Item | Value |
---|---|
geneid | 375248 |
ensemblid | ENSG00000135976.21 |
hgncid | 24079 |
symbol | ANKRD36 |
name | ankyrin repeat domain 36 |
refseq_nuc | NM_001354587.1 |
refseq_prot | NP_001341516.1 |
ensembl_nuc | ENST00000420699.9 |
ensembl_prot | ENSP00000391950.4 |
mane_status | MANE Select |
chr | chr2 |
start | 97113153 |
end | 97264521 |
strand | + |
ver | v1.2 |
region | chr2:97113153-97264521 |
region5000 | chr2:97108153-97269521 |
regionname0 | ANKRD36_chr2_97113153_97264521 |
regionname5000 | ANKRD36_chr2_97108153_97269521 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1915 | 51 | 15 | 14 | 15 | 0 | 6 | 11 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0002 | 0/0 | 1915 | 31 | 4 | 10 | 9 | 2 | 6 | 8 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0003 | 0/0 | 1881 | 23 | 23 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1876): Show |
chr2 | 97108153 | 97269521 |
a0004 | 0/0 | 1903 | 16 | 0 | 0 | 13 | 0 | 3 | 10 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MERLC others(1898): Show |
chr2 | 97108153 | 97269521 |
a0005 | 0/0 | 1881 | 12 | 4 | 6 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1876): Show |
chr2 | 97108153 | 97269521 |
a0006 | 1/0 | 1915 | 8 | 0 | 0 | 7 | 0 | 0 | 6 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0007 | 0/0 | 1915 | 8 | 1 | 7 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0008 | 0/0 | 1915 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0009 | 0/0 | 1915 | 6 | 0 | 2 | 0 | 0 | 4 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0010 | 0/0 | 1915 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0011 | 0/0 | 1134 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1129): Show |
chr2 | 97108153 | 97269521 |
a0012 | 0/0 | 1430 | 5 | 0 | 1 | 4 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1425): Show |
chr2 | 97108153 | 97269521 |
a0013 | 0/0 | 1915 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0014 | 0/0 | 1914 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1909): Show |
chr2 | 97108153 | 97269521 |
a0015 | 0/0 | 1881 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1876): Show |
chr2 | 97108153 | 97269521 |
a0016 | 0/0 | 1881 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1876): Show |
chr2 | 97108153 | 97269521 |
a0017 | 0/0 | 1915 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0018 | 0/0 | 1881 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1876): Show |
chr2 | 97108153 | 97269521 |
a0019 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1706): Show |
chr2 | 97108153 | 97269521 |
a0020 | 0/0 | 1915 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0021 | 0/0 | 1915 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0022 | 0/0 | 1915 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0023 | 0/0 | 1915 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0024 | 0/0 | 1881 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1876): Show |
chr2 | 97108153 | 97269521 |
a0025 | 0/0 | 173 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(168): Show |
chr2 | 97108153 | 97269521 |
a0026 | 0/0 | 1915 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0027 | 0/0 | 1915 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0028 | 0/0 | 1915 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0029 | 0/0 | 1847 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1842): Show |
chr2 | 97108153 | 97269521 |
a0030 | 0/0 | 1915 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0031 | 0/0 | 1915 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0032 | 0/0 | 1915 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0033 | 0/0 | 362 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(357): Show |
chr2 | 97108153 | 97269521 |
a0034 | 0/0 | 1915 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
a0035 | 0/0 | 1819 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1814): Show |
chr2 | 97108153 | 97269521 |
a0036 | 0/0 | 1915 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | MEDGK others(1910): Show |
chr2 | 97108153 | 97269521 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 5745 | 47 | 14 | 12 | 15 | 0 | 5 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0001c0029 | 0/0 | 5745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0001c0032 | 0/0 | 5745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0001c0034 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0001c0035 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0002c0002 | 0/0 | 5745 | 31 | 4 | 10 | 9 | 2 | 6 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0003c0003 | 0/0 | 5643 | 22 | 22 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5638): Show |
chr2 | 97108153 | 97269521 | ||
a0003c0030 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5638): Show |
chr2 | 97108153 | 97269521 | ||
a0004c0004 | 0/0 | 5745 | 9 | 0 | 0 | 9 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | AAGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0004c0009 | 0/0 | 5745 | 5 | 0 | 0 | 2 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | AAGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0004c0017 | 0/0 | 5745 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | AAGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0005c0005 | 0/0 | 5643 | 9 | 2 | 5 | 0 | 2 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5638): Show |
chr2 | 97108153 | 97269521 | ||
a0005c0021 | 0/0 | 5643 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5638): Show |
chr2 | 97108153 | 97269521 | ||
a0005c0031 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5638): Show |
chr2 | 97108153 | 97269521 | ||
a0006c0006 | 1/0 | 5745 | 8 | 0 | 0 | 7 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0007c0007 | 0/0 | 5745 | 7 | 0 | 7 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0007c0027 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0008c0008 | 0/0 | 5745 | 7 | 5 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0009c0012 | 0/0 | 5745 | 5 | 0 | 2 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0009c0046 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0010c0010 | 0/0 | 5745 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0010c0026 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0011c0011 | 0/0 | 5641 | 5 | 0 | 0 | 4 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5636): Show |
chr2 | 97108153 | 97269521 | ||
a0012c0014 | 0/0 | 5163 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5158): Show |
chr2 | 97108153 | 97269521 | ||
a0012c0036 | 0/0 | 5745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0013c0013 | 0/0 | 5745 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0014c0015 | 0/0 | 5742 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5737): Show |
chr2 | 97108153 | 97269521 | ||
a0015c0016 | 0/0 | 5643 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5638): Show |
chr2 | 97108153 | 97269521 | ||
a0016c0020 | 0/0 | 5643 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5638): Show |
chr2 | 97108153 | 97269521 | ||
a0017c0019 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0018c0018 | 0/0 | 5643 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5638): Show |
chr2 | 97108153 | 97269521 | ||
a0019c0028 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5128): Show |
chr2 | 97108153 | 97269521 | ||
a0020c0044 | 0/0 | 5745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0021c0042 | 0/0 | 5745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0022c0047 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0023c0024 | 0/0 | 5745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0024c0039 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5638): Show |
chr2 | 97108153 | 97269521 | ||
a0025c0043 | 0/0 | 5745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0026c0041 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0027c0023 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0028c0045 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0029c0049 | 0/0 | 5541 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5536): Show |
chr2 | 97108153 | 97269521 | ||
a0030c0037 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0031c0033 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0032c0038 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0033c0025 | 0/0 | 5678 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5673): Show |
chr2 | 97108153 | 97269521 | ||
a0034c0048 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 | ||
a0035c0040 | 0/0 | 5457 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5452): Show |
chr2 | 97108153 | 97269521 | ||
a0036c0022 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | ATGGA others(5740): Show |
chr2 | 97108153 | 97269521 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6534 | 40 | 8 | 11 | 15 | 0 | 5 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0001c0001t0004 | 0/0 | 6534 | 7 | 6 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0001c0029t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0001c0032t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0001c0034t0001 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0001c0035t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0002c0002t0001 | 0/0 | 6534 | 31 | 4 | 10 | 9 | 2 | 6 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0003c0003t0001 | 0/0 | 6432 | 22 | 22 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0003c0030t0001 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0004c0004t0002 | 0/0 | 6534 | 9 | 0 | 0 | 9 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0004c0009t0002 | 0/0 | 6534 | 5 | 0 | 0 | 2 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0004c0017t0002 | 0/0 | 6534 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0005c0005t0003 | 0/0 | 6432 | 8 | 2 | 4 | 0 | 2 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0005c0005t0007 | 0/0 | 6432 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0005c0021t0003 | 0/0 | 6432 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0005c0031t0001 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0006c0006t0001 | 1/0 | 6534 | 8 | 0 | 0 | 7 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0007c0007t0001 | 0/0 | 6534 | 6 | 0 | 6 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0007c0007t0006 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0007c0027t0001 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0008c0008t0001 | 0/0 | 6534 | 7 | 5 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0009c0012t0001 | 0/0 | 6534 | 5 | 0 | 2 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0009c0046t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0010c0010t0001 | 0/0 | 6534 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0010c0026t0001 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0011c0011t0001 | 0/0 | 6430 | 5 | 0 | 0 | 4 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6425): Show |
chr2 | 97108153 | 97269521 |
a0012c0014t0005 | 0/0 | 5750 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(5745): Show |
chr2 | 97108153 | 97269521 |
a0012c0036t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0013c0013t0001 | 0/0 | 6534 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0014c0015t0001 | 0/0 | 6531 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6526): Show |
chr2 | 97108153 | 97269521 |
a0015c0016t0001 | 0/0 | 6432 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0016c0020t0001 | 0/0 | 6432 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0017c0019t0001 | 0/0 | 6534 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0018c0018t0001 | 0/0 | 6432 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0019c0028t0001 | 0/0 | 5922 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(5917): Show |
chr2 | 97108153 | 97269521 |
a0020c0044t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0021c0042t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0022c0047t0001 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0023c0024t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0024c0039t0001 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6427): Show |
chr2 | 97108153 | 97269521 |
a0025c0043t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0026c0041t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0027c0023t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0028c0045t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0029c0049t0003 | 0/0 | 6330 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6325): Show |
chr2 | 97108153 | 97269521 |
a0030c0037t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0031c0033t0001 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0032c0038t0001 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0033c0025t0001 | 0/0 | 6467 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6462): Show |
chr2 | 97108153 | 97269521 |
a0034c0048t0001 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
a0035c0040t0001 | 0/0 | 6246 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6241): Show |
chr2 | 97108153 | 97269521 |
a0036c0022t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | GCCGG others(6529): Show |
chr2 | 97108153 | 97269521 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0029t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0032t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0034t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0001c0035t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0003c0030t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0004t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0004t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0004t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0004t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0004t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0009t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0009t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0009t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0009t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0009t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0017t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0004c0017t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0005t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0005t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0005t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0005t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0005t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0005t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0005t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0005t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0005t0007g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0021t0003g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0005c0031t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0006c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0006c0006t0001g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0006c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0006c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0006c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0006c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0006c0006t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0006c0006t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0007c0007t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0007c0007t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0007c0007t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0007c0007t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0007c0007t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0007c0007t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0007c0007t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0007c0027t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0008c0008t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0008c0008t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0008c0008t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0008c0008t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0008c0008t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0008c0008t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0008c0008t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0009c0012t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0009c0012t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0009c0012t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0009c0012t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0009c0012t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0009c0046t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0010c0010t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0010c0010t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0010c0010t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0010c0010t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0010c0010t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0010c0026t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0011c0011t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0011c0011t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0011c0011t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0011c0011t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0011c0011t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0012c0014t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0012c0014t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0012c0014t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0012c0014t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0012c0036t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0013c0013t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0013c0013t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0013c0013t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0013c0013t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0014c0015t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0014c0015t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0014c0015t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0015c0016t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0015c0016t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0015c0016t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0016c0020t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0016c0020t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0017c0019t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0017c0019t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0018c0018t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0018c0018t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0019c0028t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0020c0044t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0021c0042t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0022c0047t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0023c0024t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0024c0039t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0025c0043t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0026c0041t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0027c0023t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0028c0045t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0029c0049t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0030c0037t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0031c0033t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0032c0038t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0033c0025t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0034c0048t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0035c0040t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
a0036c0022t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0005 | t0003 | g0019 | EUR | GBR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0137 | EUR | GBR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00423 | hp1 | a0011 | c0011 | t0001 | g0047 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00423 | hp2 | a0014 | c0015 | t0001 | g0099 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00558 | hp1 | a0013 | c0013 | t0001 | g0146 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00558 | hp2 | a0006 | c0006 | t0001 | g0086 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00597 | hp1 | a0019 | c0028 | t0001 | g0132 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00597 | hp2 | a0004 | c0004 | t0002 | g0180 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00639 | hp1 | a0020 | c0044 | t0001 | g0130 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00639 | hp2 | a0001 | c0032 | t0001 | g0001 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00642 | hp1 | a0007 | c0007 | t0001 | g0011 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG00741 | hp2 | a0007 | c0007 | t0001 | g0144 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01099 | hp2 | a0005 | c0005 | t0003 | g0040 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01106 | hp1 | a0009 | c0012 | t0001 | g0094 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01175 | hp1 | a0005 | c0005 | t0003 | g0039 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01243 | hp1 | a0021 | c0042 | t0001 | g0026 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01257 | hp2 | a0005 | c0005 | t0003 | g0042 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01261 | hp1 | a0008 | c0008 | t0001 | g0170 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01261 | hp2 | a0005 | c0021 | t0003 | g0002 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01358 | hp2 | a0008 | c0008 | t0001 | g0174 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01361 | hp1 | a0009 | c0012 | t0001 | g0079 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0161 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0153 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01515 | hp1 | a0005 | c0005 | t0003 | g0037 | EUR | IBS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0135 | EUR | IBS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01891 | hp1 | a0022 | c0047 | t0001 | g0027 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01934 | hp1 | a0012 | c0036 | t0001 | g0080 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0202 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01943 | hp1 | a0001 | c0029 | t0001 | g0001 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01943 | hp2 | a0007 | c0007 | t0001 | g0143 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01975 | hp1 | a0007 | c0007 | t0001 | g0009 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01975 | hp2 | a0023 | c0024 | t0001 | g0118 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01981 | hp1 | a0005 | c0005 | t0003 | g0041 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01993 | hp1 | a0007 | c0007 | t0001 | g0008 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02004 | hp1 | a0007 | c0007 | t0001 | g0010 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02040 | hp1 | a0012 | c0014 | t0005 | g0089 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02040 | hp2 | a0014 | c0015 | t0001 | g0007 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02055 | hp2 | a0005 | c0031 | t0001 | g0012 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02071 | hp1 | a0004 | c0009 | t0002 | g0181 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02083 | hp2 | a0004 | c0009 | t0002 | g0182 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02145 | hp1 | a0024 | c0039 | t0001 | g0124 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02145 | hp2 | a0003 | c0003 | t0001 | g0062 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02257 | hp1 | a0003 | c0003 | t0001 | g0056 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02257 | hp2 | a0005 | c0005 | t0003 | g0036 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02293 | hp1 | a0025 | c0043 | t0001 | g0167 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02300 | hp1 | a0007 | c0007 | t0006 | g0142 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02451 | hp1 | a0008 | c0008 | t0001 | g0171 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02451 | hp2 | a0003 | c0003 | t0001 | g0057 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02572 | hp1 | a0003 | c0003 | t0001 | g0034 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02572 | hp2 | a0016 | c0020 | t0001 | g0033 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02602 | hp1 | a0009 | c0012 | t0001 | g0074 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02602 | hp2 | a0011 | c0011 | t0001 | g0046 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02630 | hp2 | a0017 | c0019 | t0001 | g0206 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02698 | hp1 | a0009 | c0046 | t0001 | g0096 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02717 | hp1 | a0010 | c0010 | t0001 | g0201 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02717 | hp2 | a0017 | c0019 | t0001 | g0205 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0179 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0053 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02738 | hp1 | a0026 | c0041 | t0001 | g0165 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0064 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02809 | hp2 | a0018 | c0018 | t0001 | g0016 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02886 | hp1 | a0005 | c0021 | t0003 | g0002 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02886 | hp2 | a0003 | c0003 | t0001 | g0068 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02895 | hp1 | a0018 | c0018 | t0001 | g0015 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02895 | hp2 | a0008 | c0008 | t0001 | g0175 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02897 | hp2 | a0008 | c0008 | t0001 | g0178 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02922 | hp2 | a0003 | c0003 | t0001 | g0020 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0060 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0055 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03041 | hp1 | a0003 | c0003 | t0001 | g0063 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03041 | hp2 | a0016 | c0020 | t0001 | g0018 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03098 | hp1 | a0010 | c0010 | t0001 | g0029 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03098 | hp2 | a0008 | c0008 | t0001 | g0173 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03195 | hp1 | a0003 | c0003 | t0001 | g0003 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03225 | hp2 | a0003 | c0003 | t0001 | g0128 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03486 | hp1 | a0010 | c0026 | t0001 | g0028 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03486 | hp2 | a0003 | c0003 | t0001 | g0061 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0065 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03579 | hp1 | a0008 | c0008 | t0001 | g0172 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0058 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03654 | hp1 | a0027 | c0023 | t0001 | g0157 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03669 | hp1 | a0009 | c0012 | t0001 | g0091 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03688 | hp2 | a0028 | c0045 | t0001 | g0073 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03834 | hp1 | a0004 | c0009 | t0002 | g0183 | SAS | BEB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03927 | hp2 | a0029 | c0049 | t0003 | g0043 | SAS | BEB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG04115 | hp1 | a0004 | c0009 | t0002 | g0185 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG04115 | hp2 | a0001 | c0035 | t0001 | g0103 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG04204 | hp1 | a0009 | c0012 | t0001 | g0071 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG04204 | hp2 | a0004 | c0009 | t0002 | g0184 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG04228 | hp1 | a0030 | c0037 | t0001 | g0116 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | CHB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18612 | hp2 | a0014 | c0015 | t0001 | g0100 | EAS | CHB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18941 | hp2 | a0004 | c0004 | t0002 | g0191 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18945 | hp1 | a0011 | c0011 | t0001 | g0045 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18946 | hp1 | a0013 | c0013 | t0001 | g0151 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18946 | hp2 | a0031 | c0033 | t0001 | g0108 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18951 | hp1 | a0015 | c0016 | t0001 | g0048 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18951 | hp2 | a0004 | c0004 | t0002 | g0190 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18952 | hp1 | a0006 | c0006 | t0001 | g0107 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18961 | hp1 | a0015 | c0016 | t0001 | g0044 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18961 | hp2 | a0006 | c0006 | t0001 | g0114 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18965 | hp1 | a0004 | c0004 | t0002 | g0187 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18965 | hp2 | a0012 | c0014 | t0005 | g0075 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18971 | hp1 | a0006 | c0006 | t0001 | g0087 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18971 | hp2 | a0004 | c0004 | t0002 | g0186 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18973 | hp1 | a0013 | c0013 | t0001 | g0152 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18973 | hp2 | a0004 | c0004 | t0002 | g0005 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18983 | hp1 | a0004 | c0004 | t0002 | g0005 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18991 | hp2 | a0011 | c0011 | t0001 | g0050 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA18999 | hp2 | a0004 | c0017 | t0002 | g0192 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19000 | hp2 | a0012 | c0014 | t0005 | g0115 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19002 | hp2 | a0032 | c0038 | t0001 | g0082 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19010 | hp2 | a0006 | c0006 | t0001 | g0101 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | LWK | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19030 | hp2 | a0003 | c0003 | t0001 | g0067 | AFR | LWK | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19043 | hp2 | a0010 | c0010 | t0001 | g0031 | AFR | LWK | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19056 | hp2 | a0033 | c0025 | t0001 | g0123 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19068 | hp1 | a0011 | c0011 | t0001 | g0014 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19070 | hp1 | a0004 | c0017 | t0002 | g0188 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19070 | hp2 | a0034 | c0048 | t0001 | g0013 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19072 | hp1 | a0015 | c0016 | t0001 | g0049 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19072 | hp2 | a0012 | c0014 | t0005 | g0021 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19074 | hp1 | a0013 | c0013 | t0001 | g0150 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19079 | hp2 | a0035 | c0040 | t0001 | g0122 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19085 | hp1 | a0004 | c0004 | t0002 | g0189 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19085 | hp2 | a0006 | c0006 | t0001 | g0088 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19088 | hp1 | a0004 | c0004 | t0002 | g0203 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19088 | hp2 | a0006 | c0006 | t0001 | g0084 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19240 | hp1 | a0001 | c0034 | t0001 | g0052 | AFR | YRI | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA19240 | hp2 | a0010 | c0010 | t0001 | g0030 | AFR | YRI | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0054 | AFR | ASW | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA20129 | hp2 | a0003 | c0030 | t0001 | g0066 | AFR | ASW | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0166 | SAS | GIH | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
NA20905 | hp2 | a0036 | c0022 | t0001 | g0070 | SAS | GIH | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG01123 | hp2 | a0005 | c0005 | t0007 | g0035 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02109 | hp1 | a0007 | c0027 | t0001 | g0169 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02109 | hp2 | a0003 | c0003 | t0001 | g0059 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02559 | hp1 | a0010 | c0010 | t0001 | g0032 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG02559 | hp2 | a0005 | c0005 | t0003 | g0038 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG06807 | hp1 | a0003 | c0003 | t0001 | g0204 | AFR | USA | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | USA | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0193 | REF | REF | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
homoSapiens | grch38p0 | a0006 | c0006 | t0001 | g0085 | REF | REF | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:97113741 | T | A | 1 | a0004 | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
start_lost | HIGH | c.2T>A | p.Met1? | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 589/6534 | 2/5748 | 1/1915 | chr2 | 97113741 | |||
chr2:97113750 | G | A | 1 | a0004 | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.11G>A | p.Gly4Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 598/6534 | 11/5748 | 4/1915 | chr2 | 97113750 | |||
chr2:97113752 | A | G | 1 | a0004 | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.13A>G | p.Lys5Glu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 600/6534 | 13/5748 | 5/1915 | chr2 | 97113752 | |||
chr2:97113814 | A | T | 1 | a0004 | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.75A>T | p.Gln25His | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 662/6534 | 75/5748 | 25/1915 | chr2 | 97113814 | |||
chr2:97113818 | C | T | 1 | a0004 | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.79C>T | p.Pro27Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 666/6534 | 79/5748 | 27/1915 | chr2 | 97113818 | |||
chr2:97113819 | C | A | 1 | a0004 | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.80C>A | p.Pro27His | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 667/6534 | 80/5748 | 27/1915 | chr2 | 97113819 | |||
chr2:97113864 | A | G | 2 | a0004 a0015 |
14 | HG00597.hp2 NA18941.hp2 NA18951.hp1 others(11): Show |
missense_variant | MODERATE | c.125A>G | p.His42Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 712/6534 | 125/5748 | 42/1915 | chr2 | 97113864 | |||
chr2:97118138 | T | C | 1 | a0036 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.272T>C | p.Leu91Pro | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 2/76 | 859/6534 | 272/5748 | 91/1915 | chr2 | 97118138 | |||
chr2:97118398 | A | G | 4 | a0009 a0020 a0022 others(1): Show |
9 | HG00639.hp1 HG01106.hp1 HG01361.hp1 others(6): Show |
missense_variant | MODERATE | c.367A>G | p.Asn123Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 954/6534 | 367/5748 | 123/1915 | chr2 | 97118398 | |||
chr2:97118398 | A | T | 1 | a0034 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.367A>T | p.Asn123Tyr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 954/6534 | 367/5748 | 123/1915 | chr2 | 97118398 | |||
chr2:97118416 | T | G | 3 | a0009 a0020 a0028 |
8 | HG00639.hp1 HG01106.hp1 HG01361.hp1 others(5): Show |
missense_variant | MODERATE | c.385T>G | p.Phe129Val | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 972/6534 | 385/5748 | 129/1915 | chr2 | 97118416 | |||
chr2:97118440 | T | C | 1 | a0027 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.409T>C | p.Tyr137His | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 996/6534 | 409/5748 | 137/1915 | chr2 | 97118440 | |||
chr2:97118443 | G | A | 1 | a0004 | 2 | NA18999.hp2 NA19070.hp1 |
missense_variant | MODERATE | c.412G>A | p.Ala138Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 999/6534 | 412/5748 | 138/1915 | chr2 | 97118443 | |||
chr2:97122920 | C | T | 1 | a0025 | 1 | HG02293.hp1 | stop_gained | HIGH | c.520C>T | p.Arg174* | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/76 | 1107/6534 | 520/5748 | 174/1915 | chr2 | 97122920 | |||
chr2:97124488 | G | A | 1 | a0023 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.622G>A | p.Gly208Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/76 | 1209/6534 | 622/5748 | 208/1915 | chr2 | 97124488 | |||
chr2:97124506 | ATTC | A | 1 | a0014 | 3 | HG00423.hp2 HG02040.hp2 NA18612.hp2 |
disruptive_inframe_deletion | MODERATE | c.648_650delTCT | p.Leu217del | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/76 | 1235/6534 | 648/5748 | 216/1915 | INFO_REALIGN_3_PRIME | chr2 | 97124506 | ||
chr2:97124536 | C | T | 1 | a0021 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.670C>T | p.Leu224Phe | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/76 | 1257/6534 | 670/5748 | 224/1915 | chr2 | 97124536 | |||
chr2:97147001 | TTAAACCA others(3856): Show |
T | 1 | a0033 | 1 | NA19056.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1034+487_1102-1014 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/76 | INFO_REALIGN_3_PRIME | chr2 | 97147001 | ||||||
chr2:97147002 | TAAACCAT others(3855): Show |
T | 1 | a0035 | 1 | NA19079.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1034+487_1102-1015 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/76 | chr2 | 97147002 | |||||||
chr2:97150885 | TCTTTCCC others(8897): Show |
T | 1 | a0035 | 1 | NA19079.hp2 | exon_loss_variant | HIGH | c.1102-993_1389+1134 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/76 | chr2 | 97150885 | |||||||
chr2:97150889 | TCCCCCTC others(8893): Show |
T | 1 | a0033 | 1 | NA19056.hp2 | exon_loss_variant | HIGH | c.1102-989_1389+1134 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/76 | chr2 | 97150889 | |||||||
chr2:97151924 | C | T | 1 | a0001 | 3 | HG03834.hp2 HG03927.hp1 HG04115.hp2 |
stop_gained | HIGH | c.1147C>T | p.Arg383* | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/76 | 1734/6534 | 1147/5748 | 383/1915 | chr2 | 97151924 | |||
chr2:97152093 | AGTGATTC others(4367): Show |
A | 2 | a0002 a0027 |
4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
exon_loss_variant | HIGH | c.1162+158_1261-1637 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/76 | INFO_REALIGN_3_PRIME | chr2 | 97152093 | ||||||
chr2:97158116 | G | C | 2 | a0001 a0014 |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
missense_variant | MODERATE | c.1270G>C | p.Glu424Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/76 | 1857/6534 | 1270/5748 | 424/1915 | chr2 | 97158116 | |||
chr2:97162132 | G | A | 2 | a0010 a0022 |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
missense_variant | MODERATE | c.1423G>A | p.Ala475Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/76 | 2010/6534 | 1423/5748 | 475/1915 | chr2 | 97162132 | |||
chr2:97167604 | C | T | 1 | a0024 | 1 | HG02145.hp1 | missense_variant&splice_region_variant | MODERATE | c.1559C>T | p.Thr520Met | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 21/76 | 2146/6534 | 1559/5748 | 520/1915 | chr2 | 97167604 | |||
chr2:97181772 | A | G | 1 | a0016 | 2 | HG02572.hp2 HG03041.hp2 |
missense_variant | MODERATE | c.1816A>G | p.Lys606Glu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/76 | 2403/6534 | 1816/5748 | 606/1915 | chr2 | 97181772 | |||
chr2:97183477 | C | T | 1 | a0032 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1856C>T | p.Ser619Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 27/76 | 2443/6534 | 1856/5748 | 619/1915 | chr2 | 97183477 | |||
chr2:97183482 | T | C | 10 | a0002 a0007 a0008 others(7): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
missense_variant | MODERATE | c.1861T>C | p.Trp621Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 27/76 | 2448/6534 | 1861/5748 | 621/1915 | chr2 | 97183482 | |||
chr2:97187219 | C | T | 1 | a0004 | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.2063C>T | p.Ala688Val | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 31/76 | 2650/6534 | 2063/5748 | 688/1915 | chr2 | 97187219 | |||
chr2:97187500 | CGAAGCTG others(11237): Show |
C | 1 | a0019 | 1 | HG00597.hp1 | exon_loss_variant | HIGH | c.2143+118_2755+104d others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/76 | INFO_REALIGN_3_PRIME | chr2 | 97187500 | ||||||
chr2:97188507 | GGTGAGAG others(1883): Show |
G | 7 | a0002 a0007 a0013 others(4): Show |
47 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(44): Show |
exon_loss_variant | HIGH | c.2144-494_2246-496d others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/76 | INFO_REALIGN_3_PRIME | chr2 | 97188507 | ||||||
chr2:97188626 | CTGTGTGC others(1883): Show |
C | 1 | a0006 | 1 | NA19010.hp2 | exon_loss_variant | HIGH | c.2144-398_2246-400d others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/76 | INFO_REALIGN_3_PRIME | chr2 | 97188626 | ||||||
chr2:97189233 | G | A | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2188G>A | p.Glu730Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/76 | 2775/6534 | 2188/5748 | 730/1915 | chr2 | 97189233 | |||
chr2:97190993 | A | C | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2261A>C | p.Gln754Pro | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/76 | 2848/6534 | 2261/5748 | 754/1915 | chr2 | 97190993 | |||
chr2:97191005 | A | C | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2273A>C | p.Lys758Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/76 | 2860/6534 | 2273/5748 | 758/1915 | chr2 | 97191005 | |||
chr2:97191115 | A | G | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2281A>G | p.Thr761Ala | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2868/6534 | 2281/5748 | 761/1915 | chr2 | 97191115 | |||
chr2:97191116 | C | G | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2282C>G | p.Thr761Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2869/6534 | 2282/5748 | 761/1915 | chr2 | 97191116 | |||
chr2:97191125 | A | C | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2291A>C | p.Lys764Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2878/6534 | 2291/5748 | 764/1915 | chr2 | 97191125 | |||
chr2:97191129 | T | G | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2295T>G | p.Asp765Glu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2882/6534 | 2295/5748 | 765/1915 | chr2 | 97191129 | |||
chr2:97191141 | C | G | 1 | a0006 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.2307C>G | p.Asn769Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2894/6534 | 2307/5748 | 769/1915 | chr2 | 97191141 | |||
chr2:97191149 | C | G | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2315C>G | p.Thr772Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2902/6534 | 2315/5748 | 772/1915 | chr2 | 97191149 | |||
chr2:97191155 | T | A | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2321T>A | p.Ile774Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2908/6534 | 2321/5748 | 774/1915 | chr2 | 97191155 | |||
chr2:97191175 | G | A | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2341G>A | p.Gly781Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2928/6534 | 2341/5748 | 781/1915 | chr2 | 97191175 | |||
chr2:97192885 | C | A | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2375C>A | p.Thr792Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/76 | 2962/6534 | 2375/5748 | 792/1915 | chr2 | 97192885 | |||
chr2:97194734 | C | T | 1 | a0004 | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.2458C>T | p.Arg820Trp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 39/76 | 3045/6534 | 2458/5748 | 820/1915 | chr2 | 97194734 | |||
chr2:97194750 | T | C | 9 | a0002 a0007 a0008 others(6): Show |
55 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(52): Show |
missense_variant | MODERATE | c.2474T>C | p.Leu825Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 39/76 | 3061/6534 | 2474/5748 | 825/1915 | chr2 | 97194750 | |||
chr2:97198471 | G | C | 1 | a0034 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.2662G>C | p.Glu888Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 43/76 | 3249/6534 | 2662/5748 | 888/1915 | chr2 | 97198471 | |||
chr2:97198596 | C | A | 10 | a0002 a0007 a0008 others(7): Show |
56 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
missense_variant | MODERATE | c.2693C>A | p.Ala898Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/76 | 3280/6534 | 2693/5748 | 898/1915 | chr2 | 97198596 | |||
chr2:97198637 | G | T | 10 | a0002 a0007 a0008 others(7): Show |
56 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
missense_variant | MODERATE | c.2734G>T | p.Asp912Tyr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/76 | 3321/6534 | 2734/5748 | 912/1915 | chr2 | 97198637 | |||
chr2:97200454 | C | T | 1 | a0030 | 1 | HG04228.hp1 | missense_variant&splice_region_variant | MODERATE | c.2786C>T | p.Ala929Val | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/76 | 3373/6534 | 2786/5748 | 929/1915 | chr2 | 97200454 | |||
chr2:97200496 | A | G | 1 | a0019 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.2828A>G | p.Glu943Gly | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/76 | 3415/6534 | 2828/5748 | 943/1915 | chr2 | 97200496 | |||
chr2:97204663 | ACTGTAGG others(1865): Show |
A | 1 | a0029 | 1 | HG03927.hp2 | exon_loss_variant | HIGH | c.3061+436_3163+435d others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 51/76 | INFO_REALIGN_3_PRIME | chr2 | 97204663 | ||||||
chr2:97205943 | C | T | 1 | a0011 | 5 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(2): Show |
missense_variant | MODERATE | c.3065C>T | p.Ser1022Phe | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 51/76 | 3652/6534 | 3065/5748 | 1022/1915 | chr2 | 97205943 | |||
chr2:97207905 | TTTATTAT others(1859): Show |
T | 8 | a0003 a0005 a0011 others(5): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
exon_loss_variant | HIGH | c.3193-14_3295-15del | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/76 | INFO_REALIGN_3_PRIME | chr2 | 97207905 | ||||||
chr2:97207985 | T | G | 2 | a0001 a0017 |
2 | HG01496.hp2 HG02630.hp2 |
missense_variant | MODERATE | c.3244T>G | p.Tyr1082Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/76 | 3831/6534 | 3244/5748 | 1082/1915 | chr2 | 97207985 | |||
chr2:97208387 | GTTGTAAC others(29496): Show |
G | 2 | a0006 a0032 |
8 | HG00558.hp2 NA18952.hp1 NA18961.hp2 others(5): Show |
exon_loss_variant | HIGH | c.3265+384_4094-3374 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 55/76 | INFO_REALIGN_3_PRIME | chr2 | 97208387 | ||||||
chr2:97211555 | C | A | 22 | a0002 a0003 a0004 others(19): Show |
130 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(127): Show |
missense_variant | MODERATE | c.3377C>A | p.Pro1126Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 57/76 | 3964/6534 | 3377/5748 | 1126/1915 | chr2 | 97211555 | |||
chr2:97211555 | C | T | 1 | a0033 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.3377C>T | p.Pro1126Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 57/76 | 3964/6534 | 3377/5748 | 1126/1915 | chr2 | 97211555 | |||
chr2:97211703 | T | C | 7 | a0002 a0007 a0019 others(4): Show |
44 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(41): Show |
missense_variant | MODERATE | c.3431T>C | p.Met1144Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/76 | 4018/6534 | 3431/5748 | 1144/1915 | chr2 | 97211703 | |||
chr2:97211731 | ATC | A | 1 | a0011 | 5 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(2): Show |
frameshift_variant | HIGH | c.3461_3462delCT | p.Ser1154fs | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/76 | 4048/6534 | 3461/5748 | 1154/1915 | INFO_REALIGN_3_PRIME | chr2 | 97211731 | ||
chr2:97211741 | G | A | 1 | a0018 | 2 | HG02809.hp2 HG02895.hp1 |
missense_variant&splice_region_variant | MODERATE | c.3469G>A | p.Val1157Met | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/76 | 4056/6534 | 3469/5748 | 1157/1915 | chr2 | 97211741 | |||
chr2:97213425 | G | C | 30 | a0001 a0002 a0003 others(27): Show |
172 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(169): Show |
missense_variant | MODERATE | c.3476G>C | p.Cys1159Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 59/76 | 4063/6534 | 3476/5748 | 1159/1915 | chr2 | 97213425 | |||
chr2:97217357 | T | G | 2 | a0007 a0013 |
12 | HG00558.hp1 HG00642.hp1 HG00741.hp2 others(9): Show |
missense_variant | MODERATE | c.3760T>G | p.Trp1254Gly | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/76 | 4347/6534 | 3760/5748 | 1254/1915 | chr2 | 97217357 | |||
chr2:97241463 | G | T | 1 | a0012 | 1 | HG01934.hp1 | stop_gained | HIGH | c.4291G>T | p.Glu1431* | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/76 | 4878/6534 | 4291/5748 | 1431/1915 | chr2 | 97241463 | |||
chr2:97243892 | G | T | 4 | a0004 a0005 a0008 others(1): Show |
28 | HG00558.hp1 HG00597.hp2 HG01261.hp1 others(25): Show |
missense_variant | MODERATE | c.4354G>T | p.Val1452Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/76 | 4941/6534 | 4354/5748 | 1452/1915 | chr2 | 97243892 | |||
chr2:97245479 | A | G | 2 | a0028 a0031 |
2 | HG03688.hp2 NA18946.hp2 |
missense_variant | MODERATE | c.4814A>G | p.His1605Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/76 | 5401/6534 | 4814/5748 | 1605/1915 | chr2 | 97245479 | |||
chr2:97245828 | TCAACTAA others(23686): Show |
T | 1 | a0012 | 4 | HG02040.hp1 NA18965.hp2 NA19000.hp2 others(1): Show |
exon_loss_variant | HIGH | c.5164_*5199del | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/76 | 5751/6534 | chr2 | 97245828 | ||||||
chr2:97246019 | A | C | 2 | a0002 a0013 |
12 | HG00099.hp2 HG00558.hp1 HG01099.hp1 others(9): Show |
missense_variant | MODERATE | c.5354A>C | p.Asn1785Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/76 | 5941/6534 | 5354/5748 | 1785/1915 | chr2 | 97246019 | |||
chr2:97247504 | G | A | 1 | a0006 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.5435G>A | p.Arg1812Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/76 | 6022/6534 | 5435/5748 | 1812/1915 | chr2 | 97247504 | |||
chr2:97250158 | T | G | 1 | a0003 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.5739T>G | p.Phe1913Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/76 | 6326/6534 | 5739/5748 | 1913/1915 | chr2 | 97250158 | |||
chr2:97264169 | TAGCATTG others(84): Show |
T | 14 | a0001 a0003 a0004 others(11): Show |
67 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(64): Show |
splice_acceptor_variant&splice_region_variant&3_prime_UTR_variant&intron_variant | HIGH | c.*7-65_*32delATTGAA others(85): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 76/76 | 14097 | INFO_REALIGN_3_PRIME | chr2 | 97264169 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:97113874 | A | G | 2 | a0004c0004 a0004c0017 |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
synonymous_variant | LOW | c.135A>G | p.Leu45Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 722/6534 | 135/5748 | 45/1915 | chr2 | 97113874 | |||
chr2:97118094 | C | T | 3 | a0005c0005 a0005c0021 a0029c0049 |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
synonymous_variant | LOW | c.228C>T | p.Gly76Gly | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 2/76 | 815/6534 | 228/5748 | 76/1915 | chr2 | 97118094 | |||
chr2:97127091 | C | T | 1 | a0026c0041 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.756C>T | p.Tyr252Tyr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/76 | 1343/6534 | 756/5748 | 252/1915 | chr2 | 97127091 | |||
chr2:97142777 | G | A | 1 | a0034c0048 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.843G>A | p.Lys281Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/76 | 1430/6534 | 843/5748 | 281/1915 | chr2 | 97142777 | |||
chr2:97183635 | T | C | 1 | a0001c0029 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.1920T>C | p.Gly640Gly | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/76 | 2507/6534 | 1920/5748 | 640/1915 | chr2 | 97183635 | |||
chr2:97185332 | A | G | 11 | a0002c0002 a0007c0007 a0007c0027 others(8): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
synonymous_variant | LOW | c.1956A>G | p.Gln652Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 29/76 | 2543/6534 | 1956/5748 | 652/1915 | chr2 | 97185332 | |||
chr2:97189100 | G | A | 1 | a0004c0004 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2157G>A | p.Lys719Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/76 | 2744/6534 | 2157/5748 | 719/1915 | chr2 | 97189100 | |||
chr2:97189229 | C | T | 1 | a0004c0004 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2184C>T | p.Asp728Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/76 | 2771/6534 | 2184/5748 | 728/1915 | chr2 | 97189229 | |||
chr2:97189250 | T | C | 1 | a0004c0004 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2205T>C | p.Asn735Asn | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/76 | 2792/6534 | 2205/5748 | 735/1915 | chr2 | 97189250 | |||
chr2:97191141 | C | T | 1 | a0004c0004 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2307C>T | p.Asn769Asn | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2894/6534 | 2307/5748 | 769/1915 | chr2 | 97191141 | |||
chr2:97198597 | C | T | 11 | a0002c0002 a0007c0007 a0007c0027 others(8): Show |
56 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
synonymous_variant | LOW | c.2694C>T | p.Ala898Ala | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/76 | 3281/6534 | 2694/5748 | 898/1915 | chr2 | 97198597 | |||
chr2:97198639 | T | C | 1 | a0004c0009 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.2736T>C | p.Asp912Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/76 | 3323/6534 | 2736/5748 | 912/1915 | chr2 | 97198639 | |||
chr2:97200476 | T | A | 1 | a0010c0026 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.2808T>A | p.Ser936Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/76 | 3395/6534 | 2808/5748 | 936/1915 | chr2 | 97200476 | |||
chr2:97207827 | A | G | 1 | a0005c0021 | 2 | HG01261.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.3180A>G | p.Pro1060Pro | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 53/76 | 3767/6534 | 3180/5748 | 1060/1915 | chr2 | 97207827 | |||
chr2:97217350 | A | G | 3 | a0007c0007 a0007c0027 a0013c0013 |
12 | HG00558.hp1 HG00642.hp1 HG00741.hp2 others(9): Show |
synonymous_variant | LOW | c.3753A>G | p.Thr1251Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/76 | 4340/6534 | 3753/5748 | 1251/1915 | chr2 | 97217350 | |||
chr2:97243924 | A | C | 5 | a0001c0035 a0003c0030 a0007c0027 others(2): Show |
6 | HG02109.hp1 HG02630.hp2 HG02698.hp1 others(3): Show |
synonymous_variant | LOW | c.4386A>C | p.Ile1462Ile | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/76 | 4973/6534 | 4386/5748 | 1462/1915 | chr2 | 97243924 | |||
chr2:97243990 | A | G | 2 | a0001c0034 a0036c0022 |
2 | NA19240.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.4452A>G | p.Ala1484Ala | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/76 | 5039/6534 | 4452/5748 | 1484/1915 | chr2 | 97243990 | |||
chr2:97245738 | A | G | 1 | a0034c0048 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.5073A>G | p.Gln1691Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/76 | 5660/6534 | 5073/5748 | 1691/1915 | chr2 | 97245738 | |||
chr2:97245820 | A | C | 1 | a0001c0032 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.5155A>C | p.Arg1719Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/76 | 5742/6534 | 5155/5748 | 1719/1915 | chr2 | 97245820 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:97113158 | A | G | 1 | a0005c0005t0007 | 1 | HG01123.hp2 | 5_prime_UTR_variant | MODIFIER | c.-582A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 582 | chr2 | 97113158 | ||||||
chr2:97113180 | A | G | 1 | a0007c0007t0006 | 1 | HG02300.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-560A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | chr2 | 97113180 | |||||||
chr2:97113428 | G | A | 1 | a0001c0001t0004 | 7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-312G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 312 | chr2 | 97113428 | ||||||
chr2:97113454 | C | G | 4 | a0005c0005t0003 a0005c0005t0007 a0005c0021t0003 others(1): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-286C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 286 | chr2 | 97113454 | ||||||
chr2:97113631 | T | C | 3 | a0004c0004t0002 a0004c0009t0002 a0004c0017t0002 |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-109T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 109 | chr2 | 97113631 | ||||||
chr2:97113645 | G | C | 3 | a0004c0004t0002 a0004c0009t0002 a0004c0017t0002 |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-95G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 95 | chr2 | 97113645 | ||||||
chr2:97113660 | T | C | 3 | a0004c0004t0002 a0004c0009t0002 a0004c0017t0002 |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-80T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 80 | chr2 | 97113660 | ||||||
chr2:97113661 | C | T | 3 | a0004c0004t0002 a0004c0009t0002 a0004c0017t0002 |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-79C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | chr2 | 97113661 | |||||||
chr2:97113735 | C | A | 3 | a0004c0004t0002 a0004c0009t0002 a0004c0017t0002 |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-5C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 5 | chr2 | 97113735 | ||||||
chr2:97264463 | C | G | 3 | a0001c0001t0001 a0033c0025t0001 a0035c0040t0001 |
3 | NA18972.hp2 NA19056.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 76/76 | 14296 | chr2 | 97264463 | ||||||
chr2:97264497 | G | A | 23 | a0001c0001t0001 a0001c0001t0004 a0001c0034t0001 others(20): Show |
75 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*175G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 76/76 | 14330 | chr2 | 97264497 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:97114099 | G | C | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.197+163G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114099 | |||||||
chr2:97114296 | G | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+360G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114296 | |||||||
chr2:97114436 | C | G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+500C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114436 | |||||||
chr2:97114508 | A | G | 1 | a0003c0003t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.197+572A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114508 | |||||||
chr2:97114758 | A | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+822A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114758 | |||||||
chr2:97114902 | C | A | 4 | a0007c0007t0001g0008 a0007c0007t0001g0009 a0007c0007t0001g0010 others(1): Show |
4 | HG00642.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+966C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114902 | |||||||
chr2:97114908 | C | T | 1 | a0004c0004t0002g0203 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.197+972C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114908 | |||||||
chr2:97115334 | A | T | 1 | a0002c0002t0001g0202 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.197+1398A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115334 | |||||||
chr2:97115374 | A | G | 1 | a0010c0010t0001g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197+1438A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115374 | |||||||
chr2:97115460 | A | G | 7 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+1524A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115460 | |||||||
chr2:97115561 | G | A | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.197+1625G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115561 | |||||||
chr2:97115571 | C | G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+1635C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115571 | |||||||
chr2:97115740 | T | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.197+1804T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115740 | |||||||
chr2:97115756 | C | G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+1820C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115756 | |||||||
chr2:97115863 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.197+1927A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115863 | |||||||
chr2:97115944 | A | G | 1 | a0003c0003t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.197+2008A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115944 | |||||||
chr2:97116155 | G | A | 1 | a0011c0011t0001g0014 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.198-1909G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97116155 | |||||||
chr2:97116270 | G | T | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.198-1794G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97116270 | |||||||
chr2:97116450 | A | G | 1 | a0003c0003t0001g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.198-1614A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97116450 | |||||||
chr2:97116926 | G | C | 3 | a0001c0001t0001g0017 a0018c0018t0001g0015 a0018c0018t0001g0016 |
3 | HG02293.hp2 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.198-1138G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97116926 | |||||||
chr2:97117047 | CT | C | 61 | a0001c0001t0001g0022 a0002c0002t0001g0129 a0002c0002t0001g0131 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.198-1001delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | INFO_REALIGN_3_PRIME | chr2 | 97117047 | ||||||
chr2:97117258 | T | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.198-806T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117258 | |||||||
chr2:97117651 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-413T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117651 | |||||||
chr2:97117671 | GTAATATC | G | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.198-389_198-383del others(7): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | INFO_REALIGN_3_PRIME | chr2 | 97117671 | ||||||
chr2:97117895 | G | C | 1 | a0002c0002t0001g0129 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.198-169G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117895 | |||||||
chr2:97117912 | C | T | 1 | a0002c0002t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.198-152C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117912 | |||||||
chr2:97117920 | T | C | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.198-144T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117920 | |||||||
chr2:97117953 | ATGT | A | 3 | a0016c0020t0001g0018 a0016c0020t0001g0033 a0022c0047t0001g0027 |
3 | HG01891.hp1 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.198-107_198-105del others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | INFO_REALIGN_3_PRIME | chr2 | 97117953 | ||||||
chr2:97118007 | G | A | 1 | a0022c0047t0001g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.198-57G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97118007 | |||||||
chr2:97118182 | T | C | 2 | a0003c0003t0001g0034 a0020c0044t0001g0130 |
2 | HG00639.hp1 HG02572.hp1 |
splice_region_variant&intron_variant | LOW | c.312+4T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 2/75 | chr2 | 97118182 | |||||||
chr2:97118328 | G | A | 3 | a0007c0007t0001g0008 a0007c0007t0001g0009 a0007c0007t0001g0010 |
3 | HG01975.hp1 HG01993.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.313-16G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 2/75 | chr2 | 97118328 | |||||||
chr2:97118558 | C | A | 70 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(67): Show |
71 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.486+41C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97118558 | |||||||
chr2:97118947 | A | AC | 79 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(76): Show |
80 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.486+430_486+431ins others(1): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97118947 | |||||||
chr2:97118959 | G | A | 1 | a0019c0028t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.486+442G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97118959 | |||||||
chr2:97118975 | T | C | 25 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(22): Show |
26 | HG00099.hp1 HG00099.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.486+458T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97118975 | |||||||
chr2:97119059 | A | C | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.486+542A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119059 | |||||||
chr2:97119231 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.486+714G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119231 | |||||||
chr2:97119294 | A | G | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.486+777A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119294 | |||||||
chr2:97119688 | G | A | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.486+1171G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119688 | |||||||
chr2:97119695 | C | A | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.486+1178C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119695 | |||||||
chr2:97119814 | C | CACA | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.486+1314_486+1316d others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | INFO_REALIGN_3_PRIME | chr2 | 97119814 | ||||||
chr2:97119816 | C | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.486+1299C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119816 | |||||||
chr2:97119817 | A | C | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.486+1300A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119817 | |||||||
chr2:97120024 | G | C | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.486+1507G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120024 | |||||||
chr2:97120142 | CTT | C | 6 | a0008c0008t0001g0171 a0008c0008t0001g0172 a0008c0008t0001g0173 others(3): Show |
6 | HG01358.hp2 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.486+1628_486+1629d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | INFO_REALIGN_3_PRIME | chr2 | 97120142 | ||||||
chr2:97120462 | C | A | 5 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(2): Show |
5 | HG00597.hp1 HG01261.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+1945C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120462 | |||||||
chr2:97120470 | T | TA | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.486+1960dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | INFO_REALIGN_3_PRIME | chr2 | 97120470 | ||||||
chr2:97120544 | T | C | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.486+2027T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120544 | |||||||
chr2:97120648 | G | A | 1 | a0002c0002t0001g0141 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.486+2131G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120648 | |||||||
chr2:97120664 | T | C | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.486+2147T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120664 | |||||||
chr2:97120735 | T | C | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-2152T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120735 | |||||||
chr2:97120736 | G | T | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-2151G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120736 | |||||||
chr2:97120748 | T | C | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-2139T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120748 | |||||||
chr2:97120827 | T | C | 2 | a0001c0001t0004g0194 a0008c0008t0001g0170 |
2 | HG01261.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.487-2060T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120827 | |||||||
chr2:97120887 | G | A | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-2000G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120887 | |||||||
chr2:97120917 | C | T | 13 | a0003c0003t0001g0020 a0003c0003t0001g0059 a0003c0003t0001g0060 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.487-1970C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120917 | |||||||
chr2:97120939 | G | A | 119 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(116): Show |
121 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.487-1948G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120939 | |||||||
chr2:97121014 | C | G | 2 | a0033c0025t0001g0123 a0035c0040t0001g0122 |
2 | NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.487-1873C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121014 | |||||||
chr2:97121103 | T | C | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1784T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121103 | |||||||
chr2:97121217 | A | G | 1 | a0003c0003t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.487-1670A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121217 | |||||||
chr2:97121282 | G | A | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1605G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121282 | |||||||
chr2:97121333 | A | G | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.487-1554A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121333 | |||||||
chr2:97121422 | C | T | 6 | a0001c0001t0004g0194 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-1465C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121422 | |||||||
chr2:97121503 | G | A | 1 | a0004c0004t0002g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.487-1384G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121503 | |||||||
chr2:97121513 | T | G | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1374T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121513 | |||||||
chr2:97121532 | C | T | 1 | a0003c0003t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.487-1355C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121532 | |||||||
chr2:97121595 | A | G | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1292A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121595 | |||||||
chr2:97121604 | C | T | 6 | a0001c0001t0004g0194 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-1283C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121604 | |||||||
chr2:97121624 | C | T | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1263C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121624 | |||||||
chr2:97121644 | C | T | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1243C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121644 | |||||||
chr2:97121665 | A | T | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1222A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121665 | |||||||
chr2:97121685 | C | T | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1202C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121685 | |||||||
chr2:97121786 | A | T | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1101A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121786 | |||||||
chr2:97121797 | T | G | 2 | a0008c0008t0001g0170 a0016c0020t0001g0018 |
2 | HG01261.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.487-1090T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121797 | |||||||
chr2:97121821 | G | A | 55 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(52): Show |
55 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.487-1066G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121821 | |||||||
chr2:97122147 | T | C | 73 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(70): Show |
74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.487-740T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122147 | |||||||
chr2:97122155 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487-732C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122155 | |||||||
chr2:97122182 | A | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.487-705A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122182 | |||||||
chr2:97122223 | C | T | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.487-664C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122223 | |||||||
chr2:97122373 | G | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.487-514G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122373 | |||||||
chr2:97122454 | G | A | 27 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(24): Show |
28 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.487-433G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122454 | |||||||
chr2:97122676 | A | G | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.487-211A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122676 | |||||||
chr2:97123283 | T | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+290T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123283 | |||||||
chr2:97123292 | G | A | 2 | a0004c0004t0002g0186 a0004c0004t0002g0187 |
2 | NA18965.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.593+299G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123292 | |||||||
chr2:97123420 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+427G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123420 | |||||||
chr2:97123435 | A | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+442A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123435 | |||||||
chr2:97123449 | T | TACTTC | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+457_593+458ins others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123449 | ||||||
chr2:97123478 | G | A | 1 | a0002c0002t0001g0177 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.593+485G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123478 | |||||||
chr2:97123491 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.593+498C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123491 | |||||||
chr2:97123538 | ATTG | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+546_593+548del others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123538 | |||||||
chr2:97123613 | T | TTA | 28 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(25): Show |
30 | HG00099.hp1 HG00609.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.593+643_593+644dup others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | ||||||
chr2:97123613 | T | TTATA | 7 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0034t0001g0052 others(4): Show |
7 | HG01975.hp2 HG02083.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.593+641_593+644dup others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | ||||||
chr2:97123613 | T | TTATATA | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.593+639_593+644dup others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | ||||||
chr2:97123613 | T | TTATATAT others(3): Show |
1 | a0017c0019t0001g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.593+635_593+644dup others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | ||||||
chr2:97123613 | TTA | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.593+643_593+644del others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | ||||||
chr2:97123613 | TTATATAT others(5): Show |
T | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+633_593+644del others(12): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | ||||||
chr2:97123664 | A | G | 1 | a0010c0010t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.593+671A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123664 | |||||||
chr2:97123798 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.594-662T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123798 | |||||||
chr2:97123839 | TA | T | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.594-619delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123839 | ||||||
chr2:97123893 | T | A | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.594-567T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123893 | |||||||
chr2:97123957 | T | TTA | 22 | a0001c0001t0001g0110 a0001c0001t0001g0120 a0004c0009t0002g0181 others(19): Show |
22 | HG00642.hp1 HG00741.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.594-486_594-485dup others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | ||||||
chr2:97123957 | T | TTATA | 26 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(23): Show |
26 | HG00558.hp1 HG00597.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.594-488_594-485dup others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | ||||||
chr2:97123957 | T | TTATATA | 20 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(17): Show |
20 | HG00639.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.594-490_594-485dup others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | ||||||
chr2:97123957 | T | TTATATAT others(1): Show |
3 | a0002c0002t0001g0141 a0002c0002t0001g0168 a0007c0027t0001g0169 |
3 | HG01070.hp2 HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.594-492_594-485dup others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | ||||||
chr2:97123957 | T | TTATATAT others(3): Show |
1 | a0002c0002t0001g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.594-494_594-485dup others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | ||||||
chr2:97123957 | TTA | T | 2 | a0003c0003t0001g0204 a0021c0042t0001g0026 |
2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.594-486_594-485del others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | ||||||
chr2:97123978 | G | A | 1 | a0017c0019t0001g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.594-482G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123978 | |||||||
chr2:97124041 | T | G | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.594-419T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97124041 | |||||||
chr2:97124146 | A | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.594-314A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97124146 | |||||||
chr2:97124402 | T | C | 1 | a0036c0022t0001g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.594-58T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97124402 | |||||||
chr2:97125069 | A | G | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.731+472A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125069 | |||||||
chr2:97125140 | T | C | 1 | a0004c0009t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.731+543T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125140 | |||||||
chr2:97125221 | C | G | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.731+624C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125221 | |||||||
chr2:97125232 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.731+635C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125232 | |||||||
chr2:97125272 | G | GT | 13 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(10): Show |
13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.731+683dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | INFO_REALIGN_3_PRIME | chr2 | 97125272 | ||||||
chr2:97125318 | T | A | 1 | a0019c0028t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.731+721T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125318 | |||||||
chr2:97125364 | A | G | 4 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0018c0018t0001g0015 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+767A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125364 | |||||||
chr2:97125588 | C | G | 1 | a0025c0043t0001g0167 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.731+991C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125588 | |||||||
chr2:97125711 | A | G | 1 | a0025c0043t0001g0167 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.731+1114A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125711 | |||||||
chr2:97125783 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.731+1186T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125783 | |||||||
chr2:97125859 | T | C | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.732-1208T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125859 | |||||||
chr2:97126492 | C | G | 1 | a0004c0017t0002g0192 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.732-575C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97126492 | |||||||
chr2:97126649 | A | G | 2 | a0011c0011t0001g0014 a0011c0011t0001g0050 |
2 | NA18991.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.732-418A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97126649 | |||||||
chr2:97127587 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+453G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97127587 | |||||||
chr2:97127692 | C | T | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.799+558C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97127692 | |||||||
chr2:97127878 | T | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+744T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97127878 | |||||||
chr2:97127913 | A | G | 2 | a0001c0001t0001g0109 a0031c0033t0001g0108 |
2 | NA18946.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.799+779A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97127913 | |||||||
chr2:97128104 | G | A | 1 | a0009c0012t0001g0071 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.799+970G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128104 | |||||||
chr2:97128158 | T | C | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+1024T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128158 | |||||||
chr2:97128162 | A | C | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.799+1028A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128162 | |||||||
chr2:97128261 | T | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+1127T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128261 | |||||||
chr2:97128269 | T | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+1135T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128269 | |||||||
chr2:97128285 | C | T | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+1151C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128285 | |||||||
chr2:97128300 | A | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.799+1166A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128300 | |||||||
chr2:97128308 | C | T | 2 | a0011c0011t0001g0014 a0011c0011t0001g0050 |
2 | NA18991.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.799+1174C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128308 | |||||||
chr2:97128441 | C | A | 1 | a0004c0009t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.799+1307C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128441 | |||||||
chr2:97128538 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.799+1404A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128538 | |||||||
chr2:97128597 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.799+1463T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128597 | |||||||
chr2:97128656 | T | A | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.799+1522T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128656 | |||||||
chr2:97128953 | C | T | 2 | a0008c0008t0001g0175 a0008c0008t0001g0178 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.799+1819C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128953 | |||||||
chr2:97129156 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.799+2022C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129156 | |||||||
chr2:97129532 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.799+2398G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129532 | |||||||
chr2:97129921 | T | C | 1 | a0003c0003t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.799+2787T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129921 | |||||||
chr2:97129947 | A | G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.799+2813A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129947 | |||||||
chr2:97129964 | C | G | 75 | a0001c0001t0001g0006 a0002c0002t0001g0129 a0002c0002t0001g0131 others(72): Show |
76 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+2830C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129964 | |||||||
chr2:97130162 | A | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.799+3028A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130162 | |||||||
chr2:97130207 | C | A | 2 | a0002c0002t0001g0141 a0027c0023t0001g0157 |
2 | HG01070.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.799+3073C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130207 | |||||||
chr2:97130242 | T | C | 2 | a0009c0012t0001g0074 a0028c0045t0001g0073 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.799+3108T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130242 | |||||||
chr2:97130332 | A | G | 1 | a0008c0008t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799+3198A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130332 | |||||||
chr2:97130434 | C | T | 1 | a0020c0044t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.799+3300C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130434 | |||||||
chr2:97130459 | G | C | 1 | a0003c0003t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.799+3325G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130459 | |||||||
chr2:97130588 | G | GA | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.799+3465dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97130588 | ||||||
chr2:97130645 | TA | T | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+3513delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97130645 | ||||||
chr2:97130858 | T | C | 1 | a0004c0009t0002g0182 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.799+3724T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130858 | |||||||
chr2:97130898 | C | G | 1 | a0001c0001t0001g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.799+3764C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130898 | |||||||
chr2:97130948 | G | GT | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.799+3815dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97130948 | ||||||
chr2:97131194 | A | AT | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0004g0194 others(6): Show |
9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.799+4073dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97131194 | ||||||
chr2:97131488 | C | T | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.799+4354C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131488 | |||||||
chr2:97131749 | G | A | 73 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(70): Show |
74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.799+4615G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131749 | |||||||
chr2:97131820 | T | C | 1 | a0012c0014t0005g0075 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.799+4686T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131820 | |||||||
chr2:97131884 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.799+4750A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131884 | |||||||
chr2:97131892 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.799+4758G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131892 | |||||||
chr2:97131897 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.799+4763C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131897 | |||||||
chr2:97131930 | G | A | 8 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(5): Show |
8 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.799+4796G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131930 | |||||||
chr2:97131943 | T | C | 27 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(24): Show |
28 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.799+4809T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131943 | |||||||
chr2:97131974 | C | A | 8 | a0002c0002t0001g0145 a0003c0003t0001g0003 a0003c0003t0001g0053 others(5): Show |
9 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.799+4840C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131974 | |||||||
chr2:97132029 | G | T | 1 | a0004c0017t0002g0192 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.799+4895G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132029 | |||||||
chr2:97132048 | G | C | 2 | a0001c0001t0004g0195 a0003c0003t0001g0053 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.799+4914G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132048 | |||||||
chr2:97132069 | T | C | 10 | a0003c0003t0001g0059 a0003c0003t0001g0060 a0003c0003t0001g0061 others(7): Show |
10 | HG00558.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.799+4935T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132069 | |||||||
chr2:97132305 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.799+5171A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132305 | |||||||
chr2:97132326 | G | A | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.799+5192G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132326 | |||||||
chr2:97132532 | C | T | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.799+5398C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132532 | |||||||
chr2:97132703 | A | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.799+5569A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132703 | |||||||
chr2:97133169 | C | T | 1 | a0004c0004t0002g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.799+6035C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97133169 | |||||||
chr2:97133254 | T | TAACATAG others(337): Show |
1 | a0002c0002t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.799+6132_799+6133i others(346): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97133254 | ||||||
chr2:97133254 | T | TAACATAG others(338): Show |
1 | a0002c0002t0001g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.799+6132_799+6133i others(347): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97133254 | ||||||
chr2:97133254 | T | TAACATAG others(342): Show |
1 | a0002c0002t0001g0147 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.799+6132_799+6133i others(351): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97133254 | ||||||
chr2:97133254 | T | TAACATAG others(334): Show |
4 | a0013c0013t0001g0146 a0013c0013t0001g0150 a0013c0013t0001g0151 others(1): Show |
4 | HG00558.hp1 NA18946.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+6132_799+6133i others(343): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97133254 | ||||||
chr2:97133548 | A | G | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.799+6414A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97133548 | |||||||
chr2:97133623 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+6489G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97133623 | |||||||
chr2:97133927 | A | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.799+6793A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97133927 | |||||||
chr2:97134230 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+7096G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97134230 | |||||||
chr2:97134510 | A | G | 1 | a0006c0006t0001g0107 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.799+7376A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97134510 | |||||||
chr2:97134517 | G | A | 1 | a0006c0006t0001g0107 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.799+7383G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97134517 | |||||||
chr2:97135140 | T | C | 1 | a0013c0013t0001g0150 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.800-7500T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135140 | |||||||
chr2:97135323 | T | C | 1 | a0015c0016t0001g0044 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.800-7317T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135323 | |||||||
chr2:97135417 | A | G | 2 | a0016c0020t0001g0018 a0016c0020t0001g0033 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.800-7223A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135417 | |||||||
chr2:97135478 | A | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.800-7162A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135478 | |||||||
chr2:97135537 | G | A | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.800-7103G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135537 | |||||||
chr2:97135606 | A | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.800-7034A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135606 | |||||||
chr2:97135631 | C | T | 142 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(139): Show |
145 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.800-7009C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135631 | |||||||
chr2:97135699 | G | A | 1 | a0004c0004t0002g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.800-6941G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135699 | |||||||
chr2:97135794 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.800-6846C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135794 | |||||||
chr2:97135926 | G | A | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.800-6714G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135926 | |||||||
chr2:97136203 | A | ATCCAGGT others(7): Show |
1 | a0003c0030t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.800-6428_800-6427i others(16): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97136203 | ||||||
chr2:97136582 | G | A | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.800-6058G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97136582 | |||||||
chr2:97136602 | C | A | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.800-6038C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97136602 | |||||||
chr2:97136688 | C | T | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.800-5952C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97136688 | |||||||
chr2:97137191 | G | T | 1 | a0002c0002t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.800-5449G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137191 | |||||||
chr2:97137592 | TACAC | T | 73 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(70): Show |
74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.800-5035_800-5032d others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97137592 | ||||||
chr2:97137594 | C | T | 5 | a0001c0001t0001g0022 a0012c0014t0005g0021 a0012c0014t0005g0075 others(2): Show |
5 | HG02040.hp1 NA18950.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-5046C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137594 | |||||||
chr2:97137607 | A | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.800-5033A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137607 | |||||||
chr2:97137745 | T | G | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.800-4895T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137745 | |||||||
chr2:97137953 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.800-4687C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137953 | |||||||
chr2:97138101 | CA | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.800-4538delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138101 | |||||||
chr2:97138122 | CG | C | 4 | a0005c0005t0003g0040 a0005c0005t0003g0041 a0005c0021t0003g0002 others(1): Show |
5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-4516delG | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97138122 | ||||||
chr2:97138195 | C | A | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.800-4445C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138195 | |||||||
chr2:97138394 | C | T | 1 | a0009c0012t0001g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.800-4246C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138394 | |||||||
chr2:97138685 | A | T | 6 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.800-3955A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138685 | |||||||
chr2:97138880 | G | A | 1 | a0003c0003t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.800-3760G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138880 | |||||||
chr2:97139548 | T | G | 1 | a0004c0009t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.800-3092T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139548 | |||||||
chr2:97139575 | G | A | 1 | a0004c0009t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.800-3065G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139575 | |||||||
chr2:97139591 | G | A | 1 | a0002c0002t0001g0145 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.800-3049G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139591 | |||||||
chr2:97139735 | T | C | 1 | a0002c0002t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.800-2905T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139735 | |||||||
chr2:97139865 | C | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.800-2775C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139865 | |||||||
chr2:97139938 | T | C | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.800-2702T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139938 | |||||||
chr2:97140055 | C | T | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.800-2585C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140055 | |||||||
chr2:97140118 | C | G | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.800-2522C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140118 | |||||||
chr2:97140273 | G | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.800-2367G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140273 | |||||||
chr2:97140281 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.800-2359G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140281 | |||||||
chr2:97140679 | C | T | 2 | a0015c0016t0001g0044 a0015c0016t0001g0049 |
2 | NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.800-1961C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140679 | |||||||
chr2:97140693 | A | G | 1 | a0003c0003t0001g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.800-1947A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140693 | |||||||
chr2:97140705 | C | A | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.800-1935C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140705 | |||||||
chr2:97140813 | G | T | 2 | a0008c0008t0001g0170 a0008c0008t0001g0174 |
2 | HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.800-1827G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140813 | |||||||
chr2:97141228 | C | CAT | 16 | a0001c0001t0004g0195 a0004c0004t0002g0005 a0004c0004t0002g0180 others(13): Show |
17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.800-1399_800-1398d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97141228 | ||||||
chr2:97141279 | AAAG | A | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.800-1357_800-1355d others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97141279 | ||||||
chr2:97141380 | AAG | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.800-1256_800-1255d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97141380 | ||||||
chr2:97141465 | T | A | 1 | a0003c0030t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.800-1175T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141465 | |||||||
chr2:97141665 | C | G | 2 | a0033c0025t0001g0123 a0035c0040t0001g0122 |
2 | NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.800-975C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141665 | |||||||
chr2:97141667 | A | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.800-973A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141667 | |||||||
chr2:97141789 | T | A | 1 | a0001c0001t0001g0006 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.800-851T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141789 | |||||||
chr2:97141885 | A | G | 20 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(17): Show |
21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.800-755A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141885 | |||||||
chr2:97142080 | T | C | 1 | a0022c0047t0001g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.800-560T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142080 | |||||||
chr2:97142098 | A | G | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.800-542A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142098 | |||||||
chr2:97142307 | C | G | 3 | a0004c0017t0002g0192 a0017c0019t0001g0205 a0017c0019t0001g0206 |
3 | HG02630.hp2 HG02717.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.800-333C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142307 | |||||||
chr2:97142310 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.800-330G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142310 | |||||||
chr2:97142461 | G | A | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.800-179G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142461 | |||||||
chr2:97142943 | C | G | 2 | a0008c0008t0001g0175 a0008c0008t0001g0178 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.901+108C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97142943 | |||||||
chr2:97143088 | C | T | 1 | a0002c0002t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.901+253C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97143088 | |||||||
chr2:97143258 | C | A | 2 | a0002c0002t0001g0129 a0002c0002t0001g0158 |
2 | HG01123.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.901+423C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97143258 | |||||||
chr2:97143446 | A | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.901+611A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97143446 | |||||||
chr2:97143587 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.901+752A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97143587 | |||||||
chr2:97144287 | T | C | 1 | a0022c0047t0001g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.902-231T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97144287 | |||||||
chr2:97144773 | A | T | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1003+61A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97144773 | |||||||
chr2:97144805 | G | A | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003+93G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97144805 | |||||||
chr2:97144860 | G | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1003+148G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97144860 | |||||||
chr2:97145061 | T | C | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1003+349T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145061 | |||||||
chr2:97145649 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG00609.hp2 NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1004-837C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145649 | |||||||
chr2:97145741 | G | T | 1 | a0003c0003t0001g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1004-745G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145741 | |||||||
chr2:97145805 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1004-681C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145805 | |||||||
chr2:97145854 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1004-632A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145854 | |||||||
chr2:97146246 | T | C | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1004-240T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97146246 | |||||||
chr2:97146273 | A | AT | 120 | a0001c0035t0001g0103 a0002c0002t0001g0129 a0002c0002t0001g0131 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1004-200dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | INFO_REALIGN_3_PRIME | chr2 | 97146273 | ||||||
chr2:97146702 | G | A | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1034+186G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146702 | |||||||
chr2:97146767 | G | C | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1034+251G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146767 | |||||||
chr2:97146852 | G | A | 2 | a0018c0018t0001g0015 a0018c0018t0001g0016 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1034+336G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146852 | |||||||
chr2:97146939 | A | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1034+423A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146939 | |||||||
chr2:97146976 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1034+460G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146976 | |||||||
chr2:97147267 | G | T | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1034+751G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147267 | |||||||
chr2:97147411 | C | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1034+895C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147411 | |||||||
chr2:97147470 | C | T | 2 | a0004c0017t0002g0188 a0004c0017t0002g0192 |
2 | NA18999.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1034+954C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147470 | |||||||
chr2:97147546 | A | G | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1034+1030A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147546 | |||||||
chr2:97147640 | A | G | 1 | a0001c0029t0001g0001 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1034+1124A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147640 | |||||||
chr2:97147682 | C | G | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1034+1166C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147682 | |||||||
chr2:97148032 | G | C | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1035-1263G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148032 | |||||||
chr2:97148567 | T | C | 8 | a0011c0011t0001g0014 a0011c0011t0001g0045 a0011c0011t0001g0046 others(5): Show |
8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1035-728T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148567 | |||||||
chr2:97148730 | CA | C | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1035-564delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148730 | |||||||
chr2:97148783 | A | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1035-512A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148783 | |||||||
chr2:97148813 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1035-482C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148813 | |||||||
chr2:97148871 | C | G | 1 | a0003c0003t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1035-424C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148871 | |||||||
chr2:97148871 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1035-424C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148871 | |||||||
chr2:97148962 | C | G | 1 | a0004c0004t0002g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1035-333C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148962 | |||||||
chr2:97149192 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1035-103T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149192 | |||||||
chr2:97149198 | A | AT | 4 | a0005c0005t0003g0040 a0005c0005t0003g0041 a0005c0021t0003g0002 others(1): Show |
5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-90dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | INFO_REALIGN_3_PRIME | chr2 | 97149198 | ||||||
chr2:97149207 | G | T | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1035-88G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149207 | |||||||
chr2:97149210 | T | G | 4 | a0005c0005t0003g0040 a0005c0005t0003g0041 a0005c0021t0003g0002 others(1): Show |
5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-85T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149210 | |||||||
chr2:97149215 | A | C | 4 | a0005c0005t0003g0040 a0005c0005t0003g0041 a0005c0021t0003g0002 others(1): Show |
5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-80A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149215 | |||||||
chr2:97149217 | A | G | 4 | a0005c0005t0003g0040 a0005c0005t0003g0041 a0005c0021t0003g0002 others(1): Show |
5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-78A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149217 | |||||||
chr2:97149219 | G | A | 77 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(74): Show |
79 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1035-76G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149219 | |||||||
chr2:97149382 | A | G | 1 | a0009c0012t0001g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1101+21A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97149382 | |||||||
chr2:97149582 | G | GA | 27 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(24): Show |
28 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1101+229dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | INFO_REALIGN_3_PRIME | chr2 | 97149582 | ||||||
chr2:97149850 | T | C | 1 | a0008c0008t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1101+489T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97149850 | |||||||
chr2:97150500 | C | A | 1 | a0008c0008t0001g0174 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1101+1139C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150500 | |||||||
chr2:97150572 | G | A | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1101+1211G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150572 | |||||||
chr2:97150706 | A | T | 9 | a0003c0003t0001g0059 a0003c0003t0001g0060 a0003c0003t0001g0061 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1102-1173A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150706 | |||||||
chr2:97150776 | T | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1102-1103T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150776 | |||||||
chr2:97150869 | A | T | 2 | a0033c0025t0001g0123 a0035c0040t0001g0122 |
2 | NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1102-1010A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150869 | |||||||
chr2:97150872 | G | T | 2 | a0033c0025t0001g0123 a0035c0040t0001g0122 |
2 | NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1102-1007G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150872 | |||||||
chr2:97150886 | C | T | 1 | a0033c0025t0001g0123 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1102-993C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150886 | |||||||
chr2:97150893 | C | T | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1102-986C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150893 | |||||||
chr2:97151083 | C | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1102-796C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151083 | |||||||
chr2:97151084 | G | T | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1102-795G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151084 | |||||||
chr2:97151167 | T | C | 1 | a0002c0002t0001g0202 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1102-712T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151167 | |||||||
chr2:97151285 | C | T | 1 | a0003c0003t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1102-594C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151285 | |||||||
chr2:97151455 | A | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1102-424A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151455 | |||||||
chr2:97151654 | A | G | 1 | a0005c0005t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1102-225A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151654 | |||||||
chr2:97151693 | T | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1102-186T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151693 | |||||||
chr2:97151827 | C | CT | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1102-51dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | INFO_REALIGN_3_PRIME | chr2 | 97151827 | ||||||
chr2:97152065 | TCACTG | T | 4 | a0002c0002t0001g0141 a0002c0002t0001g0161 a0002c0002t0001g0162 others(1): Show |
4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+129_1162+133d others(7): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/75 | INFO_REALIGN_3_PRIME | chr2 | 97152065 | ||||||
chr2:97152236 | C | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1163-268C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/75 | chr2 | 97152236 | |||||||
chr2:97152239 | T | C | 1 | a0006c0006t0001g0107 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1163-265T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/75 | chr2 | 97152239 | |||||||
chr2:97152394 | C | T | 1 | a0016c0020t0001g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1163-110C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/75 | chr2 | 97152394 | |||||||
chr2:97152611 | A | G | 52 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(49): Show |
52 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1193+77A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97152611 | |||||||
chr2:97153107 | C | T | 1 | a0003c0003t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1193+573C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97153107 | |||||||
chr2:97153117 | T | A | 1 | a0003c0003t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1193+583T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97153117 | |||||||
chr2:97153261 | T | G | 1 | a0009c0012t0001g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1193+727T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97153261 | |||||||
chr2:97153973 | A | C | 2 | a0001c0001t0001g0051 a0001c0034t0001g0052 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1194-702A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97153973 | |||||||
chr2:97154154 | C | G | 1 | a0003c0003t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1194-521C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154154 | |||||||
chr2:97154300 | A | G | 2 | a0016c0020t0001g0018 a0016c0020t0001g0033 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1194-375A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154300 | |||||||
chr2:97154539 | T | C | 2 | a0003c0003t0001g0064 a0012c0036t0001g0080 |
2 | HG01934.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1194-136T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154539 | |||||||
chr2:97154653 | G | T | 3 | a0001c0001t0001g0022 a0002c0002t0001g0154 a0002c0002t0001g0155 |
3 | NA18612.hp1 NA18950.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1194-22G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154653 | |||||||
chr2:97154655 | A | C | 3 | a0001c0001t0001g0022 a0002c0002t0001g0154 a0002c0002t0001g0155 |
3 | NA18612.hp1 NA18950.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1194-20A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154655 | |||||||
chr2:97154925 | T | TG | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+185dupG | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | INFO_REALIGN_3_PRIME | chr2 | 97154925 | ||||||
chr2:97155015 | T | C | 52 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(49): Show |
52 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1260+274T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155015 | |||||||
chr2:97155027 | C | T | 1 | a0005c0005t0003g0039 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1260+286C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155027 | |||||||
chr2:97155083 | A | C | 52 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(49): Show |
52 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1260+342A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155083 | |||||||
chr2:97155761 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1260+1020A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155761 | |||||||
chr2:97155765 | C | T | 52 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(49): Show |
52 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1260+1024C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155765 | |||||||
chr2:97155837 | G | T | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1260+1096G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155837 | |||||||
chr2:97155933 | A | G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1260+1192A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155933 | |||||||
chr2:97156026 | T | C | 3 | a0003c0003t0001g0060 a0003c0003t0001g0063 a0003c0003t0001g0065 |
3 | HG02976.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1260+1285T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156026 | |||||||
chr2:97156100 | G | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0004g0194 others(6): Show |
9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260+1359G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156100 | |||||||
chr2:97156398 | G | A | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1260+1657G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156398 | |||||||
chr2:97156489 | C | T | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1261-1618C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156489 | |||||||
chr2:97156605 | T | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-1502T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156605 | |||||||
chr2:97156674 | T | TA | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-1430dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | INFO_REALIGN_3_PRIME | chr2 | 97156674 | ||||||
chr2:97156726 | G | A | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1261-1381G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156726 | |||||||
chr2:97156750 | T | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0105 |
2 | HG00609.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1261-1357T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156750 | |||||||
chr2:97156826 | C | T | 73 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(70): Show |
74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1261-1281C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156826 | |||||||
chr2:97156827 | A | C | 73 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(70): Show |
74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1261-1280A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156827 | |||||||
chr2:97156853 | C | G | 9 | a0003c0003t0001g0059 a0003c0003t0001g0060 a0003c0003t0001g0061 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-1254C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156853 | |||||||
chr2:97156982 | C | T | 1 | a0002c0002t0001g0163 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1261-1125C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156982 | |||||||
chr2:97157130 | CCT | C | 7 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-958_1261-957d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | INFO_REALIGN_3_PRIME | chr2 | 97157130 | ||||||
chr2:97157131 | C | CTCTCTCT others(1): Show |
56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1261-969_1261-968i others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | INFO_REALIGN_3_PRIME | chr2 | 97157131 | ||||||
chr2:97157143 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1261-964C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157143 | |||||||
chr2:97157275 | A | G | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1261-832A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157275 | |||||||
chr2:97157500 | A | G | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1261-607A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157500 | |||||||
chr2:97157592 | C | T | 1 | a0002c0002t0001g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1261-515C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157592 | |||||||
chr2:97157821 | T | G | 2 | a0016c0020t0001g0018 a0016c0020t0001g0033 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1261-286T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157821 | |||||||
chr2:97157846 | A | G | 1 | a0002c0002t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1261-261A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157846 | |||||||
chr2:97158215 | TTTTCTTT others(7): Show |
T | 2 | a0001c0001t0001g0051 a0001c0034t0001g0052 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1321+55_1321+68del others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/75 | INFO_REALIGN_3_PRIME | chr2 | 97158215 | ||||||
chr2:97158234 | T | C | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1321+67T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/75 | chr2 | 97158234 | |||||||
chr2:97158306 | C | T | 13 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(10): Show |
13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.1321+139C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/75 | chr2 | 97158306 | |||||||
chr2:97158308 | A | G | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1321+141A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/75 | chr2 | 97158308 | |||||||
chr2:97158773 | A | G | 1 | a0005c0005t0007g0035 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1389+118A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97158773 | |||||||
chr2:97158824 | G | A | 3 | a0015c0016t0001g0044 a0015c0016t0001g0048 a0015c0016t0001g0049 |
3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1389+169G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97158824 | |||||||
chr2:97158959 | T | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1389+304T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97158959 | |||||||
chr2:97159112 | A | G | 1 | a0003c0003t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1389+457A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159112 | |||||||
chr2:97159154 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1389+499T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159154 | |||||||
chr2:97159213 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1389+558C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159213 | |||||||
chr2:97159257 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1389+602G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159257 | |||||||
chr2:97159292 | A | G | 2 | a0002c0002t0001g0164 a0020c0044t0001g0130 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1389+637A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159292 | |||||||
chr2:97159476 | T | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1389+821T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159476 | |||||||
chr2:97159624 | G | T | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1389+969G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159624 | |||||||
chr2:97159913 | C | T | 1 | a0013c0013t0001g0152 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1389+1258C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159913 | |||||||
chr2:97159955 | T | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+1300T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159955 | |||||||
chr2:97160262 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1389+1607A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160262 | |||||||
chr2:97160366 | C | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+1711C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160366 | |||||||
chr2:97160402 | G | A | 2 | a0001c0001t0001g0069 a0011c0011t0001g0045 |
2 | NA18945.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1390-1697G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160402 | |||||||
chr2:97160576 | G | A | 3 | a0002c0002t0001g0159 a0002c0002t0001g0168 a0007c0027t0001g0169 |
3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1390-1523G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160576 | |||||||
chr2:97160694 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1390-1405G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160694 | |||||||
chr2:97160722 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1390-1377T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160722 | |||||||
chr2:97160959 | T | A | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1390-1140T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160959 | |||||||
chr2:97160969 | G | A | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1390-1130G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160969 | |||||||
chr2:97161004 | A | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1390-1095A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161004 | |||||||
chr2:97161036 | G | C | 1 | a0002c0002t0001g0177 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1390-1063G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161036 | |||||||
chr2:97161115 | T | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1390-984T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161115 | |||||||
chr2:97161231 | T | C | 120 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1390-868T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161231 | |||||||
chr2:97161690 | G | A | 1 | a0005c0005t0003g0040 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1390-409G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161690 | |||||||
chr2:97161732 | T | C | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1390-367T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161732 | |||||||
chr2:97161852 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1390-247C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161852 | |||||||
chr2:97162044 | CTGAT | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1390-51_1390-48del others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | INFO_REALIGN_3_PRIME | chr2 | 97162044 | ||||||
chr2:97162053 | T | C | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1390-46T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97162053 | |||||||
chr2:97162081 | C | CT | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
splice_region_variant&intron_variant | LOW | c.1390-6dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | INFO_REALIGN_3_PRIME | chr2 | 97162081 | ||||||
chr2:97162145 | G | A | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1429+7G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162145 | |||||||
chr2:97162158 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1429+20T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162158 | |||||||
chr2:97162354 | T | G | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1429+216T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162354 | |||||||
chr2:97162460 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1429+322A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162460 | |||||||
chr2:97162516 | G | C | 3 | a0001c0001t0001g0081 a0009c0012t0001g0079 a0012c0036t0001g0080 |
3 | HG01169.hp1 HG01361.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1429+378G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162516 | |||||||
chr2:97162556 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1429+418G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162556 | |||||||
chr2:97162699 | G | A | 1 | a0031c0033t0001g0108 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1429+561G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162699 | |||||||
chr2:97162876 | G | T | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1429+738G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162876 | |||||||
chr2:97162917 | C | A | 8 | a0011c0011t0001g0014 a0011c0011t0001g0045 a0011c0011t0001g0046 others(5): Show |
8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429+779C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162917 | |||||||
chr2:97162947 | A | G | 1 | a0005c0005t0003g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1429+809A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162947 | |||||||
chr2:97163049 | T | C | 73 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(70): Show |
74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1429+911T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163049 | |||||||
chr2:97163127 | C | T | 47 | a0002c0002t0001g0129 a0002c0002t0001g0133 a0002c0002t0001g0134 others(44): Show |
47 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1429+989C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163127 | |||||||
chr2:97163192 | A | G | 131 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1429+1054A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163192 | |||||||
chr2:97163589 | T | C | 1 | a0032c0038t0001g0082 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1430-694T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163589 | |||||||
chr2:97163711 | T | G | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1430-572T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163711 | |||||||
chr2:97163721 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1430-562G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163721 | |||||||
chr2:97163751 | A | G | 1 | a0012c0014t0005g0115 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1430-532A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163751 | |||||||
chr2:97163847 | T | C | 1 | a0002c0002t0001g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1430-436T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163847 | |||||||
chr2:97163876 | C | T | 2 | a0016c0020t0001g0018 a0016c0020t0001g0033 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1430-407C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163876 | |||||||
chr2:97163877 | G | A | 20 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(17): Show |
21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1430-406G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163877 | |||||||
chr2:97163912 | C | T | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1430-371C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163912 | |||||||
chr2:97164125 | T | A | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1430-158T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97164125 | |||||||
chr2:97164616 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1531+147A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97164616 | |||||||
chr2:97164863 | C | T | 1 | a0001c0035t0001g0103 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1531+394C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97164863 | |||||||
chr2:97164878 | G | A | 1 | a0003c0003t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1531+409G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97164878 | |||||||
chr2:97165029 | C | T | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1531+560C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165029 | |||||||
chr2:97165117 | A | G | 1 | a0002c0002t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1531+648A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165117 | |||||||
chr2:97165143 | A | G | 1 | a0003c0003t0001g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1531+674A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165143 | |||||||
chr2:97165657 | G | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1531+1188G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165657 | |||||||
chr2:97165720 | A | G | 6 | a0001c0001t0004g0194 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1531+1251A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165720 | |||||||
chr2:97165876 | T | G | 2 | a0016c0020t0001g0018 a0016c0020t0001g0033 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1531+1407T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165876 | |||||||
chr2:97166049 | GT | G | 73 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(70): Show |
74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1532-1526delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | INFO_REALIGN_3_PRIME | chr2 | 97166049 | ||||||
chr2:97166168 | G | T | 3 | a0006c0006t0001g0101 a0006c0006t0001g0107 a0006c0006t0001g0114 |
3 | NA18952.hp1 NA18961.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1532-1409G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97166168 | |||||||
chr2:97166354 | A | G | 6 | a0001c0001t0004g0194 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1532-1223A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97166354 | |||||||
chr2:97166990 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1532-587C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97166990 | |||||||
chr2:97167141 | A | G | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1532-436A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97167141 | |||||||
chr2:97167500 | T | G | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0004g0194 others(6): Show |
9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1532-77T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97167500 | |||||||
chr2:97167536 | G | A | 2 | a0003c0003t0001g0020 a0003c0003t0001g0067 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1532-41G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97167536 | |||||||
chr2:97167779 | A | G | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1633+12A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97167779 | |||||||
chr2:97168028 | A | G | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+261A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168028 | |||||||
chr2:97168033 | A | C | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1633+266A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168033 | |||||||
chr2:97168140 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1633+373C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168140 | |||||||
chr2:97168335 | C | G | 1 | a0016c0020t0001g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1633+568C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168335 | |||||||
chr2:97168336 | G | A | 1 | a0001c0001t0004g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1633+569G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168336 | |||||||
chr2:97168373 | C | T | 3 | a0001c0001t0001g0098 a0014c0015t0001g0099 a0014c0015t0001g0100 |
3 | HG00423.hp2 NA18612.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1633+606C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168373 | |||||||
chr2:97168631 | C | T | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1633+864C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168631 | |||||||
chr2:97168632 | G | A | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1633+865G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168632 | |||||||
chr2:97168883 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1633+1116G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168883 | |||||||
chr2:97169403 | G | C | 1 | a0001c0001t0004g0197 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1633+1636G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97169403 | |||||||
chr2:97169497 | T | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1633+1730T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97169497 | |||||||
chr2:97169652 | G | A | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1633+1885G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97169652 | |||||||
chr2:97169743 | C | A | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1633+1976C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97169743 | |||||||
chr2:97170005 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1633+2238C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170005 | |||||||
chr2:97170034 | G | C | 1 | a0009c0012t0001g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1633+2267G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170034 | |||||||
chr2:97170134 | G | A | 1 | a0002c0002t0001g0161 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1633+2367G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170134 | |||||||
chr2:97170396 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1633+2629C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170396 | |||||||
chr2:97170733 | A | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1633+2966A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170733 | |||||||
chr2:97170886 | C | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+3119C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170886 | |||||||
chr2:97170896 | G | A | 4 | a0002c0002t0001g0141 a0002c0002t0001g0161 a0002c0002t0001g0162 others(1): Show |
4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633+3129G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170896 | |||||||
chr2:97170962 | A | C | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1633+3195A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170962 | |||||||
chr2:97171029 | GTCATTAA others(7120): Show |
G | 1 | a0035c0040t0001g0122 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1633+3376_1634-146 others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97171029 | ||||||
chr2:97171264 | C | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1633+3497C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171264 | |||||||
chr2:97171399 | A | T | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1633+3632A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171399 | |||||||
chr2:97171544 | A | C | 3 | a0006c0006t0001g0101 a0006c0006t0001g0107 a0006c0006t0001g0114 |
3 | NA18952.hp1 NA18961.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1633+3777A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171544 | |||||||
chr2:97171549 | G | T | 3 | a0006c0006t0001g0101 a0006c0006t0001g0107 a0006c0006t0001g0114 |
3 | NA18952.hp1 NA18961.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1633+3782G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171549 | |||||||
chr2:97171557 | G | C | 10 | a0006c0006t0001g0101 a0006c0006t0001g0107 a0006c0006t0001g0114 others(7): Show |
10 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1633+3790G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171557 | |||||||
chr2:97171563 | A | G | 1 | a0004c0009t0002g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1633+3796A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171563 | |||||||
chr2:97171728 | A | C | 2 | a0018c0018t0001g0015 a0018c0018t0001g0016 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1633+3961A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171728 | |||||||
chr2:97172132 | T | A | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1633+4365T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172132 | |||||||
chr2:97172174 | C | T | 73 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(70): Show |
74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1633+4407C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172174 | |||||||
chr2:97172337 | A | C | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+4570A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172337 | |||||||
chr2:97172395 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1633+4628C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172395 | |||||||
chr2:97172496 | T | G | 44 | a0002c0002t0001g0129 a0002c0002t0001g0133 a0002c0002t0001g0134 others(41): Show |
44 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1633+4729T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172496 | |||||||
chr2:97172696 | A | G | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1633+4929A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172696 | |||||||
chr2:97172740 | C | T | 1 | a0006c0006t0001g0107 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1633+4973C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172740 | |||||||
chr2:97172831 | A | ATG | 72 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(69): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1633+5090_1633+509 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97172831 | ||||||
chr2:97172831 | A | ATGTG | 15 | a0002c0002t0001g0158 a0003c0003t0001g0034 a0003c0003t0001g0128 others(12): Show |
15 | HG00423.hp1 HG01123.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1633+5088_1633+509 others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97172831 | ||||||
chr2:97172831 | ATGTG | A | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1633+5088_1633+509 others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97172831 | ||||||
chr2:97172859 | A | G | 2 | a0001c0001t0001g0023 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1633+5092A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172859 | |||||||
chr2:97172859 | ATG | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1633+5100_1633+510 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97172859 | ||||||
chr2:97172861 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1633+5094G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172861 | |||||||
chr2:97172908 | C | A | 9 | a0001c0001t0001g0121 a0002c0002t0001g0133 a0003c0003t0001g0003 others(6): Show |
10 | HG02257.hp1 HG02451.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1633+5141C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172908 | |||||||
chr2:97173407 | T | G | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1633+5640T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97173407 | |||||||
chr2:97173630 | C | T | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1633+5863C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97173630 | |||||||
chr2:97173721 | G | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+5954G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97173721 | |||||||
chr2:97173876 | G | T | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1634-5862G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97173876 | |||||||
chr2:97174203 | A | T | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1634-5535A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174203 | |||||||
chr2:97174204 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1634-5534G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174204 | |||||||
chr2:97174206 | C | T | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1634-5532C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174206 | |||||||
chr2:97174529 | G | A | 1 | a0005c0005t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1634-5209G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174529 | |||||||
chr2:97174951 | C | G | 1 | a0006c0006t0001g0084 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1634-4787C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174951 | |||||||
chr2:97174964 | C | A | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4774C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174964 | |||||||
chr2:97174965 | A | C | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4773A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174965 | |||||||
chr2:97174966 | G | A | 2 | a0002c0002t0001g0145 a0003c0003t0001g0064 |
2 | HG02809.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1634-4772G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174966 | |||||||
chr2:97174967 | G | A | 13 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(10): Show |
13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.1634-4771G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174967 | |||||||
chr2:97174967 | G | C | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4771G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174967 | |||||||
chr2:97174968 | G | A | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4770G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174968 | |||||||
chr2:97174969 | A | C | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4769A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174969 | |||||||
chr2:97174971 | G | C | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4767G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174971 | |||||||
chr2:97174972 | A | T | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4766A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174972 | |||||||
chr2:97175003 | T | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1634-4735T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175003 | |||||||
chr2:97175007 | G | A | 1 | a0014c0015t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1634-4731G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175007 | |||||||
chr2:97175019 | T | C | 1 | a0004c0004t0002g0005 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1634-4719T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175019 | |||||||
chr2:97175094 | T | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1634-4644T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175094 | |||||||
chr2:97175159 | T | C | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4579T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175159 | |||||||
chr2:97175160 | T | A | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4578T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175160 | |||||||
chr2:97175162 | C | A | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4576C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175162 | |||||||
chr2:97175167 | T | A | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4571T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175167 | |||||||
chr2:97175169 | T | C | 28 | a0003c0003t0001g0034 a0003c0003t0001g0064 a0003c0003t0001g0128 others(25): Show |
29 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1634-4569T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175169 | |||||||
chr2:97175170 | T | A | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4568T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175170 | |||||||
chr2:97175171 | C | G | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4567C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175171 | |||||||
chr2:97175172 | T | A | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4566T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175172 | |||||||
chr2:97175173 | A | T | 1 | a0003c0003t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4565A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175173 | |||||||
chr2:97175198 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1634-4540A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175198 | |||||||
chr2:97175354 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-4384G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175354 | |||||||
chr2:97175360 | T | C | 1 | a0013c0013t0001g0151 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1634-4378T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175360 | |||||||
chr2:97175411 | C | T | 4 | a0002c0002t0001g0141 a0002c0002t0001g0161 a0002c0002t0001g0162 others(1): Show |
4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-4327C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175411 | |||||||
chr2:97175467 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1634-4271G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175467 | |||||||
chr2:97175535 | C | G | 1 | a0002c0002t0001g0158 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1634-4203C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175535 | |||||||
chr2:97175547 | C | G | 1 | a0004c0004t0002g0005 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1634-4191C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175547 | |||||||
chr2:97175603 | G | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-4135G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175603 | |||||||
chr2:97175759 | C | T | 129 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0002c0002t0001g0129 others(126): Show |
132 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1634-3979C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175759 | |||||||
chr2:97175986 | G | C | 2 | a0018c0018t0001g0015 a0018c0018t0001g0016 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3752G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175986 | |||||||
chr2:97175990 | T | C | 2 | a0018c0018t0001g0015 a0018c0018t0001g0016 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3748T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175990 | |||||||
chr2:97175992 | G | C | 2 | a0018c0018t0001g0015 a0018c0018t0001g0016 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3746G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175992 | |||||||
chr2:97176002 | A | C | 2 | a0018c0018t0001g0015 a0018c0018t0001g0016 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3736A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176002 | |||||||
chr2:97176008 | G | C | 2 | a0018c0018t0001g0015 a0018c0018t0001g0016 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3730G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176008 | |||||||
chr2:97176147 | G | C | 1 | a0002c0002t0001g0135 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1634-3591G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176147 | |||||||
chr2:97176185 | C | T | 1 | a0017c0019t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1634-3553C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176185 | |||||||
chr2:97176308 | C | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1634-3430C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176308 | |||||||
chr2:97176315 | G | T | 1 | a0017c0019t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1634-3423G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176315 | |||||||
chr2:97176399 | G | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1634-3339G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176399 | |||||||
chr2:97176453 | CT | C | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1634-3277delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97176453 | ||||||
chr2:97176580 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1634-3158A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176580 | |||||||
chr2:97176669 | C | T | 57 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(54): Show |
57 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.1634-3069C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176669 | |||||||
chr2:97176787 | C | T | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1634-2951C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176787 | |||||||
chr2:97176840 | G | T | 6 | a0001c0001t0004g0194 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-2898G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176840 | |||||||
chr2:97176856 | A | G | 6 | a0001c0001t0004g0194 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-2882A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176856 | |||||||
chr2:97177172 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1634-2566A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177172 | |||||||
chr2:97177369 | A | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1634-2369A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177369 | |||||||
chr2:97177432 | A | G | 1 | a0022c0047t0001g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1634-2306A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177432 | |||||||
chr2:97177436 | G | T | 2 | a0002c0002t0001g0147 a0002c0002t0001g0148 |
2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1634-2302G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177436 | |||||||
chr2:97177502 | G | A | 1 | a0003c0003t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1634-2236G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177502 | |||||||
chr2:97177730 | G | C | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1634-2008G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177730 | |||||||
chr2:97177926 | C | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-1812C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177926 | |||||||
chr2:97178370 | C | T | 3 | a0003c0003t0001g0063 a0003c0003t0001g0064 a0003c0003t0001g0065 |
3 | HG02809.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1634-1368C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178370 | |||||||
chr2:97178379 | G | A | 7 | a0001c0001t0001g0069 a0001c0001t0001g0081 a0001c0001t0001g0083 others(4): Show |
7 | HG01169.hp1 HG01361.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-1359G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178379 | |||||||
chr2:97178490 | A | C | 1 | a0005c0005t0003g0039 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1634-1248A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178490 | |||||||
chr2:97178571 | C | T | 3 | a0002c0002t0001g0154 a0002c0002t0001g0155 a0002c0002t0001g0177 |
3 | NA18612.hp1 NA18952.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1634-1167C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178571 | |||||||
chr2:97178654 | A | T | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1634-1084A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178654 | |||||||
chr2:97178674 | T | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1634-1064T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178674 | |||||||
chr2:97178676 | T | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1634-1062T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178676 | |||||||
chr2:97178692 | G | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-1046G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178692 | |||||||
chr2:97178704 | G | A | 1 | a0031c0033t0001g0108 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1634-1034G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178704 | |||||||
chr2:97178804 | T | G | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1634-934T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178804 | |||||||
chr2:97178805 | G | GT | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1634-932dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97178805 | ||||||
chr2:97178843 | T | G | 1 | a0016c0020t0001g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1634-895T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178843 | |||||||
chr2:97178847 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1634-891A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178847 | |||||||
chr2:97179249 | C | G | 8 | a0011c0011t0001g0014 a0011c0011t0001g0045 a0011c0011t0001g0046 others(5): Show |
8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1634-489C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179249 | |||||||
chr2:97179363 | C | T | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1634-375C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179363 | |||||||
chr2:97179498 | T | C | 2 | a0002c0002t0001g0154 a0002c0002t0001g0155 |
2 | NA18612.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1634-240T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179498 | |||||||
chr2:97179635 | C | T | 13 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(10): Show |
13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.1634-103C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179635 | |||||||
chr2:97179678 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1634-60T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179678 | |||||||
chr2:97179736 | A | G | 1 | a0002c0002t0001g0149 | 1 | NA19000.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1634-2A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179736 | |||||||
chr2:97179792 | G | A | 1 | a0007c0007t0006g0142 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1662+26G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 23/75 | chr2 | 97179792 | |||||||
chr2:97179844 | C | T | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1663-17C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 23/75 | chr2 | 97179844 | |||||||
chr2:97180054 | T | G | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1735+121T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180054 | |||||||
chr2:97180204 | A | G | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1735+271A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180204 | |||||||
chr2:97180266 | A | C | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1735+333A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180266 | |||||||
chr2:97180284 | C | T | 44 | a0002c0002t0001g0129 a0002c0002t0001g0133 a0002c0002t0001g0134 others(41): Show |
44 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1735+351C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180284 | |||||||
chr2:97180383 | C | T | 1 | a0002c0002t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1735+450C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180383 | |||||||
chr2:97180547 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1735+614G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180547 | |||||||
chr2:97180592 | CT | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1735+660delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180592 | |||||||
chr2:97180691 | G | A | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1735+758G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180691 | |||||||
chr2:97180715 | G | A | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1735+782G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180715 | |||||||
chr2:97180837 | A | G | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1736-761A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180837 | |||||||
chr2:97180888 | T | C | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1736-710T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180888 | |||||||
chr2:97181105 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1736-493T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97181105 | |||||||
chr2:97181113 | T | C | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1736-485T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97181113 | |||||||
chr2:97181202 | A | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1736-396A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97181202 | |||||||
chr2:97181821 | A | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1837+28A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181821 | |||||||
chr2:97181836 | A | G | 2 | a0002c0002t0001g0168 a0007c0027t0001g0169 |
2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1837+43A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181836 | |||||||
chr2:97181869 | A | G | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1837+76A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181869 | |||||||
chr2:97181869 | A | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1837+76A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181869 | |||||||
chr2:97181952 | C | T | 1 | a0003c0003t0001g0057 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1837+159C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181952 | |||||||
chr2:97182192 | C | T | 4 | a0002c0002t0001g0141 a0002c0002t0001g0161 a0002c0002t0001g0162 others(1): Show |
4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837+399C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182192 | |||||||
chr2:97182268 | T | TAAG | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1837+476_1837+478d others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | INFO_REALIGN_3_PRIME | chr2 | 97182268 | ||||||
chr2:97182327 | T | C | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1837+534T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182327 | |||||||
chr2:97182407 | A | C | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1837+614A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182407 | |||||||
chr2:97182552 | A | G | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1837+759A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182552 | |||||||
chr2:97182578 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1837+785A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182578 | |||||||
chr2:97182858 | A | G | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1838-601A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182858 | |||||||
chr2:97182951 | C | T | 1 | a0002c0002t0001g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1838-508C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182951 | |||||||
chr2:97183087 | A | G | 1 | a0003c0003t0001g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1838-372A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97183087 | |||||||
chr2:97183399 | T | C | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1838-60T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97183399 | |||||||
chr2:97183401 | T | C | 1 | a0007c0007t0001g0143 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1838-58T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97183401 | |||||||
chr2:97183555 | G | C | 1 | a0016c0020t0001g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1867-27G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 27/75 | chr2 | 97183555 | |||||||
chr2:97183726 | C | T | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1939+72C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97183726 | |||||||
chr2:97183827 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1939+173A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97183827 | |||||||
chr2:97183880 | A | G | 7 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(4): Show |
7 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+226A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97183880 | |||||||
chr2:97183932 | T | G | 142 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(139): Show |
145 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.1939+278T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97183932 | |||||||
chr2:97184138 | G | T | 4 | a0004c0004t0002g0005 a0004c0004t0002g0190 a0004c0004t0002g0191 others(1): Show |
5 | NA18941.hp2 NA18951.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+484G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184138 | |||||||
chr2:97184218 | G | A | 44 | a0002c0002t0001g0129 a0002c0002t0001g0133 a0002c0002t0001g0134 others(41): Show |
44 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1939+564G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184218 | |||||||
chr2:97184331 | C | T | 1 | a0003c0003t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1939+677C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184331 | |||||||
chr2:97184686 | A | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1940-630A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184686 | |||||||
chr2:97184693 | G | T | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1940-623G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184693 | |||||||
chr2:97184738 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0119 |
2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1940-578A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184738 | |||||||
chr2:97184808 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1940-508A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184808 | |||||||
chr2:97184940 | C | T | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1940-376C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184940 | |||||||
chr2:97185021 | G | A | 2 | a0002c0002t0001g0154 a0002c0002t0001g0155 |
2 | NA18612.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1940-295G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97185021 | |||||||
chr2:97185073 | T | A | 1 | a0006c0006t0001g0101 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1940-243T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97185073 | |||||||
chr2:97185576 | A | G | 1 | a0005c0005t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2041+66A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185576 | |||||||
chr2:97185594 | C | T | 1 | a0027c0023t0001g0157 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2041+84C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185594 | |||||||
chr2:97185683 | C | A | 1 | a0001c0001t0004g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2041+173C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185683 | |||||||
chr2:97185692 | G | A | 1 | a0001c0001t0004g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2041+182G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185692 | |||||||
chr2:97185846 | A | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2041+336A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185846 | |||||||
chr2:97185927 | T | C | 1 | a0002c0002t0001g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2041+417T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185927 | |||||||
chr2:97186091 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2041+581A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186091 | |||||||
chr2:97186099 | A | C | 8 | a0011c0011t0001g0014 a0011c0011t0001g0045 a0011c0011t0001g0046 others(5): Show |
8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+589A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186099 | |||||||
chr2:97186155 | G | A | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2041+645G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186155 | |||||||
chr2:97186244 | G | A | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2041+734G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186244 | |||||||
chr2:97186445 | A | G | 4 | a0005c0005t0003g0019 a0005c0005t0003g0037 a0005c0005t0003g0039 others(1): Show |
4 | HG00099.hp1 HG01175.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-753A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186445 | |||||||
chr2:97186532 | G | T | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2042-666G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186532 | |||||||
chr2:97186647 | A | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2042-551A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186647 | |||||||
chr2:97186800 | C | T | 2 | a0018c0018t0001g0015 a0018c0018t0001g0016 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2042-398C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186800 | |||||||
chr2:97186835 | T | C | 1 | a0030c0037t0001g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2042-363T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186835 | |||||||
chr2:97187011 | G | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2042-187G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97187011 | |||||||
chr2:97187307 | T | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2071-22T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 31/75 | chr2 | 97187307 | |||||||
chr2:97187465 | T | G | 1 | a0003c0003t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2143+64T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187465 | |||||||
chr2:97187490 | G | C | 1 | a0005c0005t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2143+89G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187490 | |||||||
chr2:97187546 | A | G | 1 | a0030c0037t0001g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2143+145A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187546 | |||||||
chr2:97187586 | A | ATGATCTT others(1881): Show |
5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2144-637_2144-636i others(1890): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | INFO_REALIGN_3_PRIME | chr2 | 97187586 | ||||||
chr2:97187728 | G | C | 1 | a0006c0006t0001g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2143+327G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187728 | |||||||
chr2:97187851 | A | G | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2143+450A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187851 | |||||||
chr2:97187861 | C | T | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2143+460C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187861 | |||||||
chr2:97187896 | A | C | 47 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(44): Show |
47 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2143+495A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187896 | |||||||
chr2:97188207 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143+806T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188207 | |||||||
chr2:97188214 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143+813C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188214 | |||||||
chr2:97188215 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143+814T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188215 | |||||||
chr2:97188235 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143+834T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188235 | |||||||
chr2:97188276 | C | A | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2144-811C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188276 | |||||||
chr2:97188287 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-800A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188287 | |||||||
chr2:97188346 | G | T | 3 | a0015c0016t0001g0044 a0015c0016t0001g0048 a0015c0016t0001g0049 |
3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2144-741G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188346 | |||||||
chr2:97188381 | G | T | 1 | a0031c0033t0001g0108 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2144-706G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188381 | |||||||
chr2:97188419 | G | C | 2 | a0001c0001t0001g0127 a0004c0004t0002g0191 |
2 | HG02071.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.2144-668G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188419 | |||||||
chr2:97188439 | T | G | 1 | a0010c0010t0001g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2144-648T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188439 | |||||||
chr2:97188447 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-640T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188447 | |||||||
chr2:97188451 | C | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG01261.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2144-636C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188451 | |||||||
chr2:97188455 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-632A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188455 | |||||||
chr2:97188458 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-629C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188458 | |||||||
chr2:97188478 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-609T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188478 | |||||||
chr2:97188498 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-589C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188498 | |||||||
chr2:97188507 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-580G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188507 | |||||||
chr2:97188593 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-494T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188593 | |||||||
chr2:97188599 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-488A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188599 | |||||||
chr2:97188603 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-484G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188603 | |||||||
chr2:97188609 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-478C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188609 | |||||||
chr2:97188614 | T | G | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-473T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188614 | |||||||
chr2:97188619 | G | A | 8 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(5): Show |
9 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2144-468G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188619 | |||||||
chr2:97188626 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-461C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188626 | |||||||
chr2:97188644 | A | G | 1 | a0003c0003t0001g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2144-443A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188644 | |||||||
chr2:97188689 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-398G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188689 | |||||||
chr2:97188761 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-326A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188761 | |||||||
chr2:97188809 | G | A | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2144-278G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188809 | |||||||
chr2:97188853 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-234A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188853 | |||||||
chr2:97188855 | A | G | 6 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2144-232A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188855 | |||||||
chr2:97188861 | C | T | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0004g0194 others(6): Show |
9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2144-226C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188861 | |||||||
chr2:97188872 | A | G | 6 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2144-215A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188872 | |||||||
chr2:97188882 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-205T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188882 | |||||||
chr2:97189047 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-40A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97189047 | |||||||
chr2:97189052 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-35C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97189052 | |||||||
chr2:97189130 | G | A | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2172+15G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189130 | |||||||
chr2:97189135 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2172+20C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189135 | |||||||
chr2:97189151 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2172+36T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189151 | |||||||
chr2:97189168 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2173-50C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189168 | |||||||
chr2:97189196 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2173-22T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189196 | |||||||
chr2:97189215 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.2173-3A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189215 | |||||||
chr2:97189300 | C | T | 2 | a0001c0001t0001g0051 a0001c0034t0001g0052 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2245+10C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189300 | |||||||
chr2:97189305 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+15C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189305 | |||||||
chr2:97189311 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+21C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189311 | |||||||
chr2:97189320 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+30G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189320 | |||||||
chr2:97189325 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+35A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189325 | |||||||
chr2:97189334 | G | T | 4 | a0012c0014t0005g0021 a0012c0014t0005g0075 a0012c0014t0005g0089 others(1): Show |
4 | HG02040.hp1 NA18965.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245+44G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189334 | |||||||
chr2:97189336 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+46A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189336 | |||||||
chr2:97189342 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+52C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189342 | |||||||
chr2:97189349 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+59A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189349 | |||||||
chr2:97189350 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+60C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189350 | |||||||
chr2:97189353 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+63C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189353 | |||||||
chr2:97189358 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+68A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189358 | |||||||
chr2:97189360 | ATCAGCGG others(4): Show |
A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+72_2245+82del others(11): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | INFO_REALIGN_3_PRIME | chr2 | 97189360 | ||||||
chr2:97189373 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+83G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189373 | |||||||
chr2:97189376 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+86T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189376 | |||||||
chr2:97189377 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+87G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189377 | |||||||
chr2:97189378 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+88G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189378 | |||||||
chr2:97189387 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+97C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189387 | |||||||
chr2:97189389 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+99T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189389 | |||||||
chr2:97189392 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+102T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189392 | |||||||
chr2:97189402 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+112C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189402 | |||||||
chr2:97189404 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+114G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189404 | |||||||
chr2:97189412 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+122A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189412 | |||||||
chr2:97189414 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+124G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189414 | |||||||
chr2:97189422 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+132G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189422 | |||||||
chr2:97189433 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+143T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189433 | |||||||
chr2:97189435 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+145A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189435 | |||||||
chr2:97189439 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+149A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189439 | |||||||
chr2:97189443 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+153C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189443 | |||||||
chr2:97189451 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+161C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189451 | |||||||
chr2:97189453 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+163C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189453 | |||||||
chr2:97189455 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+165A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189455 | |||||||
chr2:97189466 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+176C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189466 | |||||||
chr2:97189467 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+177T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189467 | |||||||
chr2:97189474 | G | A | 4 | a0001c0001t0001g0110 a0001c0001t0001g0120 a0003c0003t0001g0064 others(1): Show |
4 | HG02683.hp2 HG02809.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245+184G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189474 | |||||||
chr2:97189491 | A | C | 8 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(5): Show |
8 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2245+201A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189491 | |||||||
chr2:97189511 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+221G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189511 | |||||||
chr2:97189517 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+227G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189517 | |||||||
chr2:97189527 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+237T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189527 | |||||||
chr2:97189529 | C | T | 23 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(20): Show |
24 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.2245+239C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189529 | |||||||
chr2:97189538 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+248A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189538 | |||||||
chr2:97189539 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+249G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189539 | |||||||
chr2:97189543 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+253C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189543 | |||||||
chr2:97189548 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+258C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189548 | |||||||
chr2:97189548 | C | T | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2245+258C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189548 | |||||||
chr2:97189574 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+284G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189574 | |||||||
chr2:97189586 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+296T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189586 | |||||||
chr2:97189598 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+308G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189598 | |||||||
chr2:97189603 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2245+313A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189603 | |||||||
chr2:97189604 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+314C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189604 | |||||||
chr2:97189617 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+327A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189617 | |||||||
chr2:97189640 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+350C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189640 | |||||||
chr2:97189645 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+355G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189645 | |||||||
chr2:97189655 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+365A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189655 | |||||||
chr2:97189666 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+376G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189666 | |||||||
chr2:97189669 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+379A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189669 | |||||||
chr2:97189677 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
161 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.2245+387G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189677 | |||||||
chr2:97189685 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+395A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189685 | |||||||
chr2:97189711 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+421C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189711 | |||||||
chr2:97189711 | C | T | 1 | a0001c0001t0004g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2245+421C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189711 | |||||||
chr2:97189716 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+426A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189716 | |||||||
chr2:97189720 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+430A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189720 | |||||||
chr2:97189731 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+441G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189731 | |||||||
chr2:97189732 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+442A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189732 | |||||||
chr2:97189759 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+469T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189759 | |||||||
chr2:97189767 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+477C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189767 | |||||||
chr2:97189770 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+480A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189770 | |||||||
chr2:97189779 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+489A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189779 | |||||||
chr2:97189792 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+502T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189792 | |||||||
chr2:97189806 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+516A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189806 | |||||||
chr2:97189814 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+524C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189814 | |||||||
chr2:97189816 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+526G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189816 | |||||||
chr2:97189826 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+536T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189826 | |||||||
chr2:97189845 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+555C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189845 | |||||||
chr2:97189847 | T | C | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2245+557T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189847 | |||||||
chr2:97189861 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+571G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189861 | |||||||
chr2:97189863 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+573G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189863 | |||||||
chr2:97189865 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+575C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189865 | |||||||
chr2:97189871 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+581A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189871 | |||||||
chr2:97189890 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+600T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189890 | |||||||
chr2:97189892 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+602C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189892 | |||||||
chr2:97189898 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+608T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189898 | |||||||
chr2:97189908 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+618C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189908 | |||||||
chr2:97189909 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+619A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189909 | |||||||
chr2:97189929 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+639G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189929 | |||||||
chr2:97189930 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+640G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189930 | |||||||
chr2:97189936 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+646G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189936 | |||||||
chr2:97189944 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+654A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189944 | |||||||
chr2:97189957 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+667T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189957 | |||||||
chr2:97189965 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+675C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189965 | |||||||
chr2:97189966 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+676T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189966 | |||||||
chr2:97189997 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+707C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189997 | |||||||
chr2:97190002 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+712C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190002 | |||||||
chr2:97190008 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+718A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190008 | |||||||
chr2:97190017 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+727T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190017 | |||||||
chr2:97190018 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+728A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190018 | |||||||
chr2:97190021 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+731G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190021 | |||||||
chr2:97190035 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+745C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190035 | |||||||
chr2:97190084 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+794C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190084 | |||||||
chr2:97190096 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+806A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190096 | |||||||
chr2:97190104 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+814C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190104 | |||||||
chr2:97190121 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+831G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190121 | |||||||
chr2:97190125 | G | A | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2245+835G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190125 | |||||||
chr2:97190138 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-840C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190138 | |||||||
chr2:97190152 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-826A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190152 | |||||||
chr2:97190160 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-818T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190160 | |||||||
chr2:97190164 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-814C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190164 | |||||||
chr2:97190166 | C | A | 23 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(20): Show |
24 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.2246-812C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190166 | |||||||
chr2:97190170 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-808A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190170 | |||||||
chr2:97190172 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-806A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190172 | |||||||
chr2:97190175 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-803G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190175 | |||||||
chr2:97190177 | A | C | 24 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(21): Show |
25 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.2246-801A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190177 | |||||||
chr2:97190188 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-790A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190188 | |||||||
chr2:97190195 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-783C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190195 | |||||||
chr2:97190197 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-781G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190197 | |||||||
chr2:97190211 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-767A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190211 | |||||||
chr2:97190218 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-760G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190218 | |||||||
chr2:97190220 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-758T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190220 | |||||||
chr2:97190235 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-743T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190235 | |||||||
chr2:97190250 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-728T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190250 | |||||||
chr2:97190266 | A | G | 5 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(2): Show |
5 | HG02559.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2246-712A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190266 | |||||||
chr2:97190294 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-684A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190294 | |||||||
chr2:97190299 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-679G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190299 | |||||||
chr2:97190299 | G | GAT | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.2246-674_2246-673d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | INFO_REALIGN_3_PRIME | chr2 | 97190299 | ||||||
chr2:97190309 | C | G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2246-669C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190309 | |||||||
chr2:97190312 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-666T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190312 | |||||||
chr2:97190321 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-657C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190321 | |||||||
chr2:97190324 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-654C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190324 | |||||||
chr2:97190341 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-637C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190341 | |||||||
chr2:97190345 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-633G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190345 | |||||||
chr2:97190348 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-630A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190348 | |||||||
chr2:97190374 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-604G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190374 | |||||||
chr2:97190388 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-590A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190388 | |||||||
chr2:97190437 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-541C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190437 | |||||||
chr2:97190438 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-540A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190438 | |||||||
chr2:97190468 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-510T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190468 | |||||||
chr2:97190471 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-507A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190471 | |||||||
chr2:97190483 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-495C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190483 | |||||||
chr2:97190492 | C | A | 1 | a0028c0045t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2246-486C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190492 | |||||||
chr2:97190493 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-485T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190493 | |||||||
chr2:97190499 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-479G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190499 | |||||||
chr2:97190504 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-474T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190504 | |||||||
chr2:97190511 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-467G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190511 | |||||||
chr2:97190512 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-466G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190512 | |||||||
chr2:97190524 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-454C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190524 | |||||||
chr2:97190549 | GA | G | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.2246-428delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190549 | |||||||
chr2:97190561 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-417T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190561 | |||||||
chr2:97190572 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-406C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190572 | |||||||
chr2:97190579 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-399A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190579 | |||||||
chr2:97190596 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-382C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190596 | |||||||
chr2:97190597 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-381C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190597 | |||||||
chr2:97190642 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-336G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190642 | |||||||
chr2:97190650 | C | G | 2 | a0001c0001t0001g0083 a0004c0004t0002g0191 |
2 | NA18941.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2246-328C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190650 | |||||||
chr2:97190651 | G | A | 1 | a0005c0021t0003g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2246-327G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190651 | |||||||
chr2:97190662 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-316G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190662 | |||||||
chr2:97190690 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-288T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190690 | |||||||
chr2:97190698 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-280C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190698 | |||||||
chr2:97190706 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-272C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190706 | |||||||
chr2:97190707 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-271C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190707 | |||||||
chr2:97190724 | G | A | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.2246-254G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190724 | |||||||
chr2:97190729 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-249T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190729 | |||||||
chr2:97190741 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-237C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190741 | |||||||
chr2:97190743 | A | G | 14 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(11): Show |
15 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2246-235A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190743 | |||||||
chr2:97190752 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-226G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190752 | |||||||
chr2:97190756 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-222C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190756 | |||||||
chr2:97190772 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-206C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190772 | |||||||
chr2:97190777 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-201A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190777 | |||||||
chr2:97190780 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-198A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190780 | |||||||
chr2:97190810 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-168A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190810 | |||||||
chr2:97190811 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-167C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190811 | |||||||
chr2:97190828 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-150T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190828 | |||||||
chr2:97190833 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-145C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190833 | |||||||
chr2:97190840 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-138A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190840 | |||||||
chr2:97190844 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-134G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190844 | |||||||
chr2:97190845 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-133A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190845 | |||||||
chr2:97190846 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-132C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190846 | |||||||
chr2:97190857 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-121A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190857 | |||||||
chr2:97190863 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-115G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190863 | |||||||
chr2:97190871 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-107A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190871 | |||||||
chr2:97190875 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-103G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190875 | |||||||
chr2:97190885 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-93A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190885 | |||||||
chr2:97190888 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-90G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190888 | |||||||
chr2:97190890 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-88T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190890 | |||||||
chr2:97190892 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-86C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190892 | |||||||
chr2:97190895 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-83C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190895 | |||||||
chr2:97190897 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-81G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190897 | |||||||
chr2:97190901 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-77G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190901 | |||||||
chr2:97190903 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-75T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190903 | |||||||
chr2:97190910 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-68G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190910 | |||||||
chr2:97190911 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-67T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190911 | |||||||
chr2:97190912 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-66G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190912 | |||||||
chr2:97190932 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-46A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190932 | |||||||
chr2:97190937 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-41G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190937 | |||||||
chr2:97190938 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-40T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190938 | |||||||
chr2:97190942 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-36T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190942 | |||||||
chr2:97191012 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.2274+6T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191012 | |||||||
chr2:97191017 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+11T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191017 | |||||||
chr2:97191035 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+29C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191035 | |||||||
chr2:97191036 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+30T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191036 | |||||||
chr2:97191040 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+34A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191040 | |||||||
chr2:97191044 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+38C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191044 | |||||||
chr2:97191048 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+42A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191048 | |||||||
chr2:97191059 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2275-50T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191059 | |||||||
chr2:97191087 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2275-22C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191087 | |||||||
chr2:97191090 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2275-19T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191090 | |||||||
chr2:97191091 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2275-18C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191091 | |||||||
chr2:97191196 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+15G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191196 | |||||||
chr2:97191198 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+17C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191198 | |||||||
chr2:97191200 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+19T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191200 | |||||||
chr2:97191207 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+26T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191207 | |||||||
chr2:97191233 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+52T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191233 | |||||||
chr2:97191241 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+60T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191241 | |||||||
chr2:97191249 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+68G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191249 | |||||||
chr2:97191253 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+72T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191253 | |||||||
chr2:97191254 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+73G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191254 | |||||||
chr2:97191257 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+76C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191257 | |||||||
chr2:97191258 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+77T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191258 | |||||||
chr2:97191265 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+84C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191265 | |||||||
chr2:97191268 | C | T | 1 | a0004c0009t0002g0182 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2347+87C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191268 | |||||||
chr2:97191269 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+88G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191269 | |||||||
chr2:97191282 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+101A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191282 | |||||||
chr2:97191284 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+103C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191284 | |||||||
chr2:97191292 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+111T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191292 | |||||||
chr2:97191294 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+113T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191294 | |||||||
chr2:97191298 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+117G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191298 | |||||||
chr2:97191305 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+124T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191305 | |||||||
chr2:97191312 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+131G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191312 | |||||||
chr2:97191313 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+132C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191313 | |||||||
chr2:97191315 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+134G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191315 | |||||||
chr2:97191325 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+144G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191325 | |||||||
chr2:97191333 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+152G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191333 | |||||||
chr2:97191348 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+167T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191348 | |||||||
chr2:97191363 | G | A | 3 | a0002c0002t0001g0154 a0002c0002t0001g0155 a0004c0004t0002g0191 |
3 | NA18612.hp1 NA18941.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.2347+182G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191363 | |||||||
chr2:97191365 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+184A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191365 | |||||||
chr2:97191391 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+210C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191391 | |||||||
chr2:97191397 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+216T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191397 | |||||||
chr2:97191423 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+242G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191423 | |||||||
chr2:97191428 | C | A | 14 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(11): Show |
15 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2347+247C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191428 | |||||||
chr2:97191430 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+249T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191430 | |||||||
chr2:97191442 | G | C | 43 | a0002c0002t0001g0129 a0002c0002t0001g0133 a0002c0002t0001g0134 others(40): Show |
43 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2347+261G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191442 | |||||||
chr2:97191449 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+268G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191449 | |||||||
chr2:97191466 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+285C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191466 | |||||||
chr2:97191470 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+289A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191470 | |||||||
chr2:97191523 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+342A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191523 | |||||||
chr2:97191526 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+345G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191526 | |||||||
chr2:97191541 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+360T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191541 | |||||||
chr2:97191544 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+363A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191544 | |||||||
chr2:97191547 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+366C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191547 | |||||||
chr2:97191565 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+384T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191565 | |||||||
chr2:97191590 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+409G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191590 | |||||||
chr2:97191592 | G | A | 5 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(2): Show |
5 | HG02559.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2347+411G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191592 | |||||||
chr2:97191594 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+413C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191594 | |||||||
chr2:97191598 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+417C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191598 | |||||||
chr2:97191598 | C | T | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2347+417C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191598 | |||||||
chr2:97191599 | G | A | 3 | a0002c0002t0001g0129 a0002c0002t0001g0158 a0002c0002t0001g0166 |
3 | HG01123.hp1 HG01169.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2347+418G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191599 | |||||||
chr2:97191609 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+428C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191609 | |||||||
chr2:97191610 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+429C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191610 | |||||||
chr2:97191628 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+447C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191628 | |||||||
chr2:97191631 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+450G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191631 | |||||||
chr2:97191673 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+492C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191673 | |||||||
chr2:97191679 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+498T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191679 | |||||||
chr2:97191681 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+500T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191681 | |||||||
chr2:97191690 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+509G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191690 | |||||||
chr2:97191695 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+514T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191695 | |||||||
chr2:97191697 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+516C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191697 | |||||||
chr2:97191698 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+517C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191698 | |||||||
chr2:97191725 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+544A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191725 | |||||||
chr2:97191735 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+554G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191735 | |||||||
chr2:97191738 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+557A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191738 | |||||||
chr2:97191739 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+558T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191739 | |||||||
chr2:97191744 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+563T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191744 | |||||||
chr2:97191750 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+569A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191750 | |||||||
chr2:97191751 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+570A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191751 | |||||||
chr2:97191752 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+571C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191752 | |||||||
chr2:97191765 | G | A | 3 | a0001c0001t0001g0109 a0004c0004t0002g0191 a0031c0033t0001g0108 |
3 | NA18941.hp2 NA18946.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.2347+584G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191765 | |||||||
chr2:97191771 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+590A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191771 | |||||||
chr2:97191773 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+592A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191773 | |||||||
chr2:97191779 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+598A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191779 | |||||||
chr2:97191781 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+600A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191781 | |||||||
chr2:97191789 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+608T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191789 | |||||||
chr2:97191790 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+609G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191790 | |||||||
chr2:97191798 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+617A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191798 | |||||||
chr2:97191810 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+629C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191810 | |||||||
chr2:97191819 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+638C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191819 | |||||||
chr2:97191820 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+639A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191820 | |||||||
chr2:97191823 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+642C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191823 | |||||||
chr2:97191826 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+645C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191826 | |||||||
chr2:97191839 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+658G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191839 | |||||||
chr2:97191847 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+666G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191847 | |||||||
chr2:97191848 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+667C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191848 | |||||||
chr2:97191866 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+685C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191866 | |||||||
chr2:97191899 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+718C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191899 | |||||||
chr2:97191900 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+719C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191900 | |||||||
chr2:97191917 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+736T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191917 | |||||||
chr2:97191958 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+777A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191958 | |||||||
chr2:97191962 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+781A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191962 | |||||||
chr2:97191965 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+784T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191965 | |||||||
chr2:97191968 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+787T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191968 | |||||||
chr2:97191983 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+802G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191983 | |||||||
chr2:97191987 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+806A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191987 | |||||||
chr2:97192001 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+820A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192001 | |||||||
chr2:97192020 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-838T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192020 | |||||||
chr2:97192042 | T | C | 9 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(6): Show |
10 | HG00597.hp2 NA18951.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2348-816T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192042 | |||||||
chr2:97192055 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-803T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192055 | |||||||
chr2:97192070 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-788G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192070 | |||||||
chr2:97192090 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-768A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192090 | |||||||
chr2:97192099 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-759T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192099 | |||||||
chr2:97192102 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-756A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192102 | |||||||
chr2:97192106 | T | A | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2348-752T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192106 | |||||||
chr2:97192117 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-741A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192117 | |||||||
chr2:97192139 | A | G | 1 | a0027c0023t0001g0157 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2348-719A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192139 | |||||||
chr2:97192149 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-709A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192149 | |||||||
chr2:97192192 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-666G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192192 | |||||||
chr2:97192196 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-662T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192196 | |||||||
chr2:97192204 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-654G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192204 | |||||||
chr2:97192207 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-651G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192207 | |||||||
chr2:97192221 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-637A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192221 | |||||||
chr2:97192222 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-636G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192222 | |||||||
chr2:97192227 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-631G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192227 | |||||||
chr2:97192241 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-617T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192241 | |||||||
chr2:97192317 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-541T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192317 | |||||||
chr2:97192318 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-540G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192318 | |||||||
chr2:97192320 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-538A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192320 | |||||||
chr2:97192348 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-510A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192348 | |||||||
chr2:97192351 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-507C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192351 | |||||||
chr2:97192372 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-486C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192372 | |||||||
chr2:97192398 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-460G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192398 | |||||||
chr2:97192402 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-456G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192402 | |||||||
chr2:97192403 | C | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-455C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192403 | |||||||
chr2:97192404 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-454T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192404 | |||||||
chr2:97192441 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-417C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192441 | |||||||
chr2:97192442 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-416G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192442 | |||||||
chr2:97192445 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-413T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192445 | |||||||
chr2:97192489 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-369C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192489 | |||||||
chr2:97192522 | C | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-336C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192522 | |||||||
chr2:97192542 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-316T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192542 | |||||||
chr2:97192562 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-296C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192562 | |||||||
chr2:97192571 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-287G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192571 | |||||||
chr2:97192575 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-283C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192575 | |||||||
chr2:97192579 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-279T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192579 | |||||||
chr2:97192583 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-275A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192583 | |||||||
chr2:97192588 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-270G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192588 | |||||||
chr2:97192604 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-254C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192604 | |||||||
chr2:97192605 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-253A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192605 | |||||||
chr2:97192610 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-248G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192610 | |||||||
chr2:97192658 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-200G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192658 | |||||||
chr2:97192673 | G | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-185G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192673 | |||||||
chr2:97192691 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-167T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192691 | |||||||
chr2:97192709 | C | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-149C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192709 | |||||||
chr2:97192726 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-132T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192726 | |||||||
chr2:97192727 | A | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-131A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192727 | |||||||
chr2:97192731 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-127G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192731 | |||||||
chr2:97192769 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-89A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192769 | |||||||
chr2:97192782 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-76A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192782 | |||||||
chr2:97192784 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-74A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192784 | |||||||
chr2:97192791 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-67T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192791 | |||||||
chr2:97192812 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-46T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192812 | |||||||
chr2:97192816 | A | G | 1 | a0014c0015t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2348-42A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192816 | |||||||
chr2:97192819 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-39G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192819 | |||||||
chr2:97192822 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-36A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192822 | |||||||
chr2:97192835 | T | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-23T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192835 | |||||||
chr2:97192839 | T | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-19T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192839 | |||||||
chr2:97192851 | T | G | 1 | a0003c0003t0001g0065 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.2348-7T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192851 | |||||||
chr2:97192891 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.2376+5T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192891 | |||||||
chr2:97192895 | A | G | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+9A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192895 | |||||||
chr2:97192897 | A | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+11A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192897 | |||||||
chr2:97192912 | G | T | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+26G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192912 | |||||||
chr2:97192915 | T | C | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+29T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192915 | |||||||
chr2:97192916 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+30G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192916 | |||||||
chr2:97192916 | G | GAGTTAAT others(1864): Show |
5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2376+36_2376+37ins others(1871): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | INFO_REALIGN_3_PRIME | chr2 | 97192916 | ||||||
chr2:97192916 | G | GAGTTAAT others(1864): Show |
9 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(6): Show |
10 | HG00597.hp2 NA18951.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2376+36_2376+37ins others(1871): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | INFO_REALIGN_3_PRIME | chr2 | 97192916 | ||||||
chr2:97192966 | T | A | 1 | a0002c0002t0001g0129 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2377-15T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192966 | |||||||
chr2:97193311 | C | T | 55 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(52): Show |
55 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2449+258C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193311 | |||||||
chr2:97193330 | A | G | 143 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(140): Show |
146 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.2449+277A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193330 | |||||||
chr2:97193407 | G | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2449+354G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193407 | |||||||
chr2:97193446 | C | T | 20 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(17): Show |
21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2449+393C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193446 | |||||||
chr2:97193490 | T | A | 70 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(67): Show |
71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2449+437T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193490 | |||||||
chr2:97193491 | A | G | 108 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(105): Show |
111 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.2449+438A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193491 | |||||||
chr2:97193537 | A | G | 70 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(67): Show |
71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2449+484A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193537 | |||||||
chr2:97193560 | G | A | 4 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0176 others(1): Show |
4 | HG01099.hp1 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.2449+507G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193560 | |||||||
chr2:97193613 | T | G | 1 | a0003c0003t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2449+560T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193613 | |||||||
chr2:97193639 | A | G | 22 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(19): Show |
23 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.2449+586A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193639 | |||||||
chr2:97193839 | A | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2449+786A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193839 | |||||||
chr2:97193859 | C | T | 2 | a0001c0001t0001g0069 a0035c0040t0001g0122 |
2 | NA19079.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2449+806C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193859 | |||||||
chr2:97193942 | T | C | 2 | a0002c0002t0001g0147 a0002c0002t0001g0148 |
2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2450-784T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193942 | |||||||
chr2:97193950 | A | C | 1 | a0004c0004t0002g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2450-776A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193950 | |||||||
chr2:97194217 | C | G | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2450-509C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194217 | |||||||
chr2:97194306 | A | G | 70 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(67): Show |
71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2450-420A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194306 | |||||||
chr2:97194341 | T | A | 1 | a0002c0002t0001g0154 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2450-385T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194341 | |||||||
chr2:97194386 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2450-340C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194386 | |||||||
chr2:97194486 | C | T | 126 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(123): Show |
129 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2450-240C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194486 | |||||||
chr2:97194627 | C | A | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2450-99C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194627 | |||||||
chr2:97194792 | G | A | 28 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(25): Show |
29 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.2478+38G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 39/75 | chr2 | 97194792 | |||||||
chr2:97194956 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2551+39A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97194956 | |||||||
chr2:97195044 | C | G | 1 | a0003c0003t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2551+127C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195044 | |||||||
chr2:97195109 | C | T | 1 | a0026c0041t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2551+192C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195109 | |||||||
chr2:97195110 | G | A | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2551+193G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195110 | |||||||
chr2:97195234 | G | A | 70 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(67): Show |
71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2551+317G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195234 | |||||||
chr2:97195260 | G | A | 2 | a0006c0006t0001g0086 a0006c0006t0001g0088 |
2 | HG00558.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2551+343G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195260 | |||||||
chr2:97195268 | G | A | 1 | a0014c0015t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+351G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195268 | |||||||
chr2:97195300 | A | T | 1 | a0014c0015t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+383A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195300 | |||||||
chr2:97195308 | A | G | 1 | a0014c0015t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+391A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195308 | |||||||
chr2:97195334 | G | A | 1 | a0014c0015t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+417G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195334 | |||||||
chr2:97195389 | T | G | 1 | a0014c0015t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+472T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195389 | |||||||
chr2:97195603 | A | C | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2551+686A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195603 | |||||||
chr2:97195712 | T | A | 1 | a0002c0002t0001g0177 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2551+795T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195712 | |||||||
chr2:97195777 | T | G | 2 | a0018c0018t0001g0015 a0018c0018t0001g0016 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2552-816T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195777 | |||||||
chr2:97195808 | T | A | 1 | a0005c0005t0003g0037 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2552-785T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195808 | |||||||
chr2:97195870 | A | G | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2552-723A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195870 | |||||||
chr2:97195899 | C | T | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2552-694C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195899 | |||||||
chr2:97195935 | C | T | 20 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(17): Show |
21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2552-658C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195935 | |||||||
chr2:97196193 | G | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2552-400G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196193 | |||||||
chr2:97196241 | G | T | 2 | a0003c0003t0001g0068 a0005c0031t0001g0012 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2552-352G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196241 | |||||||
chr2:97196292 | A | G | 1 | a0010c0010t0001g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2552-301A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196292 | |||||||
chr2:97196323 | G | GC | 70 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(67): Show |
71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2552-270_2552-269i others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196323 | |||||||
chr2:97196375 | G | A | 1 | a0009c0046t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2552-218G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196375 | |||||||
chr2:97196481 | G | A | 1 | a0002c0002t0001g0177 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2552-112G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196481 | |||||||
chr2:97196523 | T | A | 137 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(134): Show |
140 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.2552-70T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196523 | |||||||
chr2:97196659 | G | A | 55 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(52): Show |
55 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2580+38G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 41/75 | chr2 | 97196659 | |||||||
chr2:97196677 | A | T | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2581-39A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 41/75 | chr2 | 97196677 | |||||||
chr2:97196900 | G | T | 9 | a0003c0003t0001g0059 a0003c0003t0001g0060 a0003c0003t0001g0061 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2653+112G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97196900 | |||||||
chr2:97196919 | C | T | 55 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(52): Show |
55 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2653+131C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97196919 | |||||||
chr2:97196990 | A | C | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2653+202A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97196990 | |||||||
chr2:97196994 | T | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2653+206T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97196994 | |||||||
chr2:97197133 | C | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2653+345C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197133 | |||||||
chr2:97197134 | C | G | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2653+346C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197134 | |||||||
chr2:97197179 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2653+391C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197179 | |||||||
chr2:97197189 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2653+401C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197189 | |||||||
chr2:97197191 | G | C | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2653+403G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197191 | |||||||
chr2:97197200 | C | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2653+412C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197200 | |||||||
chr2:97197283 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2653+495G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197283 | |||||||
chr2:97197501 | A | G | 1 | a0005c0005t0003g0040 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2653+713A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197501 | |||||||
chr2:97197588 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0105 |
2 | HG00609.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2653+800G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197588 | |||||||
chr2:97197751 | C | A | 1 | a0001c0001t0004g0200 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2654-712C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197751 | |||||||
chr2:97197788 | G | T | 70 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(67): Show |
71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2654-675G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197788 | |||||||
chr2:97197794 | A | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2654-669A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197794 | |||||||
chr2:97197881 | C | A | 1 | a0016c0020t0001g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2654-582C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197881 | |||||||
chr2:97198123 | A | C | 2 | a0002c0002t0001g0168 a0007c0027t0001g0169 |
2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2654-340A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198123 | |||||||
chr2:97198142 | T | G | 1 | a0015c0016t0001g0048 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2654-321T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198142 | |||||||
chr2:97198285 | T | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2654-178T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198285 | |||||||
chr2:97198331 | A | T | 1 | a0003c0003t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2654-132A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198331 | |||||||
chr2:97198332 | C | A | 1 | a0003c0003t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2654-131C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198332 | |||||||
chr2:97198536 | C | T | 6 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2682+45C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 43/75 | chr2 | 97198536 | |||||||
chr2:97198551 | T | C | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.2683-35T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 43/75 | chr2 | 97198551 | |||||||
chr2:97198578 | C | G | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.2683-8C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 43/75 | chr2 | 97198578 | |||||||
chr2:97198839 | G | A | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2755+181G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97198839 | |||||||
chr2:97198916 | C | T | 57 | a0001c0001t0001g0023 a0002c0002t0001g0129 a0002c0002t0001g0131 others(54): Show |
57 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2755+258C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97198916 | |||||||
chr2:97198926 | C | T | 2 | a0003c0003t0001g0068 a0005c0031t0001g0012 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2755+268C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97198926 | |||||||
chr2:97199063 | A | G | 1 | a0009c0046t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2755+405A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199063 | |||||||
chr2:97199112 | T | C | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2755+454T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199112 | |||||||
chr2:97199192 | C | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2755+534C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199192 | |||||||
chr2:97199235 | A | C | 3 | a0001c0001t0001g0006 a0014c0015t0001g0007 a0034c0048t0001g0013 |
3 | HG00609.hp1 HG02040.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2755+577A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199235 | |||||||
chr2:97199304 | C | A | 16 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(13): Show |
17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2755+646C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199304 | |||||||
chr2:97199307 | A | T | 15 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(12): Show |
15 | HG00423.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2755+649A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199307 | |||||||
chr2:97199323 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2755+665G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199323 | |||||||
chr2:97199324 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2755+666G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199324 | |||||||
chr2:97199329 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2755+671C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199329 | |||||||
chr2:97199398 | T | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2755+740T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199398 | |||||||
chr2:97199404 | G | A | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2755+746G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199404 | |||||||
chr2:97199420 | G | C | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.2755+762G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199420 | |||||||
chr2:97199466 | G | A | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2755+808G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199466 | |||||||
chr2:97199719 | C | G | 6 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2756-615C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199719 | |||||||
chr2:97199788 | G | A | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2756-546G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199788 | |||||||
chr2:97199825 | G | C | 1 | a0031c0033t0001g0108 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2756-509G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199825 | |||||||
chr2:97199887 | G | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2756-447G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199887 | |||||||
chr2:97199963 | G | T | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2756-371G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199963 | |||||||
chr2:97200092 | A | G | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2756-242A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97200092 | |||||||
chr2:97200277 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2756-57A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97200277 | |||||||
chr2:97200584 | C | T | 2 | a0010c0010t0001g0030 a0010c0010t0001g0031 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2857+59C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200584 | |||||||
chr2:97200633 | A | G | 16 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(13): Show |
17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2857+108A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200633 | |||||||
chr2:97200699 | C | A | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2857+174C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200699 | |||||||
chr2:97200705 | T | C | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.2857+180T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200705 | |||||||
chr2:97200717 | C | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2857+192C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200717 | |||||||
chr2:97200946 | C | A | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2857+421C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200946 | |||||||
chr2:97200997 | G | T | 7 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(4): Show |
7 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.2857+472G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200997 | |||||||
chr2:97201031 | T | G | 9 | a0001c0001t0001g0112 a0008c0008t0001g0170 a0008c0008t0001g0171 others(6): Show |
9 | HG01261.hp1 HG01358.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.2857+506T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201031 | |||||||
chr2:97201125 | T | C | 1 | a0005c0005t0003g0040 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2857+600T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201125 | |||||||
chr2:97201167 | A | G | 1 | a0019c0028t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2857+642A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201167 | |||||||
chr2:97201191 | A | G | 16 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(13): Show |
17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2857+666A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201191 | |||||||
chr2:97201192 | C | T | 74 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(71): Show |
75 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2857+667C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201192 | |||||||
chr2:97201343 | T | A | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2857+818T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201343 | |||||||
chr2:97201447 | A | T | 1 | a0010c0010t0001g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2858-755A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201447 | |||||||
chr2:97201685 | G | A | 7 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2858-517G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201685 | |||||||
chr2:97201697 | G | T | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2858-505G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201697 | |||||||
chr2:97201733 | A | G | 2 | a0002c0002t0001g0135 a0010c0026t0001g0028 |
2 | HG01515.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2858-469A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201733 | |||||||
chr2:97201751 | C | T | 3 | a0009c0012t0001g0074 a0009c0012t0001g0094 a0028c0045t0001g0073 |
3 | HG01106.hp1 HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2858-451C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201751 | |||||||
chr2:97201765 | A | G | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2858-437A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201765 | |||||||
chr2:97201829 | A | G | 2 | a0004c0009t0002g0184 a0004c0009t0002g0185 |
2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2858-373A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201829 | |||||||
chr2:97201889 | A | C | 10 | a0002c0002t0001g0176 a0003c0003t0001g0059 a0003c0003t0001g0060 others(7): Show |
10 | HG01106.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2858-313A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201889 | |||||||
chr2:97202053 | C | T | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2858-149C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97202053 | |||||||
chr2:97202093 | T | C | 1 | a0008c0008t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2858-109T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97202093 | |||||||
chr2:97202118 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2858-84A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97202118 | |||||||
chr2:97202133 | G | C | 74 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(71): Show |
75 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2858-69G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97202133 | |||||||
chr2:97202237 | A | G | 1 | a0002c0002t0001g0145 | 1 | HG03688.hp1 | splice_region_variant&intron_variant | LOW | c.2886+7A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 47/75 | chr2 | 97202237 | |||||||
chr2:97202425 | C | G | 1 | a0017c0019t0001g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2959+32C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202425 | |||||||
chr2:97202433 | G | A | 1 | a0004c0004t0002g0203 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2959+40G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202433 | |||||||
chr2:97202476 | C | T | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2959+83C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202476 | |||||||
chr2:97202503 | A | G | 6 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2959+110A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202503 | |||||||
chr2:97202576 | T | C | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2959+183T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202576 | |||||||
chr2:97202774 | C | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG01106.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2959+381C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202774 | |||||||
chr2:97202946 | G | C | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2959+553G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202946 | |||||||
chr2:97203006 | C | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2959+613C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203006 | |||||||
chr2:97203100 | T | G | 2 | a0007c0007t0006g0142 a0010c0026t0001g0028 |
2 | HG02300.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2959+707T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203100 | |||||||
chr2:97203165 | C | A | 1 | a0010c0010t0001g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2959+772C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203165 | |||||||
chr2:97203168 | A | T | 3 | a0002c0002t0001g0159 a0002c0002t0001g0168 a0007c0027t0001g0169 |
3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2959+775A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203168 | |||||||
chr2:97203189 | T | C | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2959+796T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203189 | |||||||
chr2:97203319 | C | T | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2960-749C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203319 | |||||||
chr2:97203416 | C | G | 2 | a0001c0001t0001g0051 a0001c0034t0001g0052 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2960-652C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203416 | |||||||
chr2:97203445 | C | A | 1 | a0009c0012t0001g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2960-623C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203445 | |||||||
chr2:97203468 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2960-600C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203468 | |||||||
chr2:97203489 | G | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2960-579G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203489 | |||||||
chr2:97203682 | T | G | 1 | a0006c0006t0001g0084 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2960-386T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203682 | |||||||
chr2:97203692 | T | C | 8 | a0001c0034t0001g0052 a0003c0003t0001g0003 a0003c0003t0001g0053 others(5): Show |
9 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2960-376T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203692 | |||||||
chr2:97203740 | G | C | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2960-328G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203740 | |||||||
chr2:97203742 | C | G | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2960-326C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203742 | |||||||
chr2:97203742 | C | T | 1 | a0010c0010t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2960-326C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203742 | |||||||
chr2:97203743 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2960-325G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203743 | |||||||
chr2:97203802 | A | G | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2960-266A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203802 | |||||||
chr2:97203871 | A | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2960-197A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203871 | |||||||
chr2:97203930 | C | G | 1 | a0014c0015t0001g0100 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2960-138C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203930 | |||||||
chr2:97204117 | A | G | 2 | a0004c0004t0002g0186 a0004c0004t0002g0187 |
2 | NA18965.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2988+21A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 49/75 | chr2 | 97204117 | |||||||
chr2:97204141 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2988+45C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 49/75 | chr2 | 97204141 | |||||||
chr2:97204153 | C | CT | 13 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(10): Show |
13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.2989-35dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 49/75 | INFO_REALIGN_3_PRIME | chr2 | 97204153 | ||||||
chr2:97204185 | A | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | splice_region_variant&intron_variant | LOW | c.2989-6A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 49/75 | chr2 | 97204185 | |||||||
chr2:97204303 | A | T | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3061+40A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204303 | |||||||
chr2:97204314 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3061+51G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204314 | |||||||
chr2:97204335 | A | T | 45 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(42): Show |
47 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.3061+72A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204335 | |||||||
chr2:97204344 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3061+81C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204344 | |||||||
chr2:97204444 | A | G | 1 | a0013c0013t0001g0151 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3061+181A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204444 | |||||||
chr2:97204492 | T | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3061+229T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204492 | |||||||
chr2:97204495 | A | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3061+232A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204495 | |||||||
chr2:97204497 | A | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3061+234A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204497 | |||||||
chr2:97204510 | A | G | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3061+247A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204510 | |||||||
chr2:97204517 | G | A | 2 | a0001c0001t0001g0051 a0001c0034t0001g0052 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3061+254G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204517 | |||||||
chr2:97204568 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3061+305G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204568 | |||||||
chr2:97204576 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3061+313G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204576 | |||||||
chr2:97204579 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3061+316G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204579 | |||||||
chr2:97204580 | A | G | 72 | a0001c0001t0001g0023 a0002c0002t0001g0129 a0002c0002t0001g0131 others(69): Show |
73 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.3061+317A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204580 | |||||||
chr2:97204602 | A | T | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3061+339A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204602 | |||||||
chr2:97204656 | C | G | 3 | a0015c0016t0001g0044 a0015c0016t0001g0048 a0015c0016t0001g0049 |
3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.3061+393C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204656 | |||||||
chr2:97204675 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3061+412C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204675 | |||||||
chr2:97204890 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0121 |
2 | HG03654.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.3061+627G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204890 | |||||||
chr2:97204898 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3061+635A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204898 | |||||||
chr2:97204948 | C | T | 1 | a0005c0005t0003g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3061+685C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204948 | |||||||
chr2:97205076 | T | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3061+813T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205076 | |||||||
chr2:97205109 | T | C | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3062-831T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205109 | |||||||
chr2:97205224 | G | A | 46 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.3062-716G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205224 | |||||||
chr2:97205304 | G | A | 20 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(17): Show |
21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3062-636G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205304 | |||||||
chr2:97205577 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3062-363G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205577 | |||||||
chr2:97205614 | T | A | 1 | a0001c0001t0001g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3062-326T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205614 | |||||||
chr2:97205705 | G | A | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3062-235G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205705 | |||||||
chr2:97205889 | A | G | 26 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(23): Show |
27 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.3062-51A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205889 | |||||||
chr2:97205998 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3090+30G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 51/75 | chr2 | 97205998 | |||||||
chr2:97206169 | G | A | 10 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(7): Show |
11 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.3163+34G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206169 | |||||||
chr2:97206182 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3163+47A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206182 | |||||||
chr2:97206209 | C | T | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3163+74C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206209 | |||||||
chr2:97206271 | C | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.3163+136C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206271 | |||||||
chr2:97206341 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3163+206G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206341 | |||||||
chr2:97206359 | A | G | 1 | a0004c0004t0002g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3163+224A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206359 | |||||||
chr2:97206411 | T | G | 56 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(53): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3163+276T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206411 | |||||||
chr2:97206708 | C | G | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3163+573C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206708 | |||||||
chr2:97207009 | C | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3164-802C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207009 | |||||||
chr2:97207070 | G | A | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3164-741G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207070 | |||||||
chr2:97207086 | G | T | 1 | a0003c0003t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3164-725G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207086 | |||||||
chr2:97207305 | A | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3164-506A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207305 | |||||||
chr2:97207324 | T | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3164-487T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207324 | |||||||
chr2:97207422 | T | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-389T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207422 | |||||||
chr2:97207425 | T | A | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-386T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207425 | |||||||
chr2:97207425 | T | G | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3164-386T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207425 | |||||||
chr2:97207430 | C | G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-381C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207430 | |||||||
chr2:97207431 | C | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-380C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207431 | |||||||
chr2:97207454 | A | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-357A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207454 | |||||||
chr2:97207482 | C | G | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3164-329C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207482 | |||||||
chr2:97207484 | G | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3164-327G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207484 | |||||||
chr2:97207584 | A | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3164-227A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207584 | |||||||
chr2:97207650 | G | A | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3164-161G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207650 | |||||||
chr2:97207656 | C | T | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.3164-155C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207656 | |||||||
chr2:97207705 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3164-106G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207705 | |||||||
chr2:97207752 | G | A | 7 | a0002c0002t0001g0147 a0002c0002t0001g0148 a0002c0002t0001g0149 others(4): Show |
7 | HG00558.hp1 NA18946.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.3164-59G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207752 | |||||||
chr2:97207778 | C | T | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3164-33C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207778 | |||||||
chr2:97207893 | A | T | 48 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(45): Show |
48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.3193-41A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 53/75 | chr2 | 97207893 | |||||||
chr2:97208087 | C | A | 3 | a0004c0009t0002g0183 a0004c0009t0002g0184 a0004c0009t0002g0185 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3265+81C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208087 | |||||||
chr2:97208172 | T | C | 1 | a0002c0002t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3265+166T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208172 | |||||||
chr2:97208187 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3265+181G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208187 | |||||||
chr2:97208262 | T | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3265+256T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208262 | |||||||
chr2:97208316 | G | A | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.3265+310G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208316 | |||||||
chr2:97208357 | C | A | 8 | a0006c0006t0001g0084 a0006c0006t0001g0086 a0006c0006t0001g0087 others(5): Show |
8 | HG00558.hp2 NA18952.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.3265+351C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208357 | |||||||
chr2:97208359 | C | T | 8 | a0006c0006t0001g0084 a0006c0006t0001g0086 a0006c0006t0001g0087 others(5): Show |
8 | HG00558.hp2 NA18952.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.3265+353C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208359 | |||||||
chr2:97208361 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3265+355T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208361 | |||||||
chr2:97208471 | G | A | 2 | a0001c0001t0004g0198 a0001c0001t0004g0199 |
2 | HG00642.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3265+465G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208471 | |||||||
chr2:97208520 | G | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG00609.hp2 NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.3265+514G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208520 | |||||||
chr2:97208588 | A | G | 71 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(68): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3265+582A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208588 | |||||||
chr2:97208613 | A | C | 1 | a0019c0028t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3265+607A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208613 | |||||||
chr2:97208621 | G | A | 1 | a0019c0028t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3265+615G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208621 | |||||||
chr2:97208952 | C | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3266-729C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208952 | |||||||
chr2:97209139 | A | T | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3266-542A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209139 | |||||||
chr2:97209161 | T | C | 1 | a0007c0007t0001g0010 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3266-520T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209161 | |||||||
chr2:97209182 | A | G | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3266-499A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209182 | |||||||
chr2:97209207 | A | T | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3266-474A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209207 | |||||||
chr2:97209249 | T | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3266-432T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209249 | |||||||
chr2:97209290 | C | G | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3266-391C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209290 | |||||||
chr2:97209452 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3266-229G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209452 | |||||||
chr2:97209472 | T | A | 1 | a0022c0047t0001g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3266-209T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209472 | |||||||
chr2:97209550 | C | CA | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3266-128dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | INFO_REALIGN_3_PRIME | chr2 | 97209550 | ||||||
chr2:97209586 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3266-95C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209586 | |||||||
chr2:97210159 | T | C | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3367+287T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210159 | |||||||
chr2:97210160 | A | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3367+288A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210160 | |||||||
chr2:97210273 | G | C | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.3367+401G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210273 | |||||||
chr2:97210359 | A | T | 1 | a0002c0002t0001g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3367+487A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210359 | |||||||
chr2:97210509 | A | T | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3367+637A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210509 | |||||||
chr2:97210543 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3367+671G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210543 | |||||||
chr2:97210757 | A | G | 7 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(4): Show |
7 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3368-789A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210757 | |||||||
chr2:97210887 | C | A | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3368-659C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210887 | |||||||
chr2:97211062 | G | A | 60 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(57): Show |
61 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.3368-484G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211062 | |||||||
chr2:97211143 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3368-403A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211143 | |||||||
chr2:97211266 | C | T | 67 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(64): Show |
68 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.3368-280C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211266 | |||||||
chr2:97211311 | G | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3368-235G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211311 | |||||||
chr2:97211403 | G | A | 1 | a0025c0043t0001g0167 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3368-143G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211403 | |||||||
chr2:97211613 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3396+39T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 57/75 | chr2 | 97211613 | |||||||
chr2:97211662 | T | C | 127 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(124): Show |
130 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(127): Show |
splice_region_variant&intron_variant | LOW | c.3397-7T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 57/75 | chr2 | 97211662 | |||||||
chr2:97211765 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3469+24A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97211765 | |||||||
chr2:97211942 | T | C | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3469+201T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97211942 | |||||||
chr2:97212200 | G | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3469+459G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212200 | |||||||
chr2:97212228 | G | A | 1 | a0022c0047t0001g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3469+487G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212228 | |||||||
chr2:97212296 | A | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3469+555A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212296 | |||||||
chr2:97212341 | C | A | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3469+600C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212341 | |||||||
chr2:97212458 | A | T | 72 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0133 others(69): Show |
73 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.3469+717A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212458 | |||||||
chr2:97213032 | C | G | 1 | a0004c0009t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3470-387C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97213032 | |||||||
chr2:97213960 | C | T | 2 | a0003c0003t0001g0020 a0003c0003t0001g0067 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3571+346C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97213960 | |||||||
chr2:97214015 | C | T | 16 | a0001c0001t0004g0195 a0004c0004t0002g0005 a0004c0004t0002g0180 others(13): Show |
17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.3571+401C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214015 | |||||||
chr2:97214290 | A | G | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.3571+676A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214290 | |||||||
chr2:97214300 | TAA | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(195): Show |
202 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.3571+688_3571+689d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | INFO_REALIGN_3_PRIME | chr2 | 97214300 | ||||||
chr2:97214307 | G | A | 1 | a0017c0019t0001g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3571+693G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214307 | |||||||
chr2:97214322 | GTTTT | G | 144 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.3571+711_3571+714d others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | INFO_REALIGN_3_PRIME | chr2 | 97214322 | ||||||
chr2:97214815 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3572-486C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214815 | |||||||
chr2:97214848 | C | T | 1 | a0016c0020t0001g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3572-453C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214848 | |||||||
chr2:97214849 | CT | C | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3572-450delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | INFO_REALIGN_3_PRIME | chr2 | 97214849 | ||||||
chr2:97215094 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3572-207T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97215094 | |||||||
chr2:97215101 | T | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3572-200T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97215101 | |||||||
chr2:97215137 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3572-164A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97215137 | |||||||
chr2:97215156 | C | G | 1 | a0002c0002t0001g0147 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3572-145C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97215156 | |||||||
chr2:97215341 | C | G | 1 | a0009c0012t0001g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3600+12C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 61/75 | chr2 | 97215341 | |||||||
chr2:97215530 | G | A | 66 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(63): Show |
68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.3673+33G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215530 | |||||||
chr2:97215558 | T | G | 1 | a0016c0020t0001g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3673+61T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215558 | |||||||
chr2:97215806 | G | A | 1 | a0004c0004t0002g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3673+309G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215806 | |||||||
chr2:97215807 | G | T | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3673+310G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215807 | |||||||
chr2:97215817 | A | C | 1 | a0003c0003t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3673+320A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215817 | |||||||
chr2:97215875 | A | C | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3673+378A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215875 | |||||||
chr2:97216210 | A | T | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3673+713A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216210 | |||||||
chr2:97216678 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3674-499A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216678 | |||||||
chr2:97216887 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3674-290G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216887 | |||||||
chr2:97216911 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.3674-266G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216911 | |||||||
chr2:97216924 | C | T | 2 | a0002c0002t0001g0155 a0002c0002t0001g0177 |
2 | NA18952.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.3674-253C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216924 | |||||||
chr2:97217137 | A | G | 1 | a0007c0007t0001g0010 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3674-40A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97217137 | |||||||
chr2:97217234 | T | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3702+29T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 63/75 | chr2 | 97217234 | |||||||
chr2:97217833 | C | T | 1 | a0003c0003t0001g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3775+461C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97217833 | |||||||
chr2:97217837 | A | G | 12 | a0007c0007t0001g0008 a0007c0007t0001g0009 a0007c0007t0001g0010 others(9): Show |
12 | HG00558.hp1 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.3775+465A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97217837 | |||||||
chr2:97217863 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3775+491G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97217863 | |||||||
chr2:97217868 | A | G | 12 | a0007c0007t0001g0008 a0007c0007t0001g0009 a0007c0007t0001g0010 others(9): Show |
12 | HG00558.hp1 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.3775+496A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97217868 | |||||||
chr2:97218090 | C | G | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3775+718C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218090 | |||||||
chr2:97218168 | A | G | 1 | a0003c0003t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3775+796A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218168 | |||||||
chr2:97218322 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.3776-728T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218322 | |||||||
chr2:97218516 | T | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3776-534T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218516 | |||||||
chr2:97218855 | G | GT | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(146): Show |
153 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.3776-191dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | INFO_REALIGN_3_PRIME | chr2 | 97218855 | ||||||
chr2:97218855 | G | GTTTTTGA others(53002): Show |
1 | a0001c0001t0001g0097 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3776-191_3776-190i others(53011): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | INFO_REALIGN_3_PRIME | chr2 | 97218855 | ||||||
chr2:97218880 | C | G | 16 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(13): Show |
16 | HG00423.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.3776-170C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218880 | |||||||
chr2:97219026 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
130 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.3776-24T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97219026 | |||||||
chr2:97219451 | T | TTTTTTTG others(10): Show |
2 | a0003c0003t0001g0020 a0003c0003t0001g0067 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3877+234_3877+250d others(19): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97219451 | ||||||
chr2:97219596 | C | G | 18 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(15): Show |
19 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3877+350C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219596 | |||||||
chr2:97219742 | A | G | 9 | a0003c0003t0001g0059 a0003c0003t0001g0060 a0003c0003t0001g0061 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3877+496A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219742 | |||||||
chr2:97219834 | A | G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3877+588A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219834 | |||||||
chr2:97219851 | T | A | 8 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(5): Show |
8 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3877+605T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219851 | |||||||
chr2:97219867 | C | T | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3877+621C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219867 | |||||||
chr2:97219880 | T | G | 3 | a0002c0002t0001g0159 a0002c0002t0001g0168 a0007c0027t0001g0169 |
3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3877+634T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219880 | |||||||
chr2:97219962 | T | G | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3877+716T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219962 | |||||||
chr2:97220051 | C | CTG | 3 | a0002c0002t0001g0147 a0002c0002t0001g0148 a0002c0002t0001g0153 |
3 | HG01496.hp1 NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.3877+839_3877+840d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | ||||||
chr2:97220051 | CTG | C | 2 | a0002c0002t0001g0202 a0007c0007t0001g0008 |
2 | HG01934.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.3877+839_3877+840d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | ||||||
chr2:97220051 | CTGTG | C | 4 | a0002c0002t0001g0177 a0007c0007t0001g0009 a0007c0007t0001g0010 others(1): Show |
4 | HG00642.hp1 HG01975.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.3877+837_3877+840d others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | ||||||
chr2:97220051 | CTGTGTG | C | 8 | a0004c0017t0002g0188 a0010c0010t0001g0029 a0010c0010t0001g0030 others(5): Show |
8 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.3877+835_3877+840d others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | ||||||
chr2:97220051 | CTGTGTGT others(1): Show |
C | 5 | a0001c0034t0001g0052 a0002c0002t0001g0131 a0004c0009t0002g0181 others(2): Show |
5 | HG02071.hp1 HG03225.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.3877+833_3877+840d others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | ||||||
chr2:97220051 | CTGTGTGT others(3): Show |
C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(135): Show |
142 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3877+831_3877+840d others(12): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | ||||||
chr2:97220051 | CTGTGTGT others(5): Show |
C | 8 | a0004c0004t0002g0180 a0008c0008t0001g0170 a0008c0008t0001g0171 others(5): Show |
8 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.3877+829_3877+840d others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | ||||||
chr2:97220085 | G | T | 2 | a0013c0013t0001g0151 a0026c0041t0001g0165 |
2 | HG02738.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.3877+839G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220085 | |||||||
chr2:97220086 | T | C | 1 | a0026c0041t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3877+840T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220086 | |||||||
chr2:97220106 | T | C | 1 | a0014c0015t0001g0100 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3877+860T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220106 | |||||||
chr2:97220189 | T | C | 1 | a0026c0041t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3877+943T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220189 | |||||||
chr2:97220241 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3877+995A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220241 | |||||||
chr2:97220248 | C | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3877+1002C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220248 | |||||||
chr2:97220269 | G | C | 2 | a0001c0001t0001g0077 a0022c0047t0001g0027 |
2 | HG01891.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.3877+1023G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220269 | |||||||
chr2:97220277 | G | GTAC | 49 | a0001c0001t0001g0006 a0001c0001t0001g0077 a0001c0001t0001g0125 others(46): Show |
50 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.3877+1031_3877+103 others(7): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220277 | |||||||
chr2:97220278 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0077 a0001c0001t0001g0125 others(46): Show |
50 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.3877+1032G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220278 | |||||||
chr2:97220289 | G | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(17): Show |
20 | HG00609.hp1 HG00642.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3877+1043G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220289 | |||||||
chr2:97220312 | G | T | 5 | a0009c0012t0001g0071 a0009c0012t0001g0074 a0009c0012t0001g0091 others(2): Show |
5 | HG01106.hp1 HG02602.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.3877+1066G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220312 | |||||||
chr2:97220375 | A | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(54): Show |
58 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.3877+1129A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220375 | |||||||
chr2:97220452 | T | G | 2 | a0031c0033t0001g0108 a0034c0048t0001g0013 |
2 | NA18946.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3877+1206T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220452 | |||||||
chr2:97220476 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(71): Show |
75 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.3877+1230T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220476 | |||||||
chr2:97220490 | A | G | 1 | a0002c0002t0001g0162 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3877+1244A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220490 | |||||||
chr2:97220558 | G | A | 66 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(63): Show |
68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.3877+1312G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220558 | |||||||
chr2:97220691 | T | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3877+1445T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220691 | |||||||
chr2:97220719 | G | A | 1 | a0002c0002t0001g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3877+1473G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220719 | |||||||
chr2:97220729 | C | CT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(113): Show |
119 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.3877+1501dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220729 | ||||||
chr2:97220729 | CT | C | 10 | a0002c0002t0001g0155 a0008c0008t0001g0170 a0008c0008t0001g0171 others(7): Show |
10 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.3877+1501delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220729 | ||||||
chr2:97220729 | CTT | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3877+1500_3877+150 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220729 | ||||||
chr2:97220761 | C | CTT | 61 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(58): Show |
63 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.3877+1526_3877+152 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220761 | ||||||
chr2:97220761 | C | CTTT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(58): Show |
62 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.3877+1525_3877+152 others(7): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220761 | ||||||
chr2:97220774 | A | T | 65 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(62): Show |
67 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.3877+1528A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220774 | |||||||
chr2:97220775 | A | T | 25 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0005c0005t0003g0019 others(22): Show |
26 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.3877+1529A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220775 | |||||||
chr2:97220776 | T | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(64): Show |
69 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.3877+1530T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220776 | |||||||
chr2:97220776 | T | TA | 14 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(11): Show |
15 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.3877+1530_3877+153 others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220776 | |||||||
chr2:97220777 | T | A | 26 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0005c0005t0003g0019 others(23): Show |
27 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.3877+1531T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220777 | |||||||
chr2:97220789 | T | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(57): Show |
61 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.3877+1543T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220789 | |||||||
chr2:97220866 | C | T | 1 | a0005c0005t0003g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3877+1620C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220866 | |||||||
chr2:97220934 | G | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(57): Show |
61 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.3877+1688G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220934 | |||||||
chr2:97220937 | C | G | 1 | a0009c0012t0001g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3877+1691C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220937 | |||||||
chr2:97220942 | C | A | 1 | a0009c0012t0001g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3877+1696C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220942 | |||||||
chr2:97220962 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3877+1716A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220962 | |||||||
chr2:97220985 | A | T | 1 | a0001c0001t0001g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3877+1739A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220985 | |||||||
chr2:97221024 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(195): Show |
202 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.3877+1778A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221024 | |||||||
chr2:97221142 | A | G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(64): Show |
69 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.3877+1896A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221142 | |||||||
chr2:97221170 | T | G | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3877+1924T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221170 | |||||||
chr2:97221259 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3877+2013G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221259 | |||||||
chr2:97221433 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3877+2187G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221433 | |||||||
chr2:97221605 | A | G | 7 | a0001c0001t0001g0104 a0005c0005t0003g0019 a0005c0005t0003g0037 others(4): Show |
7 | HG00099.hp1 HG01123.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.3877+2359A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221605 | |||||||
chr2:97221653 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3877+2407G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221653 | |||||||
chr2:97221707 | A | T | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3877+2461A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221707 | |||||||
chr2:97221740 | C | T | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3877+2494C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221740 | |||||||
chr2:97221772 | CT | C | 9 | a0003c0003t0001g0059 a0003c0003t0001g0060 a0003c0003t0001g0061 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3877+2529delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97221772 | ||||||
chr2:97221806 | G | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3877+2560G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221806 | |||||||
chr2:97221883 | G | A | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3877+2637G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221883 | |||||||
chr2:97221945 | TG | T | 7 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(4): Show |
7 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3877+2700delG | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221945 | |||||||
chr2:97222088 | T | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3878-2718T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222088 | |||||||
chr2:97222159 | C | A | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3878-2647C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222159 | |||||||
chr2:97222178 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3878-2628G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222178 | |||||||
chr2:97222250 | T | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(65): Show |
69 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.3878-2556T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222250 | |||||||
chr2:97222310 | G | A | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3878-2496G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222310 | |||||||
chr2:97222415 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(150): Show |
157 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.3878-2391G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222415 | |||||||
chr2:97222499 | G | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(64): Show |
69 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.3878-2307G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222499 | |||||||
chr2:97222543 | C | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3878-2263C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222543 | |||||||
chr2:97222591 | C | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3878-2215C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222591 | |||||||
chr2:97222691 | A | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3878-2115A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222691 | |||||||
chr2:97222872 | T | A | 2 | a0016c0020t0001g0018 a0016c0020t0001g0033 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3878-1934T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222872 | |||||||
chr2:97222883 | C | T | 1 | a0002c0002t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3878-1923C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222883 | |||||||
chr2:97222913 | A | G | 2 | a0001c0001t0001g0051 a0001c0034t0001g0052 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3878-1893A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222913 | |||||||
chr2:97222958 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3878-1848A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222958 | |||||||
chr2:97222997 | C | T | 2 | a0003c0003t0001g0020 a0003c0003t0001g0067 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3878-1809C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222997 | |||||||
chr2:97223098 | C | CT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(87): Show |
92 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3878-1688dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97223098 | ||||||
chr2:97223098 | C | CTT | 21 | a0001c0001t0001g0092 a0001c0001t0001g0102 a0001c0001t0001g0106 others(18): Show |
22 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3878-1689_3878-168 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97223098 | ||||||
chr2:97223098 | CT | C | 9 | a0004c0004t0002g0005 a0004c0004t0002g0186 a0004c0004t0002g0187 others(6): Show |
10 | NA18941.hp2 NA18951.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3878-1688delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97223098 | ||||||
chr2:97223098 | CTT | C | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3878-1689_3878-168 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97223098 | ||||||
chr2:97223123 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1683C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223123 | |||||||
chr2:97223124 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1682A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223124 | |||||||
chr2:97223131 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1675T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223131 | |||||||
chr2:97223155 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1651T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223155 | |||||||
chr2:97223176 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1630C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223176 | |||||||
chr2:97223186 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1620C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223186 | |||||||
chr2:97223222 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1584C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223222 | |||||||
chr2:97223235 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1571A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223235 | |||||||
chr2:97223261 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1545C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223261 | |||||||
chr2:97223262 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1544A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223262 | |||||||
chr2:97223320 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1486T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223320 | |||||||
chr2:97223337 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1469G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223337 | |||||||
chr2:97223344 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1462T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223344 | |||||||
chr2:97223345 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1461T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223345 | |||||||
chr2:97223346 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1460G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223346 | |||||||
chr2:97223359 | A | G | 1 | a0007c0027t0001g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3878-1447A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223359 | |||||||
chr2:97223539 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(122): Show |
128 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.3878-1267T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223539 | |||||||
chr2:97223637 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1169T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223637 | |||||||
chr2:97223665 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1141C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223665 | |||||||
chr2:97223689 | A | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3878-1117A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223689 | |||||||
chr2:97224066 | T | C | 2 | a0002c0002t0001g0163 a0026c0041t0001g0165 |
2 | HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3878-740T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224066 | |||||||
chr2:97224179 | T | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
130 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.3878-627T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224179 | |||||||
chr2:97224263 | G | T | 1 | a0003c0003t0001g0057 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3878-543G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224263 | |||||||
chr2:97224431 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(57): Show |
61 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.3878-375G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224431 | |||||||
chr2:97224436 | G | GT | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3878-363dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97224436 | ||||||
chr2:97224444 | G | GT | 8 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(5): Show |
9 | HG00597.hp2 HG04115.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.3878-355dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97224444 | ||||||
chr2:97224444 | G | T | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3878-362G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224444 | |||||||
chr2:97224452 | G | GT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(56): Show |
60 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.3878-341dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97224452 | ||||||
chr2:97224452 | G | T | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3878-354G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224452 | |||||||
chr2:97224453 | T | G | 1 | a0004c0009t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3878-353T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224453 | |||||||
chr2:97224456 | T | G | 3 | a0005c0005t0003g0040 a0005c0005t0003g0041 a0029c0049t0003g0043 |
3 | HG01099.hp2 HG01981.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.3878-350T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224456 | |||||||
chr2:97224606 | C | T | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3878-200C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224606 | |||||||
chr2:97224730 | G | A | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3878-76G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224730 | |||||||
chr2:97224796 | A | AT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
splice_acceptor_variant&intron_variant | HIGH | c.3878-3dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97224796 | ||||||
chr2:97225227 | C | T | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3951+348C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225227 | |||||||
chr2:97225266 | G | C | 20 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(17): Show |
21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3951+387G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225266 | |||||||
chr2:97225484 | T | C | 3 | a0015c0016t0001g0044 a0015c0016t0001g0048 a0015c0016t0001g0049 |
3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.3951+605T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225484 | |||||||
chr2:97225699 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3951+820C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225699 | |||||||
chr2:97225803 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3951+924G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225803 | |||||||
chr2:97225990 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3951+1111G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225990 | |||||||
chr2:97226002 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
159 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.3951+1123T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226002 | |||||||
chr2:97226066 | A | C | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3951+1187A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226066 | |||||||
chr2:97226073 | C | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3951+1194C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226073 | |||||||
chr2:97226075 | G | A | 3 | a0001c0001t0001g0069 a0028c0045t0001g0073 a0033c0025t0001g0123 |
3 | HG03688.hp2 NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3951+1196G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226075 | |||||||
chr2:97226086 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
143 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.3951+1207T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226086 | |||||||
chr2:97226087 | G | A | 1 | a0029c0049t0003g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3951+1208G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226087 | |||||||
chr2:97226157 | G | A | 2 | a0002c0002t0001g0131 a0003c0003t0001g0204 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3951+1278G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226157 | |||||||
chr2:97226257 | C | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
161 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.3951+1378C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226257 | |||||||
chr2:97226442 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(148): Show |
155 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.3951+1563C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226442 | |||||||
chr2:97226445 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(148): Show |
155 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.3951+1566G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226445 | |||||||
chr2:97226550 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.3951+1671G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226550 | |||||||
chr2:97226561 | C | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(88): Show |
94 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.3951+1682C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226561 | |||||||
chr2:97226562 | C | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(88): Show |
94 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.3951+1683C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226562 | |||||||
chr2:97226566 | G | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(88): Show |
94 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.3951+1687G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226566 | |||||||
chr2:97226635 | T | C | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3951+1756T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226635 | |||||||
chr2:97226828 | G | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(148): Show |
155 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.3951+1949G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226828 | |||||||
chr2:97226839 | C | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3951+1960C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226839 | |||||||
chr2:97226894 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3951+2015G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226894 | |||||||
chr2:97226923 | A | C | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3951+2044A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226923 | |||||||
chr2:97226943 | C | T | 2 | a0002c0002t0001g0154 a0002c0002t0001g0155 |
2 | NA18612.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.3951+2064C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226943 | |||||||
chr2:97226958 | T | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3951+2079T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226958 | |||||||
chr2:97226979 | G | A | 1 | a0008c0008t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3951+2100G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226979 | |||||||
chr2:97227106 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3951+2227C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227106 | |||||||
chr2:97227185 | T | G | 4 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0154 others(1): Show |
4 | HG01099.hp1 HG01515.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3951+2306T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227185 | |||||||
chr2:97227254 | A | G | 2 | a0003c0003t0001g0020 a0003c0003t0001g0067 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3951+2375A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227254 | |||||||
chr2:97227345 | G | C | 1 | a0035c0040t0001g0122 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3951+2466G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227345 | |||||||
chr2:97227379 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3951+2500T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227379 | |||||||
chr2:97227615 | A | C | 2 | a0003c0003t0001g0020 a0003c0003t0001g0067 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3951+2736A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227615 | |||||||
chr2:97227950 | G | A | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3951+3071G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227950 | |||||||
chr2:97228023 | C | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3951+3144C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228023 | |||||||
chr2:97228196 | G | A | 27 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(24): Show |
28 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.3951+3317G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228196 | |||||||
chr2:97228238 | A | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG00609.hp2 NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.3951+3359A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228238 | |||||||
chr2:97228265 | C | T | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3951+3386C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228265 | |||||||
chr2:97228368 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
162 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.3951+3489T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228368 | |||||||
chr2:97228391 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3951+3512G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228391 | |||||||
chr2:97228473 | G | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3951+3594G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228473 | |||||||
chr2:97228586 | G | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3951+3707G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228586 | |||||||
chr2:97228635 | C | T | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3951+3756C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228635 | |||||||
chr2:97228638 | C | T | 4 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0154 others(1): Show |
4 | HG01099.hp1 HG01515.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3951+3759C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228638 | |||||||
chr2:97228646 | T | C | 47 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0034 others(44): Show |
49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.3951+3767T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228646 | |||||||
chr2:97228743 | G | T | 1 | a0003c0003t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3951+3864G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228743 | |||||||
chr2:97228792 | C | G | 2 | a0003c0003t0001g0020 a0003c0003t0001g0067 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3951+3913C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228792 | |||||||
chr2:97228849 | T | C | 3 | a0002c0002t0001g0159 a0002c0002t0001g0168 a0007c0027t0001g0169 |
3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3951+3970T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228849 | |||||||
chr2:97228862 | A | G | 4 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0154 others(1): Show |
4 | HG01099.hp1 HG01515.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3951+3983A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228862 | |||||||
chr2:97229068 | A | G | 8 | a0011c0011t0001g0014 a0011c0011t0001g0045 a0011c0011t0001g0046 others(5): Show |
8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.3951+4189A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229068 | |||||||
chr2:97229089 | G | A | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3951+4210G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229089 | |||||||
chr2:97229375 | T | C | 6 | a0001c0001t0004g0194 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3952-4355T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229375 | |||||||
chr2:97229538 | C | T | 1 | a0003c0003t0001g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3952-4192C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229538 | |||||||
chr2:97229547 | G | A | 4 | a0005c0005t0003g0040 a0005c0005t0003g0041 a0005c0021t0003g0002 others(1): Show |
5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.3952-4183G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229547 | |||||||
chr2:97229713 | A | G | 11 | a0002c0002t0001g0131 a0008c0008t0001g0170 a0008c0008t0001g0171 others(8): Show |
11 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3952-4017A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229713 | |||||||
chr2:97229772 | G | A | 20 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(17): Show |
21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3952-3958G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229772 | |||||||
chr2:97230239 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(137): Show |
144 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3952-3491C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230239 | |||||||
chr2:97230473 | C | T | 5 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0154 others(2): Show |
5 | HG01099.hp1 HG01515.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.3952-3257C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230473 | |||||||
chr2:97230563 | A | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.3952-3167A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230563 | |||||||
chr2:97230621 | A | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3952-3109A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230621 | |||||||
chr2:97230712 | G | A | 4 | a0013c0013t0001g0146 a0013c0013t0001g0150 a0013c0013t0001g0151 others(1): Show |
4 | HG00558.hp1 NA18946.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3952-3018G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230712 | |||||||
chr2:97230713 | C | T | 4 | a0013c0013t0001g0146 a0013c0013t0001g0150 a0013c0013t0001g0151 others(1): Show |
4 | HG00558.hp1 NA18946.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3952-3017C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230713 | |||||||
chr2:97230803 | A | G | 2 | a0001c0001t0001g0069 a0033c0025t0001g0123 |
2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3952-2927A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230803 | |||||||
chr2:97230950 | A | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.3952-2780A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230950 | |||||||
chr2:97231061 | CT | C | 2 | a0001c0001t0001g0069 a0033c0025t0001g0123 |
2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3952-2668delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231061 | |||||||
chr2:97231137 | G | T | 1 | a0009c0012t0001g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3952-2593G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231137 | |||||||
chr2:97231240 | C | G | 1 | a0002c0002t0001g0177 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3952-2490C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231240 | |||||||
chr2:97231245 | G | A | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3952-2485G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231245 | |||||||
chr2:97231402 | A | G | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3952-2328A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231402 | |||||||
chr2:97231423 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3952-2307C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231423 | |||||||
chr2:97231546 | C | T | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3952-2184C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231546 | |||||||
chr2:97231622 | A | G | 1 | a0003c0003t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3952-2108A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231622 | |||||||
chr2:97231647 | A | C | 1 | a0004c0009t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3952-2083A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231647 | |||||||
chr2:97231724 | C | T | 1 | a0005c0005t0003g0040 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3952-2006C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231724 | |||||||
chr2:97231864 | A | G | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3952-1866A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231864 | |||||||
chr2:97231871 | G | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3952-1859G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231871 | |||||||
chr2:97231948 | G | A | 2 | a0003c0003t0001g0068 a0005c0031t0001g0012 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3952-1782G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231948 | |||||||
chr2:97231963 | A | G | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3952-1767A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231963 | |||||||
chr2:97232024 | A | T | 1 | a0001c0001t0004g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3952-1706A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232024 | |||||||
chr2:97232036 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
130 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.3952-1694T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232036 | |||||||
chr2:97232280 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
158 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.3952-1450G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232280 | |||||||
chr2:97232385 | G | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
159 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.3952-1345G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232385 | |||||||
chr2:97232410 | A | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
87 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.3952-1320A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232410 | |||||||
chr2:97232412 | A | G | 1 | a0014c0015t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3952-1318A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232412 | |||||||
chr2:97232418 | A | G | 1 | a0005c0005t0007g0035 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3952-1312A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232418 | |||||||
chr2:97232457 | A | C | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3952-1273A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232457 | |||||||
chr2:97232501 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3952-1229T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232501 | |||||||
chr2:97232559 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3952-1171G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232559 | |||||||
chr2:97232596 | T | C | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3952-1134T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232596 | |||||||
chr2:97232645 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3952-1085T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232645 | |||||||
chr2:97232684 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0119 |
2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3952-1046C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232684 | |||||||
chr2:97232810 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3952-920T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232810 | |||||||
chr2:97232875 | T | C | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3952-855T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232875 | |||||||
chr2:97232927 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(131): Show |
138 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.3952-803C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232927 | |||||||
chr2:97233009 | TA | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
158 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.3952-706delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | INFO_REALIGN_3_PRIME | chr2 | 97233009 | ||||||
chr2:97233011 | A | T | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3952-719A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233011 | |||||||
chr2:97233087 | G | A | 1 | a0003c0003t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3952-643G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233087 | |||||||
chr2:97233094 | G | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3952-636G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233094 | |||||||
chr2:97233249 | G | C | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3952-481G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233249 | |||||||
chr2:97233560 | T | C | 1 | a0002c0002t0001g0135 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3952-170T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233560 | |||||||
chr2:97233932 | T | C | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4093+61T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97233932 | |||||||
chr2:97234350 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4093+479A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234350 | |||||||
chr2:97234492 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(156): Show |
163 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.4093+621T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234492 | |||||||
chr2:97234813 | T | C | 11 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(8): Show |
12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.4093+942T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234813 | |||||||
chr2:97234898 | T | A | 1 | a0005c0031t0001g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4093+1027T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234898 | |||||||
chr2:97234972 | T | TA | 2 | a0004c0017t0002g0188 a0004c0017t0002g0192 |
2 | NA18999.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.4093+1101_4093+110 others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234972 | |||||||
chr2:97234973 | C | A | 2 | a0004c0017t0002g0188 a0004c0017t0002g0192 |
2 | NA18999.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.4093+1102C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234973 | |||||||
chr2:97235015 | C | T | 1 | a0003c0003t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4093+1144C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235015 | |||||||
chr2:97235016 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(158): Show |
165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.4093+1145A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235016 | |||||||
chr2:97235106 | G | T | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+1235G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235106 | |||||||
chr2:97235168 | C | T | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+1297C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235168 | |||||||
chr2:97235240 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4093+1369A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235240 | |||||||
chr2:97235253 | C | T | 1 | a0010c0010t0001g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4093+1382C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235253 | |||||||
chr2:97235373 | A | G | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+1502A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235373 | |||||||
chr2:97235418 | G | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
164 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.4093+1547G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235418 | |||||||
chr2:97235436 | C | T | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4093+1565C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235436 | |||||||
chr2:97235518 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(80): Show |
85 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.4093+1647A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235518 | |||||||
chr2:97236163 | T | C | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4093+2292T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236163 | |||||||
chr2:97236339 | T | C | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4093+2468T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236339 | |||||||
chr2:97236534 | T | C | 1 | a0009c0046t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4093+2663T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236534 | |||||||
chr2:97236887 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4093+3016C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236887 | |||||||
chr2:97236973 | C | T | 7 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0202 others(4): Show |
7 | HG00558.hp1 HG01099.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.4093+3102C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236973 | |||||||
chr2:97237215 | A | G | 2 | a0001c0034t0001g0052 a0034c0048t0001g0013 |
2 | NA19070.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4093+3344A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237215 | |||||||
chr2:97237273 | C | T | 12 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(9): Show |
12 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.4093+3402C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237273 | |||||||
chr2:97237276 | G | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(51): Show |
55 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.4093+3405G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237276 | |||||||
chr2:97237358 | T | C | 1 | a0015c0016t0001g0048 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4093+3487T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237358 | |||||||
chr2:97237427 | T | C | 7 | a0001c0034t0001g0052 a0004c0009t0002g0181 a0004c0009t0002g0182 others(4): Show |
7 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+3556T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237427 | |||||||
chr2:97237531 | C | T | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+3660C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237531 | |||||||
chr2:97237761 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.4094-3505G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237761 | |||||||
chr2:97237801 | T | C | 2 | a0003c0003t0001g0054 a0003c0030t0001g0066 |
2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4094-3465T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237801 | |||||||
chr2:97237903 | A | G | 10 | a0001c0034t0001g0052 a0006c0006t0001g0084 a0006c0006t0001g0086 others(7): Show |
10 | HG00558.hp2 NA18952.hp1 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.4094-3363A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237903 | |||||||
chr2:97238131 | A | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.4094-3135A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238131 | |||||||
chr2:97238349 | G | A | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4094-2917G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238349 | |||||||
chr2:97238479 | G | A | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4094-2787G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238479 | |||||||
chr2:97238527 | C | T | 69 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
72 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.4094-2739C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238527 | |||||||
chr2:97238951 | C | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
132 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.4094-2315C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238951 | |||||||
chr2:97239014 | A | G | 2 | a0003c0003t0001g0061 a0003c0003t0001g0179 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4094-2252A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239014 | |||||||
chr2:97239170 | A | C | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-2096A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239170 | |||||||
chr2:97239239 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4094-2027G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239239 | |||||||
chr2:97239295 | C | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4094-1971C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239295 | |||||||
chr2:97239339 | G | GT | 9 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(6): Show |
9 | HG01261.hp1 HG01358.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.4094-1914dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97239339 | ||||||
chr2:97239339 | GT | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.4094-1914delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97239339 | ||||||
chr2:97239339 | GTT | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.4094-1915_4094-191 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97239339 | ||||||
chr2:97239715 | C | T | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4094-1551C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239715 | |||||||
chr2:97239771 | T | C | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4094-1495T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239771 | |||||||
chr2:97239951 | A | G | 1 | a0008c0008t0001g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4094-1315A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239951 | |||||||
chr2:97240109 | G | GT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(131): Show |
137 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.4094-1150dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240109 | ||||||
chr2:97240117 | A | T | 5 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0004c0004t0002g0186 others(2): Show |
5 | HG01123.hp2 HG01496.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-1149A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240117 | |||||||
chr2:97240273 | G | A | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4094-993G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240273 | |||||||
chr2:97240348 | T | G | 4 | a0001c0035t0001g0103 a0002c0002t0001g0163 a0003c0003t0001g0179 others(1): Show |
4 | HG02683.hp1 HG02723.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.4094-918T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240348 | |||||||
chr2:97240467 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4094-799G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240467 | |||||||
chr2:97240541 | C | T | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4094-725C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240541 | |||||||
chr2:97240732 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
158 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.4094-534G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240732 | |||||||
chr2:97240912 | A | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.4094-354A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240912 | |||||||
chr2:97240982 | G | GT | 14 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(11): Show |
14 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.4094-248dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | G | GTT | 5 | a0002c0002t0001g0131 a0002c0002t0001g0139 a0002c0002t0001g0154 others(2): Show |
5 | HG01175.hp2 HG01358.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-249_4094-248d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | GT | G | 5 | a0002c0002t0001g0141 a0002c0002t0001g0153 a0002c0002t0001g0168 others(2): Show |
5 | HG00741.hp2 HG01070.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-248delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | GTTTTTT | G | 28 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0069 others(25): Show |
28 | HG00423.hp2 HG00558.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4094-253_4094-248d others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | GTTTTTTT | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(86): Show |
92 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.4094-254_4094-248d others(9): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | GTTTTTTT others(1): Show |
G | 16 | a0003c0003t0001g0054 a0003c0003t0001g0059 a0003c0003t0001g0061 others(13): Show |
16 | HG00558.hp2 HG01243.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.4094-255_4094-248d others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | GTTTTTTT others(4): Show |
G | 1 | a0004c0009t0002g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4094-258_4094-248d others(13): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | GTTTTTTT others(5): Show |
G | 4 | a0004c0004t0002g0187 a0004c0009t0002g0183 a0004c0009t0002g0184 others(1): Show |
4 | HG03834.hp1 HG04204.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4094-259_4094-248d others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | GTTTTTTT others(6): Show |
G | 9 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(6): Show |
10 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.4094-260_4094-248d others(15): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | GTTTTTTT others(7): Show |
G | 3 | a0002c0002t0001g0163 a0003c0003t0001g0179 a0026c0041t0001g0165 |
3 | HG02683.hp1 HG02723.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4094-261_4094-248d others(16): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240982 | GTTTTTTT others(10): Show |
G | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4094-264_4094-248d others(19): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | ||||||
chr2:97240999 | T | G | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0004g0194 others(6): Show |
9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4094-267T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240999 | |||||||
chr2:97241086 | A | G | 1 | a0002c0002t0001g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4094-180A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97241086 | |||||||
chr2:97241173 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0120 |
2 | HG02683.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.4094-93G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97241173 | |||||||
chr2:97241244 | C | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0179 |
3 | HG02258.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4094-22C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97241244 | |||||||
chr2:97241501 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(131): Show |
137 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.4307+22A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241501 | |||||||
chr2:97241507 | G | C | 1 | a0016c0020t0001g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4307+28G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241507 | |||||||
chr2:97241556 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(58): Show |
62 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.4307+77C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241556 | |||||||
chr2:97241604 | T | C | 1 | a0005c0005t0007g0035 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4307+125T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241604 | |||||||
chr2:97241794 | A | G | 1 | a0002c0002t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4307+315A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241794 | |||||||
chr2:97241933 | T | G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4307+454T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241933 | |||||||
chr2:97242014 | G | A | 1 | a0002c0002t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4307+535G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242014 | |||||||
chr2:97242031 | C | A | 1 | a0002c0002t0001g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4307+552C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242031 | |||||||
chr2:97242076 | G | A | 6 | a0001c0001t0001g0072 a0001c0001t0001g0098 a0001c0001t0001g0104 others(3): Show |
6 | HG00423.hp2 HG00609.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.4307+597G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242076 | |||||||
chr2:97242145 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4307+666G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242145 | |||||||
chr2:97242205 | G | A | 3 | a0003c0003t0001g0179 a0005c0005t0003g0041 a0029c0049t0003g0043 |
3 | HG01981.hp1 HG02723.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4307+726G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242205 | |||||||
chr2:97242288 | C | CA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(129): Show |
135 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.4307+826dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | INFO_REALIGN_3_PRIME | chr2 | 97242288 | ||||||
chr2:97242288 | C | CAA | 5 | a0003c0003t0001g0179 a0005c0031t0001g0012 a0010c0010t0001g0030 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4307+825_4307+826d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | INFO_REALIGN_3_PRIME | chr2 | 97242288 | ||||||
chr2:97242306 | T | A | 6 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0055 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4307+827T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242306 | |||||||
chr2:97242339 | G | A | 1 | a0003c0003t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4307+860G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242339 | |||||||
chr2:97242445 | G | A | 1 | a0006c0006t0001g0107 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4307+966G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242445 | |||||||
chr2:97242524 | T | G | 5 | a0002c0002t0001g0160 a0013c0013t0001g0146 a0013c0013t0001g0150 others(2): Show |
5 | HG00558.hp1 HG01358.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.4307+1045T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242524 | |||||||
chr2:97242551 | A | G | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.4307+1072A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242551 | |||||||
chr2:97242555 | G | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.4307+1076G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242555 | |||||||
chr2:97242580 | C | A | 1 | a0003c0003t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4307+1101C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242580 | |||||||
chr2:97242770 | T | C | 1 | a0005c0005t0003g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4308-1076T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242770 | |||||||
chr2:97243012 | C | T | 25 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(22): Show |
26 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.4308-834C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243012 | |||||||
chr2:97243038 | T | C | 25 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(22): Show |
26 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.4308-808T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243038 | |||||||
chr2:97243097 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(67): Show |
71 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.4308-749G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243097 | |||||||
chr2:97243115 | T | C | 25 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(22): Show |
26 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.4308-731T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243115 | |||||||
chr2:97243126 | G | A | 24 | a0001c0001t0004g0195 a0003c0003t0001g0034 a0003c0003t0001g0128 others(21): Show |
25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-720G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243126 | |||||||
chr2:97243134 | C | T | 24 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(21): Show |
25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-712C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243134 | |||||||
chr2:97243135 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.4308-711G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243135 | |||||||
chr2:97243149 | G | T | 24 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(21): Show |
25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-697G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243149 | |||||||
chr2:97243171 | G | A | 24 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(21): Show |
25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-675G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243171 | |||||||
chr2:97243173 | G | A | 3 | a0002c0002t0001g0160 a0012c0014t0005g0021 a0034c0048t0001g0013 |
3 | HG01358.hp1 NA19070.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.4308-673G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243173 | |||||||
chr2:97243179 | C | T | 24 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(21): Show |
25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-667C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243179 | |||||||
chr2:97243183 | G | T | 24 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(21): Show |
25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-663G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243183 | |||||||
chr2:97243184 | T | C | 24 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(21): Show |
25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-662T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243184 | |||||||
chr2:97243202 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(60): Show |
64 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.4308-644A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243202 | |||||||
chr2:97243246 | A | C | 1 | a0005c0021t0003g0002 | 2 | HG01261.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.4308-600A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243246 | |||||||
chr2:97243247 | C | T | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.4308-599C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243247 | |||||||
chr2:97243252 | G | A | 5 | a0002c0002t0001g0160 a0013c0013t0001g0146 a0013c0013t0001g0150 others(2): Show |
5 | HG00558.hp1 HG01358.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.4308-594G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243252 | |||||||
chr2:97243303 | G | A | 22 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(19): Show |
23 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.4308-543G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243303 | |||||||
chr2:97243334 | C | G | 26 | a0001c0001t0001g0110 a0003c0003t0001g0034 a0003c0003t0001g0128 others(23): Show |
27 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.4308-512C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243334 | |||||||
chr2:97243400 | G | A | 28 | a0001c0001t0001g0069 a0003c0003t0001g0020 a0003c0003t0001g0034 others(25): Show |
29 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.4308-446G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243400 | |||||||
chr2:97243401 | G | A | 28 | a0001c0001t0001g0069 a0003c0003t0001g0020 a0003c0003t0001g0034 others(25): Show |
29 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.4308-445G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243401 | |||||||
chr2:97243447 | G | C | 30 | a0001c0001t0001g0069 a0002c0002t0001g0164 a0003c0003t0001g0020 others(27): Show |
31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.4308-399G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243447 | |||||||
chr2:97243453 | A | G | 27 | a0002c0002t0001g0164 a0003c0003t0001g0034 a0003c0003t0001g0128 others(24): Show |
28 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.4308-393A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243453 | |||||||
chr2:97243463 | G | A | 27 | a0002c0002t0001g0164 a0003c0003t0001g0034 a0003c0003t0001g0128 others(24): Show |
28 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.4308-383G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243463 | |||||||
chr2:97243473 | G | A | 33 | a0002c0002t0001g0133 a0002c0002t0001g0164 a0003c0003t0001g0034 others(30): Show |
34 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.4308-373G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243473 | |||||||
chr2:97243493 | C | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(114): Show |
119 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.4308-353C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243493 | |||||||
chr2:97243556 | C | T | 1 | a0002c0002t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4308-290C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243556 | |||||||
chr2:97243781 | C | T | 1 | a0003c0003t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4308-65C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243781 | |||||||
chr2:97244039 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4491+10T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244039 | |||||||
chr2:97244091 | C | A | 2 | a0002c0002t0001g0164 a0020c0044t0001g0130 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.4491+62C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244091 | |||||||
chr2:97244103 | G | A | 19 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(16): Show |
20 | HG00558.hp1 HG00597.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.4491+74G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244103 | |||||||
chr2:97244192 | C | T | 20 | a0002c0002t0001g0160 a0004c0004t0002g0005 a0004c0004t0002g0180 others(17): Show |
21 | HG00558.hp1 HG00597.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.4491+163C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244192 | |||||||
chr2:97244207 | T | A | 1 | a0003c0030t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4491+178T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244207 | |||||||
chr2:97244376 | G | C | 16 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(13): Show |
17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.4491+347G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244376 | |||||||
chr2:97244520 | G | C | 4 | a0012c0014t0005g0021 a0012c0014t0005g0075 a0012c0014t0005g0089 others(1): Show |
4 | HG02040.hp1 NA18965.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.4491+491G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244520 | |||||||
chr2:97244635 | C | T | 2 | a0016c0020t0001g0018 a0016c0020t0001g0033 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4492-522C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244635 | |||||||
chr2:97244807 | T | TTA | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4492-349_4492-348d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | INFO_REALIGN_3_PRIME | chr2 | 97244807 | ||||||
chr2:97245076 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.4492-81A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97245076 | |||||||
chr2:97246274 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.5406+203A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246274 | |||||||
chr2:97246385 | A | G | 10 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(7): Show |
11 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5406+314A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246385 | |||||||
chr2:97246400 | T | C | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.5406+329T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246400 | |||||||
chr2:97246460 | T | C | 14 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(11): Show |
14 | HG00099.hp2 HG00558.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.5406+389T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246460 | |||||||
chr2:97246585 | T | C | 5 | a0004c0009t0002g0181 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.5406+514T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246585 | |||||||
chr2:97246629 | C | T | 5 | a0002c0002t0001g0160 a0013c0013t0001g0146 a0013c0013t0001g0150 others(2): Show |
5 | HG00558.hp1 HG01358.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.5406+558C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246629 | |||||||
chr2:97246654 | A | C | 1 | a0002c0002t0001g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5406+583A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246654 | |||||||
chr2:97246679 | C | A | 5 | a0002c0002t0001g0160 a0013c0013t0001g0146 a0013c0013t0001g0150 others(2): Show |
5 | HG00558.hp1 HG01358.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.5406+608C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246679 | |||||||
chr2:97246866 | A | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5407-610A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246866 | |||||||
chr2:97246959 | G | A | 10 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(7): Show |
11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.5407-517G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246959 | |||||||
chr2:97247163 | C | G | 1 | a0006c0006t0001g0086 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5407-313C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97247163 | |||||||
chr2:97247276 | C | T | 3 | a0004c0009t0002g0183 a0004c0009t0002g0184 a0004c0009t0002g0185 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.5407-200C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97247276 | |||||||
chr2:97247725 | T | TTTGTATT others(316): Show |
1 | a0002c0002t0001g0145 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5559+107_5559+108i others(325): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | INFO_REALIGN_3_PRIME | chr2 | 97247725 | ||||||
chr2:97247847 | T | C | 1 | a0003c0030t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5559+219T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97247847 | |||||||
chr2:97248104 | T | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(61): Show |
65 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.5559+476T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248104 | |||||||
chr2:97248130 | G | A | 2 | a0001c0001t0001g0125 a0003c0030t0001g0066 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5559+502G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248130 | |||||||
chr2:97248190 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5559+562G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248190 | |||||||
chr2:97248279 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
159 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.5559+651G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248279 | |||||||
chr2:97248427 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
159 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.5560-717C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248427 | |||||||
chr2:97248515 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(8): Show |
11 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.5560-629C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248515 | |||||||
chr2:97248528 | G | A | 1 | a0002c0002t0001g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5560-616G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248528 | |||||||
chr2:97248636 | T | A | 1 | a0032c0038t0001g0082 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.5560-508T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248636 | |||||||
chr2:97248705 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5560-439C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248705 | |||||||
chr2:97248852 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0119 a0001c0001t0001g0125 others(8): Show |
12 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5560-292G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248852 | |||||||
chr2:97248890 | A | G | 1 | a0003c0003t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5560-254A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248890 | |||||||
chr2:97248959 | G | A | 1 | a0003c0003t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5560-185G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248959 | |||||||
chr2:97249030 | T | A | 1 | a0003c0030t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5560-114T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97249030 | |||||||
chr2:97249031 | A | T | 1 | a0003c0030t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5560-113A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97249031 | |||||||
chr2:97249057 | T | C | 7 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 others(4): Show |
7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5560-87T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97249057 | |||||||
chr2:97249089 | C | T | 3 | a0004c0009t0002g0183 a0004c0009t0002g0184 a0004c0009t0002g0185 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.5560-55C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97249089 | |||||||
chr2:97249334 | A | G | 1 | a0032c0038t0001g0082 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.5630+120A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 73/75 | chr2 | 97249334 | |||||||
chr2:97249714 | A | G | 1 | a0001c0001t0004g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5724+69A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249714 | |||||||
chr2:97249800 | A | G | 1 | a0024c0039t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5724+155A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249800 | |||||||
chr2:97249832 | G | A | 12 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(9): Show |
13 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.5724+187G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249832 | |||||||
chr2:97249960 | C | T | 2 | a0001c0001t0001g0051 a0001c0034t0001g0052 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5725-184C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249960 | |||||||
chr2:97249961 | G | A | 1 | a0010c0010t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5725-183G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249961 | |||||||
chr2:97249984 | G | A | 2 | a0004c0009t0002g0181 a0004c0009t0002g0182 |
2 | HG02071.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.5725-160G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249984 | |||||||
chr2:97250013 | T | C | 12 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(9): Show |
13 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.5725-131T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97250013 | |||||||
chr2:97250043 | G | A | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.5725-101G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97250043 | |||||||
chr2:97250063 | G | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.5725-81G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97250063 | |||||||
chr2:97250204 | A | C | 71 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(68): Show |
73 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.*6+31A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250204 | |||||||
chr2:97250346 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(55): Show |
59 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.*6+173A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250346 | |||||||
chr2:97250394 | G | A | 1 | a0013c0013t0001g0150 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.*6+221G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250394 | |||||||
chr2:97250404 | T | G | 2 | a0008c0008t0001g0175 a0008c0008t0001g0178 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.*6+231T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250404 | |||||||
chr2:97250539 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.*6+366C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250539 | |||||||
chr2:97250553 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(150): Show |
157 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.*6+380A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250553 | |||||||
chr2:97250627 | ATTGACTT others(14): Show |
A | 1 | a0003c0030t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*6+457_*6+477delGA others(19): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97250627 | ||||||
chr2:97250637 | T | C | 1 | a0001c0034t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*6+464T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250637 | |||||||
chr2:97250932 | A | C | 3 | a0015c0016t0001g0044 a0015c0016t0001g0048 a0015c0016t0001g0049 |
3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.*6+759A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250932 | |||||||
chr2:97251067 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.*6+894C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251067 | |||||||
chr2:97251171 | A | G | 18 | a0003c0003t0001g0020 a0003c0003t0001g0034 a0003c0003t0001g0067 others(15): Show |
18 | HG00423.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.*6+998A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251171 | |||||||
chr2:97251285 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.*6+1112T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251285 | |||||||
chr2:97251388 | C | A | 5 | a0006c0006t0001g0084 a0006c0006t0001g0086 a0006c0006t0001g0087 others(2): Show |
5 | HG00558.hp2 NA18971.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.*6+1215C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251388 | |||||||
chr2:97251518 | T | C | 6 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0055 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+1345T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251518 | |||||||
chr2:97252478 | T | C | 2 | a0005c0005t0007g0035 a0005c0031t0001g0012 |
2 | HG01123.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.*6+2305T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252478 | |||||||
chr2:97252579 | G | A | 2 | a0004c0004t0002g0186 a0004c0004t0002g0187 |
2 | NA18965.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.*6+2406G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252579 | |||||||
chr2:97252689 | A | G | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.*6+2516A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252689 | |||||||
chr2:97252713 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(67): Show |
71 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.*6+2540A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252713 | |||||||
chr2:97252758 | A | G | 1 | a0005c0005t0003g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*6+2585A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252758 | |||||||
chr2:97252761 | G | A | 1 | a0005c0005t0003g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*6+2588G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252761 | |||||||
chr2:97253368 | C | T | 4 | a0005c0005t0003g0040 a0005c0005t0003g0041 a0005c0021t0003g0002 others(1): Show |
5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.*6+3195C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253368 | |||||||
chr2:97253453 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.*6+3280T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253453 | |||||||
chr2:97253524 | C | A | 1 | a0004c0004t0002g0005 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.*6+3351C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253524 | |||||||
chr2:97253552 | A | G | 1 | a0017c0019t0001g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*6+3379A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253552 | |||||||
chr2:97253685 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.*6+3512G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253685 | |||||||
chr2:97253931 | A | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0125 others(10): Show |
13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.*6+3758A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253931 | |||||||
chr2:97254539 | C | A | 8 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(5): Show |
9 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.*6+4366C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254539 | |||||||
chr2:97254746 | A | G | 4 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0009c0012t0001g0079 others(1): Show |
4 | HG01169.hp1 HG01361.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.*6+4573A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254746 | |||||||
chr2:97254758 | C | T | 7 | a0003c0003t0001g0003 a0003c0003t0001g0020 a0003c0003t0001g0053 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*6+4585C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254758 | |||||||
chr2:97254785 | C | CAGA | 6 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0055 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4613_*6+4614ins others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97254785 | ||||||
chr2:97254787 | T | A | 6 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0055 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4614T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254787 | |||||||
chr2:97254789 | T | A | 6 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0055 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4616T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254789 | |||||||
chr2:97254790 | T | A | 6 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0055 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4617T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254790 | |||||||
chr2:97254790 | T | G | 1 | a0002c0002t0001g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.*6+4617T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254790 | |||||||
chr2:97254791 | G | A | 6 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0055 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4618G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254791 | |||||||
chr2:97254845 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
142 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.*6+4672A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254845 | |||||||
chr2:97254897 | A | G | 3 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0019c0028t0001g0132 |
3 | HG00597.hp1 NA18972.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.*6+4724A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254897 | |||||||
chr2:97255184 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.*6+5011C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97255184 | |||||||
chr2:97255237 | A | G | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.*6+5064A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97255237 | |||||||
chr2:97255720 | G | A | 1 | a0005c0005t0003g0037 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.*6+5547G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97255720 | |||||||
chr2:97256211 | G | C | 78 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(75): Show |
81 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*6+6038G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256211 | |||||||
chr2:97256238 | T | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(61): Show |
65 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.*6+6065T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256238 | |||||||
chr2:97256252 | A | G | 70 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(67): Show |
73 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.*6+6079A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256252 | |||||||
chr2:97256289 | G | A | 12 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(9): Show |
12 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.*6+6116G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256289 | |||||||
chr2:97256357 | CA | C | 71 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(68): Show |
74 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.*6+6196delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97256357 | ||||||
chr2:97256449 | GT | G | 55 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(52): Show |
57 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.*6+6279delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97256449 | ||||||
chr2:97256596 | T | C | 70 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(67): Show |
73 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.*6+6423T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256596 | |||||||
chr2:97256803 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(131): Show |
138 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.*6+6630A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256803 | |||||||
chr2:97256938 | C | T | 3 | a0004c0009t0002g0183 a0004c0009t0002g0184 a0004c0009t0002g0185 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.*6+6765C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256938 | |||||||
chr2:97257623 | A | G | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*7-6706A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97257623 | |||||||
chr2:97257878 | T | G | 1 | a0002c0002t0001g0158 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.*7-6451T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97257878 | |||||||
chr2:97258059 | CT | C | 2 | a0002c0002t0001g0159 a0002c0002t0001g0168 |
2 | HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*7-6267delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97258059 | ||||||
chr2:97258066 | A | G | 6 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.*7-6263A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258066 | |||||||
chr2:97258177 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(63): Show |
67 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.*7-6152T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258177 | |||||||
chr2:97258371 | G | A | 2 | a0001c0001t0001g0006 a0014c0015t0001g0007 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.*7-5958G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258371 | |||||||
chr2:97258770 | T | G | 1 | a0028c0045t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*7-5559T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258770 | |||||||
chr2:97258908 | C | T | 1 | a0017c0019t0001g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*7-5421C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258908 | |||||||
chr2:97258954 | G | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(60): Show |
64 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.*7-5375G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258954 | |||||||
chr2:97258991 | T | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
65 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.*7-5338T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258991 | |||||||
chr2:97259024 | C | A | 1 | a0017c0019t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*7-5305C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259024 | |||||||
chr2:97259046 | G | A | 1 | a0004c0004t0002g0005 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.*7-5283G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259046 | |||||||
chr2:97259059 | G | A | 1 | a0004c0004t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.*7-5270G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259059 | |||||||
chr2:97259140 | G | T | 1 | a0017c0019t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*7-5189G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259140 | |||||||
chr2:97259574 | G | T | 3 | a0004c0009t0002g0183 a0004c0009t0002g0184 a0004c0009t0002g0185 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.*7-4755G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259574 | |||||||
chr2:97259688 | G | A | 1 | a0001c0001t0004g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*7-4641G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259688 | |||||||
chr2:97259755 | G | A | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-4574G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259755 | |||||||
chr2:97259922 | C | T | 65 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(62): Show |
67 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.*7-4407C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259922 | |||||||
chr2:97260191 | C | T | 1 | a0002c0002t0001g0168 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.*7-4138C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260191 | |||||||
chr2:97260347 | G | GAT | 14 | a0002c0002t0001g0136 a0002c0002t0001g0138 a0002c0002t0001g0139 others(11): Show |
14 | HG00597.hp1 HG01123.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.*7-3950_*7-3949dup others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260347 | G | GATAT | 5 | a0002c0002t0001g0131 a0002c0002t0001g0133 a0002c0002t0001g0135 others(2): Show |
5 | HG01515.hp2 HG02698.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.*7-3952_*7-3949dup others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260347 | G | GATATAT | 4 | a0002c0002t0001g0134 a0002c0002t0001g0137 a0002c0002t0001g0163 others(1): Show |
4 | HG00099.hp2 HG01099.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.*7-3954_*7-3949dup others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260347 | G | GATATATA others(3): Show |
1 | a0002c0002t0001g0162 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.*7-3958_*7-3949dup others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260347 | GAT | G | 22 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0002c0002t0001g0153 others(19): Show |
23 | HG01261.hp1 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.*7-3950_*7-3949del others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260347 | GATAT | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(57): Show |
61 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.*7-3952_*7-3949del others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260347 | GATATAT | G | 5 | a0001c0001t0001g0077 a0004c0009t0002g0182 a0004c0009t0002g0183 others(2): Show |
5 | HG02083.hp2 HG02300.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.*7-3954_*7-3949del others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260347 | GATATATA others(3): Show |
G | 3 | a0002c0002t0001g0159 a0002c0002t0001g0168 a0007c0027t0001g0169 |
3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*7-3958_*7-3949del others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260347 | GATATATA others(7): Show |
G | 1 | a0001c0001t0001g0006 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*7-3962_*7-3949del others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260347 | GATATATA others(11): Show |
G | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.*7-3966_*7-3949del others(18): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | ||||||
chr2:97260377 | T | C | 3 | a0001c0001t0001g0081 a0009c0012t0001g0079 a0012c0036t0001g0080 |
3 | HG01169.hp1 HG01361.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.*7-3952T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260377 | |||||||
chr2:97260379 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(85): Show |
90 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.*7-3950T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260379 | |||||||
chr2:97260379 | T | TAC | 16 | a0001c0001t0001g0126 a0003c0003t0001g0034 a0003c0003t0001g0068 others(13): Show |
16 | HG00597.hp2 HG01123.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-3944_*7-3943dup others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | ||||||
chr2:97260379 | T | TATAC | 22 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0125 others(19): Show |
22 | HG00642.hp2 HG01891.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | ||||||
chr2:97260379 | T | TATATAC | 6 | a0003c0003t0001g0003 a0003c0003t0001g0054 a0003c0003t0001g0056 others(3): Show |
6 | HG02257.hp1 HG03130.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | ||||||
chr2:97260379 | T | TATATATA others(1): Show |
3 | a0001c0001t0004g0197 a0003c0003t0001g0057 a0003c0003t0001g0061 |
3 | HG02451.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | ||||||
chr2:97260379 | T | TATATATA others(3): Show |
3 | a0001c0001t0001g0023 a0001c0034t0001g0052 a0022c0047t0001g0027 |
3 | HG01891.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | ||||||
chr2:97260379 | T | TATATATA others(5): Show |
1 | a0003c0030t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(12): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | ||||||
chr2:97260379 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | ||||||
chr2:97260379 | T | TATATATA others(9): Show |
1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(16): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | ||||||
chr2:97260387 | T | C | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-3942T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260387 | |||||||
chr2:97260388 | A | G | 66 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(63): Show |
68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.*7-3941A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260388 | |||||||
chr2:97260389 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0113 |
3 | HG01070.hp1 HG01257.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.*7-3940T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260389 | |||||||
chr2:97260410 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(61): Show |
65 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.*7-3919A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260410 | |||||||
chr2:97260425 | AAC | A | 81 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(78): Show |
84 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.*7-3885_*7-3884del others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260425 | ||||||
chr2:97260425 | AACAC | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(61): Show |
65 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.*7-3887_*7-3884del others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260425 | ||||||
chr2:97260488 | G | A | 2 | a0017c0019t0001g0205 a0017c0019t0001g0206 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.*7-3841G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260488 | |||||||
chr2:97260759 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0113 |
3 | HG01070.hp1 HG01257.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.*7-3570T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260759 | |||||||
chr2:97260845 | C | T | 7 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-3484C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260845 | |||||||
chr2:97260855 | T | C | 1 | a0003c0003t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.*7-3474T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260855 | |||||||
chr2:97260977 | T | TTAC | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(140): Show |
147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-3350_*7-3349ins others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260977 | ||||||
chr2:97260980 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(140): Show |
147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-3349G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260980 | |||||||
chr2:97261214 | C | T | 1 | a0017c0019t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*7-3115C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261214 | |||||||
chr2:97261296 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.*7-3033C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261296 | |||||||
chr2:97261388 | G | A | 3 | a0013c0013t0001g0146 a0013c0013t0001g0150 a0013c0013t0001g0151 |
3 | HG00558.hp1 NA18946.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.*7-2941G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261388 | |||||||
chr2:97261452 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(129): Show |
135 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.*7-2877C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261452 | |||||||
chr2:97261462 | G | A | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-2867G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261462 | |||||||
chr2:97261567 | A | C | 1 | a0034c0048t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.*7-2762A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261567 | |||||||
chr2:97261672 | G | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-2657G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261672 | |||||||
chr2:97261689 | C | T | 2 | a0003c0003t0001g0020 a0003c0003t0001g0067 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.*7-2640C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261689 | |||||||
chr2:97261828 | C | G | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-2501C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261828 | |||||||
chr2:97262618 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.*7-1711A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262618 | |||||||
chr2:97262698 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.*7-1631C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262698 | |||||||
chr2:97262710 | T | C | 7 | a0008c0008t0001g0170 a0008c0008t0001g0171 a0008c0008t0001g0172 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-1619T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262710 | |||||||
chr2:97262761 | C | T | 13 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0054 others(10): Show |
14 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.*7-1568C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262761 | |||||||
chr2:97262779 | G | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.*7-1550G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262779 | |||||||
chr2:97262785 | T | TC | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.*7-1543dupC | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97262785 | ||||||
chr2:97262930 | C | T | 1 | a0021c0042t0001g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.*7-1399C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262930 | |||||||
chr2:97262943 | A | ACCTAGTC others(21): Show |
59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(56): Show |
60 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.*7-1386_*7-1385ins others(28): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262943 | |||||||
chr2:97262944 | A | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(56): Show |
60 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.*7-1385A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262944 | |||||||
chr2:97262963 | A | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.*7-1366A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262963 | |||||||
chr2:97262998 | G | A | 30 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(27): Show |
31 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.*7-1331G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262998 | |||||||
chr2:97263074 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.*7-1255T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263074 | |||||||
chr2:97263123 | T | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.*7-1206T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263123 | |||||||
chr2:97263174 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.*7-1155T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263174 | |||||||
chr2:97263185 | A | G | 1 | a0028c0045t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*7-1144A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263185 | |||||||
chr2:97263317 | G | A | 6 | a0010c0010t0001g0029 a0010c0010t0001g0030 a0010c0010t0001g0031 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.*7-1012G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263317 | |||||||
chr2:97263339 | A | G | 1 | a0010c0026t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*7-990A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263339 | |||||||
chr2:97263578 | C | T | 1 | a0028c0045t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*7-751C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263578 | |||||||
chr2:97263580 | CTT | C | 24 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(21): Show |
25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.*7-746_*7-745delTT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97263580 | ||||||
chr2:97263590 | A | C | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-739A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263590 | |||||||
chr2:97263713 | T | C | 3 | a0002c0002t0001g0159 a0002c0002t0001g0168 a0007c0027t0001g0169 |
3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*7-616T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263713 | |||||||
chr2:97263815 | A | AT | 9 | a0005c0005t0003g0019 a0005c0005t0003g0036 a0005c0005t0003g0037 others(6): Show |
10 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.*7-504dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97263815 | ||||||
chr2:97263815 | AT | A | 15 | a0004c0004t0002g0005 a0004c0004t0002g0180 a0004c0004t0002g0186 others(12): Show |
16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-504delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97263815 | ||||||
chr2:97263939 | G | A | 1 | a0003c0030t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*7-390G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263939 | |||||||
chr2:97263964 | G | A | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0004g0194 others(6): Show |
9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.*7-365G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263964 | |||||||
chr2:97264107 | A | G | 15 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(12): Show |
15 | HG00423.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.*7-222A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97264107 | |||||||
chr2:97264123 | G | T | 41 | a0003c0003t0001g0034 a0003c0003t0001g0128 a0003c0003t0001g0204 others(38): Show |
43 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.*7-206G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97264123 | |||||||
chr2:97264249 | T | C | 6 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0055 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*7-80T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97264249 |