Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr2 | 102614553 | 102716355 |
| a0002 | 0/0 | 812 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0003 | 0/0 | 812 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0004 | 0/0 | 812 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2439 | 335 | 87 | 62 | 133 | 9 | 42 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| c0002 | 0/0 | 2439 | 3 | 0 | 0 | 3 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| c0003 | 0/0 | 2439 | 2 | 0 | 1 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| c0004 | 0/0 | 2439 | 2 | 0 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| c0005 | 0/0 | 2439 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| c0006 | 0/0 | 2439 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3163 | 178 | 21 | 30 | 100 | 3 | 24 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0002 | 1/0 | 3163 | 73 | 16 | 11 | 30 | 4 | 11 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0003 | 0/1 | 3161 | 32 | 9 | 16 | 0 | 2 | 4 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0004 | 0/0 | 3159 | 5 | 4 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0005 | 0/0 | 3163 | 5 | 5 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0006 | 0/0 | 3163 | 5 | 3 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0007 | 0/0 | 3163 | 4 | 4 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0008 | 0/0 | 3163 | 3 | 3 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0009 | 0/0 | 3163 | 3 | 0 | 0 | 2 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0010 | 0/0 | 3163 | 3 | 0 | 3 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0011 | 0/0 | 3163 | 3 | 3 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0012 | 0/0 | 3163 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0013 | 0/0 | 3163 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0014 | 0/0 | 3163 | 2 | 0 | 0 | 2 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0015 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0016 | 0/0 | 3161 | 2 | 1 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0017 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0018 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0019 | 0/0 | 3163 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0020 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0021 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0022 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0023 | 0/0 | 3161 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0024 | 0/0 | 3161 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0025 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0026 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0027 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0028 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0029 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0030 | 0/0 | 3163 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0031 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0032 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0033 | 0/0 | 3163 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0034 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0035 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| t0036 | 0/0 | 3161 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2439 | 335 | 87 | 62 | 133 | 9 | 42 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0002 | 0/0 | 2439 | 3 | 0 | 0 | 3 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0003 | 0/0 | 2439 | 2 | 0 | 1 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0002c0004 | 0/0 | 2439 | 2 | 0 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0003c0006 | 0/0 | 2439 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0004c0005 | 0/0 | 2439 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | 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 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0002 | 1/0 | 5601 | 70 | 16 | 11 | 27 | 4 | 11 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0003 | 0/1 | 5599 | 30 | 9 | 15 | 0 | 1 | 4 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0004 | 0/0 | 5597 | 4 | 3 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0005 | 0/0 | 5601 | 5 | 5 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0006 | 0/0 | 5601 | 5 | 3 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0007 | 0/0 | 5601 | 4 | 4 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0008 | 0/0 | 5601 | 3 | 3 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0009 | 0/0 | 5601 | 3 | 0 | 0 | 2 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0010 | 0/0 | 5601 | 3 | 0 | 3 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0011 | 0/0 | 5601 | 3 | 3 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0012 | 0/0 | 5601 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0013 | 0/0 | 5601 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0014 | 0/0 | 5601 | 2 | 0 | 0 | 2 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0015 | 0/0 | 5597 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0016 | 0/0 | 5599 | 2 | 1 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0017 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0018 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0019 | 0/0 | 5601 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0020 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0021 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0022 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0023 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0024 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0025 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0026 | 0/0 | 5601 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0027 | 0/0 | 5601 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0028 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0029 | 0/0 | 5601 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0030 | 0/0 | 5601 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0031 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0032 | 0/0 | 5601 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0033 | 0/0 | 5601 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0034 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0035 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0001t0036 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0002t0002 | 0/0 | 5601 | 3 | 0 | 0 | 3 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0001c0003t0003 | 0/0 | 5599 | 2 | 0 | 1 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0002c0004t0001 | 0/0 | 5601 | 2 | 0 | 2 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0003c0006t0004 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| a0004c0005t0001 | 0/0 | 5601 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | copy fasta | chr2 | 102614553 | 102716355 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0149 | 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 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0169 | 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 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0180 | 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 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0218 | 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 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0229 | 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 |
| a0001c0001t0001g0239 | 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 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0250 | 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 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0304 | 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 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0001g0312 | 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 |
| a0001c0001t0001g0320 | 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 |
| a0001c0001t0001g0337 | 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 |
| a0001c0001t0002g0054 | 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 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0181 | 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 |
| a0001c0001t0002g0224 | 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 |
| a0001c0001t0002g0228 | 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 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0242 | 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 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0306 | 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 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0002g0321 | 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 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0315 | 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 |
| a0001c0001t0004g0317 | 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 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0005g0318 | 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 |
| a0001c0001t0009g0219 | 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 |
| a0001c0001t0012g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0013g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0013g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0014g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0014g0225 | 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 |
| a0001c0001t0019g0055 | 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 |
| a0001c0001t0024g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0001c0001t0025g0341 | 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 |
| a0001c0001t0028g0182 | 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 |
| a0001c0001t0032g0230 | 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 |
| a0001c0002t0002g0241 | 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 |
| a0001c0003t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0002c0004t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0002c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0003c0006t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| a0004c0005t0001g0130 | 0/0 | 1 | 0 | 1 | 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 | g0141 | 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 | g0225 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0224 | 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 | g0181 | EAS | CHS | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0306 | 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 | g0219 | 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 | g0161 | 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 | g0137 | 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 | g0139 | 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 | g0140 | 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 | g0317 | 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 | g0155 | 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 | g0154 | 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 | g0138 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01358 | hp1 | a0004 | c0005 | t0001 | g0130 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01358 | hp2 | a0001 | c0003 | t0003 | g0233 | 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 | g0247 | 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 | g0145 | 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 | g0212 | AMR | PEL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG01993 | hp1 | a0002 | c0004 | t0001 | g0147 | 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 | g0135 | 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 | g0157 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0218 | 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 | g0047 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0237 | 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 | g0314 | 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 | g0178 | 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 | g0174 | 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 | g0171 | 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 | g0168 | 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 | g0055 | 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 | g0167 | AFR | GWD | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0318 | 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 | g0341 | 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 | g0143 | 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 | g0313 | 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 | g0160 | 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 | g0170 | 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 | g0182 | 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 | g0337 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0315 | AFR | ESN | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0316 | AFR | MSL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0312 | 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 | g0338 | 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 | g0066 | 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 | g0214 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0248 | 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 | g0250 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0153 | 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 | g0180 | SAS | BEB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0054 | 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 | a0003 | 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 | g0221 | 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 | g0172 | AFR | YRI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0148 | 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 | g0223 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0323 | 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 | g0150 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0246 | 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 | g0301 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0067 | 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 | g0308 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0240 | 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 | g0068 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0241 | 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 | g0163 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0239 | 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 | g0222 | 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 | g0216 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0325 | 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 | g0144 | 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 | g0220 | 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 | g0045 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0298 | 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 | g0230 | 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 | g0231 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0156 | 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 | g0146 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0303 | 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 | g0149 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0245 | 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 | g0046 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19030 | hp2 | a0001 | c0001 | t0024 | g0340 | 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 | g0227 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0242 | 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 | g0302 | 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 | g0232 | 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 | g0234 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0215 | 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 | g0162 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0226 | 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 | g0322 | EAS | JPT | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0236 | 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 | g0169 | AFR | YRI | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0311 | 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 | g0142 | 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 | g0159 | 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 | g0136 | AMR | CLM | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0173 | 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 | g0213 | AFR | ACB | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0166 | 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 | g0133 | 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 | g0310 | AFR | LWK | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0211 | REF | REF | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0254 | REF | REF | SLC9A2_chr2_102614553_102716355 | SLC9A2 | chr2 | 102614553 | 102716355 |
| 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 | a0003 | 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 | a0004 | 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 |
| 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 |
| 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 | a0001c0001t0017a0001c0001t0018 | 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 | a0001c0001t0006a0001c0001t0011a0001c0001t0015others(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 | a0001c0001t0008a0001c0001t0020a0001c0001t0021others(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 | a0001c0001t0024a0001c0001t0025 | 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 | a0001c0001t0007a0001c0001t0017 | 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 | a0001c0001t0004a0001c0001t0015a0001c0001t0020others(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 | a0001c0001t0013a0001c0001t0025 | 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 | a0001c0001t0004a0001c0001t0015a0001c0001t0020others(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 | a0001c0001t0005a0001c0001t0013a0001c0001t0021others(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 | a0001c0001t0007a0001c0001t0017 | 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 | a0001c0001t0003a0001c0001t0016a0001c0001t0023others(3): Show | 37 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(34): 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 | a0001c0001t0004a0001c0001t0015a0001c0001t0020others(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 | a0001c0001t0003a0001c0001t0016a0001c0003t0003 | 34 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(31): 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 | a0001c0001t0012a0001c0001t0035 | 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 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(30): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): 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 |
| 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0024g0340a0001c0001t0025g0341 | 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0002g0339others(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 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0100others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(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 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(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 | a0001c0001t0001g0266a0001c0001t0002g0267a0001c0001t0005g0332others(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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0012g0338 | 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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0012g0338 | 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 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0017g0094a0001c0001t0018g0265 | 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 | a0001c0001t0001g0095a0001c0001t0001g0109a0001c0001t0001g0110others(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 | a0001c0001t0002g0339a0001c0001t0007g0335 | 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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0012g0338 | 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 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0259 | 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 | a0001c0001t0011g0278a0001c0001t0035g0331 | 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 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(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 | a0001c0001t0017g0094a0001c0001t0018g0265 | 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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0024g0340a0001c0001t0025g0341 | 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 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0119a0001c0001t0002g0104a0001c0001t0002g0118others(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 | a0001c0001t0002g0188a0001c0001t0006g0270a0001c0001t0006g0271others(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 | a0001c0001t0001g0119a0001c0001t0001g0336a0001c0001t0002g0104others(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 | a0001c0001t0002g0086a0001c0001t0033g0204 | 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 | 245 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0091others(242): Show | 247 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(244): 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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | a0001c0001t0001g0002a0001c0001t0001g0319a0001c0001t0001g0320others(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 | 236 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0095others(233): Show | 238 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(235): 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 | a0001c0001t0001g0183a0001c0001t0001g0184 | 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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0001g0119a0001c0001t0002g0118a0001c0001t0003g0096others(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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | a0001c0001t0001g0119a0001c0001t0002g0118a0001c0001t0002g0339others(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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0001g0336others(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 | a0001c0001t0001g0085a0001c0001t0002g0084 | 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 | 154 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(151): Show | 155 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(152): 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0091a0001c0001t0001g0100a0001c0001t0001g0107others(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 | a0001c0001t0001g0107a0001c0001t0018g0265 | 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 | a0001c0001t0001g0002a0001c0001t0001g0100a0001c0001t0001g0180others(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 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0186others(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 | a0001c0001t0001g0106a0001c0001t0007g0105 | 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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0002g0339others(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 | a0001c0001t0001g0109a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0002g0339others(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 | 328 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(325): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): 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 | a0001c0001t0001g0337 | 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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | 245 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0091others(242): Show | 247 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(244): 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0024g0340 | 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 | a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0024g0340 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0012g0329 | 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 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0001t0002g0092others(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 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0003g0022others(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 | a0001c0001t0001g0091a0001c0001t0001g0107a0001c0001t0001g0119others(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 | a0001c0001t0001g0091a0001c0001t0001g0119a0001c0001t0001g0330others(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 | a0001c0001t0001g0336a0001c0001t0012g0338 | 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 | a0001c0001t0024g0340 | 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 | 245 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0091others(242): Show | 247 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(244): 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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0001g0124a0001c0001t0001g0266 | 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 | a0001c0001t0001g0126a0001c0001t0001g0127 | 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 | a0001c0001t0001g0015a0001c0001t0002g0014 | 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 | a0001c0001t0001g0312a0001c0001t0002g0104a0001c0001t0007g0328others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0080others(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 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0034others(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 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0030others(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 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0298others(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 | a0001c0001t0001g0258a0001c0001t0005g0332 | 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 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0281others(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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(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 | 141 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(138): Show | 142 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(139): 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 | a0001c0001t0001g0023a0001c0001t0001g0040a0001c0001t0001g0132 | 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 | a0001c0001t0001g0091a0001c0001t0001g0119a0001c0001t0001g0286others(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 | a0001c0001t0001g0283a0001c0001t0001g0319a0001c0001t0001g0326 | 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 | a0001c0001t0001g0002a0001c0001t0001g0310a0001c0001t0001g0320others(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 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0298others(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 | a0001c0001t0001g0281a0001c0001t0001g0292a0001c0001t0002g0274others(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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(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 | 141 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(138): Show | 142 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(139): 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 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0132others(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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0008g0004others(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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0001g0119a0001c0001t0002g0118a0001c0001t0003g0096others(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 | a0001c0001t0001g0192a0001c0001t0008g0004a0001c0001t0008g0005others(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 | 176 | a0001c0001t0001g0031a0001c0001t0001g0043a0001c0001t0001g0095others(173): Show | 177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0119a0001c0001t0001g0275others(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 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0327others(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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0001g0119a0001c0001t0002g0118a0001c0001t0003g0096others(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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | 234 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0091others(231): Show | 236 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(233): 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 | a0001c0001t0001g0091a0001c0001t0001g0119a0001c0001t0001g0330others(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 | a0001c0001t0003g0315 | 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 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0047others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0336a0001c0001t0012g0338 | 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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0002g0104others(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 | a0001c0001t0002g0025a0001c0001t0018g0265a0001c0001t0024g0340 | 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 | 158 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(155): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): 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 | a0001c0001t0003g0315 | 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 | 158 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(155): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.289+11994T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102632131 | ||||||
| chr2:102632137
|
T | TATACAC | 158 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(155): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): 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 | 160 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(157): Show | 161 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(158): 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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0001g0091a0001c0001t0001g0119a0001c0001t0001g0330others(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 |
114 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0100others(111): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(112): 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 | a0001c0001t0001g0091a0001c0001t0001g0119a0001c0001t0001g0330others(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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0001g0123others(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 | 168 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(165): Show | 169 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(166): 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 | a0001c0001t0001g0011a0001c0001t0001g0091a0001c0001t0001g0119others(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 | a0001c0001t0025g0341 | 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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0001g0119a0001c0001t0002g0118a0001c0001t0003g0096others(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 | 320 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0027others(317): Show | 322 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(319): 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0024g0340 | 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 | a0001c0001t0001g0091a0001c0001t0001g0107a0001c0001t0001g0119others(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 | a0001c0001t0001g0119a0001c0001t0002g0104a0001c0001t0002g0118others(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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0002g0339others(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 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0001t0002g0092others(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 | a0001c0001t0001g0119a0001c0001t0002g0118a0001c0001t0003g0096others(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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0014g0144others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0263 | 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 | a0001c0001t0003g0315 | 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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | 160 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(157): Show | 161 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(158): 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 | a0001c0001t0002g0089a0001c0001t0002g0092a0001c0001t0002g0093 | 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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0002g0339others(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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0005g0318a0001c0001t0005g0333a0001c0001t0035g0331 | 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 | 320 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0027others(317): Show | 322 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(319): 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 | a0001c0001t0001g0281a0001c0001t0001g0292 | 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 | a0001c0001t0001g0107a0001c0001t0018g0265a0001c0001t0024g0340 | 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 | 185 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(182): Show | 186 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(183): 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(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 | a0001c0001t0013g0313 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0281others(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 | 179 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(176): Show | 180 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(177): 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 | 158 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(155): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): 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 | 2 | a0001c0001t0001g0210a0001c0001t0003g0211 | 2 | HG01258.hp2 homoSapiens_chm13v2.hp1 |
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 | a0001c0001t0001g0164a0001c0001t0001g0165 | 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 | a0001c0001t0001g0120a0001c0001t0001g0140a0001c0001t0001g0187others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(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 | a0001c0001t0001g0337 | 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 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0003g0024others(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 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(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 | a0001c0001t0001g0100a0001c0001t0002g0181 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0336a0001c0001t0012g0338a0001c0001t0028g0182 | 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 | 328 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(325): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): 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 | 173 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(170): Show | 174 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(171): 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 | 251 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0090others(248): Show | 253 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(250): 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0002g0089a0001c0001t0002g0092a0001c0001t0002g0093others(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 | a0001c0001t0001g0310a0001c0001t0002g0311 | 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 | 173 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(170): Show | 174 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(171): 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0107others(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 | a0001c0001t0003g0213 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0001g0281a0001c0001t0001g0292a0001c0001t0002g0274others(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 | a0001c0001t0001g0248a0001c0001t0001g0249 | 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 | a0001c0001t0001g0041a0001c0001t0001g0042 | 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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0001g0028a0001c0001t0001g0078 | 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 | 205 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(202): Show | 206 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(203): 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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | 250 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0090others(247): Show | 252 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(249): 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 | a0001c0001t0002g0314a0001c0001t0003g0342a0001c0001t0013g0313 | 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 | a0001c0001t0002g0001a0001c0001t0002g0194 | 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 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0119others(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 | 201 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(198): Show | 202 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(199): 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0107others(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 | a0001c0001t0001g0091a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | a0001c0001t0001g0260a0001c0001t0002g0259 | 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 | 245 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0090others(242): Show | 247 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(244): 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 | a0001c0001t0022g0007a0001c0001t0023g0008 | 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 | 152 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(149): Show | 153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.290-15540delG | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102642023 | ||||||
| chr2:102642042
|
T | TATA | 80 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0081a0001c0001t0006g0290a0001c0001t0010g0082others(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 | 152 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(149): Show | 153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0001t0002g0092others(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 | 186 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0095others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(184): 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | 152 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(149): Show | 153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | 228 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0090others(225): Show | 230 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(227): 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 | a0001c0001t0001g0109a0001c0001t0001g0123a0001c0001t0003g0125others(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 | a0001c0001t0002g0104a0001c0001t0024g0340 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0002g0001a0001c0001t0002g0194 | 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 | 217 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0095others(214): Show | 219 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(216): 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 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0073others(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 | 195 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0095others(192): Show | 197 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(194): 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 | a0001c0001t0001g0028a0001c0001t0001g0078 | 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 | a0001c0001t0001g0119a0001c0001t0002g0118a0001c0001t0003g0096others(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 | a0001c0001t0001g0180 | 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 | 228 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0090others(225): Show | 230 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.290-13578T>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102643986 | ||||||
| chr2:102644085
|
T | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0090others(225): Show | 230 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(227): 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 | 228 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0090others(225): Show | 230 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(227): 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 | a0001c0001t0002g0142 | 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 | a0001c0001t0013g0313 | 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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0002g0185others(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 | a0001c0001t0006g0294a0001c0001t0006g0295a0001c0001t0016g0293 | 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | 153 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(150): Show | 154 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(151): 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 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(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 | 319 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0027others(316): Show | 321 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(318): 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0107others(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 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0119others(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 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0119others(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 | a0001c0001t0024g0340 | 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 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0002g0138others(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 | a0001c0001t0002g0001a0001c0001t0002g0194 | 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0107others(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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0150a0001c0001t0001g0183a0001c0001t0001g0184 | 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 | a0001c0001t0001g0029a0001c0001t0003g0072 | 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 | 246 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0090others(243): Show | 248 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(245): 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 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0002g0102 | 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 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0001g0123others(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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0001g0336others(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 | a0001c0001t0002g0178 | 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 | a0001c0001t0005g0318a0001c0001t0005g0333 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0002g0104a0001c0001t0024g0340 | 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0101others(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 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(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 | a0001c0001t0001g0091a0001c0001t0001g0100a0001c0001t0001g0106others(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 |
5 | a0001c0001t0001g0131a0001c0001t0001g0210a0001c0001t0001g0251others(2): Show | 5 | HG01258.hp2 HG02129.hp1 HG02738.hp1 others(2): 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 | a0001c0001t0001g0143a0001c0001t0001g0165a0001c0001t0002g0097others(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 | a0001c0001t0001g0133a0001c0001t0001g0151a0001c0001t0001g0170others(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 | a0001c0001t0001g0164a0001c0001t0001g0169a0001c0001t0001g0180others(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 | a0001c0001t0001g0250a0001c0001t0003g0096 | 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 | a0001c0001t0001g0119a0001c0001t0001g0167a0001c0001t0002g0188others(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 | a0001c0001t0001g0090a0001c0001t0002g0093a0001c0001t0011g0297 | 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 | a0001c0001t0007g0328a0001c0001t0031g0117 | 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 | a0001c0001t0001g0107a0001c0001t0002g0092a0001c0001t0002g0118others(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 | a0001c0001t0001g0330a0001c0001t0036g0296 | 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 | a0001c0001t0002g0104a0001c0001t0002g0280a0001c0001t0024g0340 | 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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0011g0278others(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 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(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 | a0001c0001t0003g0279a0001c0001t0004g0317a0001c0001t0013g0316 | 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0006g0270a0001c0001t0006g0271a0001c0001t0006g0290others(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 | a0001c0001t0001g0281a0001c0001t0001g0292 | 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 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0128others(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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0040others(202): Show | 207 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(204): 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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0095others(201): Show | 206 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(203): 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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0001g0151a0001c0001t0001g0215a0001c0001t0002g0152 | 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 | a0001c0001t0001g0337 | 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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0091a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0091a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0091a0001c0001t0001g0283a0001c0001t0001g0286others(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 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0001g0336others(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 | a0001c0001t0001g0243 | 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 | a0001c0001t0005g0318a0001c0001t0005g0333a0001c0001t0018g0265others(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 | 237 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0090others(234): Show | 239 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(236): 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 | a0001c0001t0001g0091a0001c0001t0001g0283a0001c0001t0001g0286others(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 | 152 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(149): Show | 153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0012g0329 | 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 | a0001c0001t0001g0091a0001c0001t0001g0330a0001c0001t0001g0336others(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 | a0001c0001t0001g0336a0001c0001t0012g0338a0001c0001t0028g0182 | 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 | 153 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0098others(150): Show | 154 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(151): 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 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0080others(197): Show | 202 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(199): 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 | a0001c0001t0002g0104a0001c0001t0024g0340 | 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 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0002g0339others(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 | a0001c0001t0006g0290a0001c0001t0011g0273 | 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 | a0003c0006t0004g0334 | 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 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0009others(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 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0107others(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 | a0001c0001t0001g0180a0001c0001t0002g0189 | 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 | a0001c0001t0001g0153 | 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 | 60 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0107others(57): Show | 60 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(57): 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0107others(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 | a0001c0001t0001g0065 | 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 | 222 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(219): Show | 223 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(220): 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 | a0001c0001t0001g0041a0001c0001t0001g0164a0001c0001t0001g0165others(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 | 114 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(111): Show | 115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.290-5581T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 1/11 | chr2 | 102651983 | ||||||
| chr2:102652052
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0002g0314a0001c0001t0004g0317a0001c0001t0005g0318others(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 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0002g0089others(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 | 254 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(251): Show | 255 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(252): 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 | a0001c0001t0002g0314a0001c0001t0004g0317a0001c0001t0005g0318others(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 | a0001c0001t0002g0035a0001c0001t0003g0213 | 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 | a0001c0001t0002g0051a0001c0001t0002g0166 | 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 | 139 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0041others(136): Show | 140 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(137): 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 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0100others(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 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0250others(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 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0312others(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 | a0001c0001t0001g0312 | 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 | a0001c0001t0009g0219 | 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 | a0001c0001t0001g0027a0001c0001t0001g0100a0001c0001t0001g0239others(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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(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 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0001t0002g0092others(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 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(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 | a0001c0001t0001g0312 | 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 | a0001c0001t0002g0314a0001c0001t0004g0317a0001c0001t0005g0318others(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 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0330others(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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(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 | a0001c0001t0001g0238 | 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 | a0001c0001t0002g0179 | 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 | a0001c0001t0001g0028a0001c0001t0001g0078a0001c0001t0001g0143others(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 | a0001c0001t0001g0134a0001c0001t0002g0104 | 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 | a0001c0001t0001g0134a0001c0001t0001g0330a0001c0001t0002g0104others(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 | 110 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(107): Show | 111 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(108): 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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0012g0329 | 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 | a0001c0001t0007g0335a0003c0006t0004g0334 | 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 | a0001c0001t0002g0314a0001c0001t0004g0317a0001c0001t0013g0316others(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 | a0001c0001t0001g0041a0001c0001t0001g0176a0001c0001t0003g0024others(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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0012g0329 | 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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0119a0001c0001t0002g0274a0001c0001t0003g0315others(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 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0107others(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 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0131others(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 | a0001c0001t0001g0081a0001c0001t0001g0124a0001c0001t0001g0266others(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 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(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 | a0001c0001t0001g0148a0001c0001t0001g0186a0001c0001t0007g0269 | 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 | a0003c0006t0004g0334 | 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 | a0001c0001t0004g0282a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0004g0284others(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 | a0001c0001t0001g0134a0001c0001t0002g0104a0001c0001t0002g0118others(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 | a0001c0001t0001g0119a0001c0001t0002g0274a0001c0001t0003g0315others(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 | a0001c0001t0002g0314a0001c0001t0004g0317a0001c0001t0005g0318others(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 | a0001c0001t0001g0134a0001c0001t0001g0312a0001c0001t0002g0104others(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 | a0001c0001t0014g0144 | 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 | a0001c0001t0002g0138 | 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 | a0001c0001t0001g0320 | 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 | 224 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(221): Show | 225 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(222): 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 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0076others(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 | a0001c0001t0001g0119a0001c0001t0023g0008 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0119a0001c0001t0001g0337a0001c0001t0002g0274others(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 | 114 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(111): Show | 115 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(112): 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 | a0003c0006t0004g0334 | 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 | a0001c0001t0002g0224 | 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 | 118 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(115): Show | 119 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.753+1897G>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 2/11 | chr2 | 102659924 | ||||||
| chr2:102659925
|
C | T | 118 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(115): Show | 119 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(116): 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 | a0001c0001t0003g0137 | 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0001g0040a0001c0001t0001g0193a0001c0001t0001g0198others(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 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(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 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(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 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0107others(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 | a0001c0001t0024g0340 | 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 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0107others(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 | 120 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(117): Show | 121 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(118): 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 | a0001c0001t0001g0028a0001c0001t0001g0078a0001c0001t0001g0140others(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 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0001t0002g0092others(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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0091others(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 | a0001c0001t0001g0091a0001c0001t0023g0008 | 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 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0033others(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 | a0001c0001t0001g0091a0001c0001t0023g0008 | 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 | a0001c0001t0002g0071a0001c0001t0010g0077 | 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 | a0001c0001t0001g0091a0001c0001t0001g0337a0001c0001t0002g0274others(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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | 89 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(86): 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 | a0001c0001t0001g0085a0001c0001t0002g0084 | 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 | a0001c0001t0003g0315 | 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 | a0001c0001t0001g0325 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0330others(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 | a0001c0001t0002g0311 | 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 | 99 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0043others(96): Show | 99 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(96): 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 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0069others(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 | a0001c0001t0001g0028a0001c0001t0001g0112a0001c0001t0001g0116others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0023others(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 | a0001c0001t0001g0040a0001c0001t0001g0149a0001c0001t0001g0190others(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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0003g0279others(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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0033g0204others(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 | a0001c0001t0001g0134a0001c0001t0001g0312a0001c0001t0002g0104 | 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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1004+143G>A | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102665493 | ||||||
| chr2:102665501
|
A | G | 341 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(338): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1004+151A>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102665501 | ||||||
| chr2:102665517
|
G | A | 1 | a0001c0003t0003g0233 | 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 | a0001c0001t0006g0270a0001c0001t0006g0271 | 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 | 247 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(244): Show | 248 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(245): 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 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(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 | a0001c0001t0001g0040a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0095others(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 | 42 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0067others(39): Show | 42 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(39): 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 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(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 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0076others(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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0087a0001c0001t0002g0089a0001c0001t0002g0092others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0061others(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 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(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 | a0001c0001t0001g0134a0001c0001t0001g0312a0001c0001t0002g0104 | 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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | 94 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(91): 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(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 | 85 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0042others(82): Show | 85 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(82): 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 | a0001c0001t0001g0062a0001c0001t0001g0076a0001c0001t0001g0098others(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 | a0001c0001t0001g0028a0001c0001t0001g0078a0001c0001t0001g0090others(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 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0170others(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 | 92 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(89): 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 | 131 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0023others(128): Show | 131 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(128): 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 | a0001c0001t0004g0282a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0134a0001c0001t0001g0312a0001c0001t0002g0104 | 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 | a0001c0001t0001g0043a0001c0001t0001g0073a0001c0001t0001g0081others(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 | a0001c0001t0001g0091a0001c0001t0016g0291a0001c0001t0023g0008 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0091a0001c0001t0016g0291a0001c0001t0023g0008 | 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 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0002g0089others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0164others(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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | a0001c0001t0025g0341 | 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 | 89 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(86): 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 | a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | 246 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(243): Show | 247 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(244): 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0302 | 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 | 94 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(91): Show | 94 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(91): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0004g0282a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0001g0134a0001c0001t0001g0312a0001c0001t0002g0104 | 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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | a0001c0001t0001g0134a0001c0001t0001g0312a0001c0001t0002g0104others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | 91 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1004+3665C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 3/11 | chr2 | 102669015 | ||||||
| chr2:102669334
|
G | A | 88 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(85): Show | 88 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(85): 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 | a0001c0001t0002g0172 | 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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | a0001c0001t0001g0030a0001c0001t0001g0095a0001c0001t0001g0100others(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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(219): Show | 223 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(220): 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0027others(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 | a0001c0001t0024g0340 | 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 | a0001c0001t0002g0280a0001c0001t0004g0284a0001c0001t0004g0285 | 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 | 230 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0030others(227): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): 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 | a0001c0001t0001g0027a0001c0001t0001g0090a0001c0001t0001g0161others(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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0004g0282a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0001g0134a0001c0001t0001g0312a0001c0001t0002g0104 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0002g0280others(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 | a0001c0001t0001g0119a0001c0001t0006g0270a0001c0001t0006g0271 | 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 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0062others(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 | 30 | a0001c0001t0001g0047a0001c0001t0001g0081a0001c0001t0001g0090others(27): Show | 30 | HG01070.hp1 HG01167.hp2 HG02129.hp2 others(27): 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 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0001g0069others(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 | a0001c0001t0001g0162a0001c0001t0002g0163 | 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 | a0001c0001t0001g0134a0001c0001t0002g0104 | 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 | a0001c0001t0001g0023a0001c0001t0003g0057 | 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 | 88 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(85): Show | 88 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(85): 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0029others(198): Show | 203 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(200): 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 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0069others(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 | a0001c0001t0001g0098a0001c0001t0001g0127a0001c0001t0001g0157others(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 | a0001c0001t0001g0281a0001c0001t0001g0312a0001c0001t0001g0330others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0222 | 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 | 251 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(248): Show | 252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): 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 | a0001c0001t0004g0282a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0095others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0001t0002g0092others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0001g0028a0001c0001t0001g0078 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0004g0282a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0012g0329 | 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 | 252 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(249): Show | 253 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(250): 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 | a0001c0001t0001g0140a0001c0001t0002g0139 | 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 | a0001c0001t0003g0171 | 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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | 104 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(101): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0164others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0134a0001c0001t0002g0104 | 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 | a0001c0001t0019g0055 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0091a0001c0001t0016g0291a0001c0001t0023g0008 | 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 | a0001c0001t0001g0337 | 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0002g0314a0001c0001t0004g0317a0001c0001t0005g0318others(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 | 88 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(85): Show | 88 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(85): 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 | 104 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(101): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0134a0001c0001t0002g0104 | 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 | a0001c0001t0001g0040a0001c0001t0001g0098a0001c0001t0001g0148others(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 | a0001c0001t0001g0119a0001c0001t0001g0133a0001c0001t0001g0287others(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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0031others(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 | 304 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(301): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0001t0001g0134a0001c0001t0002g0104 | 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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0001t0002g0092others(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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0119a0001c0001t0001g0312a0001c0001t0006g0270others(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 | a0001c0001t0004g0282a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0001g0106a0001c0001t0007g0105 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | 251 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(248): Show | 252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): 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 | a0001c0001t0002g0118a0001c0001t0031g0117 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0157 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0004g0282a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0001g0034a0001c0001t0001g0222 | 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 | a0001c0001t0002g0314a0001c0001t0004g0317a0001c0001t0005g0318others(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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0002g0311 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0013g0313 | 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0069others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | 251 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(248): Show | 252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | 250 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(247): Show | 251 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(248): 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | 113 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(110): Show | 113 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(110): 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | 113 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(110): Show | 113 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(110): 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 | a0001c0001t0001g0150a0001c0001t0002g0059a0003c0006t0004g0334 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0043a0001c0001t0001g0073a0001c0001t0001g0081others(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 | a0001c0001t0001g0050a0001c0001t0001g0183a0001c0001t0001g0184others(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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0002g0242 | 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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | a0001c0001t0001g0134a0001c0001t0002g0104 | 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 | a0001c0001t0001g0212a0001c0001t0002g0001a0001c0001t0002g0194 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0119a0001c0001t0006g0270a0001c0001t0006g0271 | 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0002g0314a0001c0001t0004g0317a0001c0001t0005g0318others(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 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0002g0084 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0336a0001c0001t0012g0338 | 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 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0001t0002g0092others(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 | a0001c0001t0001g0134a0001c0001t0002g0104 | 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 | 249 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(246): Show | 250 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(247): 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | a0001c0001t0002g0314 | 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 | a0001c0001t0001g0330a0001c0001t0002g0185a0001c0001t0012g0329 | 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 | 91 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): 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 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0031others(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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | 107 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(104): Show | 107 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(104): 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0004g0282a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | 255 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(252): Show | 256 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(253): 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0002g0166 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0218a0001c0001t0009g0219 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0164others(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 | 220 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(217): Show | 221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0002g0231 | 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 | 251 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(248): Show | 252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): 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 | a0001c0001t0002g0314a0001c0001t0004g0317a0001c0001t0005g0318others(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 | a0001c0001t0001g0337a0001c0001t0002g0099a0001c0001t0002g0142others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | 2 | a0001c0001t0001g0210a0001c0001t0003g0211 | 2 | HG01258.hp2 homoSapiens_chm13v2.hp1 |
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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0001g0052a0001c0001t0001g0109 | 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0132others(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 | a0001c0001t0018g0265a0001c0001t0028g0182 | 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 | 251 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(248): Show | 252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0164others(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 | a0001c0001t0009g0264a0001c0001t0013g0313 | 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 | a0001c0001t0001g0129a0001c0001t0001g0176a0001c0001t0001g0212others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0090others(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 | 101 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(98): Show | 101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): 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 | a0001c0001t0001g0119a0001c0001t0006g0270a0001c0001t0006g0271 | 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 | a0001c0001t0001g0031a0001c0001t0001g0128 | 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 | 254 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(251): Show | 255 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(252): 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0123a0001c0001t0010g0082a0001c0001t0010g0083 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0002g0099a0001c0001t0002g0142a0001c0001t0002g0267others(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 | a0001c0001t0001g0112a0001c0001t0001g0116 | 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 | a0001c0001t0003g0315a0001c0001t0003g0342 | 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0069a0001c0001t0001g0129a0001c0001t0001g0176others(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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0001g0330others(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 | a0001c0001t0001g0215a0001c0001t0001g0235a0001c0001t0002g0152others(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 | 105 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(102): Show | 105 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(102): 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 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0133others(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 | a0001c0001t0001g0324 | 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 | 305 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0164others(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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0002g0280others(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 | 215 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0164others(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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0164others(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 | a0001c0001t0001g0143 | 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 | a0001c0001t0024g0340 | 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 | a0001c0001t0013g0313 | 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 | a0001c0001t0013g0313 | 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 | a0001c0001t0013g0313 | 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 | a0001c0001t0001g0337a0001c0001t0002g0274a0001c0001t0011g0278 | 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 | 251 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(248): Show | 252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): 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 | a0001c0001t0001g0050a0001c0001t0001g0098a0001c0001t0001g0158others(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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0002g0089others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0164others(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 | 300 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(297): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): 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 | a0001c0001t0001g0133a0001c0001t0001g0287a0001c0001t0002g0280others(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 | 86 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0043others(83): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(83): 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 | a0001c0001t0001g0312 | 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 | 224 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(221): Show | 225 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(222): 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 | a0001c0001t0001g0029a0001c0001t0003g0072 | 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0004g0317a0001c0001t0013g0316a0001c0001t0025g0341 | 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 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0002g0089others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | 86 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0043others(83): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(83): 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 | a0001c0001t0001g0287a0001c0001t0002g0280a0001c0001t0003g0279others(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 | 240 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(237): Show | 241 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(238): 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 | a0001c0001t0001g0312 | 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 | 86 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0043others(83): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(83): 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 | a0001c0001t0002g0138 | 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 | 87 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0043others(84): Show | 87 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(84): 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 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0002g0089others(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 | a0001c0001t0002g0089a0001c0001t0002g0092a0001c0001t0002g0093 | 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 | a0001c0001t0001g0106a0001c0001t0007g0105 | 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0015a0001c0001t0002g0014a0001c0001t0003g0255 | 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 | 90 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0034others(87): Show | 90 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(87): 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 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(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 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0001g0015a0001c0001t0001g0119a0001c0001t0001g0276others(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 | 210 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(207): Show | 211 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(208): 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 | a0001c0001t0001g0030a0001c0001t0001g0045a0001c0001t0001g0095others(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 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0030others(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 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0066others(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 | a0001c0001t0007g0328a0001c0001t0017g0094 | 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 | a0001c0001t0002g0166a0001c0001t0011g0278a0001c0001t0022g0007 | 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 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(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 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0119others(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 | 127 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(124): 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 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0119others(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 | a0001c0001t0001g0251a0001c0001t0002g0102 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0007g0105a0001c0001t0007g0269a0001c0001t0031g0117 | 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 | 266 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(263): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): 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 | a0001c0001t0003g0136 | 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 | a0001c0001t0002g0099a0001c0001t0002g0139a0001c0001t0002g0141others(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 | 33 | a0001c0001t0002g0191a0001c0001t0003g0022a0001c0001t0003g0024others(30): Show | 33 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(30): 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0003g0096a0001c0001t0003g0342a0001c0001t0015g0272others(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 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0002g0054a0001c0001t0031g0117 | 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 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0023g0008a0001c0001t0024g0340a0001c0001t0036g0296 | 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 | a0001c0001t0023g0008a0001c0001t0024g0340a0001c0001t0036g0296 | 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 | a0001c0001t0003g0057a0001c0001t0005g0064a0001c0001t0005g0318others(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 | a0001c0001t0003g0213 | 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 | a0001c0001t0001g0154a0001c0001t0001g0155 | 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 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0283a0001c0001t0002g0104a0001c0001t0002g0314 | 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 | a0001c0001t0003g0057a0001c0001t0005g0064a0001c0001t0005g0318others(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 | a0001c0001t0003g0057a0001c0001t0005g0064a0001c0001t0005g0318others(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 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0005g0168a0001c0001t0028g0182 | 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 | a0001c0001t0002g0099a0001c0001t0002g0139a0001c0001t0002g0141others(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 | a0001c0001t0007g0328a0001c0001t0007g0335a0001c0001t0017g0094 | 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 | a0001c0001t0004g0285a0001c0001t0004g0317a0003c0006t0004g0334 | 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 | 37 | a0001c0001t0001g0337a0001c0001t0003g0022a0001c0001t0003g0024others(34): Show | 37 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(34): 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 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0030others(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 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0003g0171 | 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 | a0001c0001t0003g0057a0001c0001t0005g0064a0001c0001t0005g0332 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0002g0188a0001c0001t0003g0342a0001c0001t0004g0284others(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 | a0001c0001t0003g0022a0001c0001t0003g0037a0001c0001t0003g0213others(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 | a0001c0001t0001g0062a0001c0001t0001g0134a0001c0001t0001g0157others(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 | a0001c0001t0001g0337a0001c0001t0008g0004a0001c0001t0008g0005 | 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 |
23 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0038others(20): Show | 23 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(20): 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 | a0001c0001t0001g0062a0001c0001t0001g0134a0001c0001t0001g0157others(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 | a0001c0001t0001g0062a0001c0001t0001g0134a0001c0001t0001g0157others(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 | a0001c0001t0005g0168a0001c0001t0028g0182 | 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 | 30 | a0001c0001t0001g0337a0001c0001t0003g0024a0001c0001t0003g0026others(27): Show | 30 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(27): 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 | a0001c0001t0003g0022a0001c0001t0003g0037a0001c0001t0003g0213others(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 | a0001c0001t0005g0318a0001c0001t0005g0333 | 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 | a0001c0001t0001g0042a0001c0001t0002g0086 | 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 | a0001c0001t0002g0099a0001c0001t0002g0139a0001c0001t0002g0141others(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 | 268 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(265): Show | 269 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(266): 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 | a0001c0001t0001g0324 | 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 | a0001c0001t0002g0084a0001c0001t0002g0242a0001c0001t0002g0306others(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 | a0001c0001t0028g0182 | 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 | 270 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(267): Show | 271 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(268): 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 | 181 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(178): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): 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 | a0001c0001t0001g0151a0001c0001t0001g0220a0001c0001t0001g0229others(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 | a0001c0001t0002g0118a0001c0001t0002g0339 | 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 | a0001c0001t0004g0285a0001c0001t0004g0317a0003c0006t0004g0334 | 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 | 252 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(249): Show | 253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0080a0001c0001t0001g0151a0001c0001t0001g0186others(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 | 260 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(257): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): 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 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0004g0285others(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 | a0001c0003t0003g0233 | 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 | a0001c0001t0003g0057a0001c0001t0003g0173a0001c0001t0003g0342 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0004g0284a0001c0001t0015g0288 | 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 | 28 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0026others(25): Show | 28 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(25): 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0169 | 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 | 260 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(257): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): 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 | 260 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(257): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): 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 | 43 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0026others(40): Show | 43 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(40): 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 | a0001c0001t0007g0105a0001c0001t0007g0269a0001c0001t0007g0328others(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 | a0001c0001t0009g0219 | 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 | a0001c0001t0001g0047a0001c0001t0001g0112a0001c0001t0001g0127 | 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 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0004g0285others(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 | 46 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0026others(43): Show | 46 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(43): 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 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0002g0014others(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 | a0001c0001t0001g0046a0001c0001t0001g0150 | 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 | a0001c0001t0005g0064a0001c0001t0005g0168a0001c0001t0005g0318others(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 | a0001c0001t0007g0105a0001c0001t0007g0269a0001c0001t0007g0328others(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 | 266 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(263): Show | 267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): 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 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0004g0285others(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 | a0001c0001t0005g0064a0001c0001t0005g0168a0001c0001t0013g0313others(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 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0031others(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 | a0001c0001t0023g0008a0001c0001t0024g0340a0001c0001t0036g0296 | 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 | a0001c0001t0001g0091a0001c0001t0001g0106 | 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 | a0001c0001t0001g0322 | 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 | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(261): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): 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 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0205others(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 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0004g0285others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0013g0316 | 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 | a0001c0001t0001g0215a0001c0001t0001g0238 | 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 | a0001c0001t0002g0152a0001c0001t0002g0197a0001c0001t0002g0207others(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 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0004g0285others(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 | a0001c0001t0001g0226 | 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 | 34 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0026others(31): Show | 34 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(31): 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 | a0001c0001t0023g0008a0001c0001t0024g0340a0001c0001t0036g0296 | 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 | a0001c0001t0001g0034a0001c0001t0005g0064a0001c0001t0005g0168others(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 | a0001c0001t0001g0153 | 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 | 259 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(256): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): 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 | a0001c0001t0002g0014a0001c0001t0002g0036a0001c0001t0002g0097others(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 | a0001c0001t0005g0064a0001c0001t0005g0168a0001c0001t0005g0318others(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 | a0002c0004t0001g0145 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0041others(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 | a0001c0001t0023g0008a0001c0001t0024g0340a0001c0001t0036g0296 | 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 | a0001c0001t0005g0064a0001c0001t0005g0168a0001c0001t0005g0318others(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 | 256 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(253): Show | 257 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.2069-1048A>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707071 | ||||||
| chr2:102707155
|
C | T | 256 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(253): Show | 257 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.2069-964C>T | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707155 | ||||||
| chr2:102707182
|
C | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(253): Show | 257 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.2069-937C>G | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102707182 | ||||||
| chr2:102707300
|
TTTA | T | 64 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0031others(61): Show | 64 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(61): 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 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0062a0001c0001t0001g0184a0001c0001t0001g0187others(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 | a0001c0001t0007g0105a0001c0001t0007g0269a0001c0001t0007g0328others(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 | a0001c0001t0002g0084a0001c0001t0002g0163 | 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 | 256 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(253): Show | 257 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(254): 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 | a0001c0001t0001g0076a0001c0001t0001g0128a0001c0001t0001g0195others(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 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0031others(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 | 47 | a0001c0001t0001g0112a0001c0001t0003g0022a0001c0001t0003g0024others(44): Show | 47 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(44): Show |
splice_region_variant&intron_variant | LOW | c.2069-3T>C | SLC9A2 | ENSG00000115616.3 | transcript | ENST00000233969.3 | protein_coding | 11/11 | chr2 | 102708116 |