Item | Value |
---|---|
geneid | 57205 |
ensemblid | ENSG00000145246.14 |
hgncid | 13549 |
symbol | ATP10D |
name | ATPase phospholipid transporting 10D (putative) |
refseq_nuc | NM_020453.4 |
refseq_prot | NP_065186.3 |
ensembl_nuc | ENST00000273859.8 |
ensembl_prot | ENSP00000273859.3 |
mane_status | MANE Select |
chr | chr4 |
start | 47485275 |
end | 47593486 |
strand | + |
ver | v1.2 |
region | chr4:47485275-47593486 |
region5000 | chr4:47480275-47598486 |
regionname0 | ATP10D_chr4_47485275_47593486 |
regionname5000 | ATP10D_chr4_47480275_47598486 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1426 | 76 | 14 | 11 | 43 | 2 | 5 | 32 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0002 | 1/0 | 1426 | 44 | 9 | 11 | 1 | 4 | 18 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0003 | 0/0 | 1426 | 28 | 15 | 3 | 7 | 0 | 3 | 5 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0004 | 0/0 | 1426 | 27 | 2 | 8 | 14 | 2 | 1 | 12 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0005 | 0/0 | 1426 | 26 | 0 | 1 | 22 | 2 | 1 | 17 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0006 | 0/0 | 1426 | 15 | 6 | 5 | 0 | 0 | 4 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0007 | 0/0 | 1426 | 12 | 0 | 0 | 12 | 0 | 0 | 10 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0008 | 0/0 | 1426 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0009 | 0/0 | 1426 | 10 | 0 | 1 | 8 | 0 | 1 | 7 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0010 | 0/0 | 1426 | 8 | 3 | 3 | 0 | 2 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0011 | 0/0 | 1426 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0012 | 0/0 | 1426 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0013 | 0/0 | 1426 | 4 | 1 | 1 | 0 | 1 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0014 | 0/0 | 1426 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0015 | 0/0 | 1426 | 4 | 1 | 2 | 1 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0016 | 0/0 | 1426 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0017 | 0/0 | 1426 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0018 | 0/0 | 1426 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0019 | 0/0 | 1426 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0020 | 0/0 | 1426 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0021 | 0/0 | 1426 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0022 | 0/0 | 1426 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0023 | 0/0 | 1426 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0024 | 0/0 | 1426 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0025 | 0/0 | 1426 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0026 | 0/0 | 1426 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0027 | 0/0 | 1426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0028 | 0/0 | 1426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0029 | 0/0 | 1426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0030 | 0/0 | 1426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0031 | 0/0 | 1426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0032 | 0/0 | 1426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0033 | 0/0 | 1426 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0034 | 0/0 | 1426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0035 | 0/0 | 1426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0036 | 0/0 | 1426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0037 | 0/0 | 1426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0038 | 0/0 | 1426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0039 | 0/0 | 1426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0040 | 0/0 | 1426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0041 | 0/0 | 1426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0042 | 0/0 | 1426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0043 | 0/0 | 1426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0044 | 0/0 | 1426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0045 | 0/0 | 1426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0046 | 0/0 | 1426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0047 | 0/0 | 1426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0048 | 0/0 | 1426 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0049 | 0/0 | 1426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
a0050 | 0/0 | 1426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | MTEAL others(1421): Show |
chr4 | 47480275 | 47598486 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4278 | 41 | 1 | 5 | 31 | 0 | 3 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0001c0003 | 0/0 | 4278 | 29 | 8 | 6 | 11 | 2 | 2 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0001c0016 | 0/0 | 4278 | 4 | 4 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0001c0031 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0001c0043 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0002c0002 | 1/0 | 4278 | 32 | 4 | 8 | 0 | 4 | 15 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0002c0008 | 0/0 | 4278 | 12 | 5 | 3 | 1 | 0 | 3 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0003c0004 | 0/0 | 4278 | 27 | 15 | 2 | 7 | 0 | 3 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0003c0048 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0004c0005 | 0/0 | 4278 | 26 | 2 | 8 | 13 | 2 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0004c0067 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0005c0006 | 0/0 | 4278 | 20 | 0 | 1 | 16 | 2 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0005c0014 | 0/0 | 4278 | 5 | 0 | 0 | 5 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0005c0044 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0006c0007 | 0/0 | 4278 | 14 | 6 | 5 | 0 | 0 | 3 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0006c0065 | 0/0 | 4278 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0007c0009 | 0/0 | 4278 | 12 | 0 | 0 | 12 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0008c0010 | 0/0 | 4278 | 11 | 10 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0009c0011 | 0/0 | 4278 | 10 | 0 | 1 | 8 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0010c0012 | 0/0 | 4278 | 8 | 3 | 3 | 0 | 2 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0011c0020 | 0/0 | 4278 | 3 | 3 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0011c0025 | 0/0 | 4278 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0011c0038 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0011c0041 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0012c0013 | 0/0 | 4278 | 5 | 5 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0013c0015 | 0/0 | 4278 | 4 | 1 | 1 | 0 | 1 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0014c0017 | 0/0 | 4278 | 4 | 0 | 4 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0015c0018 | 0/0 | 4278 | 3 | 0 | 2 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0015c0034 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0016c0019 | 0/0 | 4278 | 3 | 0 | 2 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0016c0042 | 0/0 | 4278 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0017c0022 | 0/0 | 4278 | 3 | 0 | 2 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0018c0023 | 0/0 | 4278 | 2 | 0 | 2 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0018c0046 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0019c0021 | 0/0 | 4278 | 3 | 3 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0020c0063 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0020c0064 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0021c0029 | 0/0 | 4278 | 2 | 0 | 2 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0022c0027 | 0/0 | 4278 | 2 | 0 | 2 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0023c0030 | 0/0 | 4278 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0024c0028 | 0/0 | 4278 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0025c0026 | 0/0 | 4278 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0026c0024 | 0/0 | 4278 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0027c0040 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0028c0061 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0029c0051 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0030c0055 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0031c0054 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0032c0056 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0033c0059 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0034c0058 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0035c0033 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0036c0047 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0037c0060 | 0/0 | 4278 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0038c0049 | 0/0 | 4278 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0039c0052 | 0/0 | 4278 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0040c0053 | 0/0 | 4278 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0041c0037 | 0/0 | 4278 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0042c0035 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0043c0036 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0044c0045 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0045c0032 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0046c0066 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0047c0050 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0048c0062 | 0/0 | 4278 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0049c0057 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 | ||
a0050c0039 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | ATGAC others(4273): Show |
chr4 | 47480275 | 47598486 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003 | 0/1 | 6667 | 25 | 0 | 4 | 18 | 0 | 2 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0001c0001t0004 | 0/0 | 6668 | 16 | 1 | 1 | 13 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0001c0003t0001 | 0/0 | 6668 | 23 | 8 | 6 | 5 | 2 | 2 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0001c0003t0002 | 0/0 | 6667 | 6 | 0 | 0 | 6 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0001c0016t0002 | 0/0 | 6667 | 4 | 4 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0001c0031t0002 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0001c0043t0003 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0002c0002t0001 | 1/0 | 6668 | 22 | 0 | 7 | 0 | 4 | 10 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0002c0002t0002 | 0/0 | 6667 | 5 | 0 | 1 | 0 | 0 | 4 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0002c0002t0003 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0002c0002t0004 | 0/0 | 6668 | 3 | 3 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0002c0002t0013 | 0/0 | 6667 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0002c0008t0001 | 0/0 | 6668 | 7 | 3 | 2 | 0 | 0 | 2 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0002c0008t0002 | 0/0 | 6667 | 4 | 2 | 1 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0002c0008t0015 | 0/0 | 6668 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0003c0004t0005 | 0/0 | 6668 | 20 | 15 | 1 | 3 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0003c0004t0006 | 0/0 | 6668 | 2 | 0 | 0 | 2 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0003c0004t0007 | 0/0 | 6667 | 3 | 0 | 1 | 1 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0003c0004t0010 | 0/0 | 6667 | 2 | 0 | 0 | 1 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0003c0048t0006 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0004c0005t0005 | 0/0 | 6668 | 3 | 0 | 2 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0004c0005t0006 | 0/0 | 6668 | 9 | 1 | 5 | 1 | 1 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0004c0005t0007 | 0/0 | 6667 | 14 | 1 | 1 | 12 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0004c0067t0007 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0005c0006t0001 | 0/0 | 6668 | 11 | 0 | 0 | 9 | 1 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0005c0006t0002 | 0/0 | 6667 | 9 | 0 | 1 | 7 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0005c0014t0003 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0005c0014t0004 | 0/0 | 6668 | 4 | 0 | 0 | 4 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0005c0044t0002 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0006c0007t0001 | 0/0 | 6668 | 12 | 6 | 4 | 0 | 0 | 2 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0006c0007t0002 | 0/0 | 6667 | 2 | 0 | 1 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0006c0065t0001 | 0/0 | 6668 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0007c0009t0001 | 0/0 | 6668 | 7 | 0 | 0 | 7 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0007c0009t0002 | 0/0 | 6667 | 5 | 0 | 0 | 5 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0008c0010t0008 | 0/0 | 6668 | 10 | 10 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0008c0010t0017 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0009c0011t0001 | 0/0 | 6668 | 8 | 0 | 1 | 6 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0009c0011t0014 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0009c0011t0016 | 0/0 | 6668 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0010c0012t0005 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0010c0012t0006 | 0/0 | 6668 | 3 | 0 | 1 | 0 | 2 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0010c0012t0009 | 0/0 | 6668 | 4 | 2 | 2 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0011c0020t0009 | 0/0 | 6668 | 3 | 3 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0011c0025t0009 | 0/0 | 6668 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0011c0038t0005 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0011c0041t0008 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0012c0013t0008 | 0/0 | 6668 | 5 | 5 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0013c0015t0005 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0013c0015t0009 | 0/0 | 6668 | 3 | 0 | 1 | 0 | 1 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0014c0017t0006 | 0/0 | 6668 | 3 | 0 | 3 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0014c0017t0007 | 0/0 | 6667 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0015c0018t0010 | 0/0 | 6667 | 3 | 0 | 2 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0015c0034t0012 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0016c0019t0004 | 0/0 | 6668 | 3 | 0 | 2 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0016c0042t0001 | 0/0 | 6668 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0017c0022t0001 | 0/0 | 6668 | 2 | 0 | 2 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0017c0022t0002 | 0/0 | 6667 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0018c0023t0003 | 0/0 | 6667 | 2 | 0 | 2 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0018c0046t0002 | 0/0 | 6667 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0019c0021t0009 | 0/0 | 6668 | 3 | 3 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0020c0063t0003 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0020c0064t0001 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0021c0029t0001 | 0/0 | 6668 | 2 | 0 | 2 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0022c0027t0011 | 0/0 | 6668 | 2 | 0 | 2 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0023c0030t0005 | 0/0 | 6668 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0024c0028t0008 | 0/0 | 6668 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0025c0026t0009 | 0/0 | 6668 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0026c0024t0004 | 0/0 | 6668 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0027c0040t0006 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0028c0061t0001 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0029c0051t0006 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0030c0055t0006 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0031c0054t0001 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0032c0056t0001 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0033c0059t0001 | 0/0 | 6668 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0034c0058t0008 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0035c0033t0001 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0036c0047t0004 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0037c0060t0001 | 0/0 | 6668 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0038c0049t0001 | 0/0 | 6668 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0039c0052t0001 | 0/0 | 6668 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0040c0053t0001 | 0/0 | 6668 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0041c0037t0002 | 0/0 | 6667 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0042c0035t0012 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0043c0036t0005 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0044c0045t0006 | 0/0 | 6668 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0045c0032t0003 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0046c0066t0007 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6662): Show |
chr4 | 47480275 | 47598486 |
a0047c0050t0004 | 0/0 | 6668 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0048c0062t0006 | 0/0 | 6668 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0049c0057t0008 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
a0050c0039t0001 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | GCAGC others(6663): Show |
chr4 | 47480275 | 47598486 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0003g0315 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0016t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0016t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0016t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0016t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0031t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0001c0043t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0002t0013g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0002c0008t0015g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0005g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0007g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0007g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0010g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0004t0010g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0003c0048t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0006g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0006g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0006g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0006g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0005t0007g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0004c0067t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0006t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0014t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0014t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0014t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0014t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0014t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0005c0044t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0007t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0006c0065t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0007c0009t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0008c0010t0017g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0014g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0009c0011t0016g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0010c0012t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0010c0012t0006g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0010c0012t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0010c0012t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0010c0012t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0010c0012t0009g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0010c0012t0009g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0011c0020t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0011c0020t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0011c0020t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0011c0025t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0011c0025t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0011c0038t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0011c0041t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0012c0013t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0012c0013t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0012c0013t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0012c0013t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0012c0013t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0013c0015t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0013c0015t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0013c0015t0009g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0013c0015t0009g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0014c0017t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0014c0017t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0014c0017t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0014c0017t0007g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0015c0018t0010g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0015c0018t0010g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0015c0018t0010g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0015c0034t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0016c0019t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0016c0019t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0016c0019t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0016c0042t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0017c0022t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0017c0022t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0017c0022t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0018c0023t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0018c0023t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0018c0046t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0019c0021t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0019c0021t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0019c0021t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0020c0063t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0020c0064t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0021c0029t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0021c0029t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0022c0027t0011g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0022c0027t0011g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0023c0030t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0023c0030t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0024c0028t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0024c0028t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0025c0026t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0025c0026t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0026c0024t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0026c0024t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0027c0040t0006g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0028c0061t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0029c0051t0006g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0030c0055t0006g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0031c0054t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0032c0056t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0033c0059t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0034c0058t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0035c0033t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0036c0047t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0037c0060t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0038c0049t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0039c0052t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0040c0053t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0041c0037t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0042c0035t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0043c0036t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0044c0045t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0045c0032t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0046c0066t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0047c0050t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0048c0062t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0049c0057t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
a0050c0039t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0006 | t0002 | g0306 | EUR | GBR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00099 | hp2 | a0004 | c0005 | t0005 | g0166 | EUR | GBR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00280 | hp1 | a0010 | c0012 | t0006 | g0066 | EUR | FIN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0165 | EUR | FIN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0293 | EUR | FIN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00323 | hp2 | a0013 | c0015 | t0009 | g0137 | EUR | FIN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00408 | hp1 | a0004 | c0005 | t0007 | g0015 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00438 | hp1 | a0005 | c0014 | t0003 | g0246 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00438 | hp2 | a0007 | c0009 | t0001 | g0012 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00558 | hp2 | a0002 | c0008 | t0002 | g0265 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00621 | hp1 | a0001 | c0003 | t0002 | g0260 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00621 | hp2 | a0020 | c0063 | t0003 | g0268 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00639 | hp2 | a0004 | c0005 | t0005 | g0063 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00642 | hp2 | a0010 | c0012 | t0009 | g0164 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00673 | hp1 | a0007 | c0009 | t0001 | g0012 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00673 | hp2 | a0005 | c0006 | t0002 | g0225 | EAS | CHS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00735 | hp1 | a0004 | c0005 | t0005 | g0131 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00735 | hp2 | a0010 | c0012 | t0006 | g0008 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0289 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00738 | hp2 | a0021 | c0029 | t0001 | g0150 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0106 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG00741 | hp2 | a0014 | c0017 | t0006 | g0157 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01069 | hp1 | a0015 | c0018 | t0010 | g0302 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01069 | hp2 | a0016 | c0019 | t0004 | g0023 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01070 | hp2 | a0027 | c0040 | t0006 | g0291 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01071 | hp1 | a0015 | c0018 | t0010 | g0267 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01081 | hp1 | a0028 | c0061 | t0001 | g0155 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01081 | hp2 | a0029 | c0051 | t0006 | g0008 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01099 | hp2 | a0017 | c0022 | t0001 | g0152 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01106 | hp1 | a0009 | c0011 | t0001 | g0167 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01106 | hp2 | a0004 | c0005 | t0006 | g0301 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0310 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01109 | hp2 | a0016 | c0019 | t0004 | g0024 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01168 | hp1 | a0021 | c0029 | t0001 | g0147 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01168 | hp2 | a0030 | c0055 | t0006 | g0311 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01175 | hp1 | a0010 | c0012 | t0009 | g0312 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01175 | hp2 | a0002 | c0008 | t0001 | g0196 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01192 | hp1 | a0013 | c0015 | t0009 | g0091 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01192 | hp2 | a0031 | c0054 | t0001 | g0313 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01243 | hp1 | a0017 | c0022 | t0001 | g0151 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01243 | hp2 | a0002 | c0008 | t0002 | g0298 | AMR | PUR | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01255 | hp1 | a0008 | c0010 | t0017 | g0211 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01255 | hp2 | a0003 | c0004 | t0005 | g0132 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01256 | hp1 | a0022 | c0027 | t0011 | g0197 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01256 | hp2 | a0004 | c0005 | t0006 | g0129 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0108 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01257 | hp2 | a0022 | c0027 | t0011 | g0198 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0215 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01346 | hp1 | a0018 | c0023 | t0003 | g0245 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01346 | hp2 | a0006 | c0007 | t0001 | g0030 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0292 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01358 | hp2 | a0014 | c0017 | t0006 | g0160 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01361 | hp1 | a0006 | c0007 | t0001 | g0314 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01433 | hp2 | a0005 | c0006 | t0002 | g0220 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01496 | hp2 | a0004 | c0005 | t0006 | g0009 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01516 | hp1 | a0005 | c0006 | t0001 | g0086 | EUR | IBS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0068 | EUR | IBS | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01884 | hp1 | a0023 | c0030 | t0005 | g0172 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01884 | hp2 | a0003 | c0004 | t0005 | g0203 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01891 | hp1 | a0008 | c0010 | t0008 | g0193 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01891 | hp2 | a0024 | c0028 | t0008 | g0119 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01934 | hp1 | a0003 | c0004 | t0007 | g0282 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01934 | hp2 | a0018 | c0023 | t0003 | g0242 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01952 | hp1 | a0006 | c0007 | t0002 | g0233 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01952 | hp2 | a0004 | c0005 | t0007 | g0227 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01978 | hp1 | a0004 | c0005 | t0006 | g0168 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0281 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01981 | hp1 | a0006 | c0007 | t0001 | g0156 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01981 | hp2 | a0014 | c0017 | t0007 | g0299 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01993 | hp1 | a0032 | c0056 | t0001 | g0064 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01993 | hp2 | a0014 | c0017 | t0006 | g0123 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0229 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02004 | hp2 | a0004 | c0005 | t0006 | g0009 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02015 | hp1 | a0005 | c0006 | t0002 | g0262 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02027 | hp1 | a0033 | c0059 | t0001 | g0112 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02027 | hp2 | a0005 | c0006 | t0002 | g0244 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02040 | hp1 | a0003 | c0004 | t0005 | g0092 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02071 | hp1 | a0005 | c0014 | t0004 | g0051 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02071 | hp2 | a0003 | c0004 | t0005 | g0096 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0059 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02135 | hp2 | a0004 | c0005 | t0007 | g0277 | EAS | KHV | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02145 | hp1 | a0001 | c0016 | t0002 | g0297 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02257 | hp1 | a0034 | c0058 | t0008 | g0075 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02257 | hp2 | a0011 | c0025 | t0009 | g0127 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02258 | hp1 | a0015 | c0034 | t0012 | g0194 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02258 | hp2 | a0011 | c0038 | t0005 | g0062 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02273 | hp1 | a0006 | c0007 | t0001 | g0161 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02273 | hp2 | a0018 | c0046 | t0002 | g0248 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02280 | hp1 | a0002 | c0002 | t0004 | g0183 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02280 | hp2 | a0003 | c0004 | t0005 | g0205 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0028 | AMR | PEL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0303 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02451 | hp2 | a0011 | c0041 | t0008 | g0214 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02572 | hp1 | a0002 | c0008 | t0001 | g0126 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02572 | hp2 | a0003 | c0004 | t0005 | g0057 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02602 | hp1 | a0006 | c0007 | t0002 | g0221 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0216 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02615 | hp2 | a0001 | c0016 | t0002 | g0295 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02622 | hp1 | a0008 | c0010 | t0008 | g0210 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02622 | hp2 | a0011 | c0025 | t0009 | g0124 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02630 | hp1 | a0023 | c0030 | t0005 | g0077 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02630 | hp2 | a0003 | c0004 | t0005 | g0041 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02647 | hp1 | a0006 | c0007 | t0001 | g0042 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02647 | hp2 | a0010 | c0012 | t0005 | g0067 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02698 | hp2 | a0002 | c0008 | t0001 | g0146 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02717 | hp1 | a0003 | c0004 | t0005 | g0046 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02717 | hp2 | a0006 | c0007 | t0001 | g0178 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02723 | hp1 | a0008 | c0010 | t0008 | g0209 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02723 | hp2 | a0013 | c0015 | t0005 | g0031 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0264 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02809 | hp1 | a0002 | c0002 | t0004 | g0045 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02809 | hp2 | a0003 | c0004 | t0005 | g0044 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02818 | hp1 | a0008 | c0010 | t0008 | g0305 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02818 | hp2 | a0002 | c0008 | t0002 | g0304 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02886 | hp1 | a0006 | c0007 | t0001 | g0040 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02886 | hp2 | a0019 | c0021 | t0009 | g0076 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02895 | hp1 | a0008 | c0010 | t0008 | g0010 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02895 | hp2 | a0019 | c0021 | t0009 | g0071 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02896 | hp1 | a0019 | c0021 | t0009 | g0074 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02896 | hp2 | a0010 | c0012 | t0009 | g0003 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02897 | hp1 | a0010 | c0012 | t0009 | g0003 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02897 | hp2 | a0008 | c0010 | t0008 | g0010 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02922 | hp1 | a0003 | c0004 | t0005 | g0204 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02922 | hp2 | a0012 | c0013 | t0008 | g0125 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02970 | hp1 | a0008 | c0010 | t0008 | g0213 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02970 | hp2 | a0036 | c0047 | t0004 | g0060 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02976 | hp1 | a0006 | c0007 | t0001 | g0043 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02976 | hp2 | a0003 | c0004 | t0005 | g0139 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03017 | hp1 | a0002 | c0002 | t0013 | g0234 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03017 | hp2 | a0003 | c0004 | t0007 | g0263 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03041 | hp1 | a0008 | c0010 | t0008 | g0212 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03041 | hp2 | a0011 | c0020 | t0009 | g0115 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03098 | hp1 | a0012 | c0013 | t0008 | g0029 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03098 | hp2 | a0026 | c0024 | t0004 | g0070 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03130 | hp1 | a0024 | c0028 | t0008 | g0202 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03130 | hp2 | a0002 | c0008 | t0001 | g0019 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03139 | hp1 | a0006 | c0007 | t0001 | g0039 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03139 | hp2 | a0026 | c0024 | t0004 | g0069 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03209 | hp1 | a0008 | c0010 | t0008 | g0201 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03209 | hp2 | a0003 | c0004 | t0005 | g0085 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03225 | hp1 | a0003 | c0004 | t0005 | g0162 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03225 | hp2 | a0011 | c0020 | t0009 | g0188 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0103 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03453 | hp2 | a0003 | c0004 | t0005 | g0061 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03486 | hp2 | a0012 | c0013 | t0008 | g0200 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03490 | hp1 | a0006 | c0007 | t0001 | g0006 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0109 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03491 | hp1 | a0016 | c0042 | t0001 | g0111 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0011 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03492 | hp1 | a0006 | c0007 | t0001 | g0006 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0011 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03516 | hp1 | a0002 | c0002 | t0004 | g0186 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0182 | AFR | ESN | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03540 | hp1 | a0003 | c0004 | t0005 | g0072 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | GWD | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03579 | hp2 | a0003 | c0004 | t0005 | g0090 | AFR | MSL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03688 | hp1 | a0002 | c0008 | t0015 | g0104 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03704 | hp1 | a0037 | c0060 | t0001 | g0308 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03704 | hp2 | a0002 | c0008 | t0001 | g0145 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03710 | hp1 | a0013 | c0015 | t0009 | g0288 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03710 | hp2 | a0038 | c0049 | t0001 | g0130 | SAS | PJL | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03831 | hp1 | a0005 | c0006 | t0001 | g0219 | SAS | BEB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03831 | hp2 | a0039 | c0052 | t0001 | g0135 | SAS | BEB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0285 | SAS | BEB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03834 | hp2 | a0003 | c0004 | t0005 | g0307 | SAS | BEB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | BEB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0163 | SAS | BEB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04115 | hp1 | a0006 | c0065 | t0001 | g0176 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04184 | hp1 | a0040 | c0053 | t0001 | g0173 | SAS | BEB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04184 | hp2 | a0004 | c0005 | t0006 | g0007 | SAS | BEB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0110 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04199 | hp2 | a0016 | c0019 | t0004 | g0022 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04204 | hp1 | a0041 | c0037 | t0002 | g0252 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04204 | hp2 | a0017 | c0022 | t0002 | g0284 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | STU | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18522 | hp1 | a0043 | c0036 | t0005 | g0184 | AFR | YRI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18522 | hp2 | a0020 | c0064 | t0001 | g0309 | AFR | YRI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18612 | hp1 | a0009 | c0011 | t0014 | g0228 | EAS | CHB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | CHB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18906 | hp1 | a0003 | c0004 | t0005 | g0140 | AFR | YRI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0177 | AFR | YRI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18939 | hp1 | a0004 | c0005 | t0007 | g0271 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18941 | hp2 | a0004 | c0005 | t0007 | g0001 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18942 | hp1 | a0005 | c0006 | t0001 | g0170 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18942 | hp2 | a0004 | c0067 | t0007 | g0148 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18944 | hp2 | a0007 | c0009 | t0002 | g0269 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18945 | hp1 | a0004 | c0005 | t0007 | g0001 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18946 | hp1 | a0007 | c0009 | t0001 | g0093 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18948 | hp2 | a0005 | c0014 | t0004 | g0053 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18949 | hp1 | a0004 | c0005 | t0007 | g0275 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18949 | hp2 | a0005 | c0044 | t0002 | g0249 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18950 | hp2 | a0015 | c0018 | t0010 | g0283 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18953 | hp1 | a0005 | c0006 | t0002 | g0247 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18953 | hp2 | a0007 | c0009 | t0002 | g0036 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18957 | hp1 | a0004 | c0005 | t0007 | g0001 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18957 | hp2 | a0001 | c0043 | t0003 | g0278 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18961 | hp1 | a0044 | c0045 | t0006 | g0049 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18961 | hp2 | a0001 | c0003 | t0002 | g0206 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18963 | hp1 | a0003 | c0004 | t0006 | g0138 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18965 | hp2 | a0005 | c0014 | t0004 | g0054 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18966 | hp1 | a0045 | c0032 | t0003 | g0223 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18966 | hp2 | a0004 | c0005 | t0007 | g0014 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18968 | hp2 | a0009 | c0011 | t0001 | g0081 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18982 | hp1 | a0004 | c0005 | t0007 | g0273 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18983 | hp1 | a0009 | c0011 | t0001 | g0153 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18983 | hp2 | a0007 | c0009 | t0002 | g0243 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18984 | hp1 | a0005 | c0006 | t0001 | g0142 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18984 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18986 | hp2 | a0005 | c0014 | t0004 | g0058 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18990 | hp1 | a0007 | c0009 | t0001 | g0094 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18990 | hp2 | a0005 | c0006 | t0002 | g0035 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18999 | hp1 | a0005 | c0006 | t0001 | g0098 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19000 | hp1 | a0009 | c0011 | t0001 | g0158 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19000 | hp2 | a0003 | c0004 | t0006 | g0033 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19002 | hp1 | a0009 | c0011 | t0001 | g0154 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19005 | hp1 | a0001 | c0003 | t0002 | g0239 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19005 | hp2 | a0005 | c0006 | t0001 | g0099 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19009 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19010 | hp1 | a0004 | c0005 | t0007 | g0015 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19012 | hp1 | a0004 | c0005 | t0007 | g0014 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19012 | hp2 | a0005 | c0006 | t0001 | g0113 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19030 | hp1 | a0025 | c0026 | t0009 | g0189 | AFR | LWK | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0073 | AFR | LWK | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19043 | hp1 | a0012 | c0013 | t0008 | g0128 | AFR | LWK | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19043 | hp2 | a0001 | c0016 | t0002 | g0218 | AFR | LWK | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19054 | hp1 | a0007 | c0009 | t0002 | g0224 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19056 | hp2 | a0005 | c0006 | t0002 | g0270 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19057 | hp1 | a0005 | c0006 | t0001 | g0055 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19057 | hp2 | a0003 | c0004 | t0005 | g0169 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19058 | hp1 | a0005 | c0006 | t0001 | g0032 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19058 | hp2 | a0001 | c0003 | t0002 | g0286 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19062 | hp1 | a0004 | c0005 | t0007 | g0272 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19062 | hp2 | a0001 | c0003 | t0002 | g0238 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19063 | hp1 | a0003 | c0004 | t0010 | g0235 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19065 | hp1 | a0001 | c0003 | t0002 | g0236 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19065 | hp2 | a0005 | c0006 | t0001 | g0100 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19066 | hp2 | a0046 | c0066 | t0007 | g0276 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19068 | hp1 | a0005 | c0006 | t0001 | g0101 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19068 | hp2 | a0007 | c0009 | t0002 | g0261 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19074 | hp1 | a0005 | c0006 | t0002 | g0191 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19074 | hp2 | a0009 | c0011 | t0001 | g0159 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19075 | hp1 | a0047 | c0050 | t0004 | g0207 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19075 | hp2 | a0007 | c0009 | t0001 | g0088 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19077 | hp1 | a0009 | c0011 | t0016 | g0056 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19081 | hp1 | a0009 | c0011 | t0001 | g0134 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19086 | hp1 | a0007 | c0009 | t0001 | g0097 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19086 | hp2 | a0003 | c0004 | t0007 | g0258 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19089 | hp1 | a0007 | c0009 | t0001 | g0095 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19240 | hp1 | a0002 | c0008 | t0002 | g0294 | AFR | YRI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA19240 | hp2 | a0001 | c0031 | t0002 | g0192 | AFR | YRI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20129 | hp1 | a0011 | c0020 | t0009 | g0187 | AFR | ASW | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20129 | hp2 | a0004 | c0005 | t0006 | g0133 | AFR | ASW | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20752 | hp1 | a0001 | c0003 | t0001 | g0180 | EUR | TSI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20752 | hp2 | a0048 | c0062 | t0006 | g0007 | EUR | TSI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20805 | hp1 | a0004 | c0005 | t0006 | g0121 | EUR | TSI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20805 | hp2 | a0010 | c0012 | t0006 | g0065 | EUR | TSI | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20905 | hp1 | a0009 | c0011 | t0001 | g0174 | SAS | GIH | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20905 | hp2 | a0003 | c0004 | t0010 | g0226 | SAS | GIH | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01123 | hp1 | a0002 | c0008 | t0001 | g0141 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG01123 | hp2 | a0003 | c0048 | t0006 | g0102 | AMR | CLM | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02109 | hp1 | a0025 | c0026 | t0009 | g0190 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02109 | hp2 | a0008 | c0010 | t0008 | g0208 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02486 | hp1 | a0012 | c0013 | t0008 | g0017 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02486 | hp2 | a0001 | c0016 | t0002 | g0296 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02559 | hp1 | a0003 | c0004 | t0005 | g0089 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG02559 | hp2 | a0035 | c0033 | t0001 | g0181 | AFR | ACB | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG06807 | hp1 | a0042 | c0035 | t0012 | g0021 | AFR | USA | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
HG06807 | hp2 | a0006 | c0007 | t0001 | g0038 | AFR | USA | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18955 | hp1 | a0004 | c0005 | t0006 | g0149 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20300 | hp1 | a0002 | c0008 | t0001 | g0016 | AFR | USA | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA20300 | hp2 | a0004 | c0005 | t0007 | g0274 | AFR | USA | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA21309 | hp1 | a0049 | c0057 | t0008 | g0120 | AFR | LWK | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
NA21309 | hp2 | a0050 | c0039 | t0001 | g0117 | AFR | LWK | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0315 | REF | REF | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0185 | REF | REF | ATP10D_chr4_47480275_47598486 | ATP10D | chr4 | 47480275 | 47598486 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:47512668 | C | T | 26 | a0004 a0006 a0009 others(23): Show |
95 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(92): Show |
missense_variant | MODERATE | c.128C>T | p.Thr43Ile | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/23 | 410/6668 | 128/4281 | 43/1426 | chr4 | 47512668 | |||
chr4:47515487 | T | C | 1 | a0045 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.302T>C | p.Leu101Ser | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/23 | 584/6668 | 302/4281 | 101/1426 | chr4 | 47515487 | |||
chr4:47523037 | T | C | 13 | a0008 a0010 a0015 others(10): Show |
34 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(31): Show |
missense_variant | MODERATE | c.511T>C | p.Cys171Arg | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/23 | 793/6668 | 511/4281 | 171/1426 | chr4 | 47523037 | |||
chr4:47523071 | G | A | 2 | a0019 a0034 |
4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
missense_variant | MODERATE | c.545G>A | p.Arg182His | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/23 | 827/6668 | 545/4281 | 182/1426 | chr4 | 47523071 | |||
chr4:47535531 | G | T | 1 | a0047 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.799G>T | p.Val267Leu | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 6/23 | 1081/6668 | 799/4281 | 267/1426 | chr4 | 47535531 | |||
chr4:47535573 | A | G | 1 | a0046 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.841A>G | p.Ile281Val | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 6/23 | 1123/6668 | 841/4281 | 281/1426 | chr4 | 47535573 | |||
chr4:47535949 | C | T | 1 | a0038 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.931C>T | p.Arg311Cys | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/23 | 1213/6668 | 931/4281 | 311/1426 | chr4 | 47535949 | |||
chr4:47535977 | C | T | 1 | a0042 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.959C>T | p.Thr320Ile | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/23 | 1241/6668 | 959/4281 | 320/1426 | chr4 | 47535977 | |||
chr4:47536027 | G | A | 4 | a0009 a0014 a0033 others(1): Show |
16 | HG00741.hp2 HG01106.hp1 HG01358.hp2 others(13): Show |
missense_variant | MODERATE | c.1009G>A | p.Ala337Thr | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/23 | 1291/6668 | 1009/4281 | 337/1426 | chr4 | 47536027 | |||
chr4:47536033 | G | C | 1 | a0029 | 1 | HG01081.hp2 | missense_variant&splice_region_variant | MODERATE | c.1015G>C | p.Gly339Arg | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/23 | 1297/6668 | 1015/4281 | 339/1426 | chr4 | 47536033 | |||
chr4:47546759 | A | G | 5 | a0008 a0023 a0026 others(2): Show |
17 | HG01255.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
missense_variant | MODERATE | c.1532A>G | p.Asn511Ser | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/23 | 1814/6668 | 1532/4281 | 511/1426 | chr4 | 47546759 | |||
chr4:47546793 | T | A | 2 | a0034 a0043 |
2 | HG02257.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1566T>A | p.Phe522Leu | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/23 | 1848/6668 | 1566/4281 | 522/1426 | chr4 | 47546793 | |||
chr4:47554735 | G | A | 1 | a0039 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.1645G>A | p.Val549Met | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/23 | 1927/6668 | 1645/4281 | 549/1426 | chr4 | 47554735 | |||
chr4:47554891 | G | A | 1 | a0022 | 2 | HG01256.hp1 HG01257.hp2 |
missense_variant | MODERATE | c.1801G>A | p.Ala601Thr | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/23 | 2083/6668 | 1801/4281 | 601/1426 | chr4 | 47554891 | |||
chr4:47557985 | C | A | 8 | a0010 a0013 a0022 others(5): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
missense_variant | MODERATE | c.2146C>A | p.Pro716Thr | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/23 | 2428/6668 | 2146/4281 | 716/1426 | chr4 | 47557985 | |||
chr4:47557998 | A | G | 5 | a0005 a0018 a0021 others(2): Show |
33 | HG00099.hp1 HG00438.hp1 HG00673.hp2 others(30): Show |
missense_variant | MODERATE | c.2159A>G | p.Asn720Ser | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/23 | 2441/6668 | 2159/4281 | 720/1426 | chr4 | 47557998 | |||
chr4:47558186 | G | C | 1 | a0050 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2347G>C | p.Val783Leu | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/23 | 2629/6668 | 2347/4281 | 783/1426 | chr4 | 47558186 | |||
chr4:47568859 | G | A | 3 | a0027 a0030 a0048 |
3 | HG01070.hp2 HG01168.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.2876G>A | p.Ser959Asn | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/23 | 3158/6668 | 2876/4281 | 959/1426 | chr4 | 47568859 | |||
chr4:47576954 | G | A | 20 | a0003 a0004 a0007 others(17): Show |
107 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(104): Show |
missense_variant | MODERATE | c.3548G>A | p.Arg1183Lys | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/23 | 3830/6668 | 3548/4281 | 1183/1426 | chr4 | 47576954 | |||
chr4:47582029 | G | A | 11 | a0001 a0007 a0012 others(8): Show |
104 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(101): Show |
missense_variant | MODERATE | c.3718G>A | p.Val1240Ile | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/23 | 4000/6668 | 3718/4281 | 1240/1426 | chr4 | 47582029 | |||
chr4:47582030 | T | G | 1 | a0001 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.3719T>G | p.Val1240Gly | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/23 | 4001/6668 | 3719/4281 | 1240/1426 | chr4 | 47582030 | |||
chr4:47591266 | G | C | 23 | a0003 a0004 a0008 others(20): Show |
117 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
missense_variant | MODERATE | c.4166G>C | p.Ser1389Thr | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 4448/6668 | 4166/4281 | 1389/1426 | chr4 | 47591266 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:47512549 | G | A | 1 | a0001c0031 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.9G>A | p.Glu3Glu | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/23 | 291/6668 | 9/4281 | 3/1426 | chr4 | 47512549 | |||
chr4:47512669 | C | T | 1 | a0011c0025 | 2 | HG02257.hp2 HG02622.hp2 |
synonymous_variant | LOW | c.129C>T | p.Thr43Thr | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/23 | 411/6668 | 129/4281 | 43/1426 | chr4 | 47512669 | |||
chr4:47523108 | A | G | 1 | a0004c0067 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.582A>G | p.Val194Val | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/23 | 864/6668 | 582/4281 | 194/1426 | chr4 | 47523108 | |||
chr4:47536718 | C | T | 1 | a0003c0048 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.1176C>T | p.Ile392Ile | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/23 | 1458/6668 | 1176/4281 | 392/1426 | chr4 | 47536718 | |||
chr4:47557801 | C | T | 1 | a0015c0034 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1962C>T | p.Asn654Asn | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/23 | 2244/6668 | 1962/4281 | 654/1426 | chr4 | 47557801 | |||
chr4:47558146 | C | A | 14 | a0002c0008 a0005c0006 a0005c0014 others(11): Show |
76 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(73): Show |
synonymous_variant | LOW | c.2307C>A | p.Ile769Ile | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/23 | 2589/6668 | 2307/4281 | 769/1426 | chr4 | 47558146 | |||
chr4:47558224 | G | A | 1 | a0041c0037 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.2385G>A | p.Thr795Thr | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/23 | 2667/6668 | 2385/4281 | 795/1426 | chr4 | 47558224 | |||
chr4:47558260 | G | A | 1 | a0001c0016 | 4 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
synonymous_variant | LOW | c.2421G>A | p.Ser807Ser | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/23 | 2703/6668 | 2421/4281 | 807/1426 | chr4 | 47558260 | |||
chr4:47563721 | C | T | 1 | a0036c0047 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2809C>T | p.Leu937Leu | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/23 | 3091/6668 | 2809/4281 | 937/1426 | chr4 | 47563721 | |||
chr4:47563753 | T | C | 1 | a0005c0044 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.2841T>C | p.Asn947Asn | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/23 | 3123/6668 | 2841/4281 | 947/1426 | chr4 | 47563753 | |||
chr4:47576835 | T | C | 1 | a0011c0041 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.3429T>C | p.Thr1143Thr | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/23 | 3711/6668 | 3429/4281 | 1143/1426 | chr4 | 47576835 | |||
chr4:47581965 | C | T | 1 | a0027c0040 | 1 | HG01070.hp2 | synonymous_variant | LOW | c.3654C>T | p.Tyr1218Tyr | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/23 | 3936/6668 | 3654/4281 | 1218/1426 | chr4 | 47581965 | |||
chr4:47587186 | G | A | 8 | a0001c0001 a0001c0043 a0005c0014 others(5): Show |
54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
synonymous_variant | LOW | c.3921G>A | p.Thr1307Thr | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/23 | 4203/6668 | 3921/4281 | 1307/1426 | chr4 | 47587186 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:47485289 | A | G | 1 | a0008c0010t0017 | 1 | HG01255.hp1 | 5_prime_UTR_variant | MODIFIER | c.-268A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/23 | 27252 | chr4 | 47485289 | ||||||
chr4:47485314 | T | A | 1 | a0022c0027t0011 | 2 | HG01256.hp1 HG01257.hp2 |
5_prime_UTR_variant | MODIFIER | c.-243T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/23 | 27227 | chr4 | 47485314 | ||||||
chr4:47485381 | AT | A | 28 | a0001c0001t0003 a0001c0003t0002 a0001c0016t0002 others(25): Show |
98 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
5_prime_UTR_variant | MODIFIER | c.-164delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/23 | 27148 | INFO_REALIGN_3_PRIME | chr4 | 47485381 | |||||
chr4:47591515 | G | A | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0043t0003 others(11): Show |
61 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*134G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 134 | chr4 | 47591515 | ||||||
chr4:47591760 | G | A | 53 | a0001c0001t0003 a0001c0001t0004 a0001c0043t0003 others(50): Show |
178 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*379G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 379 | chr4 | 47591760 | ||||||
chr4:47591838 | A | G | 2 | a0009c0011t0014 a0009c0011t0016 |
2 | NA18612.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*457A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 457 | chr4 | 47591838 | ||||||
chr4:47591959 | A | G | 30 | a0003c0004t0005 a0003c0004t0006 a0003c0004t0007 others(27): Show |
94 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*578A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 578 | chr4 | 47591959 | ||||||
chr4:47592187 | A | G | 6 | a0010c0012t0009 a0011c0020t0009 a0011c0025t0009 others(3): Show |
17 | HG00323.hp2 HG00642.hp2 HG01175.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*806A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 806 | chr4 | 47592187 | ||||||
chr4:47592203 | G | A | 15 | a0003c0004t0006 a0003c0004t0007 a0003c0048t0006 others(12): Show |
43 | HG00280.hp1 HG00408.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*822G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 822 | chr4 | 47592203 | ||||||
chr4:47592760 | T | C | 2 | a0015c0034t0012 a0042c0035t0012 |
2 | HG02258.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1379T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 1379 | chr4 | 47592760 | ||||||
chr4:47593141 | A | C | 1 | a0002c0002t0013 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1760A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 1760 | chr4 | 47593141 | ||||||
chr4:47593281 | A | G | 1 | a0002c0008t0015 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1900A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 23/23 | 1900 | chr4 | 47593281 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:47485685 | C | CT | 5 | a0001c0003t0001g0310 a0006c0007t0001g0314 a0010c0012t0009g0312 others(2): Show |
5 | HG01109.hp1 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+167dupT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47485685 | ||||||
chr4:47485687 | A | T | 305 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(302): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.-38+168A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47485687 | |||||||
chr4:47485688 | A | T | 3 | a0003c0004t0005g0307 a0020c0064t0001g0309 a0037c0060t0001g0308 |
3 | HG03704.hp1 HG03834.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-38+169A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47485688 | |||||||
chr4:47485808 | CACACGGG others(45): Show |
C | 182 | a0001c0001t0004g0005 a0001c0001t0004g0047 a0001c0001t0004g0078 others(179): Show |
187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.-38+301_-38+352del others(52): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47485808 | ||||||
chr4:47485823 | A | C | 125 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(122): Show |
135 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-38+304A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47485823 | |||||||
chr4:47485835 | T | TCACA | 129 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(126): Show |
139 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-38+320_-38+323dup others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47485835 | ||||||
chr4:47485860 | T | G | 5 | a0002c0002t0001g0195 a0002c0002t0001g0199 a0002c0008t0001g0196 others(2): Show |
5 | HG01175.hp2 HG01256.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+341T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47485860 | |||||||
chr4:47486021 | T | A | 1 | a0035c0033t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-38+502T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486021 | |||||||
chr4:47486037 | C | T | 1 | a0001c0003t0001g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-38+518C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486037 | |||||||
chr4:47486259 | G | A | 6 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0002c0008t0001g0016 others(3): Show |
6 | HG02486.hp1 HG03130.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+740G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486259 | |||||||
chr4:47486284 | A | G | 1 | a0001c0001t0004g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-38+765A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486284 | |||||||
chr4:47486414 | A | G | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+895A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486414 | |||||||
chr4:47486463 | G | C | 55 | a0001c0001t0004g0047 a0001c0003t0001g0028 a0001c0003t0001g0034 others(52): Show |
56 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-38+944G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486463 | |||||||
chr4:47486531 | T | C | 49 | a0001c0001t0004g0078 a0001c0001t0004g0079 a0001c0001t0004g0080 others(46): Show |
50 | HG00642.hp1 HG00741.hp1 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.-38+1012T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486531 | |||||||
chr4:47486546 | C | T | 1 | a0005c0006t0002g0306 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-38+1027C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486546 | |||||||
chr4:47486799 | T | A | 1 | a0005c0006t0002g0191 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-38+1280T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486799 | |||||||
chr4:47486991 | G | T | 1 | a0008c0010t0008g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-38+1472G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47486991 | |||||||
chr4:47487031 | G | A | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+1512G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487031 | |||||||
chr4:47487118 | A | G | 304 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(301): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.-38+1599A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487118 | |||||||
chr4:47487121 | C | T | 1 | a0002c0008t0002g0304 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-38+1602C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487121 | |||||||
chr4:47487153 | C | T | 2 | a0008c0010t0008g0193 a0015c0034t0012g0194 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-38+1634C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487153 | |||||||
chr4:47487226 | TC | T | 179 | a0001c0001t0003g0217 a0001c0001t0004g0005 a0001c0001t0004g0047 others(176): Show |
185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.-38+1712delC | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47487226 | ||||||
chr4:47487226 | TCC | T | 96 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(93): Show |
105 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-38+1711_-38+1712d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47487226 | ||||||
chr4:47487229 | C | CA | 10 | a0001c0003t0001g0116 a0001c0031t0002g0192 a0002c0002t0001g0118 others(7): Show |
10 | HG01256.hp1 HG01257.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+1710_-38+1711i others(3): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487229 | |||||||
chr4:47487229 | C | CAA | 4 | a0002c0002t0001g0195 a0002c0008t0001g0196 a0008c0010t0008g0193 others(1): Show |
4 | HG01175.hp2 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+1710_-38+1711i others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487229 | |||||||
chr4:47487230 | C | A | 30 | a0001c0003t0001g0028 a0001c0003t0001g0116 a0001c0031t0002g0192 others(27): Show |
30 | HG00639.hp1 HG01069.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-38+1711C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487230 | |||||||
chr4:47487231 | C | A | 209 | a0001c0001t0003g0217 a0001c0001t0004g0005 a0001c0001t0004g0047 others(206): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-38+1712C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487231 | |||||||
chr4:47487232 | A | C | 4 | a0011c0020t0009g0187 a0011c0020t0009g0188 a0025c0026t0009g0189 others(1): Show |
4 | HG02109.hp1 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+1713A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487232 | |||||||
chr4:47487252 | A | G | 11 | a0001c0003t0001g0116 a0001c0031t0002g0192 a0002c0002t0001g0118 others(8): Show |
11 | HG01175.hp2 HG01256.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+1733A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487252 | |||||||
chr4:47487291 | G | A | 36 | a0001c0001t0004g0047 a0001c0003t0001g0028 a0001c0003t0001g0034 others(33): Show |
36 | HG00639.hp1 HG01069.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-38+1772G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487291 | |||||||
chr4:47487321 | T | C | 1 | a0001c0003t0001g0310 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-38+1802T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487321 | |||||||
chr4:47487343 | T | C | 1 | a0003c0004t0005g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-38+1824T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487343 | |||||||
chr4:47487607 | G | C | 1 | a0001c0016t0002g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+2088G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487607 | |||||||
chr4:47487709 | C | T | 2 | a0008c0010t0008g0193 a0015c0034t0012g0194 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-38+2190C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487709 | |||||||
chr4:47487765 | T | C | 1 | a0049c0057t0008g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-38+2246T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487765 | |||||||
chr4:47487793 | A | C | 1 | a0006c0065t0001g0176 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-38+2274A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487793 | |||||||
chr4:47487828 | C | T | 2 | a0008c0010t0008g0193 a0015c0034t0012g0194 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-38+2309C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47487828 | |||||||
chr4:47488001 | T | C | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-38+2482T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488001 | |||||||
chr4:47488042 | T | C | 1 | a0005c0006t0001g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-38+2523T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488042 | |||||||
chr4:47488156 | T | G | 47 | a0001c0001t0004g0078 a0001c0001t0004g0079 a0001c0001t0004g0080 others(44): Show |
48 | HG00642.hp1 HG00741.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.-38+2637T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488156 | |||||||
chr4:47488169 | G | A | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+2650G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488169 | |||||||
chr4:47488241 | T | C | 1 | a0005c0006t0002g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-38+2722T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488241 | |||||||
chr4:47488246 | T | C | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+2727T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488246 | |||||||
chr4:47488247 | G | A | 3 | a0002c0002t0001g0122 a0004c0005t0006g0121 a0014c0017t0006g0123 |
3 | HG01361.hp2 HG01993.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-38+2728G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488247 | |||||||
chr4:47488400 | G | A | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+2881G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488400 | |||||||
chr4:47488497 | C | T | 1 | a0035c0033t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-38+2978C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488497 | |||||||
chr4:47488612 | CA | C | 9 | a0001c0003t0001g0182 a0002c0002t0004g0183 a0002c0002t0004g0186 others(6): Show |
9 | HG02280.hp1 HG03098.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+3115delA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47488612 | ||||||
chr4:47488612 | CAA | C | 95 | a0001c0001t0003g0217 a0001c0001t0004g0005 a0001c0001t0004g0143 others(92): Show |
99 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.-38+3114_-38+3115d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47488612 | ||||||
chr4:47488612 | CAAA | C | 191 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(188): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-38+3113_-38+3115d others(5): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47488612 | ||||||
chr4:47488612 | CAAAA | C | 11 | a0001c0003t0001g0073 a0001c0031t0002g0192 a0002c0002t0001g0002 others(8): Show |
11 | HG01517.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+3112_-38+3115d others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47488612 | ||||||
chr4:47488612 | CAAAAAAA others(6): Show |
C | 6 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0002c0008t0001g0016 others(3): Show |
6 | HG02486.hp1 HG03130.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+3103_-38+3115d others(15): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47488612 | ||||||
chr4:47488617 | A | C | 1 | a0011c0020t0009g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-38+3098A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488617 | |||||||
chr4:47488742 | G | A | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+3223G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488742 | |||||||
chr4:47488896 | G | A | 1 | a0008c0010t0008g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-38+3377G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488896 | |||||||
chr4:47488960 | G | A | 1 | a0008c0010t0008g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-38+3441G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47488960 | |||||||
chr4:47489069 | C | T | 63 | a0001c0001t0003g0217 a0001c0001t0004g0005 a0001c0001t0004g0143 others(60): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.-38+3550C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489069 | |||||||
chr4:47489134 | G | A | 7 | a0001c0003t0001g0073 a0003c0004t0005g0072 a0019c0021t0009g0071 others(4): Show |
7 | HG02257.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+3615G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489134 | |||||||
chr4:47489157 | G | T | 8 | a0001c0003t0001g0116 a0002c0002t0001g0118 a0002c0002t0001g0195 others(5): Show |
8 | HG01175.hp2 HG01256.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+3638G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489157 | |||||||
chr4:47489217 | G | A | 1 | a0013c0015t0005g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-38+3698G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489217 | |||||||
chr4:47489284 | G | T | 304 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(301): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.-38+3765G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489284 | |||||||
chr4:47489342 | G | T | 1 | a0001c0003t0001g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-38+3823G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489342 | |||||||
chr4:47489389 | G | GA | 47 | a0001c0001t0004g0078 a0001c0001t0004g0079 a0001c0001t0004g0080 others(44): Show |
48 | HG00642.hp1 HG00741.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.-38+3879dupA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47489389 | ||||||
chr4:47489406 | A | G | 2 | a0001c0003t0001g0177 a0006c0007t0001g0178 |
2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-38+3887A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489406 | |||||||
chr4:47489469 | G | A | 1 | a0006c0007t0002g0221 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-38+3950G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489469 | |||||||
chr4:47489472 | A | G | 1 | a0001c0001t0004g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-38+3953A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489472 | |||||||
chr4:47489669 | T | C | 1 | a0005c0006t0001g0032 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-38+4150T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489669 | |||||||
chr4:47489772 | G | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-38+4253G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489772 | |||||||
chr4:47489802 | T | G | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+4283T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489802 | |||||||
chr4:47489905 | T | C | 2 | a0001c0001t0003g0222 a0045c0032t0003g0223 |
2 | NA18612.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-38+4386T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489905 | |||||||
chr4:47489964 | C | T | 4 | a0001c0003t0001g0310 a0010c0012t0009g0312 a0030c0055t0006g0311 others(1): Show |
4 | HG01109.hp1 HG01168.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+4445C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47489964 | |||||||
chr4:47490053 | T | C | 125 | a0001c0001t0003g0217 a0001c0001t0004g0005 a0001c0001t0004g0047 others(122): Show |
129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-38+4534T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47490053 | |||||||
chr4:47490096 | T | G | 124 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(121): Show |
134 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-38+4577T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47490096 | |||||||
chr4:47490129 | C | T | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+4610C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47490129 | |||||||
chr4:47490163 | A | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-38+4644A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47490163 | |||||||
chr4:47490333 | G | A | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+4814G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47490333 | |||||||
chr4:47490417 | A | G | 1 | a0004c0005t0006g0301 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-38+4898A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47490417 | |||||||
chr4:47490651 | G | A | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-38+5132G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47490651 | |||||||
chr4:47490719 | A | C | 8 | a0001c0003t0001g0116 a0002c0002t0001g0118 a0002c0002t0001g0195 others(5): Show |
8 | HG01175.hp2 HG01256.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+5200A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47490719 | |||||||
chr4:47490950 | A | C | 1 | a0005c0006t0002g0306 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-38+5431A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47490950 | |||||||
chr4:47491193 | C | G | 124 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(121): Show |
134 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-38+5674C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47491193 | |||||||
chr4:47491291 | G | GTAACAC | 125 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(122): Show |
135 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-38+5774_-38+5779d others(8): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47491291 | ||||||
chr4:47491353 | G | A | 4 | a0001c0003t0001g0034 a0003c0004t0006g0033 a0005c0006t0002g0035 others(1): Show |
4 | HG02056.hp1 NA18953.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+5834G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47491353 | |||||||
chr4:47491635 | G | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-38+6116G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47491635 | |||||||
chr4:47491890 | T | C | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+6371T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47491890 | |||||||
chr4:47491891 | G | C | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-38+6372G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47491891 | |||||||
chr4:47491962 | A | G | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-38+6443A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47491962 | |||||||
chr4:47491969 | T | A | 6 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0002c0008t0001g0016 others(3): Show |
6 | HG02486.hp1 HG03130.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+6450T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47491969 | |||||||
chr4:47492073 | C | T | 47 | a0001c0001t0004g0078 a0001c0001t0004g0079 a0001c0001t0004g0080 others(44): Show |
48 | HG00642.hp1 HG00741.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.-38+6554C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47492073 | |||||||
chr4:47492466 | C | T | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-38+6947C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47492466 | |||||||
chr4:47492467 | C | A | 1 | a0007c0009t0002g0224 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-38+6948C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47492467 | |||||||
chr4:47492479 | C | A | 313 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-38+6960C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47492479 | |||||||
chr4:47492508 | T | C | 1 | a0004c0005t0006g0129 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-38+6989T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47492508 | |||||||
chr4:47492619 | C | T | 1 | a0009c0011t0001g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-38+7100C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47492619 | |||||||
chr4:47492620 | G | A | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+7101G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47492620 | |||||||
chr4:47492732 | A | G | 5 | a0002c0008t0001g0126 a0011c0025t0009g0124 a0011c0025t0009g0127 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+7213A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47492732 | |||||||
chr4:47492820 | A | G | 1 | a0001c0001t0004g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-38+7301A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47492820 | |||||||
chr4:47493083 | A | T | 1 | a0001c0001t0003g0300 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-38+7564A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47493083 | |||||||
chr4:47493102 | T | C | 1 | a0011c0025t0009g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-38+7583T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47493102 | |||||||
chr4:47493128 | C | T | 1 | a0014c0017t0007g0299 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-38+7609C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47493128 | |||||||
chr4:47493180 | G | T | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+7661G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47493180 | |||||||
chr4:47493288 | A | G | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+7769A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47493288 | |||||||
chr4:47493427 | A | G | 2 | a0002c0008t0002g0304 a0008c0010t0008g0193 |
2 | HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-38+7908A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47493427 | |||||||
chr4:47493522 | G | A | 3 | a0001c0003t0001g0073 a0003c0004t0005g0072 a0019c0021t0009g0071 |
3 | HG02895.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+8003G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47493522 | |||||||
chr4:47493571 | CT | C | 4 | a0001c0003t0001g0018 a0002c0008t0001g0016 a0002c0008t0001g0019 others(1): Show |
4 | HG02486.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+8056delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47493571 | ||||||
chr4:47493824 | A | C | 1 | a0014c0017t0006g0123 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-38+8305A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47493824 | |||||||
chr4:47493848 | T | A | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+8329T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47493848 | |||||||
chr4:47494003 | C | T | 6 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(3): Show |
6 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+8484C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494003 | |||||||
chr4:47494231 | G | A | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+8712G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494231 | |||||||
chr4:47494242 | C | A | 2 | a0001c0003t0001g0177 a0006c0007t0001g0178 |
2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-38+8723C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494242 | |||||||
chr4:47494360 | G | A | 36 | a0001c0001t0004g0047 a0001c0003t0001g0028 a0001c0003t0001g0034 others(33): Show |
36 | HG00639.hp1 HG01069.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-38+8841G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494360 | |||||||
chr4:47494500 | T | TAAAGTTA others(315): Show |
2 | a0011c0025t0009g0127 a0012c0013t0008g0128 |
2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(324): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(316): Show |
3 | a0002c0008t0001g0126 a0011c0025t0009g0124 a0012c0013t0008g0125 |
3 | HG02572.hp1 HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(325): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(293): Show |
1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(302): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(297): Show |
2 | a0005c0014t0004g0058 a0010c0012t0005g0067 |
2 | HG02647.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(306): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(300): Show |
2 | a0003c0004t0005g0057 a0037c0060t0001g0308 |
2 | HG02572.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(309): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(301): Show |
1 | a0040c0053t0001g0173 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(310): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(304): Show |
1 | a0007c0009t0002g0036 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(313): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(305): Show |
1 | a0005c0006t0002g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(314): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(306): Show |
1 | a0001c0003t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(315): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(307): Show |
3 | a0001c0003t0001g0310 a0010c0012t0006g0065 a0010c0012t0006g0066 |
3 | HG00280.hp1 HG01109.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(316): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(308): Show |
5 | a0004c0005t0005g0063 a0010c0012t0009g0003 a0010c0012t0009g0312 others(2): Show |
6 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(317): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(309): Show |
1 | a0030c0055t0006g0311 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(318): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(313): Show |
3 | a0002c0002t0001g0027 a0009c0011t0016g0056 a0011c0038t0005g0062 |
3 | HG02258.hp2 HG03239.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(322): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(314): Show |
10 | a0001c0003t0001g0052 a0001c0003t0001g0059 a0002c0002t0001g0025 others(7): Show |
10 | HG00639.hp1 HG01433.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(323): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(315): Show |
10 | a0001c0001t0004g0047 a0001c0003t0001g0048 a0002c0002t0001g0050 others(7): Show |
10 | HG01069.hp2 HG01109.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(324): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(316): Show |
2 | a0002c0002t0004g0045 a0003c0004t0005g0046 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(325): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(318): Show |
1 | a0003c0004t0006g0033 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(327): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(319): Show |
3 | a0003c0004t0005g0044 a0006c0007t0001g0042 a0006c0007t0001g0043 |
3 | HG02647.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(328): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(320): Show |
3 | a0003c0004t0005g0041 a0006c0007t0001g0039 a0006c0007t0001g0040 |
3 | HG02630.hp2 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(329): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(321): Show |
2 | a0002c0002t0001g0293 a0006c0007t0001g0038 |
2 | HG00323.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(330): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(322): Show |
2 | a0002c0002t0001g0002 a0002c0002t0001g0292 |
4 | HG01358.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(331): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(323): Show |
5 | a0001c0001t0004g0290 a0001c0003t0001g0215 a0001c0003t0001g0216 others(2): Show |
5 | HG01070.hp2 HG01261.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(332): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(324): Show |
1 | a0004c0005t0006g0301 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(333): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(325): Show |
3 | a0001c0003t0001g0037 a0001c0003t0001g0289 a0003c0004t0005g0307 |
3 | HG00738.hp1 HG03540.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-38+8993_-38+8994i others(334): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(326): Show |
1 | a0013c0015t0009g0288 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(335): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(307): Show |
1 | a0001c0003t0001g0068 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(316): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(309): Show |
1 | a0006c0007t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(318): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494500 | T | TAAAGTTA others(315): Show |
1 | a0001c0003t0001g0028 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-38+8993_-38+8994i others(324): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47494500 | ||||||
chr4:47494518 | C | T | 17 | a0001c0001t0003g0217 a0001c0001t0004g0171 a0002c0002t0001g0165 others(14): Show |
18 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.-38+8999C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494518 | |||||||
chr4:47494639 | T | G | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+9120T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494639 | |||||||
chr4:47494645 | A | G | 1 | a0002c0002t0001g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-38+9126A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494645 | |||||||
chr4:47494832 | A | G | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+9313A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494832 | |||||||
chr4:47494894 | A | G | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+9375A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494894 | |||||||
chr4:47494945 | T | C | 37 | a0001c0001t0004g0047 a0001c0003t0001g0028 a0001c0003t0001g0034 others(34): Show |
37 | HG00639.hp1 HG00673.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-38+9426T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47494945 | |||||||
chr4:47495187 | T | C | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+9668T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495187 | |||||||
chr4:47495188 | G | T | 1 | a0002c0008t0002g0304 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-38+9669G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495188 | |||||||
chr4:47495236 | C | G | 307 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-38+9717C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495236 | |||||||
chr4:47495436 | A | G | 61 | a0001c0001t0003g0287 a0001c0001t0004g0082 a0001c0001t0004g0083 others(58): Show |
62 | HG00642.hp1 HG00741.hp1 HG01123.hp2 others(59): Show |
intron_variant | MODIFIER | c.-38+9917A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495436 | |||||||
chr4:47495463 | T | A | 197 | a0001c0001t0003g0217 a0001c0001t0003g0287 a0001c0001t0004g0005 others(194): Show |
202 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.-38+9944T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495463 | |||||||
chr4:47495641 | A | G | 1 | a0035c0033t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-38+10122A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495641 | |||||||
chr4:47495653 | A | T | 1 | a0005c0006t0001g0113 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-38+10134A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495653 | |||||||
chr4:47495737 | CT | C | 64 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(61): Show |
68 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-38+10235delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47495737 | ||||||
chr4:47495754 | T | G | 102 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(99): Show |
108 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-38+10235T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495754 | |||||||
chr4:47495794 | A | G | 89 | a0001c0001t0003g0217 a0001c0001t0004g0005 a0001c0001t0004g0047 others(86): Show |
91 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.-38+10275A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495794 | |||||||
chr4:47495831 | G | A | 38 | a0001c0001t0004g0290 a0001c0003t0001g0020 a0001c0003t0001g0048 others(35): Show |
40 | HG01123.hp1 HG01175.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.-38+10312G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495831 | |||||||
chr4:47495887 | G | A | 2 | a0001c0003t0001g0004 a0009c0011t0014g0228 |
3 | NA18612.hp1 NA18984.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-38+10368G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495887 | |||||||
chr4:47495909 | G | A | 1 | a0011c0020t0009g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+10390G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495909 | |||||||
chr4:47495956 | C | T | 24 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(21): Show |
24 | HG01884.hp2 HG02257.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.-38+10437C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495956 | |||||||
chr4:47495969 | T | C | 194 | a0001c0001t0003g0217 a0001c0001t0003g0230 a0001c0001t0003g0231 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.-38+10450T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47495969 | |||||||
chr4:47496156 | C | CT | 132 | a0001c0001t0003g0300 a0001c0001t0004g0047 a0001c0003t0001g0028 others(129): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-38+10655dupT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47496156 | ||||||
chr4:47496156 | C | CTT | 7 | a0003c0004t0005g0139 a0003c0004t0005g0140 a0003c0004t0005g0162 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+10654_-38+1065 others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47496156 | ||||||
chr4:47496156 | CT | C | 7 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+10655delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47496156 | ||||||
chr4:47496156 | CTTTTTTT | C | 91 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(88): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.-38+10649_-38+1065 others(11): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47496156 | ||||||
chr4:47496160 | T | C | 61 | a0001c0001t0003g0217 a0001c0001t0004g0082 a0001c0001t0004g0083 others(58): Show |
65 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.-38+10641T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496160 | |||||||
chr4:47496218 | C | G | 7 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+10699C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496218 | |||||||
chr4:47496229 | C | T | 1 | a0003c0004t0007g0282 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-38+10710C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496229 | |||||||
chr4:47496277 | C | A | 92 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(89): Show |
96 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-38+10758C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496277 | |||||||
chr4:47496314 | C | T | 34 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(31): Show |
36 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-38+10795C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496314 | |||||||
chr4:47496355 | C | T | 1 | a0035c0033t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-38+10836C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496355 | |||||||
chr4:47496446 | C | T | 62 | a0002c0008t0001g0141 a0004c0005t0005g0131 a0004c0005t0005g0166 others(59): Show |
68 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.-38+10927C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496446 | |||||||
chr4:47496514 | A | G | 3 | a0001c0003t0001g0073 a0003c0004t0005g0046 a0003c0004t0005g0072 |
3 | HG02717.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+10995A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496514 | |||||||
chr4:47496559 | T | A | 1 | a0010c0012t0009g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-38+11040T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496559 | |||||||
chr4:47496560 | A | G | 1 | a0010c0012t0009g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-38+11041A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496560 | |||||||
chr4:47496561 | A | C | 1 | a0010c0012t0009g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-38+11042A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496561 | |||||||
chr4:47496662 | A | G | 1 | a0007c0009t0001g0097 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-38+11143A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496662 | |||||||
chr4:47496882 | C | T | 2 | a0026c0024t0004g0069 a0026c0024t0004g0070 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-38+11363C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496882 | |||||||
chr4:47496899 | T | G | 1 | a0001c0001t0004g0082 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-38+11380T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47496899 | |||||||
chr4:47497031 | G | A | 1 | a0010c0012t0009g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-38+11512G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497031 | |||||||
chr4:47497040 | C | T | 6 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+11521C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497040 | |||||||
chr4:47497092 | C | T | 63 | a0002c0008t0001g0141 a0004c0005t0005g0131 a0004c0005t0005g0166 others(60): Show |
69 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.-38+11573C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497092 | |||||||
chr4:47497131 | G | A | 1 | a0005c0006t0001g0098 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-38+11612G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497131 | |||||||
chr4:47497185 | G | A | 1 | a0005c0006t0002g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-38+11666G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497185 | |||||||
chr4:47497316 | G | A | 1 | a0035c0033t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-38+11797G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497316 | |||||||
chr4:47497450 | C | T | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-38+11931C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497450 | |||||||
chr4:47497451 | G | A | 1 | a0006c0007t0001g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-38+11932G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497451 | |||||||
chr4:47497489 | G | C | 90 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(87): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-38+11970G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497489 | |||||||
chr4:47497659 | G | A | 3 | a0003c0004t0005g0061 a0011c0038t0005g0062 a0036c0047t0004g0060 |
3 | HG02258.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-38+12140G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497659 | |||||||
chr4:47497694 | A | G | 1 | a0006c0007t0001g0161 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-38+12175A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497694 | |||||||
chr4:47497697 | G | A | 35 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(32): Show |
37 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38+12178G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497697 | |||||||
chr4:47497977 | T | C | 310 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-38+12458T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47497977 | |||||||
chr4:47498129 | G | T | 17 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(14): Show |
18 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-38+12610G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47498129 | |||||||
chr4:47498175 | C | T | 2 | a0024c0028t0008g0119 a0024c0028t0008g0202 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-38+12656C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47498175 | |||||||
chr4:47498339 | T | C | 310 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-38+12820T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47498339 | |||||||
chr4:47498383 | G | A | 1 | a0005c0014t0004g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-38+12864G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47498383 | |||||||
chr4:47498635 | T | C | 58 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(55): Show |
63 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-38+13116T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47498635 | |||||||
chr4:47498647 | G | T | 309 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(306): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.-38+13128G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47498647 | |||||||
chr4:47498716 | G | T | 39 | a0001c0001t0004g0047 a0001c0003t0001g0028 a0001c0003t0001g0037 others(36): Show |
39 | HG00558.hp2 HG00639.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.-38+13197G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47498716 | |||||||
chr4:47498797 | A | G | 59 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(56): Show |
64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-38+13278A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47498797 | |||||||
chr4:47499066 | G | A | 17 | a0001c0003t0001g0310 a0003c0004t0005g0061 a0004c0005t0005g0063 others(14): Show |
18 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-37-13438G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47499066 | |||||||
chr4:47499200 | G | A | 17 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(14): Show |
18 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37-13304G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47499200 | |||||||
chr4:47499372 | C | T | 1 | a0012c0013t0008g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-37-13132C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47499372 | |||||||
chr4:47499405 | A | G | 41 | a0001c0001t0003g0217 a0001c0001t0004g0082 a0001c0001t0004g0171 others(38): Show |
41 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.-37-13099A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47499405 | |||||||
chr4:47499512 | GA | G | 35 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(32): Show |
37 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-12986delA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47499512 | ||||||
chr4:47499714 | A | C | 17 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(14): Show |
18 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37-12790A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47499714 | |||||||
chr4:47499751 | G | A | 1 | a0003c0004t0010g0235 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-37-12753G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47499751 | |||||||
chr4:47499816 | C | T | 1 | a0003c0004t0007g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-37-12688C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47499816 | |||||||
chr4:47499817 | G | A | 1 | a0001c0001t0003g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-37-12687G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47499817 | |||||||
chr4:47499840 | G | A | 35 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(32): Show |
37 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-12664G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47499840 | |||||||
chr4:47500022 | T | C | 67 | a0002c0008t0001g0141 a0004c0005t0005g0131 a0004c0005t0005g0166 others(64): Show |
73 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.-37-12482T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500022 | |||||||
chr4:47500197 | C | G | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-37-12307C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500197 | |||||||
chr4:47500283 | G | A | 2 | a0003c0004t0005g0203 a0003c0004t0005g0204 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-37-12221G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500283 | |||||||
chr4:47500367 | G | A | 9 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(6): Show |
9 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37-12137G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500367 | |||||||
chr4:47500626 | C | G | 9 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(6): Show |
9 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37-11878C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500626 | |||||||
chr4:47500631 | A | C | 35 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(32): Show |
37 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-11873A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500631 | |||||||
chr4:47500643 | C | T | 2 | a0003c0004t0005g0203 a0003c0004t0005g0204 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-37-11861C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500643 | |||||||
chr4:47500650 | G | C | 1 | a0003c0004t0005g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-37-11854G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500650 | |||||||
chr4:47500659 | G | A | 1 | a0004c0005t0006g0129 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-37-11845G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500659 | |||||||
chr4:47500670 | C | A | 1 | a0007c0009t0001g0012 | 2 | HG00438.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.-37-11834C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500670 | |||||||
chr4:47500763 | T | C | 18 | a0001c0003t0001g0310 a0003c0004t0005g0061 a0004c0005t0005g0063 others(15): Show |
19 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-37-11741T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500763 | |||||||
chr4:47500834 | G | A | 1 | a0001c0003t0002g0286 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-37-11670G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500834 | |||||||
chr4:47500844 | A | C | 17 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(14): Show |
18 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37-11660A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500844 | |||||||
chr4:47500907 | G | C | 310 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-37-11597G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500907 | |||||||
chr4:47500940 | T | C | 35 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(32): Show |
37 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-11564T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500940 | |||||||
chr4:47500960 | G | A | 1 | a0005c0006t0001g0086 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-37-11544G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47500960 | |||||||
chr4:47501086 | C | CAAGA | 310 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-37-11416_-37-1141 others(8): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47501086 | ||||||
chr4:47501126 | A | G | 35 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(32): Show |
37 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-11378A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501126 | |||||||
chr4:47501174 | A | G | 9 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37-11330A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501174 | |||||||
chr4:47501236 | C | T | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-37-11268C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501236 | |||||||
chr4:47501264 | A | G | 1 | a0002c0002t0013g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-37-11240A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501264 | |||||||
chr4:47501308 | T | C | 17 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(14): Show |
18 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37-11196T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501308 | |||||||
chr4:47501410 | A | G | 35 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(32): Show |
37 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-11094A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501410 | |||||||
chr4:47501469 | T | C | 4 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-11035T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501469 | |||||||
chr4:47501644 | T | C | 136 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(133): Show |
142 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-37-10860T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501644 | |||||||
chr4:47501802 | G | C | 3 | a0003c0004t0005g0061 a0011c0038t0005g0062 a0036c0047t0004g0060 |
3 | HG02258.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-37-10702G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501802 | |||||||
chr4:47501909 | C | T | 133 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0230 others(130): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-37-10595C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501909 | |||||||
chr4:47501938 | T | A | 22 | a0001c0003t0001g0116 a0001c0003t0001g0215 a0001c0003t0001g0289 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-10566T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47501938 | |||||||
chr4:47502033 | C | T | 1 | a0001c0003t0001g0216 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-37-10471C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502033 | |||||||
chr4:47502125 | C | T | 6 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-10379C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502125 | |||||||
chr4:47502140 | T | C | 1 | a0005c0006t0002g0270 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-37-10364T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502140 | |||||||
chr4:47502144 | T | G | 159 | a0001c0001t0003g0217 a0001c0001t0003g0237 a0001c0001t0004g0047 others(156): Show |
165 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.-37-10360T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502144 | |||||||
chr4:47502257 | G | A | 6 | a0003c0004t0005g0139 a0003c0004t0005g0140 a0003c0004t0005g0162 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-10247G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502257 | |||||||
chr4:47502395 | A | G | 1 | a0001c0001t0004g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-37-10109A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502395 | |||||||
chr4:47502442 | C | A | 5 | a0001c0003t0001g0116 a0002c0002t0001g0165 a0002c0002t0002g0011 others(2): Show |
6 | HG00280.hp2 HG02040.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-10062C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502442 | |||||||
chr4:47502471 | TA | T | 87 | a0001c0001t0003g0217 a0001c0001t0003g0237 a0001c0001t0004g0047 others(84): Show |
88 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.-37-10020delA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47502471 | ||||||
chr4:47502496 | T | C | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-37-10008T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502496 | |||||||
chr4:47502504 | G | A | 22 | a0001c0003t0001g0116 a0001c0003t0001g0215 a0001c0003t0001g0289 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-10000G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502504 | |||||||
chr4:47502816 | T | G | 87 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(84): Show |
91 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-37-9688T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502816 | |||||||
chr4:47502902 | C | A | 310 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-37-9602C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47502902 | |||||||
chr4:47503031 | A | G | 22 | a0001c0003t0001g0116 a0001c0003t0001g0215 a0001c0003t0001g0289 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-37-9473A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503031 | |||||||
chr4:47503163 | C | G | 13 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-37-9341C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503163 | |||||||
chr4:47503193 | C | T | 2 | a0001c0003t0001g0028 a0002c0002t0001g0026 |
2 | HG00639.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-37-9311C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503193 | |||||||
chr4:47503197 | A | G | 7 | a0003c0004t0005g0139 a0003c0004t0005g0140 a0003c0004t0005g0162 others(4): Show |
7 | HG02258.hp1 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-9307A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503197 | |||||||
chr4:47503221 | A | G | 1 | a0001c0003t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-37-9283A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503221 | |||||||
chr4:47503227 | T | G | 70 | a0001c0003t0001g0310 a0002c0008t0001g0141 a0004c0005t0005g0131 others(67): Show |
76 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.-37-9277T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503227 | |||||||
chr4:47503290 | T | C | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-37-9214T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503290 | |||||||
chr4:47503342 | T | A | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-37-9162T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503342 | |||||||
chr4:47503382 | T | C | 7 | a0004c0005t0006g0149 a0004c0005t0007g0001 a0004c0005t0007g0271 others(4): Show |
9 | NA18939.hp1 NA18941.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37-9122T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503382 | |||||||
chr4:47503451 | G | C | 6 | a0003c0004t0005g0139 a0003c0004t0005g0140 a0003c0004t0005g0162 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-9053G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503451 | |||||||
chr4:47503619 | G | A | 86 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(83): Show |
90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-37-8885G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503619 | |||||||
chr4:47503909 | T | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-37-8595T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503909 | |||||||
chr4:47503915 | A | AAAAAT | 22 | a0001c0003t0001g0116 a0001c0003t0001g0215 a0001c0003t0001g0289 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-37-8568_-37-8564d others(7): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47503915 | ||||||
chr4:47503964 | G | A | 1 | a0003c0048t0006g0102 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-37-8540G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47503964 | |||||||
chr4:47504180 | A | C | 6 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-8324A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504180 | |||||||
chr4:47504196 | G | A | 1 | a0005c0014t0004g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-37-8308G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504196 | |||||||
chr4:47504213 | T | C | 1 | a0019c0021t0009g0074 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-37-8291T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504213 | |||||||
chr4:47504623 | C | T | 1 | a0011c0020t0009g0188 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-7881C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504623 | |||||||
chr4:47504651 | C | T | 1 | a0001c0003t0002g0239 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-37-7853C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504651 | |||||||
chr4:47504765 | G | C | 21 | a0004c0005t0006g0133 a0004c0005t0006g0149 a0004c0005t0006g0301 others(18): Show |
25 | HG00408.hp1 HG00738.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-7739G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504765 | |||||||
chr4:47504771 | G | A | 92 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(89): Show |
96 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-37-7733G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504771 | |||||||
chr4:47504776 | A | G | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-37-7728A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504776 | |||||||
chr4:47504784 | C | T | 16 | a0004c0005t0005g0063 a0005c0006t0001g0219 a0005c0006t0002g0306 others(13): Show |
17 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.-37-7720C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504784 | |||||||
chr4:47504798 | G | T | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-37-7706G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504798 | |||||||
chr4:47504862 | A | T | 1 | a0002c0008t0001g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-37-7642A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504862 | |||||||
chr4:47504944 | G | A | 68 | a0001c0001t0004g0082 a0001c0001t0004g0171 a0001c0003t0001g0028 others(65): Show |
68 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.-37-7560G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504944 | |||||||
chr4:47504974 | G | A | 67 | a0004c0005t0005g0131 a0004c0005t0005g0166 a0004c0005t0006g0007 others(64): Show |
73 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-37-7530G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47504974 | |||||||
chr4:47505108 | C | A | 4 | a0001c0001t0003g0231 a0001c0001t0003g0240 a0001c0001t0003g0241 others(1): Show |
4 | HG00558.hp1 NA18955.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-7396C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505108 | |||||||
chr4:47505176 | C | T | 102 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(99): Show |
106 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-37-7328C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505176 | |||||||
chr4:47505180 | G | C | 11 | a0005c0006t0002g0191 a0005c0006t0002g0220 a0005c0006t0002g0244 others(8): Show |
11 | HG00438.hp1 HG01346.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-7324G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505180 | |||||||
chr4:47505244 | G | C | 18 | a0001c0003t0001g0020 a0004c0005t0005g0063 a0005c0006t0001g0219 others(15): Show |
19 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-7260G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505244 | |||||||
chr4:47505251 | C | T | 2 | a0001c0001t0003g0281 a0003c0004t0007g0282 |
2 | HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-37-7253C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505251 | |||||||
chr4:47505451 | T | C | 5 | a0001c0001t0003g0237 a0001c0003t0002g0206 a0001c0003t0002g0236 others(2): Show |
5 | NA18961.hp2 NA18968.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-7053T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505451 | |||||||
chr4:47505531 | C | G | 2 | a0006c0007t0001g0038 a0006c0007t0001g0043 |
2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-37-6973C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505531 | |||||||
chr4:47505603 | A | G | 136 | a0001c0001t0004g0082 a0001c0001t0004g0171 a0001c0003t0001g0018 others(133): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-37-6901A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505603 | |||||||
chr4:47505738 | C | T | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-37-6766C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505738 | |||||||
chr4:47505739 | G | A | 15 | a0004c0005t0005g0063 a0010c0012t0005g0067 a0010c0012t0006g0065 others(12): Show |
16 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.-37-6765G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47505739 | |||||||
chr4:47506088 | T | G | 1 | a0013c0015t0009g0288 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-37-6416T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47506088 | |||||||
chr4:47506350 | AATT | A | 20 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(17): Show |
21 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-37-6146_-37-6144d others(5): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47506350 | ||||||
chr4:47506523 | C | A | 175 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(172): Show |
185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-37-5981C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47506523 | |||||||
chr4:47506868 | G | A | 1 | a0004c0005t0005g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-37-5636G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47506868 | |||||||
chr4:47506990 | T | G | 44 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(41): Show |
48 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.-37-5514T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47506990 | |||||||
chr4:47507103 | T | G | 24 | a0001c0003t0001g0116 a0001c0003t0001g0215 a0001c0003t0001g0289 others(21): Show |
27 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-37-5401T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47507103 | |||||||
chr4:47507218 | G | A | 7 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-5286G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47507218 | |||||||
chr4:47507581 | A | G | 4 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-4923A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47507581 | |||||||
chr4:47507589 | A | G | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-37-4915A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47507589 | |||||||
chr4:47507716 | G | A | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-37-4788G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47507716 | |||||||
chr4:47507754 | A | G | 1 | a0002c0002t0001g0107 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-37-4750A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47507754 | |||||||
chr4:47507873 | A | G | 4 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-4631A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47507873 | |||||||
chr4:47507904 | G | A | 2 | a0002c0002t0001g0144 a0002c0002t0001g0163 |
2 | HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-37-4600G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47507904 | |||||||
chr4:47507993 | T | C | 1 | a0002c0002t0001g0199 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-37-4511T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47507993 | |||||||
chr4:47508003 | T | C | 5 | a0001c0001t0003g0250 a0001c0001t0004g0083 a0001c0001t0004g0084 others(2): Show |
5 | HG02015.hp2 NA18939.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-4501T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508003 | |||||||
chr4:47508161 | A | G | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-37-4343A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508161 | |||||||
chr4:47508273 | C | T | 1 | a0025c0026t0009g0190 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-37-4231C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508273 | |||||||
chr4:47508365 | T | C | 1 | a0001c0003t0001g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-37-4139T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508365 | |||||||
chr4:47508373 | A | G | 1 | a0009c0011t0001g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-37-4131A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508373 | |||||||
chr4:47508445 | T | C | 7 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-4059T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508445 | |||||||
chr4:47508542 | A | G | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-37-3962A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508542 | |||||||
chr4:47508611 | C | T | 20 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(17): Show |
21 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-37-3893C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508611 | |||||||
chr4:47508749 | T | A | 2 | a0001c0003t0001g0037 a0003c0004t0005g0057 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-37-3755T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508749 | |||||||
chr4:47508764 | T | A | 2 | a0002c0002t0001g0087 a0002c0002t0002g0229 |
2 | HG01496.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-37-3740T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508764 | |||||||
chr4:47508782 | C | T | 1 | a0002c0008t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-37-3722C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47508782 | |||||||
chr4:47509001 | A | G | 15 | a0004c0005t0005g0063 a0010c0012t0005g0067 a0010c0012t0006g0065 others(12): Show |
16 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.-37-3503A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509001 | |||||||
chr4:47509210 | A | G | 2 | a0003c0004t0006g0138 a0007c0009t0001g0012 |
3 | HG00438.hp2 HG00673.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.-37-3294A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509210 | |||||||
chr4:47509211 | T | A | 1 | a0003c0004t0010g0235 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-37-3293T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509211 | |||||||
chr4:47509237 | T | G | 6 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-3267T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509237 | |||||||
chr4:47509248 | G | GT | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-37-3253dupT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47509248 | ||||||
chr4:47509272 | A | G | 1 | a0013c0015t0009g0288 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-37-3232A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509272 | |||||||
chr4:47509359 | A | G | 115 | a0001c0001t0004g0082 a0001c0001t0004g0171 a0001c0003t0001g0018 others(112): Show |
119 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-37-3145A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509359 | |||||||
chr4:47509431 | T | C | 98 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(95): Show |
102 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-37-3073T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509431 | |||||||
chr4:47509488 | T | C | 1 | a0004c0067t0007g0148 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-37-3016T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509488 | |||||||
chr4:47509593 | C | T | 175 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(172): Show |
185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-37-2911C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509593 | |||||||
chr4:47509596 | A | T | 65 | a0001c0001t0004g0082 a0001c0001t0004g0171 a0001c0003t0001g0028 others(62): Show |
65 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.-37-2908A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509596 | |||||||
chr4:47509700 | C | A | 6 | a0003c0004t0005g0139 a0003c0004t0005g0140 a0003c0004t0005g0162 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-2804C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509700 | |||||||
chr4:47509764 | T | C | 210 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(207): Show |
223 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-37-2740T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509764 | |||||||
chr4:47509943 | G | GGT | 18 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(15): Show |
19 | HG00280.hp1 HG00642.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-2522_-37-2521d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47509943 | ||||||
chr4:47509943 | GGT | G | 26 | a0001c0001t0003g0253 a0001c0003t0001g0004 a0001c0003t0001g0073 others(23): Show |
27 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.-37-2522_-37-2521d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47509943 | ||||||
chr4:47509943 | GGTGT | G | 127 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(124): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-37-2524_-37-2521d others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47509943 | ||||||
chr4:47509943 | GGTGTGT | G | 92 | a0001c0003t0001g0028 a0001c0003t0001g0037 a0001c0003t0001g0108 others(89): Show |
97 | HG00408.hp1 HG00558.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.-37-2526_-37-2521d others(8): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47509943 | ||||||
chr4:47509943 | GGTGTGTG others(1): Show |
G | 11 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(8): Show |
11 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-2528_-37-2521d others(10): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47509943 | ||||||
chr4:47509943 | GGTGTGTG others(3): Show |
G | 8 | a0002c0002t0001g0109 a0004c0005t0005g0131 a0004c0005t0006g0007 others(5): Show |
8 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-2530_-37-2521d others(12): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47509943 | ||||||
chr4:47509949 | T | TGTGTGTG others(7855): Show |
1 | a0006c0007t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-37-2527_-37-2526i others(7864): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47509949 | ||||||
chr4:47509955 | T | C | 23 | a0001c0003t0001g0116 a0001c0003t0001g0215 a0001c0003t0001g0289 others(20): Show |
26 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-37-2549T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47509955 | |||||||
chr4:47510035 | G | A | 175 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(172): Show |
185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-37-2469G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47510035 | |||||||
chr4:47510106 | A | C | 6 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-2398A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47510106 | |||||||
chr4:47510156 | C | G | 1 | a0010c0012t0009g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-37-2348C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47510156 | |||||||
chr4:47510347 | C | G | 24 | a0001c0003t0001g0116 a0001c0003t0001g0215 a0001c0003t0001g0289 others(21): Show |
27 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-37-2157C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47510347 | |||||||
chr4:47510579 | G | C | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-37-1925G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47510579 | |||||||
chr4:47510746 | A | G | 24 | a0001c0003t0001g0116 a0001c0003t0001g0215 a0001c0003t0001g0289 others(21): Show |
27 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-37-1758A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47510746 | |||||||
chr4:47510748 | T | C | 64 | a0001c0001t0004g0082 a0001c0001t0004g0171 a0001c0003t0001g0028 others(61): Show |
64 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.-37-1756T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47510748 | |||||||
chr4:47510814 | T | TA | 6 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-1689dupA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47510814 | ||||||
chr4:47510859 | A | G | 206 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(203): Show |
219 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-37-1645A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47510859 | |||||||
chr4:47511165 | C | T | 85 | a0001c0001t0004g0082 a0001c0001t0004g0171 a0001c0003t0001g0028 others(82): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-37-1339C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511165 | |||||||
chr4:47511248 | T | C | 68 | a0001c0001t0004g0082 a0001c0001t0004g0171 a0001c0003t0001g0028 others(65): Show |
69 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-37-1256T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511248 | |||||||
chr4:47511285 | GT | G | 20 | a0004c0005t0005g0063 a0005c0006t0001g0219 a0005c0006t0002g0306 others(17): Show |
21 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.-37-1210delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 47511285 | ||||||
chr4:47511307 | A | G | 15 | a0004c0005t0005g0063 a0010c0012t0005g0067 a0010c0012t0006g0065 others(12): Show |
16 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.-37-1197A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511307 | |||||||
chr4:47511364 | A | G | 1 | a0002c0002t0001g0087 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-37-1140A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511364 | |||||||
chr4:47511375 | G | A | 1 | a0009c0011t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-37-1129G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511375 | |||||||
chr4:47511425 | A | C | 1 | a0045c0032t0003g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-37-1079A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511425 | |||||||
chr4:47511434 | G | A | 4 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-1070G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511434 | |||||||
chr4:47511475 | A | G | 4 | a0004c0005t0006g0009 a0004c0005t0006g0129 a0004c0005t0006g0168 others(1): Show |
5 | HG01256.hp2 HG01496.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-1029A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511475 | |||||||
chr4:47511600 | G | A | 7 | a0001c0003t0002g0260 a0003c0004t0006g0138 a0007c0009t0001g0012 others(4): Show |
8 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-904G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511600 | |||||||
chr4:47511860 | G | A | 11 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(8): Show |
12 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37-644G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511860 | |||||||
chr4:47511899 | A | G | 1 | a0013c0015t0005g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-37-605A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511899 | |||||||
chr4:47511963 | C | T | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-37-541C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511963 | |||||||
chr4:47511998 | G | A | 3 | a0022c0027t0011g0197 a0022c0027t0011g0198 a0028c0061t0001g0155 |
3 | HG01081.hp1 HG01256.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.-37-506G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47511998 | |||||||
chr4:47512097 | A | G | 22 | a0004c0005t0005g0063 a0010c0012t0005g0067 a0010c0012t0006g0008 others(19): Show |
23 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-37-407A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47512097 | |||||||
chr4:47512196 | A | G | 11 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(8): Show |
12 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37-308A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47512196 | |||||||
chr4:47512297 | G | A | 2 | a0010c0012t0006g0008 a0029c0051t0006g0008 |
2 | HG00735.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-37-207G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47512297 | |||||||
chr4:47512338 | T | C | 2 | a0001c0001t0003g0230 a0001c0001t0003g0232 |
2 | HG01099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-37-166T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47512338 | |||||||
chr4:47512406 | G | A | 22 | a0001c0003t0001g0215 a0001c0003t0001g0289 a0002c0002t0001g0002 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-37-98G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | chr4 | 47512406 | |||||||
chr4:47512836 | G | A | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | splice_region_variant&intron_variant | LOW | c.290+6G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47512836 | |||||||
chr4:47512896 | T | C | 1 | a0001c0003t0001g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.290+66T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47512896 | |||||||
chr4:47512950 | A | C | 66 | a0004c0005t0005g0131 a0004c0005t0005g0166 a0004c0005t0006g0007 others(63): Show |
72 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.290+120A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47512950 | |||||||
chr4:47513001 | A | G | 12 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(9): Show |
13 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.290+171A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513001 | |||||||
chr4:47513084 | T | G | 6 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+254T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513084 | |||||||
chr4:47513164 | T | A | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.290+334T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513164 | |||||||
chr4:47513172 | T | G | 257 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(254): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.290+342T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513172 | |||||||
chr4:47513400 | T | C | 1 | a0003c0004t0005g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.290+570T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513400 | |||||||
chr4:47513453 | G | T | 3 | a0002c0002t0001g0195 a0002c0002t0002g0285 a0038c0049t0001g0130 |
3 | HG03688.hp2 HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.290+623G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513453 | |||||||
chr4:47513514 | G | A | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.290+684G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513514 | |||||||
chr4:47513685 | G | T | 1 | a0044c0045t0006g0049 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.290+855G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513685 | |||||||
chr4:47513843 | A | G | 279 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(276): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.290+1013A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513843 | |||||||
chr4:47513977 | G | A | 88 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(85): Show |
95 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.290+1147G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47513977 | |||||||
chr4:47514185 | C | T | 279 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(276): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.291-1291C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47514185 | |||||||
chr4:47514509 | A | G | 66 | a0004c0005t0005g0131 a0004c0005t0005g0166 a0004c0005t0006g0007 others(63): Show |
72 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.291-967A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47514509 | |||||||
chr4:47514575 | G | T | 1 | a0010c0012t0009g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.291-901G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47514575 | |||||||
chr4:47514633 | T | C | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.291-843T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47514633 | |||||||
chr4:47514717 | G | T | 6 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-759G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47514717 | |||||||
chr4:47514807 | GTTAA | G | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.291-662_291-659del others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | 47514807 | ||||||
chr4:47514893 | C | CT | 89 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(86): Show |
96 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.291-577dupT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | 47514893 | ||||||
chr4:47514925 | G | A | 2 | a0001c0001t0004g0143 a0005c0006t0001g0142 |
2 | HG02132.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.291-551G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47514925 | |||||||
chr4:47515152 | G | A | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.291-324G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47515152 | |||||||
chr4:47515160 | C | T | 6 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-316C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47515160 | |||||||
chr4:47515181 | G | A | 65 | a0002c0008t0001g0146 a0004c0005t0005g0131 a0004c0005t0005g0166 others(62): Show |
71 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.291-295G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47515181 | |||||||
chr4:47515354 | A | G | 6 | a0003c0004t0005g0139 a0003c0004t0005g0140 a0003c0004t0005g0162 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-122A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | chr4 | 47515354 | |||||||
chr4:47515914 | A | G | 17 | a0004c0005t0005g0063 a0010c0012t0005g0067 a0010c0012t0006g0008 others(14): Show |
18 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.485+244A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47515914 | |||||||
chr4:47516000 | C | T | 1 | a0001c0001t0004g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.485+330C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516000 | |||||||
chr4:47516007 | A | C | 1 | a0004c0005t0007g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.485+337A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516007 | |||||||
chr4:47516075 | C | A | 5 | a0002c0008t0002g0265 a0005c0014t0004g0051 a0005c0014t0004g0053 others(2): Show |
5 | HG00558.hp2 HG02071.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+405C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516075 | |||||||
chr4:47516102 | T | G | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.485+432T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516102 | |||||||
chr4:47516222 | C | T | 90 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(87): Show |
93 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.485+552C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516222 | |||||||
chr4:47516243 | C | CA | 9 | a0001c0003t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0110 others(6): Show |
10 | HG00438.hp2 HG00673.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+588dupA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 47516243 | ||||||
chr4:47516323 | G | A | 66 | a0004c0005t0005g0131 a0004c0005t0005g0166 a0004c0005t0006g0007 others(63): Show |
72 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.485+653G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516323 | |||||||
chr4:47516678 | T | C | 1 | a0022c0027t0011g0197 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.485+1008T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516678 | |||||||
chr4:47516790 | G | A | 20 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(17): Show |
21 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+1120G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516790 | |||||||
chr4:47516805 | CAT | C | 27 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(24): Show |
30 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.485+1136_485+1137d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516805 | |||||||
chr4:47516843 | A | G | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.485+1173A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47516843 | |||||||
chr4:47517005 | A | G | 192 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(189): Show |
197 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.485+1335A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47517005 | |||||||
chr4:47517007 | G | A | 89 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(86): Show |
96 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.485+1337G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47517007 | |||||||
chr4:47517341 | G | A | 1 | a0010c0012t0006g0065 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.485+1671G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47517341 | |||||||
chr4:47517650 | T | G | 67 | a0004c0005t0005g0131 a0004c0005t0005g0166 a0004c0005t0006g0007 others(64): Show |
73 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.485+1980T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47517650 | |||||||
chr4:47517694 | G | A | 1 | a0002c0008t0015g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.485+2024G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47517694 | |||||||
chr4:47517903 | T | C | 1 | a0003c0004t0005g0061 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.485+2233T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47517903 | |||||||
chr4:47518071 | C | T | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.485+2401C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47518071 | |||||||
chr4:47518262 | G | A | 1 | a0006c0007t0002g0233 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.485+2592G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47518262 | |||||||
chr4:47518467 | A | G | 67 | a0004c0005t0005g0131 a0004c0005t0005g0166 a0004c0005t0006g0007 others(64): Show |
73 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.485+2797A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47518467 | |||||||
chr4:47518485 | C | T | 95 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(92): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.485+2815C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47518485 | |||||||
chr4:47518654 | A | G | 1 | a0001c0001t0003g0231 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.485+2984A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47518654 | |||||||
chr4:47518734 | G | A | 1 | a0002c0002t0001g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.485+3064G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47518734 | |||||||
chr4:47518883 | A | G | 4 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3213A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47518883 | |||||||
chr4:47519022 | T | A | 1 | a0011c0020t0009g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.485+3352T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519022 | |||||||
chr4:47519178 | A | C | 179 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(176): Show |
184 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.485+3508A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519178 | |||||||
chr4:47519192 | A | G | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.485+3522A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519192 | |||||||
chr4:47519324 | T | A | 6 | a0003c0004t0005g0139 a0003c0004t0005g0140 a0003c0004t0005g0162 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3654T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519324 | |||||||
chr4:47519428 | C | T | 163 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(160): Show |
167 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.486-3584C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519428 | |||||||
chr4:47519444 | C | G | 230 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(227): Show |
240 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.486-3568C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519444 | |||||||
chr4:47519622 | G | A | 4 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-3390G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519622 | |||||||
chr4:47519625 | C | T | 1 | a0001c0003t0002g0239 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.486-3387C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519625 | |||||||
chr4:47519739 | G | A | 1 | a0018c0023t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.486-3273G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519739 | |||||||
chr4:47519855 | C | T | 1 | a0005c0044t0002g0249 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.486-3157C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519855 | |||||||
chr4:47519920 | G | A | 1 | a0022c0027t0011g0197 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.486-3092G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47519920 | |||||||
chr4:47520012 | A | G | 185 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(182): Show |
192 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.486-3000A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47520012 | |||||||
chr4:47520252 | A | G | 1 | a0001c0003t0001g0004 | 2 | NA18984.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.486-2760A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47520252 | |||||||
chr4:47520365 | G | T | 1 | a0026c0024t0004g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.486-2647G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47520365 | |||||||
chr4:47520547 | C | G | 74 | a0004c0005t0005g0131 a0004c0005t0005g0166 a0004c0005t0006g0007 others(71): Show |
80 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.486-2465C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47520547 | |||||||
chr4:47520629 | C | T | 1 | a0013c0015t0009g0288 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.486-2383C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47520629 | |||||||
chr4:47520794 | T | C | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.486-2218T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47520794 | |||||||
chr4:47520810 | G | A | 29 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(26): Show |
32 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.486-2202G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47520810 | |||||||
chr4:47520818 | C | T | 1 | a0020c0063t0003g0268 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.486-2194C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47520818 | |||||||
chr4:47521038 | G | A | 1 | a0003c0004t0005g0307 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.486-1974G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521038 | |||||||
chr4:47521277 | T | G | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.486-1735T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521277 | |||||||
chr4:47521352 | A | C | 1 | a0003c0004t0005g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.486-1660A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521352 | |||||||
chr4:47521409 | C | T | 27 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(24): Show |
30 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.486-1603C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521409 | |||||||
chr4:47521448 | G | T | 17 | a0004c0005t0005g0063 a0010c0012t0005g0067 a0010c0012t0006g0008 others(14): Show |
18 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.486-1564G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521448 | |||||||
chr4:47521493 | A | G | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.486-1519A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521493 | |||||||
chr4:47521532 | C | A | 4 | a0001c0003t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0110 others(1): Show |
4 | HG01255.hp2 HG01257.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-1480C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521532 | |||||||
chr4:47521584 | G | A | 1 | a0008c0010t0008g0208 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.486-1428G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521584 | |||||||
chr4:47521648 | A | C | 4 | a0001c0003t0001g0037 a0003c0004t0005g0057 a0011c0020t0009g0115 others(1): Show |
4 | HG02572.hp2 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-1364A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521648 | |||||||
chr4:47521684 | C | T | 2 | a0018c0023t0003g0242 a0018c0046t0002g0248 |
2 | HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.486-1328C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521684 | |||||||
chr4:47521719 | T | A | 1 | a0005c0006t0002g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.486-1293T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521719 | |||||||
chr4:47521722 | C | G | 71 | a0001c0003t0001g0037 a0003c0004t0005g0057 a0004c0005t0005g0131 others(68): Show |
77 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.486-1290C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521722 | |||||||
chr4:47521730 | T | A | 10 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(7): Show |
10 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.486-1282T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521730 | |||||||
chr4:47521782 | A | T | 1 | a0003c0004t0005g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.486-1230A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47521782 | |||||||
chr4:47522165 | T | C | 67 | a0004c0005t0005g0131 a0004c0005t0005g0166 a0004c0005t0006g0007 others(64): Show |
73 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.486-847T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522165 | |||||||
chr4:47522276 | C | T | 1 | a0008c0010t0008g0213 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.486-736C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522276 | |||||||
chr4:47522397 | T | A | 27 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(24): Show |
30 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.486-615T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522397 | |||||||
chr4:47522497 | C | T | 1 | a0002c0008t0001g0141 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.486-515C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522497 | |||||||
chr4:47522681 | C | T | 16 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(13): Show |
17 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.486-331C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522681 | |||||||
chr4:47522870 | C | T | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.486-142C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522870 | |||||||
chr4:47522872 | T | A | 3 | a0015c0018t0010g0267 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.486-140T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522872 | |||||||
chr4:47522915 | T | A | 32 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(29): Show |
35 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.486-97T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522915 | |||||||
chr4:47522943 | T | A | 1 | a0014c0017t0006g0123 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.486-69T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522943 | |||||||
chr4:47522944 | T | A | 70 | a0001c0003t0001g0020 a0004c0005t0005g0131 a0004c0005t0005g0166 others(67): Show |
76 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.486-68T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522944 | |||||||
chr4:47522980 | CT | C | 63 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(60): Show |
68 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.486-20delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 47522980 | ||||||
chr4:47522991 | T | A | 5 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 others(2): Show |
5 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-21T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522991 | |||||||
chr4:47522992 | T | A | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.486-20T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 3/22 | chr4 | 47522992 | |||||||
chr4:47523228 | G | A | 1 | a0038c0049t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.690+12G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47523228 | |||||||
chr4:47523664 | T | C | 27 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(24): Show |
30 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.690+448T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47523664 | |||||||
chr4:47523733 | A | T | 49 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(46): Show |
53 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.690+517A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47523733 | |||||||
chr4:47523805 | G | GTATTA | 16 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(13): Show |
17 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.690+590_690+591ins others(5): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 47523805 | ||||||
chr4:47523807 | T | A | 16 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(13): Show |
17 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.690+591T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47523807 | |||||||
chr4:47523822 | T | G | 3 | a0001c0003t0001g0073 a0003c0004t0005g0046 a0003c0004t0005g0072 |
3 | HG02717.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.690+606T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47523822 | |||||||
chr4:47523925 | TTTG | T | 4 | a0001c0001t0003g0259 a0001c0001t0003g0287 a0001c0001t0004g0080 others(1): Show |
4 | NA18946.hp2 NA18963.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+724_690+726del others(3): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 47523925 | ||||||
chr4:47523963 | A | G | 1 | a0005c0006t0001g0101 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.690+747A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47523963 | |||||||
chr4:47524005 | C | T | 1 | a0050c0039t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.690+789C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524005 | |||||||
chr4:47524073 | C | T | 22 | a0001c0003t0001g0215 a0001c0003t0001g0289 a0002c0002t0001g0002 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.690+857C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524073 | |||||||
chr4:47524298 | G | T | 50 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(47): Show |
54 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.690+1082G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524298 | |||||||
chr4:47524314 | C | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.690+1098C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524314 | |||||||
chr4:47524398 | T | TG | 28 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(25): Show |
31 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.691-1158dupG | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 47524398 | ||||||
chr4:47524456 | G | T | 160 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(157): Show |
164 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.691-1101G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524456 | |||||||
chr4:47524559 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.691-998G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524559 | |||||||
chr4:47524639 | C | G | 8 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-918C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524639 | |||||||
chr4:47524724 | A | T | 1 | a0003c0004t0005g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.691-833A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524724 | |||||||
chr4:47524784 | T | A | 28 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(25): Show |
31 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.691-773T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524784 | |||||||
chr4:47524803 | C | T | 241 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(238): Show |
251 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.691-754C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524803 | |||||||
chr4:47524806 | C | T | 4 | a0003c0004t0005g0044 a0003c0004t0005g0203 a0003c0004t0005g0204 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-751C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524806 | |||||||
chr4:47524840 | TAAATC | T | 50 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(47): Show |
54 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.691-715_691-711del others(5): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 47524840 | ||||||
chr4:47524854 | T | G | 8 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-703T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47524854 | |||||||
chr4:47524899 | TATATC | T | 28 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(25): Show |
31 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.691-656_691-652del others(5): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 47524899 | ||||||
chr4:47525053 | A | G | 10 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(7): Show |
10 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.691-504A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525053 | |||||||
chr4:47525110 | T | G | 1 | a0001c0001t0003g0266 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.691-447T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525110 | |||||||
chr4:47525170 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.691-387G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525170 | |||||||
chr4:47525181 | A | G | 1 | a0012c0013t0008g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.691-376A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525181 | |||||||
chr4:47525248 | C | T | 3 | a0011c0020t0009g0188 a0011c0025t0009g0124 a0011c0025t0009g0127 |
3 | HG02257.hp2 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.691-309C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525248 | |||||||
chr4:47525356 | A | T | 80 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(77): Show |
85 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.691-201A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525356 | |||||||
chr4:47525389 | G | A | 1 | a0049c0057t0008g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-168G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525389 | |||||||
chr4:47525399 | A | G | 1 | a0003c0004t0007g0258 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.691-158A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525399 | |||||||
chr4:47525453 | A | G | 10 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(7): Show |
10 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.691-104A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525453 | |||||||
chr4:47525520 | T | G | 28 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(25): Show |
31 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.691-37T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 4/22 | chr4 | 47525520 | |||||||
chr4:47525654 | A | G | 12 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(9): Show |
13 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.776+12A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47525654 | |||||||
chr4:47525871 | C | T | 1 | a0003c0048t0006g0102 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.776+229C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47525871 | |||||||
chr4:47526260 | A | C | 2 | a0026c0024t0004g0069 a0026c0024t0004g0070 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.776+618A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526260 | |||||||
chr4:47526351 | T | C | 12 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(9): Show |
13 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.776+709T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526351 | |||||||
chr4:47526472 | A | T | 27 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(24): Show |
30 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.776+830A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526472 | |||||||
chr4:47526503 | A | G | 50 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(47): Show |
54 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.776+861A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526503 | |||||||
chr4:47526546 | G | A | 11 | a0010c0012t0006g0008 a0010c0012t0006g0065 a0010c0012t0006g0066 others(8): Show |
11 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.776+904G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526546 | |||||||
chr4:47526598 | A | G | 1 | a0004c0005t0007g0273 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.776+956A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526598 | |||||||
chr4:47526601 | G | A | 7 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(4): Show |
7 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.776+959G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526601 | |||||||
chr4:47526706 | G | A | 11 | a0004c0005t0005g0131 a0006c0007t0001g0006 a0006c0007t0001g0030 others(8): Show |
12 | HG00735.hp1 HG01081.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.776+1064G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526706 | |||||||
chr4:47526729 | G | T | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.776+1087G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526729 | |||||||
chr4:47526921 | A | G | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.776+1279A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526921 | |||||||
chr4:47526954 | C | A | 1 | a0043c0036t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.776+1312C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47526954 | |||||||
chr4:47527106 | T | C | 291 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(288): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.776+1464T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47527106 | |||||||
chr4:47527473 | C | T | 22 | a0001c0003t0001g0215 a0001c0003t0001g0289 a0002c0002t0001g0002 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.776+1831C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47527473 | |||||||
chr4:47527508 | G | A | 93 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(90): Show |
96 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.776+1866G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47527508 | |||||||
chr4:47527585 | G | A | 28 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(25): Show |
31 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.776+1943G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47527585 | |||||||
chr4:47527850 | A | G | 3 | a0006c0007t0001g0006 a0006c0007t0002g0221 a0006c0065t0001g0176 |
4 | HG02602.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+2208A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47527850 | |||||||
chr4:47528047 | A | G | 2 | a0015c0018t0010g0267 a0015c0018t0010g0302 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.776+2405A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528047 | |||||||
chr4:47528059 | C | T | 5 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(2): Show |
5 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.776+2417C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528059 | |||||||
chr4:47528332 | G | A | 12 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(9): Show |
13 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.776+2690G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528332 | |||||||
chr4:47528336 | G | T | 8 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.776+2694G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528336 | |||||||
chr4:47528458 | GGT | G | 13 | a0001c0001t0003g0232 a0001c0001t0003g0251 a0001c0001t0004g0105 others(10): Show |
13 | HG01099.hp1 HG02056.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.776+2871_776+2872d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528458 | GGTGT | G | 59 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0230 others(56): Show |
60 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.776+2869_776+2872d others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528458 | GGTGTGT | G | 62 | a0001c0001t0003g0222 a0001c0001t0003g0231 a0001c0001t0003g0253 others(59): Show |
65 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.776+2867_776+2872d others(8): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528458 | GGTGTGTG others(1): Show |
G | 18 | a0001c0001t0003g0241 a0001c0001t0004g0114 a0002c0002t0001g0026 others(15): Show |
18 | HG00280.hp1 HG00639.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.776+2865_776+2872d others(10): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528458 | GGTGTGTG others(3): Show |
G | 19 | a0001c0001t0004g0143 a0001c0003t0001g0059 a0001c0003t0001g0068 others(16): Show |
19 | HG00741.hp1 HG01168.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.776+2863_776+2872d others(12): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528458 | GGTGTGTG others(5): Show |
G | 3 | a0001c0003t0001g0004 a0005c0006t0001g0142 a0040c0053t0001g0173 |
4 | HG04184.hp1 NA18984.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.776+2861_776+2872d others(14): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528458 | GGTGTGTG others(7): Show |
G | 2 | a0013c0015t0005g0031 a0049c0057t0008g0120 |
2 | HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.776+2859_776+2872d others(16): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528458 | GGTGTGTG others(11): Show |
G | 8 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.776+2855_776+2872d others(20): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528458 | GGTGTGTG others(13): Show |
G | 2 | a0004c0005t0006g0133 a0009c0011t0001g0154 |
2 | NA19002.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.776+2853_776+2872d others(22): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528458 | GGTGTGTG others(15): Show |
G | 57 | a0004c0005t0005g0131 a0004c0005t0006g0007 a0004c0005t0006g0009 others(54): Show |
61 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.776+2851_776+2872d others(24): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528458 | ||||||
chr4:47528483 | GTGTGTGT others(27): Show |
G | 1 | a0002c0002t0002g0285 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.776+2843_776+2876d others(36): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528483 | ||||||
chr4:47528493 | GTGTGTGT others(15): Show |
G | 6 | a0004c0005t0005g0166 a0004c0005t0007g0015 a0006c0007t0001g0006 others(3): Show |
7 | HG00099.hp2 HG00408.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.776+2853_776+2874d others(24): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528493 | ||||||
chr4:47528493 | GTGTGTGT others(17): Show |
G | 1 | a0002c0002t0001g0199 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.776+2853_776+2876d others(26): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528493 | ||||||
chr4:47528495 | GTGTGTGT others(13): Show |
G | 4 | a0006c0007t0001g0039 a0006c0007t0001g0040 a0006c0007t0001g0042 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+2855_776+2874d others(22): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528495 | ||||||
chr4:47528495 | GTGTGTGT others(15): Show |
G | 4 | a0008c0010t0008g0010 a0011c0038t0005g0062 a0012c0013t0008g0125 others(1): Show |
5 | HG02258.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.776+2855_776+2876d others(24): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528495 | ||||||
chr4:47528497 | GTGTGTGT others(11): Show |
G | 1 | a0006c0007t0001g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.776+2857_776+2874d others(20): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528497 | ||||||
chr4:47528497 | GTGTGTGT others(13): Show |
G | 24 | a0001c0003t0001g0048 a0002c0002t0001g0118 a0002c0002t0001g0144 others(21): Show |
25 | HG00280.hp2 HG01123.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.776+2857_776+2876d others(22): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528497 | ||||||
chr4:47528497 | GTGTGTGT others(17): Show |
G | 7 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(4): Show |
7 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.776+2857_776+2880d others(26): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528497 | ||||||
chr4:47528501 | GTGTGTGT others(9): Show |
G | 11 | a0001c0003t0001g0018 a0001c0003t0001g0052 a0001c0003t0001g0215 others(8): Show |
13 | HG00323.hp1 HG00738.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.776+2861_776+2876d others(18): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528501 | ||||||
chr4:47528503 | GTGTGTGT others(7): Show |
G | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.776+2863_776+2876d others(16): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528503 | ||||||
chr4:47528505 | G | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.776+2863G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528505 | |||||||
chr4:47528505 | GTGTGTGT others(5): Show |
G | 1 | a0034c0058t0008g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.776+2865_776+2876d others(14): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528505 | ||||||
chr4:47528507 | G | A | 14 | a0001c0003t0001g0028 a0001c0003t0001g0108 a0003c0004t0005g0041 others(11): Show |
14 | HG01257.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.776+2865G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528507 | |||||||
chr4:47528507 | GTGTGTGT others(3): Show |
G | 3 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 |
3 | HG02886.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.776+2867_776+2876d others(12): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47528507 | ||||||
chr4:47528509 | G | A | 64 | a0001c0001t0003g0250 a0001c0001t0004g0082 a0001c0001t0004g0083 others(61): Show |
65 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.776+2867G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528509 | |||||||
chr4:47528511 | G | A | 159 | a0001c0001t0003g0013 a0001c0001t0003g0230 a0001c0001t0003g0232 others(156): Show |
164 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.776+2869G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528511 | |||||||
chr4:47528513 | G | A | 189 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(186): Show |
194 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.776+2871G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528513 | |||||||
chr4:47528526 | T | C | 13 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(10): Show |
14 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.776+2884T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528526 | |||||||
chr4:47528528 | T | C | 43 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0001c0003t0001g0048 others(40): Show |
47 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.776+2886T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528528 | |||||||
chr4:47528626 | G | A | 2 | a0003c0004t0005g0061 a0036c0047t0004g0060 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.776+2984G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528626 | |||||||
chr4:47528716 | G | A | 10 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(7): Show |
10 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.776+3074G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528716 | |||||||
chr4:47528741 | C | T | 2 | a0011c0020t0009g0115 a0011c0020t0009g0187 |
2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.776+3099C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528741 | |||||||
chr4:47528907 | G | A | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.776+3265G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528907 | |||||||
chr4:47528917 | C | G | 1 | a0033c0059t0001g0112 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.776+3275C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47528917 | |||||||
chr4:47529054 | A | G | 71 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(68): Show |
76 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.776+3412A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529054 | |||||||
chr4:47529186 | T | C | 1 | a0014c0017t0006g0157 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.776+3544T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529186 | |||||||
chr4:47529188 | G | A | 1 | a0001c0003t0001g0108 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.776+3546G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529188 | |||||||
chr4:47529212 | G | A | 12 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(9): Show |
13 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.776+3570G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529212 | |||||||
chr4:47529293 | A | G | 1 | a0001c0016t0002g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.776+3651A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529293 | |||||||
chr4:47529478 | A | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.776+3836A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529478 | |||||||
chr4:47529547 | T | C | 29 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(26): Show |
32 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.776+3905T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529547 | |||||||
chr4:47529671 | T | C | 28 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(25): Show |
31 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.776+4029T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529671 | |||||||
chr4:47529696 | T | C | 1 | a0004c0005t0005g0131 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.776+4054T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529696 | |||||||
chr4:47529706 | G | A | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.776+4064G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529706 | |||||||
chr4:47529837 | T | C | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.776+4195T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529837 | |||||||
chr4:47529944 | T | C | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.776+4302T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47529944 | |||||||
chr4:47530217 | G | A | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.776+4575G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47530217 | |||||||
chr4:47530222 | G | A | 1 | a0001c0001t0003g0287 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.776+4580G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47530222 | |||||||
chr4:47530262 | CT | C | 11 | a0010c0012t0006g0008 a0010c0012t0006g0065 a0010c0012t0006g0066 others(8): Show |
11 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.776+4627delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47530262 | ||||||
chr4:47530325 | C | T | 1 | a0002c0002t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.776+4683C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47530325 | |||||||
chr4:47530342 | T | A | 1 | a0002c0002t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.776+4700T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47530342 | |||||||
chr4:47530446 | TTTTG | T | 70 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(67): Show |
75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.776+4828_776+4831d others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47530446 | ||||||
chr4:47530451 | T | C | 1 | a0027c0040t0006g0291 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.776+4809T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47530451 | |||||||
chr4:47530474 | T | A | 2 | a0003c0004t0005g0044 a0013c0015t0005g0031 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.776+4832T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47530474 | |||||||
chr4:47530476 | C | T | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.776+4834C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47530476 | |||||||
chr4:47530747 | C | T | 16 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0254 others(13): Show |
18 | HG00408.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.777-4762C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47530747 | |||||||
chr4:47530806 | G | A | 3 | a0006c0007t0001g0156 a0006c0007t0001g0161 a0006c0007t0002g0233 |
3 | HG01952.hp1 HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.777-4703G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47530806 | |||||||
chr4:47531086 | A | AT | 162 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(159): Show |
166 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.777-4414dupT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47531086 | ||||||
chr4:47531114 | G | C | 1 | a0001c0001t0004g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.777-4395G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531114 | |||||||
chr4:47531237 | A | G | 1 | a0002c0002t0001g0144 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777-4272A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531237 | |||||||
chr4:47531291 | G | A | 27 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(24): Show |
30 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.777-4218G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531291 | |||||||
chr4:47531452 | A | G | 3 | a0011c0038t0005g0062 a0012c0013t0008g0125 a0012c0013t0008g0200 |
3 | HG02258.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.777-4057A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531452 | |||||||
chr4:47531470 | G | A | 1 | a0002c0002t0002g0011 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.777-4039G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531470 | |||||||
chr4:47531502 | A | C | 10 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(7): Show |
10 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.777-4007A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531502 | |||||||
chr4:47531552 | A | C | 23 | a0001c0003t0001g0215 a0001c0003t0001g0289 a0002c0002t0001g0002 others(20): Show |
26 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.777-3957A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531552 | |||||||
chr4:47531584 | G | A | 73 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(70): Show |
78 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.777-3925G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531584 | |||||||
chr4:47531606 | T | C | 8 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.777-3903T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531606 | |||||||
chr4:47531821 | C | T | 28 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(25): Show |
31 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.777-3688C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531821 | |||||||
chr4:47531888 | C | T | 3 | a0011c0025t0009g0124 a0011c0025t0009g0127 a0020c0064t0001g0309 |
3 | HG02257.hp2 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.777-3621C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47531888 | |||||||
chr4:47532070 | C | T | 1 | a0005c0006t0002g0270 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.777-3439C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532070 | |||||||
chr4:47532183 | A | T | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.777-3326A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532183 | |||||||
chr4:47532344 | A | T | 28 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(25): Show |
31 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.777-3165A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532344 | |||||||
chr4:47532372 | T | C | 44 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(41): Show |
48 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.777-3137T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532372 | |||||||
chr4:47532681 | C | T | 2 | a0011c0020t0009g0115 a0011c0020t0009g0187 |
2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.777-2828C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532681 | |||||||
chr4:47532711 | A | T | 1 | a0006c0007t0002g0233 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.777-2798A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532711 | |||||||
chr4:47532713 | G | A | 240 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(237): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.777-2796G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532713 | |||||||
chr4:47532735 | C | T | 2 | a0026c0024t0004g0069 a0026c0024t0004g0070 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.777-2774C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532735 | |||||||
chr4:47532944 | G | C | 11 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(8): Show |
11 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.777-2565G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532944 | |||||||
chr4:47532977 | G | A | 86 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(83): Show |
88 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.777-2532G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47532977 | |||||||
chr4:47533000 | G | T | 294 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(291): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.777-2509G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47533000 | |||||||
chr4:47533121 | A | T | 163 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(160): Show |
166 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.777-2388A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47533121 | |||||||
chr4:47533193 | G | A | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.777-2316G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47533193 | |||||||
chr4:47533200 | G | GA | 17 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(14): Show |
18 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.777-2299dupA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47533200 | ||||||
chr4:47533200 | GA | G | 25 | a0001c0003t0001g0028 a0002c0002t0001g0025 a0002c0002t0001g0026 others(22): Show |
25 | HG00558.hp2 HG00639.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.777-2299delA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47533200 | ||||||
chr4:47533388 | A | T | 2 | a0015c0018t0010g0267 a0015c0018t0010g0302 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.777-2121A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47533388 | |||||||
chr4:47533589 | G | A | 2 | a0001c0003t0001g0037 a0003c0004t0005g0057 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.777-1920G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47533589 | |||||||
chr4:47533768 | G | A | 2 | a0011c0041t0008g0214 a0015c0034t0012g0194 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.777-1741G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47533768 | |||||||
chr4:47533790 | A | G | 4 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-1719A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47533790 | |||||||
chr4:47533920 | C | T | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.777-1589C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47533920 | |||||||
chr4:47533977 | C | T | 1 | a0004c0005t0005g0131 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.777-1532C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47533977 | |||||||
chr4:47534506 | A | C | 2 | a0003c0004t0005g0061 a0036c0047t0004g0060 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.777-1003A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47534506 | |||||||
chr4:47534518 | C | G | 1 | a0005c0006t0002g0262 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.777-991C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47534518 | |||||||
chr4:47534549 | T | C | 181 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(178): Show |
186 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.777-960T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47534549 | |||||||
chr4:47534577 | C | A | 1 | a0012c0013t0008g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.777-932C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47534577 | |||||||
chr4:47534650 | C | G | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.777-859C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47534650 | |||||||
chr4:47534678 | C | T | 65 | a0004c0005t0005g0131 a0004c0005t0005g0166 a0004c0005t0006g0007 others(62): Show |
71 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.777-831C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47534678 | |||||||
chr4:47535011 | T | G | 6 | a0001c0001t0003g0237 a0001c0003t0002g0206 a0001c0003t0002g0236 others(3): Show |
6 | NA18961.hp2 NA18968.hp1 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.777-498T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47535011 | |||||||
chr4:47535091 | C | T | 2 | a0012c0013t0008g0125 a0012c0013t0008g0200 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.777-418C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47535091 | |||||||
chr4:47535106 | T | C | 22 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(19): Show |
23 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.777-403T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47535106 | |||||||
chr4:47535250 | A | G | 208 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(205): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.777-259A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47535250 | |||||||
chr4:47535289 | G | A | 1 | a0037c0060t0001g0308 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.777-220G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47535289 | |||||||
chr4:47535300 | A | C | 208 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(205): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.777-209A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47535300 | |||||||
chr4:47535317 | T | TA | 200 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(197): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.777-179dupA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47535317 | ||||||
chr4:47535317 | T | TAA | 6 | a0001c0001t0003g0254 a0001c0003t0001g0018 a0001c0003t0001g0048 others(3): Show |
6 | HG00408.hp2 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.777-180_777-179dup others(2): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 47535317 | ||||||
chr4:47535373 | T | C | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.777-136T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | chr4 | 47535373 | |||||||
chr4:47535804 | T | C | 7 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(4): Show |
7 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.884-98T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 6/22 | chr4 | 47535804 | |||||||
chr4:47536102 | T | C | 22 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(19): Show |
23 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1015+69T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/22 | chr4 | 47536102 | |||||||
chr4:47536218 | G | A | 2 | a0001c0003t0001g0004 a0001c0003t0001g0034 |
3 | HG02056.hp1 NA18984.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1015+185G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/22 | chr4 | 47536218 | |||||||
chr4:47536222 | T | C | 2 | a0011c0041t0008g0214 a0015c0034t0012g0194 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1015+189T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/22 | chr4 | 47536222 | |||||||
chr4:47536261 | A | AAG | 4 | a0004c0005t0007g0015 a0004c0005t0007g0277 a0008c0010t0008g0201 others(1): Show |
5 | HG00408.hp1 HG02135.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016-158_1016-157d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 47536261 | ||||||
chr4:47536261 | AAGAG | A | 3 | a0001c0003t0001g0028 a0002c0002t0001g0025 a0002c0002t0001g0026 |
3 | HG00639.hp1 HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1016-160_1016-157d others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 47536261 | ||||||
chr4:47536343 | T | C | 214 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(211): Show |
222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1016-94T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/22 | chr4 | 47536343 | |||||||
chr4:47536591 | A | C | 5 | a0001c0016t0002g0295 a0001c0016t0002g0296 a0001c0016t0002g0297 others(2): Show |
5 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+27A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 8/22 | chr4 | 47536591 | |||||||
chr4:47537053 | A | G | 1 | a0002c0002t0001g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1396+115A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537053 | |||||||
chr4:47537066 | A | T | 1 | a0001c0003t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1396+128A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537066 | |||||||
chr4:47537116 | G | C | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1396+178G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537116 | |||||||
chr4:47537186 | T | C | 11 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(8): Show |
12 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396+248T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537186 | |||||||
chr4:47537187 | G | A | 10 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(7): Show |
11 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396+249G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537187 | |||||||
chr4:47537203 | T | C | 10 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(7): Show |
11 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396+265T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537203 | |||||||
chr4:47537223 | C | T | 311 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1396+285C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537223 | |||||||
chr4:47537533 | A | G | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1396+595A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537533 | |||||||
chr4:47537563 | A | G | 1 | a0004c0005t0007g0277 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1396+625A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537563 | |||||||
chr4:47537685 | A | T | 2 | a0011c0041t0008g0214 a0015c0034t0012g0194 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1396+747A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537685 | |||||||
chr4:47537870 | G | A | 1 | a0007c0009t0002g0243 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1396+932G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47537870 | |||||||
chr4:47538081 | G | C | 239 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(236): Show |
248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1396+1143G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538081 | |||||||
chr4:47538170 | G | A | 309 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(306): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1396+1232G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538170 | |||||||
chr4:47538457 | C | G | 72 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(69): Show |
78 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1396+1519C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538457 | |||||||
chr4:47538489 | A | G | 26 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(23): Show |
27 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1396+1551A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538489 | |||||||
chr4:47538491 | C | G | 1 | a0001c0003t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1396+1553C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538491 | |||||||
chr4:47538492 | A | G | 100 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(97): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1396+1554A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538492 | |||||||
chr4:47538542 | T | C | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1396+1604T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538542 | |||||||
chr4:47538563 | A | C | 11 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(8): Show |
12 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396+1625A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538563 | |||||||
chr4:47538677 | G | A | 1 | a0020c0064t0001g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1396+1739G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538677 | |||||||
chr4:47538822 | T | C | 14 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1396+1884T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538822 | |||||||
chr4:47538908 | C | T | 1 | a0001c0003t0001g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1396+1970C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538908 | |||||||
chr4:47538935 | G | A | 2 | a0001c0003t0001g0310 a0003c0004t0005g0307 |
2 | HG01109.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1396+1997G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47538935 | |||||||
chr4:47539128 | A | T | 7 | a0001c0003t0002g0260 a0003c0004t0006g0138 a0007c0009t0001g0012 others(4): Show |
8 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396+2190A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47539128 | |||||||
chr4:47539162 | A | C | 5 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(2): Show |
5 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396+2224A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47539162 | |||||||
chr4:47539222 | G | A | 163 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(160): Show |
166 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.1396+2284G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47539222 | |||||||
chr4:47539338 | C | G | 12 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(9): Show |
13 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1396+2400C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47539338 | |||||||
chr4:47539448 | A | T | 1 | a0010c0012t0005g0067 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1396+2510A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47539448 | |||||||
chr4:47539701 | G | A | 6 | a0001c0001t0003g0250 a0001c0001t0003g0251 a0001c0001t0004g0083 others(3): Show |
6 | HG02015.hp2 NA18939.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396+2763G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47539701 | |||||||
chr4:47539832 | A | G | 66 | a0001c0003t0001g0004 a0004c0005t0005g0131 a0004c0005t0005g0166 others(63): Show |
73 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1396+2894A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47539832 | |||||||
chr4:47539886 | C | T | 5 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(2): Show |
5 | HG02559.hp2 HG02615.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396+2948C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47539886 | |||||||
chr4:47540018 | C | T | 1 | a0002c0002t0002g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1396+3080C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540018 | |||||||
chr4:47540143 | A | G | 220 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(217): Show |
227 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1396+3205A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540143 | |||||||
chr4:47540254 | C | T | 231 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(228): Show |
239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1396+3316C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540254 | |||||||
chr4:47540335 | A | G | 4 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+3397A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540335 | |||||||
chr4:47540393 | C | T | 2 | a0011c0041t0008g0214 a0015c0034t0012g0194 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1396+3455C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540393 | |||||||
chr4:47540395 | C | T | 2 | a0005c0006t0001g0032 a0005c0006t0001g0219 |
2 | HG03831.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1396+3457C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540395 | |||||||
chr4:47540412 | T | A | 79 | a0001c0003t0001g0004 a0001c0003t0001g0037 a0001c0016t0002g0295 others(76): Show |
86 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1396+3474T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540412 | |||||||
chr4:47540500 | C | A | 180 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(177): Show |
185 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1396+3562C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540500 | |||||||
chr4:47540629 | G | A | 3 | a0011c0038t0005g0062 a0012c0013t0008g0125 a0012c0013t0008g0200 |
3 | HG02258.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1396+3691G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540629 | |||||||
chr4:47540772 | C | G | 1 | a0002c0008t0001g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1396+3834C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540772 | |||||||
chr4:47540775 | G | C | 2 | a0004c0005t0005g0131 a0006c0007t0001g0030 |
2 | HG00735.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1396+3837G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47540775 | |||||||
chr4:47541222 | CTGT | C | 4 | a0001c0003t0001g0037 a0003c0004t0005g0057 a0011c0020t0009g0115 others(1): Show |
4 | HG02572.hp2 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+4297_1396+429 others(7): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47541222 | ||||||
chr4:47541289 | G | A | 2 | a0003c0004t0005g0061 a0036c0047t0004g0060 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1396+4351G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47541289 | |||||||
chr4:47541397 | A | C | 22 | a0001c0003t0001g0215 a0001c0003t0001g0289 a0002c0002t0001g0002 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1396+4459A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47541397 | |||||||
chr4:47541629 | T | G | 10 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(7): Show |
10 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1396+4691T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47541629 | |||||||
chr4:47541640 | A | G | 90 | a0001c0003t0001g0037 a0001c0016t0002g0295 a0001c0016t0002g0296 others(87): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1396+4702A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47541640 | |||||||
chr4:47541778 | A | T | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1396+4840A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47541778 | |||||||
chr4:47541829 | C | T | 1 | a0003c0004t0005g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1397-4795C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47541829 | |||||||
chr4:47541830 | G | T | 11 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(8): Show |
11 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1397-4794G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47541830 | |||||||
chr4:47541874 | T | C | 175 | a0001c0003t0001g0018 a0001c0003t0001g0028 a0001c0003t0001g0037 others(172): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1397-4750T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47541874 | |||||||
chr4:47541995 | C | T | 177 | a0001c0003t0001g0018 a0001c0003t0001g0028 a0001c0003t0001g0037 others(174): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1397-4629C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47541995 | |||||||
chr4:47542100 | A | ACAATATA others(333): Show |
1 | a0005c0014t0004g0058 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(344): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(315): Show |
1 | a0005c0014t0004g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(326): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(333): Show |
1 | a0002c0008t0002g0265 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(344): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(334): Show |
1 | a0003c0004t0005g0169 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(345): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(335): Show |
2 | a0005c0014t0004g0051 a0044c0045t0006g0049 |
2 | HG02071.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(346): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(336): Show |
1 | a0005c0014t0004g0054 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(347): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(334): Show |
4 | a0001c0003t0001g0028 a0002c0002t0001g0026 a0005c0006t0001g0101 others(1): Show |
4 | HG00639.hp1 HG02300.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(345): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(335): Show |
5 | a0002c0002t0001g0107 a0005c0006t0001g0055 a0005c0006t0001g0098 others(2): Show |
5 | HG03942.hp1 NA18999.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(346): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(336): Show |
2 | a0003c0004t0005g0203 a0005c0006t0001g0113 |
2 | HG01884.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(347): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(317): Show |
1 | a0005c0006t0002g0270 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(328): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(331): Show |
2 | a0008c0010t0008g0201 a0008c0010t0008g0208 |
2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(342): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(332): Show |
2 | a0008c0010t0008g0209 a0008c0010t0008g0210 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(343): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(333): Show |
5 | a0005c0006t0002g0262 a0008c0010t0008g0193 a0008c0010t0008g0213 others(2): Show |
5 | HG01255.hp1 HG01891.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(344): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(334): Show |
3 | a0002c0002t0001g0027 a0015c0018t0010g0283 a0015c0018t0010g0302 |
3 | HG01069.hp1 HG03239.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(345): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(334): Show |
1 | a0016c0019t0004g0023 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(345): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(335): Show |
4 | a0002c0002t0001g0025 a0003c0004t0005g0204 a0015c0018t0010g0267 others(1): Show |
4 | HG01071.hp1 HG01433.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(346): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(335): Show |
1 | a0016c0019t0004g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(346): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(336): Show |
1 | a0003c0004t0005g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(347): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(331): Show |
1 | a0008c0010t0008g0212 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1397-4516_1397-451 others(342): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542100 | A | ACAATATA others(332): Show |
1 | a0008c0010t0008g0010 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1397-4516_1397-451 others(343): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47542100 | ||||||
chr4:47542131 | C | G | 9 | a0011c0038t0005g0062 a0012c0013t0008g0125 a0012c0013t0008g0200 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1397-4493C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542131 | |||||||
chr4:47542253 | C | T | 2 | a0001c0031t0002g0192 a0005c0006t0002g0270 |
2 | NA19056.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1397-4371C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542253 | |||||||
chr4:47542379 | A | G | 245 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(242): Show |
251 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.1397-4245A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542379 | |||||||
chr4:47542464 | A | G | 105 | a0001c0003t0001g0108 a0001c0003t0001g0215 a0001c0003t0001g0289 others(102): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1397-4160A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542464 | |||||||
chr4:47542509 | T | C | 8 | a0001c0001t0004g0082 a0001c0003t0001g0073 a0001c0003t0001g0177 others(5): Show |
8 | HG00642.hp1 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1397-4115T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542509 | |||||||
chr4:47542521 | A | C | 5 | a0001c0003t0001g0037 a0002c0002t0001g0025 a0002c0002t0001g0136 others(2): Show |
5 | HG01255.hp2 HG01261.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1397-4103A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542521 | |||||||
chr4:47542581 | A | G | 9 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(6): Show |
9 | HG02258.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1397-4043A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542581 | |||||||
chr4:47542603 | T | G | 3 | a0003c0004t0005g0041 a0011c0038t0005g0062 a0019c0021t0009g0071 |
3 | HG02258.hp2 HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1397-4021T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542603 | |||||||
chr4:47542615 | T | C | 71 | a0001c0001t0003g0217 a0001c0001t0003g0222 a0001c0001t0003g0230 others(68): Show |
73 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1397-4009T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542615 | |||||||
chr4:47542622 | T | C | 263 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(260): Show |
276 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1397-4002T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542622 | |||||||
chr4:47542649 | G | T | 312 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(309): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1397-3975G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542649 | |||||||
chr4:47542668 | G | A | 3 | a0011c0038t0005g0062 a0012c0013t0008g0125 a0012c0013t0008g0200 |
3 | HG02258.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1397-3956G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542668 | |||||||
chr4:47542730 | C | T | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1397-3894C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542730 | |||||||
chr4:47542930 | C | T | 83 | a0001c0001t0003g0257 a0001c0003t0001g0108 a0001c0003t0002g0260 others(80): Show |
89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1397-3694C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542930 | |||||||
chr4:47542966 | A | T | 1 | a0005c0006t0001g0086 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1397-3658A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542966 | |||||||
chr4:47542977 | T | C | 2 | a0009c0011t0001g0167 a0010c0012t0009g0312 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1397-3647T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47542977 | |||||||
chr4:47543111 | A | G | 170 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(167): Show |
177 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.1397-3513A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543111 | |||||||
chr4:47543124 | C | A | 73 | a0001c0003t0001g0018 a0001c0003t0001g0048 a0001c0003t0001g0052 others(70): Show |
74 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1397-3500C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543124 | |||||||
chr4:47543128 | A | G | 3 | a0011c0038t0005g0062 a0012c0013t0008g0125 a0012c0013t0008g0200 |
3 | HG02258.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1397-3496A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543128 | |||||||
chr4:47543156 | T | A | 2 | a0003c0004t0005g0092 a0003c0004t0005g0096 |
2 | HG02040.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1397-3468T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543156 | |||||||
chr4:47543158 | A | T | 2 | a0003c0004t0005g0092 a0003c0004t0005g0096 |
2 | HG02040.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1397-3466A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543158 | |||||||
chr4:47543164 | T | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1397-3460T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543164 | |||||||
chr4:47543264 | G | A | 248 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(245): Show |
259 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1397-3360G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543264 | |||||||
chr4:47543298 | T | C | 9 | a0001c0003t0001g0004 a0009c0011t0001g0081 a0009c0011t0001g0134 others(6): Show |
10 | NA18612.hp1 NA18968.hp2 NA18983.hp1 others(7): Show |
intron_variant | MODIFIER | c.1397-3326T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543298 | |||||||
chr4:47543304 | C | A | 3 | a0006c0007t0001g0156 a0006c0007t0001g0161 a0006c0007t0002g0233 |
3 | HG01952.hp1 HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1397-3320C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543304 | |||||||
chr4:47543358 | G | A | 267 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(264): Show |
278 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.1397-3266G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543358 | |||||||
chr4:47543534 | A | G | 82 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(79): Show |
88 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1397-3090A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543534 | |||||||
chr4:47543599 | T | C | 79 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(76): Show |
85 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1397-3025T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543599 | |||||||
chr4:47543637 | G | T | 3 | a0011c0038t0005g0062 a0012c0013t0008g0125 a0012c0013t0008g0200 |
3 | HG02258.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1397-2987G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543637 | |||||||
chr4:47543698 | A | G | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-2926A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543698 | |||||||
chr4:47543764 | G | A | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-2860G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543764 | |||||||
chr4:47543795 | T | C | 8 | a0002c0008t0001g0141 a0002c0008t0001g0145 a0002c0008t0001g0146 others(5): Show |
8 | HG01123.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1397-2829T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543795 | |||||||
chr4:47543834 | TGTAC | T | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-2789_1397-278 others(8): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47543834 | |||||||
chr4:47543836 | T | TAC | 86 | a0001c0003t0001g0004 a0001c0003t0001g0018 a0001c0003t0001g0048 others(83): Show |
88 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1397-2772_1397-277 others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47543836 | ||||||
chr4:47544044 | TA | T | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-2575delA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47544044 | ||||||
chr4:47544154 | T | C | 8 | a0007c0009t0001g0012 a0007c0009t0001g0088 a0007c0009t0001g0097 others(5): Show |
9 | HG00438.hp2 HG00673.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.1397-2470T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544154 | |||||||
chr4:47544247 | C | T | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1397-2377C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544247 | |||||||
chr4:47544368 | C | G | 2 | a0025c0026t0009g0189 a0025c0026t0009g0190 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1397-2256C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544368 | |||||||
chr4:47544396 | G | A | 1 | a0043c0036t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1397-2228G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544396 | |||||||
chr4:47544531 | G | T | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1397-2093G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544531 | |||||||
chr4:47544751 | C | T | 286 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1397-1873C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544751 | |||||||
chr4:47544819 | A | G | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-1805A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544819 | |||||||
chr4:47544883 | C | T | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-1741C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544883 | |||||||
chr4:47544892 | C | T | 2 | a0034c0058t0008g0075 a0043c0036t0005g0184 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1397-1732C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544892 | |||||||
chr4:47544919 | C | T | 3 | a0007c0009t0001g0093 a0007c0009t0001g0094 a0007c0009t0001g0095 |
3 | NA18946.hp1 NA18990.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1397-1705C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544919 | |||||||
chr4:47544988 | T | A | 3 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 |
3 | HG02886.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1397-1636T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47544988 | |||||||
chr4:47545034 | T | C | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-1590T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47545034 | |||||||
chr4:47545132 | G | A | 3 | a0007c0009t0002g0036 a0007c0009t0002g0224 a0007c0009t0002g0243 |
3 | NA18953.hp2 NA18983.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1397-1492G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47545132 | |||||||
chr4:47545593 | TAAGA | T | 79 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(76): Show |
85 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1397-1025_1397-102 others(8): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47545593 | ||||||
chr4:47545664 | G | C | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1397-960G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47545664 | |||||||
chr4:47545800 | T | G | 1 | a0001c0001t0003g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1397-824T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47545800 | |||||||
chr4:47546220 | A | G | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-404A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47546220 | |||||||
chr4:47546237 | A | G | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-387A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47546237 | |||||||
chr4:47546333 | G | T | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1397-291G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47546333 | |||||||
chr4:47546337 | C | CAAAG | 286 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1397-286_1397-285i others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 47546337 | ||||||
chr4:47546374 | G | A | 1 | a0001c0016t0002g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1397-250G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47546374 | |||||||
chr4:47546414 | C | T | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-210C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47546414 | |||||||
chr4:47546425 | G | A | 1 | a0013c0015t0009g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1397-199G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | 47546425 | |||||||
chr4:47546937 | G | A | 1 | a0005c0006t0002g0244 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1635+75G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47546937 | |||||||
chr4:47546967 | G | A | 1 | a0005c0006t0002g0244 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1635+105G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47546967 | |||||||
chr4:47547090 | G | GA | 26 | a0002c0002t0001g0002 a0002c0002t0001g0025 a0002c0002t0001g0026 others(23): Show |
29 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1635+239dupA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 47547090 | ||||||
chr4:47547090 | GA | G | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1635+239delA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 47547090 | ||||||
chr4:47547103 | G | T | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1635+241G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547103 | |||||||
chr4:47547412 | G | A | 7 | a0009c0011t0001g0081 a0009c0011t0001g0134 a0009c0011t0001g0153 others(4): Show |
7 | NA18612.hp1 NA18968.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1635+550G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547412 | |||||||
chr4:47547415 | C | T | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1635+553C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547415 | |||||||
chr4:47547491 | G | A | 2 | a0034c0058t0008g0075 a0043c0036t0005g0184 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1635+629G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547491 | |||||||
chr4:47547511 | A | G | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+649A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547511 | |||||||
chr4:47547559 | A | G | 3 | a0003c0004t0005g0085 a0003c0004t0005g0089 a0003c0004t0005g0090 |
3 | HG02559.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1635+697A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547559 | |||||||
chr4:47547656 | C | CAT | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+795_1635+796i others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 47547656 | ||||||
chr4:47547665 | T | C | 2 | a0001c0003t0001g0073 a0001c0003t0001g0177 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1635+803T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547665 | |||||||
chr4:47547677 | G | A | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1635+815G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547677 | |||||||
chr4:47547688 | A | G | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+826A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547688 | |||||||
chr4:47547703 | A | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1635+841A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547703 | |||||||
chr4:47547710 | A | G | 1 | a0003c0004t0006g0138 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1635+848A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547710 | |||||||
chr4:47547781 | A | G | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+919A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547781 | |||||||
chr4:47547965 | G | A | 2 | a0034c0058t0008g0075 a0043c0036t0005g0184 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1635+1103G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547965 | |||||||
chr4:47547983 | G | A | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+1121G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47547983 | |||||||
chr4:47548005 | G | A | 1 | a0032c0056t0001g0064 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1635+1143G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548005 | |||||||
chr4:47548034 | C | G | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1635+1172C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548034 | |||||||
chr4:47548035 | G | A | 99 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(96): Show |
103 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1635+1173G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548035 | |||||||
chr4:47548116 | G | A | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+1254G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548116 | |||||||
chr4:47548154 | A | ATTAAGCT others(4): Show |
1 | a0004c0005t0006g0149 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1635+1293_1635+129 others(15): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 47548154 | ||||||
chr4:47548302 | C | T | 1 | a0005c0014t0003g0246 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1635+1440C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548302 | |||||||
chr4:47548427 | C | G | 1 | a0001c0001t0003g0253 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1635+1565C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548427 | |||||||
chr4:47548429 | C | T | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1635+1567C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548429 | |||||||
chr4:47548466 | T | A | 1 | a0014c0017t0006g0160 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1635+1604T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548466 | |||||||
chr4:47548535 | A | G | 3 | a0004c0005t0006g0133 a0017c0022t0001g0151 a0017c0022t0001g0152 |
3 | HG01099.hp2 HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1635+1673A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548535 | |||||||
chr4:47548551 | T | C | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+1689T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548551 | |||||||
chr4:47548624 | C | A | 1 | a0005c0006t0001g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1635+1762C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548624 | |||||||
chr4:47548683 | T | G | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+1821T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548683 | |||||||
chr4:47548757 | T | C | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+1895T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548757 | |||||||
chr4:47548803 | A | G | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+1941A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548803 | |||||||
chr4:47548805 | A | C | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1635+1943A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548805 | |||||||
chr4:47548809 | T | C | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1635+1947T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548809 | |||||||
chr4:47548853 | C | T | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1635+1991C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548853 | |||||||
chr4:47548854 | A | G | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+1992A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47548854 | |||||||
chr4:47549144 | G | A | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+2282G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549144 | |||||||
chr4:47549169 | A | G | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+2307A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549169 | |||||||
chr4:47549221 | C | T | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+2359C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549221 | |||||||
chr4:47549246 | G | A | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+2384G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549246 | |||||||
chr4:47549408 | T | C | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+2546T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549408 | |||||||
chr4:47549619 | T | C | 2 | a0026c0024t0004g0069 a0026c0024t0004g0070 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1635+2757T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549619 | |||||||
chr4:47549764 | G | T | 1 | a0010c0012t0009g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1635+2902G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549764 | |||||||
chr4:47549784 | G | A | 2 | a0010c0012t0006g0065 a0010c0012t0006g0066 |
2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1635+2922G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549784 | |||||||
chr4:47549846 | T | G | 78 | a0001c0001t0003g0253 a0001c0003t0001g0004 a0002c0008t0001g0016 others(75): Show |
80 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1635+2984T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549846 | |||||||
chr4:47549905 | A | G | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+3043A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549905 | |||||||
chr4:47549910 | G | A | 81 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+3048G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47549910 | |||||||
chr4:47549950 | CT | C | 24 | a0001c0003t0002g0238 a0003c0004t0005g0169 a0003c0004t0005g0205 others(21): Show |
26 | HG00408.hp1 HG01255.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1635+3105delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 47549950 | ||||||
chr4:47549950 | CTT | C | 83 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(80): Show |
85 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1635+3104_1635+310 others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 47549950 | ||||||
chr4:47549950 | CTTT | C | 8 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1635+3103_1635+310 others(7): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 47549950 | ||||||
chr4:47550093 | A | G | 287 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(284): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1635+3231A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550093 | |||||||
chr4:47550095 | C | T | 1 | a0003c0004t0010g0235 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1635+3233C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550095 | |||||||
chr4:47550181 | A | G | 15 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(12): Show |
16 | HG01255.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1635+3319A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550181 | |||||||
chr4:47550233 | A | G | 1 | a0005c0006t0001g0100 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1635+3371A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550233 | |||||||
chr4:47550242 | T | G | 1 | a0001c0003t0001g0116 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1635+3380T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550242 | |||||||
chr4:47550395 | T | C | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1635+3533T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550395 | |||||||
chr4:47550489 | G | T | 1 | a0011c0020t0009g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1635+3627G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550489 | |||||||
chr4:47550530 | G | T | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1635+3668G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550530 | |||||||
chr4:47550612 | G | A | 82 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(79): Show |
88 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1635+3750G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550612 | |||||||
chr4:47550644 | G | A | 1 | a0004c0005t0005g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1635+3782G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550644 | |||||||
chr4:47550672 | T | C | 3 | a0002c0002t0001g0050 a0002c0002t0001g0144 a0002c0002t0001g0163 |
3 | HG03942.hp2 HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1635+3810T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550672 | |||||||
chr4:47550680 | G | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1635+3818G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550680 | |||||||
chr4:47550719 | A | G | 2 | a0005c0006t0001g0219 a0005c0006t0002g0306 |
2 | HG00099.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1635+3857A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550719 | |||||||
chr4:47550745 | A | G | 84 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(81): Show |
90 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1635+3883A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550745 | |||||||
chr4:47550762 | A | G | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1635+3900A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550762 | |||||||
chr4:47550817 | G | A | 1 | a0014c0017t0006g0160 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1636-3909G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550817 | |||||||
chr4:47550947 | A | G | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1636-3779A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550947 | |||||||
chr4:47550956 | C | T | 1 | a0005c0006t0001g0100 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1636-3770C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47550956 | |||||||
chr4:47551039 | C | T | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1636-3687C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551039 | |||||||
chr4:47551043 | C | G | 83 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(80): Show |
89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1636-3683C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551043 | |||||||
chr4:47551230 | C | T | 1 | a0010c0012t0009g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1636-3496C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551230 | |||||||
chr4:47551302 | A | G | 1 | a0009c0011t0001g0158 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1636-3424A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551302 | |||||||
chr4:47551468 | G | A | 1 | a0008c0010t0008g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1636-3258G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551468 | |||||||
chr4:47551471 | A | G | 1 | a0006c0007t0001g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1636-3255A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551471 | |||||||
chr4:47551604 | G | A | 1 | a0011c0038t0005g0062 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1636-3122G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551604 | |||||||
chr4:47551655 | G | A | 8 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1636-3071G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551655 | |||||||
chr4:47551896 | C | A | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1636-2830C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551896 | |||||||
chr4:47551901 | C | T | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1636-2825C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551901 | |||||||
chr4:47551957 | A | C | 286 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1636-2769A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551957 | |||||||
chr4:47551985 | G | A | 1 | a0026c0024t0004g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1636-2741G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47551985 | |||||||
chr4:47552216 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1636-2510G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552216 | |||||||
chr4:47552251 | C | T | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1636-2475C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552251 | |||||||
chr4:47552315 | A | G | 83 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(80): Show |
89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1636-2411A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552315 | |||||||
chr4:47552316 | G | A | 3 | a0011c0038t0005g0062 a0012c0013t0008g0125 a0012c0013t0008g0200 |
3 | HG02258.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1636-2410G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552316 | |||||||
chr4:47552328 | A | G | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1636-2398A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552328 | |||||||
chr4:47552333 | C | T | 1 | a0034c0058t0008g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1636-2393C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552333 | |||||||
chr4:47552338 | T | G | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1636-2388T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552338 | |||||||
chr4:47552371 | G | T | 99 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(96): Show |
102 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.1636-2355G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552371 | |||||||
chr4:47552471 | T | A | 76 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(73): Show |
77 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1636-2255T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552471 | |||||||
chr4:47552767 | A | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1636-1959A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552767 | |||||||
chr4:47552786 | C | T | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1636-1940C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552786 | |||||||
chr4:47552920 | G | A | 1 | a0046c0066t0007g0276 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1636-1806G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552920 | |||||||
chr4:47552977 | A | C | 1 | a0049c0057t0008g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1636-1749A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47552977 | |||||||
chr4:47553040 | T | C | 1 | a0001c0001t0004g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1636-1686T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553040 | |||||||
chr4:47553179 | T | C | 287 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(284): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1636-1547T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553179 | |||||||
chr4:47553375 | A | G | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1636-1351A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553375 | |||||||
chr4:47553403 | T | C | 2 | a0005c0006t0001g0099 a0005c0006t0001g0101 |
2 | NA19005.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1636-1323T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553403 | |||||||
chr4:47553528 | T | G | 1 | a0006c0007t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1636-1198T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553528 | |||||||
chr4:47553561 | A | G | 2 | a0025c0026t0009g0189 a0025c0026t0009g0190 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1636-1165A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553561 | |||||||
chr4:47553604 | G | T | 9 | a0001c0003t0001g0037 a0011c0020t0009g0115 a0011c0020t0009g0187 others(6): Show |
9 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1636-1122G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553604 | |||||||
chr4:47553676 | T | A | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1636-1050T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553676 | |||||||
chr4:47553682 | G | C | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1636-1044G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553682 | |||||||
chr4:47553864 | T | C | 2 | a0015c0018t0010g0267 a0015c0018t0010g0302 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1636-862T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47553864 | |||||||
chr4:47554054 | C | T | 1 | a0011c0020t0009g0188 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1636-672C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47554054 | |||||||
chr4:47554057 | G | A | 1 | a0019c0021t0009g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1636-669G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47554057 | |||||||
chr4:47554287 | A | G | 83 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(80): Show |
89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1636-439A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47554287 | |||||||
chr4:47554359 | G | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1636-367G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47554359 | |||||||
chr4:47554577 | C | T | 8 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1636-149C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47554577 | |||||||
chr4:47554650 | A | C | 3 | a0001c0031t0002g0192 a0024c0028t0008g0119 a0024c0028t0008g0202 |
3 | HG01891.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1636-76A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47554650 | |||||||
chr4:47554684 | A | G | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1636-42A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 10/22 | chr4 | 47554684 | |||||||
chr4:47555080 | T | A | 1 | a0034c0058t0008g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1824+166T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555080 | |||||||
chr4:47555105 | G | A | 9 | a0008c0010t0008g0193 a0008c0010t0008g0201 a0008c0010t0008g0208 others(6): Show |
9 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1824+191G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555105 | |||||||
chr4:47555112 | G | A | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1824+198G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555112 | |||||||
chr4:47555237 | C | T | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1824+323C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555237 | |||||||
chr4:47555238 | G | A | 1 | a0003c0004t0005g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1824+324G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555238 | |||||||
chr4:47555238 | G | C | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1824+324G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555238 | |||||||
chr4:47555352 | G | A | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1824+438G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555352 | |||||||
chr4:47555361 | T | G | 1 | a0036c0047t0004g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1824+447T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555361 | |||||||
chr4:47555383 | G | A | 10 | a0001c0003t0001g0037 a0011c0020t0009g0115 a0011c0020t0009g0187 others(7): Show |
10 | HG02257.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1824+469G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555383 | |||||||
chr4:47555417 | G | A | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1824+503G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555417 | |||||||
chr4:47555437 | T | A | 78 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(75): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1824+523T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555437 | |||||||
chr4:47555468 | A | T | 286 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1824+554A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555468 | |||||||
chr4:47555577 | G | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1824+663G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555577 | |||||||
chr4:47555591 | A | G | 1 | a0037c0060t0001g0308 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1824+677A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555591 | |||||||
chr4:47555716 | C | T | 5 | a0001c0003t0001g0020 a0001c0003t0001g0073 a0001c0003t0001g0177 others(2): Show |
5 | HG03453.hp1 HG03516.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1824+802C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555716 | |||||||
chr4:47555774 | G | A | 1 | a0001c0003t0002g0286 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1824+860G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555774 | |||||||
chr4:47555815 | G | A | 1 | a0001c0001t0003g0281 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1824+901G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555815 | |||||||
chr4:47555840 | A | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1824+926A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555840 | |||||||
chr4:47555883 | T | A | 287 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(284): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1824+969T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555883 | |||||||
chr4:47555976 | A | T | 3 | a0005c0006t0001g0142 a0005c0006t0002g0244 a0005c0044t0002g0249 |
3 | HG02027.hp2 NA18949.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1824+1062A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555976 | |||||||
chr4:47555991 | C | T | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1824+1077C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47555991 | |||||||
chr4:47556051 | A | G | 286 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1824+1137A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47556051 | |||||||
chr4:47556115 | A | G | 174 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(171): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.1824+1201A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47556115 | |||||||
chr4:47556137 | C | T | 101 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(98): Show |
108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1824+1223C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47556137 | |||||||
chr4:47556154 | A | G | 1 | a0001c0001t0003g0300 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1824+1240A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47556154 | |||||||
chr4:47556185 | C | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1824+1271C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47556185 | |||||||
chr4:47556191 | C | T | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1824+1277C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47556191 | |||||||
chr4:47556265 | G | A | 1 | a0006c0007t0001g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1824+1351G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47556265 | |||||||
chr4:47556440 | A | C | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1825-1224A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47556440 | |||||||
chr4:47556549 | A | G | 2 | a0002c0002t0001g0122 a0002c0002t0001g0292 |
2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1825-1115A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47556549 | |||||||
chr4:47557103 | T | C | 1 | a0001c0003t0001g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1825-561T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47557103 | |||||||
chr4:47557149 | C | T | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1825-515C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47557149 | |||||||
chr4:47557245 | A | C | 185 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(182): Show |
190 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1825-419A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47557245 | |||||||
chr4:47557277 | T | A | 9 | a0001c0003t0001g0037 a0011c0020t0009g0115 a0011c0020t0009g0187 others(6): Show |
9 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1825-387T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 11/22 | chr4 | 47557277 | |||||||
chr4:47558322 | T | C | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2434+49T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/22 | chr4 | 47558322 | |||||||
chr4:47558369 | C | T | 101 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(98): Show |
108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.2434+96C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/22 | chr4 | 47558369 | |||||||
chr4:47558386 | T | C | 76 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(73): Show |
79 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.2434+113T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/22 | chr4 | 47558386 | |||||||
chr4:47558534 | A | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2434+261A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/22 | chr4 | 47558534 | |||||||
chr4:47558681 | G | A | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.2435-242G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/22 | chr4 | 47558681 | |||||||
chr4:47558842 | A | C | 25 | a0002c0002t0001g0002 a0002c0002t0001g0025 a0002c0002t0001g0026 others(22): Show |
28 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2435-81A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/22 | chr4 | 47558842 | |||||||
chr4:47558853 | A | C | 2 | a0004c0005t0005g0063 a0004c0005t0005g0166 |
2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.2435-70A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/22 | chr4 | 47558853 | |||||||
chr4:47558894 | G | A | 1 | a0008c0010t0017g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2435-29G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 12/22 | chr4 | 47558894 | |||||||
chr4:47559047 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2541+18G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559047 | |||||||
chr4:47559099 | G | C | 2 | a0004c0005t0005g0063 a0004c0005t0005g0166 |
2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.2541+70G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559099 | |||||||
chr4:47559124 | G | A | 102 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(99): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.2541+95G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559124 | |||||||
chr4:47559162 | C | T | 102 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(99): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.2541+133C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559162 | |||||||
chr4:47559247 | T | C | 1 | a0001c0001t0003g0231 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2541+218T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559247 | |||||||
chr4:47559393 | G | A | 1 | a0003c0004t0006g0033 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2541+364G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559393 | |||||||
chr4:47559459 | C | T | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2541+430C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559459 | |||||||
chr4:47559503 | T | C | 1 | a0003c0004t0006g0138 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2541+474T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559503 | |||||||
chr4:47559703 | C | T | 1 | a0009c0011t0001g0158 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2541+674C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559703 | |||||||
chr4:47559718 | A | G | 15 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(12): Show |
16 | HG01255.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2541+689A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47559718 | |||||||
chr4:47560180 | G | A | 177 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.2542-769G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560180 | |||||||
chr4:47560232 | T | G | 1 | a0036c0047t0004g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2542-717T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560232 | |||||||
chr4:47560357 | T | C | 1 | a0037c0060t0001g0308 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2542-592T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560357 | |||||||
chr4:47560360 | T | G | 10 | a0001c0003t0001g0037 a0011c0020t0009g0115 a0011c0020t0009g0187 others(7): Show |
10 | HG02257.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2542-589T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560360 | |||||||
chr4:47560396 | A | G | 1 | a0022c0027t0011g0198 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2542-553A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560396 | |||||||
chr4:47560521 | A | C | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.2542-428A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560521 | |||||||
chr4:47560634 | A | G | 1 | a0008c0010t0008g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2542-315A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560634 | |||||||
chr4:47560785 | G | GC | 75 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(72): Show |
76 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.2542-163dupC | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 47560785 | ||||||
chr4:47560803 | T | C | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.2542-146T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560803 | |||||||
chr4:47560815 | T | C | 2 | a0003c0004t0005g0139 a0003c0004t0005g0140 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2542-134T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560815 | |||||||
chr4:47560882 | G | A | 15 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(12): Show |
16 | HG01255.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2542-67G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560882 | |||||||
chr4:47560907 | C | T | 2 | a0011c0041t0008g0214 a0049c0057t0008g0120 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2542-42C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 13/22 | chr4 | 47560907 | |||||||
chr4:47561175 | T | C | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2668+100T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561175 | |||||||
chr4:47561322 | C | T | 1 | a0003c0004t0010g0235 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2668+247C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561322 | |||||||
chr4:47561426 | T | C | 2 | a0001c0001t0003g0279 a0001c0001t0003g0280 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2668+351T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561426 | |||||||
chr4:47561428 | C | T | 84 | a0001c0003t0001g0048 a0001c0003t0001g0052 a0002c0002t0001g0107 others(81): Show |
90 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.2668+353C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561428 | |||||||
chr4:47561431 | G | A | 75 | a0002c0008t0001g0016 a0002c0008t0001g0019 a0002c0008t0001g0126 others(72): Show |
76 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.2668+356G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561431 | |||||||
chr4:47561466 | A | G | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.2668+391A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561466 | |||||||
chr4:47561498 | A | C | 1 | a0002c0008t0001g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2668+423A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561498 | |||||||
chr4:47561504 | A | G | 1 | a0001c0001t0003g0253 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2668+429A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561504 | |||||||
chr4:47561521 | A | G | 1 | a0013c0015t0009g0288 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2668+446A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561521 | |||||||
chr4:47561543 | C | G | 1 | a0013c0015t0009g0288 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2668+468C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561543 | |||||||
chr4:47561792 | T | A | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2668+717T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561792 | |||||||
chr4:47561835 | G | C | 1 | a0003c0004t0005g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2668+760G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561835 | |||||||
chr4:47561849 | T | C | 2 | a0002c0002t0002g0011 a0002c0002t0013g0234 |
3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2668+774T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47561849 | |||||||
chr4:47562335 | A | G | 2 | a0034c0058t0008g0075 a0043c0036t0005g0184 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2669-1246A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562335 | |||||||
chr4:47562351 | C | T | 268 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(265): Show |
279 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.2669-1230C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562351 | |||||||
chr4:47562424 | C | A | 20 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(17): Show |
21 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.2669-1157C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562424 | |||||||
chr4:47562500 | T | A | 1 | a0036c0047t0004g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2669-1081T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562500 | |||||||
chr4:47562542 | C | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2669-1039C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562542 | |||||||
chr4:47562656 | G | A | 15 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(12): Show |
16 | HG01255.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2669-925G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562656 | |||||||
chr4:47562692 | A | G | 3 | a0005c0006t0001g0086 a0021c0029t0001g0147 a0032c0056t0001g0064 |
3 | HG01168.hp1 HG01516.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2669-889A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562692 | |||||||
chr4:47562752 | A | G | 3 | a0001c0003t0001g0020 a0001c0003t0001g0182 a0020c0064t0001g0309 |
3 | HG03453.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2669-829A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562752 | |||||||
chr4:47562790 | T | A | 286 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.2669-791T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562790 | |||||||
chr4:47562832 | A | AAT | 21 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(18): Show |
22 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.2669-737_2669-736d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr4 | 47562832 | ||||||
chr4:47562832 | A | AATAT | 8 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2669-739_2669-736d others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr4 | 47562832 | ||||||
chr4:47562923 | A | G | 1 | a0013c0015t0005g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2669-658A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47562923 | |||||||
chr4:47563199 | C | A | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2669-382C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47563199 | |||||||
chr4:47563200 | G | A | 2 | a0024c0028t0008g0119 a0024c0028t0008g0202 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2669-381G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47563200 | |||||||
chr4:47563337 | T | C | 1 | a0002c0002t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2669-244T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47563337 | |||||||
chr4:47563339 | G | A | 4 | a0001c0003t0001g0180 a0001c0003t0001g0215 a0001c0003t0001g0289 others(1): Show |
4 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.2669-242G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47563339 | |||||||
chr4:47563374 | T | A | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2669-207T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47563374 | |||||||
chr4:47563464 | G | C | 85 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(82): Show |
88 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.2669-117G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 14/22 | chr4 | 47563464 | |||||||
chr4:47563789 | GTTC | G | 4 | a0005c0014t0004g0051 a0005c0014t0004g0053 a0005c0014t0004g0054 others(1): Show |
4 | HG02071.hp1 NA18948.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2853+29_2853+31del others(3): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 47563789 | ||||||
chr4:47563845 | TA | T | 85 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(82): Show |
88 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.2853+90delA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 47563845 | ||||||
chr4:47563898 | T | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2853+133T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47563898 | |||||||
chr4:47564109 | C | G | 1 | a0006c0007t0002g0221 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2853+344C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564109 | |||||||
chr4:47564157 | G | A | 1 | a0004c0005t0006g0301 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2853+392G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564157 | |||||||
chr4:47564252 | A | G | 3 | a0034c0058t0008g0075 a0042c0035t0012g0021 a0043c0036t0005g0184 |
3 | HG02257.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2853+487A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564252 | |||||||
chr4:47564271 | C | T | 94 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(91): Show |
97 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.2853+506C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564271 | |||||||
chr4:47564317 | G | T | 3 | a0034c0058t0008g0075 a0042c0035t0012g0021 a0043c0036t0005g0184 |
3 | HG02257.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2853+552G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564317 | |||||||
chr4:47564331 | G | GT | 13 | a0001c0001t0003g0259 a0011c0020t0009g0115 a0011c0020t0009g0187 others(10): Show |
13 | HG02257.hp1 HG02257.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2853+578dupT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 47564331 | ||||||
chr4:47564343 | T | A | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.2853+578T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564343 | |||||||
chr4:47564353 | C | A | 19 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(16): Show |
20 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.2853+588C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564353 | |||||||
chr4:47564376 | G | A | 3 | a0007c0009t0001g0093 a0007c0009t0001g0094 a0007c0009t0001g0095 |
3 | NA18946.hp1 NA18990.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2853+611G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564376 | |||||||
chr4:47564582 | A | G | 15 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(12): Show |
16 | HG01255.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2853+817A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564582 | |||||||
chr4:47564630 | A | T | 1 | a0021c0029t0001g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2853+865A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564630 | |||||||
chr4:47564705 | A | G | 1 | a0008c0010t0008g0010 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2853+940A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564705 | |||||||
chr4:47564753 | G | A | 1 | a0004c0005t0005g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2853+988G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564753 | |||||||
chr4:47564843 | T | C | 2 | a0021c0029t0001g0147 a0032c0056t0001g0064 |
2 | HG01168.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2853+1078T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564843 | |||||||
chr4:47564958 | C | CGTTT | 6 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0139 others(3): Show |
6 | HG02280.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2853+1198_2853+120 others(8): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 47564958 | ||||||
chr4:47564967 | A | G | 79 | a0002c0002t0001g0109 a0002c0002t0001g0110 a0003c0004t0005g0041 others(76): Show |
85 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.2853+1202A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47564967 | |||||||
chr4:47565011 | C | T | 1 | a0036c0047t0004g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2853+1246C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565011 | |||||||
chr4:47565014 | T | A | 1 | a0036c0047t0004g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2853+1249T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565014 | |||||||
chr4:47565015 | A | G | 1 | a0036c0047t0004g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2853+1250A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565015 | |||||||
chr4:47565019 | C | T | 1 | a0036c0047t0004g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2853+1254C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565019 | |||||||
chr4:47565020 | G | A | 1 | a0036c0047t0004g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2853+1255G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565020 | |||||||
chr4:47565035 | T | C | 1 | a0020c0063t0003g0268 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2853+1270T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565035 | |||||||
chr4:47565087 | T | C | 1 | a0011c0025t0009g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2853+1322T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565087 | |||||||
chr4:47565104 | T | G | 80 | a0002c0002t0001g0107 a0002c0002t0001g0109 a0002c0002t0001g0110 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.2853+1339T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565104 | |||||||
chr4:47565212 | G | A | 176 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(173): Show |
185 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.2853+1447G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565212 | |||||||
chr4:47565239 | C | T | 78 | a0002c0002t0001g0107 a0003c0004t0005g0041 a0003c0004t0005g0044 others(75): Show |
84 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.2853+1474C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565239 | |||||||
chr4:47565562 | A | G | 275 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(272): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.2853+1797A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565562 | |||||||
chr4:47565619 | A | G | 1 | a0001c0001t0004g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2853+1854A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565619 | |||||||
chr4:47565656 | G | A | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2853+1891G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565656 | |||||||
chr4:47565749 | TA | T | 8 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2853+1991delA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 47565749 | ||||||
chr4:47565750 | A | T | 86 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(83): Show |
89 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.2853+1985A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565750 | |||||||
chr4:47565832 | A | G | 1 | a0017c0022t0002g0284 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2853+2067A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565832 | |||||||
chr4:47565931 | G | T | 72 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(69): Show |
75 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.2853+2166G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565931 | |||||||
chr4:47565943 | C | G | 1 | a0001c0001t0003g0253 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2853+2178C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47565943 | |||||||
chr4:47566064 | T | G | 2 | a0034c0058t0008g0075 a0043c0036t0005g0184 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2853+2299T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47566064 | |||||||
chr4:47566123 | A | G | 2 | a0025c0026t0009g0189 a0025c0026t0009g0190 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2853+2358A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47566123 | |||||||
chr4:47566438 | A | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2854-2399A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47566438 | |||||||
chr4:47566522 | ATC | A | 3 | a0011c0038t0005g0062 a0012c0013t0008g0125 a0012c0013t0008g0200 |
3 | HG02258.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2854-2313_2854-231 others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 47566522 | ||||||
chr4:47566547 | A | G | 87 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(84): Show |
90 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.2854-2290A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47566547 | |||||||
chr4:47566611 | G | A | 167 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(164): Show |
176 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.2854-2226G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47566611 | |||||||
chr4:47566706 | T | G | 2 | a0006c0007t0001g0156 a0006c0007t0002g0233 |
2 | HG01952.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.2854-2131T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47566706 | |||||||
chr4:47566709 | G | A | 2 | a0002c0002t0001g0109 a0002c0002t0001g0110 |
2 | HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2854-2128G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47566709 | |||||||
chr4:47566947 | A | G | 86 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(83): Show |
89 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.2854-1890A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47566947 | |||||||
chr4:47567051 | CTT | C | 167 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(164): Show |
176 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.2854-1784_2854-178 others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 47567051 | ||||||
chr4:47567089 | T | A | 167 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(164): Show |
176 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.2854-1748T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47567089 | |||||||
chr4:47567275 | T | A | 1 | a0005c0006t0002g0191 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2854-1562T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47567275 | |||||||
chr4:47567682 | T | A | 1 | a0001c0001t0004g0105 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2854-1155T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47567682 | |||||||
chr4:47567765 | A | G | 1 | a0002c0002t0001g0107 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2854-1072A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47567765 | |||||||
chr4:47567894 | T | C | 168 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(165): Show |
177 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.2854-943T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47567894 | |||||||
chr4:47568102 | A | G | 168 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(165): Show |
177 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.2854-735A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47568102 | |||||||
chr4:47568152 | T | C | 1 | a0004c0005t0006g0301 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2854-685T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47568152 | |||||||
chr4:47568218 | T | A | 2 | a0006c0007t0001g0006 a0006c0007t0002g0221 |
3 | HG02602.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2854-619T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47568218 | |||||||
chr4:47568437 | A | G | 81 | a0002c0002t0001g0107 a0003c0004t0005g0041 a0003c0004t0005g0044 others(78): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2854-400A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47568437 | |||||||
chr4:47568592 | T | C | 8 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2854-245T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47568592 | |||||||
chr4:47568678 | C | T | 86 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(83): Show |
89 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.2854-159C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 15/22 | chr4 | 47568678 | |||||||
chr4:47569236 | C | A | 1 | a0012c0013t0008g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3163+90C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47569236 | |||||||
chr4:47569395 | T | TCAGACCC | 168 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(165): Show |
177 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.3163+251_3163+257d others(9): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 47569395 | ||||||
chr4:47569642 | C | A | 1 | a0002c0002t0013g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3163+496C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47569642 | |||||||
chr4:47569741 | G | A | 1 | a0005c0006t0002g0225 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3163+595G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47569741 | |||||||
chr4:47569831 | A | C | 3 | a0006c0007t0001g0156 a0006c0007t0001g0161 a0006c0007t0002g0233 |
3 | HG01952.hp1 HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.3163+685A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47569831 | |||||||
chr4:47569897 | C | T | 169 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(166): Show |
178 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.3163+751C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47569897 | |||||||
chr4:47570426 | G | A | 9 | a0001c0003t0001g0037 a0011c0020t0009g0115 a0011c0020t0009g0187 others(6): Show |
9 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3163+1280G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570426 | |||||||
chr4:47570483 | G | C | 1 | a0012c0013t0008g0017 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3163+1337G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570483 | |||||||
chr4:47570494 | T | C | 1 | a0034c0058t0008g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3163+1348T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570494 | |||||||
chr4:47570541 | C | A | 1 | a0002c0002t0003g0303 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3163+1395C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570541 | |||||||
chr4:47570547 | T | G | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3163+1401T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570547 | |||||||
chr4:47570759 | T | C | 1 | a0012c0013t0008g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3164-1395T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570759 | |||||||
chr4:47570774 | G | T | 20 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(17): Show |
21 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.3164-1380G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570774 | |||||||
chr4:47570794 | T | A | 1 | a0011c0020t0009g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3164-1360T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570794 | |||||||
chr4:47570802 | CA | C | 74 | a0001c0001t0003g0280 a0001c0003t0001g0037 a0001c0003t0001g0052 others(71): Show |
79 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.3164-1340delA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 47570802 | ||||||
chr4:47570925 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3164-1229C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570925 | |||||||
chr4:47570957 | C | G | 1 | a0005c0006t0002g0306 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3164-1197C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570957 | |||||||
chr4:47570988 | T | C | 1 | a0006c0007t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3164-1166T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47570988 | |||||||
chr4:47571089 | G | A | 1 | a0028c0061t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3164-1065G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47571089 | |||||||
chr4:47571227 | A | T | 26 | a0002c0002t0001g0002 a0002c0002t0001g0025 a0002c0002t0001g0026 others(23): Show |
29 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.3164-927A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47571227 | |||||||
chr4:47571529 | A | G | 35 | a0001c0003t0001g0037 a0002c0002t0001g0002 a0002c0002t0001g0025 others(32): Show |
38 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.3164-625A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47571529 | |||||||
chr4:47571643 | A | G | 33 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(30): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.3164-511A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47571643 | |||||||
chr4:47571693 | C | A | 13 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(10): Show |
14 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3164-461C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47571693 | |||||||
chr4:47572038 | C | T | 1 | a0034c0058t0008g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3164-116C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47572038 | |||||||
chr4:47572063 | T | G | 1 | a0003c0004t0005g0169 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3164-91T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 16/22 | chr4 | 47572063 | |||||||
chr4:47572379 | AT | A | 169 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(166): Show |
178 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.3240+158delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572379 | ||||||
chr4:47572450 | A | C | 9 | a0001c0003t0001g0037 a0011c0020t0009g0115 a0011c0020t0009g0187 others(6): Show |
9 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3240+220A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | chr4 | 47572450 | |||||||
chr4:47572579 | A | G | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.3241-293A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | chr4 | 47572579 | |||||||
chr4:47572633 | A | G | 1 | a0002c0008t0002g0265 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3241-239A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | chr4 | 47572633 | |||||||
chr4:47572641 | G | A | 4 | a0003c0004t0010g0226 a0007c0009t0001g0093 a0007c0009t0001g0094 others(1): Show |
4 | NA18946.hp1 NA18990.hp1 NA19089.hp1 others(1): Show |
intron_variant | MODIFIER | c.3241-231G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | chr4 | 47572641 | |||||||
chr4:47572644 | C | CGT | 26 | a0001c0001t0003g0013 a0001c0001t0003g0237 a0001c0001t0003g0251 others(23): Show |
28 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3241-193_3241-192d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572644 | ||||||
chr4:47572644 | C | CGTGT | 67 | a0001c0001t0003g0217 a0001c0001t0003g0230 a0001c0001t0003g0231 others(64): Show |
68 | HG00280.hp1 HG00408.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.3241-195_3241-192d others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572644 | ||||||
chr4:47572644 | C | CGTGTGT | 24 | a0001c0001t0003g0222 a0001c0003t0001g0018 a0001c0003t0001g0048 others(21): Show |
25 | HG00738.hp1 HG01175.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.3241-197_3241-192d others(8): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572644 | ||||||
chr4:47572644 | C | CGTGTGTG others(1): Show |
31 | a0001c0001t0003g0240 a0001c0001t0004g0078 a0002c0002t0001g0002 others(28): Show |
34 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.3241-199_3241-192d others(10): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572644 | ||||||
chr4:47572644 | C | CGTGTGTG others(3): Show |
5 | a0001c0003t0001g0310 a0002c0002t0001g0144 a0002c0002t0001g0165 others(2): Show |
6 | HG00280.hp2 HG01109.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3241-201_3241-192d others(12): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572644 | ||||||
chr4:47572644 | CGT | C | 58 | a0002c0002t0001g0109 a0002c0002t0001g0110 a0002c0008t0001g0016 others(55): Show |
59 | HG00099.hp1 HG00438.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.3241-193_3241-192d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572644 | ||||||
chr4:47572644 | CGTGT | C | 4 | a0002c0008t0001g0196 a0004c0005t0005g0131 a0016c0019t0004g0023 others(1): Show |
4 | HG00735.hp1 HG01069.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3241-195_3241-192d others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572644 | ||||||
chr4:47572644 | CGTGTGT | C | 77 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(74): Show |
83 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.3241-197_3241-192d others(8): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572644 | ||||||
chr4:47572644 | CGTGTGTG others(1): Show |
C | 4 | a0003c0004t0006g0138 a0004c0005t0006g0149 a0004c0067t0007g0148 others(1): Show |
4 | NA18942.hp2 NA18955.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.3241-199_3241-192d others(10): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 47572644 | ||||||
chr4:47572689 | A | G | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3241-183A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | chr4 | 47572689 | |||||||
chr4:47572720 | T | C | 26 | a0002c0002t0001g0002 a0002c0002t0001g0025 a0002c0002t0001g0026 others(23): Show |
29 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.3241-152T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | chr4 | 47572720 | |||||||
chr4:47572809 | G | A | 6 | a0001c0003t0001g0180 a0001c0003t0001g0215 a0001c0003t0001g0289 others(3): Show |
6 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.3241-63G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | chr4 | 47572809 | |||||||
chr4:47573069 | G | A | 2 | a0024c0028t0008g0119 a0024c0028t0008g0202 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3366+72G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573069 | |||||||
chr4:47573378 | T | A | 1 | a0015c0034t0012g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3366+381T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573378 | |||||||
chr4:47573417 | A | G | 1 | a0001c0003t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3366+420A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573417 | |||||||
chr4:47573438 | A | G | 1 | a0028c0061t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3366+441A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573438 | |||||||
chr4:47573444 | T | C | 169 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(166): Show |
178 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.3366+447T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573444 | |||||||
chr4:47573655 | C | G | 169 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(166): Show |
178 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.3366+658C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573655 | |||||||
chr4:47573704 | T | C | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3366+707T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573704 | |||||||
chr4:47573768 | T | G | 33 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(30): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.3366+771T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573768 | |||||||
chr4:47573837 | G | A | 2 | a0017c0022t0001g0151 a0017c0022t0001g0152 |
2 | HG01099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.3366+840G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573837 | |||||||
chr4:47573867 | T | C | 1 | a0003c0004t0005g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3366+870T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47573867 | |||||||
chr4:47573884 | AT | A | 192 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(189): Show |
202 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.3366+898delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 47573884 | ||||||
chr4:47574364 | C | A | 1 | a0019c0021t0009g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3366+1367C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47574364 | |||||||
chr4:47574465 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3366+1468G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47574465 | |||||||
chr4:47574513 | C | A | 18 | a0010c0012t0005g0067 a0010c0012t0006g0008 a0010c0012t0006g0065 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.3366+1516C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47574513 | |||||||
chr4:47574553 | G | A | 1 | a0002c0008t0001g0145 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3366+1556G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47574553 | |||||||
chr4:47574652 | C | T | 1 | a0003c0004t0010g0235 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3366+1655C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47574652 | |||||||
chr4:47574653 | G | A | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3366+1656G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47574653 | |||||||
chr4:47574868 | T | C | 17 | a0001c0003t0001g0004 a0001c0003t0001g0028 a0001c0003t0001g0034 others(14): Show |
18 | HG00621.hp1 HG00741.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3366+1871T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47574868 | |||||||
chr4:47574894 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3367-1879G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47574894 | |||||||
chr4:47574948 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3367-1825G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47574948 | |||||||
chr4:47575101 | G | A | 2 | a0003c0004t0007g0282 a0004c0005t0006g0168 |
2 | HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.3367-1672G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47575101 | |||||||
chr4:47575375 | T | C | 8 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3367-1398T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47575375 | |||||||
chr4:47575399 | T | C | 1 | a0013c0015t0009g0288 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3367-1374T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47575399 | |||||||
chr4:47575438 | G | A | 85 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(82): Show |
91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.3367-1335G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47575438 | |||||||
chr4:47575573 | T | G | 1 | a0001c0001t0003g0237 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3367-1200T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47575573 | |||||||
chr4:47575788 | A | T | 1 | a0004c0005t0007g0001 | 3 | NA18941.hp2 NA18945.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.3367-985A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47575788 | |||||||
chr4:47575900 | G | A | 1 | a0034c0058t0008g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3367-873G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47575900 | |||||||
chr4:47575924 | C | CT | 23 | a0001c0031t0002g0192 a0002c0002t0001g0110 a0002c0002t0001g0122 others(20): Show |
23 | HG01175.hp2 HG01192.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.3367-824dupT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 47575924 | ||||||
chr4:47575924 | C | CTT | 7 | a0005c0006t0001g0219 a0011c0020t0009g0115 a0011c0020t0009g0187 others(4): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3367-825_3367-824d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 47575924 | ||||||
chr4:47575924 | CT | C | 88 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(85): Show |
92 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.3367-824delT | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 47575924 | ||||||
chr4:47575924 | CTT | C | 8 | a0001c0001t0003g0253 a0001c0001t0004g0047 a0001c0001t0004g0290 others(5): Show |
8 | HG00639.hp2 HG02572.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.3367-825_3367-824d others(4): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 47575924 | ||||||
chr4:47575924 | CTTT | C | 80 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(77): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.3367-826_3367-824d others(5): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 47575924 | ||||||
chr4:47575939 | T | C | 1 | a0001c0001t0004g0105 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3367-834T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47575939 | |||||||
chr4:47575994 | C | T | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3367-779C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47575994 | |||||||
chr4:47576035 | C | T | 1 | a0050c0039t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3367-738C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576035 | |||||||
chr4:47576118 | T | A | 199 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(196): Show |
210 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.3367-655T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576118 | |||||||
chr4:47576141 | C | T | 1 | a0001c0001t0003g0259 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3367-632C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576141 | |||||||
chr4:47576174 | A | G | 200 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(197): Show |
211 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.3367-599A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576174 | |||||||
chr4:47576179 | C | A | 1 | a0014c0017t0006g0160 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3367-594C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576179 | |||||||
chr4:47576192 | A | T | 1 | a0047c0050t0004g0207 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3367-581A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576192 | |||||||
chr4:47576215 | G | T | 8 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3367-558G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576215 | |||||||
chr4:47576330 | C | T | 13 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(10): Show |
14 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3367-443C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576330 | |||||||
chr4:47576567 | T | G | 83 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(80): Show |
86 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.3367-206T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576567 | |||||||
chr4:47576723 | A | G | 1 | a0003c0004t0010g0235 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3367-50A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 18/22 | chr4 | 47576723 | |||||||
chr4:47577065 | A | C | 7 | a0001c0001t0003g0013 a0001c0001t0003g0255 a0001c0001t0003g0256 others(4): Show |
9 | HG02135.hp1 NA18945.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.3567+92A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47577065 | |||||||
chr4:47577083 | T | C | 1 | a0034c0058t0008g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3567+110T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47577083 | |||||||
chr4:47577541 | C | CA | 87 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(84): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.3567+568_3567+569i others(3): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47577541 | |||||||
chr4:47577701 | G | A | 1 | a0042c0035t0012g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3567+728G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47577701 | |||||||
chr4:47577830 | AG | A | 68 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(65): Show |
71 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.3567+859delG | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 47577830 | ||||||
chr4:47577951 | G | A | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3567+978G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47577951 | |||||||
chr4:47577998 | C | A | 86 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(83): Show |
92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.3567+1025C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47577998 | |||||||
chr4:47578096 | C | T | 87 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(84): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.3567+1123C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578096 | |||||||
chr4:47578112 | G | A | 1 | a0006c0007t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3567+1139G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578112 | |||||||
chr4:47578420 | T | C | 200 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(197): Show |
211 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.3567+1447T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578420 | |||||||
chr4:47578432 | C | G | 1 | a0046c0066t0007g0276 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3567+1459C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578432 | |||||||
chr4:47578526 | A | G | 86 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(83): Show |
92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.3567+1553A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578526 | |||||||
chr4:47578568 | C | G | 1 | a0034c0058t0008g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3567+1595C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578568 | |||||||
chr4:47578640 | C | A | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3567+1667C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578640 | |||||||
chr4:47578737 | C | G | 1 | a0036c0047t0004g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3568-1661C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578737 | |||||||
chr4:47578806 | C | T | 4 | a0001c0001t0003g0241 a0001c0001t0004g0079 a0001c0043t0003g0278 others(1): Show |
4 | NA18955.hp2 NA18957.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.3568-1592C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578806 | |||||||
chr4:47578879 | T | A | 14 | a0002c0002t0004g0045 a0008c0010t0008g0010 a0008c0010t0008g0193 others(11): Show |
15 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.3568-1519T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578879 | |||||||
chr4:47578939 | C | T | 3 | a0002c0002t0004g0045 a0026c0024t0004g0069 a0026c0024t0004g0070 |
3 | HG02809.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3568-1459C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578939 | |||||||
chr4:47578958 | A | G | 2 | a0001c0003t0002g0238 a0001c0003t0002g0239 |
2 | NA19005.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.3568-1440A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578958 | |||||||
chr4:47578974 | C | T | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3568-1424C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47578974 | |||||||
chr4:47579005 | A | C | 3 | a0002c0002t0001g0195 a0002c0002t0002g0264 a0038c0049t0001g0130 |
3 | HG02738.hp2 HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3568-1393A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47579005 | |||||||
chr4:47579031 | A | G | 1 | a0002c0002t0001g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3568-1367A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47579031 | |||||||
chr4:47579383 | C | T | 37 | a0002c0002t0001g0002 a0002c0002t0001g0025 a0002c0002t0001g0026 others(34): Show |
40 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.3568-1015C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47579383 | |||||||
chr4:47579415 | G | A | 1 | a0002c0002t0001g0107 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3568-983G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47579415 | |||||||
chr4:47579727 | G | A | 1 | a0001c0001t0003g0266 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3568-671G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47579727 | |||||||
chr4:47579761 | G | A | 5 | a0001c0003t0001g0020 a0001c0003t0001g0073 a0001c0003t0001g0177 others(2): Show |
5 | HG03453.hp1 HG03516.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.3568-637G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47579761 | |||||||
chr4:47579837 | G | T | 1 | a0002c0002t0002g0011 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3568-561G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47579837 | |||||||
chr4:47580089 | A | C | 4 | a0001c0003t0001g0180 a0001c0003t0001g0215 a0001c0003t0001g0289 others(1): Show |
4 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.3568-309A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47580089 | |||||||
chr4:47580161 | T | C | 3 | a0012c0013t0008g0017 a0012c0013t0008g0029 a0012c0013t0008g0128 |
3 | HG02486.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3568-237T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47580161 | |||||||
chr4:47580221 | T | A | 2 | a0012c0013t0008g0125 a0012c0013t0008g0200 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3568-177T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47580221 | |||||||
chr4:47580259 | C | T | 2 | a0001c0001t0003g0230 a0001c0001t0003g0232 |
2 | HG01099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.3568-139C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47580259 | |||||||
chr4:47580370 | A | C | 230 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(227): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.3568-28A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 19/22 | chr4 | 47580370 | |||||||
chr4:47580526 | G | A | 2 | a0002c0002t0001g0087 a0002c0002t0002g0229 |
2 | HG01496.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.3648+48G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47580526 | |||||||
chr4:47580660 | A | G | 4 | a0001c0003t0001g0180 a0001c0003t0001g0215 a0001c0003t0001g0289 others(1): Show |
4 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.3648+182A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47580660 | |||||||
chr4:47580802 | C | T | 2 | a0003c0004t0005g0203 a0003c0004t0005g0204 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3648+324C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47580802 | |||||||
chr4:47581012 | G | A | 1 | a0001c0003t0001g0116 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3648+534G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47581012 | |||||||
chr4:47581145 | G | A | 95 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(92): Show |
99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.3648+667G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47581145 | |||||||
chr4:47581165 | T | C | 1 | a0002c0002t0004g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3648+687T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47581165 | |||||||
chr4:47581274 | G | A | 98 | a0002c0002t0001g0002 a0002c0002t0001g0025 a0002c0002t0001g0026 others(95): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.3649-686G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47581274 | |||||||
chr4:47581379 | A | C | 1 | a0002c0002t0004g0045 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3649-581A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47581379 | |||||||
chr4:47581393 | C | T | 1 | a0003c0004t0005g0092 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3649-567C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47581393 | |||||||
chr4:47581603 | G | A | 1 | a0001c0001t0003g0254 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3649-357G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47581603 | |||||||
chr4:47581829 | T | C | 3 | a0007c0009t0001g0093 a0007c0009t0001g0094 a0007c0009t0001g0095 |
3 | NA18946.hp1 NA18990.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.3649-131T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 20/22 | chr4 | 47581829 | |||||||
chr4:47582100 | T | C | 3 | a0001c0031t0002g0192 a0024c0028t0008g0119 a0024c0028t0008g0202 |
3 | HG01891.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3753+36T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47582100 | |||||||
chr4:47582368 | T | A | 29 | a0002c0002t0001g0002 a0002c0002t0001g0025 a0002c0002t0001g0026 others(26): Show |
32 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.3753+304T>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47582368 | |||||||
chr4:47582386 | A | G | 11 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3753+322A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47582386 | |||||||
chr4:47582665 | G | A | 196 | a0001c0001t0004g0143 a0001c0003t0001g0180 a0001c0003t0001g0182 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.3753+601G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47582665 | |||||||
chr4:47582760 | C | T | 1 | a0002c0002t0001g0136 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3753+696C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47582760 | |||||||
chr4:47582878 | A | C | 1 | a0008c0010t0008g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3753+814A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47582878 | |||||||
chr4:47583147 | A | G | 1 | a0011c0041t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3753+1083A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583147 | |||||||
chr4:47583171 | C | T | 1 | a0001c0031t0002g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3753+1107C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583171 | |||||||
chr4:47583258 | A | G | 1 | a0035c0033t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3753+1194A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583258 | |||||||
chr4:47583278 | G | A | 99 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(96): Show |
103 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3753+1214G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583278 | |||||||
chr4:47583403 | A | T | 1 | a0008c0010t0008g0208 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3753+1339A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583403 | |||||||
chr4:47583447 | A | T | 1 | a0013c0015t0009g0137 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3753+1383A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583447 | |||||||
chr4:47583522 | A | G | 2 | a0001c0003t0001g0073 a0001c0003t0001g0177 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3753+1458A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583522 | |||||||
chr4:47583552 | G | A | 1 | a0012c0013t0008g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3753+1488G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583552 | |||||||
chr4:47583628 | G | T | 112 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(109): Show |
117 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.3753+1564G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583628 | |||||||
chr4:47583774 | T | TA | 133 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(130): Show |
139 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.3753+1716dupA | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr4 | 47583774 | ||||||
chr4:47583926 | T | C | 1 | a0007c0009t0001g0095 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3753+1862T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47583926 | |||||||
chr4:47584132 | C | T | 1 | a0028c0061t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3753+2068C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47584132 | |||||||
chr4:47584607 | A | G | 169 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(166): Show |
178 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.3754-2412A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47584607 | |||||||
chr4:47584632 | G | A | 1 | a0022c0027t0011g0198 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3754-2387G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47584632 | |||||||
chr4:47584643 | A | G | 169 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(166): Show |
178 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.3754-2376A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47584643 | |||||||
chr4:47584855 | A | C | 1 | a0010c0012t0009g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3754-2164A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47584855 | |||||||
chr4:47585019 | A | G | 1 | a0001c0003t0001g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3754-2000A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47585019 | |||||||
chr4:47585194 | A | G | 1 | a0001c0016t0002g0296 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3754-1825A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47585194 | |||||||
chr4:47585271 | C | T | 10 | a0011c0020t0009g0115 a0011c0020t0009g0187 a0011c0020t0009g0188 others(7): Show |
10 | HG02109.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.3754-1748C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47585271 | |||||||
chr4:47585300 | T | C | 1 | a0019c0021t0009g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3754-1719T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47585300 | |||||||
chr4:47585340 | A | ATT | 299 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(296): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.3754-1678_3754-167 others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr4 | 47585340 | ||||||
chr4:47585397 | G | A | 77 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(74): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.3754-1622G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47585397 | |||||||
chr4:47585533 | T | C | 26 | a0003c0004t0005g0085 a0010c0012t0009g0003 a0010c0012t0009g0164 others(23): Show |
27 | HG00323.hp2 HG00642.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.3754-1486T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47585533 | |||||||
chr4:47585648 | A | G | 30 | a0001c0003t0001g0289 a0002c0002t0001g0002 a0002c0002t0001g0025 others(27): Show |
33 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.3754-1371A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47585648 | |||||||
chr4:47585739 | A | C | 8 | a0003c0004t0005g0057 a0011c0041t0008g0214 a0012c0013t0008g0017 others(5): Show |
8 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3754-1280A>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47585739 | |||||||
chr4:47585764 | GC | G | 36 | a0001c0003t0001g0020 a0001c0003t0001g0028 a0001c0003t0001g0034 others(33): Show |
37 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.3754-1253delC | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr4 | 47585764 | ||||||
chr4:47585860 | G | A | 6 | a0010c0012t0009g0003 a0010c0012t0009g0164 a0010c0012t0009g0312 others(3): Show |
7 | HG00323.hp2 HG00642.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.3754-1159G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47585860 | |||||||
chr4:47586082 | A | G | 1 | a0006c0065t0001g0176 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3754-937A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47586082 | |||||||
chr4:47586279 | T | C | 11 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(8): Show |
12 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3754-740T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47586279 | |||||||
chr4:47586328 | C | T | 3 | a0001c0003t0001g0052 a0001c0016t0002g0296 a0001c0016t0002g0297 |
3 | HG02145.hp1 HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3754-691C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47586328 | |||||||
chr4:47586392 | A | G | 9 | a0011c0041t0008g0214 a0012c0013t0008g0017 a0012c0013t0008g0029 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3754-627A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47586392 | |||||||
chr4:47586765 | T | C | 1 | a0001c0001t0003g0256 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3754-254T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47586765 | |||||||
chr4:47586777 | A | G | 38 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(35): Show |
40 | HG00323.hp2 HG00642.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.3754-242A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47586777 | |||||||
chr4:47586831 | T | C | 170 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(167): Show |
179 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.3754-188T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47586831 | |||||||
chr4:47586967 | A | G | 1 | a0003c0004t0005g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3754-52A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 21/22 | chr4 | 47586967 | |||||||
chr4:47587282 | C | A | 169 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(166): Show |
178 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.3941+76C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587282 | |||||||
chr4:47587296 | C | G | 38 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(35): Show |
40 | HG00323.hp2 HG00642.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.3941+90C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587296 | |||||||
chr4:47587299 | A | G | 1 | a0006c0007t0001g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3941+93A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587299 | |||||||
chr4:47587373 | A | G | 38 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(35): Show |
40 | HG00323.hp2 HG00642.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.3941+167A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587373 | |||||||
chr4:47587377 | G | T | 1 | a0007c0009t0001g0095 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3941+171G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587377 | |||||||
chr4:47587378 | T | G | 1 | a0007c0009t0001g0095 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3941+172T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587378 | |||||||
chr4:47587379 | G | T | 1 | a0007c0009t0001g0095 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3941+173G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587379 | |||||||
chr4:47587393 | G | C | 9 | a0011c0041t0008g0214 a0012c0013t0008g0017 a0012c0013t0008g0029 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3941+187G>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587393 | |||||||
chr4:47587552 | G | A | 1 | a0001c0003t0001g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3941+346G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587552 | |||||||
chr4:47587569 | T | TACCACAG others(5): Show |
9 | a0011c0041t0008g0214 a0012c0013t0008g0017 a0012c0013t0008g0029 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3941+363_3941+364i others(14): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587569 | |||||||
chr4:47587837 | G | A | 169 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(166): Show |
178 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.3941+631G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587837 | |||||||
chr4:47587879 | A | G | 38 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(35): Show |
40 | HG00323.hp2 HG00642.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.3941+673A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47587879 | |||||||
chr4:47587968 | T | TTTTG | 9 | a0011c0041t0008g0214 a0012c0013t0008g0017 a0012c0013t0008g0029 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3941+778_3941+781d others(6): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 47587968 | ||||||
chr4:47588071 | C | T | 1 | a0004c0005t0007g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3941+865C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588071 | |||||||
chr4:47588074 | G | T | 1 | a0010c0012t0009g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3941+868G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588074 | |||||||
chr4:47588104 | A | G | 11 | a0008c0010t0008g0010 a0008c0010t0008g0193 a0008c0010t0008g0201 others(8): Show |
12 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3941+898A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588104 | |||||||
chr4:47588130 | C | A | 9 | a0011c0041t0008g0214 a0012c0013t0008g0017 a0012c0013t0008g0029 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3941+924C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588130 | |||||||
chr4:47588185 | T | C | 9 | a0011c0041t0008g0214 a0012c0013t0008g0017 a0012c0013t0008g0029 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3941+979T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588185 | |||||||
chr4:47588348 | C | G | 237 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(234): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.3941+1142C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588348 | |||||||
chr4:47588383 | G | A | 1 | a0004c0005t0007g0015 | 2 | HG00408.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3941+1177G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588383 | |||||||
chr4:47588419 | A | G | 1 | a0001c0003t0001g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3941+1213A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588419 | |||||||
chr4:47588464 | T | G | 72 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(69): Show |
77 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3941+1258T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588464 | |||||||
chr4:47588539 | TC | T | 6 | a0002c0002t0003g0303 a0002c0002t0004g0045 a0002c0002t0004g0183 others(3): Show |
6 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3941+1336delC | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 47588539 | ||||||
chr4:47588594 | T | C | 1 | a0002c0002t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3941+1388T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588594 | |||||||
chr4:47588646 | G | T | 1 | a0001c0001t0004g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3941+1440G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588646 | |||||||
chr4:47588676 | C | A | 1 | a0007c0009t0001g0095 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3941+1470C>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588676 | |||||||
chr4:47588726 | C | T | 2 | a0015c0034t0012g0194 a0042c0035t0012g0021 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3941+1520C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588726 | |||||||
chr4:47588893 | A | G | 8 | a0011c0041t0008g0214 a0012c0013t0008g0017 a0012c0013t0008g0029 others(5): Show |
8 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3941+1687A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588893 | |||||||
chr4:47588925 | G | A | 2 | a0003c0004t0005g0203 a0003c0004t0005g0204 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3941+1719G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47588925 | |||||||
chr4:47589075 | C | G | 1 | a0011c0038t0005g0062 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3941+1869C>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47589075 | |||||||
chr4:47589106 | G | A | 9 | a0011c0041t0008g0214 a0012c0013t0008g0017 a0012c0013t0008g0029 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3941+1900G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47589106 | |||||||
chr4:47589409 | T | C | 3 | a0019c0021t0009g0071 a0019c0021t0009g0074 a0019c0021t0009g0076 |
3 | HG02886.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3942-1633T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47589409 | |||||||
chr4:47589513 | G | A | 1 | a0003c0004t0005g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3942-1529G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47589513 | |||||||
chr4:47589537 | T | G | 1 | a0026c0024t0004g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3942-1505T>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47589537 | |||||||
chr4:47589597 | T | C | 1 | a0010c0012t0009g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3942-1445T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47589597 | |||||||
chr4:47590065 | C | T | 72 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(69): Show |
77 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3942-977C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590065 | |||||||
chr4:47590070 | G | T | 1 | a0007c0009t0002g0269 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3942-972G>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590070 | |||||||
chr4:47590121 | T | C | 1 | a0007c0009t0001g0093 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3942-921T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590121 | |||||||
chr4:47590274 | A | G | 1 | a0001c0016t0002g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3942-768A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590274 | |||||||
chr4:47590485 | G | A | 1 | a0006c0007t0002g0233 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3942-557G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590485 | |||||||
chr4:47590632 | C | T | 2 | a0001c0003t0002g0206 a0001c0003t0002g0236 |
2 | NA18961.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3942-410C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590632 | |||||||
chr4:47590633 | G | A | 70 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(67): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.3942-409G>A | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590633 | |||||||
chr4:47590764 | A | T | 72 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(69): Show |
77 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3942-278A>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590764 | |||||||
chr4:47590794 | A | G | 1 | a0003c0004t0005g0307 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3942-248A>G | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590794 | |||||||
chr4:47590903 | C | T | 1 | a0005c0014t0004g0054 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3942-139C>T | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590903 | |||||||
chr4:47590976 | T | TGG | 57 | a0001c0001t0003g0013 a0001c0001t0003g0230 a0001c0001t0003g0231 others(54): Show |
58 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.3942-56_3942-55dup others(2): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 47590976 | ||||||
chr4:47590980 | G | GT | 72 | a0003c0004t0005g0041 a0003c0004t0005g0044 a0003c0004t0005g0046 others(69): Show |
77 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3942-62_3942-61ins others(1): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590980 | |||||||
chr4:47590991 | T | C | 170 | a0001c0001t0003g0013 a0001c0001t0003g0217 a0001c0001t0003g0222 others(167): Show |
179 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.3942-51T>C | ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 22/22 | chr4 | 47590991 |