0152 |
2 | NA18971.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1004+5270A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670620 | |||||||
| chr2:102670627 | C | G | 2 | a0001c0001t0001g0154 a0001c0001t0002g0104 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1004+5277C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670627 | |||||||
| chr2:102670671 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0003g0057 |
2 | HG01884.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1004+5321C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670671 | |||||||
| chr2:102670677 | T | C | 1 | a0001c0001t0023g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1004+5327T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670677 | |||||||
| chr2:102670740 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1004+5390G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670740 | |||||||
| chr2:102670802 | A | C | 87 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(84): Show |
87 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1004+5452A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670802 | |||||||
| chr2:102670842 | A | T | 110 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(107): Show |
111 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1004+5492A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670842 | |||||||
| chr2:102670849 | C | CT | 39 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
39 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.1004+5520dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670849 | ||||||
| chr2:102670849 | C | CTT | 200 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0029 others(197): Show |
202 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.1004+5519_1004+552 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670849 | ||||||
| chr2:102670849 | C | CTTT | 39 | a0001c0001t0001g0028 a0001c0001t0001g0047 a0001c0001t0001g0069 others(36): Show |
39 | HG00438.hp2 HG00609.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1004+5518_1004+552 others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670849 | ||||||
| chr2:102670849 | C | CTTTT | 7 | a0001c0001t0001g0098 a0001c0001t0001g0127 a0001c0001t0001g0146 others(4): Show |
7 | HG00408.hp1 HG01123.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.1004+5517_1004+552 others(8): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670849 | ||||||
| chr2:102670849 | CTT | C | 9 | a0001c0001t0001g0281 a0001c0001t0001g0314 a0001c0001t0001g0330 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1004+5519_1004+552 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670849 | ||||||
| chr2:102670849 | CTTT | C | 20 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(17): Show |
20 | HG01175.hp1 HG01255.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1004+5518_1004+552 others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102670849 | ||||||
| chr2:102670911 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1004+5561G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670911 | |||||||
| chr2:102670989 | T | C | 250 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(247): Show |
251 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1004+5639T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102670989 | |||||||
| chr2:102671070 | T | A | 3 | a0001c0001t0004g0282 a0001c0001t0018g0265 a0001c0001t0028g0178 |
3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1004+5720T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671070 | |||||||
| chr2:102671079 | C | T | 1 | a0001c0001t0016g0293 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1004+5729C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671079 | |||||||
| chr2:102671165 | C | T | 101 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1004+5815C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671165 | |||||||
| chr2:102671233 | C | CCTCACAA others(25): Show |
1 | a0001c0001t0028g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1004+5883_1004+588 others(36): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671233 | |||||||
| chr2:102671233 | C | T | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1004+5883C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671233 | |||||||
| chr2:102671234 | G | A | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1004+5884G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671234 | |||||||
| chr2:102671258 | GTTTTAC | G | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1004+5914_1004+591 others(10): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102671258 | ||||||
| chr2:102671431 | T | G | 27 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(24): Show |
27 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1004+6081T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671431 | |||||||
| chr2:102671507 | A | C | 66 | a0001c0001t0001g0030 a0001c0001t0001g0069 a0001c0001t0001g0095 others(63): Show |
67 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1004+6157A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671507 | |||||||
| chr2:102671508 | T | C | 102 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1004+6158T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671508 | |||||||
| chr2:102671563 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1004+6213G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671563 | |||||||
| chr2:102671630 | T | C | 6 | a0001c0001t0001g0090 a0001c0001t0002g0089 a0001c0001t0002g0092 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1004+6280T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671630 | |||||||
| chr2:102671641 | T | G | 22 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(19): Show |
22 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1004+6291T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671641 | |||||||
| chr2:102671711 | G | A | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1004+6361G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671711 | |||||||
| chr2:102671714 | G | A | 1 | a0001c0001t0002g0339 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1004+6364G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671714 | |||||||
| chr2:102671748 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(31): Show |
34 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1004+6398A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671748 | |||||||
| chr2:102671963 | A | G | 33 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(30): Show |
33 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1004+6613A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102671963 | |||||||
| chr2:102672017 | G | A | 2 | a0001c0001t0018g0265 a0001c0001t0028g0178 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1004+6667G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672017 | |||||||
| chr2:102672038 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0078 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1004+6688G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672038 | |||||||
| chr2:102672074 | A | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1004+6724A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672074 | |||||||
| chr2:102672086 | G | T | 106 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(103): Show |
107 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1004+6736G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672086 | |||||||
| chr2:102672134 | A | G | 3 | a0001c0001t0004g0282 a0001c0001t0018g0265 a0001c0001t0028g0178 |
3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1004+6784A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672134 | |||||||
| chr2:102672137 | T | C | 3 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0012g0329 |
3 | HG02647.hp1 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1004+6787T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672137 | |||||||
| chr2:102672138 | A | T | 1 | a0001c0001t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1004+6788A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672138 | |||||||
| chr2:102672147 | T | C | 251 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(248): Show |
252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1004+6797T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672147 | |||||||
| chr2:102672182 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0002g0159 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1004+6832T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672182 | |||||||
| chr2:102672189 | T | C | 1 | a0001c0001t0003g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1004+6839T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672189 | |||||||
| chr2:102672290 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1004+6940C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672290 | |||||||
| chr2:102672322 | A | C | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1004+6972A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672322 | |||||||
| chr2:102672359 | CTG | C | 103 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(100): Show |
103 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1004+7011_1004+701 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102672359 | ||||||
| chr2:102672368 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1004+7018T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672368 | |||||||
| chr2:102672378 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1004+7028A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672378 | |||||||
| chr2:102672396 | T | G | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1004+7046T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672396 | |||||||
| chr2:102672433 | CT | C | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1004+7087delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102672433 | ||||||
| chr2:102672496 | C | G | 1 | a0001c0001t0002g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1004+7146C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672496 | |||||||
| chr2:102672575 | G | A | 14 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0164 others(11): Show |
14 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1004+7225G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672575 | |||||||
| chr2:102672683 | C | T | 102 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1004+7333C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672683 | |||||||
| chr2:102672768 | A | T | 2 | a0001c0001t0001g0154 a0001c0001t0002g0104 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1004+7418A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672768 | |||||||
| chr2:102672769 | G | A | 1 | a0001c0001t0019g0054 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1004+7419G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672769 | |||||||
| chr2:102672827 | T | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1004+7477T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672827 | |||||||
| chr2:102672971 | G | C | 3 | a0001c0001t0001g0091 a0001c0001t0016g0291 a0001c0001t0023g0008 |
3 | HG02486.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1004+7621G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672971 | |||||||
| chr2:102672992 | G | C | 1 | a0001c0001t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1004+7642G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672992 | |||||||
| chr2:102672993 | CT | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1004+7644delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102672993 | |||||||
| chr2:102673026 | C | CA | 23 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(20): Show |
23 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1004+7685dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102673026 | ||||||
| chr2:102673083 | G | A | 110 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(107): Show |
111 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1004+7733G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673083 | |||||||
| chr2:102673149 | G | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1004+7799G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673149 | |||||||
| chr2:102673226 | A | C | 1 | a0001c0001t0001g0262 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1004+7876A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673226 | |||||||
| chr2:102673257 | T | A | 6 | a0001c0001t0002g0300 a0001c0001t0004g0316 a0001c0001t0005g0317 others(3): Show |
6 | HG01167.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1004+7907T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673257 | |||||||
| chr2:102673278 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1004+7928A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673278 | |||||||
| chr2:102673380 | CT | C | 87 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(84): Show |
87 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1004+8037delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102673380 | ||||||
| chr2:102673390 | T | C | 103 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(100): Show |
103 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1004+8040T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673390 | |||||||
| chr2:102673480 | A | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1004+8130A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673480 | |||||||
| chr2:102673667 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0002g0104 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1004+8317A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673667 | |||||||
| chr2:102673782 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1004+8432T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673782 | |||||||
| chr2:102673788 | C | CT | 26 | a0001c0001t0001g0040 a0001c0001t0001g0098 a0001c0001t0001g0137 others(23): Show |
26 | HG00280.hp2 HG01071.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1004+8454dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102673788 | ||||||
| chr2:102673788 | CT | C | 14 | a0001c0001t0001g0119 a0001c0001t0001g0153 a0001c0001t0001g0287 others(11): Show |
14 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1004+8454delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102673788 | ||||||
| chr2:102673825 | C | T | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1004+8475C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673825 | |||||||
| chr2:102673841 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1004+8491T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673841 | |||||||
| chr2:102673848 | G | A | 1 | a0001c0001t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1004+8498G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673848 | |||||||
| chr2:102673883 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1004+8533T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673883 | |||||||
| chr2:102673936 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1004+8586C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673936 | |||||||
| chr2:102673944 | C | T | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1004+8594C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673944 | |||||||
| chr2:102673948 | C | T | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1004+8598C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673948 | |||||||
| chr2:102673992 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0031 others(27): Show |
31 | HG00609.hp2 HG01106.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1004+8642T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102673992 | |||||||
| chr2:102674180 | C | G | 303 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(300): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1004+8830C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102674180 | |||||||
| chr2:102674387 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0002g0104 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1005-8874G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102674387 | |||||||
| chr2:102674444 | C | T | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1005-8817C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102674444 | |||||||
| chr2:102674735 | G | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-8526G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102674735 | |||||||
| chr2:102674923 | T | G | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1005-8338T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102674923 | |||||||
| chr2:102675023 | A | G | 6 | a0001c0001t0001g0090 a0001c0001t0002g0089 a0001c0001t0002g0092 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1005-8238A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102675023 | |||||||
| chr2:102675184 | A | G | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1005-8077A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102675184 | |||||||
| chr2:102675461 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1005-7800C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102675461 | |||||||
| chr2:102675533 | G | C | 1 | a0001c0001t0002g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1005-7728G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102675533 | |||||||
| chr2:102675582 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1005-7679G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102675582 | |||||||
| chr2:102675698 | A | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0314 a0001c0001t0006g0270 others(1): Show |
4 | HG03130.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005-7563A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102675698 | |||||||
| chr2:102675819 | G | A | 3 | a0001c0001t0004g0282 a0001c0001t0018g0265 a0001c0001t0028g0178 |
3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1005-7442G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102675819 | |||||||
| chr2:102675861 | C | A | 2 | a0001c0001t0001g0106 a0001c0001t0007g0105 |
2 | HG02258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1005-7400C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102675861 | |||||||
| chr2:102675981 | T | C | 24 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(21): Show |
24 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1005-7280T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102675981 | |||||||
| chr2:102676234 | C | A | 250 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(247): Show |
251 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1005-7027C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102676234 | |||||||
| chr2:102676299 | G | A | 2 | a0001c0001t0002g0118 a0001c0001t0031g0117 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1005-6962G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102676299 | |||||||
| chr2:102676503 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1005-6758T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102676503 | |||||||
| chr2:102676657 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-6604G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102676657 | |||||||
| chr2:102676769 | A | T | 30 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(27): Show |
30 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1005-6492A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102676769 | |||||||
| chr2:102677072 | C | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0146 |
3 | HG00408.hp1 HG02040.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1005-6189C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677072 | |||||||
| chr2:102677084 | A | G | 1 | a0001c0001t0015g0288 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1005-6177A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677084 | |||||||
| chr2:102677149 | T | G | 1 | a0001c0001t0001g0135 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1005-6112T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677149 | |||||||
| chr2:102677159 | T | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-6102T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677159 | |||||||
| chr2:102677197 | G | C | 1 | a0001c0001t0003g0342 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1005-6064G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677197 | |||||||
| chr2:102677258 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1005-6003G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677258 | |||||||
| chr2:102677270 | GTC | G | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-5989_1005-598 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102677270 | ||||||
| chr2:102677297 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1005-5964G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677297 | |||||||
| chr2:102677298 | GA | G | 30 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(27): Show |
30 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1005-5953delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102677298 | ||||||
| chr2:102677299 | A | G | 1 | a0001c0001t0008g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1005-5962A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677299 | |||||||
| chr2:102677438 | T | C | 30 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(27): Show |
30 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1005-5823T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677438 | |||||||
| chr2:102677512 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1005-5749C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677512 | |||||||
| chr2:102677557 | G | T | 3 | a0001c0001t0004g0282 a0001c0001t0018g0265 a0001c0001t0028g0178 |
3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1005-5704G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677557 | |||||||
| chr2:102677595 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0221 |
2 | NA18972.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1005-5666C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677595 | |||||||
| chr2:102677785 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1005-5476A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677785 | |||||||
| chr2:102677812 | A | G | 12 | a0001c0001t0002g0300 a0001c0001t0004g0316 a0001c0001t0005g0317 others(9): Show |
12 | HG01167.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1005-5449A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677812 | |||||||
| chr2:102677967 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1005-5294A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677967 | |||||||
| chr2:102677993 | TCCCTGAA others(4): Show |
T | 111 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(108): Show |
112 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1005-5267_1005-525 others(15): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102677993 | |||||||
| chr2:102678080 | C | T | 1 | a0001c0001t0002g0318 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1005-5181C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102678080 | |||||||
| chr2:102678133 | C | T | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-5128C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102678133 | |||||||
| chr2:102678134 | G | A | 1 | a0001c0001t0013g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1005-5127G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102678134 | |||||||
| chr2:102678328 | T | TA | 126 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(123): Show |
127 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1005-4921dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102678328 | ||||||
| chr2:102678328 | TA | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(19): Show |
22 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1005-4921delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102678328 | ||||||
| chr2:102678509 | T | C | 250 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(247): Show |
251 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1005-4752T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102678509 | |||||||
| chr2:102678660 | G | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-4601G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102678660 | |||||||
| chr2:102678803 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1005-4458T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102678803 | |||||||
| chr2:102678903 | T | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-4358T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102678903 | |||||||
| chr2:102679054 | G | A | 249 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(246): Show |
250 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1005-4207G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679054 | |||||||
| chr2:102679131 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1005-4130T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679131 | |||||||
| chr2:102679236 | T | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-4025T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679236 | |||||||
| chr2:102679289 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1005-3972G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679289 | |||||||
| chr2:102679301 | C | T | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1005-3960C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679301 | |||||||
| chr2:102679370 | CTA | C | 113 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(110): Show |
114 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1005-3878_1005-387 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102679370 | ||||||
| chr2:102679381 | TATA | T | 112 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(109): Show |
112 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1005-3877_1005-387 others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102679381 | ||||||
| chr2:102679382 | AT | A | 23 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(20): Show |
23 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1005-3878delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679382 | |||||||
| chr2:102679385 | A | T | 23 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(20): Show |
23 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1005-3876A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679385 | |||||||
| chr2:102679386 | T | A | 112 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(109): Show |
112 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1005-3875T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679386 | |||||||
| chr2:102679387 | T | A | 3 | a0001c0001t0001g0139 a0001c0001t0002g0059 a0004c0006t0004g0334 |
3 | HG00673.hp1 NA18522.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1005-3874T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679387 | |||||||
| chr2:102679387 | T | G | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-3874T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679387 | |||||||
| chr2:102679444 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0073 a0001c0001t0001g0081 others(12): Show |
15 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1005-3817C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679444 | |||||||
| chr2:102679538 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG00438.hp1 NA18942.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005-3723C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679538 | |||||||
| chr2:102679614 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1005-3647G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679614 | |||||||
| chr2:102679658 | G | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-3603G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679658 | |||||||
| chr2:102679669 | C | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-3592C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679669 | |||||||
| chr2:102679712 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1005-3549A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679712 | |||||||
| chr2:102679804 | G | C | 1 | a0001c0001t0002g0241 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1005-3457G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679804 | |||||||
| chr2:102679859 | T | A | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1005-3402T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102679859 | |||||||
| chr2:102680050 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0002g0104 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1005-3211G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680050 | |||||||
| chr2:102680081 | T | TTTTGTAT others(12): Show |
3 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0194 |
4 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005-3167_1005-316 others(23): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102680081 | ||||||
| chr2:102680129 | G | C | 30 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(27): Show |
30 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1005-3132G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680129 | |||||||
| chr2:102680158 | A | AT | 102 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1005-3094dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102680158 | ||||||
| chr2:102680163 | T | G | 3 | a0001c0001t0001g0119 a0001c0001t0006g0270 a0001c0001t0006g0271 |
3 | HG03130.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1005-3098T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680163 | |||||||
| chr2:102680251 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1005-3010T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680251 | |||||||
| chr2:102680303 | T | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-2958T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680303 | |||||||
| chr2:102680387 | C | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-2874C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680387 | |||||||
| chr2:102680477 | C | G | 105 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(102): Show |
106 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1005-2784C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680477 | |||||||
| chr2:102680503 | G | A | 12 | a0001c0001t0002g0300 a0001c0001t0004g0316 a0001c0001t0005g0317 others(9): Show |
12 | HG01167.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1005-2758G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680503 | |||||||
| chr2:102680593 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1005-2668C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680593 | |||||||
| chr2:102680809 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0085 a0001c0001t0002g0084 |
3 | HG02135.hp1 NA18747.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1005-2452T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680809 | |||||||
| chr2:102680810 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1005-2451A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680810 | |||||||
| chr2:102680872 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-2389G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680872 | |||||||
| chr2:102680899 | C | T | 30 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(27): Show |
30 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1005-2362C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680899 | |||||||
| chr2:102680904 | C | G | 2 | a0001c0001t0001g0336 a0001c0001t0012g0337 |
2 | HG01361.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1005-2357C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680904 | |||||||
| chr2:102680918 | G | GGGCCTCT others(339): Show |
6 | a0001c0001t0001g0090 a0001c0001t0002g0089 a0001c0001t0002g0092 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1005-2206_1005-220 others(350): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102680918 | ||||||
| chr2:102680918 | G | GGGCCTCT others(339): Show |
1 | a0001c0001t0001g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1005-2206_1005-220 others(350): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 102680918 | ||||||
| chr2:102680921 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0002g0104 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1005-2340C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102680921 | |||||||
| chr2:102681056 | C | T | 248 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(245): Show |
249 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1005-2205C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102681056 | |||||||
| chr2:102681245 | G | A | 105 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(102): Show |
106 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1005-2016G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102681245 | |||||||
| chr2:102681403 | T | A | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1005-1858T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102681403 | |||||||
| chr2:102681597 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1005-1664G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102681597 | |||||||
| chr2:102681626 | T | A | 1 | a0001c0001t0002g0300 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1005-1635T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102681626 | |||||||
| chr2:102681689 | C | A | 3 | a0001c0001t0001g0330 a0001c0001t0002g0185 a0001c0001t0012g0329 |
3 | HG02647.hp1 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1005-1572C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102681689 | |||||||
| chr2:102681899 | G | C | 90 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(87): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1005-1362G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102681899 | |||||||
| chr2:102681904 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0031 others(27): Show |
31 | HG00609.hp2 HG01106.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1005-1357G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102681904 | |||||||
| chr2:102681970 | T | G | 1 | a0001c0001t0009g0264 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1005-1291T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102681970 | |||||||
| chr2:102682093 | T | G | 1 | a0001c0001t0006g0294 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1005-1168T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682093 | |||||||
| chr2:102682120 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-1141G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682120 | |||||||
| chr2:102682140 | C | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-1121C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682140 | |||||||
| chr2:102682229 | G | A | 114 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(111): Show |
115 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1005-1032G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682229 | |||||||
| chr2:102682351 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1005-910G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682351 | |||||||
| chr2:102682420 | G | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-841G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682420 | |||||||
| chr2:102682446 | A | G | 106 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(103): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1005-815A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682446 | |||||||
| chr2:102682490 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1005-771C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682490 | |||||||
| chr2:102682790 | A | T | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005-471A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682790 | |||||||
| chr2:102682791 | T | C | 3 | a0001c0001t0004g0282 a0001c0001t0018g0265 a0001c0001t0028g0178 |
3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1005-470T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682791 | |||||||
| chr2:102682854 | C | T | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1005-407C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682854 | |||||||
| chr2:102682877 | G | A | 1 | a0001c0001t0005g0332 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1005-384G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682877 | |||||||
| chr2:102682972 | T | C | 254 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(251): Show |
255 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1005-289T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682972 | |||||||
| chr2:102682992 | C | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-269C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102682992 | |||||||
| chr2:102683095 | A | T | 1 | a0001c0001t0002g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1005-166A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102683095 | |||||||
| chr2:102683108 | G | A | 30 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(27): Show |
30 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1005-153G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102683108 | |||||||
| chr2:102683152 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0009g0218 |
2 | HG00621.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1005-109T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102683152 | |||||||
| chr2:102683178 | T | C | 31 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(28): Show |
31 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1005-83T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102683178 | |||||||
| chr2:102683563 | T | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+85T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 4/11 | chr2 | 102683563 | |||||||
| chr2:102683611 | G | A | 14 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0164 others(11): Show |
14 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1222+133G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 4/11 | chr2 | 102683611 | |||||||
| chr2:102683752 | TCTC | T | 219 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(216): Show |
220 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.1222+281_1222+283d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 102683752 | ||||||
| chr2:102683917 | T | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1223-217T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 4/11 | chr2 | 102683917 | |||||||
| chr2:102683948 | A | G | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1223-186A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 4/11 | chr2 | 102683948 | |||||||
| chr2:102684046 | C | T | 1 | a0001c0001t0002g0230 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1223-88C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 4/11 | chr2 | 102684046 | |||||||
| chr2:102684047 | A | G | 250 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(247): Show |
251 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1223-87A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 4/11 | chr2 | 102684047 | |||||||
| chr2:102684356 | T | C | 6 | a0001c0001t0002g0300 a0001c0001t0004g0316 a0001c0001t0005g0317 others(3): Show |
6 | HG01167.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1425+20T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102684356 | |||||||
| chr2:102684422 | G | A | 8 | a0001c0001t0001g0338 a0001c0001t0002g0099 a0001c0001t0002g0162 others(5): Show |
8 | HG00738.hp2 HG01069.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1425+86G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102684422 | |||||||
| chr2:102684606 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1425+270T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102684606 | |||||||
| chr2:102684708 | G | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1425+372G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102684708 | |||||||
| chr2:102684739 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(46): Show |
50 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1425+403G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102684739 | |||||||
| chr2:102684754 | G | T | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1425+418G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102684754 | |||||||
| chr2:102684786 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1425+450A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102684786 | |||||||
| chr2:102684809 | A | G | 111 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(108): Show |
112 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1425+473A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102684809 | |||||||
| chr2:102684992 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1425+656A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102684992 | |||||||
| chr2:102685077 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1425+741G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685077 | |||||||
| chr2:102685110 | G | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(8): Show |
11 | HG00099.hp2 HG00140.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1425+774G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685110 | |||||||
| chr2:102685284 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0109 |
2 | HG00642.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1425+948G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685284 | |||||||
| chr2:102685298 | C | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1425+962C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685298 | |||||||
| chr2:102685422 | G | A | 2 | a0001c0001t0002g0148 a0001c0001t0002g0149 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1425+1086G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685422 | |||||||
| chr2:102685462 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0132 others(2): Show |
5 | NA18957.hp2 NA18960.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1425+1126T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685462 | |||||||
| chr2:102685527 | G | A | 2 | a0001c0001t0018g0265 a0001c0001t0028g0178 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1425+1191G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685527 | |||||||
| chr2:102685530 | A | C | 250 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(247): Show |
251 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1425+1194A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685530 | |||||||
| chr2:102685641 | A | G | 31 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(28): Show |
31 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1425+1305A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685641 | |||||||
| chr2:102685655 | C | T | 14 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0164 others(11): Show |
14 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1425+1319C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685655 | |||||||
| chr2:102685660 | G | A | 2 | a0001c0001t0009g0264 a0001c0001t0013g0299 |
2 | HG02965.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1425+1324G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685660 | |||||||
| chr2:102685745 | C | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0176 a0001c0001t0001g0211 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1425+1409C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685745 | |||||||
| chr2:102685752 | T | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(18): Show |
21 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1425+1416T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685752 | |||||||
| chr2:102685878 | T | A | 30 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0090 others(27): Show |
30 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1425+1542T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685878 | |||||||
| chr2:102685908 | G | A | 100 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(97): Show |
100 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1425+1572G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685908 | |||||||
| chr2:102685924 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0006g0270 a0001c0001t0006g0271 |
3 | HG03130.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1425+1588T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685924 | |||||||
| chr2:102685962 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0128 |
2 | HG01975.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1425+1626G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685962 | |||||||
| chr2:102685982 | T | C | 253 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(250): Show |
254 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.1425+1646T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102685982 | |||||||
| chr2:102686050 | A | G | 106 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(103): Show |
107 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1425+1714A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102686050 | |||||||
| chr2:102686109 | T | C | 3 | a0001c0001t0001g0123 a0001c0001t0010g0082 a0001c0001t0010g0083 |
3 | HG01167.hp1 HG01169.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1425+1773T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102686109 | |||||||
| chr2:102686121 | A | G | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1425+1785A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102686121 | |||||||
| chr2:102686370 | C | T | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1425+2034C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102686370 | |||||||
| chr2:102686638 | C | T | 5 | a0001c0001t0002g0099 a0001c0001t0002g0162 a0001c0001t0002g0267 others(2): Show |
5 | HG00738.hp2 HG01069.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1425+2302C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102686638 | |||||||
| chr2:102686905 | T | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0116 |
2 | HG02080.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1425+2569T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102686905 | |||||||
| chr2:102686937 | C | T | 2 | a0001c0001t0003g0298 a0001c0001t0003g0342 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1425+2601C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102686937 | |||||||
| chr2:102686971 | T | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1425+2635T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102686971 | |||||||
| chr2:102687067 | A | G | 14 | a0001c0001t0001g0069 a0001c0001t0001g0129 a0001c0001t0001g0176 others(11): Show |
15 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1425+2731A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102687067 | |||||||
| chr2:102687191 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0001g0330 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1425+2855G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102687191 | |||||||
| chr2:102687278 | C | G | 1 | a0001c0001t0002g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1425+2942C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102687278 | |||||||
| chr2:102687283 | AAC | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0234 a0001c0001t0002g0141 others(1): Show |
4 | HG00408.hp2 NA18982.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1425+2956_1425+295 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102687283 | ||||||
| chr2:102687659 | A | G | 104 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(101): Show |
104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1425+3323A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102687659 | |||||||
| chr2:102687783 | A | AT | 18 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0001g0153 others(15): Show |
18 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1425+3460dupT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102687783 | ||||||
| chr2:102687868 | T | G | 1 | a0001c0001t0001g0323 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1425+3532T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102687868 | |||||||
| chr2:102687979 | T | C | 304 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(301): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1425+3643T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102687979 | |||||||
| chr2:102687990 | G | A | 1 | a0001c0001t0030g0010 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1425+3654G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102687990 | |||||||
| chr2:102688008 | G | A | 1 | a0001c0001t0009g0264 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1425+3672G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688008 | |||||||
| chr2:102688225 | T | A | 14 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0164 others(11): Show |
14 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1425+3889T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688225 | |||||||
| chr2:102688322 | G | T | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1425+3986G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688322 | |||||||
| chr2:102688390 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1425+4054G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688390 | |||||||
| chr2:102688403 | C | T | 6 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0002g0280 others(3): Show |
6 | HG01891.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1425+4067C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688403 | |||||||
| chr2:102688453 | T | C | 214 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1425+4117T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688453 | |||||||
| chr2:102688503 | G | T | 14 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0164 others(11): Show |
14 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1425+4167G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688503 | |||||||
| chr2:102688511 | C | T | 14 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0164 others(11): Show |
14 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1425+4175C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688511 | |||||||
| chr2:102688512 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1425+4176G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688512 | |||||||
| chr2:102688545 | T | C | 1 | a0001c0001t0024g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1425+4209T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688545 | |||||||
| chr2:102688596 | C | T | 1 | a0001c0001t0013g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1425+4260C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688596 | |||||||
| chr2:102688597 | A | G | 1 | a0001c0001t0013g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1425+4261A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688597 | |||||||
| chr2:102688598 | C | T | 1 | a0001c0001t0013g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1425+4262C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688598 | |||||||
| chr2:102688658 | T | G | 3 | a0001c0001t0001g0338 a0001c0001t0002g0274 a0001c0001t0011g0278 |
3 | HG02922.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1425+4322T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688658 | |||||||
| chr2:102688721 | T | C | 250 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(247): Show |
251 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1425+4385T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688721 | |||||||
| chr2:102688727 | AAAACAAA others(1): Show |
A | 7 | a0001c0001t0001g0050 a0001c0001t0001g0098 a0001c0001t0001g0147 others(4): Show |
7 | HG00438.hp1 HG02165.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1425+4403_1425+441 others(12): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102688727 | ||||||
| chr2:102688734 | A | G | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1425+4398A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688734 | |||||||
| chr2:102688739 | C | T | 9 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0002g0089 others(6): Show |
9 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1425+4403C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688739 | |||||||
| chr2:102688792 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1425+4456T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688792 | |||||||
| chr2:102688797 | T | C | 15 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0164 others(12): Show |
15 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1425+4461T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688797 | |||||||
| chr2:102688801 | T | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(296): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1425+4465T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688801 | |||||||
| chr2:102688998 | C | T | 8 | a0001c0001t0001g0153 a0001c0001t0001g0287 a0001c0001t0002g0280 others(5): Show |
8 | HG01891.hp2 HG02818.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1425+4662C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102688998 | |||||||
| chr2:102689011 | C | T | 85 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0043 others(82): Show |
85 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1425+4675C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102689011 | |||||||
| chr2:102689012 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1425+4676G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102689012 | |||||||
| chr2:102689067 | T | C | 1 | a0001c0001t0003g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1425+4731T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102689067 | |||||||
| chr2:102689205 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1425+4869G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102689205 | |||||||
| chr2:102689207 | G | A | 223 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(220): Show |
224 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1425+4871G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102689207 | |||||||
| chr2:102689448 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0003g0072 |
2 | HG02258.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1426-4966G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102689448 | |||||||
| chr2:102689506 | CT | C | 110 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(107): Show |
111 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1426-4906delT | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102689506 | ||||||
| chr2:102689631 | A | G | 3 | a0001c0001t0004g0316 a0001c0001t0013g0315 a0001c0001t0025g0340 |
3 | HG01167.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1426-4783A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102689631 | |||||||
| chr2:102689670 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1426-4744C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102689670 | |||||||
| chr2:102690042 | T | G | 15 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0002g0089 others(12): Show |
15 | HG01167.hp2 HG02055.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1426-4372T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690042 | |||||||
| chr2:102690168 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1426-4246C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690168 | |||||||
| chr2:102690193 | C | T | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1426-4221C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690193 | |||||||
| chr2:102690309 | C | G | 1 | a0001c0001t0002g0339 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1426-4105C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690309 | |||||||
| chr2:102690310 | G | A | 85 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0043 others(82): Show |
85 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1426-4104G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690310 | |||||||
| chr2:102690312 | C | T | 5 | a0001c0001t0001g0287 a0001c0001t0002g0280 a0001c0001t0003g0279 others(2): Show |
5 | HG01891.hp2 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1426-4102C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690312 | |||||||
| chr2:102690313 | G | A | 239 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(236): Show |
240 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1426-4101G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690313 | |||||||
| chr2:102690387 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1426-4027G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690387 | |||||||
| chr2:102690430 | T | C | 85 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0043 others(82): Show |
85 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1426-3984T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690430 | |||||||
| chr2:102690509 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1426-3905G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690509 | |||||||
| chr2:102690523 | G | A | 86 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0043 others(83): Show |
86 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1426-3891G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690523 | |||||||
| chr2:102690831 | A | C | 14 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0002g0089 others(11): Show |
14 | HG01167.hp2 HG02055.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426-3583A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690831 | |||||||
| chr2:102690839 | C | T | 3 | a0001c0001t0002g0089 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02723.hp2 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1426-3575C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690839 | |||||||
| chr2:102690862 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0007g0105 |
2 | HG02258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1426-3552A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690862 | |||||||
| chr2:102690879 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1426-3535A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102690879 | |||||||
| chr2:102690948 | AAACAAG | A | 3 | a0001c0001t0001g0015 a0001c0001t0002g0014 a0001c0001t0003g0255 |
3 | HG00140.hp2 HG01496.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1426-3462_1426-345 others(10): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102690948 | ||||||
| chr2:102690968 | C | CA | 89 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0034 others(86): Show |
89 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1426-3427dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102690968 | ||||||
| chr2:102690968 | CA | C | 152 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(149): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1426-3427delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102690968 | ||||||
| chr2:102690968 | CAA | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(53): Show |
57 | HG00609.hp2 HG00621.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1426-3428_1426-342 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102690968 | ||||||
| chr2:102690968 | CAAA | C | 12 | a0001c0001t0001g0015 a0001c0001t0001g0119 a0001c0001t0001g0276 others(9): Show |
12 | HG00140.hp2 HG01167.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1426-3429_1426-342 others(7): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102690968 | ||||||
| chr2:102691068 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(206): Show |
210 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.1426-3346G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691068 | |||||||
| chr2:102691261 | C | T | 70 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0095 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1426-3153C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691261 | |||||||
| chr2:102691291 | A | ATT | 56 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(53): Show |
56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1426-3116_1426-311 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102691291 | ||||||
| chr2:102691315 | T | C | 39 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0065 others(36): Show |
40 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1426-3099T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691315 | |||||||
| chr2:102691346 | C | T | 2 | a0001c0001t0007g0328 a0001c0001t0017g0094 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1426-3068C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691346 | |||||||
| chr2:102691414 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0011g0278 a0001c0001t0022g0007 |
3 | HG02922.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1426-3000C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691414 | |||||||
| chr2:102691462 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1426-2952T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691462 | |||||||
| chr2:102691526 | T | C | 51 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(48): Show |
51 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.1426-2888T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691526 | |||||||
| chr2:102691647 | G | C | 27 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0119 others(24): Show |
27 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1426-2767G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691647 | |||||||
| chr2:102691650 | G | T | 126 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1426-2764G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691650 | |||||||
| chr2:102691668 | A | G | 28 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0119 others(25): Show |
28 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.1426-2746A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102691668 | |||||||
| chr2:102691849 | C | CTGGGGTA others(9): Show |
2 | a0001c0001t0001g0251 a0001c0001t0002g0102 |
2 | HG02738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1426-2563_1426-254 others(20): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102691849 | ||||||
| chr2:102692019 | C | A | 1 | a0001c0001t0028g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1426-2395C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692019 | |||||||
| chr2:102692302 | TG | T | 3 | a0001c0001t0007g0105 a0001c0001t0007g0269 a0001c0001t0031g0117 |
3 | HG02970.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1426-2110delG | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102692302 | ||||||
| chr2:102692343 | A | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(262): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1426-2071A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692343 | |||||||
| chr2:102692506 | G | A | 1 | a0001c0001t0009g0264 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1426-1908G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692506 | |||||||
| chr2:102692558 | T | C | 1 | a0001c0001t0003g0156 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1426-1856T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692558 | |||||||
| chr2:102692566 | C | T | 6 | a0001c0001t0002g0099 a0001c0001t0002g0159 a0001c0001t0002g0161 others(3): Show |
6 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1426-1848C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692566 | |||||||
| chr2:102692571 | C | G | 1 | a0001c0001t0004g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1426-1843C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692571 | |||||||
| chr2:102692687 | T | C | 32 | a0001c0001t0002g0191 a0001c0001t0003g0022 a0001c0001t0003g0024 others(29): Show |
32 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1426-1727T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692687 | |||||||
| chr2:102692699 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1426-1715T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692699 | |||||||
| chr2:102692774 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1426-1640G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692774 | |||||||
| chr2:102692776 | T | C | 8 | a0001c0001t0003g0096 a0001c0001t0003g0342 a0001c0001t0015g0272 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1426-1638T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102692776 | |||||||
| chr2:102693055 | T | TTA | 7 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(4): Show |
7 | HG02895.hp1 HG02970.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1426-1344_1426-134 others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102693055 | ||||||
| chr2:102693070 | T | C | 2 | a0001c0001t0002g0055 a0001c0001t0031g0117 |
2 | HG03540.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1426-1344T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102693070 | |||||||
| chr2:102693107 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1426-1307C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102693107 | |||||||
| chr2:102693190 | C | T | 6 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG02895.hp1 HG02970.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1426-1224C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102693190 | |||||||
| chr2:102693527 | G | T | 3 | a0001c0001t0023g0008 a0001c0001t0024g0341 a0001c0001t0036g0296 |
3 | HG03486.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1426-887G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102693527 | |||||||
| chr2:102693528 | A | T | 3 | a0001c0001t0023g0008 a0001c0001t0024g0341 a0001c0001t0036g0296 |
3 | HG03486.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1426-886A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102693528 | |||||||
| chr2:102693550 | C | T | 5 | a0001c0001t0003g0057 a0001c0001t0005g0064 a0001c0001t0005g0317 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1426-864C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102693550 | |||||||
| chr2:102693811 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1426-603C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102693811 | |||||||
| chr2:102693818 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1426-596G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102693818 | |||||||
| chr2:102693973 | C | CTAT | 4 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG02895.hp1 HG03041.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1426-430_1426-428d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102693973 | ||||||
| chr2:102694018 | A | T | 3 | a0001c0001t0001g0283 a0001c0001t0002g0104 a0001c0001t0002g0300 |
3 | HG02572.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1426-396A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102694018 | |||||||
| chr2:102694174 | A | T | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1426-240A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102694174 | |||||||
| chr2:102694326 | TA | T | 5 | a0001c0001t0003g0057 a0001c0001t0005g0064 a0001c0001t0005g0317 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1426-82delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 102694326 | ||||||
| chr2:102694369 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1426-45T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 5/11 | chr2 | 102694369 | |||||||
| chr2:102694789 | T | C | 5 | a0001c0001t0003g0057 a0001c0001t0005g0064 a0001c0001t0005g0317 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516-254T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 6/11 | chr2 | 102694789 | |||||||
| chr2:102694879 | AGTTT | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(227): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1516-158_1516-155d others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 102694879 | ||||||
| chr2:102695001 | T | C | 2 | a0001c0001t0005g0169 a0001c0001t0028g0178 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1516-42T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 6/11 | chr2 | 102695001 | |||||||
| chr2:102695215 | G | A | 5 | a0001c0001t0002g0099 a0001c0001t0002g0159 a0001c0001t0002g0161 others(2): Show |
5 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1586+102G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695215 | |||||||
| chr2:102695379 | C | T | 3 | a0001c0001t0007g0328 a0001c0001t0007g0335 a0001c0001t0017g0094 |
3 | HG02055.hp1 HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1586+266C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695379 | |||||||
| chr2:102695465 | G | C | 1 | a0001c0001t0006g0294 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1586+352G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695465 | |||||||
| chr2:102695614 | G | A | 3 | a0001c0001t0004g0285 a0001c0001t0004g0316 a0004c0006t0004g0334 |
3 | HG01167.hp2 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1586+501G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695614 | |||||||
| chr2:102695629 | G | A | 36 | a0001c0001t0001g0338 a0001c0001t0003g0022 a0001c0001t0003g0024 others(33): Show |
36 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1586+516G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695629 | |||||||
| chr2:102695756 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1586+643G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695756 | |||||||
| chr2:102695770 | A | AATATATA others(4): Show |
1 | a0001c0001t0002g0032 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1586+688_1586+698d others(13): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695770 | ||||||
| chr2:102695770 | AATATATA others(4): Show |
A | 67 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(64): Show |
67 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1586+688_1586+698d others(13): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695770 | ||||||
| chr2:102695770 | AATATATA others(15): Show |
A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(140): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1586+677_1586+698d others(24): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695770 | ||||||
| chr2:102695771 | A | ATATATAT others(24): Show |
1 | a0001c0001t0003g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1586+687_1586+688i others(33): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695771 | ||||||
| chr2:102695771 | A | T | 1 | a0001c0003t0003g0012 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1586+658A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695771 | |||||||
| chr2:102695781 | T | TATATATA others(62): Show |
3 | a0001c0001t0003g0057 a0001c0001t0005g0064 a0001c0001t0005g0332 |
3 | HG01884.hp1 HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1586+676_1586+677i others(71): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695781 | ||||||
| chr2:102695781 | T | TATATATA others(44): Show |
1 | a0001c0001t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1586+686_1586+687i others(53): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695781 | ||||||
| chr2:102695781 | T | TATATATA others(15): Show |
5 | a0001c0001t0002g0188 a0001c0001t0003g0342 a0001c0001t0004g0284 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1586+687_1586+688i others(24): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695781 | ||||||
| chr2:102695781 | T | TATATATT others(205): Show |
1 | a0001c0001t0031g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1586+674_1586+675i others(214): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695781 | ||||||
| chr2:102695789 | T | TATTA | 4 | a0001c0001t0003g0022 a0001c0001t0003g0037 a0001c0001t0003g0212 others(1): Show |
4 | HG01192.hp1 HG01192.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1586+676_1586+677i others(6): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695789 | |||||||
| chr2:102695789 | TTATATAT others(6): Show |
T | 1 | a0001c0002t0002g0200 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1586+688_1586+700d others(15): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695789 | ||||||
| chr2:102695790 | T | A | 10 | a0001c0001t0001g0062 a0001c0001t0001g0146 a0001c0001t0001g0154 others(7): Show |
10 | HG01358.hp1 HG02080.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1586+677T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695790 | |||||||
| chr2:102695791 | A | ATATATAT others(140): Show |
1 | a0001c0001t0007g0105 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1586+686_1586+687i others(149): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695791 | ||||||
| chr2:102695791 | A | ATATATAT others(165): Show |
1 | a0001c0001t0007g0269 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1586+686_1586+687i others(174): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695791 | ||||||
| chr2:102695791 | A | ATATATAT others(77): Show |
3 | a0001c0001t0001g0338 a0001c0001t0008g0004 a0001c0001t0008g0005 |
3 | HG02896.hp1 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1586+687_1586+688i others(86): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695791 | ||||||
| chr2:102695791 | A | ATATATAT others(110): Show |
1 | a0001c0001t0008g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1586+687_1586+688i others(119): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695791 | ||||||
| chr2:102695791 | A | ATATATAT others(42): Show |
22 | a0001c0001t0003g0024 a0001c0001t0003g0026 a0001c0001t0003g0038 others(19): Show |
22 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1586+687_1586+688i others(51): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695791 | ||||||
| chr2:102695791 | A | T | 10 | a0001c0001t0001g0062 a0001c0001t0001g0146 a0001c0001t0001g0154 others(7): Show |
10 | HG01358.hp1 HG02080.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1586+678A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695791 | |||||||
| chr2:102695792 | T | A | 10 | a0001c0001t0001g0062 a0001c0001t0001g0146 a0001c0001t0001g0154 others(7): Show |
10 | HG01358.hp1 HG02080.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1586+679T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695792 | |||||||
| chr2:102695800 | T | TATAATAT others(41): Show |
2 | a0001c0001t0005g0169 a0001c0001t0028g0178 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1586+687_1586+688i others(50): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695800 | |||||||
| chr2:102695801 | T | A | 29 | a0001c0001t0001g0338 a0001c0001t0003g0024 a0001c0001t0003g0026 others(26): Show |
29 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1586+688T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695801 | |||||||
| chr2:102695801 | T | TATATATT others(40): Show |
5 | a0001c0001t0003g0022 a0001c0001t0003g0037 a0001c0001t0003g0212 others(2): Show |
5 | HG01192.hp1 HG01192.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1586+694_1586+695i others(49): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695801 | ||||||
| chr2:102695803 | T | TATATATA others(56): Show |
2 | a0001c0001t0005g0317 a0001c0001t0005g0333 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1586+698_1586+699i others(65): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 102695803 | ||||||
| chr2:102695817 | A | T | 2 | a0001c0001t0001g0042 a0001c0001t0002g0086 |
2 | HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1586+704A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695817 | |||||||
| chr2:102695826 | A | T | 6 | a0001c0001t0002g0099 a0001c0001t0002g0159 a0001c0001t0002g0161 others(3): Show |
6 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1586+713A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695826 | |||||||
| chr2:102695829 | A | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(264): Show |
268 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1586+716A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102695829 | |||||||
| chr2:102696058 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1586+945C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696058 | |||||||
| chr2:102696067 | G | C | 1 | a0001c0001t0001g0323 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1586+954G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696067 | |||||||
| chr2:102696244 | G | A | 6 | a0001c0001t0002g0084 a0001c0001t0002g0241 a0001c0001t0002g0307 others(3): Show |
6 | HG00609.hp2 NA18962.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1586+1131G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696244 | |||||||
| chr2:102696313 | A | G | 1 | a0001c0001t0031g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1586+1200A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696313 | |||||||
| chr2:102696422 | A | T | 1 | a0001c0001t0028g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1586+1309A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696422 | |||||||
| chr2:102696559 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(266): Show |
270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1586+1446C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696559 | |||||||
| chr2:102696574 | C | A | 1 | a0001c0001t0015g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1586+1461C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696574 | |||||||
| chr2:102696724 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1586+1611G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696724 | |||||||
| chr2:102696876 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1586+1763A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696876 | |||||||
| chr2:102696971 | G | A | 1 | a0001c0001t0015g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1586+1858G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696971 | |||||||
| chr2:102696992 | A | C | 1 | a0001c0001t0015g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1586+1879A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102696992 | |||||||
| chr2:102697196 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1586+2083C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102697196 | |||||||
| chr2:102697289 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(177): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1586+2176G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102697289 | |||||||
| chr2:102697388 | A | G | 1 | a0001c0001t0015g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1586+2275A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102697388 | |||||||
| chr2:102697593 | C | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0219 a0001c0001t0001g0228 others(1): Show |
4 | NA18990.hp2 NA19000.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.1586+2480C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102697593 | |||||||
| chr2:102697598 | C | T | 2 | a0001c0001t0002g0118 a0001c0001t0002g0339 |
2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1586+2485C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102697598 | |||||||
| chr2:102697660 | T | A | 3 | a0001c0001t0004g0285 a0001c0001t0004g0316 a0004c0006t0004g0334 |
3 | HG01167.hp2 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1586+2547T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102697660 | |||||||
| chr2:102697713 | T | A | 251 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(248): Show |
252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1586+2600T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102697713 | |||||||
| chr2:102697737 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1586+2624A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102697737 | |||||||
| chr2:102698070 | C | T | 8 | a0001c0001t0001g0080 a0001c0001t0001g0140 a0001c0001t0001g0186 others(5): Show |
8 | NA18952.hp1 NA18960.hp1 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1586+2957C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698070 | |||||||
| chr2:102698201 | G | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(256): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1587-2869G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698201 | |||||||
| chr2:102698246 | G | A | 8 | a0001c0001t0004g0282 a0001c0001t0004g0284 a0001c0001t0004g0285 others(5): Show |
8 | HG01167.hp2 HG01891.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1587-2824G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698246 | |||||||
| chr2:102698330 | A | G | 1 | a0001c0003t0003g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1587-2740A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698330 | |||||||
| chr2:102698332 | C | T | 3 | a0001c0001t0003g0057 a0001c0001t0003g0174 a0001c0001t0003g0342 |
3 | HG01884.hp1 HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1587-2738C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698332 | |||||||
| chr2:102698344 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1587-2726C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698344 | |||||||
| chr2:102698526 | T | A | 2 | a0001c0001t0004g0284 a0001c0001t0015g0288 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1587-2544T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698526 | |||||||
| chr2:102698626 | C | A | 27 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0026 others(24): Show |
27 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1587-2444C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698626 | |||||||
| chr2:102698681 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1587-2389G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698681 | |||||||
| chr2:102698830 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1587-2240C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698830 | |||||||
| chr2:102698863 | G | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(256): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1587-2207G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698863 | |||||||
| chr2:102698951 | C | T | 1 | a0001c0001t0020g0003 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1587-2119C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698951 | |||||||
| chr2:102698959 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(256): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1587-2111C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102698959 | |||||||
| chr2:102699343 | C | T | 1 | a0001c0001t0018g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1587-1727C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102699343 | |||||||
| chr2:102699379 | C | G | 42 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0026 others(39): Show |
42 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.1587-1691C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102699379 | |||||||
| chr2:102699637 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1587-1433A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102699637 | |||||||
| chr2:102699772 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1587-1298C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102699772 | |||||||
| chr2:102699811 | G | A | 5 | a0001c0001t0007g0105 a0001c0001t0007g0269 a0001c0001t0007g0328 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587-1259G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102699811 | |||||||
| chr2:102700049 | C | A | 1 | a0001c0001t0009g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1587-1021C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102700049 | |||||||
| chr2:102700380 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0127 |
3 | HG00408.hp1 HG02129.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1587-690G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102700380 | |||||||
| chr2:102700384 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1587-686C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102700384 | |||||||
| chr2:102700578 | G | C | 9 | a0001c0001t0004g0282 a0001c0001t0004g0284 a0001c0001t0004g0285 others(6): Show |
9 | HG01167.hp2 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1587-492G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102700578 | |||||||
| chr2:102700628 | G | A | 1 | a0001c0001t0007g0269 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1587-442G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102700628 | |||||||
| chr2:102700685 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1587-385G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102700685 | |||||||
| chr2:102700708 | G | C | 45 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0026 others(42): Show |
45 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1587-362G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102700708 | |||||||
| chr2:102700813 | A | G | 11 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0002g0014 others(8): Show |
11 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1587-257A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102700813 | |||||||
| chr2:102700978 | T | C | 1 | a0001c0001t0021g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1587-92T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 7/11 | chr2 | 102700978 | |||||||
| chr2:102701243 | CTTGCAAA others(6): Show |
C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0139 |
2 | NA18949.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1748+15_1748+27del others(13): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 102701243 | ||||||
| chr2:102701317 | A | G | 10 | a0001c0001t0005g0064 a0001c0001t0005g0169 a0001c0001t0005g0317 others(7): Show |
10 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1748+86A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701317 | |||||||
| chr2:102701334 | C | A | 1 | a0001c0001t0002g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1748+103C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701334 | |||||||
| chr2:102701335 | G | A | 5 | a0001c0001t0007g0105 a0001c0001t0007g0269 a0001c0001t0007g0328 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1748+104G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701335 | |||||||
| chr2:102701381 | T | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(262): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1748+150T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701381 | |||||||
| chr2:102701422 | A | G | 9 | a0001c0001t0004g0282 a0001c0001t0004g0284 a0001c0001t0004g0285 others(6): Show |
9 | HG01167.hp2 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1748+191A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701422 | |||||||
| chr2:102701432 | G | A | 6 | a0001c0001t0005g0064 a0001c0001t0005g0169 a0001c0001t0013g0299 others(3): Show |
6 | HG02647.hp2 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1748+201G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701432 | |||||||
| chr2:102701465 | T | C | 45 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0031 others(42): Show |
45 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1748+234T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701465 | |||||||
| chr2:102701509 | C | T | 3 | a0001c0001t0023g0008 a0001c0001t0024g0341 a0001c0001t0036g0296 |
3 | HG03486.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1748+278C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701509 | |||||||
| chr2:102701737 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1748+506T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701737 | |||||||
| chr2:102701935 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0106 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1749-471G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102701935 | |||||||
| chr2:102702179 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1749-227G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 8/11 | chr2 | 102702179 | |||||||
| chr2:102702681 | A | G | 1 | a0001c0001t0001g0321 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1845+179A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102702681 | |||||||
| chr2:102702998 | T | C | 1 | a0001c0001t0008g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1845+496T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102702998 | |||||||
| chr2:102703017 | G | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(260): Show |
264 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1845+515G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102703017 | |||||||
| chr2:102703091 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1845+589C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102703091 | |||||||
| chr2:102703189 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1845+687C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102703189 | |||||||
| chr2:102703207 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0205 others(3): Show |
6 | HG00642.hp1 HG01074.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1845+705C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102703207 | |||||||
| chr2:102703387 | C | T | 9 | a0001c0001t0004g0282 a0001c0001t0004g0284 a0001c0001t0004g0285 others(6): Show |
9 | HG01167.hp2 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1845+885C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102703387 | |||||||
| chr2:102703482 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1845+980C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102703482 | |||||||
| chr2:102703734 | G | A | 1 | a0001c0001t0013g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1846-810G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102703734 | |||||||
| chr2:102703781 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0237 |
2 | NA18979.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1846-763T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102703781 | |||||||
| chr2:102703821 | G | C | 4 | a0001c0001t0002g0141 a0001c0001t0002g0197 a0001c0001t0002g0207 others(1): Show |
4 | NA18941.hp2 NA18998.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1846-723G>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102703821 | |||||||
| chr2:102704097 | A | C | 9 | a0001c0001t0004g0282 a0001c0001t0004g0284 a0001c0001t0004g0285 others(6): Show |
9 | HG01167.hp2 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1846-447A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102704097 | |||||||
| chr2:102704195 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1846-349A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102704195 | |||||||
| chr2:102704449 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1846-95A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102704449 | |||||||
| chr2:102704498 | G | T | 1 | a0001c0002t0002g0200 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1846-46G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 9/11 | chr2 | 102704498 | |||||||
| chr2:102704953 | T | C | 33 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0026 others(30): Show |
33 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.1977+278T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 10/11 | chr2 | 102704953 | |||||||
| chr2:102705028 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1977+353C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 10/11 | chr2 | 102705028 | |||||||
| chr2:102705232 | G | GAT | 3 | a0001c0001t0023g0008 a0001c0001t0024g0341 a0001c0001t0036g0296 |
3 | HG03486.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1977+562_1977+563d others(4): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 102705232 | ||||||
| chr2:102705468 | G | GA | 12 | a0001c0001t0001g0034 a0001c0001t0005g0064 a0001c0001t0005g0169 others(9): Show |
12 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1978-368dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 102705468 | ||||||
| chr2:102705707 | G | A | 1 | a0001c0001t0007g0269 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1978-139G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 10/11 | chr2 | 102705707 | |||||||
| chr2:102706000 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2068+64A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706000 | |||||||
| chr2:102706024 | TAAGAATG others(328): Show |
T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(255): Show |
259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.2068+102_2068+436d others(2): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 102706024 | ||||||
| chr2:102706133 | C | G | 1 | a0001c0001t0002g0036 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2068+197C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706133 | |||||||
| chr2:102706348 | G | GA | 9 | a0001c0001t0002g0014 a0001c0001t0002g0036 a0001c0001t0002g0097 others(6): Show |
9 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.2068+425dupA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 102706348 | ||||||
| chr2:102706360 | A | G | 1 | a0001c0001t0016g0293 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2068+424A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706360 | |||||||
| chr2:102706431 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2068+495C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706431 | |||||||
| chr2:102706439 | T | C | 10 | a0001c0001t0005g0064 a0001c0001t0005g0169 a0001c0001t0005g0317 others(7): Show |
10 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.2068+503T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706439 | |||||||
| chr2:102706532 | A | G | 1 | a0002c0004t0001g0134 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2068+596A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706532 | |||||||
| chr2:102706575 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2068+639A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706575 | |||||||
| chr2:102706583 | A | T | 33 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0041 others(30): Show |
33 | HG01106.hp1 HG01358.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+647A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706583 | |||||||
| chr2:102706730 | C | G | 1 | a0001c0001t0035g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2068+794C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706730 | |||||||
| chr2:102706734 | A | G | 3 | a0001c0001t0023g0008 a0001c0001t0024g0341 a0001c0001t0036g0296 |
3 | HG03486.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2068+798A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102706734 | |||||||
| chr2:102707066 | G | A | 10 | a0001c0001t0005g0064 a0001c0001t0005g0169 a0001c0001t0005g0317 others(7): Show |
10 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.2069-1053G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707066 | |||||||
| chr2:102707071 | A | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(252): Show |
256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.2069-1048A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707071 | |||||||
| chr2:102707155 | C | T | 255 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(252): Show |
256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.2069-964C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707155 | |||||||
| chr2:102707182 | C | G | 255 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(252): Show |
256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.2069-937C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707182 | |||||||
| chr2:102707300 | TTTA | T | 63 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0031 others(60): Show |
63 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2069-816_2069-814d others(5): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 102707300 | ||||||
| chr2:102707301 | TTA | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(177): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.2069-816_2069-815d others(4): Show |
SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 102707301 | ||||||
| chr2:102707302 | TA | T | 6 | a0001c0001t0001g0062 a0001c0001t0001g0184 a0001c0001t0001g0187 others(3): Show |
6 | HG01517.hp1 HG02602.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.2069-816delA | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707302 | |||||||
| chr2:102707303 | A | T | 5 | a0001c0001t0007g0105 a0001c0001t0007g0269 a0001c0001t0007g0328 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2069-816A>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707303 | |||||||
| chr2:102707310 | T | A | 2 | a0001c0001t0002g0084 a0001c0001t0002g0152 |
2 | NA18971.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2069-809T>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707310 | |||||||
| chr2:102707356 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2069-763T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707356 | |||||||
| chr2:102707510 | T | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(252): Show |
256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.2069-609T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707510 | |||||||
| chr2:102707876 | C | G | 9 | a0001c0001t0001g0076 a0001c0001t0001g0128 a0001c0001t0001g0195 others(6): Show |
9 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2069-243C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707876 | |||||||
| chr2:102707886 | C | A | 45 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0031 others(42): Show |
45 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.2069-233C>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707886 | |||||||
| chr2:102707894 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2069-225A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707894 | |||||||
| chr2:102708116 | T | C | 46 | a0001c0001t0001g0112 a0001c0001t0003g0022 a0001c0001t0003g0024 others(43): Show |
46 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(43): Show |
splice_region_variant&intron_variant | LOW | c.2069-3T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102708116 |