Item | Value |
---|---|
geneid | 55334 |
ensemblid | ENSG00000029364.12 |
hgncid | 20182 |
symbol | SLC39A9 |
name | solute carrier family 39 member 9 |
refseq_nuc | NM_018375.5 |
refseq_prot | NP_060845.2 |
ensembl_nuc | ENST00000336643.10 |
ensembl_prot | ENSP00000336887.5 |
mane_status | MANE Select |
chr | chr14 |
start | 69398692 |
end | 69462390 |
strand | + |
ver | v1.2 |
region | chr14:69398692-69462390 |
region5000 | chr14:69393692-69467390 |
regionname0 | SLC39A9_chr14_69398692_69462390 |
regionname5000 | SLC39A9_chr14_69393692_69467390 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 307 | 306 | 89 | 45 | 114 | 18 | 38 | 85 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | MDDFI others(302): Show |
chr14 | 69393692 | 69467390 |
a0002 | 0/0 | 307 | 17 | 0 | 0 | 17 | 0 | 0 | 12 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | MDDFI others(302): Show |
chr14 | 69393692 | 69467390 |
a0003 | 0/0 | 307 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | MDDFI others(302): Show |
chr14 | 69393692 | 69467390 |
a0004 | 0/0 | 307 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | MDDFI others(302): Show |
chr14 | 69393692 | 69467390 |
a0005 | 0/0 | 307 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | MDDFI others(302): Show |
chr14 | 69393692 | 69467390 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 921 | 302 | 87 | 43 | 114 | 18 | 38 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | ATGGA others(916): Show |
chr14 | 69393692 | 69467390 | ||
a0001c0003 | 0/0 | 921 | 3 | 2 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | ATGGA others(916): Show |
chr14 | 69393692 | 69467390 | ||
a0001c0004 | 0/0 | 921 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | ATGGA others(916): Show |
chr14 | 69393692 | 69467390 | ||
a0002c0002 | 0/0 | 921 | 17 | 0 | 0 | 17 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | ATGGA others(916): Show |
chr14 | 69393692 | 69467390 | ||
a0003c0005 | 0/0 | 921 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | ATGGA others(916): Show |
chr14 | 69393692 | 69467390 | ||
a0004c0006 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | ATGGA others(916): Show |
chr14 | 69393692 | 69467390 | ||
a0005c0007 | 0/0 | 921 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | ATGGA others(916): Show |
chr14 | 69393692 | 69467390 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5399 | 129 | 19 | 19 | 64 | 8 | 18 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0002 | 0/1 | 5398 | 80 | 27 | 11 | 25 | 6 | 10 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0003 | 0/0 | 5398 | 17 | 4 | 4 | 0 | 3 | 6 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0004 | 0/0 | 5398 | 15 | 0 | 1 | 12 | 1 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0005 | 0/0 | 5399 | 14 | 13 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0006 | 0/0 | 5397 | 6 | 4 | 2 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5392): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0007 | 0/0 | 5399 | 6 | 6 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0008 | 0/0 | 5399 | 5 | 4 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0009 | 0/0 | 5398 | 3 | 0 | 0 | 3 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0010 | 0/0 | 5399 | 3 | 0 | 0 | 3 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0011 | 0/0 | 5397 | 2 | 0 | 0 | 2 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5392): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0012 | 0/0 | 5399 | 2 | 2 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0013 | 0/0 | 5398 | 2 | 2 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0014 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0015 | 0/0 | 5398 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0016 | 0/0 | 5398 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0017 | 0/0 | 5398 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0018 | 0/0 | 5398 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0019 | 0/0 | 5398 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0020 | 0/0 | 5398 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0021 | 0/0 | 5398 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0022 | 0/0 | 5398 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0023 | 0/0 | 5398 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0024 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0025 | 0/0 | 5399 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0026 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0027 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0028 | 0/0 | 5399 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0029 | 0/0 | 5398 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0030 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0001c0001t0031 | 0/0 | 5398 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0003t0002 | 0/0 | 5398 | 3 | 2 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0001c0004t0001 | 0/0 | 5399 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0002c0002t0001 | 0/0 | 5399 | 17 | 0 | 0 | 17 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5394): Show |
chr14 | 69393692 | 69467390 |
a0003c0005t0002 | 0/0 | 5398 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0004c0006t0002 | 0/0 | 5398 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
a0005c0007t0003 | 0/0 | 5398 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | GAAGA others(5393): Show |
chr14 | 69393692 | 69467390 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0007g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0009g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0010g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0010g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0011g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0011g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0013g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0014g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0015g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0016g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0017g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0018g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0019g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0020g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0021g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0022g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0023g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0024g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0025g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0026g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0027g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0028g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0029g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0030g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0001t0031g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0003t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0001c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0003c0005t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0004c0006t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
a0005c0007t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | GBR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0105 | EUR | GBR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0074 | EUR | GBR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | FIN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0127 | EUR | FIN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00733 | hp1 | a0001 | c0001 | t0021 | g0077 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0096 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG00741 | hp2 | a0003 | c0005 | t0002 | g0073 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01074 | hp1 | a0001 | c0003 | t0002 | g0064 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0143 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0122 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0103 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | CLM | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0089 | EUR | IBS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0092 | EUR | IBS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01891 | hp2 | a0001 | c0003 | t0002 | g0010 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01952 | hp1 | a0001 | c0001 | t0017 | g0063 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01981 | hp2 | a0001 | c0001 | t0018 | g0044 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG01993 | hp2 | a0001 | c0004 | t0001 | g0232 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02145 | hp2 | a0004 | c0006 | t0002 | g0182 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02148 | hp1 | a0001 | c0001 | t0025 | g0189 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | CDX | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02280 | hp1 | a0001 | c0001 | t0013 | g0025 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02602 | hp2 | a0001 | c0001 | t0028 | g0169 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0147 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02717 | hp2 | a0001 | c0001 | t0027 | g0213 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02738 | hp2 | a0001 | c0001 | t0015 | g0038 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0158 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0010 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0178 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0145 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0148 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0149 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0141 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0144 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03098 | hp1 | a0001 | c0001 | t0030 | g0146 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03209 | hp2 | a0001 | c0001 | t0019 | g0121 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03490 | hp2 | a0001 | c0001 | t0031 | g0053 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03579 | hp1 | a0001 | c0001 | t0024 | g0094 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03579 | hp2 | a0001 | c0001 | t0013 | g0024 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0079 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | STU | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | STU | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0179 | AFR | YRI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | CHB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | YRI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | YRI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18945 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18963 | hp1 | a0001 | c0001 | t0011 | g0098 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18964 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18967 | hp2 | a0001 | c0001 | t0011 | g0097 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18975 | hp1 | a0001 | c0001 | t0016 | g0132 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18977 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18991 | hp1 | a0005 | c0007 | t0003 | g0084 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18993 | hp1 | a0001 | c0001 | t0023 | g0114 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19010 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19030 | hp1 | a0001 | c0001 | t0029 | g0026 | AFR | LWK | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | LWK | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0142 | AFR | LWK | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19055 | hp1 | a0001 | c0001 | t0010 | g0135 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19072 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19072 | hp2 | a0001 | c0001 | t0014 | g0255 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19077 | hp1 | a0001 | c0001 | t0020 | g0134 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19086 | hp1 | a0001 | c0001 | t0010 | g0136 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19091 | hp2 | a0001 | c0001 | t0026 | g0183 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | YRI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | YRI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0153 | AFR | ASW | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0082 | EUR | TSI | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0123 | SAS | GIH | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0101 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0140 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG03471 | hp2 | a0001 | c0001 | t0022 | g0095 | AFR | MSL | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | USA | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | USA | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | USA | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0071 | REF | REF | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0216 | REF | REF | SLC39A9_chr14_69393692_69467390 | SLC39A9 | chr14 | 69393692 | 69467390 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69424189 | A | C | 1 | a0005 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.192A>C | p.Glu64Asp | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/7 | 870/5399 | 192/924 | 64/307 | chr14 | 69424189 | |||
chr14:69455835 | T | C | 1 | a0002 | 17 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(14): Show |
missense_variant | MODERATE | c.662T>C | p.Met221Thr | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/7 | 1340/5399 | 662/924 | 221/307 | chr14 | 69455835 | |||
chr14:69458495 | G | A | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.826G>A | p.Asp276Asn | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 1504/5399 | 826/924 | 276/307 | chr14 | 69458495 | |||
chr14:69458514 | G | C | 1 | a0004 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.845G>C | p.Gly282Ala | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 1523/5399 | 845/924 | 282/307 | chr14 | 69458514 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69399414 | G | A | 1 | a0001c0004 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.45G>A | p.Leu15Leu | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/7 | 723/5399 | 45/924 | 15/307 | chr14 | 69399414 | |||
chr14:69458404 | G | A | 1 | a0001c0003 | 3 | HG01074.hp1 HG01891.hp2 HG02818.hp1 |
synonymous_variant | LOW | c.735G>A | p.Val245Val | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 1413/5399 | 735/924 | 245/307 | chr14 | 69458404 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69398730 | C | G | 1 | a0001c0001t0031 | 1 | HG03490.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-640C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/7 | chr14 | 69398730 | |||||||
chr14:69398802 | T | C | 1 | a0001c0001t0014 | 1 | NA19072.hp2 | 5_prime_UTR_variant | MODIFIER | c.-568T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/7 | 568 | chr14 | 69398802 | ||||||
chr14:69399290 | C | G | 1 | a0001c0001t0030 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/7 | 80 | chr14 | 69399290 | ||||||
chr14:69399304 | T | C | 1 | a0001c0001t0015 | 1 | HG02738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/7 | 66 | chr14 | 69399304 | ||||||
chr14:69399349 | G | A | 1 | a0001c0001t0016 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-21G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/7 | 21 | chr14 | 69399349 | ||||||
chr14:69458652 | C | T | 1 | a0001c0001t0007 | 6 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*59C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 59 | chr14 | 69458652 | ||||||
chr14:69458821 | T | C | 2 | a0001c0001t0017 a0001c0001t0018 |
2 | HG01952.hp1 HG01981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*228T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 228 | chr14 | 69458821 | ||||||
chr14:69458914 | A | G | 2 | a0001c0001t0013 a0001c0001t0029 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*321A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 321 | chr14 | 69458914 | ||||||
chr14:69459069 | G | A | 1 | a0001c0001t0030 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 476 | chr14 | 69459069 | ||||||
chr14:69459157 | A | G | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*564A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 564 | chr14 | 69459157 | ||||||
chr14:69459236 | G | C | 1 | a0001c0001t0007 | 6 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*643G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 643 | chr14 | 69459236 | ||||||
chr14:69459341 | G | T | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0012 others(1): Show |
22 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*748G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 748 | chr14 | 69459341 | ||||||
chr14:69459556 | GT | G | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*977delT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 977 | INFO_REALIGN_3_PRIME | chr14 | 69459556 | |||||
chr14:69459557 | T | G | 1 | a0001c0001t0012 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*964T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 964 | chr14 | 69459557 | ||||||
chr14:69459579 | C | A | 1 | a0001c0001t0009 | 3 | NA18945.hp2 NA18964.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*986C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 986 | chr14 | 69459579 | ||||||
chr14:69459583 | T | C | 1 | a0001c0001t0024 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*990T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 990 | chr14 | 69459583 | ||||||
chr14:69459717 | A | G | 2 | a0001c0001t0013 a0001c0001t0029 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1124A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 1124 | chr14 | 69459717 | ||||||
chr14:69459921 | G | A | 1 | a0001c0001t0019 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1328G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 1328 | chr14 | 69459921 | ||||||
chr14:69460224 | A | G | 2 | a0001c0001t0013 a0001c0001t0029 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1631A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 1631 | chr14 | 69460224 | ||||||
chr14:69460242 | G | A | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0010 others(2): Show |
23 | HG00323.hp2 HG00544.hp1 HG01167.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1649G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 1649 | chr14 | 69460242 | ||||||
chr14:69460401 | T | C | 1 | a0001c0001t0029 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1808T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 1808 | chr14 | 69460401 | ||||||
chr14:69460541 | AT | A | 2 | a0001c0001t0006 a0001c0001t0011 |
8 | HG00738.hp1 HG01192.hp2 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1950delT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 1950 | INFO_REALIGN_3_PRIME | chr14 | 69460541 | |||||
chr14:69460670 | A | C | 1 | a0001c0001t0018 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2077A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 2077 | chr14 | 69460670 | ||||||
chr14:69460706 | A | G | 1 | a0001c0001t0023 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2113A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 2113 | chr14 | 69460706 | ||||||
chr14:69460798 | T | G | 1 | a0001c0001t0025 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2205T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 2205 | chr14 | 69460798 | ||||||
chr14:69460801 | A | G | 1 | a0001c0001t0005 | 14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2208A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 2208 | chr14 | 69460801 | ||||||
chr14:69460833 | C | T | 1 | a0001c0001t0027 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2240C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 2240 | chr14 | 69460833 | ||||||
chr14:69460998 | A | G | 2 | a0001c0001t0013 a0001c0001t0029 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2405A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 2405 | chr14 | 69460998 | ||||||
chr14:69461302 | A | G | 1 | a0001c0001t0026 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2709A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 2709 | chr14 | 69461302 | ||||||
chr14:69461590 | G | T | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 others(6): Show |
33 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2997G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 2997 | chr14 | 69461590 | ||||||
chr14:69461640 | T | G | 2 | a0001c0001t0013 a0001c0001t0029 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3047T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 3047 | chr14 | 69461640 | ||||||
chr14:69461696 | G | A | 1 | a0001c0001t0006 | 6 | HG00738.hp1 HG01192.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3103G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 3103 | chr14 | 69461696 | ||||||
chr14:69461782 | A | G | 1 | a0001c0001t0012 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3189A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 3189 | chr14 | 69461782 | ||||||
chr14:69462117 | C | A | 1 | a0001c0001t0021 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3524C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 3524 | chr14 | 69462117 | ||||||
chr14:69462166 | T | C | 1 | a0001c0001t0020 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3573T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 3573 | chr14 | 69462166 | ||||||
chr14:69462226 | A | G | 2 | a0001c0001t0003 a0005c0007t0003 |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3633A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 7/7 | 3633 | chr14 | 69462226 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69399608 | C | G | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+143C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69399608 | |||||||
chr14:69399941 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+476T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69399941 | |||||||
chr14:69400121 | G | A | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.96+656G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69400121 | |||||||
chr14:69400130 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+665C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69400130 | |||||||
chr14:69400291 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.96+826A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69400291 | |||||||
chr14:69400363 | T | C | 179 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0068 others(176): Show |
198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.96+898T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69400363 | |||||||
chr14:69400374 | G | T | 1 | a0001c0001t0021g0077 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.96+909G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69400374 | |||||||
chr14:69400593 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.96+1128G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69400593 | |||||||
chr14:69400682 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+1217C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69400682 | |||||||
chr14:69400772 | T | C | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.96+1307T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69400772 | |||||||
chr14:69400976 | C | G | 1 | a0001c0001t0002g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+1511C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69400976 | |||||||
chr14:69400980 | TA | T | 10 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0280 others(7): Show |
10 | HG02165.hp2 HG02886.hp1 HG03490.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+1530delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69400980 | ||||||
chr14:69401036 | C | A | 14 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(11): Show |
14 | HG00733.hp1 HG01433.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.96+1571C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69401036 | |||||||
chr14:69401128 | T | C | 1 | a0001c0001t0013g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.96+1663T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69401128 | |||||||
chr14:69401333 | C | G | 24 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0159 others(21): Show |
25 | HG00735.hp2 HG02015.hp2 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.96+1868C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69401333 | |||||||
chr14:69401434 | T | A | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+1969T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69401434 | |||||||
chr14:69401542 | T | TAACTTTA others(34): Show |
1 | a0001c0001t0026g0183 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.96+2079_96+2119dup others(41): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69401542 | ||||||
chr14:69402212 | A | C | 1 | a0001c0001t0002g0290 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.96+2747A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402212 | |||||||
chr14:69402225 | T | TA | 8 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
8 | HG00323.hp1 HG00673.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+2772dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69402225 | ||||||
chr14:69402249 | A | C | 1 | a0001c0001t0003g0015 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.96+2784A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402249 | |||||||
chr14:69402318 | C | A | 1 | a0002c0002t0001g0191 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.96+2853C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402318 | |||||||
chr14:69402370 | T | C | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+2905T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402370 | |||||||
chr14:69402428 | A | T | 190 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0048 others(187): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.96+2963A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402428 | |||||||
chr14:69402741 | A | T | 1 | a0001c0001t0001g0271 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.96+3276A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402741 | |||||||
chr14:69402861 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+3396T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402861 | |||||||
chr14:69402913 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.96+3448C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402913 | |||||||
chr14:69402914 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.96+3449T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402914 | |||||||
chr14:69402954 | T | C | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.96+3489T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402954 | |||||||
chr14:69402975 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0078 |
3 | HG02451.hp1 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.96+3510A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69402975 | |||||||
chr14:69403087 | AAAATAAA others(7): Show |
A | 18 | a0001c0001t0004g0017 a0001c0001t0004g0124 a0001c0001t0004g0125 others(15): Show |
21 | HG00323.hp2 HG00544.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+3644_96+3657del others(14): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69403087 | ||||||
chr14:69403155 | CCTGTTTG others(1): Show |
C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0074 a0001c0001t0002g0075 |
5 | HG00140.hp2 HG01433.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+3691_96+3698del others(8): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69403155 | |||||||
chr14:69403179 | C | T | 20 | a0001c0001t0004g0017 a0001c0001t0004g0122 a0001c0001t0004g0123 others(17): Show |
23 | HG00323.hp2 HG00544.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.96+3714C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69403179 | |||||||
chr14:69403527 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.96+4062A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69403527 | |||||||
chr14:69403701 | C | T | 74 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(71): Show |
82 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.96+4236C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69403701 | |||||||
chr14:69403766 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.96+4301A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69403766 | |||||||
chr14:69403997 | T | C | 8 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(5): Show |
9 | HG02109.hp1 HG02280.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+4532T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69403997 | |||||||
chr14:69404083 | G | A | 55 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(52): Show |
61 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.96+4618G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69404083 | |||||||
chr14:69404159 | A | G | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.96+4694A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69404159 | |||||||
chr14:69404227 | A | G | 19 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(16): Show |
22 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+4762A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69404227 | |||||||
chr14:69404338 | G | T | 11 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(8): Show |
14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+4873G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69404338 | |||||||
chr14:69404427 | T | A | 1 | a0001c0001t0005g0150 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+4962T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69404427 | |||||||
chr14:69404505 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+5040T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69404505 | |||||||
chr14:69404633 | G | A | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+5168G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69404633 | |||||||
chr14:69404860 | A | G | 1 | a0001c0001t0005g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.96+5395A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69404860 | |||||||
chr14:69405053 | C | T | 1 | a0001c0001t0002g0014 | 2 | NA18950.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.96+5588C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405053 | |||||||
chr14:69405153 | A | G | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG02165.hp2 NA18939.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+5688A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405153 | |||||||
chr14:69405162 | A | G | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG01192.hp1 HG01257.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.96+5697A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405162 | |||||||
chr14:69405227 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | NA18946.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.96+5762G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405227 | |||||||
chr14:69405240 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.96+5775T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405240 | |||||||
chr14:69405267 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.96+5802C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405267 | |||||||
chr14:69405268 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+5803G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405268 | |||||||
chr14:69405474 | G | T | 1 | a0002c0002t0001g0283 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.96+6009G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405474 | |||||||
chr14:69405833 | A | C | 28 | a0001c0001t0004g0017 a0001c0001t0004g0122 a0001c0001t0004g0123 others(25): Show |
31 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+6368A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405833 | |||||||
chr14:69405860 | C | T | 55 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(52): Show |
61 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.96+6395C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405860 | |||||||
chr14:69405877 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.96+6412G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69405877 | |||||||
chr14:69406154 | C | T | 1 | a0003c0005t0002g0073 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+6689C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406154 | |||||||
chr14:69406159 | G | GTA | 28 | a0001c0001t0004g0017 a0001c0001t0004g0122 a0001c0001t0004g0123 others(25): Show |
31 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+6698_96+6699dup others(2): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69406159 | ||||||
chr14:69406300 | A | G | 55 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(52): Show |
61 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.96+6835A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406300 | |||||||
chr14:69406343 | C | T | 24 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0159 others(21): Show |
25 | HG00735.hp2 HG02015.hp2 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.96+6878C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406343 | |||||||
chr14:69406528 | G | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(11): Show |
17 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.96+7063G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406528 | |||||||
chr14:69406549 | G | A | 19 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(16): Show |
22 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+7084G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406549 | |||||||
chr14:69406618 | T | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+7153T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406618 | |||||||
chr14:69406685 | T | TA | 30 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0159 others(27): Show |
31 | HG00735.hp2 HG01081.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.96+7237dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69406685 | ||||||
chr14:69406685 | TA | T | 6 | a0001c0001t0001g0267 a0001c0001t0002g0041 a0001c0001t0002g0120 others(3): Show |
7 | HG01517.hp1 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+7237delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69406685 | ||||||
chr14:69406702 | A | T | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | NA18946.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.96+7237A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406702 | |||||||
chr14:69406805 | G | A | 8 | a0001c0001t0006g0096 a0001c0001t0006g0099 a0001c0001t0006g0100 others(5): Show |
8 | HG00738.hp1 HG01192.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+7340G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406805 | |||||||
chr14:69406848 | G | GT | 80 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0159 others(77): Show |
88 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.96+7403dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69406848 | ||||||
chr14:69406848 | G | GTT | 81 | a0001c0001t0001g0048 a0001c0001t0001g0171 a0001c0001t0001g0172 others(78): Show |
91 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.96+7402_96+7403dup others(2): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69406848 | ||||||
chr14:69406848 | G | GTTT | 22 | a0001c0001t0001g0068 a0001c0001t0002g0037 a0001c0001t0002g0067 others(19): Show |
23 | HG00280.hp1 HG00639.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.96+7401_96+7403dup others(3): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69406848 | ||||||
chr14:69406848 | G | GTTTT | 6 | a0001c0001t0002g0072 a0001c0001t0003g0079 a0001c0001t0003g0090 others(3): Show |
6 | HG01106.hp2 HG02145.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+7400_96+7403dup others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69406848 | ||||||
chr14:69406971 | C | T | 57 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0270 others(54): Show |
64 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.96+7506C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406971 | |||||||
chr14:69406994 | G | A | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.96+7529G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69406994 | |||||||
chr14:69407027 | T | C | 1 | a0001c0001t0002g0016 | 2 | HG00408.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.96+7562T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407027 | |||||||
chr14:69407275 | T | C | 2 | a0001c0001t0006g0096 a0001c0001t0006g0101 |
2 | HG00738.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.96+7810T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407275 | |||||||
chr14:69407277 | T | C | 2 | a0001c0001t0006g0096 a0001c0001t0006g0101 |
2 | HG00738.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.96+7812T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407277 | |||||||
chr14:69407282 | T | TTTCCTTC others(23): Show |
15 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0105 others(12): Show |
18 | HG00099.hp2 HG00408.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.96+7830_96+7859dup others(30): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407282 | ||||||
chr14:69407284 | T | C | 2 | a0001c0001t0006g0096 a0001c0001t0006g0101 |
2 | HG00738.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.96+7819T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407284 | |||||||
chr14:69407284 | T | TCCTTCCT others(32): Show |
1 | a0001c0001t0002g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.96+7821_96+7859dup others(39): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407284 | ||||||
chr14:69407302 | C | CCCTT | 3 | a0001c0001t0001g0078 a0001c0001t0006g0102 a0001c0001t0019g0121 |
3 | HG03209.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.96+7862_96+7865dup others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | C | CCCTTCCT others(5): Show |
5 | a0001c0001t0003g0079 a0001c0001t0003g0088 a0001c0001t0003g0091 others(2): Show |
5 | HG00733.hp2 HG02145.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+7854_96+7865dup others(12): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | C | CCCTTCCT others(9): Show |
9 | a0001c0001t0002g0115 a0001c0001t0003g0015 a0001c0001t0003g0080 others(6): Show |
10 | HG01106.hp2 HG01346.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+7850_96+7865dup others(16): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | C | CCCTTCCT others(13): Show |
1 | a0001c0001t0003g0082 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.96+7846_96+7865dup others(20): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | C | CCCTTCCT others(36): Show |
1 | a0001c0001t0002g0104 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.96+7859_96+7860ins others(43): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | C | CCCTTCCT others(17): Show |
2 | a0001c0001t0003g0081 a0001c0001t0003g0138 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.96+7842_96+7865dup others(24): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | C | CCTTCCTT others(4): Show |
2 | a0001c0001t0013g0024 a0001c0001t0029g0026 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+7838_96+7839ins others(11): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | C | CCTTCCTT others(16): Show |
1 | a0001c0001t0013g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.96+7838_96+7839ins others(23): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | CCCTT | C | 4 | a0001c0001t0001g0170 a0001c0001t0001g0271 a0002c0002t0001g0253 others(1): Show |
4 | HG02080.hp1 HG02145.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+7862_96+7865del others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | CCCTTCCT others(1): Show |
C | 3 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 |
3 | HG01081.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.96+7858_96+7865del others(8): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407302 | CCCTTCCT others(5): Show |
C | 1 | a0001c0001t0001g0023 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.96+7854_96+7865del others(12): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407302 | ||||||
chr14:69407319 | CCTTCCTT others(5): Show |
C | 1 | a0001c0001t0005g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.96+7871_96+7882del others(12): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407319 | ||||||
chr14:69407331 | T | C | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+7866T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407331 | |||||||
chr14:69407495 | G | T | 2 | a0001c0001t0012g0148 a0001c0001t0012g0149 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.96+8030G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407495 | |||||||
chr14:69407499 | C | T | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+8034C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407499 | |||||||
chr14:69407518 | GT | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+8055delT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69407518 | ||||||
chr14:69407701 | C | T | 5 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(2): Show |
6 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+8236C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407701 | |||||||
chr14:69407783 | C | T | 1 | a0001c0001t0028g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.96+8318C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407783 | |||||||
chr14:69407843 | G | C | 7 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG00558.hp2 HG02015.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+8378G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407843 | |||||||
chr14:69407919 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.96+8454C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69407919 | |||||||
chr14:69408151 | T | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+8686T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69408151 | |||||||
chr14:69408478 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+9013A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69408478 | |||||||
chr14:69408483 | A | G | 1 | a0001c0001t0023g0114 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.96+9018A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69408483 | |||||||
chr14:69408638 | T | C | 1 | a0001c0001t0013g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.96+9173T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69408638 | |||||||
chr14:69408674 | C | T | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00323.hp1 HG00673.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+9209C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69408674 | |||||||
chr14:69408749 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+9284A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69408749 | |||||||
chr14:69408846 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.96+9381C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69408846 | |||||||
chr14:69408970 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.96+9505A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69408970 | |||||||
chr14:69409071 | A | G | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01175.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.96+9606A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409071 | |||||||
chr14:69409161 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+9696A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409161 | |||||||
chr14:69409165 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.96+9700T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409165 | |||||||
chr14:69409286 | G | GTAGTATA others(36): Show |
1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+9826_96+9868dup others(43): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69409286 | ||||||
chr14:69409333 | T | A | 1 | a0001c0001t0001g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.96+9868T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409333 | |||||||
chr14:69409444 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.96+9979T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409444 | |||||||
chr14:69409512 | A | AT | 19 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(16): Show |
22 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+10054dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69409512 | ||||||
chr14:69409583 | G | A | 1 | a0002c0002t0001g0256 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.96+10118G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409583 | |||||||
chr14:69409614 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.96+10149T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409614 | |||||||
chr14:69409797 | G | T | 1 | a0001c0001t0002g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.96+10332G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409797 | |||||||
chr14:69409812 | A | C | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.96+10347A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409812 | |||||||
chr14:69409983 | G | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+10518G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69409983 | |||||||
chr14:69410030 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+10565A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410030 | |||||||
chr14:69410126 | T | G | 1 | a0001c0001t0004g0125 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.96+10661T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410126 | |||||||
chr14:69410359 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0254 |
2 | HG02015.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.96+10894T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410359 | |||||||
chr14:69410579 | A | G | 1 | a0001c0001t0006g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.96+11114A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410579 | |||||||
chr14:69410632 | A | G | 1 | a0001c0001t0010g0136 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.96+11167A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410632 | |||||||
chr14:69410724 | T | C | 5 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(2): Show |
6 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+11259T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410724 | |||||||
chr14:69410808 | AAGAGATG others(7): Show |
A | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+11344_96+11357d others(16): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410808 | |||||||
chr14:69410828 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+11363T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410828 | |||||||
chr14:69410866 | A | T | 11 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(8): Show |
14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+11401A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410866 | |||||||
chr14:69410940 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+11475G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410940 | |||||||
chr14:69410994 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.96+11529T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69410994 | |||||||
chr14:69411011 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+11546A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411011 | |||||||
chr14:69411211 | C | CA | 50 | a0001c0001t0001g0068 a0001c0001t0001g0159 a0001c0001t0001g0171 others(47): Show |
51 | HG00733.hp2 HG00738.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.96+11767dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69411211 | ||||||
chr14:69411211 | CA | C | 21 | a0001c0001t0001g0251 a0001c0001t0002g0006 a0001c0001t0002g0016 others(18): Show |
24 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.96+11767delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69411211 | ||||||
chr14:69411248 | G | A | 2 | a0001c0001t0011g0097 a0001c0001t0011g0098 |
2 | NA18963.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.96+11783G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411248 | |||||||
chr14:69411257 | T | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+11792T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411257 | |||||||
chr14:69411279 | G | C | 1 | a0001c0001t0026g0183 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.96+11814G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411279 | |||||||
chr14:69411404 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+11939G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411404 | |||||||
chr14:69411460 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+11995A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411460 | |||||||
chr14:69411465 | ATAAAACC others(28): Show |
A | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+12002_96+12036d others(37): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69411465 | ||||||
chr14:69411500 | C | T | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+12035C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411500 | |||||||
chr14:69411545 | A | T | 1 | a0001c0001t0001g0250 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.96+12080A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411545 | |||||||
chr14:69411613 | T | A | 57 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(54): Show |
64 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.96+12148T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411613 | |||||||
chr14:69411712 | C | A | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+12247C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411712 | |||||||
chr14:69411713 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+12248A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411713 | |||||||
chr14:69411724 | G | A | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.96+12259G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411724 | |||||||
chr14:69411730 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+12265A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411730 | |||||||
chr14:69411738 | G | A | 19 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(16): Show |
22 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+12273G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411738 | |||||||
chr14:69411743 | A | T | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.96+12278A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411743 | |||||||
chr14:69411780 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12314A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411780 | |||||||
chr14:69411781 | A | AT | 7 | a0001c0001t0001g0198 a0001c0001t0001g0265 a0001c0001t0001g0266 others(4): Show |
7 | HG01106.hp1 HG01192.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-12294dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69411781 | ||||||
chr14:69411781 | AT | A | 9 | a0001c0001t0001g0048 a0001c0001t0001g0202 a0001c0001t0001g0207 others(6): Show |
9 | HG03098.hp2 HG03139.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-12294delT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69411781 | ||||||
chr14:69411782 | T | A | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12312T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411782 | |||||||
chr14:69411792 | T | TCAAGTTA others(939): Show |
2 | a0001c0001t0013g0024 a0001c0001t0029g0026 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-12302_97-12301i others(948): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411792 | |||||||
chr14:69411792 | T | TCAAGTTA others(938): Show |
1 | a0001c0001t0013g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.97-12302_97-12301i others(947): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411792 | |||||||
chr14:69411795 | T | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-12299T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411795 | |||||||
chr14:69411805 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-12289C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411805 | |||||||
chr14:69411821 | CG | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-12272delG | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411821 | |||||||
chr14:69411823 | C | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-12271C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411823 | |||||||
chr14:69411845 | G | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-12249G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411845 | |||||||
chr14:69411968 | A | ATGGTTCA others(27): Show |
1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12126_97-12125i others(36): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411968 | |||||||
chr14:69411972 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12122G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411972 | |||||||
chr14:69411974 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12120G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411974 | |||||||
chr14:69411975 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12119G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411975 | |||||||
chr14:69411977 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12117T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69411977 | |||||||
chr14:69412031 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12063T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412031 | |||||||
chr14:69412034 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12060A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412034 | |||||||
chr14:69412036 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.97-12058C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412036 | |||||||
chr14:69412037 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12057T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412037 | |||||||
chr14:69412040 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12054C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412040 | |||||||
chr14:69412043 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12051A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412043 | |||||||
chr14:69412045 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12049T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412045 | |||||||
chr14:69412046 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-12048G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412046 | |||||||
chr14:69412056 | C | T | 1 | a0001c0001t0013g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.97-12038C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412056 | |||||||
chr14:69412063 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0208 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.97-12031G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412063 | |||||||
chr14:69412070 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.97-12024C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412070 | |||||||
chr14:69412096 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11998A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412096 | |||||||
chr14:69412111 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11983T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412111 | |||||||
chr14:69412128 | G | A | 16 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(13): Show |
17 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.97-11966G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412128 | |||||||
chr14:69412146 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11948T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412146 | |||||||
chr14:69412148 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11946G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412148 | |||||||
chr14:69412160 | C | T | 4 | a0001c0001t0001g0277 a0001c0001t0013g0024 a0001c0001t0013g0025 others(1): Show |
4 | HG02280.hp1 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-11934C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412160 | |||||||
chr14:69412205 | C | G | 1 | a0001c0003t0002g0064 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.97-11889C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412205 | |||||||
chr14:69412210 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11884A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412210 | |||||||
chr14:69412211 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11883A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412211 | |||||||
chr14:69412216 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11878T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412216 | |||||||
chr14:69412218 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11876T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412218 | |||||||
chr14:69412219 | C | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11875C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412219 | |||||||
chr14:69412222 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11872T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412222 | |||||||
chr14:69412224 | C | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11870C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412224 | |||||||
chr14:69412225 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11869T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412225 | |||||||
chr14:69412227 | A | T | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11867A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412227 | |||||||
chr14:69412228 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11866A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412228 | |||||||
chr14:69412229 | A | T | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11865A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412229 | |||||||
chr14:69412230 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11864A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412230 | |||||||
chr14:69412231 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11863T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412231 | |||||||
chr14:69412244 | C | T | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | NA18960.hp2 NA18966.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-11850C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412244 | |||||||
chr14:69412313 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.97-11781C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412313 | |||||||
chr14:69412349 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97-11745A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412349 | |||||||
chr14:69412367 | C | T | 1 | a0001c0001t0017g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.97-11727C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412367 | |||||||
chr14:69412390 | A | AAAAT | 46 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(43): Show |
55 | HG00544.hp1 HG01167.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.97-11659_97-11656d others(6): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69412390 | ||||||
chr14:69412390 | A | AAAATAAA others(1): Show |
10 | a0001c0001t0001g0209 a0001c0001t0002g0108 a0001c0001t0002g0118 others(7): Show |
10 | HG00323.hp2 HG00673.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-11663_97-11656d others(10): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69412390 | ||||||
chr14:69412390 | AAAAT | A | 64 | a0001c0001t0001g0068 a0001c0001t0001g0194 a0001c0001t0001g0195 others(61): Show |
71 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.97-11659_97-11656d others(6): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69412390 | ||||||
chr14:69412390 | AAAATAAA others(5): Show |
A | 4 | a0001c0001t0001g0264 a0001c0001t0008g0142 a0001c0001t0008g0143 others(1): Show |
4 | HG00544.hp2 HG01081.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-11667_97-11656d others(14): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69412390 | ||||||
chr14:69412390 | AAAATAAA others(9): Show |
A | 4 | a0001c0001t0002g0062 a0001c0001t0013g0024 a0001c0001t0013g0025 others(1): Show |
4 | HG02280.hp1 HG03041.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-11671_97-11656d others(18): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69412390 | ||||||
chr14:69412436 | A | G | 5 | a0001c0001t0002g0047 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
5 | HG02922.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-11658A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412436 | |||||||
chr14:69412499 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.97-11595T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412499 | |||||||
chr14:69412585 | A | G | 1 | a0001c0001t0003g0015 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.97-11509A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412585 | |||||||
chr14:69412586 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.97-11508T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412586 | |||||||
chr14:69412679 | G | C | 1 | a0001c0001t0001g0250 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.97-11415G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412679 | |||||||
chr14:69412698 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-11396A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412698 | |||||||
chr14:69412791 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-11303T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412791 | |||||||
chr14:69412865 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-11229A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412865 | |||||||
chr14:69412879 | C | T | 2 | a0001c0001t0022g0095 a0001c0001t0024g0094 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.97-11215C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412879 | |||||||
chr14:69412892 | C | A | 1 | a0001c0001t0002g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.97-11202C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412892 | |||||||
chr14:69412899 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.97-11195A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412899 | |||||||
chr14:69412939 | T | C | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-11155T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69412939 | |||||||
chr14:69413072 | C | A | 192 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0048 others(189): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.97-11022C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413072 | |||||||
chr14:69413079 | A | G | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.97-11015A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413079 | |||||||
chr14:69413122 | C | T | 1 | a0003c0005t0002g0073 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.97-10972C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413122 | |||||||
chr14:69413161 | C | G | 1 | a0001c0001t0013g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.97-10933C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413161 | |||||||
chr14:69413215 | G | C | 7 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG00558.hp2 HG02015.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-10879G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413215 | |||||||
chr14:69413273 | A | G | 274 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(271): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.97-10821A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413273 | |||||||
chr14:69413281 | G | A | 2 | a0001c0003t0002g0010 a0001c0003t0002g0064 |
3 | HG01074.hp1 HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.97-10813G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413281 | |||||||
chr14:69413311 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-10783A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413311 | |||||||
chr14:69413369 | A | T | 2 | a0001c0001t0002g0115 a0004c0006t0002g0182 |
2 | HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.97-10725A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413369 | |||||||
chr14:69413414 | G | A | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.97-10680G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413414 | |||||||
chr14:69413446 | A | G | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97-10648A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413446 | |||||||
chr14:69413682 | A | G | 1 | a0001c0001t0008g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.97-10412A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413682 | |||||||
chr14:69413767 | G | C | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00323.hp1 HG00673.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-10327G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413767 | |||||||
chr14:69413972 | A | G | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97-10122A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413972 | |||||||
chr14:69413973 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.97-10121T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69413973 | |||||||
chr14:69414049 | T | C | 1 | a0001c0001t0008g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.97-10045T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414049 | |||||||
chr14:69414050 | C | CT | 27 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(24): Show |
27 | HG00323.hp1 HG00673.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.97-10026dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69414050 | ||||||
chr14:69414050 | CT | C | 19 | a0001c0001t0001g0166 a0001c0001t0002g0115 a0001c0001t0003g0015 others(16): Show |
20 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.97-10026delT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69414050 | ||||||
chr14:69414081 | C | T | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-10013C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414081 | |||||||
chr14:69414137 | G | A | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-9957G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414137 | |||||||
chr14:69414156 | TTC | T | 5 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0031 others(2): Show |
5 | HG00733.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-9931_97-9930del others(2): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69414156 | ||||||
chr14:69414215 | G | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-9879G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414215 | |||||||
chr14:69414586 | T | C | 1 | a0001c0001t0002g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.97-9508T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414586 | |||||||
chr14:69414619 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.97-9475C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414619 | |||||||
chr14:69414687 | G | C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG02165.hp2 NA18939.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-9407G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414687 | |||||||
chr14:69414695 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-9399G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414695 | |||||||
chr14:69414797 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.97-9297C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414797 | |||||||
chr14:69414876 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.97-9218C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414876 | |||||||
chr14:69414923 | T | G | 54 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(51): Show |
60 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.97-9171T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414923 | |||||||
chr14:69414961 | G | A | 156 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(153): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.97-9133G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69414961 | |||||||
chr14:69415063 | A | G | 180 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0068 others(177): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.97-9031A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69415063 | |||||||
chr14:69415308 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.97-8786A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69415308 | |||||||
chr14:69415507 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-8587C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69415507 | |||||||
chr14:69415651 | CA | C | 129 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(126): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.97-8442delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69415651 | |||||||
chr14:69415675 | A | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(126): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.97-8419A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69415675 | |||||||
chr14:69415699 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.97-8395C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69415699 | |||||||
chr14:69415716 | C | G | 3 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 |
3 | HG01081.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.97-8378C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69415716 | |||||||
chr14:69415918 | T | TTTA | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-8159_97-8157dup others(3): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69415918 | ||||||
chr14:69415982 | A | G | 1 | a0001c0001t0008g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-8112A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69415982 | |||||||
chr14:69416040 | A | G | 1 | a0001c0001t0017g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.97-8054A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416040 | |||||||
chr14:69416430 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-7664A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416430 | |||||||
chr14:69416469 | G | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-7625G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416469 | |||||||
chr14:69416579 | C | G | 1 | a0001c0001t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.97-7515C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416579 | |||||||
chr14:69416588 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.97-7506G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416588 | |||||||
chr14:69416657 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.97-7437C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416657 | |||||||
chr14:69416687 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.97-7407C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416687 | |||||||
chr14:69416726 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.97-7368T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416726 | |||||||
chr14:69416728 | A | G | 2 | a0001c0001t0011g0097 a0001c0001t0011g0098 |
2 | NA18963.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.97-7366A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416728 | |||||||
chr14:69416947 | T | C | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-7147T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69416947 | |||||||
chr14:69417105 | G | GT | 5 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0031 others(2): Show |
5 | HG00733.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-6988dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69417105 | ||||||
chr14:69417159 | G | A | 7 | a0001c0001t0001g0068 a0001c0001t0002g0014 a0001c0001t0002g0040 others(4): Show |
8 | HG02129.hp1 HG04184.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-6935G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69417159 | |||||||
chr14:69417405 | G | A | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97-6689G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69417405 | |||||||
chr14:69417412 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-6682C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69417412 | |||||||
chr14:69417455 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-6639A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69417455 | |||||||
chr14:69417952 | C | T | 6 | a0001c0001t0002g0047 a0001c0001t0002g0057 a0001c0001t0002g0060 others(3): Show |
6 | HG02922.hp2 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-6142C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69417952 | |||||||
chr14:69417995 | C | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-6099C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69417995 | |||||||
chr14:69418031 | T | C | 1 | a0001c0001t0007g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97-6063T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418031 | |||||||
chr14:69418164 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.97-5930T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418164 | |||||||
chr14:69418224 | A | G | 19 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(16): Show |
22 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-5870A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418224 | |||||||
chr14:69418530 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-5564A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418530 | |||||||
chr14:69418619 | C | T | 1 | a0001c0001t0024g0094 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.97-5475C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418619 | |||||||
chr14:69418684 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.97-5410A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418684 | |||||||
chr14:69418713 | A | G | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.97-5381A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418713 | |||||||
chr14:69418794 | G | A | 1 | a0001c0001t0006g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.97-5300G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418794 | |||||||
chr14:69418794 | G | T | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-5300G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418794 | |||||||
chr14:69418803 | T | C | 1 | a0002c0002t0001g0222 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.97-5291T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418803 | |||||||
chr14:69418899 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.97-5195T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418899 | |||||||
chr14:69418903 | T | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-5191T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418903 | |||||||
chr14:69418919 | G | A | 55 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(52): Show |
61 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.97-5175G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69418919 | |||||||
chr14:69419128 | G | T | 1 | a0001c0001t0005g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97-4966G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419128 | |||||||
chr14:69419161 | C | T | 55 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(52): Show |
61 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.97-4933C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419161 | |||||||
chr14:69419257 | T | C | 1 | a0001c0001t0003g0079 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.97-4837T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419257 | |||||||
chr14:69419319 | A | G | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.97-4775A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419319 | |||||||
chr14:69419372 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-4722A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419372 | |||||||
chr14:69419384 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-4710G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419384 | |||||||
chr14:69419499 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0215 |
2 | NA18977.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.97-4595T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419499 | |||||||
chr14:69419596 | T | C | 74 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(71): Show |
82 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.97-4498T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419596 | |||||||
chr14:69419653 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.97-4441T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419653 | |||||||
chr14:69419718 | G | T | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97-4376G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419718 | |||||||
chr14:69419792 | C | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(46): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.97-4302C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419792 | |||||||
chr14:69419883 | A | T | 1 | a0001c0001t0001g0245 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.97-4211A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419883 | |||||||
chr14:69419908 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.97-4186G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419908 | |||||||
chr14:69419974 | A | T | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.97-4120A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419974 | |||||||
chr14:69419981 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.97-4113C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69419981 | |||||||
chr14:69420120 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.97-3974T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69420120 | |||||||
chr14:69420168 | C | G | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-3926C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69420168 | |||||||
chr14:69420357 | T | C | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97-3737T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69420357 | |||||||
chr14:69420546 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.97-3548C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69420546 | |||||||
chr14:69420559 | G | A | 1 | a0001c0001t0015g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.97-3535G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69420559 | |||||||
chr14:69420703 | ACT | A | 2 | a0001c0001t0005g0007 a0001c0001t0005g0152 |
4 | HG01243.hp1 HG01884.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-3388_97-3387del others(2): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69420703 | ||||||
chr14:69420862 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.97-3232T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69420862 | |||||||
chr14:69421050 | C | T | 1 | a0001c0001t0012g0149 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97-3044C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421050 | |||||||
chr14:69421096 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-2998C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421096 | |||||||
chr14:69421150 | G | T | 55 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(52): Show |
61 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.97-2944G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421150 | |||||||
chr14:69421278 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-2816T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421278 | |||||||
chr14:69421312 | T | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-2782T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421312 | |||||||
chr14:69421345 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-2749C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421345 | |||||||
chr14:69421423 | C | T | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.97-2671C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421423 | |||||||
chr14:69421464 | C | G | 8 | a0001c0001t0006g0096 a0001c0001t0006g0099 a0001c0001t0006g0100 others(5): Show |
8 | HG00738.hp1 HG01192.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-2630C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421464 | |||||||
chr14:69421604 | C | G | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-2490C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421604 | |||||||
chr14:69421619 | C | T | 55 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(52): Show |
61 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.97-2475C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421619 | |||||||
chr14:69421647 | A | G | 4 | a0001c0001t0004g0124 a0001c0001t0004g0139 a0001c0001t0009g0001 others(1): Show |
6 | NA18945.hp2 NA18964.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-2447A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421647 | |||||||
chr14:69421716 | G | A | 1 | a0001c0001t0002g0011 | 2 | HG01081.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.97-2378G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421716 | |||||||
chr14:69421803 | G | A | 2 | a0001c0001t0004g0017 a0001c0001t0004g0137 |
3 | HG00544.hp1 NA18981.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.97-2291G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421803 | |||||||
chr14:69421812 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.97-2282G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421812 | |||||||
chr14:69421863 | C | T | 24 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0159 others(21): Show |
25 | HG00735.hp2 HG02015.hp2 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.97-2231C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421863 | |||||||
chr14:69421978 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.97-2116C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69421978 | |||||||
chr14:69422012 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-2082T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69422012 | |||||||
chr14:69422087 | C | T | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-2007C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69422087 | |||||||
chr14:69422214 | G | A | 1 | a0001c0001t0003g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97-1880G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69422214 | |||||||
chr14:69422513 | C | T | 7 | a0001c0001t0001g0068 a0001c0001t0002g0014 a0001c0001t0002g0040 others(4): Show |
8 | HG02129.hp1 HG04184.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-1581C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69422513 | |||||||
chr14:69422583 | C | T | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-1511C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69422583 | |||||||
chr14:69422664 | A | G | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.97-1430A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69422664 | |||||||
chr14:69422837 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.97-1257T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69422837 | |||||||
chr14:69423002 | C | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0172 a0001c0001t0028g0169 |
3 | HG00735.hp2 HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.97-1092C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423002 | |||||||
chr14:69423318 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-776T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423318 | |||||||
chr14:69423421 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.97-673A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423421 | |||||||
chr14:69423515 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-579C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423515 | |||||||
chr14:69423565 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-529A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423565 | |||||||
chr14:69423597 | A | G | 6 | a0001c0001t0002g0047 a0001c0001t0002g0057 a0001c0001t0002g0060 others(3): Show |
6 | HG02922.hp2 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-497A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423597 | |||||||
chr14:69423713 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-381C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423713 | |||||||
chr14:69423726 | C | T | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-368C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423726 | |||||||
chr14:69423791 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.97-303G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423791 | |||||||
chr14:69423830 | G | A | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-264G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423830 | |||||||
chr14:69423896 | CA | C | 160 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0048 others(157): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.97-179delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 69423896 | ||||||
chr14:69423899 | A | C | 1 | a0001c0001t0029g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-195A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423899 | |||||||
chr14:69423914 | A | G | 24 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0159 others(21): Show |
25 | HG00735.hp2 HG02015.hp2 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.97-180A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423914 | |||||||
chr14:69423939 | A | T | 5 | a0001c0001t0004g0124 a0001c0001t0004g0139 a0001c0001t0009g0001 others(2): Show |
7 | NA18945.hp2 NA18964.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-155A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423939 | |||||||
chr14:69423951 | A | G | 1 | a0001c0001t0027g0213 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.97-143A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423951 | |||||||
chr14:69423971 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-123G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 1/6 | chr14 | 69423971 | |||||||
chr14:69424248 | G | C | 1 | a0001c0001t0002g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.205+46G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69424248 | |||||||
chr14:69424485 | C | G | 1 | a0001c0001t0006g0103 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.205+283C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69424485 | |||||||
chr14:69424582 | T | C | 1 | a0001c0001t0004g0126 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.205+380T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69424582 | |||||||
chr14:69424638 | C | T | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.205+436C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69424638 | |||||||
chr14:69424987 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.205+785C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69424987 | |||||||
chr14:69425138 | G | C | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205+936G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69425138 | |||||||
chr14:69425376 | C | A | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.205+1174C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69425376 | |||||||
chr14:69425424 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.205+1222G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69425424 | |||||||
chr14:69425430 | GA | G | 5 | a0001c0001t0002g0047 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
5 | HG02922.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.205+1232delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69425430 | ||||||
chr14:69425617 | A | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0271 |
2 | NA18971.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.205+1415A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69425617 | |||||||
chr14:69425661 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.205+1459G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69425661 | |||||||
chr14:69425761 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.205+1559A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69425761 | |||||||
chr14:69425809 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0162 |
2 | HG02015.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.205+1607C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69425809 | |||||||
chr14:69425828 | A | G | 5 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(2): Show |
6 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+1626A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69425828 | |||||||
chr14:69425904 | A | T | 1 | a0001c0001t0004g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.205+1702A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69425904 | |||||||
chr14:69426007 | T | A | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.205+1805T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426007 | |||||||
chr14:69426108 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.205+1906A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426108 | |||||||
chr14:69426228 | T | C | 49 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(46): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.205+2026T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426228 | |||||||
chr14:69426308 | A | G | 10 | a0001c0001t0002g0005 a0001c0001t0002g0046 a0001c0001t0002g0050 others(7): Show |
12 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.205+2106A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426308 | |||||||
chr14:69426342 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.205+2140G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426342 | |||||||
chr14:69426400 | AAGGATAC others(8): Show |
A | 21 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(18): Show |
24 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.205+2201_205+2215d others(17): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69426400 | ||||||
chr14:69426581 | TC | T | 7 | a0001c0001t0001g0068 a0001c0001t0002g0014 a0001c0001t0002g0040 others(4): Show |
8 | HG02129.hp1 HG04184.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.205+2382delC | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69426581 | ||||||
chr14:69426591 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.205+2389C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426591 | |||||||
chr14:69426715 | CAGG | C | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.205+2516_205+2518d others(5): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69426715 | ||||||
chr14:69426736 | C | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.205+2534C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426736 | |||||||
chr14:69426740 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.205+2538T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426740 | |||||||
chr14:69426746 | C | G | 1 | a0001c0001t0004g0125 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.205+2544C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426746 | |||||||
chr14:69426799 | G | A | 5 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(2): Show |
6 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+2597G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426799 | |||||||
chr14:69426929 | C | T | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00323.hp1 HG00673.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+2727C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426929 | |||||||
chr14:69426980 | A | G | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.205+2778A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69426980 | |||||||
chr14:69427007 | AT | A | 84 | a0001c0001t0001g0068 a0001c0001t0001g0175 a0001c0001t0001g0225 others(81): Show |
92 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.205+2824delT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69427007 | ||||||
chr14:69427007 | ATT | A | 8 | a0001c0001t0001g0048 a0001c0001t0002g0013 a0001c0001t0002g0052 others(5): Show |
9 | HG02083.hp2 HG02523.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.205+2823_205+2824d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69427007 | ||||||
chr14:69427026 | T | C | 16 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(13): Show |
17 | HG00733.hp2 HG01346.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.205+2824T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427026 | |||||||
chr14:69427092 | C | T | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.205+2890C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427092 | |||||||
chr14:69427192 | C | A | 1 | a0001c0001t0002g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.205+2990C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427192 | |||||||
chr14:69427207 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.205+3005T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427207 | |||||||
chr14:69427398 | A | G | 1 | a0001c0001t0029g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.205+3196A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427398 | |||||||
chr14:69427436 | A | T | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.205+3234A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427436 | |||||||
chr14:69427475 | A | T | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.205+3273A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427475 | |||||||
chr14:69427559 | C | T | 12 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0030 others(9): Show |
12 | HG00733.hp1 HG01433.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.205+3357C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427559 | |||||||
chr14:69427659 | T | C | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205+3457T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427659 | |||||||
chr14:69427948 | G | T | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.205+3746G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69427948 | |||||||
chr14:69428075 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.205+3873C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69428075 | |||||||
chr14:69428208 | C | T | 5 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0013g0024 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.205+4006C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69428208 | |||||||
chr14:69428274 | C | CA | 8 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(5): Show |
9 | HG02109.hp1 HG02280.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.205+4089dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69428274 | ||||||
chr14:69428274 | CA | C | 21 | a0001c0001t0001g0277 a0001c0001t0002g0107 a0001c0001t0005g0007 others(18): Show |
24 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.205+4089delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69428274 | ||||||
chr14:69428297 | T | C | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.205+4095T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69428297 | |||||||
chr14:69428456 | A | G | 49 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(46): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.205+4254A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69428456 | |||||||
chr14:69428509 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.205+4307C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69428509 | |||||||
chr14:69428572 | A | G | 156 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(153): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.205+4370A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69428572 | |||||||
chr14:69428595 | A | T | 1 | a0001c0001t0008g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.205+4393A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69428595 | |||||||
chr14:69428672 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.205+4470A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69428672 | |||||||
chr14:69428695 | A | AGT | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.205+4493_205+4494i others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69428695 | |||||||
chr14:69428864 | CTGCGTAT others(7): Show |
C | 1 | a0001c0001t0025g0189 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.205+4674_205+4687d others(16): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69428864 | ||||||
chr14:69429057 | C | A | 1 | a0001c0001t0003g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.205+4855C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69429057 | |||||||
chr14:69429365 | G | A | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.205+5163G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69429365 | |||||||
chr14:69429427 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.205+5225A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69429427 | |||||||
chr14:69429483 | G | T | 187 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0048 others(184): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.205+5281G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69429483 | |||||||
chr14:69429524 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.205+5322G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69429524 | |||||||
chr14:69429550 | A | G | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.205+5348A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69429550 | |||||||
chr14:69429582 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.205+5380G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69429582 | |||||||
chr14:69429823 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.205+5621A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69429823 | |||||||
chr14:69430418 | T | G | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.205+6216T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69430418 | |||||||
chr14:69430496 | A | G | 2 | a0001c0001t0002g0287 a0001c0001t0003g0093 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.205+6294A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69430496 | |||||||
chr14:69430628 | C | CT | 53 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0159 others(50): Show |
58 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.205+6441dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69430628 | ||||||
chr14:69430628 | C | CTT | 118 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(115): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.205+6440_205+6441d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69430628 | ||||||
chr14:69430628 | C | CTTT | 8 | a0001c0001t0002g0111 a0001c0001t0002g0286 a0001c0001t0002g0287 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.205+6439_205+6441d others(5): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69430628 | ||||||
chr14:69430710 | G | A | 1 | a0001c0001t0006g0103 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.205+6508G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69430710 | |||||||
chr14:69430725 | T | A | 49 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(46): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.205+6523T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69430725 | |||||||
chr14:69430755 | C | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0200 a0001c0001t0001g0204 others(9): Show |
15 | HG00423.hp1 HG00609.hp1 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.205+6553C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69430755 | |||||||
chr14:69430775 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.205+6573T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69430775 | |||||||
chr14:69430804 | A | T | 1 | a0001c0001t0015g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.205+6602A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69430804 | |||||||
chr14:69430895 | T | G | 3 | a0001c0001t0002g0060 a0001c0001t0002g0062 a0001c0001t0002g0076 |
3 | HG02965.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.205+6693T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69430895 | |||||||
chr14:69431131 | G | T | 5 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(2): Show |
6 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+6929G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69431131 | |||||||
chr14:69431212 | T | C | 1 | a0001c0001t0030g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.205+7010T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69431212 | |||||||
chr14:69431371 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.205+7169T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69431371 | |||||||
chr14:69431405 | C | CT | 7 | a0001c0001t0001g0171 a0001c0001t0007g0018 a0001c0001t0007g0140 others(4): Show |
8 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.205+7216dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69431405 | ||||||
chr14:69431459 | T | G | 19 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(16): Show |
22 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.205+7257T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69431459 | |||||||
chr14:69431559 | C | CT | 48 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(45): Show |
54 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.205+7369dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69431559 | ||||||
chr14:69431631 | C | T | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.205+7429C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69431631 | |||||||
chr14:69431783 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.205+7581G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69431783 | |||||||
chr14:69431884 | A | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0061 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.205+7682A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69431884 | |||||||
chr14:69431926 | G | A | 24 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0159 others(21): Show |
25 | HG00735.hp2 HG02015.hp2 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.205+7724G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69431926 | |||||||
chr14:69432179 | A | G | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | NA18946.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.205+7977A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69432179 | |||||||
chr14:69432477 | G | T | 1 | a0001c0001t0003g0087 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.205+8275G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69432477 | |||||||
chr14:69432539 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.205+8337G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69432539 | |||||||
chr14:69432569 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.205+8367C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69432569 | |||||||
chr14:69432570 | G | A | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205+8368G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69432570 | |||||||
chr14:69433111 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.205+8909G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433111 | |||||||
chr14:69433210 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-8859G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433210 | |||||||
chr14:69433259 | A | G | 2 | a0001c0001t0022g0095 a0001c0001t0024g0094 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.206-8810A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433259 | |||||||
chr14:69433277 | C | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.206-8792C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433277 | |||||||
chr14:69433291 | C | T | 4 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0279 others(1): Show |
4 | HG01175.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-8778C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433291 | |||||||
chr14:69433320 | G | T | 1 | a0001c0001t0008g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.206-8749G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433320 | |||||||
chr14:69433542 | A | G | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.206-8527A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433542 | |||||||
chr14:69433560 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0272 a0001c0001t0001g0277 |
4 | HG02896.hp2 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-8509G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433560 | |||||||
chr14:69433707 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.206-8362T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433707 | |||||||
chr14:69433824 | C | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-8245C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433824 | |||||||
chr14:69433828 | CA | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-8240delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433828 | |||||||
chr14:69433920 | A | C | 5 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(2): Show |
6 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-8149A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433920 | |||||||
chr14:69433922 | C | T | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.206-8147C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433922 | |||||||
chr14:69433957 | G | A | 1 | a0001c0001t0008g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.206-8112G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69433957 | |||||||
chr14:69434073 | C | A | 19 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(16): Show |
22 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.206-7996C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434073 | |||||||
chr14:69434078 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-7991C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434078 | |||||||
chr14:69434083 | C | CT | 28 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0159 others(25): Show |
29 | HG00735.hp2 HG01934.hp2 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.206-7970dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69434083 | ||||||
chr14:69434083 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-7986C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434083 | |||||||
chr14:69434083 | CT | C | 127 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(124): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.206-7970delT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69434083 | ||||||
chr14:69434127 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.206-7942A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434127 | |||||||
chr14:69434241 | G | C | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.206-7828G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434241 | |||||||
chr14:69434406 | C | G | 1 | a0001c0001t0002g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.206-7663C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434406 | |||||||
chr14:69434516 | T | C | 5 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(2): Show |
5 | HG01433.hp1 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-7553T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434516 | |||||||
chr14:69434568 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206-7501T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434568 | |||||||
chr14:69434749 | G | A | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-7320G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434749 | |||||||
chr14:69434791 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.206-7278T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434791 | |||||||
chr14:69434901 | C | T | 1 | a0001c0001t0003g0015 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.206-7168C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69434901 | |||||||
chr14:69435097 | C | T | 1 | a0001c0001t0013g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.206-6972C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435097 | |||||||
chr14:69435195 | T | G | 3 | a0001c0001t0002g0043 a0001c0001t0002g0049 a0001c0001t0002g0065 |
3 | HG02129.hp1 NA18944.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.206-6874T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435195 | |||||||
chr14:69435380 | G | A | 4 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-6689G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435380 | |||||||
chr14:69435536 | G | A | 1 | a0001c0001t0029g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.206-6533G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435536 | |||||||
chr14:69435668 | G | T | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.206-6401G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435668 | |||||||
chr14:69435765 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0215 |
2 | NA18977.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.206-6304C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435765 | |||||||
chr14:69435776 | G | A | 3 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 |
3 | HG01081.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.206-6293G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435776 | |||||||
chr14:69435820 | G | A | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.206-6249G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435820 | |||||||
chr14:69435829 | C | T | 1 | a0001c0001t0022g0095 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.206-6240C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435829 | |||||||
chr14:69435860 | A | G | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.206-6209A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69435860 | |||||||
chr14:69436171 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.206-5898G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436171 | |||||||
chr14:69436173 | G | T | 1 | a0001c0001t0030g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.206-5896G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436173 | |||||||
chr14:69436190 | G | T | 1 | a0002c0002t0001g0240 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.206-5879G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436190 | |||||||
chr14:69436370 | C | G | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.206-5699C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436370 | |||||||
chr14:69436470 | C | T | 2 | a0001c0001t0005g0150 a0001c0001t0005g0154 |
2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.206-5599C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436470 | |||||||
chr14:69436561 | T | G | 19 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(16): Show |
22 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.206-5508T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436561 | |||||||
chr14:69436704 | T | C | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.206-5365T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436704 | |||||||
chr14:69436920 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0239 |
3 | NA18971.hp1 NA18992.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.206-5149A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436920 | |||||||
chr14:69436946 | CT | C | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | NA18960.hp2 NA18966.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-5122delT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436946 | |||||||
chr14:69436949 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | NA18960.hp2 NA18966.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-5120G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436949 | |||||||
chr14:69436953 | C | T | 6 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(3): Show |
7 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.206-5116C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436953 | |||||||
chr14:69436961 | G | A | 1 | a0001c0001t0008g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.206-5108G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436961 | |||||||
chr14:69436992 | C | T | 1 | a0001c0001t0006g0103 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.206-5077C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69436992 | |||||||
chr14:69437124 | C | A | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.206-4945C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437124 | |||||||
chr14:69437155 | C | T | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-4914C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437155 | |||||||
chr14:69437162 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.206-4907C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437162 | |||||||
chr14:69437196 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-4873A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437196 | |||||||
chr14:69437207 | G | T | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.206-4862G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437207 | |||||||
chr14:69437268 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.206-4801C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437268 | |||||||
chr14:69437292 | G | A | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.206-4777G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437292 | |||||||
chr14:69437590 | G | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-4479G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437590 | |||||||
chr14:69437594 | G | GT | 18 | a0001c0001t0001g0238 a0001c0001t0003g0015 a0001c0001t0003g0079 others(15): Show |
19 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.206-4462dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69437594 | ||||||
chr14:69437621 | A | T | 1 | a0001c0001t0001g0237 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.206-4448A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437621 | |||||||
chr14:69437683 | G | A | 2 | a0001c0001t0004g0122 a0001c0001t0004g0123 |
2 | HG01167.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.206-4386G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437683 | |||||||
chr14:69437766 | T | C | 20 | a0001c0001t0004g0017 a0001c0001t0004g0122 a0001c0001t0004g0123 others(17): Show |
23 | HG00323.hp2 HG00544.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.206-4303T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437766 | |||||||
chr14:69437995 | T | C | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-4074T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69437995 | |||||||
chr14:69438017 | C | T | 4 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0279 others(1): Show |
4 | HG01175.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-4052C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438017 | |||||||
chr14:69438024 | C | CT | 53 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0279 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.206-4031dupT | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69438024 | ||||||
chr14:69438024 | C | CTT | 6 | a0001c0001t0002g0012 a0001c0001t0002g0051 a0001c0001t0002g0054 others(3): Show |
7 | HG02280.hp1 HG03209.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.206-4032_206-4031d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69438024 | ||||||
chr14:69438025 | T | C | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.206-4044T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438025 | |||||||
chr14:69438246 | A | G | 16 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(13): Show |
17 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.206-3823A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438246 | |||||||
chr14:69438247 | C | T | 19 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(16): Show |
22 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.206-3822C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438247 | |||||||
chr14:69438375 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.206-3694C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438375 | |||||||
chr14:69438419 | G | A | 49 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(46): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.206-3650G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438419 | |||||||
chr14:69438491 | T | G | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.206-3578T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438491 | |||||||
chr14:69438590 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.206-3479G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438590 | |||||||
chr14:69438764 | G | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0202 |
2 | NA18955.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.206-3305G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438764 | |||||||
chr14:69438917 | T | C | 20 | a0001c0001t0004g0017 a0001c0001t0004g0122 a0001c0001t0004g0123 others(17): Show |
23 | HG00323.hp2 HG00544.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.206-3152T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438917 | |||||||
chr14:69438970 | C | G | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.206-3099C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69438970 | |||||||
chr14:69439008 | G | A | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.206-3061G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69439008 | |||||||
chr14:69439062 | GAACT | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-3004_206-3001d others(6): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 69439062 | ||||||
chr14:69439199 | G | A | 3 | a0001c0001t0002g0043 a0001c0001t0002g0049 a0001c0001t0002g0065 |
3 | HG02129.hp1 NA18944.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.206-2870G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69439199 | |||||||
chr14:69439413 | C | G | 19 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(16): Show |
22 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.206-2656C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69439413 | |||||||
chr14:69439534 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.206-2535C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69439534 | |||||||
chr14:69439536 | A | G | 5 | a0001c0001t0007g0018 a0001c0001t0007g0140 a0001c0001t0007g0141 others(2): Show |
6 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-2533A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69439536 | |||||||
chr14:69439641 | G | A | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-2428G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69439641 | |||||||
chr14:69439681 | G | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-2388G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69439681 | |||||||
chr14:69439856 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-2213G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69439856 | |||||||
chr14:69440018 | A | C | 18 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(15): Show |
21 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.206-2051A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440018 | |||||||
chr14:69440018 | A | T | 1 | a0001c0001t0002g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.206-2051A>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440018 | |||||||
chr14:69440045 | A | G | 180 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0068 others(177): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.206-2024A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440045 | |||||||
chr14:69440075 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.206-1994G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440075 | |||||||
chr14:69440077 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.206-1992C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440077 | |||||||
chr14:69440179 | G | A | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.206-1890G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440179 | |||||||
chr14:69440277 | C | A | 1 | a0001c0001t0005g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.206-1792C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440277 | |||||||
chr14:69440334 | A | G | 2 | a0001c0001t0022g0095 a0001c0001t0024g0094 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.206-1735A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440334 | |||||||
chr14:69440428 | A | G | 1 | a0001c0001t0002g0016 | 2 | HG00408.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.206-1641A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440428 | |||||||
chr14:69440472 | A | C | 14 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(11): Show |
17 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.206-1597A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440472 | |||||||
chr14:69440690 | T | G | 1 | a0001c0001t0013g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.206-1379T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440690 | |||||||
chr14:69440728 | C | T | 1 | a0001c0001t0014g0255 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.206-1341C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440728 | |||||||
chr14:69440811 | T | C | 23 | a0001c0001t0001g0048 a0001c0001t0002g0005 a0001c0001t0002g0011 others(20): Show |
27 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.206-1258T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440811 | |||||||
chr14:69440820 | C | T | 8 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 others(5): Show |
8 | HG01081.hp1 HG02615.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.206-1249C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440820 | |||||||
chr14:69440821 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.206-1248G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440821 | |||||||
chr14:69440822 | C | T | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.206-1247C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440822 | |||||||
chr14:69440881 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.206-1188C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440881 | |||||||
chr14:69440910 | C | G | 4 | a0001c0001t0008g0145 a0001c0001t0013g0024 a0001c0001t0013g0025 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-1159C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440910 | |||||||
chr14:69440933 | G | A | 1 | a0001c0001t0030g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.206-1136G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440933 | |||||||
chr14:69440960 | G | C | 59 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0223 others(56): Show |
66 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.206-1109G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440960 | |||||||
chr14:69440968 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.206-1101T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69440968 | |||||||
chr14:69441017 | A | G | 15 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(12): Show |
16 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.206-1052A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69441017 | |||||||
chr14:69441618 | T | G | 133 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0237 others(130): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.206-451T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69441618 | |||||||
chr14:69441717 | A | G | 16 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(13): Show |
17 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.206-352A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69441717 | |||||||
chr14:69441785 | G | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-284G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69441785 | |||||||
chr14:69441977 | G | A | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.206-92G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69441977 | |||||||
chr14:69442012 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.206-57A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69442012 | |||||||
chr14:69442037 | A | G | 1 | a0001c0001t0008g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.206-32A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 2/6 | chr14 | 69442037 | |||||||
chr14:69443083 | T | C | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.403+817T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443083 | |||||||
chr14:69443108 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0249 |
2 | HG02300.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.403+842C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443108 | |||||||
chr14:69443234 | C | G | 1 | a0001c0001t0002g0113 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.403+968C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443234 | |||||||
chr14:69443270 | C | A | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+1004C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443270 | |||||||
chr14:69443490 | T | C | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.403+1224T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443490 | |||||||
chr14:69443643 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.403+1377C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443643 | |||||||
chr14:69443682 | C | T | 2 | a0001c0001t0012g0148 a0001c0001t0012g0149 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.403+1416C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443682 | |||||||
chr14:69443901 | T | C | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403+1635T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443901 | |||||||
chr14:69443911 | C | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(46): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.403+1645C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443911 | |||||||
chr14:69443922 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.403+1656A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69443922 | |||||||
chr14:69444191 | A | C | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.403+1925A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444191 | |||||||
chr14:69444448 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.403+2182A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444448 | |||||||
chr14:69444540 | C | G | 2 | a0001c0001t0001g0009 a0001c0001t0002g0227 |
4 | HG00099.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+2274C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444540 | |||||||
chr14:69444573 | A | G | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.403+2307A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444573 | |||||||
chr14:69444574 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.403+2308A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444574 | |||||||
chr14:69444593 | T | C | 23 | a0001c0001t0001g0192 a0001c0001t0001g0221 a0001c0001t0001g0236 others(20): Show |
26 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.403+2327T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444593 | |||||||
chr14:69444770 | G | A | 2 | a0001c0001t0012g0148 a0001c0001t0012g0149 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.403+2504G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444770 | |||||||
chr14:69444780 | A | G | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403+2514A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444780 | |||||||
chr14:69444803 | A | G | 4 | a0001c0001t0001g0184 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG01934.hp2 HG01952.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+2537A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444803 | |||||||
chr14:69444873 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.403+2607G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69444873 | |||||||
chr14:69445052 | G | GA | 73 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(70): Show |
81 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.403+2796dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69445052 | ||||||
chr14:69445082 | T | C | 1 | a0001c0001t0002g0016 | 2 | HG00408.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.403+2816T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445082 | |||||||
chr14:69445183 | A | G | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.403+2917A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445183 | |||||||
chr14:69445287 | G | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.403+3021G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445287 | |||||||
chr14:69445291 | A | G | 138 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0263 others(135): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.403+3025A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445291 | |||||||
chr14:69445434 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.403+3168T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445434 | |||||||
chr14:69445469 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0239 |
3 | NA18971.hp1 NA18992.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.403+3203A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445469 | |||||||
chr14:69445487 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.403+3221G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445487 | |||||||
chr14:69445553 | G | T | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.403+3287G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445553 | |||||||
chr14:69445563 | A | AAGTT | 17 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(14): Show |
20 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.403+3298_403+3301d others(6): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69445563 | ||||||
chr14:69445668 | G | A | 16 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(13): Show |
17 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.403+3402G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445668 | |||||||
chr14:69445714 | G | A | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+3448G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445714 | |||||||
chr14:69445789 | T | C | 1 | a0001c0001t0002g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.403+3523T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445789 | |||||||
chr14:69445862 | C | T | 2 | a0001c0003t0002g0010 a0001c0003t0002g0064 |
3 | HG01074.hp1 HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.403+3596C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445862 | |||||||
chr14:69445901 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.403+3635T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69445901 | |||||||
chr14:69446021 | CGTT | C | 6 | a0001c0001t0001g0275 a0001c0001t0005g0150 a0001c0001t0005g0154 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+3780_403+3782d others(5): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446021 | ||||||
chr14:69446021 | CGTTGTT | C | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.403+3777_403+3782d others(8): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446021 | ||||||
chr14:69446021 | CGTTGTTG others(5): Show |
C | 2 | a0001c0001t0012g0148 a0001c0001t0012g0149 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.403+3771_403+3782d others(14): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446021 | ||||||
chr14:69446068 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.403+3802C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446068 | |||||||
chr14:69446177 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.403+3911G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446177 | |||||||
chr14:69446279 | C | CAT | 24 | a0001c0001t0001g0209 a0001c0001t0002g0059 a0001c0001t0002g0110 others(21): Show |
25 | HG00733.hp2 HG00738.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.403+4028_403+4029d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446279 | ||||||
chr14:69446279 | CAT | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.403+4028_403+4029d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446279 | ||||||
chr14:69446290 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.403+4024A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446290 | |||||||
chr14:69446598 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.403+4332C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446598 | |||||||
chr14:69446720 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0267 |
2 | NA18612.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.403+4454A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446720 | |||||||
chr14:69446873 | C | CA | 81 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0218 others(78): Show |
92 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.403+4623dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446873 | ||||||
chr14:69446873 | CA | C | 59 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0020 others(56): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.403+4623delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446873 | ||||||
chr14:69446896 | G | GA | 49 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(46): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.403+4639dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446896 | ||||||
chr14:69446941 | T | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0051 a0001c0001t0002g0054 others(2): Show |
6 | HG02145.hp1 HG03209.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+4675T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446941 | |||||||
chr14:69446941 | T | TAG | 8 | a0001c0001t0001g0068 a0001c0001t0002g0014 a0001c0001t0002g0040 others(5): Show |
9 | HG02129.hp1 HG03927.hp1 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+4676_403+4677i others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446941 | ||||||
chr14:69446943 | T | G | 59 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0068 others(56): Show |
67 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.403+4677T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446943 | |||||||
chr14:69446943 | T | TAG | 5 | a0001c0001t0003g0081 a0001c0001t0003g0085 a0001c0001t0003g0138 others(2): Show |
5 | HG01346.hp2 HG02809.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+4678_403+4679i others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446943 | ||||||
chr14:69446945 | T | G | 137 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0023 others(134): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.403+4679T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446945 | |||||||
chr14:69446945 | T | TAG | 9 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0082 others(6): Show |
10 | HG00733.hp2 HG01106.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.403+4680_403+4681i others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446945 | ||||||
chr14:69446945 | TATAG | T | 3 | a0001c0001t0001g0171 a0001c0001t0002g0111 a0001c0001t0013g0024 |
3 | HG02630.hp1 HG03579.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.403+4681_403+4684d others(6): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446945 | ||||||
chr14:69446947 | T | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(239): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.403+4681T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446947 | |||||||
chr14:69446949 | G | T | 4 | a0001c0001t0004g0017 a0001c0001t0004g0126 a0001c0001t0004g0137 others(1): Show |
5 | HG00544.hp1 NA18981.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+4683G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446949 | |||||||
chr14:69446964 | A | C | 4 | a0001c0001t0004g0124 a0001c0001t0004g0139 a0001c0001t0009g0001 others(1): Show |
6 | NA18945.hp2 NA18964.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+4698A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446964 | |||||||
chr14:69446966 | A | AGAGC | 6 | a0001c0001t0002g0112 a0001c0001t0002g0286 a0001c0001t0002g0287 others(3): Show |
6 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+4701_403+4702i others(6): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446966 | ||||||
chr14:69446966 | A | C | 1 | a0001c0001t0002g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.403+4700A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446966 | |||||||
chr14:69446968 | C | A | 9 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0286 others(6): Show |
9 | HG01192.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+4702C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446968 | |||||||
chr14:69446968 | C | CGA | 43 | a0001c0001t0001g0193 a0001c0001t0001g0202 a0001c0001t0001g0233 others(40): Show |
49 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.403+4718_403+4719d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446968 | ||||||
chr14:69446968 | C | CGAGA | 7 | a0001c0001t0006g0096 a0001c0001t0006g0099 a0001c0001t0006g0100 others(4): Show |
7 | HG00738.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+4716_403+4719d others(6): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69446968 | ||||||
chr14:69446972 | A | C | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.403+4706A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446972 | |||||||
chr14:69446977 | G | A | 1 | a0001c0004t0001g0232 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.403+4711G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446977 | |||||||
chr14:69446978 | A | G | 1 | a0001c0001t0002g0029 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.403+4712A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69446978 | |||||||
chr14:69447137 | T | C | 1 | a0001c0001t0024g0094 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.403+4871T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69447137 | |||||||
chr14:69447191 | C | T | 3 | a0001c0001t0008g0142 a0001c0001t0008g0143 a0001c0001t0008g0144 |
3 | HG01081.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.403+4925C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69447191 | |||||||
chr14:69447698 | G | T | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.403+5432G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69447698 | |||||||
chr14:69447739 | T | C | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.403+5473T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69447739 | |||||||
chr14:69447773 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.404-5468C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69447773 | |||||||
chr14:69447774 | G | T | 55 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(52): Show |
61 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.404-5467G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69447774 | |||||||
chr14:69447913 | C | CA | 44 | a0001c0001t0001g0204 a0001c0001t0001g0230 a0001c0001t0001g0242 others(41): Show |
48 | HG00323.hp2 HG00544.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.404-5311dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69447913 | ||||||
chr14:69447913 | C | CAA | 31 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(28): Show |
34 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.404-5312_404-5311d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69447913 | ||||||
chr14:69447927 | A | AG | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404-5314_404-5313i others(3): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69447927 | |||||||
chr14:69447947 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404-5294A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69447947 | |||||||
chr14:69448042 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.404-5199G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69448042 | |||||||
chr14:69448069 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0254 |
2 | HG02015.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.404-5172G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69448069 | |||||||
chr14:69448144 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0074 a0001c0001t0002g0075 |
5 | HG00140.hp2 HG01433.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-5097G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69448144 | |||||||
chr14:69448201 | T | C | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.404-5040T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69448201 | |||||||
chr14:69448214 | C | CA | 176 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.404-5008dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69448214 | ||||||
chr14:69448214 | C | CAA | 84 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0078 others(81): Show |
92 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.404-5009_404-5008d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69448214 | ||||||
chr14:69448214 | C | CAAA | 8 | a0001c0001t0001g0068 a0001c0001t0001g0170 a0001c0001t0002g0034 others(5): Show |
8 | HG01358.hp1 HG02080.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.404-5010_404-5008d others(5): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69448214 | ||||||
chr14:69448346 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0173 |
2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.404-4895A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69448346 | |||||||
chr14:69448464 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.404-4777G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69448464 | |||||||
chr14:69448538 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.404-4703T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69448538 | |||||||
chr14:69448888 | AAG | A | 16 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(13): Show |
17 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-4351_404-4350d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69448888 | ||||||
chr14:69448912 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.404-4329C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69448912 | |||||||
chr14:69449024 | T | G | 11 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(8): Show |
14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.404-4217T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69449024 | |||||||
chr14:69449370 | T | C | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.404-3871T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69449370 | |||||||
chr14:69449435 | G | A | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.404-3806G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69449435 | |||||||
chr14:69449454 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.404-3787G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69449454 | |||||||
chr14:69449845 | C | CTG | 10 | a0001c0001t0001g0250 a0001c0001t0002g0047 a0001c0001t0002g0057 others(7): Show |
11 | HG02109.hp1 HG02922.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.404-3378_404-3377d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69449845 | ||||||
chr14:69450106 | T | C | 1 | a0001c0001t0008g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.404-3135T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450106 | |||||||
chr14:69450193 | T | TA | 20 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(17): Show |
23 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(20): Show |
intron_variant | MODIFIER | c.404-3038dupA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69450193 | ||||||
chr14:69450285 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.404-2956C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450285 | |||||||
chr14:69450286 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.404-2955T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450286 | |||||||
chr14:69450452 | T | A | 1 | a0001c0001t0001g0254 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.404-2789T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450452 | |||||||
chr14:69450572 | T | A | 5 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0288 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-2669T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450572 | |||||||
chr14:69450671 | A | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0150 others(11): Show |
17 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.404-2570A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450671 | |||||||
chr14:69450685 | C | G | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.404-2556C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450685 | |||||||
chr14:69450701 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.404-2540C>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450701 | |||||||
chr14:69450845 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.404-2396G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450845 | |||||||
chr14:69450903 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.404-2338G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450903 | |||||||
chr14:69450904 | T | G | 1 | a0001c0001t0002g0041 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.404-2337T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450904 | |||||||
chr14:69450983 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404-2258T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450983 | |||||||
chr14:69450995 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.404-2246C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69450995 | |||||||
chr14:69451064 | T | C | 1 | a0001c0001t0019g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.404-2177T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69451064 | |||||||
chr14:69451083 | TA | T | 4 | a0001c0001t0002g0041 a0001c0001t0013g0024 a0001c0001t0013g0025 others(1): Show |
4 | HG02280.hp1 HG03579.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-2151delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 69451083 | ||||||
chr14:69451166 | G | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404-2075G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69451166 | |||||||
chr14:69451299 | G | A | 49 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(46): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.404-1942G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69451299 | |||||||
chr14:69451392 | A | G | 3 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0108 |
3 | HG00099.hp2 HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.404-1849A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69451392 | |||||||
chr14:69451415 | G | T | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.404-1826G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69451415 | |||||||
chr14:69451604 | T | C | 2 | a0001c0001t0012g0148 a0001c0001t0012g0149 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.404-1637T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69451604 | |||||||
chr14:69451931 | G | T | 1 | a0001c0001t0002g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.404-1310G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69451931 | |||||||
chr14:69452310 | A | G | 7 | a0001c0001t0001g0068 a0001c0001t0002g0014 a0001c0001t0002g0040 others(4): Show |
8 | HG02129.hp1 HG04184.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.404-931A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452310 | |||||||
chr14:69452344 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.404-897T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452344 | |||||||
chr14:69452351 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404-890C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452351 | |||||||
chr14:69452396 | C | T | 73 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(70): Show |
81 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.404-845C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452396 | |||||||
chr14:69452473 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0027g0213 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.404-768C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452473 | |||||||
chr14:69452519 | G | A | 54 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(51): Show |
60 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.404-722G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452519 | |||||||
chr14:69452538 | CA | C | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.404-702delA | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452538 | |||||||
chr14:69452582 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404-659G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452582 | |||||||
chr14:69452600 | G | T | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.404-641G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452600 | |||||||
chr14:69452608 | G | T | 1 | a0001c0001t0002g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.404-633G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452608 | |||||||
chr14:69452960 | A | C | 2 | a0001c0001t0006g0099 a0001c0001t0006g0100 |
2 | HG02622.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.404-281A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69452960 | |||||||
chr14:69453058 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.404-183C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69453058 | |||||||
chr14:69453111 | C | T | 2 | a0001c0001t0004g0129 a0001c0001t0004g0131 |
2 | NA18982.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.404-130C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69453111 | |||||||
chr14:69453112 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404-129G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 3/6 | chr14 | 69453112 | |||||||
chr14:69453461 | T | C | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+152T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69453461 | |||||||
chr14:69453534 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+225G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69453534 | |||||||
chr14:69453563 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.472+254G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69453563 | |||||||
chr14:69453606 | C | T | 1 | a0001c0001t0005g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.472+297C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69453606 | |||||||
chr14:69453641 | A | C | 1 | a0001c0001t0001g0275 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.472+332A>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69453641 | |||||||
chr14:69453672 | C | G | 1 | a0001c0001t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.472+363C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69453672 | |||||||
chr14:69453694 | T | C | 1 | a0001c0001t0008g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.472+385T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69453694 | |||||||
chr14:69453971 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.472+662C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69453971 | |||||||
chr14:69454013 | A | G | 132 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(129): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.472+704A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69454013 | |||||||
chr14:69454044 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0265 |
2 | HG01106.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.472+735G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69454044 | |||||||
chr14:69454262 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.473-550A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69454262 | |||||||
chr14:69454762 | A | G | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.473-50A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 4/6 | chr14 | 69454762 | |||||||
chr14:69454957 | T | C | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.558+60T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 5/6 | chr14 | 69454957 | |||||||
chr14:69455030 | A | G | 1 | a0001c0001t0030g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.558+133A>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 5/6 | chr14 | 69455030 | |||||||
chr14:69455045 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.558+148G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 5/6 | chr14 | 69455045 | |||||||
chr14:69455311 | T | G | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.558+414T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 5/6 | chr14 | 69455311 | |||||||
chr14:69455319 | G | T | 5 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0151 others(2): Show |
8 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.559-413G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 5/6 | chr14 | 69455319 | |||||||
chr14:69455930 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0197 |
2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.693+64C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69455930 | |||||||
chr14:69456022 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.693+156C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456022 | |||||||
chr14:69456043 | T | A | 1 | a0001c0001t0001g0023 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.693+177T>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456043 | |||||||
chr14:69456245 | G | T | 1 | a0004c0006t0002g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.693+379G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456245 | |||||||
chr14:69456301 | C | T | 28 | a0001c0001t0004g0017 a0001c0001t0004g0122 a0001c0001t0004g0123 others(25): Show |
31 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.693+435C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456301 | |||||||
chr14:69456317 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.693+451G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456317 | |||||||
chr14:69456451 | G | A | 1 | a0001c0001t0003g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.693+585G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456451 | |||||||
chr14:69456479 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0284 |
3 | HG01175.hp2 HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.693+613C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456479 | |||||||
chr14:69456645 | C | G | 1 | a0001c0001t0011g0098 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.693+779C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456645 | |||||||
chr14:69456650 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.693+784G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456650 | |||||||
chr14:69456900 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.693+1034T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456900 | |||||||
chr14:69456985 | T | C | 17 | a0001c0001t0003g0015 a0001c0001t0003g0079 a0001c0001t0003g0080 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+1119T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69456985 | |||||||
chr14:69457175 | C | CAT | 65 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(62): Show |
72 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.694-1180_694-1179d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 69457175 | ||||||
chr14:69457183 | TAC | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.694-1158_694-1157d others(4): Show |
SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 69457183 | ||||||
chr14:69457185 | C | T | 265 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(262): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.694-1178C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457185 | |||||||
chr14:69457187 | C | T | 122 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(119): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.694-1176C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457187 | |||||||
chr14:69457189 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.694-1174C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457189 | |||||||
chr14:69457191 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.694-1172C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457191 | |||||||
chr14:69457193 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.694-1170C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457193 | |||||||
chr14:69457252 | G | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.694-1111G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457252 | |||||||
chr14:69457348 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.694-1015G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457348 | |||||||
chr14:69457444 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.694-919G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457444 | |||||||
chr14:69457585 | G | C | 56 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0002g0005 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.694-778G>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457585 | |||||||
chr14:69457632 | G | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0074 a0001c0001t0002g0075 |
5 | HG00140.hp2 HG01433.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-731G>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457632 | |||||||
chr14:69457712 | T | G | 19 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0104 others(16): Show |
22 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.694-651T>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457712 | |||||||
chr14:69457755 | C | T | 2 | a0001c0001t0002g0104 a0001c0001t0002g0117 |
2 | HG00642.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.694-608C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457755 | |||||||
chr14:69457781 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.694-582G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69457781 | |||||||
chr14:69458012 | C | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0025 a0001c0001t0029g0026 |
3 | HG02280.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.694-351C>G | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69458012 | |||||||
chr14:69458169 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.694-194G>A | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69458169 | |||||||
chr14:69458321 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.694-42T>C | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69458321 | |||||||
chr14:69458349 | C | T | 7 | a0001c0001t0001g0068 a0001c0001t0002g0014 a0001c0001t0002g0040 others(4): Show |
8 | HG02129.hp1 HG04184.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-14C>T | SLC39A9 | ENSG00000029364.12 | transcript | ENST00000336643.10 | protein_coding | 6/6 | chr14 | 69458349 |