Item | Value |
---|---|
geneid | 83986 |
ensemblid | ENSG00000167930.17 |
hgncid | 14163 |
symbol | FAM234A |
name | family with sequence similarity 234 member A |
refseq_nuc | NM_032039.4 |
refseq_prot | NP_114428.1 |
ensembl_nuc | ENST00000399932.8 |
ensembl_prot | ENSP00000382814.3 |
mane_status | MANE Select |
chr | chr16 |
start | 234821 |
end | 266096 |
strand | + |
ver | v1.2 |
region | chr16:234821-266096 |
region5000 | chr16:229821-271096 |
regionname0 | FAM234A_chr16_234821_266096 |
regionname5000 | FAM234A_chr16_229821_271096 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 552 | 368 | 87 | 70 | 152 | 14 | 43 | 115 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0002 | 0/0 | 552 | 14 | 0 | 1 | 13 | 0 | 0 | 9 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0003 | 0/0 | 552 | 8 | 0 | 3 | 5 | 0 | 0 | 4 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0004 | 0/0 | 552 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0005 | 0/0 | 552 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0006 | 0/0 | 552 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0007 | 0/0 | 552 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0008 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0009 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0010 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0011 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0012 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0013 | 0/0 | 552 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0014 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0015 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
a0016 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | MLDHK others(547): Show |
chr16 | 229821 | 271096 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1656 | 262 | 67 | 52 | 100 | 11 | 30 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0002 | 0/0 | 1656 | 84 | 10 | 14 | 45 | 3 | 12 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0005 | 0/0 | 1656 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0006 | 0/0 | 1656 | 5 | 3 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0009 | 0/0 | 1656 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0012 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0017 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0018 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0019 | 0/0 | 1656 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0020 | 0/0 | 1656 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0021 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0024 | 0/0 | 1656 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0027 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0001c0029 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0002c0003 | 0/0 | 1656 | 14 | 0 | 1 | 13 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0003c0004 | 0/0 | 1656 | 8 | 0 | 3 | 5 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0004c0007 | 0/0 | 1656 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0005c0010 | 0/0 | 1656 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0006c0011 | 0/0 | 1656 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0007c0008 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0008c0013 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0009c0026 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0010c0023 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0011c0015 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0012c0028 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0013c0014 | 0/0 | 1656 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0014c0016 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0015c0022 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 | ||
a0016c0025 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | ATGTT others(1651): Show |
chr16 | 229821 | 271096 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2909 | 218 | 38 | 47 | 94 | 10 | 28 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0002 | 0/0 | 2909 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0003 | 0/0 | 2909 | 18 | 8 | 3 | 5 | 1 | 1 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0004 | 0/0 | 2909 | 5 | 5 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0005 | 0/0 | 2909 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0007 | 0/0 | 2909 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0008 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0009 | 0/0 | 2909 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0010 | 0/0 | 2909 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0011 | 0/1 | 2909 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0012 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0014 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0016 | 0/0 | 2909 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0001t0017 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0002t0001 | 0/0 | 2909 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0002t0002 | 0/0 | 2909 | 80 | 10 | 13 | 43 | 3 | 11 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0002t0013 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0002t0015 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0002t0018 | 0/0 | 2909 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0005t0002 | 0/0 | 2909 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0006t0001 | 0/0 | 2909 | 3 | 2 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0006t0006 | 0/0 | 2909 | 2 | 1 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0009t0003 | 0/0 | 2909 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0012t0004 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0017t0001 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0018t0001 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0019t0001 | 0/0 | 2909 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0020t0001 | 0/0 | 2909 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0021t0003 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0024t0002 | 0/0 | 2909 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0027t0002 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0001c0029t0002 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0002c0003t0001 | 0/0 | 2909 | 14 | 0 | 1 | 13 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0003c0004t0002 | 0/0 | 2909 | 8 | 0 | 3 | 5 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0004c0007t0001 | 0/0 | 2909 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0005c0010t0001 | 0/0 | 2909 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0006c0011t0002 | 0/0 | 2909 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0007c0008t0002 | 0/0 | 2909 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0008c0013t0008 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0009c0026t0002 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0010c0023t0003 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0011c0015t0001 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0012c0028t0002 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0013c0014t0001 | 0/0 | 2909 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0014c0016t0001 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0015c0022t0001 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
a0016c0025t0002 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | GCCAG others(2904): Show |
chr16 | 229821 | 271096 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0004 | 1/0 | 4 | 0 | 2 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0007 | 0/0 | 4 | 1 | 0 | 0 | 1 | 2 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0007g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0007g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0009g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0009g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0011g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0014g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0016g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0017g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0015g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0018g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0006g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0009t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0009t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0012t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0017t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0018t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0019t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0020t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0021t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0024t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0027t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0029t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0004c0007t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0004c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0004c0007t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0005c0010t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0005c0010t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0006c0011t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0006c0011t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0007c0008t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0007c0008t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0008c0013t0008g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0009c0026t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0010c0023t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0011c0015t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0012c0028t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0013c0014t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0014c0016t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0015c0022t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0016c0025t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0263 | EUR | GBR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00423 | hp2 | a0005 | c0010 | t0001 | g0077 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00438 | hp2 | a0003 | c0004 | t0002 | g0014 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00597 | hp1 | a0001 | c0027 | t0002 | g0294 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0355 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00621 | hp2 | a0001 | c0021 | t0003 | g0205 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00642 | hp1 | a0003 | c0004 | t0002 | g0014 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0289 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0295 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00738 | hp1 | a0001 | c0006 | t0006 | g0346 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0126 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0127 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0240 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01099 | hp2 | a0001 | c0020 | t0001 | g0184 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0339 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01168 | hp2 | a0006 | c0011 | t0002 | g0296 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01169 | hp1 | a0006 | c0011 | t0002 | g0020 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0292 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01192 | hp1 | a0001 | c0002 | t0018 | g0033 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01243 | hp2 | a0001 | c0006 | t0001 | g0060 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0297 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0035 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0350 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0038 | EUR | IBS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0039 | EUR | IBS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0071 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0226 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0308 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01975 | hp1 | a0003 | c0004 | t0002 | g0142 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0304 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01978 | hp2 | a0003 | c0004 | t0002 | g0145 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01981 | hp1 | a0001 | c0019 | t0001 | g0084 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0302 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0356 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02027 | hp1 | a0002 | c0003 | t0001 | g0357 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0323 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02056 | hp2 | a0001 | c0009 | t0003 | g0279 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0360 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02080 | hp2 | a0001 | c0009 | t0003 | g0246 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02083 | hp2 | a0008 | c0013 | t0008 | g0352 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02132 | hp1 | a0001 | c0002 | t0015 | g0307 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02132 | hp2 | a0009 | c0026 | t0002 | g0020 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | CDX | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | CDX | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0280 | EAS | CDX | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0288 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02258 | hp2 | a0001 | c0006 | t0001 | g0042 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0331 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02523 | hp1 | a0010 | c0023 | t0003 | g0278 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0342 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02572 | hp2 | a0007 | c0008 | t0002 | g0344 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02630 | hp1 | a0011 | c0015 | t0001 | g0064 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0244 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0313 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0290 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0341 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02809 | hp2 | a0001 | c0005 | t0002 | g0013 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02818 | hp2 | a0001 | c0005 | t0002 | g0131 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0316 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02896 | hp2 | a0007 | c0008 | t0002 | g0343 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02976 | hp2 | a0012 | c0028 | t0002 | g0245 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03098 | hp1 | a0001 | c0001 | t0010 | g0237 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0361 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03130 | hp2 | a0001 | c0005 | t0002 | g0132 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03209 | hp2 | a0001 | c0006 | t0006 | g0347 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03225 | hp2 | a0001 | c0012 | t0004 | g0227 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0239 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03491 | hp1 | a0013 | c0014 | t0001 | g0258 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03516 | hp2 | a0001 | c0005 | t0002 | g0133 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03540 | hp1 | a0001 | c0005 | t0002 | g0048 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03579 | hp1 | a0001 | c0001 | t0017 | g0012 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03927 | hp1 | a0001 | c0001 | t0016 | g0095 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0034 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0037 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0283 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0243 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04228 | hp1 | a0001 | c0024 | t0002 | g0299 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | CHB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0228 | AFR | YRI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18943 | hp1 | a0002 | c0003 | t0001 | g0024 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18950 | hp1 | a0003 | c0004 | t0002 | g0322 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18954 | hp2 | a0001 | c0029 | t0002 | g0001 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0349 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18969 | hp1 | a0002 | c0003 | t0001 | g0353 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18978 | hp2 | a0001 | c0001 | t0012 | g0108 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18982 | hp2 | a0002 | c0003 | t0001 | g0354 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0311 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18997 | hp2 | a0001 | c0018 | t0001 | g0149 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18998 | hp2 | a0003 | c0004 | t0002 | g0021 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18999 | hp2 | a0001 | c0017 | t0001 | g0176 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19001 | hp1 | a0002 | c0003 | t0001 | g0359 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19003 | hp2 | a0002 | c0003 | t0001 | g0348 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19004 | hp1 | a0002 | c0003 | t0001 | g0024 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19005 | hp1 | a0003 | c0004 | t0002 | g0177 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19007 | hp1 | a0002 | c0003 | t0001 | g0351 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19012 | hp1 | a0014 | c0016 | t0001 | g0118 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19043 | hp2 | a0004 | c0007 | t0001 | g0054 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19060 | hp1 | a0015 | c0022 | t0001 | g0116 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19064 | hp2 | a0002 | c0003 | t0001 | g0358 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19079 | hp1 | a0001 | c0002 | t0013 | g0001 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19079 | hp2 | a0003 | c0004 | t0002 | g0310 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19082 | hp1 | a0005 | c0010 | t0001 | g0078 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0327 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19090 | hp1 | a0016 | c0025 | t0002 | g0018 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19240 | hp1 | a0004 | c0007 | t0001 | g0056 | AFR | YRI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0362 | AFR | ASW | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | ASW | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0363 | EUR | TSI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0330 | EUR | TSI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0317 | SAS | GIH | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | GIH | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02109 | hp1 | a0001 | c0006 | t0001 | g0043 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0236 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02559 | hp1 | a0001 | c0005 | t0002 | g0013 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | USA | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | USA | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20300 | hp2 | a0004 | c0007 | t0001 | g0055 | AFR | USA | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA21309 | hp1 | a0001 | c0001 | t0014 | g0040 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
homoSapiens | chm13v2 | a0001 | c0001 | t0011 | g0241 | REF | REF | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:254562 | C | T | 1 | a0010 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.149C>T | p.Ala50Val | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | 325/2909 | 149/1659 | 50/552 | chr16 | 254562 | |||
chr16:259525 | G | A | 1 | a0006 | 2 | HG01168.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.311G>A | p.Arg104Lys | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/13 | 487/2909 | 311/1659 | 104/552 | chr16 | 259525 | |||
chr16:259593 | G | A | 1 | a0008 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.379G>A | p.Asp127Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/13 | 555/2909 | 379/1659 | 127/552 | chr16 | 259593 | |||
chr16:259999 | C | T | 2 | a0002 a0008 |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
missense_variant | MODERATE | c.416C>T | p.Ala139Val | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/13 | 592/2909 | 416/1659 | 139/552 | chr16 | 259999 | |||
chr16:260031 | G | A | 1 | a0013 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.448G>A | p.Glu150Lys | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/13 | 624/2909 | 448/1659 | 150/552 | chr16 | 260031 | |||
chr16:260139 | A | G | 1 | a0015 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.556A>G | p.Ile186Val | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/13 | 732/2909 | 556/1659 | 186/552 | chr16 | 260139 | |||
chr16:261417 | G | A | 1 | a0011 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.611G>A | p.Ser204Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/13 | 787/2909 | 611/1659 | 204/552 | chr16 | 261417 | |||
chr16:261462 | T | G | 1 | a0016 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.656T>G | p.Val219Gly | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/13 | 832/2909 | 656/1659 | 219/552 | chr16 | 261462 | |||
chr16:261507 | G | A | 1 | a0004 | 3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.701G>A | p.Arg234Gln | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/13 | 877/2909 | 701/1659 | 234/552 | chr16 | 261507 | |||
chr16:264166 | G | A | 1 | a0009 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1339G>A | p.Glu447Lys | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/13 | 1515/2909 | 1339/1659 | 447/552 | chr16 | 264166 | |||
chr16:264659 | C | G | 1 | a0012 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1390C>G | p.Leu464Val | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/13 | 1566/2909 | 1390/1659 | 464/552 | chr16 | 264659 | |||
chr16:264665 | C | T | 1 | a0005 | 2 | HG00423.hp2 NA19082.hp1 |
missense_variant | MODERATE | c.1396C>T | p.Arg466Cys | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/13 | 1572/2909 | 1396/1659 | 466/552 | chr16 | 264665 | |||
chr16:264963 | G | A | 1 | a0007 | 2 | HG02572.hp2 HG02896.hp2 |
missense_variant | MODERATE | c.1600G>A | p.Asp534Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1776/2909 | 1600/1659 | 534/552 | chr16 | 264963 | |||
chr16:264997 | G | A | 1 | a0014 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.1634G>A | p.Arg545Gln | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1810/2909 | 1634/1659 | 545/552 | chr16 | 264997 | |||
chr16:265009 | A | G | 1 | a0003 | 8 | HG00438.hp2 HG00642.hp1 HG01975.hp1 others(5): Show |
missense_variant | MODERATE | c.1646A>G | p.Gln549Arg | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1822/2909 | 1646/1659 | 549/552 | chr16 | 265009 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:254515 | C | T | 10 | a0001c0002 a0001c0005 a0001c0024 others(7): Show |
106 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(103): Show |
synonymous_variant | LOW | c.102C>T | p.Asn34Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | 278/2909 | 102/1659 | 34/552 | chr16 | 254515 | |||
chr16:254579 | T | C | 1 | a0001c0024 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.166T>C | p.Leu56Leu | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | 342/2909 | 166/1659 | 56/552 | chr16 | 254579 | |||
chr16:254662 | G | A | 1 | a0001c0012 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.249G>A | p.Arg83Arg | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | 425/2909 | 249/1659 | 83/552 | chr16 | 254662 | |||
chr16:259517 | C | T | 1 | a0001c0005 | 6 | HG02559.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
synonymous_variant | LOW | c.303C>T | p.Asn101Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/13 | 479/2909 | 303/1659 | 101/552 | chr16 | 259517 | |||
chr16:260006 | G | A | 1 | a0001c0006 | 5 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(2): Show |
synonymous_variant | LOW | c.423G>A | p.Ser141Ser | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/13 | 599/2909 | 423/1659 | 141/552 | chr16 | 260006 | |||
chr16:261496 | C | T | 1 | a0001c0021 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.690C>T | p.Leu230Leu | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/13 | 866/2909 | 690/1659 | 230/552 | chr16 | 261496 | |||
chr16:263262 | C | T | 1 | a0001c0020 | 1 | HG01099.hp2 | splice_region_variant&synonymous_variant | LOW | c.972C>T | p.Ser324Ser | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/13 | 1148/2909 | 972/1659 | 324/552 | chr16 | 263262 | |||
chr16:263766 | C | T | 1 | a0001c0029 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.1179C>T | p.Thr393Thr | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 10/13 | 1355/2909 | 1179/1659 | 393/552 | chr16 | 263766 | |||
chr16:264144 | C | G | 1 | a0001c0019 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.1317C>G | p.Leu439Leu | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/13 | 1493/2909 | 1317/1659 | 439/552 | chr16 | 264144 | |||
chr16:264812 | C | T | 1 | a0001c0018 | 1 | NA18997.hp2 | splice_region_variant&synonymous_variant | LOW | c.1449C>T | p.Ala483Ala | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1625/2909 | 1449/1659 | 483/552 | chr16 | 264812 | |||
chr16:264830 | C | T | 1 | a0001c0009 | 2 | HG02056.hp2 HG02080.hp2 |
synonymous_variant | LOW | c.1467C>T | p.Ser489Ser | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1643/2909 | 1467/1659 | 489/552 | chr16 | 264830 | |||
chr16:264863 | G | T | 1 | a0001c0027 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.1500G>T | p.Pro500Pro | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1676/2909 | 1500/1659 | 500/552 | chr16 | 264863 | |||
chr16:264971 | C | T | 1 | a0001c0017 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.1608C>T | p.Asp536Asp | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1784/2909 | 1608/1659 | 536/552 | chr16 | 264971 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:234850 | G | C | 1 | a0001c0006t0006 | 2 | HG00738.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-147G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/13 | 19564 | chr16 | 234850 | ||||||
chr16:249611 | A | G | 1 | a0001c0001t0010 | 2 | HG03098.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-77A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/13 | 4803 | chr16 | 249611 | ||||||
chr16:254410 | C | T | 1 | a0001c0002t0018 | 1 | HG01192.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-4C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | chr16 | 254410 | |||||||
chr16:265028 | C | A | 1 | a0001c0001t0012 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 6 | chr16 | 265028 | ||||||
chr16:265205 | G | A | 1 | a0001c0001t0012 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 183 | chr16 | 265205 | ||||||
chr16:265286 | C | T | 1 | a0001c0001t0009 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*264C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 264 | chr16 | 265286 | ||||||
chr16:265308 | T | G | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0012t0004 |
8 | HG02486.hp2 HG02717.hp2 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*286T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 286 | chr16 | 265308 | ||||||
chr16:265355 | C | T | 2 | a0001c0001t0009 a0001c0001t0017 |
3 | HG01069.hp1 HG01071.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*333C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 333 | chr16 | 265355 | ||||||
chr16:265382 | C | T | 1 | a0001c0001t0016 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 360 | chr16 | 265382 | ||||||
chr16:265413 | C | T | 1 | a0001c0001t0007 | 2 | HG03130.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*391C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 391 | chr16 | 265413 | ||||||
chr16:265437 | G | A | 18 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0014 others(15): Show |
117 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*415G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 415 | chr16 | 265437 | ||||||
chr16:265446 | C | T | 1 | a0001c0001t0005 | 6 | HG02559.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*424C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 424 | chr16 | 265446 | ||||||
chr16:265558 | C | G | 27 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(24): Show |
150 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*536C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 536 | chr16 | 265558 | ||||||
chr16:265587 | G | A | 2 | a0001c0001t0009 a0001c0001t0017 |
3 | HG01069.hp1 HG01071.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*565G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 565 | chr16 | 265587 | ||||||
chr16:265703 | C | T | 2 | a0001c0001t0009 a0001c0001t0017 |
3 | HG01069.hp1 HG01071.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*681C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 681 | chr16 | 265703 | ||||||
chr16:265840 | G | A | 4 | a0001c0001t0003 a0001c0009t0003 a0001c0021t0003 others(1): Show |
22 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*818G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 818 | chr16 | 265840 | ||||||
chr16:265876 | C | A | 1 | a0001c0002t0013 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*854C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 854 | chr16 | 265876 | ||||||
chr16:265915 | G | A | 1 | a0001c0001t0014 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*893G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 893 | chr16 | 265915 | ||||||
chr16:265986 | T | C | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0017 |
5 | HG01069.hp1 HG01071.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*964T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 964 | chr16 | 265986 | ||||||
chr16:265988 | C | T | 1 | a0001c0002t0015 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*966C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 966 | chr16 | 265988 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:234909 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-140+52G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234909 | |||||||
chr16:234914 | C | T | 1 | a0001c0001t0001g0364 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-140+57C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234914 | |||||||
chr16:234920 | C | G | 1 | a0001c0001t0001g0363 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-140+63C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234920 | |||||||
chr16:234931 | C | T | 2 | a0001c0001t0007g0361 a0001c0001t0007g0362 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-140+74C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234931 | |||||||
chr16:234939 | C | T | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+82C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234939 | |||||||
chr16:234987 | C | T | 10 | a0001c0001t0001g0338 a0001c0001t0001g0340 a0001c0001t0001g0345 others(7): Show |
10 | HG00738.hp1 HG01109.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-140+130C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234987 | |||||||
chr16:235044 | A | C | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-140+187A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235044 | |||||||
chr16:235064 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-140+207A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235064 | |||||||
chr16:235118 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
7 | HG01256.hp1 HG01517.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140+261G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235118 | |||||||
chr16:235120 | T | G | 2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-140+263T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235120 | |||||||
chr16:235300 | G | A | 13 | a0001c0001t0003g0041 a0001c0001t0007g0361 a0001c0001t0007g0362 others(10): Show |
13 | HG01192.hp1 HG01361.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-140+443G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235300 | |||||||
chr16:235314 | C | T | 132 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(129): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-140+457C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235314 | |||||||
chr16:235340 | C | G | 1 | a0001c0001t0008g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-140+483C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235340 | |||||||
chr16:235362 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-140+505C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235362 | |||||||
chr16:235382 | A | C | 2 | a0001c0001t0004g0233 a0001c0001t0004g0234 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-140+525A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235382 | |||||||
chr16:235440 | A | G | 1 | a0001c0001t0001g0334 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-140+583A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235440 | |||||||
chr16:235511 | A | T | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-140+654A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235511 | |||||||
chr16:235513 | A | C | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+656A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235513 | |||||||
chr16:235590 | C | T | 1 | a0001c0001t0005g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-140+733C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235590 | |||||||
chr16:235683 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-140+826A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235683 | |||||||
chr16:235789 | A | C | 1 | a0001c0001t0005g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-140+932A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235789 | |||||||
chr16:235811 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-140+954G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235811 | |||||||
chr16:235927 | C | T | 20 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(17): Show |
20 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-140+1070C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235927 | |||||||
chr16:235946 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | NA19005.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-140+1089A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235946 | |||||||
chr16:235969 | A | G | 2 | a0001c0006t0001g0042 a0001c0006t0001g0043 |
2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-140+1112A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235969 | |||||||
chr16:235983 | T | G | 1 | a0001c0001t0001g0213 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-140+1126T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235983 | |||||||
chr16:235998 | A | C | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+1141A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235998 | |||||||
chr16:236009 | T | C | 120 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(117): Show |
126 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-140+1152T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236009 | |||||||
chr16:236088 | G | C | 5 | a0001c0001t0002g0238 a0001c0001t0010g0237 a0001c0001t0010g0239 others(2): Show |
5 | HG00738.hp1 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+1231G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236088 | |||||||
chr16:236243 | A | G | 9 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0003g0202 others(6): Show |
9 | HG00621.hp2 HG00673.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.-140+1386A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236243 | |||||||
chr16:236249 | A | C | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1392A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236249 | |||||||
chr16:236334 | A | T | 3 | a0001c0001t0001g0201 a0001c0006t0006g0346 a0001c0006t0006g0347 |
3 | HG00738.hp1 HG03209.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-140+1477A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236334 | |||||||
chr16:236353 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-140+1496A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236353 | |||||||
chr16:236358 | C | G | 1 | a0001c0002t0002g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-140+1501C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236358 | |||||||
chr16:236388 | T | G | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1531T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236388 | |||||||
chr16:236389 | T | C | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1532T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236389 | |||||||
chr16:236502 | A | G | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1645A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236502 | |||||||
chr16:236568 | A | C | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1711A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236568 | |||||||
chr16:236580 | A | G | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1723A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236580 | |||||||
chr16:236588 | G | A | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1731G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236588 | |||||||
chr16:236595 | A | C | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1738A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236595 | |||||||
chr16:236629 | G | A | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1772G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236629 | |||||||
chr16:236644 | C | A | 2 | a0001c0002t0002g0018 a0016c0025t0002g0018 |
2 | NA18975.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-140+1787C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236644 | |||||||
chr16:236681 | C | T | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+1824C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236681 | |||||||
chr16:236712 | G | C | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1855G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236712 | |||||||
chr16:236797 | G | T | 130 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(127): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-140+1940G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236797 | |||||||
chr16:236798 | C | T | 130 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(127): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-140+1941C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236798 | |||||||
chr16:236803 | G | A | 4 | a0001c0001t0001g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 others(1): Show |
4 | HG02486.hp2 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+1946G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236803 | |||||||
chr16:236824 | G | T | 129 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(126): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+1967G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236824 | |||||||
chr16:236825 | A | G | 131 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(128): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-140+1968A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236825 | |||||||
chr16:236827 | AC | A | 129 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(126): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+1974delC | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236827 | ||||||
chr16:236835 | G | A | 128 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(125): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-140+1978G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236835 | |||||||
chr16:236844 | C | T | 128 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(125): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-140+1987C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236844 | |||||||
chr16:236862 | G | C | 129 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(126): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+2005G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236862 | |||||||
chr16:236885 | C | CGA | 129 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(126): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+2028_-140+202 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236885 | |||||||
chr16:236888 | C | G | 129 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(126): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+2031C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236888 | |||||||
chr16:236897 | T | TCC | 129 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(126): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+2040_-140+204 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236897 | |||||||
chr16:236903 | A | AAAAAAAA others(8): Show |
2 | a0001c0006t0001g0042 a0001c0006t0001g0043 |
2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-140+2052_-140+205 others(19): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236903 | ||||||
chr16:236903 | A | AAAAAAAT others(8): Show |
1 | a0001c0001t0014g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140+2056_-140+205 others(19): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236903 | ||||||
chr16:236905 | A | AAAAAAAA others(13): Show |
10 | a0001c0001t0007g0361 a0001c0001t0007g0362 a0001c0002t0002g0034 others(7): Show |
10 | HG01074.hp1 HG01192.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.-140+2052_-140+205 others(24): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236905 | ||||||
chr16:236905 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-140+2052_-140+205 others(25): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236905 | ||||||
chr16:236905 | A | AAAAAAAA others(13): Show |
114 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(111): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.-140+2052_-140+205 others(24): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236905 | ||||||
chr16:236905 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0002g0333 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-140+2052_-140+205 others(24): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236905 | ||||||
chr16:236929 | A | T | 1 | a0001c0001t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-140+2072A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236929 | |||||||
chr16:236983 | T | C | 281 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(278): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-140+2126T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236983 | |||||||
chr16:237058 | T | C | 1 | a0001c0002t0002g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-140+2201T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237058 | |||||||
chr16:237071 | A | AT | 85 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(82): Show |
90 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-140+2221dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 237071 | ||||||
chr16:237078 | T | A | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+2221T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237078 | |||||||
chr16:237079 | A | T | 263 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(260): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-140+2222A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237079 | |||||||
chr16:237080 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0005g0231 |
2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-140+2223A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237080 | |||||||
chr16:237092 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-140+2235G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237092 | |||||||
chr16:237211 | T | C | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+2354T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237211 | |||||||
chr16:237235 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
5 | NA18612.hp1 NA18949.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-140+2378C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237235 | |||||||
chr16:237324 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-140+2467T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237324 | |||||||
chr16:237383 | G | A | 17 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(14): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-140+2526G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237383 | |||||||
chr16:237389 | C | T | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+2532C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237389 | |||||||
chr16:237485 | A | G | 1 | a0001c0002t0002g0332 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-140+2628A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237485 | |||||||
chr16:237557 | C | T | 1 | a0001c0002t0002g0240 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-140+2700C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237557 | |||||||
chr16:237713 | C | CT | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(79): Show |
88 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-140+2872dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 237713 | ||||||
chr16:237742 | T | C | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+2885T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237742 | |||||||
chr16:237791 | G | A | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+2934G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237791 | |||||||
chr16:237844 | C | A | 2 | a0001c0002t0002g0045 a0001c0002t0002g0046 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-140+2987C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237844 | |||||||
chr16:237892 | C | T | 12 | a0001c0001t0001g0338 a0001c0001t0001g0340 a0001c0001t0001g0345 others(9): Show |
13 | HG01109.hp2 HG02109.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-140+3035C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237892 | |||||||
chr16:237918 | C | G | 111 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(108): Show |
118 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-140+3061C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237918 | |||||||
chr16:237951 | G | T | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3094G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237951 | |||||||
chr16:238007 | GTTATTTA others(3): Show |
G | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3161_-140+317 others(14): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238007 | ||||||
chr16:238010 | ATTTATT | A | 264 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(261): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-140+3161_-140+316 others(10): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238010 | ||||||
chr16:238045 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-140+3188T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238045 | |||||||
chr16:238185 | A | G | 13 | a0002c0003t0001g0024 a0002c0003t0001g0349 a0002c0003t0001g0350 others(10): Show |
14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-140+3328A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238185 | |||||||
chr16:238216 | G | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02135.hp2 NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-140+3359G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238216 | |||||||
chr16:238303 | A | G | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3446A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238303 | |||||||
chr16:238325 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+3468G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238325 | |||||||
chr16:238519 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-140+3662C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238519 | |||||||
chr16:238542 | A | G | 4 | a0001c0001t0004g0233 a0001c0001t0004g0234 a0001c0006t0006g0346 others(1): Show |
4 | HG00738.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+3685A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238542 | |||||||
chr16:238543 | G | A | 1 | a0001c0009t0003g0246 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-140+3686G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238543 | |||||||
chr16:238562 | C | G | 110 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0076 others(107): Show |
116 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(113): Show |
intron_variant | MODIFIER | c.-140+3705C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238562 | |||||||
chr16:238562 | C | T | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3705C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238562 | |||||||
chr16:238583 | A | G | 18 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0003g0242 others(15): Show |
19 | HG00733.hp2 HG02056.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.-140+3726A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238583 | |||||||
chr16:238619 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-140+3762A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238619 | |||||||
chr16:238691 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-140+3834G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238691 | |||||||
chr16:238720 | C | A | 1 | a0001c0002t0002g0280 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-140+3863C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238720 | |||||||
chr16:238727 | C | T | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3870C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238727 | |||||||
chr16:238763 | C | G | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3906C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238763 | |||||||
chr16:238765 | C | CA | 127 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(124): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.-140+3929dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238765 | ||||||
chr16:238765 | C | CAA | 31 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0027 others(28): Show |
34 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.-140+3928_-140+392 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238765 | ||||||
chr16:238765 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03831.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-140+3919_-140+392 others(15): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238765 | ||||||
chr16:238775 | A | G | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3918A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238775 | |||||||
chr16:238776 | AAAAAAAA others(4): Show |
A | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3930_-140+394 others(15): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238776 | ||||||
chr16:238780 | A | G | 81 | a0001c0001t0001g0198 a0001c0001t0001g0273 a0001c0001t0001g0318 others(78): Show |
86 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.-140+3923A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238780 | |||||||
chr16:238781 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0156 a0001c0001t0001g0169 |
3 | NA18999.hp1 NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-140+3924A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238781 | |||||||
chr16:238782 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-140+3925A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238782 | |||||||
chr16:238850 | T | C | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(83): Show |
92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-140+3993T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238850 | |||||||
chr16:238896 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0130 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-140+4039A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238896 | |||||||
chr16:238919 | C | CAAAAAA | 8 | a0002c0003t0001g0024 a0002c0003t0001g0353 a0002c0003t0001g0354 others(5): Show |
9 | HG00621.hp1 HG02015.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-140+4070_-140+407 others(10): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238919 | ||||||
chr16:238919 | C | CAAAAAAA | 6 | a0001c0001t0003g0041 a0002c0003t0001g0349 a0002c0003t0001g0350 others(3): Show |
6 | HG01361.hp2 HG03486.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.-140+4069_-140+407 others(11): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238919 | ||||||
chr16:239021 | G | A | 3 | a0001c0001t0002g0238 a0001c0001t0010g0237 a0001c0001t0010g0239 |
3 | HG03098.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-140+4164G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239021 | |||||||
chr16:239022 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-140+4165C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239022 | |||||||
chr16:239076 | C | T | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0002t0002g0051 others(1): Show |
4 | HG00140.hp2 HG02698.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-140+4219C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239076 | |||||||
chr16:239168 | C | T | 1 | a0002c0003t0001g0357 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-140+4311C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239168 | |||||||
chr16:239175 | C | CTGTAGTC others(1020): Show |
1 | a0001c0001t0007g0361 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1013): Show |
1 | a0001c0001t0001g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1024): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1013): Show |
1 | a0001c0001t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1024): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
1 | a0001c0002t0018g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1030): Show |
1 | a0004c0007t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1041): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1029): Show |
1 | a0004c0007t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1040): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1027): Show |
3 | a0001c0001t0001g0220 a0001c0001t0010g0237 a0001c0002t0002g0218 |
3 | HG01106.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1038): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1026): Show |
4 | a0001c0001t0001g0221 a0001c0001t0002g0238 a0001c0001t0003g0339 others(1): Show |
4 | HG01109.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1037): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1025): Show |
1 | a0004c0007t0001g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1036): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1025): Show |
10 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0224 others(7): Show |
10 | HG02109.hp2 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1036): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1024): Show |
1 | a0001c0001t0001g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1035): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1024): Show |
1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1035): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1023): Show |
1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1034): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1023): Show |
3 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 |
3 | HG01243.hp2 HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1034): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1023): Show |
5 | a0001c0001t0001g0345 a0001c0002t0002g0341 a0001c0002t0002g0342 others(2): Show |
5 | HG02572.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1034): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
1 | a0001c0002t0002g0282 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1022): Show |
1 | a0001c0005t0002g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1020): Show |
5 | a0001c0002t0002g0283 a0001c0002t0002g0284 a0001c0002t0002g0285 others(2): Show |
5 | HG04199.hp1 NA18946.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
2 | a0001c0001t0014g0040 a0001c0005t0002g0132 |
2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
9 | a0001c0002t0002g0034 a0001c0002t0002g0035 a0001c0002t0002g0243 others(6): Show |
9 | HG00642.hp2 HG01361.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1020): Show |
1 | a0001c0002t0002g0226 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1019): Show |
28 | a0001c0002t0002g0001 a0001c0002t0002g0195 a0001c0002t0002g0271 others(25): Show |
32 | HG00597.hp1 HG00733.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1020): Show |
3 | a0001c0005t0002g0013 a0001c0005t0002g0133 a0001c0012t0004g0227 |
4 | HG02559.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1020): Show |
32 | a0001c0001t0001g0198 a0001c0001t0001g0273 a0001c0001t0001g0318 others(29): Show |
33 | HG01074.hp1 HG01515.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1019): Show |
1 | a0012c0028t0002g0245 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1019): Show |
1 | a0001c0002t0002g0228 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1018): Show |
2 | a0001c0002t0002g0328 a0001c0002t0002g0329 |
2 | NA19068.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1029): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1019): Show |
1 | a0001c0002t0002g0330 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1013): Show |
5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0002g0128 others(2): Show |
5 | HG00609.hp2 HG01978.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1024): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1011): Show |
13 | a0002c0003t0001g0024 a0002c0003t0001g0349 a0002c0003t0001g0350 others(10): Show |
14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1022): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1011): Show |
1 | a0001c0001t0001g0181 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1022): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1011): Show |
13 | a0001c0001t0001g0029 a0001c0001t0001g0182 a0001c0001t0001g0183 others(10): Show |
13 | HG00738.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1022): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1008): Show |
7 | a0001c0001t0001g0247 a0001c0001t0003g0275 a0001c0001t0003g0276 others(4): Show |
7 | HG00733.hp2 HG02080.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1019): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1009): Show |
1 | a0001c0009t0003g0279 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1020): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1005): Show |
4 | a0001c0001t0001g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 others(1): Show |
4 | HG02486.hp2 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1016): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1005): Show |
1 | a0001c0001t0003g0203 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1016): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1012): Show |
1 | a0001c0001t0001g0269 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1023): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1011): Show |
2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1022): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1007): Show |
1 | a0001c0001t0003g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1018): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1022): Show |
5 | a0001c0001t0001g0059 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
5 | HG02027.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1022): Show |
5 | a0001c0001t0001g0076 a0001c0001t0001g0107 a0001c0001t0001g0109 others(2): Show |
5 | HG01123.hp1 NA18967.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
18 | a0001c0001t0001g0025 a0001c0001t0001g0047 a0001c0001t0001g0049 others(15): Show |
18 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
15 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0111 others(12): Show |
15 | HG01255.hp1 HG01993.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1020): Show |
14 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0074 others(11): Show |
16 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1022): Show |
1 | a0001c0001t0001g0123 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
1 | a0001c0001t0001g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1019): Show |
1 | a0001c0001t0016g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1019): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0096 others(2): Show |
7 | HG00738.hp2 HG01167.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
1 | a0001c0001t0001g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1020): Show |
10 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0063 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1019): Show |
1 | a0001c0001t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
1 | a0001c0001t0001g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1020): Show |
1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1020): Show |
3 | a0001c0001t0001g0023 a0001c0001t0003g0081 a0001c0001t0003g0098 |
4 | HG01074.hp2 HG01106.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1022): Show |
2 | a0001c0001t0001g0099 a0001c0002t0002g0125 |
2 | HG00140.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239175 | C | CTGTAGTC others(1021): Show |
2 | a0001c0001t0001g0100 a0001c0002t0002g0051 |
2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | ||||||
chr16:239199 | A | G | 1 | a0001c0001t0005g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-140+4342A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239199 | |||||||
chr16:239278 | C | T | 1 | a0001c0002t0002g0327 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-140+4421C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239278 | |||||||
chr16:239294 | T | C | 5 | a0001c0001t0002g0238 a0001c0001t0004g0233 a0001c0001t0004g0234 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-140+4437T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239294 | |||||||
chr16:239336 | G | A | 22 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0220 others(19): Show |
22 | HG01106.hp1 HG01109.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-140+4479G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239336 | |||||||
chr16:239342 | G | A | 1 | a0001c0001t0014g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140+4485G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239342 | |||||||
chr16:239410 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-140+4553G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239410 | |||||||
chr16:239614 | C | CA | 35 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0075 others(32): Show |
36 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-140+4775dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239614 | ||||||
chr16:239614 | C | CAA | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(83): Show |
92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-140+4774_-140+477 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239614 | ||||||
chr16:239614 | CA | C | 19 | a0001c0001t0001g0175 a0001c0001t0001g0266 a0001c0001t0003g0242 others(16): Show |
20 | HG00621.hp1 HG01167.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-140+4775delA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239614 | ||||||
chr16:239688 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+4831G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239688 | |||||||
chr16:239695 | T | C | 234 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(231): Show |
247 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-140+4838T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239695 | |||||||
chr16:239699 | T | C | 3 | a0001c0001t0001g0220 a0001c0001t0003g0222 a0001c0001t0003g0223 |
3 | HG01106.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-140+4842T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239699 | |||||||
chr16:239840 | T | C | 3 | a0004c0007t0001g0054 a0004c0007t0001g0055 a0004c0007t0001g0056 |
3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-140+4983T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239840 | |||||||
chr16:239938 | G | C | 1 | a0001c0001t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-140+5081G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239938 | |||||||
chr16:239977 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-140+5120A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239977 | |||||||
chr16:240166 | C | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG00099.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-140+5309C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240166 | |||||||
chr16:240193 | G | A | 1 | a0001c0001t0005g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-140+5336G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240193 | |||||||
chr16:240305 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(30): Show |
38 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(35): Show |
intron_variant | MODIFIER | c.-140+5448C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240305 | |||||||
chr16:240500 | GTA | G | 9 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0220 others(6): Show |
9 | HG01106.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-140+5645_-140+564 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 240500 | ||||||
chr16:240502 | A | AT | 18 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0088 others(15): Show |
18 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-140+5662dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 240502 | ||||||
chr16:240502 | AT | A | 107 | a0001c0001t0001g0089 a0001c0001t0001g0122 a0001c0001t0001g0198 others(104): Show |
113 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.-140+5662delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 240502 | ||||||
chr16:240543 | C | T | 1 | a0001c0002t0002g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-140+5686C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240543 | |||||||
chr16:240593 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-140+5736C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240593 | |||||||
chr16:240602 | A | T | 1 | a0001c0002t0018g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-140+5745A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240602 | |||||||
chr16:240626 | C | T | 7 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0221 others(4): Show |
7 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140+5769C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240626 | |||||||
chr16:240925 | C | T | 1 | a0001c0001t0001g0364 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-140+6068C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240925 | |||||||
chr16:240927 | TTTAAAAC others(4): Show |
T | 1 | a0001c0001t0001g0094 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-140+6073_-140+608 others(15): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 240927 | ||||||
chr16:241048 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-140+6191C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241048 | |||||||
chr16:241275 | G | GAA | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(228): Show |
244 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.-140+6428_-140+642 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241275 | ||||||
chr16:241350 | G | C | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+6493G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241350 | |||||||
chr16:241406 | G | T | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+6549G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241406 | |||||||
chr16:241476 | C | A | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+6619C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241476 | |||||||
chr16:241535 | G | A | 1 | a0004c0007t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-140+6678G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241535 | |||||||
chr16:241588 | C | CA | 16 | a0001c0001t0001g0147 a0001c0002t0002g0312 a0002c0003t0001g0024 others(13): Show |
17 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.-140+6743dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241588 | ||||||
chr16:241645 | C | T | 12 | a0001c0001t0001g0247 a0001c0001t0003g0274 a0001c0001t0003g0275 others(9): Show |
12 | HG00733.hp2 HG02056.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.-140+6788C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241645 | |||||||
chr16:241655 | G | C | 12 | a0001c0001t0001g0247 a0001c0001t0003g0274 a0001c0001t0003g0275 others(9): Show |
12 | HG00733.hp2 HG02056.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.-140+6798G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241655 | |||||||
chr16:241671 | A | C | 21 | a0001c0002t0002g0001 a0001c0002t0002g0195 a0001c0002t0002g0280 others(18): Show |
25 | HG01070.hp2 HG01071.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.-140+6814A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241671 | |||||||
chr16:241683 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-140+6826C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241683 | |||||||
chr16:241708 | C | G | 19 | a0001c0001t0001g0214 a0001c0001t0003g0242 a0001c0001t0004g0215 others(16): Show |
20 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.-140+6851C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241708 | |||||||
chr16:241734 | A | G | 2 | a0001c0002t0002g0038 a0001c0002t0002g0039 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-140+6877A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241734 | |||||||
chr16:241745 | A | G | 1 | a0001c0001t0014g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140+6888A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241745 | |||||||
chr16:241905 | C | CA | 18 | a0001c0001t0001g0072 a0001c0001t0001g0110 a0001c0001t0001g0111 others(15): Show |
18 | HG00438.hp1 HG00735.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-140+7066dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241905 | ||||||
chr16:241905 | CA | C | 103 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 others(100): Show |
108 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.-140+7066delA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241905 | ||||||
chr16:241905 | CAA | C | 25 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0220 others(22): Show |
26 | HG00621.hp1 HG01106.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.-140+7065_-140+706 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241905 | ||||||
chr16:242066 | G | A | 3 | a0001c0002t0002g0293 a0001c0002t0002g0328 a0001c0002t0002g0329 |
3 | NA18979.hp1 NA19068.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-140+7209G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242066 | |||||||
chr16:242079 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0182 |
3 | HG01109.hp1 HG01496.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-140+7222G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242079 | |||||||
chr16:242251 | A | G | 2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-139-7298A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242251 | |||||||
chr16:242325 | G | A | 1 | a0001c0002t0002g0314 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-139-7224G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242325 | |||||||
chr16:242389 | T | A | 1 | a0001c0001t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-139-7160T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242389 | |||||||
chr16:242394 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-139-7155A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242394 | |||||||
chr16:242406 | G | C | 1 | a0001c0002t0002g0328 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-139-7143G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242406 | |||||||
chr16:242495 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG01123.hp1 HG01255.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-139-7054C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242495 | |||||||
chr16:242578 | C | T | 1 | a0001c0001t0003g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-139-6971C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242578 | |||||||
chr16:242612 | C | CT | 6 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0001g0171 others(3): Show |
6 | HG01993.hp2 NA18967.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.-139-6921dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 242612 | ||||||
chr16:242612 | CT | C | 19 | a0001c0001t0001g0112 a0001c0001t0001g0136 a0001c0001t0001g0183 others(16): Show |
19 | HG00733.hp2 HG00738.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-139-6921delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 242612 | ||||||
chr16:242669 | A | G | 10 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0005g0012 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-139-6880A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242669 | |||||||
chr16:242706 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-139-6843G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242706 | |||||||
chr16:242770 | G | A | 6 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG01884.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-139-6779G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242770 | |||||||
chr16:242773 | T | C | 246 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(243): Show |
259 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.-139-6776T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242773 | |||||||
chr16:242913 | G | A | 1 | a0001c0002t0002g0195 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-139-6636G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242913 | |||||||
chr16:242981 | C | CT | 5 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0144 others(2): Show |
8 | HG00609.hp2 HG02083.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.-139-6552dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 242981 | ||||||
chr16:242981 | CT | C | 9 | a0001c0001t0001g0075 a0001c0001t0001g0151 a0001c0001t0001g0175 others(6): Show |
9 | HG01081.hp1 HG01257.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.-139-6552delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 242981 | ||||||
chr16:243022 | C | G | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-139-6527C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243022 | |||||||
chr16:243156 | T | G | 1 | a0001c0001t0007g0362 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-139-6393T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243156 | |||||||
chr16:243168 | G | T | 10 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0220 others(7): Show |
10 | HG01106.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-139-6381G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243168 | |||||||
chr16:243198 | C | T | 1 | a0001c0002t0002g0308 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-139-6351C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243198 | |||||||
chr16:243258 | C | T | 13 | a0002c0003t0001g0024 a0002c0003t0001g0349 a0002c0003t0001g0350 others(10): Show |
14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139-6291C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243258 | |||||||
chr16:243275 | G | A | 1 | a0001c0017t0001g0176 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-139-6274G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243275 | |||||||
chr16:243315 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0002t0002g0065 |
4 | HG02257.hp1 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139-6234C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243315 | |||||||
chr16:243496 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-139-6053A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243496 | |||||||
chr16:243530 | A | G | 3 | a0004c0007t0001g0054 a0004c0007t0001g0055 a0004c0007t0001g0056 |
3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-139-6019A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243530 | |||||||
chr16:243563 | T | C | 188 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(185): Show |
200 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.-139-5986T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243563 | |||||||
chr16:243588 | G | C | 3 | a0001c0001t0002g0238 a0001c0001t0010g0237 a0001c0001t0010g0239 |
3 | HG03098.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-5961G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243588 | |||||||
chr16:243594 | C | T | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-139-5955C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243594 | |||||||
chr16:243779 | G | T | 5 | a0001c0001t0001g0340 a0001c0001t0001g0345 a0001c0001t0003g0339 others(2): Show |
5 | HG01109.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-139-5770G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243779 | |||||||
chr16:243916 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0072 others(26): Show |
31 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-139-5633G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243916 | |||||||
chr16:243942 | C | T | 1 | a0001c0002t0002g0313 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-139-5607C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243942 | |||||||
chr16:243972 | A | AT | 84 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0168 others(81): Show |
89 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.-139-5563dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 243972 | ||||||
chr16:244008 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-139-5541A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244008 | |||||||
chr16:244024 | A | G | 3 | a0001c0001t0001g0338 a0001c0002t0002g0341 a0001c0002t0002g0342 |
3 | HG02109.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-139-5525A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244024 | |||||||
chr16:244028 | G | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0080 others(2): Show |
7 | HG00738.hp2 HG01099.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-139-5521G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244028 | |||||||
chr16:244029 | T | C | 1 | a0002c0003t0001g0357 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-139-5520T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244029 | |||||||
chr16:244030 | G | A | 1 | a0002c0003t0001g0357 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-139-5519G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244030 | |||||||
chr16:244031 | C | T | 1 | a0002c0003t0001g0357 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-139-5518C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244031 | |||||||
chr16:244032 | C | G | 2 | a0001c0001t0001g0338 a0002c0003t0001g0357 |
2 | HG02027.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-139-5517C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244032 | |||||||
chr16:244037 | C | A | 1 | a0002c0003t0001g0357 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-139-5512C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244037 | |||||||
chr16:244050 | C | G | 1 | a0001c0001t0001g0338 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-139-5499C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244050 | |||||||
chr16:244070 | A | G | 2 | a0001c0001t0007g0361 a0001c0001t0007g0362 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-139-5479A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244070 | |||||||
chr16:244080 | T | C | 3 | a0004c0007t0001g0054 a0004c0007t0001g0055 a0004c0007t0001g0056 |
3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-139-5469T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244080 | |||||||
chr16:244086 | A | C | 1 | a0001c0009t0003g0246 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-139-5463A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244086 | |||||||
chr16:244093 | T | C | 2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-139-5456T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244093 | |||||||
chr16:244094 | G | C | 2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-139-5455G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244094 | |||||||
chr16:244103 | G | A | 2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-139-5446G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244103 | |||||||
chr16:244104 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-139-5445G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244104 | |||||||
chr16:244114 | A | G | 17 | a0001c0001t0001g0198 a0001c0001t0001g0213 a0001c0001t0001g0219 others(14): Show |
17 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-139-5435A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244114 | |||||||
chr16:244130 | G | A | 1 | a0001c0001t0004g0233 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-139-5419G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244130 | |||||||
chr16:244158 | T | C | 99 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-139-5391T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244158 | |||||||
chr16:244162 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-139-5387G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244162 | |||||||
chr16:244170 | G | A | 2 | a0002c0003t0001g0353 a0008c0013t0008g0352 |
2 | HG02083.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-139-5379G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244170 | |||||||
chr16:244178 | T | C | 206 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-139-5371T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244178 | |||||||
chr16:244182 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-139-5367A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244182 | |||||||
chr16:244183 | T | C | 1 | a0001c0002t0002g0302 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-139-5366T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244183 | |||||||
chr16:244190 | G | A | 7 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0224 others(4): Show |
7 | HG01891.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-139-5359G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244190 | |||||||
chr16:244190 | G | C | 55 | a0001c0001t0001g0073 a0001c0001t0001g0096 a0001c0001t0001g0097 others(52): Show |
59 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.-139-5359G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244190 | |||||||
chr16:244203 | T | C | 11 | a0001c0001t0001g0088 a0001c0001t0001g0220 a0001c0001t0003g0222 others(8): Show |
11 | HG00423.hp2 HG00609.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-139-5346T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244203 | |||||||
chr16:244211 | A | G | 205 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(202): Show |
216 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-139-5338A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244211 | |||||||
chr16:244215 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0100 |
2 | HG02055.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-139-5334G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244215 | |||||||
chr16:244219 | T | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0100 others(6): Show |
12 | HG00738.hp2 HG02280.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-139-5330T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244219 | |||||||
chr16:244219 | TG | T | 3 | a0001c0001t0002g0238 a0001c0001t0010g0237 a0001c0001t0010g0239 |
3 | HG03098.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-5328delG | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244219 | ||||||
chr16:244244 | A | G | 65 | a0001c0001t0001g0023 a0001c0001t0001g0214 a0001c0001t0001g0318 others(62): Show |
70 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.-139-5305A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244244 | |||||||
chr16:244248 | G | A | 2 | a0001c0002t0002g0052 a0001c0002t0002g0053 |
2 | NA19010.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-139-5301G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244248 | |||||||
chr16:244255 | A | C | 5 | a0001c0001t0001g0340 a0001c0001t0001g0345 a0001c0001t0003g0274 others(2): Show |
5 | HG02280.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-139-5294A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244255 | |||||||
chr16:244260 | G | A | 2 | a0001c0001t0004g0233 a0001c0001t0004g0234 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-139-5289G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244260 | |||||||
chr16:244263 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0003g0242 |
2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-139-5286C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244263 | |||||||
chr16:244264 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-139-5285G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244264 | |||||||
chr16:244386 | C | T | 2 | a0001c0001t0005g0229 a0001c0001t0008g0236 |
2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-139-5163C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244386 | |||||||
chr16:244387 | A | G | 21 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0221 others(18): Show |
21 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-139-5162A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244387 | |||||||
chr16:244401 | T | C | 1 | a0001c0002t0002g0281 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-139-5148T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244401 | |||||||
chr16:244533 | C | G | 1 | a0001c0001t0003g0275 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-139-5016C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244533 | |||||||
chr16:244672 | A | G | 2 | a0001c0001t0010g0237 a0001c0001t0010g0239 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-4877A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244672 | |||||||
chr16:244682 | C | CT | 20 | a0001c0001t0001g0147 a0001c0001t0001g0190 a0001c0001t0001g0199 others(17): Show |
20 | HG01071.hp1 HG01256.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-139-4844dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244682 | ||||||
chr16:244682 | CT | C | 121 | a0001c0001t0001g0063 a0001c0001t0001g0089 a0001c0001t0001g0094 others(118): Show |
126 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(123): Show |
intron_variant | MODIFIER | c.-139-4844delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244682 | ||||||
chr16:244682 | CTT | C | 19 | a0001c0001t0001g0214 a0001c0002t0002g0038 a0001c0002t0002g0240 others(16): Show |
20 | HG00621.hp1 HG01074.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-139-4845_-139-484 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244682 | ||||||
chr16:244683 | T | C | 1 | a0001c0009t0003g0279 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-139-4866T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244683 | |||||||
chr16:244710 | C | T | 14 | a0001c0001t0008g0236 a0002c0003t0001g0024 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-139-4839C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244710 | |||||||
chr16:244750 | A | G | 161 | a0001c0001t0001g0070 a0001c0001t0001g0213 a0001c0001t0001g0214 others(158): Show |
168 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(165): Show |
intron_variant | MODIFIER | c.-139-4799A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244750 | |||||||
chr16:244751 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-139-4798C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244751 | |||||||
chr16:244798 | C | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0120 others(1): Show |
4 | HG01123.hp1 HG01255.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-139-4751C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244798 | |||||||
chr16:244854 | A | G | 2 | a0001c0002t0002g0037 a0001c0002t0002g0240 |
2 | HG01074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-139-4695A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244854 | |||||||
chr16:244872 | A | G | 13 | a0002c0003t0001g0024 a0002c0003t0001g0349 a0002c0003t0001g0350 others(10): Show |
14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139-4677A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244872 | |||||||
chr16:244879 | ATGGGGTT others(2076): Show |
A | 1 | a0001c0001t0007g0362 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-139-4660_-139-257 others(4): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244879 | ||||||
chr16:244892 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0101 others(1): Show |
6 | HG00738.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-139-4657A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244892 | |||||||
chr16:244912 | A | T | 1 | a0001c0001t0001g0334 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-139-4637A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244912 | |||||||
chr16:244919 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-139-4630C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244919 | |||||||
chr16:244982 | G | A | 1 | a0001c0001t0007g0361 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-139-4567G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244982 | |||||||
chr16:245054 | C | G | 1 | a0001c0002t0002g0295 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-139-4495C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245054 | |||||||
chr16:245085 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-139-4464C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245085 | |||||||
chr16:245118 | A | G | 89 | a0001c0001t0004g0233 a0001c0001t0004g0234 a0001c0002t0001g0317 others(86): Show |
94 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.-139-4431A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245118 | |||||||
chr16:245353 | A | G | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-4196A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245353 | |||||||
chr16:245365 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-139-4184G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245365 | |||||||
chr16:245446 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG01074.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-139-4103C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245446 | |||||||
chr16:245602 | G | A | 15 | a0001c0001t0004g0233 a0001c0001t0004g0234 a0002c0003t0001g0024 others(12): Show |
16 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.-139-3947G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245602 | |||||||
chr16:245626 | A | G | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-3923A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245626 | |||||||
chr16:245664 | GA | G | 119 | a0001c0001t0001g0345 a0001c0001t0002g0238 a0001c0001t0003g0081 others(116): Show |
125 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.-139-3874delA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 245664 | ||||||
chr16:245715 | A | C | 26 | a0001c0001t0003g0081 a0001c0001t0003g0098 a0001c0001t0003g0202 others(23): Show |
27 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-139-3834A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245715 | |||||||
chr16:245719 | A | G | 174 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(171): Show |
181 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.-139-3830A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245719 | |||||||
chr16:245793 | A | G | 13 | a0002c0003t0001g0024 a0002c0003t0001g0349 a0002c0003t0001g0350 others(10): Show |
14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139-3756A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245793 | |||||||
chr16:245796 | T | C | 135 | a0001c0001t0002g0238 a0001c0001t0003g0041 a0001c0001t0003g0081 others(132): Show |
142 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.-139-3753T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245796 | |||||||
chr16:245825 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-3724C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245825 | |||||||
chr16:245839 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-139-3710G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245839 | |||||||
chr16:245958 | G | A | 16 | a0001c0001t0003g0041 a0001c0001t0004g0233 a0001c0001t0004g0234 others(13): Show |
17 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.-139-3591G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245958 | |||||||
chr16:245964 | T | A | 2 | a0001c0001t0004g0233 a0001c0001t0004g0234 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-139-3585T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245964 | |||||||
chr16:246055 | T | C | 2 | a0001c0001t0010g0237 a0001c0001t0010g0239 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-3494T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246055 | |||||||
chr16:246185 | C | A | 174 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(171): Show |
181 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.-139-3364C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246185 | |||||||
chr16:246219 | A | AAAT | 17 | a0001c0001t0001g0002 a0001c0001t0003g0041 a0001c0001t0004g0233 others(14): Show |
19 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.-139-3311_-139-330 others(7): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246219 | ||||||
chr16:246219 | A | T | 18 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(15): Show |
18 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-139-3330A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246219 | |||||||
chr16:246222 | T | A | 4 | a0001c0001t0001g0005 a0001c0001t0010g0237 a0001c0001t0010g0239 others(1): Show |
4 | HG02165.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139-3327T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246222 | |||||||
chr16:246283 | A | AT | 18 | a0001c0001t0001g0011 a0001c0001t0001g0110 a0001c0001t0001g0144 others(15): Show |
18 | HG02257.hp1 HG02293.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.-139-3251dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246283 | ||||||
chr16:246293 | T | G | 3 | a0001c0002t0002g0065 a0001c0002t0002g0244 a0012c0028t0002g0245 |
3 | HG02647.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-139-3256T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246293 | |||||||
chr16:246295 | T | G | 3 | a0001c0002t0002g0065 a0001c0002t0002g0244 a0012c0028t0002g0245 |
3 | HG02647.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-139-3254T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246295 | |||||||
chr16:246297 | T | G | 3 | a0001c0002t0002g0065 a0001c0002t0002g0244 a0012c0028t0002g0245 |
3 | HG02647.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-139-3252T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246297 | |||||||
chr16:246355 | C | T | 2 | a0001c0001t0001g0028 a0001c0002t0002g0036 |
2 | HG01978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-139-3194C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246355 | |||||||
chr16:246382 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-139-3167A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246382 | |||||||
chr16:246383 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-139-3166G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246383 | |||||||
chr16:246417 | C | CT | 33 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0072 others(30): Show |
33 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.-139-3110dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | ||||||
chr16:246417 | C | CTT | 102 | a0001c0001t0001g0004 a0001c0001t0002g0238 a0001c0001t0003g0098 others(99): Show |
107 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.-139-3111_-139-311 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | ||||||
chr16:246417 | C | CTTT | 16 | a0001c0001t0003g0081 a0001c0001t0003g0276 a0001c0001t0003g0331 others(13): Show |
16 | HG00733.hp2 HG01106.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-139-3112_-139-311 others(7): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | ||||||
chr16:246417 | CT | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0138 others(11): Show |
14 | HG01069.hp2 HG01106.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139-3110delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | ||||||
chr16:246417 | CTTT | C | 12 | a0002c0003t0001g0024 a0002c0003t0001g0349 a0002c0003t0001g0350 others(9): Show |
13 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.-139-3112_-139-311 others(7): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | ||||||
chr16:246458 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-139-3091C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246458 | |||||||
chr16:246459 | G | A | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-3090G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246459 | |||||||
chr16:246503 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-139-3046T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246503 | |||||||
chr16:246512 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-139-3037C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246512 | |||||||
chr16:246513 | G | A | 1 | a0001c0002t0002g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-139-3036G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246513 | |||||||
chr16:246524 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-139-3025A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246524 | |||||||
chr16:246568 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0197 |
2 | HG01261.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-139-2981C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246568 | |||||||
chr16:246666 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-139-2883G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246666 | |||||||
chr16:246691 | T | C | 2 | a0001c0001t0004g0233 a0001c0001t0004g0234 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-139-2858T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246691 | |||||||
chr16:246726 | GT | G | 10 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
10 | HG00735.hp1 HG01099.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.-139-2811delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246726 | ||||||
chr16:246739 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-139-2810C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246739 | |||||||
chr16:246749 | GTGTTT | G | 9 | a0001c0002t0001g0317 a0001c0002t0002g0051 a0001c0002t0002g0125 others(6): Show |
9 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-139-2778_-139-277 others(9): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246749 | ||||||
chr16:246801 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-139-2748G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246801 | |||||||
chr16:246997 | A | G | 15 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0004g0215 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-139-2552A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246997 | |||||||
chr16:247025 | G | A | 2 | a0001c0002t0002g0341 a0001c0002t0002g0342 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-139-2524G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247025 | |||||||
chr16:247027 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-139-2522C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247027 | |||||||
chr16:247077 | G | T | 2 | a0001c0001t0010g0237 a0001c0001t0010g0239 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-2472G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247077 | |||||||
chr16:247202 | C | G | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-2347C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247202 | |||||||
chr16:247232 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-139-2317G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247232 | |||||||
chr16:247265 | G | A | 31 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(28): Show |
31 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-139-2284G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247265 | |||||||
chr16:247289 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-139-2260C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247289 | |||||||
chr16:247322 | C | T | 13 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0004g0215 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-139-2227C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247322 | |||||||
chr16:247426 | G | T | 2 | a0001c0001t0007g0361 a0001c0001t0007g0362 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-139-2123G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247426 | |||||||
chr16:247511 | C | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0096 others(152): Show |
166 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.-139-2038C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247511 | |||||||
chr16:247525 | C | G | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-2024C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247525 | |||||||
chr16:247604 | G | A | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-1945G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247604 | |||||||
chr16:247672 | C | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0096 others(213): Show |
228 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(225): Show |
intron_variant | MODIFIER | c.-139-1877C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247672 | |||||||
chr16:247751 | T | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0096 others(215): Show |
230 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(227): Show |
intron_variant | MODIFIER | c.-139-1798T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247751 | |||||||
chr16:247782 | T | C | 4 | a0001c0001t0003g0242 a0001c0001t0003g0339 a0007c0008t0002g0343 others(1): Show |
4 | HG01109.hp2 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139-1767T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247782 | |||||||
chr16:247836 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-139-1713T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247836 | |||||||
chr16:247939 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-139-1610C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247939 | |||||||
chr16:248098 | T | C | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-1451T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248098 | |||||||
chr16:248132 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-139-1417C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248132 | |||||||
chr16:248138 | A | C | 365 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(362): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.-139-1411A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248138 | |||||||
chr16:248241 | C | G | 2 | a0001c0002t0002g0341 a0001c0002t0002g0342 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-139-1308C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248241 | |||||||
chr16:248251 | C | T | 5 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0224 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-139-1298C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248251 | |||||||
chr16:248588 | G | A | 11 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0217 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-139-961G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248588 | |||||||
chr16:248589 | A | G | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-960A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248589 | |||||||
chr16:248690 | C | G | 26 | a0001c0001t0003g0041 a0001c0001t0003g0242 a0001c0001t0004g0233 others(23): Show |
27 | HG00621.hp1 HG00738.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-139-859C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248690 | |||||||
chr16:248755 | G | A | 1 | a0001c0002t0001g0317 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-139-794G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248755 | |||||||
chr16:248861 | C | A | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-688C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248861 | |||||||
chr16:249003 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-139-546C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 249003 | |||||||
chr16:249466 | T | C | 1 | a0001c0002t0002g0301 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-139-83T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 249466 | |||||||
chr16:249503 | G | A | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-46G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 249503 | |||||||
chr16:249716 | C | T | 8 | a0001c0002t0002g0022 a0001c0002t0002g0270 a0001c0002t0002g0315 others(5): Show |
9 | HG02040.hp2 HG02074.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34+62C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249716 | |||||||
chr16:249808 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-34+154G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249808 | |||||||
chr16:249924 | A | G | 5 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(2): Show |
5 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+270A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249924 | |||||||
chr16:249946 | A | T | 10 | a0001c0001t0005g0012 a0001c0001t0005g0031 a0001c0001t0005g0032 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34+292A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249946 | |||||||
chr16:249959 | C | T | 3 | a0001c0001t0003g0242 a0001c0001t0010g0237 a0001c0001t0010g0239 |
3 | HG02886.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-34+305C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249959 | |||||||
chr16:249981 | T | C | 93 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(90): Show |
98 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.-34+327T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249981 | |||||||
chr16:250007 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG01256.hp2 HG01258.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-34+353G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250007 | |||||||
chr16:250008 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-34+354C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250008 | |||||||
chr16:250077 | G | C | 17 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(14): Show |
17 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34+423G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250077 | |||||||
chr16:250097 | A | G | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34+443A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250097 | |||||||
chr16:250174 | T | G | 15 | a0001c0001t0003g0041 a0002c0003t0001g0024 a0002c0003t0001g0348 others(12): Show |
16 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34+520T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250174 | |||||||
chr16:250178 | A | G | 146 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(143): Show |
153 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.-34+524A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250178 | |||||||
chr16:250240 | T | C | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34+586T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250240 | |||||||
chr16:250264 | T | G | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-34+610T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250264 | |||||||
chr16:250277 | T | C | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34+623T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250277 | |||||||
chr16:250389 | T | C | 139 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0101 others(136): Show |
148 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.-34+735T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250389 | |||||||
chr16:250394 | AC | A | 23 | a0001c0001t0003g0041 a0001c0001t0003g0242 a0001c0001t0004g0215 others(20): Show |
23 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-34+742delC | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 250394 | ||||||
chr16:250396 | C | T | 16 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(13): Show |
16 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34+742C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250396 | |||||||
chr16:250396 | CT | C | 10 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(7): Show |
10 | HG02055.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34+746delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 250396 | ||||||
chr16:250400 | T | C | 128 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0003g0081 others(125): Show |
137 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.-34+746T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250400 | |||||||
chr16:250491 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-34+837G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250491 | |||||||
chr16:250642 | G | A | 177 | a0001c0001t0001g0090 a0001c0001t0001g0152 a0001c0001t0001g0213 others(174): Show |
184 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(181): Show |
intron_variant | MODIFIER | c.-34+988G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250642 | |||||||
chr16:250682 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+1028C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250682 | |||||||
chr16:250697 | T | A | 175 | a0001c0001t0001g0090 a0001c0001t0001g0213 a0001c0001t0001g0214 others(172): Show |
181 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.-34+1043T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250697 | |||||||
chr16:250773 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-34+1119T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250773 | |||||||
chr16:250993 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-34+1339A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250993 | |||||||
chr16:251012 | A | AAT | 6 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(3): Show |
6 | HG02027.hp2 NA18949.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+1359_-34+1360d others(4): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251012 | ||||||
chr16:251013 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-34+1359A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251013 | |||||||
chr16:251025 | T | C | 1 | a0001c0002t0002g0323 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-34+1371T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251025 | |||||||
chr16:251042 | C | T | 2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-34+1388C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251042 | |||||||
chr16:251113 | T | C | 1 | a0002c0003t0001g0357 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-34+1459T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251113 | |||||||
chr16:251147 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-34+1493T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251147 | |||||||
chr16:251182 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-34+1528G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251182 | |||||||
chr16:251325 | A | G | 3 | a0004c0007t0001g0054 a0004c0007t0001g0055 a0004c0007t0001g0056 |
3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-34+1671A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251325 | |||||||
chr16:251396 | A | G | 1 | a0001c0002t0002g0306 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-34+1742A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251396 | |||||||
chr16:251397 | T | A | 1 | a0001c0002t0002g0306 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-34+1743T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251397 | |||||||
chr16:251398 | G | T | 1 | a0001c0002t0002g0306 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-34+1744G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251398 | |||||||
chr16:251499 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-34+1845C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251499 | |||||||
chr16:251515 | C | T | 1 | a0001c0002t0002g0313 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-34+1861C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251515 | |||||||
chr16:251524 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0178 |
2 | NA19063.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-34+1870G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251524 | |||||||
chr16:251526 | C | T | 1 | a0001c0002t0018g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-34+1872C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251526 | |||||||
chr16:251528 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+1874C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251528 | |||||||
chr16:251679 | G | GT | 43 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0050 others(40): Show |
43 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.-34+2052dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | ||||||
chr16:251679 | G | GTT | 24 | a0001c0001t0001g0259 a0001c0001t0005g0031 a0001c0001t0005g0129 others(21): Show |
25 | HG00621.hp1 HG01361.hp2 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.-34+2051_-34+2052d others(4): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | ||||||
chr16:251679 | G | GTTT | 90 | a0001c0001t0001g0165 a0001c0001t0002g0128 a0001c0001t0002g0130 others(87): Show |
96 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-34+2050_-34+2052d others(5): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | ||||||
chr16:251679 | G | GTTTT | 29 | a0001c0001t0003g0274 a0001c0001t0003g0275 a0001c0001t0003g0277 others(26): Show |
30 | HG00642.hp2 HG01109.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+2049_-34+2052d others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | ||||||
chr16:251679 | GT | G | 10 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0063 others(7): Show |
10 | HG01256.hp1 HG01256.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34+2052delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | ||||||
chr16:251679 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-34+2041_-34+2052d others(14): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | ||||||
chr16:251687 | T | TTTG | 14 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0220 others(11): Show |
14 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34+2035_-34+2036i others(5): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251687 | ||||||
chr16:251741 | T | C | 183 | a0001c0001t0001g0165 a0001c0001t0001g0213 a0001c0001t0001g0214 others(180): Show |
191 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.-34+2087T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251741 | |||||||
chr16:251895 | C | T | 4 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0217 others(1): Show |
4 | HG02486.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+2241C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251895 | |||||||
chr16:251896 | G | A | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-34+2242G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251896 | |||||||
chr16:251942 | A | G | 185 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0165 others(182): Show |
193 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.-34+2288A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251942 | |||||||
chr16:251952 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+2298A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251952 | |||||||
chr16:251972 | T | C | 1 | a0001c0002t0002g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-34+2318T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251972 | |||||||
chr16:252002 | C | CA | 24 | a0001c0001t0001g0066 a0001c0001t0001g0091 a0001c0001t0001g0144 others(21): Show |
24 | HG00597.hp1 HG01261.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-33-2360dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252002 | ||||||
chr16:252002 | CA | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0143 |
6 | HG02040.hp1 HG02080.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-2360delA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252002 | ||||||
chr16:252003 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-34+2349A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252003 | |||||||
chr16:252029 | G | A | 1 | a0001c0001t0005g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-33-2352G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252029 | |||||||
chr16:252033 | C | CT | 111 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(108): Show |
118 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.-33-2347dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252033 | ||||||
chr16:252086 | G | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0257 a0001c0001t0001g0264 |
3 | HG00140.hp1 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-33-2295G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252086 | |||||||
chr16:252162 | A | G | 2 | a0001c0006t0006g0346 a0001c0006t0006g0347 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-33-2219A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252162 | |||||||
chr16:252185 | G | GT | 54 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(51): Show |
58 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-33-2180dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252185 | ||||||
chr16:252185 | G | T | 9 | a0001c0001t0001g0174 a0001c0001t0001g0251 a0001c0001t0001g0252 others(6): Show |
9 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-2196G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252185 | |||||||
chr16:252185 | GT | G | 131 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(128): Show |
137 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.-33-2180delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252185 | ||||||
chr16:252190 | T | G | 1 | a0001c0001t0001g0259 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-33-2191T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252190 | |||||||
chr16:252326 | C | A | 1 | a0001c0002t0002g0321 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-33-2055C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252326 | |||||||
chr16:252405 | T | C | 3 | a0001c0002t0002g0065 a0001c0002t0002g0244 a0012c0028t0002g0245 |
3 | HG02647.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-33-1976T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252405 | |||||||
chr16:252433 | G | A | 13 | a0001c0001t0003g0081 a0001c0001t0003g0098 a0001c0001t0003g0202 others(10): Show |
13 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33-1948G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252433 | |||||||
chr16:252507 | G | T | 1 | a0001c0001t0007g0362 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33-1874G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252507 | |||||||
chr16:252627 | C | G | 1 | a0001c0002t0002g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-33-1754C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252627 | |||||||
chr16:253021 | G | T | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33-1360G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253021 | |||||||
chr16:253024 | C | A | 27 | a0001c0002t0002g0018 a0001c0002t0002g0021 a0001c0002t0002g0022 others(24): Show |
29 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-33-1357C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253024 | |||||||
chr16:253028 | A | T | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33-1353A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253028 | |||||||
chr16:253400 | A | T | 113 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(110): Show |
120 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.-33-981A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253400 | |||||||
chr16:253422 | G | A | 4 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0292 others(1): Show |
4 | HG01175.hp2 HG01255.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-959G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253422 | |||||||
chr16:253567 | C | T | 1 | a0001c0027t0002g0294 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-33-814C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253567 | |||||||
chr16:253663 | A | G | 1 | a0001c0001t0001g0334 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-33-718A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253663 | |||||||
chr16:253664 | T | C | 182 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(179): Show |
190 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.-33-717T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253664 | |||||||
chr16:253699 | C | T | 2 | a0001c0001t0007g0361 a0001c0001t0007g0362 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-33-682C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253699 | |||||||
chr16:253725 | C | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-33-656C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253725 | |||||||
chr16:253725 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-33-656C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253725 | |||||||
chr16:253859 | C | T | 1 | a0001c0002t0002g0320 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-33-522C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253859 | |||||||
chr16:253964 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-33-417A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253964 | |||||||
chr16:254023 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-33-358G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254023 | |||||||
chr16:254041 | G | T | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33-340G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254041 | |||||||
chr16:254119 | A | G | 1 | a0001c0002t0002g0034 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-33-262A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254119 | |||||||
chr16:254270 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-33-111A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254270 | |||||||
chr16:254316 | C | T | 3 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 |
3 | HG01243.hp2 HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-33-65C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254316 | |||||||
chr16:254737 | G | A | 3 | a0004c0007t0001g0054 a0004c0007t0001g0055 a0004c0007t0001g0056 |
3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.268+56G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 254737 | |||||||
chr16:254787 | A | C | 4 | a0001c0001t0007g0361 a0001c0001t0007g0362 a0001c0001t0010g0237 others(1): Show |
4 | HG03098.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+106A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 254787 | |||||||
chr16:254804 | A | T | 260 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(257): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.268+123A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 254804 | |||||||
chr16:254850 | G | A | 4 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(1): Show |
4 | HG02055.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+169G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 254850 | |||||||
chr16:255089 | C | T | 5 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | HG01261.hp2 HG01993.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+408C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255089 | |||||||
chr16:255139 | C | T | 17 | a0001c0001t0003g0081 a0001c0001t0003g0098 a0001c0001t0003g0202 others(14): Show |
17 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.268+458C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255139 | |||||||
chr16:255146 | G | A | 10 | a0001c0001t0005g0012 a0001c0001t0005g0031 a0001c0001t0005g0032 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+465G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255146 | |||||||
chr16:255146 | G | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0196 |
2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.268+465G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255146 | |||||||
chr16:255269 | T | C | 183 | a0001c0001t0001g0059 a0001c0001t0001g0213 a0001c0001t0001g0214 others(180): Show |
191 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.268+588T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255269 | |||||||
chr16:255270 | G | A | 1 | a0002c0003t0001g0355 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.268+589G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255270 | |||||||
chr16:255274 | G | A | 1 | a0001c0002t0002g0034 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268+593G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255274 | |||||||
chr16:255302 | T | C | 2 | a0001c0002t0002g0022 a0001c0002t0002g0325 |
3 | NA18953.hp1 NA18963.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.268+621T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255302 | |||||||
chr16:255378 | G | C | 166 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(163): Show |
174 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.268+697G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255378 | |||||||
chr16:255400 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0338 |
2 | HG02109.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.268+719C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255400 | |||||||
chr16:255426 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.268+745C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255426 | |||||||
chr16:255457 | C | G | 1 | a0001c0002t0002g0323 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.268+776C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255457 | |||||||
chr16:255541 | T | A | 2 | a0001c0001t0007g0361 a0001c0001t0007g0362 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.268+860T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255541 | |||||||
chr16:255647 | C | A | 1 | a0001c0002t0002g0280 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.268+966C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255647 | |||||||
chr16:255732 | C | A | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+1051C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255732 | |||||||
chr16:255829 | A | G | 111 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(108): Show |
118 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.268+1148A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255829 | |||||||
chr16:255863 | G | A | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+1182G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255863 | |||||||
chr16:255873 | G | A | 1 | a0001c0002t0002g0295 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.268+1192G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255873 | |||||||
chr16:255888 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.268+1207C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255888 | |||||||
chr16:256045 | G | A | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+1364G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256045 | |||||||
chr16:256063 | C | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0091 |
3 | NA18969.hp2 NA18981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.268+1382C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256063 | |||||||
chr16:256161 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0075 |
2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.268+1480G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256161 | |||||||
chr16:256173 | G | A | 1 | a0014c0016t0001g0118 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.268+1492G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256173 | |||||||
chr16:256239 | A | T | 1 | a0001c0001t0001g0334 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.268+1558A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256239 | |||||||
chr16:256244 | A | G | 139 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(136): Show |
146 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.268+1563A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256244 | |||||||
chr16:256317 | T | TA | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+1636_268+1637i others(3): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256317 | |||||||
chr16:256403 | T | C | 2 | a0001c0001t0003g0081 a0001c0001t0003g0098 |
2 | HG01106.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.268+1722T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256403 | |||||||
chr16:256609 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.268+1928A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256609 | |||||||
chr16:256673 | C | T | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+1992C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256673 | |||||||
chr16:256740 | A | AT | 105 | a0001c0001t0001g0164 a0001c0001t0001g0181 a0001c0001t0001g0198 others(102): Show |
112 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.268+2078dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 256740 | ||||||
chr16:256740 | AT | A | 24 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0097 others(21): Show |
24 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.268+2078delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 256740 | ||||||
chr16:256743 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.268+2062T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256743 | |||||||
chr16:256989 | G | A | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+2308G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256989 | |||||||
chr16:257068 | G | A | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+2387G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257068 | |||||||
chr16:257075 | C | T | 1 | a0001c0001t0003g0210 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.268+2394C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257075 | |||||||
chr16:257083 | T | C | 15 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0219 others(12): Show |
15 | HG01106.hp1 HG01891.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.269-2400T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257083 | |||||||
chr16:257170 | C | T | 2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.269-2313C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257170 | |||||||
chr16:257189 | C | G | 1 | a0001c0002t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.269-2294C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257189 | |||||||
chr16:257236 | C | CT | 54 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(51): Show |
54 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.269-2221dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 257236 | ||||||
chr16:257236 | CT | C | 55 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0001g0136 others(52): Show |
56 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.269-2221delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 257236 | ||||||
chr16:257236 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.269-2230_269-2221d others(12): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 257236 | ||||||
chr16:257236 | CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0002g0280 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.269-2233_269-2221d others(15): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 257236 | ||||||
chr16:257257 | T | G | 10 | a0001c0001t0005g0012 a0001c0001t0005g0031 a0001c0001t0005g0032 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-2226T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257257 | |||||||
chr16:257435 | G | A | 1 | a0001c0001t0008g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.269-2048G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257435 | |||||||
chr16:257539 | C | T | 2 | a0001c0001t0007g0361 a0001c0001t0007g0362 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.269-1944C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257539 | |||||||
chr16:257560 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0156 |
2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.269-1923A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257560 | |||||||
chr16:257615 | T | C | 104 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(101): Show |
111 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.269-1868T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257615 | |||||||
chr16:257618 | A | G | 10 | a0001c0001t0005g0012 a0001c0001t0005g0031 a0001c0001t0005g0032 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-1865A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257618 | |||||||
chr16:257780 | G | C | 2 | a0001c0001t0010g0237 a0001c0001t0010g0239 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.269-1703G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257780 | |||||||
chr16:257858 | T | G | 32 | a0001c0001t0003g0081 a0001c0001t0003g0098 a0001c0001t0003g0202 others(29): Show |
32 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.269-1625T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257858 | |||||||
chr16:257983 | G | A | 2 | a0007c0008t0002g0343 a0007c0008t0002g0344 |
2 | HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.269-1500G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257983 | |||||||
chr16:258003 | G | A | 9 | a0001c0001t0003g0242 a0001c0006t0001g0042 a0001c0006t0001g0043 others(6): Show |
9 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-1480G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258003 | |||||||
chr16:258004 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.269-1479C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258004 | |||||||
chr16:258023 | A | G | 1 | a0001c0001t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.269-1460A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258023 | |||||||
chr16:258056 | G | A | 9 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0122 others(6): Show |
9 | HG02015.hp1 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.269-1427G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258056 | |||||||
chr16:258109 | C | G | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.269-1374C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258109 | |||||||
chr16:258150 | G | A | 3 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0217 |
3 | HG02486.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.269-1333G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258150 | |||||||
chr16:258155 | A | AT | 35 | a0001c0001t0001g0059 a0001c0001t0001g0139 a0001c0001t0001g0214 others(32): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.269-1310dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 258155 | ||||||
chr16:258155 | AT | A | 37 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0067 others(34): Show |
37 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.269-1310delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 258155 | ||||||
chr16:258173 | T | A | 19 | a0001c0001t0003g0041 a0001c0001t0003g0081 a0001c0001t0003g0098 others(16): Show |
19 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.269-1310T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258173 | |||||||
chr16:258192 | T | G | 1 | a0001c0001t0001g0188 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.269-1291T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258192 | |||||||
chr16:258319 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.269-1164G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258319 | |||||||
chr16:258361 | C | A | 1 | a0001c0001t0003g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.269-1122C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258361 | |||||||
chr16:258501 | CAGA | C | 152 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(149): Show |
159 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.269-976_269-974del others(3): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 258501 | ||||||
chr16:258563 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.269-920C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258563 | |||||||
chr16:258609 | C | A | 1 | a0005c0010t0001g0078 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.269-874C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258609 | |||||||
chr16:258650 | G | T | 1 | a0001c0002t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.269-833G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258650 | |||||||
chr16:258683 | C | T | 1 | a0001c0001t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.269-800C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258683 | |||||||
chr16:258733 | G | A | 2 | a0007c0008t0002g0343 a0007c0008t0002g0344 |
2 | HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.269-750G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258733 | |||||||
chr16:258761 | G | C | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.269-722G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258761 | |||||||
chr16:258929 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.269-554C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258929 | |||||||
chr16:258940 | A | G | 5 | a0001c0005t0002g0013 a0001c0005t0002g0048 a0001c0005t0002g0131 others(2): Show |
6 | HG02559.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-543A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258940 | |||||||
chr16:259032 | C | T | 1 | a0001c0002t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.269-451C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259032 | |||||||
chr16:259061 | G | A | 1 | a0013c0014t0001g0258 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.269-422G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259061 | |||||||
chr16:259092 | T | G | 2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.269-391T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259092 | |||||||
chr16:259156 | C | A | 73 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
80 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.269-327C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259156 | |||||||
chr16:259358 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.269-125C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259358 | |||||||
chr16:259378 | A | C | 1 | a0001c0001t0001g0338 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.269-105A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259378 | |||||||
chr16:259413 | G | A | 1 | a0001c0002t0002g0034 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.269-70G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259413 | |||||||
chr16:259427 | C | T | 10 | a0001c0001t0005g0012 a0001c0001t0005g0031 a0001c0001t0005g0032 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-56C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259427 | |||||||
chr16:259446 | TG | T | 14 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0220 others(11): Show |
14 | HG01106.hp1 HG01891.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.269-35delG | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 259446 | ||||||
chr16:259448 | G | C | 14 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0220 others(11): Show |
14 | HG01106.hp1 HG01891.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.269-35G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259448 | |||||||
chr16:259706 | T | C | 1 | a0001c0001t0005g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.385+107T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259706 | |||||||
chr16:259721 | C | T | 107 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(104): Show |
114 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.385+122C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259721 | |||||||
chr16:259837 | A | C | 1 | a0001c0001t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.386-132A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259837 | |||||||
chr16:259895 | C | T | 6 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0217 others(3): Show |
6 | HG02486.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-74C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259895 | |||||||
chr16:259937 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.386-32C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259937 | |||||||
chr16:259951 | C | T | 36 | a0001c0002t0001g0317 a0001c0002t0002g0018 a0001c0002t0002g0021 others(33): Show |
38 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.386-18C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259951 | |||||||
chr16:260244 | G | A | 110 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(107): Show |
117 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.577+84G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260244 | |||||||
chr16:260246 | C | T | 1 | a0001c0012t0004g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.577+86C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260246 | |||||||
chr16:260294 | T | C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02615.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.577+134T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260294 | |||||||
chr16:260355 | C | T | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.577+195C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260355 | |||||||
chr16:260381 | G | A | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.577+221G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260381 | |||||||
chr16:260469 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.577+309C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260469 | |||||||
chr16:260503 | C | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0156 a0001c0001t0001g0169 others(1): Show |
4 | NA18989.hp2 NA18999.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.577+343C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260503 | |||||||
chr16:260508 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.577+348C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260508 | |||||||
chr16:260598 | C | T | 1 | a0001c0001t0005g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577+438C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260598 | |||||||
chr16:260845 | G | C | 3 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0217 |
3 | HG02486.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.578-539G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260845 | |||||||
chr16:260871 | T | G | 2 | a0001c0001t0007g0361 a0001c0001t0007g0362 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.578-513T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260871 | |||||||
chr16:260887 | C | T | 2 | a0001c0001t0001g0340 a0001c0001t0001g0345 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.578-497C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260887 | |||||||
chr16:260968 | G | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0156 |
2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.578-416G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260968 | |||||||
chr16:261108 | G | A | 5 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(2): Show |
5 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.578-276G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261108 | |||||||
chr16:261133 | G | A | 8 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.578-251G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261133 | |||||||
chr16:261181 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.578-203C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261181 | |||||||
chr16:261235 | T | G | 4 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0238 others(1): Show |
4 | HG02055.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.578-149T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261235 | |||||||
chr16:261362 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0185 |
3 | NA18948.hp1 NA18975.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.578-22G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261362 | |||||||
chr16:261368 | G | A | 8 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0217 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.578-16G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261368 | |||||||
chr16:261651 | G | A | 1 | a0002c0003t0001g0359 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.708+137G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261651 | |||||||
chr16:261671 | C | T | 2 | a0001c0001t0010g0237 a0001c0001t0010g0239 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.708+157C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261671 | |||||||
chr16:261823 | C | T | 14 | a0002c0003t0001g0024 a0002c0003t0001g0348 a0002c0003t0001g0349 others(11): Show |
15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.709-270C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261823 | |||||||
chr16:261854 | A | G | 170 | a0001c0001t0001g0338 a0001c0001t0002g0128 a0001c0001t0002g0130 others(167): Show |
178 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.709-239A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261854 | |||||||
chr16:261860 | C | T | 1 | a0001c0001t0001g0363 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.709-233C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261860 | |||||||
chr16:261971 | CTCTCTTC others(38): Show |
C | 156 | a0001c0001t0001g0338 a0001c0001t0002g0128 a0001c0001t0002g0130 others(153): Show |
163 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.709-100_709-56delA others(44): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 261971 | ||||||
chr16:262250 | G | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0144 others(3): Show |
10 | HG00423.hp1 HG00609.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.841+25G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 7/12 | chr16 | 262250 | |||||||
chr16:262254 | A | G | 176 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0144 others(173): Show |
188 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.841+29A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 7/12 | chr16 | 262254 | |||||||
chr16:262288 | C | T | 1 | a0002c0003t0001g0353 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.841+63C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 7/12 | chr16 | 262288 | |||||||
chr16:262369 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.842-55G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 7/12 | chr16 | 262369 | |||||||
chr16:262621 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.971+68C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262621 | |||||||
chr16:262636 | T | C | 113 | a0001c0001t0001g0070 a0001c0001t0001g0338 a0001c0001t0002g0128 others(110): Show |
120 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.971+83T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262636 | |||||||
chr16:262806 | G | GT | 33 | a0001c0001t0001g0072 a0001c0001t0001g0140 a0001c0001t0001g0153 others(30): Show |
34 | HG00621.hp1 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.971+267dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 262806 | ||||||
chr16:262814 | T | A | 6 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0217 others(3): Show |
6 | HG02486.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.971+261T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262814 | |||||||
chr16:262824 | T | G | 14 | a0001c0001t0001g0059 a0001c0001t0001g0213 a0001c0001t0001g0214 others(11): Show |
14 | HG01106.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.971+271T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262824 | |||||||
chr16:262888 | C | T | 2 | a0001c0001t0010g0237 a0001c0001t0010g0239 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.971+335C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262888 | |||||||
chr16:263203 | C | A | 131 | a0001c0001t0001g0338 a0001c0001t0002g0128 a0001c0001t0002g0130 others(128): Show |
138 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.972-59C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 263203 | |||||||
chr16:263206 | G | A | 1 | a0001c0021t0003g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.972-56G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 263206 | |||||||
chr16:263407 | A | G | 172 | a0001c0001t0001g0080 a0001c0001t0001g0338 a0001c0001t0002g0128 others(169): Show |
180 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(177): Show |
splice_region_variant&intron_variant | LOW | c.1112+5A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263407 | |||||||
chr16:263466 | C | T | 6 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0217 others(3): Show |
6 | HG02486.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1112+64C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263466 | |||||||
chr16:263510 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1112+108G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263510 | |||||||
chr16:263520 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1112+118G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263520 | |||||||
chr16:263574 | C | T | 2 | a0001c0001t0001g0104 a0001c0012t0004g0227 |
2 | HG03225.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1113-126C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263574 | |||||||
chr16:263645 | C | T | 3 | a0004c0007t0001g0054 a0004c0007t0001g0055 a0004c0007t0001g0056 |
3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1113-55C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263645 | |||||||
chr16:263647 | T | C | 1 | a0001c0001t0003g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1113-53T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263647 | |||||||
chr16:263849 | C | T | 99 | a0001c0001t0001g0338 a0001c0001t0002g0128 a0001c0001t0002g0130 others(96): Show |
106 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1188+74C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 10/12 | chr16 | 263849 | |||||||
chr16:263983 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1189-33C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 10/12 | chr16 | 263983 | |||||||
chr16:264256 | C | T | 8 | a0001c0001t0005g0012 a0001c0001t0005g0129 a0001c0001t0005g0229 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344+85C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | chr16 | 264256 | |||||||
chr16:264262 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1344+91G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | chr16 | 264262 | |||||||
chr16:264452 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1345-162G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | chr16 | 264452 | |||||||
chr16:264520 | AGACATAG others(35): Show |
A | 5 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0292 others(2): Show |
5 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345-92_1345-51del others(42): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 264520 | ||||||
chr16:264535 | G | T | 9 | a0001c0001t0005g0012 a0001c0001t0005g0031 a0001c0001t0005g0032 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-79G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | chr16 | 264535 | |||||||
chr16:264754 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1447+38G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/12 | chr16 | 264754 | |||||||
chr16:264757 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1447+41G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/12 | chr16 | 264757 | |||||||
chr16:264781 | G | T | 5 | a0001c0006t0001g0042 a0001c0006t0001g0043 a0001c0006t0001g0060 others(2): Show |
5 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1448-30G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/12 | chr16 | 264781 |